Literature DB >> 11267761

Isolation and phenotypic characterization of Pseudomonas aeruginosa pseudorevertants containing suppressors of the catabolite repression control-defective crc-10 allele.

D N Collier1, C Spence, M J Cox, P V Phibbs.   

Abstract

The amiE gene encodes an aliphatic amidase capable of converting fluoroacetamide to the toxic compound fluoroacetate and is one of many genes whose expression is subject to catabolite repression control in Pseudomonas aeruginosa. The protein product of the crc gene, Crc, is required for repression of amiE and most other genes subject to catabolite repression control in this bacterium. When grown in a carbon source such as succinate, wild-type P. aeruginosa is insensitive to fluoroacetamide (due to repression of amiE expression). In contrast, mutants harboring the crc-10 null allele cannot grow in the presence of fluoroacetamide (due to lack of repression of amiE). Selection for succinate-dependent, fluoroacetamide-resistant derivatives of the crc-10 mutant yielded three independent pseudorevertants containing suppressors that restored a degree of catabolite repression control. Synthesis of Crc protein was not reestablished in these pseudorevertants. All three suppressors of crc-10 were extragenic, and all three also suppressed a Delta crc::tetA allele. In each of the three pseudorevertants, catabolite repression control of amidase expression was restored. Catabolite repression control of mannitol dehydrogenase production was also restored in two of the three isolates. None of the suppressors restored repression of glucose-6-phosphate dehydrogenase or pyocyanin production.

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Year:  2001        PMID: 11267761     DOI: 10.1111/j.1574-6968.2001.tb10546.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  6 in total

1.  The global carbon metabolism regulator Crc is a component of a signal transduction pathway required for biofilm development by Pseudomonas aeruginosa.

Authors:  G A O'Toole; K A Gibbs; P W Hager; P V Phibbs; R Kolter
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

2.  Integration of signals through Crc and PtsN in catabolite repression of Pseudomonas putida TOL plasmid pWW0.

Authors:  Isabel Aranda-Olmedo; Juan L Ramos; Silvia Marqués
Journal:  Appl Environ Microbiol       Date:  2005-08       Impact factor: 4.792

3.  Genetic evidence that catabolites of the Entner-Doudoroff pathway signal C source repression of the sigma54 Pu promoter of Pseudomonas putida.

Authors:  Francisco Velázquez; Ilaria di Bartolo; Víctor de Lorenzo
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

4.  Simultaneous catabolite repression between glucose and toluene metabolism in Pseudomonas putida is channeled through different signaling pathways.

Authors:  Teresa del Castillo; Juan L Ramos
Journal:  J Bacteriol       Date:  2007-07-06       Impact factor: 3.490

5.  Metabolic basis for the evolution of a common pathogenic Pseudomonas aeruginosa variant.

Authors:  Dallas L Mould; Mirjana Stevanovic; Alix Ashare; Daniel Schultz; Deborah A Hogan
Journal:  Elife       Date:  2022-05-03       Impact factor: 8.713

6.  The aliphatic amidase AmiE is involved in regulation of Pseudomonas aeruginosa virulence.

Authors:  Thomas Clamens; Thibaut Rosay; Alexandre Crépin; Teddy Grandjean; Takfarinas Kentache; Julie Hardouin; Perrine Bortolotti; Anke Neidig; Marlies Mooij; Mélanie Hillion; Julien Vieillard; Pascal Cosette; Joerg Overhage; Fergal O'Gara; Emeline Bouffartigues; Alain Dufour; Sylvie Chevalier; Benoit Guery; Pierre Cornelis; Marc G J Feuilloley; Olivier Lesouhaitier
Journal:  Sci Rep       Date:  2017-01-24       Impact factor: 4.379

  6 in total

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