96 results on '"FLAVIN mononucleotide"'
Search Results
2. Isolation and Characterisation of Subcomplexes of the Mitochondrial NADH: Ubiquinone Oxidoreductase (Complex I)
- Author
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Jaana Tyynelä, Simon P. J. Albracht, Måtin Wikström, A. Mariette P. De Jong, Anna Majander, Moshe Finel, and SILS Other Research (FNWI)
- Subjects
Iron-Sulfur Proteins ,Stereochemistry ,Flavin Mononucleotide ,Molecular Sequence Data ,Centrifugation ,Biology ,Biochemistry ,law.invention ,Electron Transport ,chemistry.chemical_compound ,03 medical and health sciences ,law ,Oxidoreductase ,Animals ,NADH, NADPH Oxidoreductases ,Amino Acid Sequence ,Electron paramagnetic resonance ,Decylubiquinone ,030304 developmental biology ,chemistry.chemical_classification ,NADH-Ubiquinone Oxidoreductase ,0303 health sciences ,Electron Transport Complex I ,030302 biochemistry & molecular biology ,Electron Spin Resonance Spectroscopy ,Rotenone ,Mitochondria ,chemistry ,Cattle ,Electrophoresis, Polyacrylamide Gel ,Reductase activity ,Ferricyanide - Abstract
Enzymically active subcomplexes were purified from bovine mitochondrial NADH:ubiquinone oxidoreductase (complex I) by sucrose-gradient centrifugation in the presence of detergents. These subcomplexes, named I lambda, IS, and I lambda S, catalyse ferricyanide and ubiquinone-1 (Q-1) reduction by NADH at similar rates to complex I, but do not catalyse the reduction of decylubiquinone. In addition, the Q-1 reductase activity of all the subcomplexes is insensitive to rotenone. Chemical and EPR analyses of the subcomplexes show that FMN and all the Fe-S clusters of complex I are present, but that the line shape of cluster 2 is modified. The smallest subcomplex, I lambda S, contains only approximately 13 subunits, as compared to approximately 22 in the previously described subcomplex I alpha [Finel, M., Skehel, J. M., Albracht, S. J. P., Fearnley, I. M.Walker, J. E. (1992) Biochemistry 31, 11425-11434], but it retains the 75-, 51-, 49-, 30-, 24-, 23- (TYKY) and 20-kDa (PSST) subunits, which are suggested to form a functional core that comprises the EPR-detectable Fe-S clusters 1-4, and FMN. The structural and functional implications of such an arrangement are discussed.
- Published
- 2008
3. Reconstitution of Liver NADH: Cytochrome b5 Oxidoreductase and of Desulfovibrio vulgaris Flavodoxin with 1-Carba-1-deazaflavin
- Author
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Denis Pompon, Florence Lederer, and Bernard Guiard
- Subjects
Semiquinone ,Flavin Mononucleotide ,Flavodoxin ,Flavoprotein ,Flavin group ,Biochemistry ,Cofactor ,Oxidoreductase ,Animals ,Anaerobiosis ,Desulfovibrio vulgaris ,Cytochrome Reductases ,Cytochrome b5 reductase ,chemistry.chemical_classification ,biology ,Chemistry ,Dithionite ,biology.organism_classification ,Kinetics ,Spectrophotometry ,Flavin-Adenine Dinucleotide ,Microsomes, Liver ,biology.protein ,Cattle ,Desulfovibrio ,Cytochrome-B(5) Reductase - Abstract
Flavin-free cytochrome b5 reductase was reconstituted with 1-deazaflavin and 5-deazaflavin mononucleotides and dinucleotides. The 5-deazaenzyme functioned in transhydrogenation reactions but lacked electron transferase activity. The 1-deazaenzyme was fully competent for both input and output reactions. The flavin reduction rate was lowered about sevenfold upon N-1 substitution of FAD, but hydrogen abstraction from NADH remained the limiting step. Autoxidation of the reduced enzyme was more rapid than with the normal cofactor. Oxidation was accompanied by appearance of a transient blue-type semiquinone and superoxide ion production. Flavin-free apoflavodoxin was reconstituted with 1-deaza-1-carbaflavin mononucleotide (1-deaza-FMN). Its behaviour toward dithionite and oxygen was qualitatively highly similar to that of native flavodoxin. These observations contrast with the fact that apoflavocytochrome b2 could not be reconstituted with 1-deaza-FMN [Pompon, D. and Lederer, F. (1979) Eur. J. Biochem. 96, 571–579]. These results, as well as other data from the literature, are discussed in the light of existing hypotheses, which try to correlate flavin protein interactions and flavoprotein function.
- Published
- 2005
4. Type 2 isopentenyl diphosphate isomerase from a thermoacidophilic archaeonSulfolobus shibatae
- Author
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Satoshi Yamashita, Toru Nakayama, Hisashi Hemmi, Tokuzo Nishino, and Yosuke Ikeda
- Subjects
chemistry.chemical_classification ,Sulfolobus shibatae ,biology ,ved/biology ,ved/biology.organism_classification_rank.species ,NADH dehydrogenase ,Flavin mononucleotide ,Isomerase ,biology.organism_classification ,Biochemistry ,Molecular biology ,NADH dehydrogenase activity ,Sulfolobus ,chemistry.chemical_compound ,Enzyme ,chemistry ,biology.protein ,Mevalonate pathway - Abstract
Although isopentenyl diphosphate-dimethylallyl diphosphate isomerase is thought to be essential for archaea because they use the mevalonate pathway, its corresponding activity has not been detected in any archaea. A novel type of the enzyme, which has no sequence similarity to the known, well-studied type of enzymes, was recently reported in some bacterial strains. In this study, we describe the cloning of a gene of a homologue of the novel bacterial isomerase from a thermoacidophilic archaeon Sulfolobus shibatae. The gene was heterologously expressed in Escherichia coli, and the recombinant enzyme was purified and characterized. The thermostable archaeal enzyme is tetrameric, and requires NAD(P)H and Mg2+ for activity, similar to its bacterial homologues. Using its apoenzyme, we were able to confirm that the archaeal enzyme is strictly dependent on FMN. Moreover, we provide evidence to show that the enzyme also has NADH dehydrogenase activity although it catalyzes the isomerase reaction without consuming any detectable amount of NADH.
- Published
- 2004
5. Selective release and function of one of the two FMN groups in the cytoplasmic NAD+-reducing [NiFe]-hydrogenase from Ralstonia eutropha
- Author
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Boris Bleijlevens, Simon P. J. Albracht, Tanja Burgdorf, Eddy van der Linden, Michael Bernhard, Bärbel Friedrich, and Bart W. Faber
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chemistry.chemical_classification ,animal structures ,Hydrogenase ,biology ,Chemistry ,Stereochemistry ,Dimer ,Cupriavidus necator ,Flavin mononucleotide ,Flavin group ,biology.organism_classification ,Biochemistry ,chemistry.chemical_compound ,Enzyme ,Ferricyanide ,NAD+ kinase - Abstract
The soluble, cytoplasmic NAD+-reducing [NiFe]-hydrogenase from Ralstonia eutropha is a heterotetrameric enzyme (HoxFUYH) and contains two FMN groups. The purified oxidized enzyme is inactive in the H2-NAD+ reaction, but can be activated by catalytic amounts of NADH. It was discovered that one of the FMN groups (FMN-a) is selectively released upon prolonged reduction of the enzyme with NADH. During this process, the enzyme maintained its tetrameric form, with one FMN group (FMN-b) firmly bound, but it lost its physiological activity--the reduction of NAD+ by H2. This activity could be reconstituted by the addition of excess FMN to the reduced enzyme. The rate of reduction of benzyl viologen by H2 was not dependent on the presence of FMN-a. Enzyme devoid of FMN-a could not be activated by NADH. As NADH-dehydrogenase activity was not dependent on the presence of FMN-a, and because FMN-b did not dissociate from the reduced enzyme, we conclude that FMN-b is functional in the NADH-dehydrogenase activity catalyzed by the HoxFU dimer. The possible function of FMN-a as a hydride acceptor in the hydrogenase reaction catalyzed by the HoxHY dimer is discussed.
- Published
- 2004
6. Interflavin electron transfer in human cytochrome P450 reductase is enhanced by coenzyme binding. Relaxation kinetic studies with coenzyme analogues
- Author
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Aldo Gutierrez, Andrew W. Munro, Nigel S. Scrutton, Alex Grunau, Gordon C. K. Roberts, and C. Roland Wolf
- Subjects
Models, Molecular ,Conformational change ,Flavin Mononucleotide ,Stereochemistry ,Coenzymes ,Flavoprotein ,Flavin group ,Biochemistry ,Redox ,Protein Structure, Secondary ,Cofactor ,Electron Transport ,Electron transfer ,Electrochemistry ,Escherichia coli ,Humans ,Coenzyme binding ,Cloning, Molecular ,NADPH-Ferrihemoprotein Reductase ,biology ,Chemistry ,Cytochrome P450 reductase ,NAD ,Kinetics ,Spectrophotometry ,Flavin-Adenine Dinucleotide ,Potentiometry ,biology.protein ,Oxidation-Reduction ,Protein Binding - Abstract
The role of coenzyme binding in regulating interflavin electron transfer in human cytochrome P450 reductase (CPR) has been studied using temperature-jump spectroscopy. Previous studies [Gutierrez, A., Paine, M., Wolf, C.R., Scrutton, N.S.,Roberts, G.C.K. Biochemistry (2002) 41, 4626-4637] have shown that the observed rate, 1/tau, of interflavin electron transfer (FADsq - FMNsq--FADox - FMNhq) in CPR reduced at the two-electron level with NADPH is 55 +/- 2 s-1, whereas with dithionite-reduced enzyme the observed rate is 11 +/- 0.5 s-1, suggesting that NADPH (or NADP+) binding has an important role in controlling the rate of internal electron transfer. In relaxation experiments performed with CPR reduced at the two-electron level with NADH, the observed rate of internal electron transfer (1/tau = 18 +/- 0.7 s-1) is intermediate in value between those seen with dithionite-reduced and NADPH-reduced enzyme, indicating that the presence of the 2'-phosphate is important for enhancing internal electron transfer. To investigate this further, temperature jump experiments were performed with dithionite-reduced enzyme in the presence of 2',5'-ADP and 2'-AMP. These two ligands increase the observed rate of interflavin electron transfer in two-electron reduced CPR from 1/tau = 11 s-1 to 35 +/- 0.2 s-1 and 32 +/- 0.6 s-1, respectively. Reduction of CPR at the two-electron level by NADPH, NADH or dithionite generates the same spectral species, consistent with an electron distribution that is equivalent regardless of reductant at the initiation of the temperature jump. Spectroelectrochemical experiments establish that the redox potentials of the flavins of CPR are unchanged on binding 2',5'-ADP, supporting the view that enhanced rates of interdomain electron transfer have their origin in a conformational change produced by binding NADPH or its fragments. Addition of 2',5'-ADP either to the isolated FAD-domain or to full-length CPR (in their oxidized and reduced forms) leads to perturbation of the optical spectra of both the flavins, consistent with a conformational change that alters the environment of these redox cofactors. The binding of 2',5'-ADP eliminates the unusual dependence of the observed flavin reduction rate on NADPH concentration (i.e. enhanced at low coenzyme concentration) observed in stopped-flow studies. The data are discussed in the context of previous kinetic studies and of the crystallographic structure of rat CPR.
- Published
- 2003
7. Determination of the redox potentials and electron transfer properties of the FAD- and FMN-binding domains of the human oxidoreductase NR1
- Author
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C. Roland Wolf, Mark J. I. Paine, Nigel S. Scrutton, Olivier Roitel, Andrew W. Munro, Robert D. Finn, and Jaswir Basran
- Subjects
chemistry.chemical_classification ,FMN Reductase ,Semiquinone ,Flavin Mononucleotide ,Stereochemistry ,Spectrum Analysis ,Cytochrome P450 reductase ,Flavin group ,Photochemistry ,Biochemistry ,Redox ,Electron transport chain ,Protein Structure, Tertiary ,Electron Transport ,Electron transfer ,FMN binding ,chemistry ,Oxidoreductase ,Flavin-Adenine Dinucleotide ,Potentiometry ,Humans ,bacteria ,2,6-Dichloroindophenol ,Ferricyanides ,Oxidation-Reduction - Abstract
Human novel reductase 1 (NR1) is an NADPH dependent diflavin oxidoreductase related to cytochrome P450 reductase (CPR). The FAD/NADPH- and FMN-binding domains of NR1 have been expressed and purified and their redox properties studied by stopped-flow and steady-state kinetic methods, and by potentiometry. The midpoint reduction potentials of the oxidized/semiquinone (-315 +/- 5 mV) and semiquinone/dihydroquinone (-365 +/- 15 mV) couples of the FAD/NADPH domain are similar to those for the FAD/NADPH domain of human CPR, but the rate of hydride transfer from NADPH to the FAD/NADPH domain of NR1 is approximately 200-fold slower. Hydride transfer is rate-limiting in steady-state reactions of the FAD/NADPH domain with artificial redox acceptors. Stopped-flow studies indicate that hydride transfer from the FAD/NADPH domain of NR1 to NADP+ is faster than hydride transfer in the physiological direction (NADPH to FAD), consistent with the measured reduction potentials of the FAD couples [midpoint potential for FAD redox couples is -340 mV, cf-320 mV for NAD(P)H]. The midpoint reduction potentials for the flavin couples in the FMN domain are -146 +/- 5 mV (oxidized/semiquinone) and -305 +/- 5 mV (semiquinone/dihydroquinone). The FMN oxidized/semiquinone couple indicates stabilization of the FMN semiquinone, consistent with (a) a need to transfer electrons from the FAD/NADPH domain to the FMN domain, and (b) the thermodynamic properties of the FMN domain in CPR and nitric oxide synthase. Despite overall structural resemblance of NR1 and CPR, our studies reveal thermodynamic similarities but major kinetic differences in the electron transfer reactions catalysed by the flavin-binding domains.
- Published
- 2003
8. The effects of pH and semiquinone formation on the oxidation-reduction potentials of flavin mononucleotide. A reappraisal
- Author
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Stephen G. Mayhew
- Subjects
Molecular Structure ,Semiquinone ,Hydroquinone ,Flavin Mononucleotide ,Chemistry ,Flavin mononucleotide ,Flavin group ,Hydrogen-Ion Concentration ,Photochemistry ,Electrochemistry ,Biochemistry ,Redox ,chemistry.chemical_compound ,Stability constants of complexes ,Flavins ,Radiolysis ,Benzoquinones ,Oxidation-Reduction ,Software - Abstract
Calculation shows that there is poor agreement between frequently cited values for the midpoint redox potentials of the two one-electron steps in the reduction of flavin mononucleotide and equations for the lines that relate these potentials to pH and that use the published pKa values for the three redox states of the flavin [Draper, R. & Ingraham, L.L. (1969) Arch. Biochem. Biophys. 125, 802-808]. Equilibrium data for the first step in the reduction obtained by pulse radiolysis [Anderson, R.F. (1983) Biochim. Biophys. Acta 722, 158-162] show much closer agreement with theory and lead to values for the semiquinone formation constant of flavin mononucleotide that are close to those derived from measurements of the radical concentration using ESR spectroscopy. It is concluded that the data from the second method are more reliable. The redox potentials for flavin mononucleotide at pH 7.0 and 20 degrees C are calculated to be -0.207 V for the overall two-electron reduction (Em), -0.313 V for reduction of the oxidized flavin to the semiquinone (E2) and -0.101 V for the reduction of the semiquinone to the hydroquinone (E1). Information is provided to allow calculation of the three redox potentials at other pH values in the physiological range.
- Published
- 1999
9. 31P Nuclear magnetic resonance study of the flavoprotein component of the Escherichia coli sulfite reductase
- Author
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Jacques Covès, Adeline Evrard, Mahel Zeghouf, Claude Roby, and Marc Fontecave
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Magnetic Resonance Spectroscopy ,Semiquinone ,Flavin Mononucleotide ,Stereochemistry ,Flavoprotein ,Photochemistry ,Dithionite ,Biochemistry ,Redox ,Sulfite reductase ,chemistry.chemical_compound ,Protein structure ,Cytochrome P-450 Enzyme System ,Escherichia coli ,Oxidoreductases Acting on Sulfur Group Donors ,Sulfite Reductase (NADPH) ,Reactive center ,Manganese ,Binding Sites ,Flavoproteins ,biology ,Chemistry ,Cytochrome P450 reductase ,NAD ,biology.protein ,NADP - Abstract
SiR-FP60, the monomeric form of the Escherichia coli sulfite reductase flavoprotein component (SiR-FP), has been analysed by 31P-NMR spectroscopy. This protein was reported previously as a reliable simplified model for native SiR-FP [Zeghouf, M., Fontecave, M., Macherel, D., & Coves, J. (1998) Biochemistry37, 6117–6123]. SiR-FP60 was examined in its native form, as a complex with NADP+ and after monoelectronic reduction either with NADPH or dithionite. In these latter cases, the stabilized FMN semiquinone radical offers a natural and internal paramagnetic probe. The paramagnetic effect of added manganese was also studied. In each case, the NMR parameters were extracted from digitalized data by a deconvolution procedure and compared with those obtained previously with cytochrome P450 reductase. Evolution of the NMR parameters and of calculated relaxation rate constants upon biochemical modifications of SiR-FP60 led us to propose that the reactive center is more compact than the one of cytochrome P450 reductase, with the redox components, FMN, FAD and NADPH, in a tighter spatial arrangement, close to the protein surface. This underlies some subtle differences between the two proteins for which a very similar overall structure is likely considering their common genetic origin and common operating cycle.
- Published
- 1999
10. Properties of the Recombinant beta Subunit of Glutamate Synthase
- Author
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E. Verzotti, Maria A. Vanoni, Bruno Curti, and Giuliana Zanetti
- Subjects
Iron-Sulfur Proteins ,Flavin Mononucleotide ,Macromolecular Substances ,Molecular Sequence Data ,Restriction Mapping ,Azospirillum brasilense ,Biology ,Polymerase Chain Reaction ,Biochemistry ,Substrate Specificity ,chemistry.chemical_compound ,Glutamate synthase ,Escherichia coli ,Anaerobiosis ,Cloning, Molecular ,DNA Primers ,Glutamine amidotransferase ,G alpha subunit ,Flavin adenine dinucleotide ,Binding Sites ,Base Sequence ,Glutamate dehydrogenase ,Glutamate Synthase ,Electron Spin Resonance Spectroscopy ,Glutamate receptor ,Molecular biology ,Recombinant Proteins ,Kinetics ,chemistry ,Spectrophotometry ,Flavin-Adenine Dinucleotide ,biology.protein ,NADPH binding ,ATP synthase alpha/beta subunits - Abstract
Glutamate synthase is a complex iron-sulfur flavoprotein containing one molecule each of FAD and FMN and three distinct iron-sulfur centers/alpha beta protomer. Production of the beta subunit was observed in total extracts of Escherichia coli BL21 (DE) cells harbouring a pT7-7 derivative carrying gltD, the gene encoding the Azospirillum brasilense glutamate synthase beta subunit. The protein was soluble, and the identity of the purified protein with the Azospirillum glutamate synthase beta subunit was confirmed by N-terminal sequence analysis. The kinetic and spectroscopic characterization of the glutamate synthase beta subunit confirmed that it contains the NADPH binding site, but, in contrast with earlier proposals that assigned both FAD and FMN binding sites to the alpha subunit of glutamate synthase, the beta subunit was shown to contain stoichiometric amounts of FAD. No iron-sulfur centers were detected by EPR spectroscopy measurements of the recombinant beta subunit. Under steady-state conditions, the glutamate synthase beta subunit can catalyze the NADPH-dependent reduction of several synthetic electron acceptors but no glutamate synthase or glutamate dehydrogenase reactions in either direction. The results are in agreement with previous data from our laboratory and, together with the absence of amino acid sequence similarity between glutamate synthase beta subunit and glutamate dehydrogenases, are against the hypothesis that glutamate synthase is evolutionarily derived from the association of an ancestral glutamate dehydrogenase (the beta subunit) and an amidotransferase (the alpha subunit). The protein-bound FAD is reduced by NADPH at a rate much faster than turnover with synthetic electron acceptors, leading to formation of a stable reduced flavin-NADP+ charge-transfer complex. The rate of reduction of the bound FAD by NADPH is also similar to the rate at which one of the flavins is reduced in the native glutamate synthase, as measured in a stopped-flow spectrophotometer under pre-steady-state conditions. The ability of FAD bound to the beta subunit of glutamate synthase to react with NADPH and the lack of reactivity with sulfite lead us to conclude that FAD is Flavin 1 of glutamate synthase [Vanoni, M.A., Edmondson, D.E., Zanetti, G. & Curti, B. (1992) Biochemistry 31, 4613-4623].
- Published
- 1996
11. Disruption of the gene encoding the NADH-binding subunit of NADH: ubiquinone oxidoreductase in Neurospora crassa. Formation of a partially assembled enzyme without FMN and the iron-sulphur cluster N-3
- Author
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Hanns Weiss, Tomoko Ohnishi, Vladimir D. Sled, and Wolfgang Fecke
- Subjects
Iron-Sulfur Proteins ,Flavin Mononucleotide ,Macromolecular Substances ,Protein Conformation ,NADH binding ,Protein subunit ,Genes, Fungal ,Genetic Vectors ,Mutant ,Biology ,Biochemistry ,Neurospora crassa ,Oxidoreductase ,Centrifugation, Density Gradient ,Escherichia coli ,NAD(P)H Dehydrogenase (Quinone) ,Cloning, Molecular ,chemistry.chemical_classification ,Binding Sites ,Electron Spin Resonance Spectroscopy ,Chromatography, Ion Exchange ,NAD ,biology.organism_classification ,Recombinant Proteins ,Enzyme assay ,Mitochondria ,Molecular Weight ,Enzyme ,chemistry ,Mutagenesis ,Chromatography, Gel ,biology.protein ,Sequence motif ,Oxidation-Reduction - Abstract
In this study, the gene of the 51-kDa NADH-binding subunit of the mitochondrial NADH:ubiquinone oxidoreductase (complex I) in Neurospora crassa was inactivated by homologous replacement with a defective gene copy. The resulting mutant, nuo51, lacks the 51-kDa subunit and shows no complex I activity but still grows at one third of the wild-type growth rate. The enzyme activity of the alternative NADH:ubiquinone oxidoreductase(s) is increased twofold while the activities of the other mitochondrial respiratory enzymes are normal. Complex I is almost completely assembled except for the NADH-binding subunit and still possesses three out of the four EPR-detectable iron-sulphur clusters. Since the deleted subunit contains the sequence motif for one tetranuclear iron-sulphur cluster, the missing cluster N-3 is considered to be bound to this subunit.
- Published
- 1994
12. Homonuclear and heteronuclear NMR studies of oxidized Desulfovibrio vulgaris flavodoxin. Sequential assignments and identification of secondary structure elements
- Author
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G. Paul Curley, Heinz Rüterjans, Franz Müller, Paul A. O'Farrell, Frank Löhr, Martin A. Knauf, and Stephen G. Mayhew
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Magnetic Resonance Spectroscopy ,Proline ,Flavin Mononucleotide ,Stereochemistry ,Flavodoxin ,Molecular Sequence Data ,Flavin mononucleotide ,Biochemistry ,Protein Structure, Secondary ,Homonuclear molecule ,chemistry.chemical_compound ,Flavins ,Side chain ,Amino Acid Sequence ,Desulfovibrio vulgaris ,Protein secondary structure ,Binding Sites ,Nitrogen Isotopes ,biology ,Nuclear magnetic resonance spectroscopy ,biology.organism_classification ,Recombinant Proteins ,Solutions ,Heteronuclear molecule ,chemistry ,biology.protein ,Oxidation-Reduction - Abstract
Recombinant Desulfovibrio vulgaris flavodoxin (molecular mass 16.3 kDa) was produced in Escherichia coli. The oxidized protein has been investigated with a combination of homonuclear and heteronuclear two-dimensional and heteronuclear three-dimensional NMR spectroscopy. Sequence-specific assignment of all backbone and most of the side chain 1H and 15N resonances has been obtained. The secondary structure has been inferred from the pattern of sequential, medium-, and long-range NOEs, together with information about slowly exchanging amide hydrogens and HN-H alpha spin-spin coupling constants. In solution, flavodoxin consists of a five-stranded parallel beta-sheet and four alpha-helices. Residues 3-9, 32-36, 52-58, 87-96, and 123-128 are involved in the beta-sheet whereas the a-helical regions comprise residues 13-28, 69-76, 104-114, and 134-148. Several proton resonances of the bound flavin mononucleotide cofactor have been assigned. NOE contacts between the prosthetic group and the apoprotein have been detected.
- Published
- 1993
13. Iron release from ferrisiderophores. A multi-step mechanism involving a NADH/FMN oxidoreductase and a chemical reduction by FMNH2
- Author
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Félix Hallé and Jean-Marie Meyer
- Subjects
Siderophore ,FMN Reductase ,Flavin Mononucleotide ,Stereochemistry ,Iron ,Kinetics ,Biochemistry ,Substrate Specificity ,chemistry.chemical_compound ,FMN reductase ,medicine ,NADH, NADPH Oxidoreductases ,Ferrichrome ,chemistry.chemical_classification ,biology ,NAD ,biology.organism_classification ,Enzyme ,chemistry ,Pseudomonas aeruginosa ,Pseudomonadales ,Ferric ,Oxidation-Reduction ,medicine.drug ,Pseudomonadaceae - Abstract
Release of iron from various ferrisiderophores (ferripyoverdines, ferrioxamines B and E, ferricrocin, ferrichrome A, ferrienterobactin and its analog ferric N,N',N''-tri(1,3,5-Tris) 2,3-dihydroxybenzoylaminomethylbenzene) was obtained through an enzymic reduction of iron, involving NADH, FMN and the ferripyoverdine reductase of Pseudomonas aeruginosa PAO1. The iron released from the same complexes was also obtained through chemical reduction of iron involving FMNH2. Evidence is given that the enzymic process acts through a FMNH2 reduction; the P. aeruginosa enzyme, purified according to its ferripyoverdine-reductase activity [Halle, F. & Meyer, J. M., Eur. J. Biochem. 209, 613-620], functions as a NADH:FMN oxidoreductase, the FMNH2 produced being able to chemically reduce the iron complexed by siderophores. The general occurrence of such a multi-step mechanism, which denies the existence of specific ferrisiderophore reductases, is discussed.
- Published
- 1992
14. Purification and characterization of a novel FMN-dependent enzyme. Membrane-bound L-(+)-pantoyl lactone dehydrogenase from Nocardia asteroides
- Author
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Sakayu Shimizu, Hideaki Yamada, and Michihiko Kataoka
- Subjects
Flavin Mononucleotide ,Detergents ,Polidocanol ,Dehydrogenase ,Biochemistry ,Catalysis ,Cofactor ,Polyethylene Glycols ,Substrate Specificity ,Sepharose ,Column chromatography ,Enzyme Stability ,chemistry.chemical_classification ,Chromatography ,Molecular mass ,biology ,Temperature ,Membrane Proteins ,Hydrogen Peroxide ,Hydrogen-Ion Concentration ,biology.organism_classification ,Propylene Glycol ,Enzyme Activation ,Oxygen ,Alcohol Oxidoreductases ,Enzyme ,chemistry ,Propylene Glycols ,Enzyme Induction ,Nocardia asteroides ,Chromatography, Gel ,biology.protein ,Electrophoresis, Polyacrylamide Gel ,Actinomycetales ,Isoelectric Focusing ,Lactone - Abstract
Membrane-bound L-(+)-pantoyl lactone dehydrogenase, an enzyme that catalyzes the formation of ketopantoyl lactone from L-(+)-pantoyl lactone, was solubilized with Brij 35 and purified 78-fold to apparent homogeneity, with a 3.7% overall recovery, from Nocardia asteroides through purification procedures including successive ammonium sulfate fractionation, and DEAE-Sephacel, Sepharose CL-6B and Cellulofine GC-700-m column chromatography in the presence of Brij 35. The relative molecular mass of the native enzyme, as estimated on high-performance gel-permeation chromatography, is at least more than 600 kDa and its subunit molecular mass is 42 kDa. The enzyme shows high specificity for L-(+)-pantoyl lactone as a substrate (Km = 26.8 mM; Vmax = 4.22 mumol.min-1.mg protein-1). Brij 35 acts as a stabilizer and also as an efficient activator of the enzyme. The prosthetic group of L-(+)-pantoyl lactone dehydrogenase was identified as noncovalently bound FMN.
- Published
- 1992
15. Redox and flavin-binding properties of recombinant flavodoxin from Desulfovibrio vulgaris (Hildenborough)
- Author
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Gerrit Voordouw, Mary C. Carr, Stephen G. Mayhew, and G. Paul Curley
- Subjects
DNA, Bacterial ,Semiquinone ,Flavin Mononucleotide ,Stereochemistry ,Flavodoxin ,Riboflavin ,Molecular Sequence Data ,Restriction Mapping ,Inorganic chemistry ,Flavoprotein ,Flavin group ,Biochemistry ,Redox ,chemistry.chemical_compound ,Escherichia coli ,Amino Acid Sequence ,Desulfovibrio vulgaris ,Cloning, Molecular ,Base Sequence ,biology ,Hydroquinone ,biology.organism_classification ,Recombinant Proteins ,Dissociation constant ,Oligodeoxyribonucleotides ,chemistry ,Genes, Bacterial ,Mutagenesis, Site-Directed ,Potentiometry ,biology.protein ,Oxidation-Reduction ,Plasmids ,Protein Binding - Abstract
Flavodoxin from Desulfovibrio vulgaris (Hildenborough) has been expressed at a high level (3-4% soluble protein) in Escherichia coli by subcloning a minimal insert carrying the gene behind the tac promoter of plasmid pDK6. The recombinant protein was readily isolated and its properties were shown to be identical to those of the wild-type protein obtained directly from D. vulgaris, with the exception that the recombinant protein lacks the N-terminal methionine residue. Detailed measurements of the redox potentials of this flavodoxin are reported for the first time. The redox potential, E2, for the couple oxidized flavodoxin/flavodoxin semiquinone at pH 7.0 is -143 mV (25 degrees C), while the value for the flavodoxin semiquinone/flavodoxin hydroquinone couple (E1) at the same pH is -440 mV. The effects of pH on the observed potentials were examined; E2 varies linearly with pH (slope = -59 mV), while E1 is independent of pH at high pH values, but below pH 7.5 the potential becomes less negative with decreasing pH, indicating a redox-linked protonation of the flavodoxin hydroquinone. D. vulgaris apoflavodoxin binds FMN very tightly, with a value of 0.24 nM for the dissociation constant (Kd) at pH 7.0 and 25 degrees C, similar to that observed with other flavodoxins. In addition, the apoflavodoxin readily binds riboflavin (Kd = 0.72 microM; 50 mM sodium phosphate, pH 7.0, 5 mM EDTA at 25 degrees C) and the complex is spectroscopically very similar to that formed with FMN. The redox potentials for the riboflavin complex were determined at pH 6.5 (E1 = -262 mV, E2 = -193 mV; 25 degrees C) and are discussed in the light of earlier proposals that charge/charge interactions between different parts of the flavin hydroquinone play a crucial role in determining E1 in flavodoxin.
- Published
- 1991
16. Flavin-photosensitized oxidation of reduced c-type cytochromes. Reaction mechanism and comparison with photoreduction of oxidized cytochromes by flavin semiquinones
- Author
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José A. Navarro, Manuel Hervás, Mercedes Roncel, Gordon Tollin, and Miguel A. De la Rosa
- Subjects
Photolysis ,biology ,Semiquinone ,Cytochrome ,Flavin Mononucleotide ,Photochemistry ,Riboflavin ,Cytochrome c ,Cytochrome c Group ,Flavin group ,Biochemistry ,Redox ,Electron Transport ,Kinetics ,chemistry.chemical_compound ,Electron transfer ,chemistry ,Flavins ,Electrochemistry ,biology.protein ,Flash photolysis ,Lumiflavin ,Oxidation-Reduction - Abstract
In order to compare the oxidation and reduction reactions of c-type cytochromes (cytochrome c552 from the green alga Monoraphidium braunii and horse heart cytochrome c) by different flavins (lumiflavin, riboflavin and FMN), laser flash photolysis studies have been carried out using either reduced or oxidized protein in the presence of triplet or semiquinone flavin, respectively. The reaction kinetics clearly demonstrate that cytochrome oxidation is mediated by the flavin triplet state. The rate constants for reduction are 20-100 times smaller than those for oxidation, indicating that the triplet state is a more effective reactant than is the semiquinone. This is attributed to its excited state nature and correspondingly high free energy content. The rate constants for both the reduction and oxidation of cytochrome c552 by riboflavin are significantly smaller than those obtained with lumiflavin, suggesting a steric interference of the ribityl side chain in the flavin-cytochrome interaction. The comparison between oxidation and reduction indicates that the former process is less affected by steric hindrance than the latter. Both reduction and oxidation of cytochrome c552 by FMN show an ionic strength dependence with the same sign, consistent with a negatively charged reaction site on the cytochrome. The magnitude of the electrostatic effect is slightly smaller for reduction than it is for oxidation. A pattern quite similar to that observed with cytochrome c552 was obtained when parallel experiments were carried out with horse cytochrome c, although differences were observed in the steric and electrostatic properties of the electron transfer site(s) in these two cytochromes. These results suggest that the same or closely adjacent sites on the proteins are involved in the oxidation and reduction reactions. The biochemical implications of this are discussed.
- Published
- 1990
17. Selective release and function of one of the two FMN groups in the cytoplasmic NAD+-reducing [NiFe]-hydrogenase from Ralstonia eutropha
- Author
-
Eddy, van der Linden, Bart W, Faber, Boris, Bleijlevens, Tanja, Burgdorf, Michael, Bernhard, Bärbel, Friedrich, and Simon P J, Albracht
- Subjects
Cytoplasm ,Flavin Mononucleotide ,NAD ,Aerobiosis ,Molecular Weight ,Glucose Oxidase ,Glucose ,Spectrometry, Fluorescence ,Hydrogenase ,Chromatography, Gel ,Cupriavidus necator ,Anaerobiosis ,Ferricyanides ,Oxidation-Reduction ,Hydrogen - Abstract
The soluble, cytoplasmic NAD+-reducing [NiFe]-hydrogenase from Ralstonia eutropha is a heterotetrameric enzyme (HoxFUYH) and contains two FMN groups. The purified oxidized enzyme is inactive in the H2-NAD+ reaction, but can be activated by catalytic amounts of NADH. It was discovered that one of the FMN groups (FMN-a) is selectively released upon prolonged reduction of the enzyme with NADH. During this process, the enzyme maintained its tetrameric form, with one FMN group (FMN-b) firmly bound, but it lost its physiological activity--the reduction of NAD+ by H2. This activity could be reconstituted by the addition of excess FMN to the reduced enzyme. The rate of reduction of benzyl viologen by H2 was not dependent on the presence of FMN-a. Enzyme devoid of FMN-a could not be activated by NADH. As NADH-dehydrogenase activity was not dependent on the presence of FMN-a, and because FMN-b did not dissociate from the reduced enzyme, we conclude that FMN-b is functional in the NADH-dehydrogenase activity catalyzed by the HoxFU dimer. The possible function of FMN-a as a hydride acceptor in the hydrogenase reaction catalyzed by the HoxHY dimer is discussed.
- Published
- 2004
18. A comparison of the urea-induced unfolding of apoflavodoxin and flavodoxin from Desulfovibrio vulgaris
- Author
-
Brian O, Nuallain and Stephen G, Mayhew
- Subjects
Protein Folding ,Flavin Mononucleotide ,Protein Conformation ,Flavodoxin ,Urea ,Desulfovibrio vulgaris ,Apoproteins ,Fluorescence - Abstract
The kinetics and thermodynamics of the urea-induced unfolding of flavodoxin and apoflavodoxin from Desulfovibrio vulgaris were investigated by measuring changes in flavin and protein fluorescence. The reaction of urea with flavodoxin is up to 5000 times slower than the reaction with the apoprotein (0.67 s(-1) in 3 m urea in 25 mm sodium phosphate at 25 degrees C), and it results in the dissociation of FMN. The rate of unfolding of apoflavodoxin depends on the urea concentration, while the reaction with the holoprotein is independent of urea. The rates decrease in high salt with the greater effect occurring with apoprotein. The fluorescence changes fit two-state models for unfolding, but they do not exclude the possibility of intermediates. Calculation suggests that 21% and 30% of the amino-acid side chains become exposed to solvent during unfolding of flavodoxin and apoflavodoxin, respectively. The equilibrium unfolding curves move to greater concentrations of urea with increase of ionic strength. This effect is larger with phosphate than with chloride, and with apoflavodoxin than with flavodoxin. In low salt the conformational stability of the holoprotein is greater than that of apoflavodoxin, but in high salt the relative stabilities are reversed. It is calculated that two ions are released during unfolding of the apoprotein. It is concluded that the urea-dependent unfolding of flavodoxin from D. vulgaris occurs because apoprotein in equilibrium with FMN and holoprotein unfolds and shifts the equilibrium so that flavodoxin dissociates. Small changes in flavin fluorescence occur at low concentrations of urea and these may reflect binding of urea to the holoprotein.
- Published
- 2002
19. A novel two-protein component flavoprotein hydroxylase
- Author
-
P, Chaiyen, C, Suadee, and P, Wilairat
- Subjects
Molecular Weight ,Kinetics ,Acinetobacter ,Flavin Mononucleotide ,Multienzyme Complexes ,Flavins ,Flavin-Adenine Dinucleotide ,Hydroxylation ,Mixed Function Oxygenases ,Substrate Specificity - Abstract
p-Hydroxyphenylacetate (HPA) hydroxylase (HPAH) was purified from Acinetobacter baumannii and shown to be a two-protein component enzyme. The small component (C1) is the reductase enzyme with a subunit molecular mass of 32 kDa. C1 alone catalyses HPA-stimulated NADH oxidation without hydroxylation of HPA. C1 is a flavoprotein with FMN as a native cofactor but can also bind to FAD. The large component (C2) is the hydroxylase component that hydroxylates HPA in the presence of C1. C2 is a tetrameric enzyme with a subunit molecular mass of 50 kDa and apparently contains no redox centre. FMN, FAD, or riboflavin could be used as coenzymes for hydroxylase activity with FMN showing the highest activity. Our data demonstrated that C2 alone was capable of utilizing reduced FMN to form the product 3,4-dihydroxyphenylacetate. Mixing reduced flavin with C2 also resulted in the formation of a flavin intermediate that resembled a C(4a)-substituted flavin species indicating that the reaction mechanism of the enzyme proceeded via C(4a)-substituted flavin intermediates. Based on the available evidence, we conclude that the reaction mechanism of HPAH from A. baumannii is similar to that of bacterial luciferase. The enzyme uses a luciferase-like mechanism and reduced flavin (FMNH2, FADH2, or reduced riboflavin) to catalyse the hydroxylation of aromatic compounds, which are usually catalysed by FAD-associated aromatic hydroxylases.
- Published
- 2001
20. Flavin-protein interactions in flavocytochrome b2 as studied by NMR after reconstitution of the enzyme with 13C- and 15N-labelled flavin
- Author
-
G, Fleischmann, F, Lederer, F, Müller, A, Bacher, and H, Rüterjans
- Subjects
Carbon Isotopes ,Binding Sites ,Flavoproteins ,L-Lactate Dehydrogenase ,Nitrogen Isotopes ,Flavin Mononucleotide ,Protein Conformation ,Riboflavin ,Molecular Conformation ,Hydrogen Bonding ,Saccharomyces cerevisiae ,Recombinant Proteins ,Escherichia coli ,Flavin-Adenine Dinucleotide ,L-Lactate Dehydrogenase (Cytochrome) ,Cloning, Molecular ,Nuclear Magnetic Resonance, Biomolecular - Abstract
A new procedure was devised for reversibly removing the flavin from flavocytochrome b2. It allowed reconstitution with selectively enriched 13C- and 15N-labelled FMN for an NMR analysis of the chemical shifts of the enriched positions as well as that of 31P. From these measurements, it was possible to deduce information about the hydrogen-bonding pattern of FMN in the protein, the hybridization states of the nitrogen atoms and (in part) the pi-electron distribution. The carbonyl groups at C(2) and C(4) and the nitrogen atoms N(1) and N(5) form hydrogen bonds to the apoenzyme in both redox states. Nevertheless, according to 15N-chemical shifts, the bond from the protein to N(3) is very weak in both redox states, whereas that to N(5) is strong for the oxidized state, and is weakened upon flavin reduction. On the other hand, the 13C-NMR results indicate that the C(2) and C(4) carbonyl oxygens form stronger hydrogen bonds with the enzyme than most other flavoproteins in both redox states. From coupling constant measurements it is shown that the N(3) proton is not solvent accessible. Although no N-H coupling constant could be measured for N(5) in the reduced state due to lack of resolution, N(5) is clearly protonated in flavocytochrome b2 as in all other known flavoproteins. With respect to N(10), it is more sp3-hybridized in the oxidized state than in free FMN, whereas the other nitrogen atoms show a nearly planar structure. In the reduced state, N(5) and N(10) in bound FMN are both more sp3-hybridized than in free FMN, but N(5) exhibits a higher degree of sp3-hybridization than N(10), which is only slightly shifted out of the isoalloxazine plane. In addition, two-electron reduction of the enzyme leads to anion formation on N(1), as indicated by its 15N-chemical shift of N(1) and characteristic upfield shifts of the resonances of C(2), C(4) and C(4a) compared to the oxidized state, as observed for most flavoproteins. 31P-NMR measurements show that the phosphate geometry has changed in enzyme bound FMN compared to the free flavin in water, indicating a strong interaction of the phosphate group with the apoenzyme.
- Published
- 2000
21. A protein factor of rat liver mitochondrial matrix involved in flavinylation of dimethylglycine dehydrogenase
- Author
-
C, Brizio, A, Otto, R, Brandsch, S, Passarella, and M, Barile
- Subjects
Male ,Reticulocytes ,Time Factors ,Transcription, Genetic ,Flavin Mononucleotide ,Blotting, Western ,Mitochondria, Liver ,Oxidoreductases, N-Demethylating ,Chaperonin 60 ,Chromatography, Affinity ,Rats ,Mitochondrial Proteins ,Adenosine Triphosphate ,Apoenzymes ,Flavins ,Protein Biosynthesis ,Dimethylglycine Dehydrogenase ,Flavin-Adenine Dinucleotide ,Animals ,HSP70 Heat-Shock Proteins ,Rabbits ,Rats, Wistar ,Plasmids - Abstract
The involvement of rat liver mitochondria in the flavinylation of the mitochondrial matrix flavoenzyme dimethylglycine dehydrogenase (Me2GlyDH) has been investigated. Me2GlyDH was synthesized as an apoenzyme in the rabbit reticulocyte lysate (RL) transcription/translation system and its flavinylation was monitored by virtue of the trypsin resistance of the holoenzyme. The rate of holoenzyme formation in the presence of FAD was stimulated with increasing efficiency by the addition of solubilized mitoplasts, mitochondrial matrix and DEAE-purified matrix fraction. Apo-Me2GlyDH was also converted into holoenzyme when the solubilized mitoplasts were supplemented with FMN and ATP. This observation is consistent with the existence of a mitochondrial FAD synthetase generating the FAD needed for holoenzyme formation from its precursors. Holoenzyme formation in the presence of FAD increased linearly with the concentration of matrix protein in the assay, and depended on the amount of externally added Me2GlyDH with saturation characteristics. These findings suggest the presence of a protein factor in the mitochondrial matrix which stimulates Me2GlyDH flavinylation. This factor was different from both mitochondrial heat shock protein (Hsp)70, as shown by immunodepletion experiments, and mitochondrial Hsp60, as demonstrated by the capability of a DEAE-purified matrix fraction devoid of Hsp60 to accelerate flavinylation of both RL translated and purified Me2GlyDH.
- Published
- 2000
22. 2-hydroxyglutaryl-CoA dehydratase from Clostridium symbiosum
- Author
-
Julia A. Vorholt, Marcus Hans, Dietmar Linder, Uta Müller, Wolfgang Buckel, Jörg Sievers, and Eckhard Bill
- Subjects
Iron-Sulfur Proteins ,Acidaminococcus fermentans ,Clostridium symbiosum ,Thauera aromatica ,Operon ,Sequence analysis ,Flavin Mononucleotide ,Molecular Sequence Data ,Iron–sulfur cluster ,Biology ,Biochemistry ,chemistry.chemical_compound ,Spectroscopy, Mossbauer ,Proteobacteria ,Amino Acid Sequence ,Cloning, Molecular ,Hydro-Lyases ,Clostridium ,Bacteria ,Sequence Homology, Amino Acid ,Electron Spin Resonance Spectroscopy ,Sequence Analysis, DNA ,biology.organism_classification ,Archaea ,chemistry ,Models, Chemical ,Genes, Bacterial ,Dehydratase ,Rhodopseudomonas palustris - Abstract
Component D (HgdAB) of 2-hydroxyglutaryl-CoA dehydratase from Clostridium symbiosum was purified to homogeneity. It is able to use component A from Acidaminococcus fermentans (HgdC) to initiate catalysis together with ATP, Mg2+ and a strong reducing agent such as Ti(III)citrate. Component D from C. symbiosum has a 6 x higher specific activity compared with that from A. fermentans and contains a second [4Fe-4S] cluster but the same amount of riboflavin 5'-phosphate (1.0 per heterodimeric enzyme, m = 100 kDa). Mossbauer spectroscopy revealed symmetric cube-type structures of the two [4Fe-4S]2+ clusters. EPR spectroscopy showed the resistance of the clusters to reducing agents, but detected a sharp signal at g = 2. 004 probably due to a stabilized flavin semiquinone. Three genes from C. symbiosum coding for components D (hgdA and hgdB) and A (hgdC) were cloned and sequenced. Primer extension experiments indicated that the genes are transcribed in the order hgdCAB from an operon only half the size of that from A. fermentans. Sequence comparisons detected a close relationship to the dehydratase system from A. fermentans and HgdA from Fusobacterium nucleatum, as well as to putative proteins of unknown function from Archaeoglobus fulgidus. Lower, but significant, identities were found with putative enzymes from several methanogenic Archaea and Escherichia coli, as well as with the mechanistically related benzoyl-CoA reductases from the Proteobacteria Rhodopseudomonas palustris and Thauera aromatica.
- Published
- 1999
23. Purification and partial characterisation of a reversible artificial mediator accepting NADH oxidoreductase from Clostridium thermoaceticum
- Author
-
Katrin Walter, Manfred G. Bayer, and Helmut Simon
- Subjects
Paraquat ,Flavin Mononucleotide ,Iron ,Molecular Sequence Data ,Dehydrogenase ,Anthraquinones ,Flavin group ,Biochemistry ,Oxidoreductase ,Enzyme Stability ,NADP Transhydrogenases ,Amino Acid Sequence ,Gel electrophoresis ,chemistry.chemical_classification ,Clostridium ,Molecular mass ,Sequence Homology, Amino Acid ,Chemistry ,NAD ,Molecular Weight ,Glycerol-3-phosphate dehydrogenase ,Enzyme ,Flavin-Adenine Dinucleotide ,2,6-Dichloroindophenol ,Spectrophotometry, Ultraviolet ,NAD+ kinase ,Sequence Analysis ,Sulfur - Abstract
An NAD(H)-dependent artificial mediator accepting pyridine nucleotide oxidoreductase present in Clostridium thermoaceticum has been purified 50-fold by three chromatographic steps to apparent electro-phoretical homogeneity with a yield of 25%. By PAGE and gel filtration the molecular mass of the native enzyme was estimated to be 200 kDa and 210 kDa, respectively. By SDS/gel electrophoresis, a single band was found at 17000 Da, suggesting a homododecamer. Reducing carbamoyl methylviologen or hexa-cyanoferrate(III) with NADH, the enzyme was most active at pH 10 and the specific activities were 100 μmol min-1 mg-1 protein and 800 μmol min-1 mg-1 protein, respectively. The Km values for hexacya-noferrate(III), carbamoylmethylviologen and NADH at pH 8.5 were determined to be 0.40, 0.55 and 1.1 mM, respectively. Other electron acceptors for the dehydrogenation of NADH were 2,6-dichlorophe-nolindophenol, anthraquinone-2,6-disulphonate, ubiquinone 0 and FAD. In the reduction of NAD+ with reduced methyl viologen (MV+), the specific activity was about 225 μmol min-1 mg-1 protein at the pH maximum of 5.0. The Km values for reduced methylviologen, NADH and NAD+ were 1.0, 1.1 and 0.25 mM, respectively. The enzyme had 10.6 atoms iron and 12.7 atoms sulphur per dodecamer. A significant content of flavin or molybdopterin cofactor could not be detected. The first 45 amino acids of the oxidoreductase show a surprisingly high degree of identity or similarity with the ribosomal L12 protein of various eubacteria, the acyl carrier proteins of microorganisms, but also with bovine heart mitochondria and a 3-phosphoglycerate dehydrogenase as well as a gyceraldehyde-3-phosphate dehydrogenase from bacteria and pea chloroplasts, respectively.
- Published
- 1996
24. Probing electron transfer in flavocytochrome P-450 BM3 and its component domains
- Author
-
John R. Coggins, Simon Daff, Stephen K Chapman, Andrew W. Munro, and J. Gordon Lindsay
- Subjects
Semiquinone ,Cytochrome ,Stereochemistry ,Flavin Mononucleotide ,Haem peroxidase ,Restriction Mapping ,Flavin group ,Heme ,Photochemistry ,Biochemistry ,Mixed Function Oxygenases ,Electron Transport ,Electron transfer ,Bacterial Proteins ,Cytochrome P-450 Enzyme System ,Escherichia coli ,Cloning, Molecular ,NADPH-Ferrihemoprotein Reductase ,chemistry.chemical_classification ,Binding Sites ,biology ,Electron Spin Resonance Spectroscopy ,Quinones ,Substrate (chemistry) ,Fatty acid ,Monooxygenase ,Peptide Fragments ,Recombinant Proteins ,Kinetics ,chemistry ,biology.protein ,Bacillus megaterium ,Flavin-Adenine Dinucleotide ,Oxidation-Reduction ,NADP - Abstract
Rapid events in the processes of electron transfer and substrate binding to cytochrome P-450 BM3 from Bacillus megaterium and its constituent haem-containing and flavin-containing domains have been investigated using stopped-flow spectrophotometry. The formation of a blue semiquinone flavin form occurs during the NADPH-dependent reduction of the flavin domain and a species with a similar absorption maximum is also seen during reduction of the holoenzyme by NADPH. EPR spectroscopy confirms the formation of the flavin semiquinone. The formation of this semiquinone is transient during fatty acid monooxygenation by the holoenzyme, but in the presence of excess NADPH the species reforms once fatty acid is exhausted. Electron transfers through the reductase domain are too rapid to limit the fatty acid monooxygenation reaction. The substrate-binding-induced haem iron spin-state shift also occurs much faster than the Kcat at 25 degrees C. The rate of first electron transfer to the haem domain is also rapid; but it is of the order of 5-10-times larger than the Kcat for the enzyme (dependent on the fatty acid used). Given that two successive electron transfers to haem iron are required for the oxygenation reaction, these rates are likely to exert some control over the rate of fatty acid oxygenation reactions. The presence of large amounts of NADPH also results in decreased rates of electron transfer from flavin to haem iron. In the difference spectrum of the active fatty acid hydroxylase, features indicative of a high-spin iron haem accumulate. These are in accordance with the presence of large amounts of an Fe(3+)-product bound enzyme during turnover and indicate that product release may also contribute to rate limitation. Taken together, these data suggest that the catalytic rate is not determined by the accumulation of a single intermediate in the reaction scheme, but rather that it is controlled in a series of steps.
- Published
- 1996
25. Roulette mutagenesis of the FMN-binding site of Klebsiella pneumoniae flavodoxin
- Author
-
Andrew J. Green, Susan Huff, and Martin Drummond
- Subjects
Threonine ,Flavodoxin ,Flavin Mononucleotide ,Mutant ,Molecular Sequence Data ,Glycine ,Biology ,Biochemistry ,Protein Structure, Secondary ,FMN binding ,Nitrogenase ,Amino Acid Sequence ,Binding site ,Site-directed mutagenesis ,Codon ,Binding Sites ,Base Sequence ,Lysine ,Mutagenesis ,Klebsiella pneumoniae ,Phenotype ,biology.protein ,Alpha helix - Abstract
A method of randomising specific regions of coding sequences has been devised which utilises the Lac phenotype to identify mutants. Intact genes can be mutagenised, making it unnecessary to reclone the mutations before examining mutant phenotypes. The method has been applied to three residues around the N-terminus of the first alpha helix of the Klebsiella pneumoniae nitrogenase flavodoxin, which are predicted to form part of the phosphate-binding subsite. Surprisingly, most substitutions at Gly12, a highly conserved residue in the chain reversal preceding the alpha helix, appeared to be fairly stable in vivo and were found to retain some function. Substitutions at Lys13, a surface residue which contributes to a patch of positive charge characteristic of the nitrogenase flavodoxins, had no major effect on stability or function. However, most substitutions at Thr14, which is predicted to hydrogen bond to the phosphate of the prosthetic group FMN, were much more destabilising and grossly reduced function. The exceptions were Ala, Cys, Ser and Val, which suggests that the bulk of the residue at this position is critical.
- Published
- 1993
26. Reduction and mobilization of iron by a NAD(P)H:flavin oxidoreductase from Escherichia coli
- Author
-
Jacques Covès and Mare Fontecave
- Subjects
Siderophore ,FMN Reductase ,Stereochemistry ,Flavin Mononucleotide ,Iron ,Riboflavin ,Flavin group ,Biochemistry ,Ferric Compounds ,Catalysis ,Ferrous ,Electron Transport ,Oxidoreductase ,FMN reductase ,medicine ,Escherichia coli ,NADH, NADPH Oxidoreductases ,Ribonucleotide Reductase Subunit ,Ferrous Compounds ,chemistry.chemical_classification ,Chemistry ,Hydrogen-Ion Concentration ,NAD ,Kinetics ,Ferritins ,Flavin-Adenine Dinucleotide ,Ferric ,NAD+ kinase ,Oxidation-Reduction ,Ferrichrome ,NADP ,medicine.drug - Abstract
Iron is an essential element in all living cells. Solubilization, uptake and transport of iron by microorganisms is controlled by highly efficient and specific Fe(3+)-chelating agents named siderophores. However, mechanisms of mobilization of iron from ferrisiderophores are still enigmatic. Here, we demonstrate that Escherichia coli contains a powerful enzymatic system for the reduction of ferrisiderophores. Siderophores have a much lower affinity for ferrous iron, which then can be liberated. This system has been previously purified and characterized as a NAD(P)H:flavin oxidoreductase [Fontecave, M., Eliasson, R. and Reichard, P. (1987) J. Biol. Chem. 262, 12,325-12,331)]. It catalyzes the reduction of free flavins, FMN, FAD or riboflavin by NADH or NADPH. Reduced flavins, in turn, transfer their electrons to physiological ferric complexes: ferrisiderophores, ferric citrate and ferritins. The reaction is inhibited by molecular oxygen and greatly stimulated by Fe(2+)-acceptors such as ferrozine or the iron-free form of ribonucleotide reductase subunit R2. We suggest that the reduction and the mobilization of iron from ferrisiderophores in the cell might be regulated by the presence of physiological ferrous traps such as apoproteins.
- Published
- 1993
27. Purification and characterisation of the NADH:acceptor reductase component of xylene monooxygenase encoded by the TOL plasmid pWW0 of Pseudomonas putida mt-2
- Author
-
J P, Shaw and S, Harayama
- Subjects
Flavin Mononucleotide ,Pseudomonas putida ,Dithionite ,Cytochrome c Group ,NADH Dehydrogenase ,NAD ,Electron Transport ,Molecular Weight ,Spectrophotometry ,Flavin-Adenine Dinucleotide ,Oxygenases ,Anaerobiosis ,Isoelectric Point ,Oxidation-Reduction ,Plasmids - Abstract
The xylene monooxygenase system encoded by the TOL plasmid pWW0 of Pseudomonas putida catalyses the hydroxylation of a methyl side-chain of toluene and xylenes. Genetic studies have suggested that this monooxygenase consists of two different proteins, products of the xylA and xylM genes, which function as an electron-transfer protein and a terminal hydroxylase, respectively. In this study, the electron-transfer component of xylene monooxygenase, the product of xylA, was purified to homogeneity. Fractions containing the xylA gene product were identified by its NADH:cytochrome c reductase activity. The molecular mass of the enzyme was determined to be 40 kDa by SDS/PAGE, and 42 kDa by gel filtration. The enzyme was found to contain 1 mol/mol of tightly but not covalently bound FAD, as well as 2 mol/mol of non-haem iron and 2 mol/mol of acid-labile sulfide, suggesting the presence of two redox centers, one FAD and one [2Fe-2S] cluster/protein molecule. The oxidised form of the protein had absorbance maxima at 457 nm and 390 nm, with shoulders at 350 nm and 550 nm. These absorbance maxima disappeared upon reduction of the protein by NADH or dithionite. The NADH:acceptor reductase was capable of reducing either one- or two-electron acceptors, such as horse heart cytochrome c or 2,6-dichloroindophenol, at an optimal pH of 8.5. The reductase was found to have a Km value for NADH of 22 microM. The oxidation of NADH was determined to be stereospecific; the enzyme is pro-R (class A enzyme). The titration of the reductase with NADH or dithionite yielded three distinct reduced forms of the enzyme: the reduction of the [2Fe-2S] center occurred with a midpoint redox potential of -171 mV; and the reduction of FAD to FAD. (semiquinone form), with a calculated midpoint redox potential of -244 mV. The reduction of FAD. to FAD.. (dihydroquinone form), the last stage of the titration, occurred with a midpoint redox potential of -297 mV. The [2Fe-2S] center could be removed from the protein by treatment with an excess of mersalyl acid. The [2Fe-2S]-depleted protein was still reduced by NADH, giving rise to the formation of the anionic flavin semiquinone observed in the native enzyme, thus suggesting that the electron flow was NADH --FAD --[2Fe-2S] in this reductase. The resulting protein could no longer reduce cytochrome c, but could reduce 2,6-dichloroindophenol at a reduced rate.
- Published
- 1992
28. Biosynthesis of vitamin B12. Transformation of riboflavin 2H-labeled in the 1'R position of 1'S position into 5,6-dimethylbenzimidazole
- Author
-
Paul Renz, Thomas A. Schild, Bernhard Vogler, and Brigitte Lingens
- Subjects
Barbituric acid ,Magnetic Resonance Spectroscopy ,Sodium cyanoborohydride ,Stereochemistry ,Flavin Mononucleotide ,Riboflavin ,Propionibacterium ,Stereoisomerism ,Riboside ,Biochemistry ,Mass Spectrometry ,Dimethylbenzimidazole ,chemistry.chemical_compound ,Vitamin B 12 ,Stereospecificity ,chemistry ,Ribose ,Proton NMR ,Benzimidazoles ,Hydrogen - Abstract
The 5,6-dimethylbenzimidazole moiety of vitamin B12 is formed from riboflavin in aerobic and some aerotolerant bacteria. Thereby C1' of riboflavin is transformed into C2 of the vitamin B12 base. In the present publication a study on this transformation with riboflavin 2H-labeled in the 1'R or 1'S position is described. This study was undertaken in order to find out if one of the two hydrogens at C1' is transferred to C2 of 5,6-dimethylbenzimidazole. The 2H-labeled riboflavin samples were synthesized starting from unlabeled or 1-2H-labeled ribose and 3,4-dimethylaniline yielding N-beta-D-ribopyranosyl-3,4-dimethylaniline. The unlabeled riboside was reduced to N-D-ribityl-3,4-dimethylaniline with sodium cyanoborotrideuteride, the 2H-labeled riboside with sodium cyanoborohydride. The ribityl derivatives were transformed into N-D-ribityl-2-phenylazo-4,5-dimethylaniline, and condensed with barbituric acid to riboflavin. The reduction of the ribosyl compound to the ribityl derivative is only partially stereospecific. Thus the riboflavin synthesized from unlabeled ribose had a 2H ratio of 3/1 (1'R/1'S), the riboflavin obtained from D-[1-2H1]ribose of 1/3 (1'R/1'S). The 2H content in these positions was determined from the 1H-NMR spectra. These spectra showed also that 1 mol 2H/mol riboflavin was present in position 1'. The deuterated riboflavin samples were incubated under aerobic conditions with broken cell preparations of Propionibacterium shermanii. The deuterium content of the 5,6-dimethylbenzimidazole isolated was determined by mass spectrometry and by 1H NMR. These measurements revealed that the hydrogen in the pro-S position at C1' of riboflavin is retained during 5,6-dimethylbenzimidazole formation, and is thus found at C2 of this base.
- Published
- 1992
29. (R)-lactyl-CoA dehydratase from Clostridium propionicum. Stereochemistry of the dehydration of (R)-2-hydroxybutyryl-CoA to crotonyl-CoA
- Author
-
Antje E. M. Hofmeister and Wolfgang Buckel
- Subjects
chemistry.chemical_classification ,Clostridium ,Threonine ,Stereochemistry ,Flavin Mononucleotide ,Riboflavin ,Crotonyl-CoA ,Substrate (chemistry) ,Water ,Dehydrogenase ,Stereoisomerism ,medicine.disease ,Biochemistry ,chemistry.chemical_compound ,Enzyme ,Stereospecificity ,chemistry ,Dehydratase ,medicine ,Propionate ,Dehydration ,Acyl Coenzyme A ,Oxidation-Reduction ,Hydro-Lyases - Abstract
1 A new two-step method for purifying component EII of lactyl-CoA dehydratase was developed. The source fo the enzyme was Clostridium propionicum grown on either d,l-alanine or l-threonine. No difference in these preparations was observed whether during purification or by SDS/PAGE of the pure enzymes. Bothe preparations exhibited similar activities towards (R)-lactyl-CoA as well as towards (R)-2-hydroxbutyryl-CoA, the latter being the superior substrate. 2 Three species of (2R)-2-hydroxybutyrate labelled with 3H at C3 were prepared containing 96%, 37% and 63% of the 3H in the 3S-position. By incubation of these species with acetyl-CoA, propionate CoA-transferse and lactyl-CoA dehydratase 104%, 32% and 70% of the 3H, respectively, was released as 3HOH. The data indicate the stereospecific abstraction of the 3Si hydrogin of (2R)-2-hydroxybutyryl-CoA during the dehydration. 3 The identity of the product of the dehydration as crotonyl-CoA was established by the combined action of the enzymes crotonase and (S)-3-hydroxybutyryl-CoA dehydrogenase. The results indicate that the elimination of water from (R)-2-hydroxybutyryl-CoA occurs in a syn mode. 4 All enzyme activities necessary for the conversion of l-threonine via (R)-2-hydroxybutyryl-CoA to butyrate were detected in cell-free extracts of C.propionicum. 5 A new mechanism for the dehydration of lactyl-CoA is proposed.
- Published
- 1992
30. Effect of KCl on the interactions between NADPH:cytochrome P-450 reductase and either cytochrome c, cytochrome b5 or cytochrome P-450 in octyl glucoside micelles
- Author
-
Yukio Nisimoto and Dale E. Edmondson
- Subjects
Magnetic Resonance Spectroscopy ,Cytochrome ,Stereochemistry ,Flavin Mononucleotide ,Detergents ,Cytochrome c Group ,Biochemistry ,Potassium Chloride ,Cytochrome C1 ,Cytochrome P-450 Enzyme System ,Glucosides ,Cytochrome c oxidase ,Animals ,Micelles ,NADPH-Ferrihemoprotein Reductase ,Binding Sites ,biology ,Cytochrome c peroxidase ,Chemistry ,Cytochrome b6f complex ,Cytochrome c ,Circular Dichroism ,Osmolar Concentration ,Cytochrome P450 reductase ,Cytochromes b5 ,Coenzyme Q – cytochrome c reductase ,biology.protein ,Microsomes, Liver ,Cytochromes ,Electrophoresis, Polyacrylamide Gel ,Rabbits - Abstract
Significant dissociation of FMN from NADPH:cytochrome P-450 reductase resulted in loss of the activity for reduction of cytochrome b5 as well as cytochrome c and cytochrome P-450. However, the ability to reduce these electron acceptors was greatly restored upon incubation of FMN-depleted enzyme with added FMN. The reductions of cytochrome c and detergent-solubilized cytochrome b5 by NADPH:cytochrome P-450 reductase were greatly increased in the presence of high concentrations of KCl, although the stimulatory effect of the salt on cytochrome P-450 reduction was less significant. No apparent effect of superoxide dismutase could be seen on the rate or extent of cytochrome reduction in solutions containing high-salt concentrations. Complex formation of the flavoprotein with cytochrome c, which is known to be involved in the mechanism of non-physiological electron transfer, caused a perturbation in the absorption spectrum in the Soret-band region of cytochrome c, and its magnitude was enhanced by addition of KCl. Similarly, an appreciable increase in ellipticity in the Soret band of cytochrome c was observed upon binding with the flavoprotein. However, only small changes were found in absorption and circular dichroism spectra for the complex of NADPH:cytochrome P-450 reductase with either cytochrome b5 or cytochrome P-450. It is suggested that the high-salt concentration allows closer contact between the heme and flavin prosthetic groups through hydrophobic-hydrophobic interactions rather than electrostatic-charge pairing between the flavoprotein and the cytochrome which causes a faster rate of electron transfer. Neither alterations in the chemical shift nor in the line width of the bound FMN and FAD phosphate resonances were observed upon complex formation of NADPH:cytochrome P-450 reductase with the cytochrome.
- Published
- 1992
31. NMR studies on p-hydroxybenzoate hydroxylase from Pseudomonas fluorescens and salicylate hydroxylase from Pseudomonas putida
- Author
-
W.J.H. van Berkel, Franz Müller, Chrit T. W. Moonen, and J.J.M. Vervoort
- Subjects
Conformational change ,Magnetic Resonance Spectroscopy ,Stereochemistry ,Flavin Mononucleotide ,Protein Conformation ,Biochemie ,Flavin group ,Pseudomonas fluorescens ,Biochemistry ,Mixed Function Oxygenases ,Pseudomonas ,Life Science ,Carbon Isotopes ,Binding Sites ,biology ,Molecular Structure ,Nitrogen Isotopes ,Hydrogen bond ,Chemistry ,Substrate (chemistry) ,Active site ,Nuclear magnetic resonance spectroscopy ,biology.organism_classification ,4-Hydroxybenzoate-3-Monooxygenase ,Pseudomonas putida ,Solvent ,biology.protein ,Flavin-Adenine Dinucleotide ,Oxidation-Reduction ,NADP - Abstract
p-Hydroxybenzoate hydroxylase from Pseudomonas fluorescens and salicylate hydroxylase from Pseudomonas putida have been reconstituted with 13C- and 15N-enriched FAD. The protein preparations were studied by 13C-NMR, 15N-NMR and 31P-NMR techniques in the oxidized and in the two-electron-reduced states. The chemical shift values are compared with those of free flavin in water or chloroform. It is shown that the pi electron distribution in oxidized free p-hydroxybenzoate hydroxylase is comparable to free flavin in water, and it is therefore suggested that the flavin ring is solvent accessible. Addition of substrate has a strong effect on several resonances, e.g. C2 and N5, which indicates that the flavin ring becomes shielded from solvent and also that a conformational change occurs involving the positive pole of an alpha-helix microdipole. In the reduced state, the flavin in p-hydroxybenzoate hydroxylase is bound in the anionic form, i.e. carrying a negative charge at N1. The flavin is bound in a more planar configuration than when free in solution. Upon binding of substrate the resonances of N1, C10a and N10 shift upfield. It is suggested that these upfield shifts are the result of a conformational change similar, but not identical, to the one observed in the oxidized state. The 13C chemical shifts of FAD bound to apo(salicylate hydroxylase) indicate that in the oxidized state the flavin ring is also fairly solvent accessible in the free enzyme. Addition of substrate has a strong effect on the hydrogen bond formed with O4 alpha. It is suggested that this is due to the exclusion of water from the active site by the binding of substrate. In the reduced state, the flavin is anionic. Addition of substrate forces the flavin ring to adopt a more planar configuration, i.e. a sp2-hybridized N5 atom and a slightly sp3-hybridized N10 atom. The NMR results are discussed in relation to the reaction catalyzed by the enzymes.
- Published
- 1991
32. Tertiary structure of two-electron reduced Megasphaera elsdenii flavodoxin and some implications, as determined by two-dimensional 1H-NMR and restrained molecular dynamics
- Author
-
Jacob de Vlieg, Carlo P. M. van Mierlo, Philip Lijnzaad, Franz Müller, Jacques Vervoort, and Herman J. C. Berendsen
- Subjects
Models, Molecular ,Magnetic Resonance Spectroscopy ,biology ,Semiquinone ,Molecular model ,Flavodoxin ,Chemistry ,Stereochemistry ,Flavin Mononucleotide ,Hydrogen Bonding ,Nuclear Overhauser effect ,Flavin group ,Veillonellaceae ,Biochemistry ,Protein tertiary structure ,NMR spectra database ,Bacterial Proteins ,biology.protein ,Proton NMR ,Computer Graphics ,Nucleic Acid Conformation ,Oxidation-Reduction - Abstract
The tertiary structure of the non-crystallizable two-electron-reduced Megasphaera elsdenii flavodoxin (15 kDa, 137 amino acid residues) has been determined using nuclear Overhauser enhancement restraints extracted from two-dimensional 1H-NMR spectra. A tertiary structure satisfying the experimental restraints very well (maximum NOE violation of 66 pm) was obtained with use of restrained molecular dynamics, using 509 distance restraints (including one non-NOE) on a starting structure modeled from the crystal structure of one-electron-reduced Clostridium MP flavodoxin. The protein consists of a central parallel beta-sheet surrounded on both sides by two alpha-helices. The flavin is positioned at the periphery of the molecule. The tertiary structure of the protein is highly defined with the exception of the flavin. The latter is expected to result from performing the restrained molecular dynamics simulation without water molecules and without proper charges on the flavin. The flavin, including the phosphate, the ribityl side chain and the isoalloxazine ring, is solvent accessible under the experimental conditions used and evidenced by a two-dimensional amide exchange experiment. This accessibility is expected to be important in the redox potential regulation of the semiquinone/hydroquinone couple of the protein. The amide exchange against deuterons and several typical line shapes in the two-dimensional NMR spectra are consistent with the structure generated. The structure is discussed in detail.
- Published
- 1990
33. A two-dimensional 1H-NMR study on Megasphaera elsdenii flavodoxin in the oxidized state and some comparisons with the two-electron-reduced state
- Author
-
B.P.J. van der Sanden, P. van Woensel, Franz Müller, C.P.M. van Mierlo, and J.J.M. Vervoort
- Subjects
Models, Molecular ,Magnetic Resonance Spectroscopy ,Pyrazine ,Flavodoxin ,Stereochemistry ,Flavin Mononucleotide ,Protein Conformation ,Molecular Sequence Data ,Flavin mononucleotide ,Nuclear Overhauser effect ,Flavin group ,Veillonellaceae ,Biochemistry ,chemistry.chemical_compound ,Protein structure ,Amino Acid Sequence ,Binding Sites ,biology ,Molecular Structure ,Chemistry ,Quinones ,Nuclear magnetic resonance spectroscopy ,Hydroquinones ,biology.protein ,Proton NMR ,Oxidation-Reduction - Abstract
Assignments for the 137 amino acid residues of oxidized Megasphaera elsdenii flavodoxin have been made using the sequential resonance assignment procedure. Great benefit was experienced from assignments of the fully reduced protein. The secondary and tertiary structures of the typical alpha/beta protein remain virtually identical on going from the oxidized to the two-electron-reduced state as judged from two-dimensional NOE spectroscopy. However, functionally important conformation changes in the flavin-binding region do occur on reduction. Considerable reduction-state-dependent chemical shift variations of protons in the immediate vicinity of the isoalloxazine moiety take place. From analysis of these shifts, it can be concluded that ring current effects of the pyrazine part of the flavin diminish on two-electron reduction.
- Published
- 1990
34. A 31P-nuclear-magnetic-resonance study of NADPH-cytochrome-P-450 reductase and of the Azotobacter flavodoxin/ferredoxin-NADP+ reductase complex
- Author
-
Franz Müller, Dale E. Edmondson, Jacques Vervoort, and Peter J. M. Bonants
- Subjects
animal structures ,Magnetic Resonance Spectroscopy ,Semiquinone ,Stereochemistry ,Flavodoxin ,Flavin Mononucleotide ,Swine ,Flavin group ,Reductase ,Biochemistry ,Pyrophosphate ,Cofactor ,chemistry.chemical_compound ,Animals ,NADH, NADPH Oxidoreductases ,NADPH-Ferrihemoprotein Reductase ,chemistry.chemical_classification ,Binding Sites ,biology ,Flavoproteins ,Phosphorus ,Ferredoxin-NADP Reductase ,Enzyme ,chemistry ,Azotobacter ,biology.protein ,Flavin-Adenine Dinucleotide ,Microsomes, Liver ,Rabbits ,Ferredoxin—NADP(+) reductase ,Protein Binding - Abstract
31P-nuclear-magnetic-resonance spectroscopy has been employed to probe the structure of the detergent-solubilized form of liver microsomal NADPH--cytochrome-P-450 reductase. In addition to the resonances due to the FMN and FAD coenzymes, additional phosphorus resonances are observed and are assigned to the tightly bound adenosine 2'-phosphate (2'-AMP) and to phospholipids. The phospholipid content was found to vary with the preparation; however, the 2'-AMP resonance was observed in all preparations tested. In agreement with published results [Otvos et al. (1986) Biochemistry 25, 7220-7228] for the protease-solubilized enzyme, the addition of Mn(II) to the oxidized enzyme did not result in any observable line-broadening of the FMN and FAD phosphorus resonances. The phospholipid resonances, however, were extensively broadened and the line width of the phosphorus resonance assigned to the bound 2'-AMP was broadened by approximately 70 Hz. The data show that only the phosphorus moieties of the phospholipids and the 2'-AMP, but not the flavin coenzymes are exposed to the bulk solvent. Removal of the FMN moiety from the enzyme substantially alters the 31P-NMR spectrum as compared with the native enzyme. The 2'-AMP is removed from the enzyme during the FMN-depletion procedure and the pyrophosphate resonances of the bound FAD are significantly altered. Reconstitution of the FMN-depleted protein with FMN results in the restoration of the coenzyme spectral properties. Reduction of FMN to its air-stable paramagnetic semiquinone form results in broadening of the FMN and 2'-AMP resonances in the detergent-solubilized enzyme. In agreement with previous results. FMN semiquinone formation had little or no effect on the line width of the FMN phosphorus resonance for the proteolytically solubilized enzyme. 31P-NMR experiments with Azotobacter flavodoxin semiquinone, both in its free form and in a complex with spinach ferredoxin-NADP+ reductase, mimic the differential paramagnetic effects of the flavin semiquinone on the line width of the FMN phosphorus resonance, observed by comparison of the detergent-solubilized and protease-solubilized forms of the reductase. The data demonstrate that assignment of the site of flavin semiquinone formation to a particular flavin coenzyme may not always be possible by 31P-NMR experiments in multi-flavin containing enzymes.
- Published
- 1990
35. The Purification and Properties of Cyclohexanone Oxygenase from Nocardia globerula CL1 and Acinetobacter NCIB 9871
- Author
-
Peter W. Trudgill, David B. Norris, and Nuala A. Donoghue
- Subjects
Oxygenase ,Spectrophotometry, Infrared ,Flavin Mononucleotide ,Stereochemistry ,Cyclohexanone ,Flavin group ,Biochemistry ,Nocardia ,Mixed Function Oxygenases ,chemistry.chemical_compound ,Oxygen Consumption ,Species Specificity ,Cyclopentanone monooxygenase ,Oxidoreductase ,Sulfhydryl Compounds ,Amino Acids ,chemistry.chemical_classification ,Acinetobacter ,Substrate (chemistry) ,Molecular Weight ,Kinetics ,Spectrometry, Fluorescence ,Enzyme ,chemistry ,Spectrophotometry ,Flavin-Adenine Dinucleotide ,Spectrophotometry, Ultraviolet ,Crystallization ,Protein Binding - Abstract
1 Cyclohexanone oxygenases from Nocardia globerula CL1 and Acinetobacter NCIB 9571 have been purified 12-fold and 35-fold respectively and each gives a single symmetrical sedimentation peak in the ultracentrifuge and a single protein band on 2.25 nm average pore radius polyacrylamide gels. 2 The enzyme from N. globerula has a molecular weight of 53000 while that from Acinetobacter has a molecular weight of about 59000. Each is a single polypeptide chain with one mole of bound FAD per mole of protein that does not dissociate during purification. Acidification of the Acinetobacter enzyme in the presence of (NH4)2SO4 releases the bound FAD and yields native apoenzyme from which the active holoenzyme can be reconstituted. The apparent dissociation constant for the FAD is 40 nM. 3 The near unitary stoichiometry of cyclohexanone, NADPH and oxygen consumption is typical of mixed function oxygenases with external electron donors. The oxygenated product has been identified as 1-oxa-2-oxocycloheptane thus placing these enzymes in the small group of lactone and ester-forming oxygenases. Their correct systematic name is cyclohexanone. NADPH: oxygen oxidoreductase (1,2-lactonizing) (EC 1.14.13.-). 4 A functionally essential sulfhydryl group is present at the catalytic centre of both enzymes but there is no reliable indication from inhibitor studies that they contain any functional metal ion. The three titratable sulfhydryl groups of the Acinetobacter enzyme are not equivalent since reaction with one of them selectively inhibits catalytic activity. Protection against sulfhydryl active agents is afforded by NADPH but not by cyclohexanone. 5 The N. globerula enzyme has a pH optimum of 8.4, apparent Km values of 1.56 μM and 31.3 μM for cyclohexanone and NADPH respectively and a catalytic centre activity of 1018 ml substrate transformed × mol enzyme−1× min−1. The Acinetobacter enzyme has a pH optimum of 9.0, apparent Km values of 6.9 tM and 17.8 μM and a catalytic centre activity of 1390 mol × mol enzyme−1× min−1. Both enzymes display absolute specificity for electron donor which contrasts with the broad specificity for ketone substrate. 6 An enzyme-cyclohexanone complex has been detected by difference spectroscopy only in the case of the Nocardia enzyme. Rapid reduction of the enzyme-bound FAD occurs upon addition of NADPH in the absence of cyclohexanone. Titration of enzyme with NADPH under anaerobic conditions and anaerobic photoreduction in the presence of EDTA have not revealed the formation of any stable flavin semiquinones. 7 These enzymes bear a strong resemblance to several of the monooxygenases that hydroxylate aromatic compounds.
- Published
- 1976
36. Structural Studies of Yeast Flavocytochrome b2: Cooperative Roles of the alpha and beta Globules in the Formation of the Flavin-Binding Sites
- Author
-
Françoise Labeyrie, Maryvonne Mevel-Ninio, and Yanick Risler
- Subjects
Protein Denaturation ,Α subunit ,Binding Sites ,Flavoproteins ,Heme binding ,Flavin Mononucleotide ,Macromolecular Substances ,Molecular Conformation ,Heme ,Protomer ,Flavin group ,Guanidines ,Biochemistry ,Yeast ,Molecular Weight ,Fusion gene ,chemistry.chemical_compound ,chemistry ,Chromatography, Gel ,Cytochromes ,Binding site ,Guanidine ,Protein Binding - Abstract
The purpose of the study reported here was the localization of the heme binding sites on the two globular fragments, alpha and beta, of the 'cleaved' form of the flavocytochrome b2 chain. These fragments were partially resolved by means of molecular sieving under denaturing conditions (3 M or 6 M guanidine in the presence of 2-mercaptoethanol). They were then renatured in the presence of excesses of FMN and protoheme. The protoheme was found to be quantitatively bound to the alpha subunit, confirming previous findings. The flavin binds neither to alpha alone nor to beta alone, but only to the reassociated alphabeta protomer. the results are discussed in terms of the possible occurrence of gene fusion in the formation of the complex flavocytochrome chain of this very particular L-lactate cytochrome c reductase found specifically in yeasts.
- Published
- 1977
37. l-alpha-Hydroxyacid Oxidase Isozymes. Purification and Molecular Properties
- Author
-
Roger S. Holmes and John Duley
- Subjects
Protein Conformation ,Protein subunit ,Flavin mononucleotide ,Kidney ,Biochemistry ,Isozyme ,Cofactor ,chemistry.chemical_compound ,Apoenzymes ,Flavins ,Animals ,Coenzyme binding ,Sulfhydryl Compounds ,Amino Acids ,Polyacrylamide gel electrophoresis ,chemistry.chemical_classification ,Binding Sites ,biology ,Molecular mass ,Molecular biology ,Rats ,Isoenzymes ,Molecular Weight ,Alcohol Oxidoreductases ,Enzyme ,Liver ,chemistry ,Organ Specificity ,Spectrophotometry ,biology.protein ,Spectrophotometry, Ultraviolet ,Hydroxy Acids ,Protein Binding - Abstract
l-α-Hydroxyacid oxidase isozymes from rat liver (A isozyme) and kidney (B isozyme) have been isolated in a high state of purity with specific activities of 61 and 14.7 microkatals per gram protein respectively. The subunit molecular weights determined by sodium dodecylsulphate polyacrylamide gel electrophoresis were 40000 ± 3000; the mouse A and B isozymes were also partially purified and their subunit molecular weights shown to be 37000. The total amino acid contents of the two rat isozymes were very similar and had identical tyrosine (9 residues per 40000) and tryptophan (5 per 40000) contents. No free suiphydryl groups were found following suiphydryl titration experiments using the purified native rat isozymes. Following denaturation with sodium dodecylsulphate, 2 (A subunit) and 3 (B subunit) suiphydryl residues were titratable. The apoenzyme form of rat isozyme B exhibited 2 of the 3 titratable suiphydryl groups in the absence of sodium dodecylsulphate which suggests an involvement of these residues in coenzyme binding. Flavin mononucleotide content was estimated from spectral studies to be I residue per subunit (40000 molecular weight) of native enzyme. Following storage in ammonium sulphate at 4°C for several months, flavin mononucleotide was irreversibly removed such that the rat A and B isozymes contained 0.3 and 0.7 residue of coenzyme per subunit. This accounts for the more pronounced loss of specific activity following storage for the A isozyme than the B isozyme as well as the comparatively high minimal molecular weights based upon flavin mononucleotide values previously reported by other workers. This evidence for chemical homology together with the previously reported immunochemical crossreactivity for these isozymes provide evidence that the A and B polypeptides are products of recently duplicated genes during evolution.
- Published
- 1976
38. Identification of NADH-Specific and NADPH-Specific FMN Reductases in Beneckea harveyi
- Author
-
Erik Gerlo and Josée Charlier
- Subjects
chemistry.chemical_classification ,Flavin Mononucleotide ,Photobacterium ,Stereochemistry ,Temperature ,Biology ,Biochemistry ,Molecular Weight ,Kinetics ,Enzyme ,Drug Stability ,chemistry ,Bioluminescence ,NADH, NADPH Oxidoreductases ,Identification (biology) ,Thermostability - Abstract
Distinct FMN reductases specific for NADH and NADPH were identified in extracts of Beneckea harveyi. These enzymes differ in their physical (molecular weight, thermostability) as well as in their chemical properties (binding constants for NADH and NADPH). The NADH-specific enzyme is more efficient then the NADPH-specific one with respect to the bioluminescent reaction.
- Published
- 1975
39. Formate Dehydrogenase from Pseudomonas oxalaticus
- Author
-
Ulrich Müller, Peter Willnow, Ulrich Ruschig, and Thomas Höpner
- Subjects
Formates ,Flavin Mononucleotide ,Stereochemistry ,Iron ,Flavoprotein ,Flavin mononucleotide ,Formate dehydrogenase ,Photochemistry ,Biochemistry ,Catalysis ,Substrate Specificity ,chemistry.chemical_compound ,Pseudomonas ,Formate ,chemistry.chemical_classification ,biology ,Formate Dehydrogenases ,Aldehyde Oxidoreductases ,Enzyme Activation ,Molecular Weight ,Kinetics ,Enzyme ,chemistry ,biology.protein ,NAD+ kinase ,Ferricyanide - Abstract
Formate dehydrogenase (EC 1.2.1.2) from Pseudomonas oxalaticus has been isolated and characterized. The enzyme (molecular weight 315000) is a complex flavoprotein containing 2 FMN, 18--25 non-heme iron atoms and 15--20 acid-labile sulphides. In the last step of the purification, a sucrose gradient centrifugation, a second catalytically active species has been found apparently originating from a dissociation of the enzyme into two equal subunits. The enzyme is specific toward its natural substrate formate. It transfers electrons to NAD+, oxygen, ferricyanide, and a lot of nonphysiological acceptors (dyes). In addition electrons are transferred from NADH to these acceptors. The (reversible) removal of FMN requires a reduction step. Reincorporation has been followed by the reappearance of the reactivity against formate and by fluorescence titration. The deflavo enzyme also binds FAD and riboflavin. The resulting enzyme species show characteristic catalytic abilities. Activity against formate is peculiar to the FMN species.
- Published
- 1978
40. Content and localization of FMN, Fe-S clusters and nickel in the NAD-linked hydrogenase of Nocardia opaca 1b
- Author
-
Hans G. Schlegel, Richard Cammack, and Klaus Schneider
- Subjects
Hydrogenase ,Flavin Mononucleotide ,Iron ,Dimer ,chemistry.chemical_element ,Electron donor ,Photochemistry ,Biochemistry ,Redox ,Nocardia ,Absorption ,03 medical and health sciences ,chemistry.chemical_compound ,Nickel ,Oxidoreductase ,Molecule ,030304 developmental biology ,chemistry.chemical_classification ,0303 health sciences ,030302 biochemistry & molecular biology ,Electron Spin Resonance Spectroscopy ,Electron acceptor ,NAD ,Molecular Weight ,chemistry ,Electrophoresis, Polyacrylamide Gel ,Oxidoreductases ,Oxidation-Reduction ,Sulfur - Abstract
By preparative polyacrylamide gel electrophoresis at pH 8.5, and in the absence of nickel ions, two types of subunit dimers of the NAD-linked hydrogenase from Nocardia opaca 1b were separated and isolated, and their properties were compared with each other as well as with the properties of the native enzyme. The intact hydrogenase contained 14.3 ± 0.4 labile sulphur, 13.6 ± 1.1 iron and 3.8 ± 0.1 nickel atoms and approximately 1 FMN molecule per enzyme molecule. The oxidized hydrogenase showed an absorption spectrum with maxima (shoulders) at 380 nm and 420 nm and an electron spin resonance (ESR) spectrum with a signal at g= 2.01. The midpoint redox potential of the Fe-S cluster giving rise to this signal was + 25 m V. In the reduced state, hydrogenase gave characteristic low-temperature (10 – 20 K) and high-temperature (>40 K) ESR spectra which were interpreted as due to [4Fe–4S] and [2Fe–2S] clusters, respectively. The midpoint redox potentials of these clusters were determined to be -420 mV and -285 mV, respectively. The large hydrogenase dimer, consisting of subunits with relative molecular masses Mr of 64000 and 31000. contained 9.9 ± 0.4 S2− and 9.3 ± 0.5 iron atoms per protein molecule. This dimer contained the FMN molecule, but no nickel. The absorption and ESR spectra of the large dimer were qualitatively similar to the spectra of the whole enzyme. This dimer did not show any hydrogenase activity, but reduced several electron acceptors with NADH as electron donor (diaphorase activity). The small hydrogenase dimer, consisting of subunits with Mr of 56000 and 27000, was demonstrated to have substantially different properties. For iron and labile sulphur average values of 3.9 and 4.3 atoms/dimer molecule have been determined, respectively. The dimer contained, in addition, about 2 atoms of nickel and was free of flavins. In the oxidized state this dimer showed an absorption spectrum with a broad band in the 400-nm region and a characteristic ESR signal at g= 2.01. The reduced form of the dimer was ESR-silent. The small dimer alone was diaphorase-inactive and did not reduce NAD with H2, but it displayed high H2-uptake activities with viologen dyes, methylene blue and FMN, and H2-evolving activity with reduced methyl viologen. Hydrogen-dependent NAD reduction was fully restored by recombining both subunit dimers, although the reconstituted enzyme differed from the original in its activity towards artificial acceptors and the, ESR spectrum in the oxidized state.
- Published
- 1984
41. Bioluminescence emission of bacterial luciferase with 1-deaza-FMN. Evidence for the noninvolvement of N(1)-protonated flavin species as emitters
- Author
-
Manfred Kurfürst, J. Woodland Hastings, Sandro Ghisla, and Peter Macheroux
- Subjects
Flavin Mononucleotide ,Stereochemistry ,Protonation ,Flavin group ,Decanal ,Biochemistry ,Fluorescence ,Absorbance ,Kinetics ,chemistry.chemical_compound ,Spectrometry, Fluorescence ,chemistry ,Spectrophotometry ,ddc:570 ,Luminescent Measurements ,Bioluminescence ,Luciferase ,Emission spectrum ,Luciferases ,Protein Binding ,Vibrio - Abstract
The reaction of reduced 1-d-FMN with oxygen and decanal results in bioluminescence with kinetic and spectral properties similar to those of the reaction with FMNH2, even though the spectral (absorbance, fluorescence) and chemical properties of the oxidized forms differ greatly. This emission, which is about 10 - 15% as efficient as with FMNH2, is postulated to involve the intermediacy of the corresponding 4a-hydroperoxide, the fluorescence of which occurred transiently. The N(l) protonated species had been proposed as the emitter in the reaction with FMNH2, but the 1-deaza analog cannot be protonated at the corresponding position, thus excluding this possibility.
- Published
- 1989
42. Nuclear magnetic resonance studies of the old yellow enzyme. 1. 15N NMR of the enzyme recombined with 15N-labeled flavin mononucleotides
- Author
-
Heinz Rüterjans, Franz Müller, and Wolf-Dieter Beinert
- Subjects
Magnetic Resonance Spectroscopy ,Chemical Phenomena ,Flavin Mononucleotide ,Protein Conformation ,Stereochemistry ,Flavoprotein ,Flavin mononucleotide ,Ring (chemistry) ,Biochemistry ,chemistry.chemical_compound ,Apoenzymes ,Nuclear magnetic resonance ,Oxidoreductase ,Atom ,Electrochemistry ,NADH, NADPH Oxidoreductases ,chemistry.chemical_classification ,Nitrogen Isotopes ,biology ,Hydrogen bond ,NADPH Dehydrogenase ,Hydrogen Bonding ,Nuclear magnetic resonance spectroscopy ,Hydrogen-Ion Concentration ,Resonance (chemistry) ,Chemistry ,chemistry ,Isotope Labeling ,biology.protein ,Isoelectric Focusing ,Oxidation-Reduction ,Protein Binding - Abstract
The apoenzyme of NADPH oxidoreductase, ‘old yellow enzyme’, was reconstituted with specifically 15N-labeled flavin mononucleotide and investigated by 15N NMR spectroscopy in the oxidized and reduced state. The results indicate that in the oxidized state a hydrogen bond is formed between the N(5) atom and the apoprotein. In addition, hydrogen bonds exist between the N(1) and N(3) atoms of FMN and the apoprotein. The resonance position of N(10) indicates that this atom is somewhat sp3-hybridized, i.e. lifted out of the molecular plane of the isoalloxazine ring system. In the reduced state the N(1) atom is negatively charged and the N(3) atom forms a hydrogen bond with the apoprotein. The N(10) atom in protein-bound FMN exhibits about the same hybridization state as in free anionic reduced FMN, i.e. it is located in the plane of the isoalloxazine ring. The chemical shift of the N(5) resonance indicates that this atom is almost completely sp3-hybridized. This interpretation can also be derived from the 15N(5)-1H coupling constant. Among the flavoproteins thus far studied by NMR techniques, old yellow enzyme is the only protein that shows a conformation of the reduced prosthetic group with the N(5) atom lifted out of the molecular plane. The isoelectric focussing properties of old yellow enzyme and a new easy method for the preparation of the apoprotein are also reported.
- Published
- 1985
43. Characterization of the Flavoenzyme Enoyl Reductase of Fatty Acid Synthetase from Yeast
- Author
-
Feodor Lynen and J. Lawrence Fox
- Subjects
Fatty Acid Desaturases ,chemistry.chemical_classification ,Circular dichroism ,Flavin Mononucleotide ,Protein Conformation ,Stereochemistry ,Circular Dichroism ,Fatty acid ,Saccharomyces cerevisiae ,Flavin group ,Reductase ,Biochemistry ,Redox ,Yeast ,Spectrometry, Fluorescence ,Enzyme ,chemistry ,Spectrophotometry ,Fatty Acid Synthases ,Binding site ,Oxidation-Reduction ,Protein Binding - Abstract
Enoyl reductase in the fatty acid synthetase from brewer's yeast, a flavoenzyme function, has been used as a specific probe for one partial activity of the multi-functional enzyme. The enzyme has an absorption maximum at 460 nm with epsilon = 18600 M-1 cm-1 and A280 = 1.37 mg-1 ml. The circular dichroism spectrum shows negative peaks at 373 and 466 nm. The fluorescence maximum is at 540 nm. The apoenzyme has an absorption maximum at 279 nm and shows fluorescence at 345 nm. The association constant for the FMN is 4 X 10(7) M-1. The redox potential was determined as Eh = --0.193 V. The reductase is characterized as a 'true' transhydrogenase as no flavin free radical can be obtained by photochemical or chemical reduction or oxidation, i.e. it only functions via two-electron steps. An interpretation of the hydrophobic nature of the flavin binding site based on spectral data is presented.
- Published
- 1980
44. The Dissociation of Flavin Coenzymes from Trypsin-Solubilized NADPH/Cytochrome c (P-450) Reductase of Pig-Liver Microsomes
- Author
-
Gordon E. Trout
- Subjects
Flavin Mononucleotide ,Swine ,Flavin group ,Reductase ,Photochemistry ,Biochemistry ,Cofactor ,Dissociation (chemistry) ,Reaction rate constant ,Animals ,Cytochrome Reductases ,NADPH-Ferrihemoprotein Reductase ,chemistry.chemical_classification ,biology ,Chemistry ,Cytochrome c ,Osmolar Concentration ,Hydrogen-Ion Concentration ,Kinetics ,Enzyme ,Computers, Analog ,Ionic strength ,Flavin-Adenine Dinucleotide ,Microsomes, Liver ,biology.protein ,Chloromercuribenzoates - Abstract
The change in fluorescence emission at 520 nm after excitation at 365 nm was used to investigate the effect of pH and ionic strength on the dissociation of flavin cofactors from microsomal NADPH/cytochrome c (P-450) reductase. In the unmodified enzyme both the FAD and FMN moieties appeared to dissociate at a similar rate and followed first-order kinetics. The rate constant for the dissociation was increased by low pH and high ionic strength, particularly in the range pH 4.4–3.8 (0.02 M acetate buffer) where the rate constants increased 80-fold. Modification of the enzyme by treatment with p-chloromercuribenzoate enhanced the rate of flavin dissociation and, in the region of pH 4, resulted in a biphasic increase in fluorescence consistent with two simultaneous parallel first-order dissociations. It was concluded that p-chloromercuribenzoate treatment modified the protein so that the two flavin cofactors dissociated at different rates. Using the measured rate constants for the dissociations, and the known variation in fluorescence of flavin nucleotides with pH, an analogue computer simulation of the dissociation as well as a manual curve-fitting procedure showed that the biphasic response could be explained as a simultaneous rapid dissociation of FAD and a slower loss of FMN from the protein.
- Published
- 1976
45. A 13C Nuclear-Magnetic-Resonance Study on Free Flavins and Megasphaera elsdenii and Azotobacter vinelandii Flavodoxin. 13C-Enriched Flavins as Probes for the Study of Flavoprotein Active Sites
- Author
-
Franz Müller and Cees G. Van Schagen
- Subjects
Magnetic Resonance Spectroscopy ,Flavin Mononucleotide ,Flavodoxin ,Riboflavin ,Flavin group ,Veillonellaceae ,Photochemistry ,Biochemistry ,Acid dissociation constant ,Nuclear magnetic resonance ,Flavins ,Molecule ,Binding Sites ,Aqueous solution ,Flavoproteins ,biology ,Hydrogen bond ,Chemistry ,Chemical shift ,Hydrogen-Ion Concentration ,biology.organism_classification ,Azotobacter vinelandii ,Azotobacter ,biology.protein ,Oxidation-Reduction - Abstract
Selectively 13C-enriched free and protein-bound flavins in the oxidized and two-electron reduced state were investigated by the 13 C nuclear magnetic resonance technique. FMN in aqueous solution and N-(3)-menthyl-2′,3′4,'5′-tetraacetylriboflavin in an apolar solvent were used as reference compounds for the protein-bound FMN A comparison of th chemical shifts of FMN in aqueous solution with those of N(3)-methyltetraacetyl- riboglavin in CHCL3 reveals that FMN is strongly polarized yielding a pseudo-ionic molecule stabilized by hydrogen bonding of H2O with C-2α of the isoalloxazine molecule. The interpretation is fully supported by the one-bond)1J) 13C coupling constants. The chemical shifts combined with the coupling constants indicate the change of charge distribution within the molecule when going from apolar to polar solutions Binding of FMN to Megasphaera elsdenii and to Azotobacter vinelandii apoflavodoxins affects the resonances due to C-2 and C-10 a as compared to free FMN.These shifts together with the coupling constants indicate the formation of a hydrogen bound between C-2α of FMN and an amino acid residue of the apoprotein. In M. Elsdenii flavodoxin such a hydrogen bond also exists with C-4α which is not observed in A vinelandii flavodoxin. The chemical shifts to the two-electron reduced derivatives of FMN and N(3)menthyl-2′,3′,4′,5′,-tetraacetyl- riboflavin clearly indicate that the FMN derivative possesses a more planar conformation than its analog; it shows pH-independent, From the pH-dependence of the chemical shifts of the atoms C-10a, C-2 and C-4a. The chemical shift of C-4 is pH-independent. From the pH- dependence of the chemical shifts an ionization constant of 6.7 is calculated. The chemical shifts of protein-bound FMN in the reduced state are very similar to those of the anionic, reduced FMN. The data show that in both flavodoxins studied the prosthetic group when reduced is bound in the anionic form an possesses approximately a coplanar confornation. The results are discussed with respect to the possible biological implications. It is suggested that specific interaction of the prosthetic group with the apoprotein, the ionization state and the degree of planarity of the reduced prosthetic group are factors determining the biological functions of flavodoxins and possibly the functions of flavoproteins in general.
- Published
- 1981
46. A comparative study on iron sources for mitochondrial haem synthesis including ferritin and models of transit pool species
- Author
-
Felix Funk, Walter Schneider, Emmanuel Lesuisse, Robert R. Crichton, and Cécile Lecrenier
- Subjects
Flavin Mononucleotide ,Iron ,Ferrozine ,Mitochondria, Liver ,Heme ,Mitochondrion ,Biochemistry ,Electron Transport Complex IV ,chemistry.chemical_compound ,Animals ,Horses ,Bovine serum albumin ,Monoamine Oxidase ,biology ,digestive, oral, and skin physiology ,Substrate (chemistry) ,Rats, Inbred Strains ,Rats ,Ferritin ,Kinetics ,Mitochondrial respiratory chain ,Models, Chemical ,chemistry ,Ferritins ,biology.protein ,Sorbitol ,Bacterial outer membrane ,Spleen ,Intracellular ,Phenanthrolines - Abstract
The rates of reaction of various exogenic iron(III) complexes with deuteroporphyrin IX in isolated mitochondria to form deuterohaem were measured. Ferritin was shown to supply iron readily for haem synthesis if the ferritin iron was reductively mobilised by the mitochondrial respiratory chain with succinate as substrate and FMN as mediator. In contrast, polynuclear complexes of iron(III) were able to form deuterohaem without added FMN. Rates of haem formation are about five times higher for the lowest polynuclear units than for ferritin. Sorbitol, gluconate, and bovine serum albumin were used as scavengers for polynuclear complexes with restricted size. Strong chelators of iron(II) compete favourably for deuterohaem formation, which supports the multistep mechanism for haem formation suggested by a priori arguments. Rates of deuterohaem formation were measured in homologous and heterologous systems of ferritins and mitochondria. Slightly differing rates of haem formation were shown to originate in different rates of iron mobilisation from the ferritins. The lack of species specificity in the interaction of ferritin with mitochondria also shows up in the linear dependence of ferritin binding on its bulk concentration as measured using 3H-labeled ferritin. Rates of haem formation are virtually the same in mitoplasts and mitochondria which indicates insignificant influences of the outer membrane. The hypothesis of low polynuclears as major components of the intracellular transit iron pool implies that both ferritin and transit iron pool species are largely equivalent sources of iron for mitochondrial haem synthesis.
- Published
- 1986
47. Biosynthesis of Vitamin B12. Some Properties of the 5, 6-Dimethylbenzimidazole-Forming System of Propionibacterium freudenreichii and Propionibacterium shermanii
- Author
-
Paul Renz and Joachim Hörig
- Subjects
Niacinamide ,biology ,Nicotinamide ,Flavin Mononucleotide ,Propionibacterium freudenreichii ,Riboflavin ,Propionibacterium ,Nicotinic Acids ,Flavin mononucleotide ,Substrate (chemistry) ,biology.organism_classification ,Biochemistry ,Vitamin B 12 ,chemistry.chemical_compound ,Dimethylbenzimidazole ,chemistry ,Biosynthesis ,Flavin-Adenine Dinucleotide ,Benzimidazoles - Abstract
1. Homogenates of Propionibacterium freudenreichii transform riboflavin into 5,6-dimethylbenzimidazole. This process is stimulated by nicotinamide. Homogenates of Propionibacterium shermanii form only small amounts of 5,6-dimethylbenzimidazole from riboflavin in the absence of nicotinamide, but also form appreciable amounts in the presence of nicotinamide. 2. The stimulation of the 5,6-dimethylbenzimidazole-forming system by nicotinamide shows a lag phase which is abolished by preincubation of the homogenate with nicotinamide. Since no lag phase is observed when nicotinamide is replaced by nicotinate, nicotinate seems to be the true stimulating agent. These observations are in agreement with the fact that nicotinamide is rapidly split to nicotinate in homogenates of P. freudenreichii. 3. The 5,6-dimethylbenzimidazole-forming homogenate system is only active at a high buffer concentration (0.3--0.5 M) and in the presence of oxygen. The system has a pronounced oxygen optimum. 4. Flavin mononucleotide and flavin-adenine dinucleotide are better substrates for the 5,6-dimethylbenzimidazole-forming homogenate system than riboflavin. But with [1'-14C]riboflavin as substrate the specific radioactivity of 5,6-dimethylbenzimidazole is higher than the specific radioactivity of flavin--adenine dinucleotide and lower than the specific radioactivie substrate for the formation of 5,6-dimethylbenzimidazole. 5. A tentative reaction sequence for the transformation of flavin mononucleotide into 5,6-dimethylbenzimidazole is discussed.
- Published
- 1980
48. Hydrolysis and rearrangement reactions of riboflavin phosphates. An explicit kinetic study
- Author
-
Jakob Harksen, Adelbert Bacher, and Peter Nielsen
- Subjects
Aqueous solution ,Flavin Mononucleotide ,Hydrolysis ,Inorganic chemistry ,Kinetics ,Riboflavin ,Hydrogen-Ion Concentration ,Phosphate ,Photochemistry ,Biochemistry ,High-performance liquid chromatography ,Catalysis ,chemistry.chemical_compound ,Reaction rate constant ,Isomerism ,chemistry ,Isomerization ,Chromatography, High Pressure Liquid ,Mathematics - Abstract
Four isomeric monophosphates and five isomeric bisphosphates of riboflavin were isolated from commercial FMN or were prepared by acid-catalyzed isomerization. The reaction of riboflavin monophosphates in aqueous solution was studied in the pH range between 0 and 9 under various conditions. The predominant reaction at pH values below 2 is the acid-catalyzed migration of the phosphate group. A detailed kinetic study of this reaction was performed by high pressure liquid chromatography. Experimental data were fitted with computer-generated curves based on an algorithm for a network of first-order reactions. Rate constants and activation parameters were obtained for the temperature range of 50-80 degrees C at pH 1. At thermodynamic equilibrium, the reaction mixture contains about 66% 5'-phosphate, 11% 4'-phosphate, 8% 3'-phosphate, and 15% 2'-phosphate (pH 1.0, 50 degrees C). In the pH range between 3 and 7, the hydrolysis of FMN is the prevailing reaction with a rate maximum at about pH 4. The same experimental approach was used in a subsequent kinetic study on the isomerization of riboflavin bisphosphates. The formation of five out of six possible isomers was studied quantitatively and rate constants for each partial reaction were obtained.
- Published
- 1985
49. Characterization of an FMN-containing cyclohexanone monooxygenase from a cyclohexane-grown Xanthobacter sp
- Author
-
R. Martin Buckland, Michael K. Trower, and Martin Griffin
- Subjects
Cyclohexane ,Flavin Mononucleotide ,Macromolecular Substances ,Stereochemistry ,Cyclohexanone ,Flavoprotein ,Flavin group ,Biochemistry ,Cofactor ,Substrate Specificity ,chemistry.chemical_compound ,Oxidoreductase ,Chromatography, High Pressure Liquid ,chemistry.chemical_classification ,Chromatography ,Gram-Negative Aerobic Bacteria ,biology ,Chemistry ,Monooxygenase ,Chromatography, Ion Exchange ,Enzyme assay ,Molecular Weight ,Kinetics ,Durapatite ,Spectrophotometry ,Chromatography, Gel ,Oxygenases ,biology.protein ,Electrophoresis, Polyacrylamide Gel ,Hydroxyapatites ,Oxidation-Reduction - Abstract
A soluble cyclohexanone monooxygenase was purified 16.1-fold to homogeneity from a Xanthobacter sp. grown upon cyclohexane as sole source of carbon and energy. The native enzyme is a 50-kDa single polypeptide chain associated with FMN rather than FAD as flavin prosthetic group in a 1:1 stoichiometric relationship. The monooxygenase catalyses the transformation of cyclohexanone to the lactone 1-oxa-2-oxocycloheptane in an oxygen ring insertion reaction. Only related cycloalkanone substrates are accepted for oxygenation, no activity is shown towards straight-chain alkanones. Enzyme activity is strongly inhibited by sulphydryl-reactive agents, but is relatively insensitive to metal chelators, electron transport inhibitors and the metal ions Fe3+ and Cu2+. Cyclohexanone monooxygenase has Km values for cyclohexanone and NADPH of less than 0.5 microM and 12.5 microM respectively. Kinetic investigations under steady-state conditions demonstrate that the flavoprotein prosthetic group, FMN, is involved in the monooxygenase catalytic mechanism. The systematic name for the enzyme is cyclohexanone, NADPH:oxygen oxidoreductase (6-hydroxylating, 1,2-lactonizing) (EC 1.14.13.22).
- Published
- 1989
50. Synthesis, Separation, Identification and Interconversion of Riboflavin Phosphates and Their Acetyl Derivatives: A Reinvestigation
- Author
-
Peter Hemmerich and Gisela Scola-Nagelschneider
- Subjects
chemistry.chemical_classification ,Chemical Phenomena ,biology ,Flavin Mononucleotide ,Flavodoxin ,Riboflavin ,Mineral acid ,Acetylation ,Flavin group ,Phosphate ,Biochemistry ,Catalysis ,Chemistry ,Hydrolysis ,chemistry.chemical_compound ,Organophosphorus Compounds ,chemistry ,Flavins ,Yield (chemistry) ,biology.protein ,Organic chemistry - Abstract
A reinvestigation of flavin phosphate synthesis, separation, identification, and interconversion was made in view of contradictory results in the literature. It has been confirmed that monochlorophosphoric acid is the best agent for selective 5′-monophosphorylation of riboflavin and derivatives. This reaction yields, however, invariably up to 20% of an isomer, which has been separated by preparative thick-layer chromatography and shown to be the 4′-monophosphate. All the earlier authors failed to detect this isomer which does not bind to flavodoxin. It equilibrates in dilute mineral acid to yield an 8:2 mixture of 5′-phosphate to 4′-phosphate by phosphate migration. The formation of 2′,3′,4′-triacetyl-flavin mononucleotide, according to Christie, S. M. H., Kenner, G. W. & Todd, A. R. (1954) J. Chem. Soc., 46–52, upon acid-catalysed acetylation of pure FMN, was confirmed. The same reaction under base catalysis, however, does not yield 2′,3′,4′-triacetyl-flavin mononucleotide as claimed by Khomutova, E. D., Shapiro, T. A., Mezentseva, M. V. & Berezovskii, V. M. (1965) Otd. Ohshch. i Tekhn. Khim., 241–244, Chem. Absir. 65, 5516a, but in fact up to 80% 2′,3′-diacetyl-flavin 4′: 5′-cyclophosphate as the main product, which is stable under neutral and weak acidic conditions and does not hydrolyse to 2′,3′-diacetyl-flavin 5′-monophosphate as claimed by McCormick, D. B. (1974) J. Heterocycl. Chem. 11, 969–974. The various flavin phosphates and their acetyl derivatives have been identified by pH-titration, electrophoresis, and proton magnetic resonance spectrometry, which permit direct analyses of crude reaction products as well as a rapid purity check of commercial FMN.
- Published
- 1976
Catalog
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