Literature DB >> 8190065

Isolation of a DNA polymerase I (polA) mutant of Rhizobium leguminosarum that has significantly reduced levels of an IncQ-group plasmid.

S F Crank1, J A Downie.   

Abstract

A population of Tn5 mutagenized Rhizobium leguminosarum cells was screened for mutants affected in protein secretion by introducing a plasmid carrying the Erwinia chrysanthemi prtB gene and screening for mutants defective in secretion of the protease PrtB. One such mutant (A301) also appeared to be defective in secretion of the R. leguminosarum nodulation protein NodO. Genetic analysis showed that the defect in A301 was caused by the Tn5 insertion. However the DNA sequence adjacent to the site of Tn5 insertion had significant homology to the Escherichia coli polA gene, which encodes DNA polymerase I. The mutant A301 showed increased sensitivity to ultraviolet light, a characteristic of polA mutants of E. coli. The apparent defect in secretion by A301 was due to a large decrease in the copy number of the IncQ group replicon on which prtB and nodO were cloned and this decreased the total amounts of PrtB or NodO protein synthesised and secreted by the polA mutant. The polA mutant had a lower growth rate than the parent strain on both rich and minimal media, but there was no obvious effect of the polA mutation on the symbiosis of R. leguminosarum bv. viciae with pea.

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Year:  1994        PMID: 8190065     DOI: 10.1007/bf00283884

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  23 in total

1.  A rapid method for the identification of plasmid desoxyribonucleic acid in bacteria.

Authors:  T Eckhardt
Journal:  Plasmid       Date:  1978-09       Impact factor: 3.466

Review 2.  Signaling and host range variation in nodulation.

Authors:  J Dénarié; F Debellé; C Rosenberg
Journal:  Annu Rev Microbiol       Date:  1992       Impact factor: 15.500

3.  Nucleotide sequence of the Escherichia coli polA gene and primary structure of DNA polymerase I.

Authors:  C M Joyce; W S Kelley; N D Grindley
Journal:  J Biol Chem       Date:  1982-02-25       Impact factor: 5.157

4.  Supercoil sequencing: a fast and simple method for sequencing plasmid DNA.

Authors:  E Y Chen; P H Seeburg
Journal:  DNA       Date:  1985-04

5.  Rapid similarity searches of nucleic acid and protein data banks.

Authors:  W J Wilbur; D J Lipman
Journal:  Proc Natl Acad Sci U S A       Date:  1983-02       Impact factor: 11.205

6.  Protein secretion in gram-negative bacteria. The extracellular metalloprotease B from Erwinia chrysanthemi contains a C-terminal secretion signal analogous to that of Escherichia coli alpha-hemolysin.

Authors:  P Delepelaire; C Wandersman
Journal:  J Biol Chem       Date:  1990-10-05       Impact factor: 5.157

7.  Protease secretion by Erwinia chrysanthemi: the specific secretion functions are analogous to those of Escherichia coli alpha-haemolysin.

Authors:  S Létoffé; P Delepelaire; C Wandersman
Journal:  EMBO J       Date:  1990-05       Impact factor: 11.598

8.  Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.

Authors:  G Ditta; S Stanfield; D Corbin; D R Helinski
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

Review 9.  E. coli hemolysin interactions with prokaryotic and eukaryotic cell membranes.

Authors:  C Hughes; P Stanley; V Koronakis
Journal:  Bioessays       Date:  1992-08       Impact factor: 4.345

10.  nodO, a new nod gene of the Rhizobium leguminosarum biovar viciae sym plasmid pRL1JI, encodes a secreted protein.

Authors:  R A de Maagd; A H Wijfjes; H P Spaink; J E Ruiz-Sainz; C A Wijffelman; R J Okker; B J Lugtenberg
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

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  1 in total

1.  DNA polymerase I is essential for growth of Methylobacterium dichloromethanicum DM4 with dichloromethane.

Authors:  M F Kayser; M T Stumpp; S Vuilleumier
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

  1 in total

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