Literature DB >> 3308849

Signal sequence mutations that alter coupling of secretion and translation of an Escherichia coli outer membrane protein.

S A Benson1, M N Hall, B A Rasmussen.   

Abstract

The lamB701-708 signal sequence mutation reduces expression of LamB, an outer membrane protein of Escherichia coli. To investigate the possibility that synthesis and export of LamB are coupled, as suggested by the expression defect of the lamB701-708 mutation, we isolated intragenic suppressors of the lamB701-708 mutation. The expression defect imposed by the lamB701-708 mutation is suppressed by an export-defective signal sequence mutation, suggesting that translation and export are coupled. The additional observation that not all export-defective signal sequence mutations suppressed the lamB701-708 expression defect suggests that translational arrest can be uncoupled from export.

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Year:  1987        PMID: 3308849      PMCID: PMC213840          DOI: 10.1128/jb.169.10.4686-4691.1987

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


  21 in total

1.  Structure of the malB region in Escherichia coli K12. I. Genetic map of the malK-lamB operon.

Authors:  O Raibaud; M Roa; C Braun-Breton; M Schwartz
Journal:  Mol Gen Genet       Date:  1979-07-24

Review 2.  Cotranslational and posttranslational protein translocation in prokaryotic systems.

Authors:  C Lee; J Beckwith
Journal:  Annu Rev Cell Biol       Date:  1986

3.  Mutations that affect lamB gene expression at a posttranscriptional level.

Authors:  M Schwartz; M Roa; M Débarbouillé
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

4.  A role for mRNA secondary structure in the control of translation initiation.

Authors:  M N Hall; J Gabay; M Débarbouillé; M Schwartz
Journal:  Nature       Date:  1982-02-18       Impact factor: 49.962

5.  Presentation of the maltose system and of the workshop.

Authors:  M Hofnung
Journal:  Ann Microbiol (Paris)       Date:  1982-01

6.  Localization and processing of outer membrane and periplasmic proteins in Escherichia coli strains harboring export-specific suppressor mutations.

Authors:  S D Emr; P J Bassford
Journal:  J Biol Chem       Date:  1982-05-25       Impact factor: 5.157

7.  Mutations affecting localization of an Escherichia coli outer membrane protein, the bacteriophage lambda receptor.

Authors:  S D Emr; T J Silhavy
Journal:  J Mol Biol       Date:  1980-07-25       Impact factor: 5.469

8.  E. coli mutant pleiotropically defective in the export of secreted proteins.

Authors:  D B Oliver; J Beckwith
Journal:  Cell       Date:  1981-09       Impact factor: 41.582

9.  Evidence for a coupling of synthesis and export of an outer membrane protein in Escherichia coli.

Authors:  M N Hall; J Gabay; M Schwartz
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

10.  Translocation of proteins across the endoplasmic reticulum III. Signal recognition protein (SRP) causes signal sequence-dependent and site-specific arrest of chain elongation that is released by microsomal membranes.

Authors:  P Walter; G Blobel
Journal:  J Cell Biol       Date:  1981-11       Impact factor: 10.539

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  4 in total

1.  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

2.  Cassette mutagenic analysis of the yeast invertase signal peptide: effects on protein translocation.

Authors:  J K Ngsee; W Hansen; P Walter; M Smith
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

Review 3.  Signal peptide mutants of Escherichia coli.

Authors:  J Gennity; J Goldstein; M Inouye
Journal:  J Bioenerg Biomembr       Date:  1990-06       Impact factor: 2.945

4.  Effect of OmpA signal peptide mutations on OmpA secretion, synthesis, and assembly.

Authors:  Y Tanji; J Gennity; S Pollitt; M Inouye
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

  4 in total

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