首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Cloning of the macrolide antibiotic biosynthesis gene acyA which encodes 3-O-acyltransferase from Streptomyces thermotolerans and its use for direct fermentative production of a hybrid macrolide antibiotic.
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Cloning of the macrolide antibiotic biosynthesis gene acyA which encodes 3-O-acyltransferase from Streptomyces thermotolerans and its use for direct fermentative production of a hybrid macrolide antibiotic.

机译:从耐热链霉菌中克隆编码3-O-酰基转移酶的大环内酯类抗生素生物合成基因acyA并将其用于直接发酵生产大环内酯类抗生素。

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摘要

A gene encoding the macrolide modification enzyme 3-O-acyltransferase (acyA) was cloned by chromosome walking onto the carbomycin biosynthetic region in Streptomyces thermotolerans TH475, with the 3' region of the gene encoding the macrolide modification enzyme 4"-O-acyltransferase (acyB1) as a probe. A shortened fragment (1.8 kb) containing acyA was subcloned with pIJ350. A high-level tylosin producer, Streptomyces fradiae MBBF, transformed with the plasmid could produce a hybrid macrolide, 3-O-acetyltylosin, most efficiently.
机译:通过染色体行走到耐热链霉菌TH475中的咔菌生物合成区域上,克隆编码大环内酯修饰酶3-O-酰基转移酶(acyA)的基因,该基因的3'区域编码大环内酯修饰酶4“ -O-酰基转移酶( pIJ350将含有acyA的短片段(1.8 kb)亚克隆到pIJ350上,用该质粒转化的高水平泰乐菌素生产者链霉菌MBBF可以最有效地产生杂交大环内酯3 -O-乙酰泰乐菌素。

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