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编码海洋蓝细菌聚球藻属PCC 7002菌株RNA聚合酶主要σ因子的sigA基因:克隆与特性分析

The sigA gene encoding the major sigma factor of RNA polymerase from the marine cyanobacterium Synechococcus sp. strain PCC 7002: cloning and characterization.

作者信息

Osborn A M, Bruce K D, Ritchie D A, Strike P

机构信息

Department of Genetics and Microbiology, Donnan Laboratories, University of Liverpool, PO Box 147, Liverpool L69 3BX, UK.

出版信息

Microbiology (Reading). 1996 Feb;142 ( Pt 2):337-345. doi: 10.1099/13500872-142-2-347.

Abstract

The gene encoding the principal sigma factor from Synechococcus sp. strain PCC 7002 was isolated and characterized. The Synechococcus sp. strain PCC 7002 sigA gene encodes a protein of 375 amino acids (43 center dot 7 kDa) that is required for viability under normal growth conditions. The SigA protein was overproduced in Escherichia coli and the purified protein was used to raise polyclonal antiserum in rabbits. This antiserum was used in immunoblot analyses of partially purified RNA polymerase from Synechococcus sp. strain PR6000. The probable in vivo translational start site was identified by a comparison of amino acid sequencing results obtained with SigA proteins overproduced in E. coli with immunoblot analyses of SigA protein in crude preparations of RNA polymerase from the cyanobacterium. The sigA gene is encoded on a transcript of 1700 bases that initiates 496 nucleotides upstream from the probable in vivo translational start site. The abundance of sigA transcripts decreases rapidly after the removal of combined nitrogen from the growth medium.

摘要

对来自聚球藻属(Synechococcus sp.)菌株PCC 7002的主要σ因子编码基因进行了分离和表征。聚球藻属菌株PCC 7002的sigA基因编码一种由375个氨基酸组成(43.7 kDa)的蛋白质,该蛋白质在正常生长条件下是生存所必需的。SigA蛋白在大肠杆菌中过量表达,纯化后的蛋白用于在兔体内制备多克隆抗血清。该抗血清用于对来自聚球藻属菌株PR6000的部分纯化RNA聚合酶进行免疫印迹分析。通过比较在大肠杆菌中过量表达的SigA蛋白的氨基酸测序结果与蓝细菌RNA聚合酶粗制品中SigA蛋白的免疫印迹分析结果,确定了可能的体内翻译起始位点。sigA基因编码在一个1700个碱基的转录本上,该转录本在可能的体内翻译起始位点上游496个核苷酸处起始。从生长培养基中去除化合态氮后,sigA转录本的丰度迅速下降。

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