Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Biosynthesis of Streptothricin Antibiotics. VI. Mechanisms of β-Lysine and Its Peptide Formation
沢田 洋介中野 史朗谷山 兵三
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キーワード: precursor
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1977 年 25 巻 12 号 p. 3210-3217

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1. Streptomyces lavendulae ISP-5069 produces racemomycin-A which yields β-lysine as a component on hydrolysis. β-Lysine was derived from an intermediate α, ε-diaminopimelic acid via lysine pathway. Exogenous lysine acted as a donor of β-lysine to form racemomycin-C and-B by S. lavendulae NT-1008 by means of incorporation of 14C-labeled lysine. 2. Two taxonomically different strains, S. lavendulae NT-1008 and S. albidoflavus S-0003, were selected as the strains producing racemomycin-A, -C, and-B as a mixture. These antibiotics were present both in the intracellular pool and in the broth. 3. Addition of 14C-racemomycin-A to the culture medium resulted in the incorporation of 14C into racemomycin-C and-B. Majority of the radioactivity was present in the extracellular racemomycin-C and-B, but a significant portion was present in the intracellular antibiotics. These data indicate that racemomycin-C and-B were transformed stepwisely from racemomycin-A and β-lysine, suggesting an endogenous formation.
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© The Pharmaceutical Society of Japan
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