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核糖体回收因子的过表达导致阿维链霉菌菌株中阿维菌素产量增加。

Overexpression of ribosome recycling factor causes increased production of avermectin in Streptomyces avermitilis strains.

机构信息

State Key Laboratories for Agro-Biotechnology and College of Biological Sciences, China Agricultural University, Beijing 100193, People's Republic of China.

出版信息

J Ind Microbiol Biotechnol. 2010 Jul;37(7):673-9. doi: 10.1007/s10295-010-0710-0. Epub 2010 Mar 30.

Abstract

Ribosome recycling factor (RRF), encoded by frr gene, is involved in the release of ribosomes from the translational post-termination complex for a new round of initiation. In this study, the frr gene with either its own promoter or with ermE p was cloned into a multi-copy vector, pKC1139, and a single-site integrative vector, pSET152, respectively. The resulting plasmids were transformed into Streptomyces avermitilis wild-type strain ATCC31267, avermectin high-producing mutant strain 76-02-e, and the engineered strain GB-165 that produces only avermectin B. The results showed that overexpression of frr increased avermectin yield (by 3- to 3.7-fold in the wild-type strain) and revealed an frr gene "copy number effect"; i.e., multiple copies of frr had a greater promoting effect on avermectin production than a single copy in each of the three transformed S. avermitilis strains. Comparison of the growth and expression of the ave genes in an frr-overexpressing strain and wild-type ATCC31267 indicated that frr overexpression promoted cell growth as well as the expression of ave genes (including pathway-specific positive regulatory gene aveR for avermectin biosynthesis and ave structural genes), leading in turn to avermectin overproduction. These findings provide an effective approach for the improvement of antibiotic production in Streptomyces.

摘要

核糖体回收因子(RRF)由 frr 基因编码,参与核糖体从翻译终止后复合物中的释放,以便进行新一轮的起始。在本研究中,frr 基因分别带有其自身的启动子或 ermE p 被克隆到多拷贝载体 pKC1139 和单一位点整合载体 pSET152 中。所得质粒分别转化到链霉菌阿维链霉菌野生型菌株 ATCC31267、阿维菌素高产突变株 76-02-e 和只生产阿维菌素 B 的工程菌株 GB-165。结果表明,frr 的过表达增加了阿维菌素的产量(在野生型菌株中增加了 3 到 3.7 倍),并揭示了 frr 基因的“拷贝数效应”;即,frr 的多个拷贝比三个转化的阿维链霉菌菌株中的单个拷贝对阿维菌素生产具有更大的促进作用。在过表达 frr 的菌株和野生型 ATCC31267 中的 ave 基因的生长和表达比较表明,frr 的过表达促进了细胞生长以及 ave 基因的表达(包括阿维菌素生物合成的途径特异性正调控基因 aveR 和 ave 结构基因),从而导致阿维菌素的过量生产。这些发现为提高链霉菌抗生素的生产提供了一种有效的方法。

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