Literature DB >> 11892929

Combinatorial biosynthesis in microorganisms as a route to new antimicrobial, antitumor and neuroregenerative drugs.

C R Hutchinson1, R McDaniel.   

Abstract

Combinatorial biosynthesis utilizes the genes of biosynthetic pathways that produce microbial products to create novel chemical structures. The engineering of mondular polyketide synthase (PKS) genes has been the major focus of this effort and has led to the production of analogs of macrolide antibiotics like the erythromycins and their derived ketolides, and of the immunosuppressive macrolide FK-520 (Fujisawa Pharmaceutical Co Ltd). Approaches to making analogs of the promising antitumor compounds known as epothilones are also being explored. Lead compounds for further study have resulted and routes to analogs of other pharmacologically important compounds have been established. To facilitate this work, many new tools for manipulating and studying the multifunctional PKSs have been developed including the development of Escherichia coli as a PKS expression last. These developments have resulted in faster ways of engineering PKS to produce new compounds for the development of chemotherapeutic agents from natural products.

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Year:  2001        PMID: 11892929

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  2 in total

1.  Human microbial metabolite mimicry as a strategy to expand the chemical space of potential drugs.

Authors:  Hao Li; Harmit S Ranhotra; Sridhar Mani; Zdeněk Dvořák; Harry Sokol; Rolf Müller
Journal:  Drug Discov Today       Date:  2020-06-17       Impact factor: 7.851

2.  Chemical diversity of polyene macrolides produced by Streptomyces noursei ATCC 11455 and recombinant strain ERD44 with genetically altered polyketide synthase NysC.

Authors:  Per Bruheim; Sven E F Borgos; Pascale Tsan; Håvard Sletta; Trond E Ellingsen; Jean-Marc Lancelin; Sergey B Zotchev
Journal:  Antimicrob Agents Chemother       Date:  2004-11       Impact factor: 5.191

  2 in total

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