Literature DB >> 1834634

The first gene in the Escherichia coli secA operon, gene X, encodes a nonessential secretory protein.

T Rajapandi1, K M Dolan, D B Oliver.   

Abstract

TnphoA insertions in the first gene of the Escherichia coli secA operon, gene X, were isolated and analyzed. Studies of the Gene X-PhoA fusion proteins showed that gene X encodes a secretory protein, since the fusion proteins possessed normal alkaline phosphatase activity and a substantial portion of this activity was found in the periplasm. In addition, the Gene X-PhoA fusion proteins were initially synthesized with a cleavable signal peptide. A gene X::TnphoA insertion was used to construct a strain containing a disrupted chromosomal copy of gene X. Analysis of this strain indicated that gene X is nonessential for cell growth and viability and does not appear to play an essential role in the process of protein export.

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Year:  1991        PMID: 1834634      PMCID: PMC209214          DOI: 10.1128/jb.173.22.7092-7097.1991

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


  26 in total

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Journal:  J Mol Biol       Date:  1975-08-05       Impact factor: 5.469

2.  Use of phoA fusions to study the topology of the Escherichia coli inner membrane protein leader peptidase.

Authors:  J L San Millan; D Boyd; R Dalbey; W Wickner; J Beckwith
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

3.  Novel secA alleles improve export of maltose-binding protein synthesized with a defective signal peptide.

Authors:  J D Fikes; P J Bassford
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

4.  A new method for predicting signal sequence cleavage sites.

Authors:  G von Heijne
Journal:  Nucleic Acids Res       Date:  1986-06-11       Impact factor: 16.971

5.  Regulation of the Escherichia coli secA gene by protein secretion defects: analysis of secA, secB, secD, and secY mutants.

Authors:  E E Rollo; D B Oliver
Journal:  J Bacteriol       Date:  1988-07       Impact factor: 3.490

6.  Vectors for selective expression of cloned DNAs by T7 RNA polymerase.

Authors:  A H Rosenberg; B N Lade; D S Chui; S W Lin; J J Dunn; F W Studier
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7.  Azide-resistant mutants of Escherichia coli alter the SecA protein, an azide-sensitive component of the protein export machinery.

Authors:  D B Oliver; R J Cabelli; K M Dolan; G P Jarosik
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

8.  Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes.

Authors:  F W Studier; B A Moffatt
Journal:  J Mol Biol       Date:  1986-05-05       Impact factor: 5.469

9.  Isolation and analysis of dominant secA mutations in Escherichia coli.

Authors:  G P Jarosik; D B Oliver
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

10.  TnphoA: a transposon probe for protein export signals.

Authors:  C Manoil; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

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  14 in total

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Authors:  H Tian; D Boyd; J Beckwith
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

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Authors:  Shameema Sarker; Donald Oliver
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3.  Revised translation start site for secM defines an atypical signal peptide that regulates Escherichia coli secA expression.

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Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

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5.  Translocon "pulling" of nascent SecM controls the duration of its translational pause and secretion-responsive secA regulation.

Authors:  Martha E Butkus; Lucia B Prundeanu; Donald B Oliver
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

6.  Translation arrest of SecM is essential for the basal and regulated expression of SecA.

Authors:  Akiko Murakami; Hitoshi Nakatogawa; Koreaki Ito
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-09       Impact factor: 11.205

7.  SecM facilitates translocase function of SecA by localizing its biosynthesis.

Authors:  Hitoshi Nakatogawa; Akiko Murakami; Hiroyuki Mori; Koreaki Ito
Journal:  Genes Dev       Date:  2005-02-15       Impact factor: 11.361

8.  Regulation of Escherichia coli secA by cellular protein secretion proficiency requires an intact gene X signal sequence and an active translocon.

Authors:  D Oliver; J Norman; S Sarker
Journal:  J Bacteriol       Date:  1998-10       Impact factor: 3.490

9.  Recruitment of a species-specific translational arrest module to monitor different cellular processes.

Authors:  Shinobu Chiba; Takashi Kanamori; Takuya Ueda; Yoshinori Akiyama; Kit Pogliano; Koreaki Ito
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-07       Impact factor: 11.205

10.  Genetic screen yields mutations in genes encoding all known components of the Escherichia coli signal recognition particle pathway.

Authors:  Hongping Tian; Jon Beckwith
Journal:  J Bacteriol       Date:  2002-01       Impact factor: 3.490

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