25 results on '"Jenke-Kodama H"'
Search Results
2. Domain configuration and phylogeny of fatty acid synthases and polyketide synthase-like proteins in protists: P27-127
- Author
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Jenke-Kodama, H., Yamaguchi, A., and Tamura, M.
- Published
- 2012
3. Emulating evolutionary processes to morph aureothin-type modular polyketide synthases and associated oxygenases.
- Author
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Peng H, Ishida K, Sugimoto Y, Jenke-Kodama H, and Hertweck C
- Subjects
- Amino Acid Sequence, Anti-Bacterial Agents chemistry, Anti-Bacterial Agents metabolism, Chromones chemistry, Genetic Engineering methods, Models, Chemical, Molecular Structure, Mutation, Phylogeny, Polyketide Synthases classification, Polyketide Synthases genetics, Polyketides chemistry, Streptomyces genetics, Chromones metabolism, Oxygenases metabolism, Polyketide Synthases metabolism, Polyketides metabolism, Streptomyces metabolism
- Abstract
Polyketides produced by modular type I polyketide synthases (PKSs) play eminent roles in the development of medicines. Yet, the production of structural analogs by genetic engineering poses a major challenge. We report an evolution-guided morphing of modular PKSs inspired by recombination processes that lead to structural diversity in nature. By deletion and insertion of PKS modules we interconvert the assembly lines for related antibiotic and antifungal agents, aureothin (aur) and neoaureothin (nor) (aka spectinabilin), in both directions. Mutational and functional analyses of the polyketide-tailoring cytochrome P450 monooxygenases, and PKS phylogenies give contradictory clues on potential evolutionary scenarios (generalist-to-specialist enzyme evolution vs. most parsimonious ancestor). The KS-AT linker proves to be well suited as fusion site for both excision and insertion of modules, which supports a model for alternative module boundaries in some PKS systems. This study teaches important lessons on the evolution of PKSs, which may guide future engineering approaches.
- Published
- 2019
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4. Unlocking the Spatial Control of Secondary Metabolism Uncovers Hidden Natural Product Diversity in Nostoc punctiforme.
- Author
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Dehm D, Krumbholz J, Baunach M, Wiebach V, Hinrichs K, Guljamow A, Tabuchi T, Jenke-Kodama H, Süssmuth RD, and Dittmann E
- Subjects
- Carbon Dioxide metabolism, Fermentation, Genes, Bacterial, Light, Mutation, Nostoc genetics, Secondary Metabolism, Signal Transduction, Transcriptome, Biological Products metabolism, Nostoc metabolism
- Abstract
Filamentous cyanobacteria belong to the most prolific producers of structurally unique and biologically active natural products, yet the majority of biosynthetic gene clusters predicted for these multicellular collectives are currently orphan. Here, we present a systems analysis of secondary metabolite gene expression in the model strain Nostoc punctiforme PCC73102 using RNA-seq and fluorescence reporter analysis. Our data demonstrate that the majority of the cryptic gene clusters are not silent but are expressed with regular or sporadic pattern. Cultivation of N. punctiforme using high-density fermentation overrules the spatial control and leads to a pronounced upregulation of more than 50% of biosynthetic gene clusters. Our data suggest that a combination of autocrine factors, a high CO
2 level, and high light account for the upregulation of individual pathways. Our overarching study not only sheds light on the strategies of filamentous cyanobacteria to share the enormous metabolic burden connected with the production of specialized molecules but provides an avenue for the genome-based discovery of natural products in multicellular cyanobacteria as exemplified by the discovery of highly unusual variants of the tricyclic peptide microviridin.- Published
- 2019
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5. Profiling soil microbial communities with next-generation sequencing: the influence of DNA kit selection and technician technical expertise.
- Author
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Soliman T, Yang SY, Yamazaki T, and Jenke-Kodama H
- Abstract
Structure and diversity of microbial communities are an important research topic in biology, since microbes play essential roles in the ecology of various environments. Different DNA isolation protocols can lead to data bias and can affect results of next-generation sequencing. To evaluate the impact of protocols for DNA isolation from soil samples and also the influence of individual handling of samples, we compared results obtained by two researchers (R and T) using two different DNA extraction kits: (1) MO BIO PowerSoil
® DNA Isolation kit (MO_R and MO_T) and (2) NucleoSpin® Soil kit (MN_R and MN_T). Samples were collected from six different sites on Okinawa Island, Japan. For all sites, differences in the results of microbial composition analyses (bacteria, archaea, fungi, and other eukaryotes), obtained by the two researchers using the two kits, were analyzed. For both researchers, the MN kit gave significantly higher yields of genomic DNA at all sites compared to the MO kit (ANOVA; P < 0.006). In addition, operational taxonomic units for some phyla and classes were missed in some cases: Micrarchaea were detected only in the MN_T and MO_R analyses; the bacterial phylum Armatimonadetes was detected only in MO_R and MO_T; and WIM5 of the phylum Amoebozoa of eukaryotes was found only in the MO_T analysis. Our results suggest the possibility of handling bias; therefore, it is crucial that replicated DNA extraction be performed by at least two technicians for thorough microbial analyses and to obtain accurate estimates of microbial diversity., Competing Interests: The authors declare there are no competing interests.- Published
- 2017
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6. Diversity of Microbial Communities and Quantitative Chemodiversity in Layers of Marine Sediment Cores from a Causeway (Kaichu-Doro) in Okinawa Island, Japan.
- Author
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Soliman T, Reimer JD, Yang SY, Villar-Briones A, Roy MC, and Jenke-Kodama H
- Abstract
Microbial community diversity and chemodiversity were investigated in marine sediments adjacent to the Okinawan "Kaichu-Doro" Causeway, which was constructed 46 years ago to connect a group of four islands (Henza-jima, Miyagi-jima, Ikei-jima, Hamahiga-jima) to the Okinawan main island. This causeway was not built on pilings, but by land reclamation; hence, it now acts as a long, thin peninsula. The construction of this causeway was previously shown to have influenced the surrounding marine ecosystem, causing ecosystem fragmentation and loss of water circulation. In this study, we collected sediment cores ( n = 10) from five paired sites in 1 m water depths. Each pair of sites consisted of one site each on the immediate north and south sides of the causeway. Originally the members of each pair were much closer to each other (<150 m) than to other pairs, but now the members of each pair are isolated by the causeway. Each core was 60-80 cm long and was divided into 15-cm layers. We examined the vertical diversity of microbial communities and chemical compounds to determine the correlation between chemodiversity and microbial communities among marine sediment cores and layers. Principal coordinate analyses (PCoA) of detected compounds and of bacterial and archaeal operational taxonomic units (OTUs) revealed that the north and south sides of the causeway are relatively isolated, with each side having unique microbial OTUs. Additionally, some bacterial families (e.g., Acidaminobacteraceae, Rhizobiaceae, and Xanthomonadaceae) were found only on the south side of Kaichu-Doro. Interestingly, we found that the relative abundance of OTUs for some microbial families increased from top to bottom, but this was reversed in some other families. We conclude that the causeway has altered microbial community composition and metabolite profiles in marine sediments.
- Published
- 2017
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7. Comparative population genetic structure of redbelly tilapia ( Coptodon zillii (Gervais, 1848)) from three different aquatic habitats in Egypt.
- Author
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Soliman T, Aly W, Fahim RM, Berumen ML, Jenke-Kodama H, and Bernardi G
- Abstract
Recently, tilapia have become increasingly important in aquaculture and fisheries worldwide. They are one of the major protein sources in many African countries and are helping to combat malnutrition. Therefore, maintenance and conservation genetics of wild populations of tilapia are of great significance. In this study, we report the population genetic structure and genetic diversity of the redbelly tilapia ( Coptodon zillii ) in three different Egyptian aquatic environments: brackish (Lake Idku), marine (Al-Max Bay), and freshwater (Lake Nasser). The habitat differences, environmental factors, and harvesting pressures are the main characteristics of the sampling sites. Three mitochondrial DNA markers (COI: cytochrome oxidase subunit I; the D-loop; CYTB: cytochrome b) were used to assess population structure differences among the three populations. The population at Lake Nasser presented the highest genetic diversity ( H
d = 0.8116, H = 6), and the marine population of Al-Max Bay the lowest ( Hd = 0.2391, H = 4) of the combined sequences. In addition, the phylogenetic haplotype network showed private haplotypes in each environmental habitat. Results presented here will be useful in aquaculture to introduce the appropriate broodstock for future aquaculture strategies of C. zillii . In addition, evidence of population structure may contribute to the management of tilapia fisheries in Egyptian waters.- Published
- 2017
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8. Genomics-Guided Exploitation of Lipopeptide Diversity in Myxobacteria.
- Author
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Burgard C, Zaburannyi N, Nadmid S, Maier J, Jenke-Kodama H, Luxenburger E, Bernauer HS, and Wenzel SC
- Subjects
- Multigene Family, Myxococcales metabolism, Genomics, Lipopeptides metabolism, Myxococcales genetics
- Abstract
Analysis of 122 myxobacterial genome sequences suggested 16 strains as producers of the myxochromide lipopeptide family. Detailed sequence comparison of the respective mch biosynthetic gene clusters informed a genome-mining approach, ultimately leading to the discovery and chemical characterization of four novel myxochromide core types. The myxochromide megasynthetase is subject to evolutionary diversification, resulting in considerable structural diversity of biosynthesis products. The observed differences are due to the number, type, sequence, and configuration of the incorporated amino acids. The analysis revealed molecular details on how point mutations and recombination events led to structural diversity. It also gave insights into the evolutionary scenarios that have led to the emergence of mch clusters in different strains and genera of myxobacteria.
- Published
- 2017
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9. Distribution of palytoxin in coral reef organisms living in close proximity to an aggregation of Palythoa tuberculosa.
- Author
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Aratake S, Taira Y, Fujii T, Roy MC, Reimer JD, Yamazaki T, and Jenke-Kodama H
- Subjects
- Acrylamides metabolism, Animals, Cnidarian Venoms, Acrylamides chemistry, Cnidaria physiology, Coral Reefs, Invertebrates chemistry, Seaweed chemistry
- Abstract
Palytoxin is a strong marine toxin that was first isolated from the zoantharian Palythoa toxica and later from other species of the genus Palythoa. How the toxin gets into the animal remains an unsolved question. To study the specificity of palytoxin distribution, the toxin content of Palythoa tuberculosa and other organisms living in close association on a coral reef in Okinawa were analysed by mass spectrometry. In contrast to earlier reports, palytoxin was only detected in P. tuberculosa colonies., (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Published
- 2016
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10. Molecular systematics of marine gregarine apicomplexans from Pacific tunicates, with descriptions of five novel species of Lankesteria.
- Author
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Rueckert S, Wakeman KC, Jenke-Kodama H, and Leander BS
- Subjects
- Animals, Apicomplexa cytology, Apicomplexa isolation & purification, DNA, Protozoan genetics, Genes, rRNA, Microscopy, Electron, Scanning, Molecular Sequence Data, Pacific Ocean, Sequence Analysis, DNA, Trophozoites cytology, Apicomplexa classification, Intestines parasitology, Phylogeny, Urochordata parasitology
- Abstract
The eugregarines are a group of apicomplexan parasites that mostly infect the intestines of invertebrates. The high level of morphological variation found within and among species of eugregarines makes it difficult to find consistent and reliable traits that unite even closely related lineages. Based mostly on traits observed with light microscopy, the majority of described eugregarines from marine invertebrates has been classified into a single group, the Lecudinidae. Our understanding of the overall diversity and phylogenetic relationships of lecudinids is very poor, mainly because only a modest amount of exploratory research has been done on the group and very few species of lecudinids have been characterized at the molecular phylogenetic level. In an attempt to understand the diversity of marine gregarines better, we surveyed lecudinids that infect the intestines of Pacific ascidians (i.e. sea squirts) using ultrastructural and molecular phylogenetic approaches; currently, these species fall within one genus, Lankesteria. We collected lecudinid gregarines from six ascidian host species, and our data demonstrated that each host was infected by a different species of Lankesteria: (i) Lankesteria hesperidiiformis sp. nov., isolated from Distaplia occidentalis, (ii) Lankesteria metandrocarpae sp. nov., isolated from Metandrocarpa taylori, (iii) Lankesteria halocynthiae sp. nov., isolated from Halocynthia aurantium, (iv) Lankesteria herdmaniae sp. nov., isolated from Herdmania momus, (v) Lankesteria cf. ritterellae, isolated from Ritterella rubra, and (vi) Lankesteria didemni sp. nov., isolated from Didemnum vexillum. Visualization of the trophozoites with scanning electron microscopy showed that four of these species were covered with epicytic folds, whereas two of the species were covered with a dense pattern of epicytic knobs. The molecular phylogenetic data suggested that species of Lankesteria with surface knobs form a clade that is nested within a paraphyletic assemblage species of Lankesteria with epicytic folds.
- Published
- 2015
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11. Effects of causeway construction on environment and biota of subtropical tidal flats in Okinawa, Japan.
- Author
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Reimer JD, Yang SY, White KN, Asami R, Fujita K, Hongo C, Ito S, Kawamura I, Maeda I, Mizuyama M, Obuchi M, Sakamaki T, Tachihara K, Tamura M, Tanahara A, Yamaguchi A, and Jenke-Kodama H
- Subjects
- Biodiversity, Biota, Construction Industry, Environment, Geologic Sediments, Japan, Risk Assessment, Transportation, Ecosystem, Environmental Monitoring, Water Pollution statistics & numerical data
- Abstract
Okinawa, Japan is known for its high marine biodiversity, yet little work has been performed on examining impacts of numerous large-scale coastal development projects on its marine ecosystems. Here, we examine apparent impacts of the construction of the Kaichu-Doro causeway, which was built over 40 years ago. The causeway is a 4.75 km long embankment that divides a large tidal flat and has only two points of water exchange along its entire length. We employed quadrats, transects, sampling, visual surveys, and microbial community analyses combined with environmental, water quality data, and 1m cores, at five stations of two paired sites each (one on each side of Kaichu-Doro) to investigate how the environment and biota have changed since the Kaichu-Doro was built. Results indicate reduction in water flow, and site S1 was particularly heavily impacted by poor water quality, with low diversity and disturbed biotic communities., (Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2015
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12. Molecular Phylogeny and Ultrastructure of Caliculium glossobalani n. gen. et sp. (Apicomplexa) from a Pacific Glossobalanus minutus (Hemichordata) Confounds the Relationships Between Marine and Terrestrial Gregarines.
- Author
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Wakeman KC, Reimer JD, Jenke-Kodama H, and Leander BS
- Subjects
- DNA, Ribosomal genetics, Apicomplexa classification, Apicomplexa genetics, Phylogeny
- Abstract
Gregarines are a diverse group of apicomplexan parasites with a conspicuous extracellular feeding stage, called a "trophozoite", that infects the intestines and other body cavities of invertebrate hosts. Although the morphology of trophozoites is very diverse in gregarines as a whole, high degrees of intraspecific variation combined with relatively low degrees of interspecific variation make the delimitation of different species based on trophozoite morphology observed with light microscopy difficult. The coupling of molecular phylogenetic data with comparative morphology has shed considerable light onto the boundaries and interrelationships of different gregarine species. In this study, we isolated a novel marine gregarine from the hepatic region of a Pacific representative of the hemichordate Glossobalanus minutus, and report the first ultrastructural and molecular data from any gregarine infecting this distinctive group of hosts. Molecular phylogenetic analyses of an SSU rDNA sequence derived from two single-cell isolates of this marine gregarine demonstrated a strong and unexpected affiliation with a clade of terrestrial gregarines (e.g. Gregarina). This molecular phylogenetic data combined with a comparison of the morphological features in previous reports of gregarines collected from Atlantic representatives of G. minutus justified the establishment of a new binomial for the new isolate, namely Caliculium glossobalani n. gen. et sp. The molecular phylogenetic analyses demonstrated a clade of terrestrial gregarines associated with a sequence acquired from a marine species, which suggest that different groups of terrestrial/freshwater gregarines evolved independently from marine ancestors., (© 2014 The Author(s) Journal of Eukaryotic Microbiology © 2014 International Society of Protistologists.)
- Published
- 2014
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13. The single cellular green microalga Botryococcus braunii, race B possesses three distinct 1-deoxy-D-xylulose 5-phosphate synthases.
- Author
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Matsushima D, Jenke-Kodama H, Sato Y, Fukunaga Y, Sumimoto K, Kuzuyama T, Matsunaga S, and Okada S
- Subjects
- Amino Acid Sequence, Chlorophyta genetics, Chlorophyta metabolism, Conserved Sequence, DNA, Complementary genetics, Gene Expression genetics, Gene Expression Regulation, Plant genetics, Gene Library, Kinetics, Microalgae genetics, Microalgae metabolism, Molecular Sequence Data, Phylogeny, Plant Leaves genetics, Plant Leaves metabolism, Plant Proteins genetics, Plant Proteins isolation & purification, Plant Proteins metabolism, Protein Isoforms, Recombinant Proteins, Sequence Alignment, Sequence Analysis, DNA, Temperature, Transferases isolation & purification, Transferases metabolism, Chlorophyta enzymology, Microalgae enzymology, Plant Leaves enzymology, Terpenes metabolism, Transferases genetics
- Abstract
Green algae exclusively use the methylerythritol 4-phosphate (MEP) pathway for the biosynthesis of isoprenoids. The first enzyme of this pathway is 1-deoxy-D-xylulose 5-phosphate synthase (DXS, EC 2.2.1.7). Green algae have been thought to possess only a single DXS, in contrast to land plants, which have at least two isoforms that serve different roles in metabolism. The green microalga Botryococcus braunii has an extraordinary isoprenoid metabolism, as it produces large amounts of triterpene hydrocarbons. Here, we did cDNA cloning of DXSs from B. braunii and examined enzyme activities of the heterologously expressed proteins. Three distinct DXS isoforms were identified, all of which were functional and had similar kinetic properties, whereas the temperature dependence of enzyme activity showed considerable differences. Transcription of the genes was examined by real time quantitative RT-PCR. The three DXS genes were simultaneously expressed, and the expression levels were highest on day six after subculturing. B. braunii is the first green microalga demonstrated to have multiple DXS isoforms like land plants. This difference to other microalgae seems to mirror its special needs for extensive triterpene production by increasing the metabolic flow through the MEP pathway., (Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2012
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14. A polyketide interferes with cellular differentiation in the symbiotic cyanobacterium Nostoc punctiforme.
- Author
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Liaimer A, Jenke-Kodama H, Ishida K, Hinrichs K, Stangeland J, Hertweck C, and Dittmann E
- Abstract
Nostoc punctiforme is a filamentous cyanobacterium capable of forming symbiotic associations with a wide range of plants. The strain exhibits extensive phenotypic characteristics and can differentiate three mutually exclusive cell types: nitrogen-fixing heterocysts, motile hormogonia and spore-like akinetes. Here, we provide evidence for a crucial role of an extracellular metabolite in balancing cellular differentiation. Insertional mutagenesis of a gene of the polyketide synthase gene cluster pks2 led to the accumulation of short filaments carrying mostly terminal heterocysts under diazotrophic conditions. The mutant has a strong tendency to form biofilms on solid surfaces as well as in liquid culture. The pks2(-) strain keeps forming hormogonia over the entire growth curve and shows an early onset of akinete formation. We could isolate two fractions of the wild-type supernatant that could restore the capability to form long filaments with intercalary heterocysts. Growth of the mutant cells in the neighbourhood of wild-type cells on plates led to a reciprocal influence and a partial reconstruction of wild-type and mutant phenotype respectively. We postulate that extracellular metabolites of Nostoc punctiforme act as life cycle governing factors (LCGFs) and that the ratio between distinct factors may guide the differentiation into different life stages., (© 2011 Society for Applied Microbiology and Blackwell Publishing Ltd.)
- Published
- 2011
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15. Evolution of metabolic diversity: insights from microbial polyketide synthases.
- Author
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Jenke-Kodama H and Dittmann E
- Subjects
- Molecular Structure, Bacteria enzymology, Bacteria metabolism, Evolution, Molecular, Polyketide Synthases genetics, Polyketide Synthases metabolism
- Abstract
Polyketides are a family of complex natural products that are built from simple carboxylic acid building blocks. In microorganisms, the majority of these secondary metabolites are produced by exceptionally large, multifunctional proteins termed polyketide synthases (PKSs). Each unit of a type I PKS assembly line resembles a mammalian type fatty acid synthase (FAS), although certain domains are optionally missing. The evolutionary analysis of microbial PKS has revealed a long joint evolution process of PKSs and FASs. The phylogenomic analysis of modular type I PKSs as the most widespread PKS type in bacteria showed a large impact of gene duplications and gene losses on the evolution of type I PKS in different bacterial groups. The majority of type I PKSs in actinobacteria and cyanobacteria may have evolved from a common ancestor, whereas in proteobacteria most type I PKSs were acquired from other bacterial groups. The modularization of type I PKSs almost unexceptionally started with multiple duplications of a single ancestor module. The repeating modules represent ideal platforms for recombination events that can lead to corresponding changes in the actual chemistry of the products. The analysis of these "natural reprogramming" events of PKSs may assist in the development of concepts for the biocombinatorial design of bioactive compounds.
- Published
- 2009
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16. Bioinformatic perspectives on NRPS/PKS megasynthases: advances and challenges.
- Author
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Jenke-Kodama H and Dittmann E
- Subjects
- Drug Design, Drug Discovery, Genetics, Microbial, Biological Products, Peptide Synthases, Polyketide Synthases
- Abstract
The increased understanding of both fundamental principles and mechanistic variations of NRPS/PKS megasynthases along with the unprecedented availability of microbial sequences has inspired a number of in silico studies of both enzyme families. The insights that can be extracted from these analyses go far beyond a rough classification of data and have turned bioinformatics into a frontier field of natural products research. As databases are flooded with NRPS/PKS gene sequence of microbial genomes and metagenomes, increasingly reliable structural prediction methods can help to uncover hidden treasures. Already, phylogenetic analyses have revealed that NRPS/PKS pathways should not simply be regarded as enzyme complexes, specifically evolved to product a selected natural product. Rather, they represent a collection of genetic opinions, allowing biosynthetic pathways to be shuffled in a process of perpetual chemical innovations and pathways diversification in nature can give impulses for specificities, protein interactions and genetic engineering of libraries of novel peptides and polyketides. The successful translation of the knowledge obtained from bioinformatic dissection of NRPS/PKS megasynthases into new techniques for drug discovery and design remain challenges for the future.
- Published
- 2009
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17. Exploiting the mosaic structure of trans-acyltransferase polyketide synthases for natural product discovery and pathway dissection.
- Author
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Nguyen T, Ishida K, Jenke-Kodama H, Dittmann E, Gurgui C, Hochmuth T, Taudien S, Platzer M, Hertweck C, and Piel J
- Subjects
- Amino Acid Sequence, Biological Products chemistry, Biological Products metabolism, Catalysis, Drug Design, Enzyme Activation, Molecular Sequence Data, Protein Structure, Tertiary, Structure-Activity Relationship, Burkholderia enzymology, Polyketide Synthases chemistry, Polyketide Synthases metabolism, Sequence Analysis, Protein methods, Signal Transduction physiology
- Abstract
Modular polyketide synthases (PKSs) are giant bacterial enzymes that synthesize many polyketides of therapeutic value. In contrast to PKSs that provide acyltransferase (AT) activities in cis, trans-AT PKSs lack integrated AT domains and exhibit unusual enzymatic features with poorly understood functions in polyketide assembly. This has retarded insight into the assembly of products such as mupirocin, leinamycin and bryostatin 1. We show that trans-AT PKSs evolved in a fundamentally different fashion from cis-AT systems, through horizontal recruitment and assembly of substrate-specific ketosynthase (KS) domains. The insights obtained from analysis of these KS mosaics will facilitate both the discovery of novel polyketides by genome mining, as we demonstrate for the thailandamides of Burkholderia thailandensis, and the extraction of chemical information from short trans-AT PCR products, as we show using metagenomic DNA of marine sponges. Our data also suggest new strategies for dissecting polyketide biosynthetic pathways and engineering polyketide assembly.
- Published
- 2008
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18. Evolutionary mechanisms underlying secondary metabolite diversity.
- Author
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Jenke-Kodama H, Müller R, and Dittmann E
- Subjects
- Adaptation, Psychological, Animals, Bacteria genetics, Gene Expression Regulation, Bacterial, Gene Expression Regulation, Enzymologic, Gene Expression Regulation, Plant, Humans, Phylogeny, Plants genetics, Polyketide Synthases genetics, Selection, Genetic, Species Specificity, Bacteria enzymology, Evolution, Molecular, Metabolic Networks and Pathways genetics, Plants enzymology, Polyketide Synthases metabolism
- Abstract
The enormous chemical diversity and the broad range of biological activities of secondary metabolites raise many questions about their role in nature and the specific traits leading to their evolution. The answers to these questions will not only be of fundamental interest but may also provide lessons that could help to improve the screening protocols of pharmaceutical companies and strategies for rational secondary metabolite engineering. In this review, we try to dissect evolutionary principles leading to the emergence, distribution, diversification and selection of genes involved in secondary metabolite biosyntheses. We give an overview about recent insights into the evolution of the different types of polyketide synthases (PKS) in microorganisms and plants and highlight unique mechanisms underlying polyketide diversity. Although phylogenetic and experimental data have significantly increased our knowledge about the role and evolution of secondary metabolites in the last decades there is still much dissent about the impact of natural selection. In order to understand the evolution towards metabolic diversity we therefore need more thorough investigations of the ecological role of secondary metabolites in the future.
- Published
- 2008
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19. Non-colinear polyketide biosynthesis in the aureothin and neoaureothin pathways: an evolutionary perspective.
- Author
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Traitcheva N, Jenke-Kodama H, He J, Dittmann E, and Hertweck C
- Subjects
- Amino Acid Sequence, Chromones chemistry, Cloning, Molecular, Molecular Sequence Data, Multigene Family, Polyenes chemistry, Polyenes metabolism, Polyketide Synthases chemistry, Polyketide Synthases genetics, Pyrones chemistry, Sequence Analysis, DNA, Streptomyces genetics, Chromones metabolism, Evolution, Molecular, Phylogeny, Polyketide Synthases metabolism, Pyrones metabolism, Streptomyces enzymology
- Abstract
Aureothin and neoaureothin (spectinabilin) represent rare nitroaryl-substituted polyketide metabolites from Streptomyces thioluteus and Streptomyces orinoci, respectively, which only differ in the lengths of the polyene backbones. Cloning and sequencing of the 39 kb neoaureothin (nor) biosynthesis gene cluster and its comparison with the aureothin (aur) pathway genes revealed that both polyketide synthase (PKS) assembly lines are remarkably similar. In both cases the module architecture breaks with the principle of colinearity, as individual PKS modules are used in an iterative fashion. Parsimony and neighbour-joining phylogenetic studies provided insights into the evolutionary process that led to the programming of these unusual type I PKS systems and to prediction of which modules act iteratively. The iterative function of the first module in the neoaureothin pathway, NorA, was confirmed by a successful cross-complementation.
- Published
- 2007
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20. A type II polyketide synthase is responsible for anthraquinone biosynthesis in Photorhabdus luminescens.
- Author
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Brachmann AO, Joyce SA, Jenke-Kodama H, Schwär G, Clarke DJ, and Bode HB
- Subjects
- Amino Acid Sequence, Bacteriocins chemistry, Bacteriocins metabolism, Chromatography, High Pressure Liquid, Genes, Bacterial, Models, Chemical, Molecular Sequence Data, Multigene Family, Mutation, Photorhabdus metabolism, Phylogeny, Polyketide Synthases chemistry, Sequence Homology, Amino Acid, Anthraquinones chemistry, Gene Expression Regulation, Bacterial, Photorhabdus enzymology, Polyketide Synthases physiology
- Abstract
Type II polyketide synthases are involved in the biosynthesis of numerous clinically relevant secondary metabolites with potent antibiotic or anticancer activity. Until recently the only known producers of type II PKSs were members of the Gram-positive actimomycetes, well-known producers of secondary metabolites in general. Here we present the second example of a type II PKS from Gram-negative bacteria. We have identified the biosynthesis gene cluster responsible for the production of anthraquinones (AQs) from the entomopathogenic bacterium Photorhabdus luminescens. This is the first example of AQ production in Gram-negative bacteria, and their heptaketide origin was confirmed by feeding experiments. Deletion of a cyclase/aromatase involved in AQ biosynthesis resulted in accumulation of mutactin and dehydromutactin, which have been described as shunt products of typical octaketide compounds from streptomycetes, and a pathway for AQ formation from octaketide intermediates is discussed.
- Published
- 2007
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21. Horizontal gene transfer of two cytoskeletal elements from a eukaryote to a cyanobacterium.
- Author
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Guljamow A, Jenke-Kodama H, Saumweber H, Quillardet P, Frangeul L, Castets AM, Bouchier C, Tandeau de Marsac N, and Dittmann E
- Subjects
- Cytoskeleton genetics, Eukaryotic Cells, Genomic Islands, Actins genetics, Gene Transfer, Horizontal, Microcystis genetics, Profilins genetics, Sequence Homology, Amino Acid
- Published
- 2007
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22. A Type II polyketide synthase from the gram-negative Bacterium Stigmatella aurantiaca is involved in Aurachin alkaloid biosynthesis.
- Author
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Sandmann A, Dickschat J, Jenke-Kodama H, Kunze B, Dittmann E, and Müller R
- Subjects
- Amino Acid Sequence, Base Sequence, Molecular Sequence Data, Alkaloids biosynthesis, Gram-Negative Bacteria enzymology, Polyketide Synthases metabolism, Quinolines chemistry, Stigmatella aurantiaca enzymology
- Published
- 2007
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23. Natural biocombinatorics in the polyketide synthase genes of the actinobacterium Streptomyces avermitilis.
- Author
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Jenke-Kodama H, Börner T, and Dittmann E
- Subjects
- Computational Biology, Macrolides chemistry, Macrolides metabolism, Molecular Structure, Multigene Family genetics, Phylogeny, Streptomyces enzymology, Polyketide Synthases genetics, Polyketide Synthases metabolism, Recombination, Genetic genetics, Streptomyces genetics, Streptomyces metabolism
- Abstract
Modular polyketide synthases (PKSs) of bacteria provide an enormous reservoir of natural chemical diversity. Studying natural biocombinatorics may aid in the development of concepts for experimental design of genes for the biosynthesis of new bioactive compounds. Here we address the question of how the modularity of biosynthetic enzymes and the prevalence of multiple gene clusters in Streptomyces drive the evolution of metabolic diversity. The phylogeny of ketosynthase (KS) domains of Streptomyces PKSs revealed that the majority of modules involved in the biosynthesis of a single compound evolved by duplication of a single ancestor module. Using Streptomyces avermitilis as a model organism, we have reconstructed the evolutionary relationships of different domain types. This analysis suggests that 65% of the modules were altered by recombinational replacements that occurred within and between biosynthetic gene clusters. The natural reprogramming of the biosynthetic pathways was unambiguously confined to domains that account for the structural diversity of the polyketide products and never observed for the KS domains. We provide examples for natural acyltransferase (AT), ketoreductase (KR), and dehydratase (DH)-KR domain replacements. Potential sites of homologous recombination could be identified in interdomain regions and within domains. Our results indicate that homologous recombination facilitated by the modularity of PKS architecture is the most important mechanism underlying polyketide diversity in bacteria.
- Published
- 2006
- Full Text
- View/download PDF
24. Bacterial type III polyketide synthases: phylogenetic analysis and potential for the production of novel secondary metabolites by heterologous expression in pseudomonads.
- Author
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Gross F, Luniak N, Perlova O, Gaitatzis N, Jenke-Kodama H, Gerth K, Gottschalk D, Dittmann E, and Müller R
- Subjects
- Acyltransferases biosynthesis, Base Sequence, Myxococcales genetics, Naphthoquinones chemistry, Phylogeny, Pseudomonas genetics, Acyltransferases genetics, Acyltransferases metabolism, Myxococcales enzymology
- Abstract
Type III polyketide synthases (PKS) were regarded as typical for plant secondary metabolism before they were found in microorganisms recently. Due to microbial genome sequencing efforts, more and more type III PKS are found, most of which of unknown function. In this manuscript, we report a comprehensive analysis of the phylogeny of bacterial type III PKS and report the expression of a type III PKS from the myxobacterium Sorangium cellulosum in pseudomonads. There is no precedent of a secondary metabolite that might be biosynthetically correlated to a type III PKS from any myxobacterium. Additionally, an inactivation mutant of the S. cellulosum gene shows no physiological difference compared to the wild-type strain which is why these type III PKS are assumed to be "silent" under the laboratory conditions administered. One type III PKS (SoceCHS1) was expressed in different Pseudomonas sp. after the heterologous expression in Escherichia coli failed. Cultures of recombinant Pseudomonas sp. harbouring SoceCHS1 turned red upon incubation and the diffusible pigment formed was identified as 2,5,7-trihydroxy-1,4-naphthoquinone, the autooxidation product of 1,3,6,8-tetrahydroxynaphthalene. The successful heterologous production of a secondary metabolite using a gene not expressed under administered laboratory conditions provides evidence for the usefulness of our approach to activate such secondary metabolite genes for the production of novel metabolites.
- Published
- 2006
- Full Text
- View/download PDF
25. Evolutionary implications of bacterial polyketide synthases.
- Author
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Jenke-Kodama H, Sandmann A, Müller R, and Dittmann E
- Subjects
- Amino Acid Sequence, Bacteria enzymology, Bacteria genetics, Bacterial Proteins chemistry, Genome, Bacterial, Polyketide Synthases chemistry, Sequence Alignment, Sequence Homology, Amino Acid, Bacteria classification, Bacterial Proteins genetics, Phylogeny, Polyketide Synthases genetics
- Abstract
Polyketide synthases (PKS) perform a stepwise biosynthesis of diverse carbon skeletons from simple activated carboxylic acid units. The products of the complex pathways possess a wide range of pharmaceutical properties, including antibiotic, antitumor, antifungal, and immunosuppressive activities. We have performed a comprehensive phylogenetic analysis of multimodular and iterative PKS of bacteria and fungi and of the distinct types of fatty acid synthases (FAS) from different groups of organisms based on the highly conserved ketoacyl synthase (KS) domains. Apart from enzymes that meet the classification standards we have included enzymes involved in the biosynthesis of mycolic acids, polyunsaturated fatty acids (PUFA), and glycolipids in bacteria. This study has revealed that PKS and FAS have passed through a long joint evolution process, in which modular PKS have a central position. They appear to have derived from bacterial FAS and primary iterative PKS and, in addition, share a common ancestor with animal FAS and secondary iterative PKS. Furthermore, we have carried out a phylogenomic analysis of all modular PKS that are encoded by the complete eubacterial genomes currently available in the database. The phylogenetic distribution of acyltransferase and KS domain sequences revealed that multiple gene duplications, gene losses, as well as horizontal gene transfer (HGT) have contributed to the evolution of PKS I in bacteria. The impact of these factors seems to vary considerably between the bacterial groups. Whereas in actinobacteria and cyanobacteria the majority of PKS I genes may have evolved from a common ancestor, several lines of evidence indicate that HGT has strongly contributed to the evolution of PKS I in proteobacteria. Discovery of new evolutionary links between PKS and FAS and between the different PKS pathways in bacteria may help us in understanding the selective advantage that has led to the evolution of multiple secondary metabolite biosyntheses within individual bacteria.
- Published
- 2005
- Full Text
- View/download PDF
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