The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
NOVEL FERMENTATION PRODUCTS FROM STREPTOMYCES FRADIAE: X-RAY CRYSTAL STRUCTURE OF 5-O-MYCAROSYLTYLACTONE AND PROOF OF THE ABSOLUTE CONFIGURATION OF TYLOSIN
NOEL D. JONESMICHAEL O. CHANEYHERBERT A. KIRSTGENE M. WILDRICHARD H. BALTZROBERT L. HAMILLJONATHAN W. PASCHAL
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1982 Volume 35 Issue 4 Pages 420-425

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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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© Japan Antibiotics Research Association
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