Literature DB >> 3305483

Export of protein in Escherichia coli: a novel mutation in ompC affects expression of other major outer membrane proteins.

K M Catron, C A Schnaitman.   

Abstract

A mutation within the ompC structural gene of Escherichia coli K-12 which affects expression of outer membrane proteins was characterized. The mutation consisted of a 6-base-pair deletion near the 3' end of the gene which removed the amino acids Val-300 and Gly-301 of the mature coding sequence but otherwise left the reading frame intact. The deletion occurred within a region highly conserved among the porins. No protein product was detected from a single copy of the mutant gene. The mutation caused a trans-dominant decrease in the expression of a wild-type ompC allele. The mutation caused a similar decrease in the amounts of OmpA, OmpF, LamB, and Lc proteins, yet it did not appear to affect the minor outer membrane proteins. It had no significant effect on transcription from either ompF or ompC promoters as measured with lacZ operon fusions. The effects of the mutation on other proteins were completely eliminated when the signal sequence was disrupted so that the mutant protein no longer interacted with the secretion machinery of the cell but instead accumulated as precursor in the cytoplasm. A model is proposed involving the translocation of proteins to the outer membrane and the importance of protein conformation in this process.

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Year:  1987        PMID: 3305483      PMCID: PMC213748          DOI: 10.1128/jb.169.9.4327-4334.1987

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  27 in total

1.  A reliable method for the recovery of DNA fragments from agarose and acrylamide gels.

Authors:  G Dretzen; M Bellard; P Sassone-Corsi; P Chambon
Journal:  Anal Biochem       Date:  1981-04       Impact factor: 3.365

2.  Selection for loss of tetracycline resistance by Escherichia coli.

Authors:  S R Maloy; W D Nunn
Journal:  J Bacteriol       Date:  1981-02       Impact factor: 3.490

Review 3.  Genetic analysis of the major outer membrane proteins of Escherichia coli.

Authors:  M N Hall; T J Silhavy
Journal:  Annu Rev Genet       Date:  1981       Impact factor: 16.830

4.  Identification of three genes controlling production of new outer membrane pore proteins in Escherichia coli K-12.

Authors:  A P Pugsley; C A Schnaitman
Journal:  J Bacteriol       Date:  1978-09       Impact factor: 3.490

5.  Outer membrane proteins of Escherichia coli. VII. Evidence that bacteriophage-directed protein 2 functions as a pore.

Authors:  A P Pugsley; C A Schnaitman
Journal:  J Bacteriol       Date:  1978-03       Impact factor: 3.490

6.  Translocation of phospholipids between the outer and inner membranes of Salmonella typhimurium.

Authors:  N C Jones; M J Osborn
Journal:  J Biol Chem       Date:  1977-10-25       Impact factor: 5.157

7.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

8.  Studies on transformation of Escherichia coli with plasmids.

Authors:  D Hanahan
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

9.  Biosynthesis of the outer membrane receptor for vitamin B12, E colicins, and bacteriophage BF23 by Escherichia coli: kinetics of phenotypic expression after the introduction of bfe+ and bfe alleles.

Authors:  P J Bassford; R J Kadner; C A Schnaitman
Journal:  J Bacteriol       Date:  1977-01       Impact factor: 3.490

10.  The ultimate localization of an outer membrane protein of Escherichia coli K-12 is not determined by the signal sequence.

Authors:  J Tommassen; H van Tol; B Lugtenberg
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

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  11 in total

1.  The Escherichia coli sigma(E)-dependent extracytoplasmic stress response is controlled by the regulated proteolysis of an anti-sigma factor.

Authors:  S E Ades; L E Connolly; B M Alba; C A Gross
Journal:  Genes Dev       Date:  1999-09-15       Impact factor: 11.361

2.  Alterations in the hydrophilic segment of the maltose-binding protein (MBP) signal peptide that affect either export or translation of MBP.

Authors:  J W Puziss; R J Harvey; P J Bassford
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

3.  Deletions or duplications in the BtuB protein affect its level in the outer membrane of Escherichia coli.

Authors:  W Köster; A Gudmundsdottir; M D Lundrigan; A Seiffert; R J Kadner
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

4.  Genetic analysis of lipopolysaccharide core biosynthesis by Escherichia coli K-12: insertion mutagenesis of the rfa locus.

Authors:  E A Austin; J F Graves; L A Hite; C T Parker; C A Schnaitman
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

5.  Export-defective lamB protein is a target for translational control caused by ompC porin overexpression.

Authors:  E M Click; C A Schnaitman
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

6.  Translational control of exported proteins that results from OmpC porin overexpression.

Authors:  E M Click; G A McDonald; C A Schnaitman
Journal:  J Bacteriol       Date:  1988-05       Impact factor: 3.490

7.  Role of lipopolysaccharide in assembly of Escherichia coli outer membrane proteins OmpA, OmpC, and OmpF.

Authors:  G Ried; I Hindennach; U Henning
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

8.  Overproduction and identification of the ftsQ gene product, an essential cell division protein in Escherichia coli K-12.

Authors:  D R Storts; O M Aparicio; J M Schoemaker; A Markovitz
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

9.  Role of the rfaG and rfaP genes in determining the lipopolysaccharide core structure and cell surface properties of Escherichia coli K-12.

Authors:  C T Parker; A W Kloser; C A Schnaitman; M A Stein; S Gottesman; B W Gibson
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

10.  DegS and YaeL participate sequentially in the cleavage of RseA to activate the sigma(E)-dependent extracytoplasmic stress response.

Authors:  Benjamin M Alba; Jennifer A Leeds; Christina Onufryk; Chi Zen Lu; Carol A Gross
Journal:  Genes Dev       Date:  2002-08-15       Impact factor: 11.361

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