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Synthesis of a non-natural glucose-2-phosphate ester able to dupe the acc system of Agrobacterium fabrum
- Source :
- Organic and Biomolecular Chemistry, Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (5), pp.1090--1096. ⟨10.1039/c8ob03086c⟩, Organic & Biomolecular Chemistry, Organic & Biomolecular Chemistry, 2019, 17 (5), pp.1090--1096. ⟨10.1039/c8ob03086c⟩
- Publication Year :
- 2019
- Publisher :
- HAL CCSD, 2019.
-
Abstract
- International audience; The first non-natural derivative of the rare D-glucose-2-phosphate (G2P), namely glucose-2-(O-lactic acid phosphate) (G2LP), has been synthesized. When used as sole carbon source, G2LP enables bacterial growth of the plant pathogenic strain Agrobacterium fabrum C58 (formerly referred to as Agrobacterium tumefa-ciens). X-ray crystallography and affinity measurements investigations reveal that G2LP binds the periplasmic binding protein (PBP) AccA similarly to the natural compounds and with the same affinity. Moreover, enzy-matic assays show that it is able to serve as substrate of the phosphodiesterase AccF. The properties found for G2LP demonstrate that the very unusual glucose-2-phosphoryl residue, present in G2LP, can be used as structural feature for designing non-natural systems fully compatible with the Acc cascade of A. fabrum.
- Subjects :
- plasmids
[SDV]Life Sciences [q-bio]
Agrobacterium
Crystallography, X-Ray
01 natural sciences
Biochemistry
Substrate Specificity
03 medical and health sciences
Residue (chemistry)
chemistry.chemical_compound
Hydrolysis
Bacterial Proteins
diesters
Physical and Theoretical Chemistry
030304 developmental biology
phosphate
0303 health sciences
opines
biology
Phosphoric Diester Hydrolases
010405 organic chemistry
Chemistry
Binding protein
Organic Chemistry
Glucosephosphates
Substrate (chemistry)
Phosphodiesterase
Esters
Agrobacterium tumefaciens
Periplasmic space
Phosphate
biology.organism_classification
0104 chemical sciences
hydrolysis
Periplasmic Binding Proteins
glycogen
Subjects
Details
- Language :
- English
- ISSN :
- 14770520 and 14770539
- Database :
- OpenAIRE
- Journal :
- Organic and Biomolecular Chemistry, Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (5), pp.1090--1096. ⟨10.1039/c8ob03086c⟩, Organic & Biomolecular Chemistry, Organic & Biomolecular Chemistry, 2019, 17 (5), pp.1090--1096. ⟨10.1039/c8ob03086c⟩
- Accession number :
- edsair.doi.dedup.....190fb8288444b25f2d4a62e6dbaddec6