Literature DB >> 428024

Bioconversion and biosynthesis of 16-membered macrolide antibiotics. X. Final steps in the biosynthesis of spiramycin, using enzyme inhibitor: cerulenin.

S Omura, C Kitao, H Hamada, H Ikeda.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1979        PMID： 428024     DOI： 10.1248/cpb.27.176

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN： 0009-2363            Impact factor:   1.645


× No keyword cloud information.
  3 in total

1.  Branched-chain fatty acids produced by mutants of Streptomyces fradiae, putative precursors of the lactone ring of tylosin.

Authors:  M L Huber; J W Paschal; J P Leeds; H A Kirst; J A Wind; F D Miller; J R Turner
Journal:  Antimicrob Agents Chemother       Date:  1990-08       Impact factor: 5.191

Review 2.  Enzymes of secondary metabolism and the biosynthesis of macrolide antibiotics.

Authors:  J Neuzil; Z Hostálek
Journal:  Folia Microbiol (Praha)       Date:  1986       Impact factor: 2.099

3.  Post-PKS tailoring steps of the spiramycin macrolactone ring in Streptomyces ambofaciens.

Authors:  Hoang-Chuong Nguyen; Emmanuelle Darbon; Robert Thai; Jean-Luc Pernodet; Sylvie Lautru
Journal:  Antimicrob Agents Chemother       Date:  2013-05-28       Impact factor: 5.191
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.