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在 24 元大环内酯抗生素英地那新的生物合成过程中,通过β-谷氨酸从 L-谷氨酸衍生出 3-氨基丁酸起始单元的独特途径。

A unique pathway for the 3-aminobutyrate starter unit from L-glutamate through β-glutamate during biosynthesis of the 24-membered macrolactam antibiotic, incednine.

机构信息

Department of Chemistry and Materials Science, Tokyo Institute of Technology, O-okayama, Tokyo 152-8551, Japan.

出版信息

Org Lett. 2012 Sep 7;14(17):4591-3. doi: 10.1021/ol302052c. Epub 2012 Aug 28.

Abstract

Incednine is a 24-membered macrolactam antibiotic produced by Streptomyces sp. ML694-90F3. A previous study demonstrated that its unique nitrogen-containing starter unit was derived from L-glutamate. To elucidate the missing link between L-glutamate and the starter unit, deuterium labeled amino acid feeding experiments were conducted. These experiments revealed that 3-[3-(2)H]aminobutyrate and β-[2,2,4,4-(2)H(4)]glutamate were incorporated into the starter moiety. The results indicate that a novel decarboxylation of β-glutamate to give 3-aminobutyrate is involved in incednine biosynthesis.

摘要

英地宁是由链霉菌 sp. ML694-90F3 产生的一种 24 元大环内酯类抗生素。先前的研究表明,其独特的含氮起始单元来自 L-谷氨酸。为了阐明 L-谷氨酸和起始单元之间缺失的环节,进行了氘标记氨基酸喂养实验。这些实验表明,3-[3-(2)H]氨基丁酸和β-[2,2,4,4-(2)H(4)]谷氨酸被掺入起始部分。结果表明,β-谷氨酸发生的一种新的脱羧反应生成 3-氨基丁酸参与了英地宁的生物合成。

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