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Mutants of Streptomyces cattleya defective in the synthesis of a factor required for thienamycin production.

作者信息

Buchan T, Roach C, Ruby C, Taylor D, Preisig C, Reeves C

机构信息

Panlabs, Inc. Bothell, WA 98011.

出版信息

J Antibiot (Tokyo). 1994 Sep;47(9):992-1000. doi: 10.7164/antibiotics.47.992.

DOI:10.7164/antibiotics.47.992
PMID:7928701
Abstract

Thienamycin non-producing mutants of Streptomydes cattleya were identified that displayed a cross-feeding relationship. A diffusible product from one of these mutants (RK-11) resulted in restoration of thienamycin production when fed to cultures of another mutant (RK-4). In vivo radiolabeling experiments were conducted to test whether the RK-11 mutant produced a late biosynthetic intermediate which contained a carbapenem ring and a cysteaminyl and/or a hydroxyethyl side chain. Both [35S]cystine and [methyl-3H]methionine were used to label the RK-11 product which was then fed to RK-4 cultures. None of the thienamycin subsequently produced by RK-4 converter cells was labeled, implying the lack of either side chain of the thienamycin molecule in the RK-11 product. Further stability studies suggested that the RK-11 product does not contain a carbapenem ring. Additional feeding experiments with RK-4 cells also ruled out the possibility that the RK-11 product is a co-factor necessary for thienamycin production. It is concluded that the RK-11 product may regulate expression of the thienamycin gene cluster.

摘要

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引用本文的文献

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Mutational analysis of the thienamycin biosynthetic gene cluster from Streptomyces cattleya.链霉菌卡特利链霉菌噻唑烷酮生物合成基因簇的突变分析。
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2
Four enzymes define the incorporation of coenzyme A in thienamycin biosynthesis.四种酶决定了辅酶A在硫霉素生物合成中的掺入。
Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11128-33. doi: 10.1073/pnas.0804500105. Epub 2008 Aug 4.