Literature DB >> 18217713

Nonribosomal peptide synthetases involved in the production of medically relevant natural products.

Elizabeth A Felnagle1, Emily E Jackson, Yolande A Chan, Angela M Podevels, Andrew D Berti, Matthew D McMahon, Michael G Thomas.   

Abstract

Natural products biosynthesized wholly or in part by nonribosomal peptide synthetases (NRPSs) are some of the most important drugs currently used clinically for the treatment of a variety of diseases. Since the initial research into NRPSs in the early 1960s, we have gained considerable insights into the mechanism by which these enzymes assemble these natural products. This review will present a brief history of how the basic mechanistic steps of NRPSs were initially deciphered and how this information has led us to understand how nature modified these systems to generate the enormous structural diversity seen in nonribosomal peptides. This review will also briefly discuss how drug development and discovery are being influenced by what we have learned from nature about nonribosomal peptide biosynthesis.

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Year:  2008        PMID: 18217713      PMCID: PMC3131160          DOI: 10.1021/mp700137g

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  162 in total

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  89 in total

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Authors:  Arnold L Demain
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Journal:  J Am Soc Mass Spectrom       Date:  2013-12-03       Impact factor: 3.109

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Authors:  Diego A Alonzo; Clarisse Chiche-Lapierre; Michael J Tarry; Jimin Wang; T Martin Schmeing
Journal:  Nat Chem Biol       Date:  2020-02-17       Impact factor: 15.040

8.  Discovery of (Dihydro)pyrazine N-Oxides via Genome Mining in Pseudomonas.

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9.  Characterization and properties of biosurfactants produced by a newly isolated strain Bacillus methylotrophicus DCS1 and their applications in enhancing solubility of hydrocarbon.

Authors:  Nawel Jemil; Hanen Ben Ayed; Noomen Hmidet; Moncef Nasri
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10.  Biosynthesis of (-)-(1S,2R)-allocoronamic acyl thioester by an Fe(II)-dependent halogenase and a cyclopropane-forming flavoprotein.

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