Literature DB >> 6337849

Hyperproduction of phosphate-binding protein, phoS, and pre-phoS proteins in Escherichia coli carrying a cloned phoS gene.

T Morita, M Amemura, K Makino, H Shinagawa, K Magota, N Otsuji, A Nakata.   

Abstract

A large amount of phosphate-binding protein, the phoS gene product, accumulated in the periplasmic space of the cells when an Escherichia coli strain carrying a multicopy plasmid containing a chromosomal fragment of the phoS-phoT region (pSN507) was grown in a low-phosphate medium. When the same strain carrying a plasmid containing only the phoS gene (pSN518 or pSN5182) was grown in low-phosphate medium, phosphate-binding protein accumulated in the periplasm, and in addition a larger protein accumulated in the non-periplasmic fraction. The apparent Mr of this protein and the phosphate-binding protein were 39000 and 35000 respectively, as judged by sodium dodecyl sulfate/polyacrylamide gel electrophoresis. This larger protein showed immunological cross-reaction with the phosphate-binding protein. The 39000-Mr protein was also detected in cells carrying pSN507 when the proteins were pulse-labeled with radioactive amino acids. From these findings, together with the fact that this protein is recovered from the membrane fraction, we conclude that this protein is an unsecreted precursor protein of the phosphate-binding protein. Kinetics and regulation of accumulation of these proteins were studied. This system will be useful for preparation and purification of the precursor protein for biochemical studies in relation to the mechanism of protein secretion.

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Year:  1983        PMID: 6337849     DOI: 10.1111/j.1432-1033.1983.tb07169.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  17 in total

1.  Activation by gene amplification of pitB, encoding a third phosphate transporter of Escherichia coli K-12.

Authors:  S M Hoffer; P Schoondermark; H W van Veen; J Tommassen
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

2.  Regulation of the phosphate regulon of Escherichia coli: characterization of the promoter of the pstS gene.

Authors:  S Kimura; K Makino; H Shinagawa; M Amemura; A Nakata
Journal:  Mol Gen Genet       Date:  1989-02

Review 3.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

Review 4.  Linkage map of Escherichia coli K-12, edition 8.

Authors:  B J Bachmann
Journal:  Microbiol Rev       Date:  1990-06

5.  Overproduction of acetate kinase activates the phosphate regulon in the absence of the phoR and phoM functions in Escherichia coli.

Authors:  T Y Lee; K Makino; H Shinagawa; A Nakata
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

6.  Expression in Escherichia coli of the 37-kilodalton endoflagellar sheath protein of Treponema pallidum by use of the polymerase chain reaction and a T7 expression system.

Authors:  R D Isaacs; J D Radolf
Journal:  Infect Immun       Date:  1990-07       Impact factor: 3.441

7.  Nucleotide sequence of the lig gene and primary structure of DNA ligase of Escherichia coli.

Authors:  Y Ishino; H Shinagawa; K Makino; S Tsunasawa; F Sakiyama; A Nakata
Journal:  Mol Gen Genet       Date:  1986-07

8.  The effect of the locus pstB on phosphate binding in the phosphate specific transport (PST) system of Escherichia coli.

Authors:  R Levitz; I Friedberg; R Brucker; A Fux; E Yagil
Journal:  Mol Gen Genet       Date:  1985

9.  Structural gene for the phosphate-repressible phosphate-binding protein of Escherichia coli has its own promoter: complete nucleotide sequence of the phoS gene.

Authors:  B P Surin; D A Jans; A L Fimmel; D C Shaw; G B Cox; H Rosenberg
Journal:  J Bacteriol       Date:  1984-03       Impact factor: 3.490

10.  Immediate entrance to the export pathway after synthesis as a requirement for export of the sak gene product in Escherichia coli.

Authors:  T Sako
Journal:  J Bacteriol       Date:  1986-09       Impact factor: 3.490

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