Literature DB >> 7096197

Novel fermentation products from Streptomyces fradiae: X-ray crystal structure of 5-O-mycarosyltylactone and proof of the absolute configuration of tylosin.

N D Jones, M O Chaney, H A Kirst, G M Wild, R H Baltz, R L Hamill, J W Paschal.   

Abstract

5-O-Mycarosyltylactone has been isolated as a predominant factor from fermentation broths of a Streptomyces fradiae mutant. The relative configurations of mycarose and tylactone (protylonolide) have been determined by X-ray crystal structure analysis. Hydrolysis of 5-O-mycarosyltylactone yielded (-)-tylactone and L-(-)-mycarose. Taken together, these two experiments establish the absolute configuration of (-)-tylactone. Bioconversion of (-)-tylactone to tylosin by tyl G mutants of S. fradiae proves the absolute configuration of tylosin. Physicochemical data for tylactone and a unique component piece of tylactone are also reported.

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Year:  1982        PMID: 7096197     DOI: 10.7164/antibiotics.35.420

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  1 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

  1 in total

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