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大肠杆菌磷酸结合蛋白的结构基因phoS的核苷酸序列。

Nucleotide sequence of the phoS gene, the structural gene for the phosphate-binding protein of Escherichia coli.

作者信息

Magota K, Otsuji N, Miki T, Horiuchi T, Tsunasawa S, Kondo J, Sakiyama F, Amemura M, Morita T, Shinagawa H

出版信息

J Bacteriol. 1984 Mar;157(3):909-17. doi: 10.1128/jb.157.3.909-917.1984.

Abstract

phoS is the structural gene for the phosphate-binding protein, which is localized in periplasm and involved in active transport of phosphate in Escherichia coli. It is also a negative regulatory gene for the pho regulon, and the gene expression is inducible by phosphate starvation. The complete nucleotide sequence of the phoS gene was determined by the method of Maxam and Gilbert (A. M. Maxam and W. Gilbert, Methods Enzymol. 65:499-560, 1980). The amino acid sequences at the amino termini of the pre-PhoS and PhoS proteins and at the carboxy terminus of the PhoS protein were determined by using the purified proteins. Furthermore, the amino acid sequence of enzymatically digested peptide fragments of the PhoS protein was determined. The combined data established the nucleotide sequence of the coding region and the amino acid sequence of the pre-PhoS and the PhoS proteins. The pre-PhoS protein contains an extension of peptide composed of 25 amino acid residues at the amino terminus of the PhoS protein, which has the general characteristics of a signal peptide. The mature PhoS protein is composed of 321 amino acid residues, with a calculated molecular weight of 34,422, and lacks the disulfide bond and methionine. The regulatory region of phoS contains a characteristic Shine-Dalgarno sequence at an appropriate position preceding the translational initiation site, as well as three possible Pribnow boxes and one -35 sequence. the nucleotide sequence of the regulatory region of phoS was compared with those of phoA and phoE, the genes constituting the pho regulon.

摘要

phoS是磷酸结合蛋白的结构基因,该蛋白定位于周质中,参与大肠杆菌中磷酸盐的主动运输。它也是pho操纵子的负调控基因,其基因表达可由磷酸盐饥饿诱导。phoS基因的完整核苷酸序列通过Maxam和Gilbert的方法(A. M. Maxam和W. Gilbert,《酶学方法》65:499 - 560,1980)测定。利用纯化的蛋白质确定了前PhoS蛋白和PhoS蛋白氨基末端以及PhoS蛋白羧基末端的氨基酸序列。此外,还确定了PhoS蛋白经酶切的肽片段的氨基酸序列。综合这些数据确定了编码区的核苷酸序列以及前PhoS蛋白和PhoS蛋白的氨基酸序列。前PhoS蛋白在PhoS蛋白的氨基末端含有一个由25个氨基酸残基组成的肽延伸段,具有信号肽的一般特征。成熟的PhoS蛋白由321个氨基酸残基组成,计算分子量为34422,且不含二硫键和甲硫氨酸。phoS的调控区在翻译起始位点之前的适当位置含有一个特征性的Shine - Dalgarno序列,以及三个可能的Pribnow框和一个 - 35序列。将phoS调控区的核苷酸序列与构成pho操纵子的phoA和phoE的核苷酸序列进行了比较。

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