NOVEL FERMENTATION PRODUCTS FROM STREPTOMYCES FRADIAE: X-RAY CRYSTAL STRUCTURE OF 5-O-MYCAROSYLTYLACTONE AND PROOF OF THE ABSOLUTE CONFIGURATION OF TYLOSIN

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 (-)...

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Veröffentlicht in:Journal of antibiotics 1982, Vol.35(4), pp.420-425
Hauptverfasser: JONES, NOEL D., CHANEY, MICHAEL O., KIRST, HERBERT A., WILD, GENE M., BALTZ, RICHARD H., HAMILL, ROBERT L., PASCHAL, JONATHAN W.
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-8820
1881-1469
DOI:10.7164/antibiotics.35.420