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      A Roadmap for Natural Product Discovery Based on Large-Scale Genomics and Metabolomics

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          Abstract

          Actinobacteria encode a wealth of natural product biosynthetic gene clusters (NPGCs), whose systematic study is complicated by numerous repetitive motifs. By combining several metrics we developed a method for global classification of these gene clusters into families (GCFs) and analyzed the biosynthetic capacity of Actinobacteria in 830 genome sequences, including 344 obtained for this project. The GCF network, comprised of 11,422 gene clusters grouped into 4,122 GCFs, was validated in hundreds of strains by correlating confident mass spectrometric detection of known small molecules with the presence/absence of their established biosynthetic gene clusters. The method also linked previously unassigned GCFs to known natural products, an approach that will enable de novo, bioassay-free discovery of novel natural products using large data sets. Extrapolation from the 830-genome dataset reveals that Actinobacteria encode hundreds of thousands of future drug leads, while the strong correlation between phylogeny and GCFs frames a roadmap to efficiently access them.

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          Most cited references24

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          Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2).

          Streptomyces coelicolor is a representative of the group of soil-dwelling, filamentous bacteria responsible for producing most natural antibiotics used in human and veterinary medicine. Here we report the 8,667,507 base pair linear chromosome of this organism, containing the largest number of genes so far discovered in a bacterium. The 7,825 predicted genes include more than 20 clusters coding for known or predicted secondary metabolites. The genome contains an unprecedented proportion of regulatory genes, predominantly those likely to be involved in responses to external stimuli and stresses, and many duplicated gene sets that may represent 'tissue-specific' isoforms operating in different phases of colonial development, a unique situation for a bacterium. An ancient synteny was revealed between the central 'core' of the chromosome and the whole chromosome of pathogens Mycobacterium tuberculosis and Corynebacterium diphtheriae. The genome sequence will greatly increase our understanding of microbial life in the soil as well as aiding the generation of new drug candidates by genetic engineering.
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            Assembly-line enzymology for polyketide and nonribosomal Peptide antibiotics: logic, machinery, and mechanisms.

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              Thoughts and facts about antibiotics: where we are now and where we are heading.

              The declining trends in microbial metabolite and natural products research and the refocusing of this research area are discussed. Renewing natural products research requires inexhaustible natural resources, as well as new genetic techniques and microbial sources, including endophytic microbes. The numbers of known bioactive metabolites are summarized according to their microbiological origin, biological activities and chemical structures. Synthetic and natural product-based libraries are also compared. Importantly, the wide range of microbial metabolite bioactivities, future trends and the importance of prioritizing natural products over synthetic compounds are emphasized.
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                Author and article information

                Journal
                101231976
                32624
                Nat Chem Biol
                Nat. Chem. Biol.
                Nature chemical biology
                1552-4450
                1552-4469
                24 September 2014
                28 September 2014
                November 2014
                01 May 2015
                : 10
                : 11
                : 963-968
                Affiliations
                [1 ] Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA
                [2 ] Departments of Chemistry, Molecular Biosciences, and the Feinberg School of Medicine, Northwestern University, 2170 Campus Drive, Evanston, IL, 60208, USA
                [3 ] Department of Microbiology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA
                [4 ] Bacterial Foodborne Pathogens and Mycology Research, USDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Peoria, IL, 61604, USA
                Author notes
                [* ] Corresponding authors: William W. Metcalf, metcalf@ 123456illinois.edu
                [†]

                Authors contributed equally to this study

                Author Contributions JRD designed and performed bioinformatic analyses. JRD, RRH and KAT produced microbial extracts. JCA designed LC-MS experiments and JCA and AWG collected and analyzed LC-MS data. KSJ received and processed germplasm and contributed to genomic library preparation. DPL selected and provided germplasm from the ARS Culture Collection. WWM and NLK designed and directed the work. JRD, JCA, WWM and NLK wrote the manuscript.

                Author Information Draft genomes sequenced as part of this project are available through NCBI BioProject PRJNA238534.

                Article
                NIHMS626187
                10.1038/nchembio.1659
                4201863
                25262415
                7ee8b2bc-0e13-468c-b992-39d0e99d19c6
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                Biochemistry
                Biochemistry

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