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Biosynthetic study of FR-900848: unusual observation on polyketide biosynthesis that did not accept acetate as origin of acetyl-CoA

机译:FR-900848的生物合成研究:不接受醋酸盐作为乙酰辅酶A的聚酮化合物生物合成的异常观察

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摘要

The biosynthetic pathway of a potent antifungal agent, FR-900848, has been examined by administration of several 13C-labeled precursors to Streptoverticillium fervens HP-891. Although none of the 13C-labeled acetate was incorporated into FR-900848, the labeling pattern of FR-900848 derived from d-[U-13C6]glucose revealed that the fatty acid backbone of FR-900848 has been biosynthesized via a polyketide pathway. These unusual results strongly show that the major pathway to provide acetyl-CoA in this microorganism is glycolysis. Feeding experiments with d-[U-13C6]glucose, [1,3-13C2]glycerol, and l-[Me-13C]methionine provided information on the biosynthetic origin of structurally unusual parts (polycyclopropane and aminonucleoside) in this antibiotic.
机译:有效的抗真菌剂FR-900848的生物合成途径已通过将数种13C标记的前体施用至链霉菌HP-891进行了研究。尽管13C标记的乙酸盐均未掺入FR-900848中,但衍生自d- [U-13C6]葡萄糖的FR-900848的标记方式表明FR-900848的脂肪酸主链已通过聚酮化合物途径进行了生物合成。这些异常结果强烈表明,在该微生物中提供乙酰辅酶A的主要途径是糖酵解。用d- [U-13C6]葡萄糖,[1,3-13C2]甘油和1- [Me-13C]蛋氨酸的饲喂实验提供了该抗生素中结构异常部分(聚环丙烷和氨基核苷)的生物合成来源的信息。

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