Literature DB >> 7657605

Genetic and transcriptional organization of the region encoding the beta subunit of Bacillus subtilis RNA polymerase.

K J Boor1, M L Duncan, C W Price.   

Abstract

The gene encoding the beta subunit of Bacillus subtilis RNA polymerase was isolated from a lambda gt11 expression library using an antibody probe. Gene identity was confirmed by the similarity of its predicted product to the Escherichia coli beta subunit and by mapping an alteration conferring rifampicin resistance within the conserved rif coding region. Including the rif region, four colinear blocks of sequence similarity were shared between the B. subtilis and E. coli beta subunits. In E. coli, these conserved blocks are separated by three regions that either were not conserved or were entirely absent from the B. subtilis protein. The B. subtilis beta gene was part of a cluster with the order rplL (encoding ribosomal protein L7/L12), orf23 (encoding a 22,513-dalton protein that is apparently essential for growth), rpoB (beta), and rpoC (beta'). This organization differs from the corresponding region in E. coli by the inclusion of orf23. Experiments using promoter probe vectors and site-directed mutagenesis located a major rpoB promoter overlapping the 3'-coding region of orf23, 250 nucleotides upstream from the beta initiation codon. Thus, the B. subtilis rpoB region differs from its E. coli counterpart in both genetic and transcriptional organization.

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Year:  1995        PMID: 7657605     DOI: 10.1074/jbc.270.35.20329

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  21 in total

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3.  Ribosomal protein gene cluster analysis in eubacterium genomics: homology between Sinorhizobium meliloti strain 1021 and Bacillus subtilis.

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5.  Barriers to genetic exchange between bacterial species: Streptococcus pneumoniae transformation.

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6.  The spectrum of spontaneous rifampin resistance mutations in the rpoB gene of Bacillus subtilis 168 spores differs from that of vegetative cells and resembles that of Mycobacterium tuberculosis.

Authors:  Wayne L Nicholson; Heather Maughan
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

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8.  Residues in the N-terminal domain of MutL required for mismatch repair in Bacillus subtilis.

Authors:  Nicholas J Bolz; Justin S Lenhart; Steven C Weindorf; Lyle A Simmons
Journal:  J Bacteriol       Date:  2012-07-27       Impact factor: 3.490

9.  rpoB-based identification of nonpigmented and late-pigmenting rapidly growing mycobacteria.

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Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

10.  Immunohistochemical localization of galectin-3 in the granulomatous lesions of paratuberculosis-infected bovine intestine.

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