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嗜热纤维梭菌groES和groEL基因的序列及转录分析

Sequence and transcriptional analysis of groES and groEL genes from the thermophilic bacterium Clostridium thermocellum.

作者信息

Ciruela A, Cross S, Freedman R B, Hazlewood G P

机构信息

Department of Cellular Physiology, The Babraham Institute, Cambridge, UK.

出版信息

Gene. 1997 Feb 20;186(1):143-7. doi: 10.1016/s0378-1119(96)00814-1.

Abstract

The groESL operon from Clostridium thermocellum (Ct) has been isolated and sequenced, revealing two ORFs of 285 and 1626 nt, separated by 48 nt. The first ORF encoded a 94-aa 10.6-kDa GroES homologue; the second encoded a 541-aa polypeptide of 57.6 kDa, that exhibited 61% and 77% sequence identity with GroEL from Escherichia coli (Ec) and Clostridium acetobutylicum (Ca), respectively. A putative tsp, preceded by -10 and -35 consensus promoters, was identified upstream of groES. This was followed by an inverted repeat observed previously in bacterial heat shock genes. A 15-nt palindrome characteristic of a Rho-independent transcription terminator, was located downstream of groEL. The first nt of the groES translational start codon was preceded (7 nt) by a putative RBS (AGGAGG); a second RBS sequence was located 8 nt upstream of the groEL start. Production of GroE homologues by Ct was constitutive, but was enhanced significantly during a temperature upshift from 60 degrees C to 70 degrees C. The Ct GroEL, expressed in Ec as a fusion protein with GST, was purified, free of contaminating Ec GroEL.

摘要

来自嗜热栖热放线菌(Ct)的groESL操纵子已被分离和测序,结果显示有两个开放阅读框,分别为285个核苷酸和1626个核苷酸,中间间隔48个核苷酸。第一个开放阅读框编码一个94个氨基酸、10.6 kDa的GroES同源物;第二个编码一个541个氨基酸、57.6 kDa的多肽,该多肽与大肠杆菌(Ec)和丙酮丁醇梭菌(Ca)的GroEL分别具有61%和77%的序列同一性。在groES上游鉴定出一个假定的转录起始点,其前面有-10和-35一致启动子。随后是先前在细菌热休克基因中观察到的反向重复序列。在groEL下游有一个15个核苷酸的回文结构,这是不依赖Rho的转录终止子的特征。groES翻译起始密码子的第一个核苷酸之前(7个核苷酸)有一个假定的核糖体结合位点(AGGAGG);第二个核糖体结合位点序列位于groEL起始位点上游8个核苷酸处。嗜热栖热放线菌产生GroE同源物是组成型的,但在温度从60℃升至70℃的过程中显著增强。在大肠杆菌中作为与GST的融合蛋白表达的嗜热栖热放线菌GroEL被纯化,不含污染的大肠杆菌GroEL。

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