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鼠伤寒沙门氏菌中pts操纵子的部分核苷酸序列:五个细菌属的比较分析

Partial nucleotide sequence of the pts operon in Salmonella typhimurium: comparative analyses in five bacterial genera.

作者信息

Schnierow B J, Yamada M, Saier M H

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093.

出版信息

Mol Microbiol. 1989 Jan;3(1):113-8. doi: 10.1111/j.1365-2958.1989.tb00110.x.

DOI:10.1111/j.1365-2958.1989.tb00110.x
PMID:2497295
Abstract

The nucleotide sequence of a Salmonella typhimurium DNA segment of 549 base pairs which encompasses the operator-promoter of the pts operon, the entirety of the ptsH gene, encoding HPr of the phosphotransferase system (PTS), the first 29 nucleotides of the ptsI gene, encoding Enzyme I of the PTS, and the intercistronic region between the ptsH and ptsI genes was determined and compared with the corresponding sequence from Escherichia coli (De Reuse et al., 1985). The two sequences showed 91% overall identity, with some regions showing sequence conservation and others exhibiting relative divergence. Two open reading frames were identified in both species: one encoded HPr on the 'sense' strand (255 nucleotides; 12 nucleotide differences, no amino acid differences); the other, on the anti-sense strand, consisted of 291 nucleotides (13 nucleotide differences, 13 amino acid differences). While HPr bears a net negative charge, the putative protein encoded by the open reading frame on the anti-sense strand is strongly basic. Computer analyses of HPr proteins from five different bacterial genera revealed four regions which show strong sequence identity and therefore are presumed to be critical for maintenance of biological activity. Two of these regions were specific to Gram-positive bacteria. Proposed functions for each of these regions are discussed. Relative evolutionary distances between the HPr proteins were also computed.

摘要

测定了鼠伤寒沙门氏菌一段549个碱基对的DNA片段的核苷酸序列,该片段包含pts操纵子的操纵子-启动子、编码磷酸转移酶系统(PTS)的HPr的ptsH基因的全部、编码PTS的酶I的ptsI基因的前29个核苷酸,以及ptsH和ptsI基因之间的基因间区域,并与大肠杆菌的相应序列进行了比较(De Reuse等人,1985年)。这两个序列总体上有91%的同一性,一些区域显示出序列保守性,而另一些区域则表现出相对的差异。在两个物种中都鉴定出了两个开放阅读框:一个在“有义”链上编码HPr(255个核苷酸;12个核苷酸差异,无氨基酸差异);另一个在反义链上,由291个核苷酸组成(13个核苷酸差异,13个氨基酸差异)。虽然HPr带有净负电荷,但反义链上开放阅读框编码的推定蛋白质具有很强的碱性。对来自五个不同细菌属的HPr蛋白进行计算机分析,发现了四个显示出强序列同一性的区域,因此推测这些区域对维持生物活性至关重要。其中两个区域是革兰氏阳性菌特有的。讨论了这些区域各自的推测功能。还计算了HPr蛋白之间的相对进化距离。

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