Literature DB >> 7768869

ccrA1: a mutation in Streptomyces coelicolor that affects the control of catabolite repression.

C Ingram1, I Delic, J Westpheling.   

Abstract

The regulation of carbon utilization is of central importance in the gene expression pathways for both morphological development and antibiotic production in Streptomyces species. We report the identification and characterization of a mutation in Streptomyces coelicolor, ccrA1, that affects the expression of several catabolite-controlled promoters. ccrA1 mutants are altered in expression of galP1, the glucose-sensitive, galactose-dependent promoter of the galactose utilization operon; in expression of the glycerol utilization operon, which is glucose sensitive and glycerol dependent; and in expression of chi63, the glucose-sensitive chitin-dependent promoter of a gene involved in chitin utilization. ccrA1 has no effect on the expression of galP2, a promoter that directs constitutive transcription of the galE and galK genes. ccrA1 maps to a region of the S. coelicolor genome which distinguishes it from other mutations known to be involved in catabolite control. We suggest that ccrA1 identifies a gene whose product may be involved in the general regulation of carbon catabolite repression in this complex bacterium.

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Year:  1995        PMID: 7768869      PMCID: PMC177065          DOI: 10.1128/jb.177.12.3579-3586.1995

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


  41 in total

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Authors:  M J Buttner; A M Smith; M J Bibb
Journal:  Cell       Date:  1988-02-26       Impact factor: 41.582

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Journal:  Biochem Biophys Res Commun       Date:  1968-03-27       Impact factor: 3.575

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Authors:  C Guidi-Rontani; A Danchin; A Ullmann
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

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Journal:  J Bacteriol       Date:  1980-10       Impact factor: 3.490

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Authors:  C J Thompson; J M Ward; D A Hopwood
Journal:  J Bacteriol       Date:  1982-08       Impact factor: 3.490

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Authors:  N D Lomovskaya; N M Mkrtumian; N L Gostimskaya; V N Danilenko
Journal:  J Virol       Date:  1972-02       Impact factor: 5.103

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Authors:  I Pastan; R Perlman
Journal:  Science       Date:  1970-07-24       Impact factor: 47.728

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  7 in total

1.  Regulation of hly expression in Listeria monocytogenes by carbon sources and pH occurs through separate mechanisms mediated by PrfA.

Authors:  J Behari; P Youngman
Journal:  Infect Immun       Date:  1998-08       Impact factor: 3.441

2.  Modulation of actinorhodin biosynthesis in Streptomyces lividans by glucose repression of afsR2 gene transcription.

Authors:  E S Kim; H J Hong; C Y Choi; S N Cohen
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

3.  A new GntR family transcriptional regulator in streptomyces coelicolor is required for morphogenesis and antibiotic production and controls transcription of an ABC transporter in response to carbon source.

Authors:  Brandan Hillerich; Janet Westpheling
Journal:  J Bacteriol       Date:  2006-08-25       Impact factor: 3.490

4.  glkA is involved in glucose repression of chitinase production in Streptomyces lividans.

Authors:  A Saito; T Fujii; T Yoneyama; K Miyashita
Journal:  J Bacteriol       Date:  1998-06       Impact factor: 3.490

5.  The synthesis of the Streptomyces reticuli cellulase (avicelase) is regulated by both activation and repression mechanisms.

Authors:  S Walter; H Schrempf
Journal:  Mol Gen Genet       Date:  1996-05-23

6.  Phosphoinositides are involved in control of the glucose-dependent growth resumption that follows the transition phase in Streptomyces lividans.

Authors:  H Chouayekh; H Nothaft; S Delaunay; M Linder; B Payrastre; N Seghezzi; F Titgemeyer; M J Virolle
Journal:  J Bacteriol       Date:  2006-11-22       Impact factor: 3.490

7.  In vivo analysis of HPr reveals a fructose-specific phosphotransferase system that confers high-affinity uptake in Streptomyces coelicolor.

Authors:  Harald Nothaft; Stephan Parche; Annette Kamionka; Fritz Titgemeyer
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

  7 in total

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