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苜蓿中华根瘤菌中的磷酸盐同化作用:一个类pit基因的鉴定

Phosphate assimilation in Rhizobium (Sinorhizobium) meliloti: identification of a pit-like gene.

作者信息

Bardin S D, Voegele R T, Finan T M

机构信息

Department of Biology, McMaster University, Hamilton, Ontario, Canada L8S 4K1.

出版信息

J Bacteriol. 1998 Aug;180(16):4219-26. doi: 10.1128/JB.180.16.4219-4226.1998.

Abstract

Rhizobium meliloti mutants defective in the phoCDET-encoded phosphate transport system form root nodules on alfalfa plants that fail to fix nitrogen (Fix-). We have previously reported that two classes of second-site mutations can suppress the Fix- phenotype of phoCDET mutants to Fix+. Here we show that one of these suppressor loci (sfx1) contains two genes, orfA and pit, which appear to form an operon transcribed in the order orfA-pit. The Pit protein is homologous to various phosphate transporters, and we present evidence that three suppressor mutations arose from a single thymidine deletion in a hepta-thymidine sequence centered 54 nucleotides upstream of the orfA transcription start site. This mutation increased the level of orfA-pit transcription. These data, together with previous biochemical evidence, show that the orfA-pit genes encode a Pi transport system that is expressed in wild-type cells grown with excess Pi but repressed in cells under conditions of Pi limitation. In phoCDET mutant cells, orfA-pit expression is repressed, but this repression is alleviated by the second-site suppressor mutations. Suppression increases orfA-pit expression compensating for the deficiencies in phosphate assimilation and symbiosis of the phoCDET mutants.

摘要

在由phoCDET编码的磷酸盐转运系统中存在缺陷的苜蓿中华根瘤菌突变体,能在无法固氮(Fix-)的苜蓿植株上形成根瘤。我们之前报道过,两类第二位点突变可将phoCDET突变体的Fix-表型抑制为Fix+。在此我们表明,其中一个抑制基因座(sfx1)包含两个基因,即orfA和pit,它们似乎形成一个以orfA-pit顺序转录的操纵子。Pit蛋白与多种磷酸盐转运蛋白同源,并且我们提供的证据表明,三个抑制突变源自一个七聚胸苷序列中的单个胸苷缺失,该序列位于orfA转录起始位点上游54个核苷酸处。此突变提高了orfA-pit的转录水平。这些数据与先前的生化证据一起表明,orfA-pit基因编码一个Pi转运系统,该系统在生长于过量Pi环境下的野生型细胞中表达,但在Pi限制条件下的细胞中受到抑制。在phoCDET突变体细胞中,orfA-pit的表达受到抑制,但第二位点抑制突变可缓解这种抑制。抑制作用增加了orfA-pit的表达,从而弥补了phoCDET突变体在磷酸盐同化和共生方面的缺陷。

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