Literature DB >> 2496297

Anaerobic growth defects resulting from gene fusions affecting succinyl-CoA synthetase in Escherichia coli K12.

F Mat-Jan1, C R Williams, D P Clark.   

Abstract

Insertion of the fusion-generating phage Mud1 (Ap, lacZ) yielded two similar isolates, DC511 and DC512, which were unable to grow aerobically on acetate or alpha-ketoglutarate but which could use succinate, malate, fumarate, glycerol, and various sugars. These mutants were unable to grow anaerobically on most sugars unless provided with methionine, lysine, and delta-aminolevulinic acid, all of which require succinyl-CoA for their synthesis. The insertions of both mutants mapped at 17 min, in the suc operon. Enzyme assays indicated a lack of succinyl-CoA synthetase; however, full activity of the alpha-ketoglutarate dehydrogenase was retained. Beta-galactosidase expression by strains containing these gene fusions was reduced under anaerobic conditions. In aerobically grown cultures, both fusions were induced about fivefold in the presence of acetate. This type of regulation would be expected of a Krebs cycle enzyme.

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Year:  1989        PMID: 2496297     DOI: 10.1007/bf00339728

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


  16 in total

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Journal:  J Gen Microbiol       Date:  1986-06

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Journal:  J Bacteriol       Date:  1982-01       Impact factor: 3.490

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  4 in total

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Authors:  Y J Avissar; S I Beale
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

2.  Change in direction of flagellar rotation in Escherichia coli mediated by acetate kinase.

Authors:  F E Dailey; H C Berg
Journal:  J Bacteriol       Date:  1993-05       Impact factor: 3.490

3.  pH dependence and gene structure of inaA in Escherichia coli.

Authors:  S White; F E Tuttle; D Blankenhorn; D C Dosch; J L Slonczewski
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

4.  Rationally designed mariner vectors for functional genomic analysis of Actinobacillus pleuropneumoniae and other Pasteurellaceae species by transposon-directed insertion-site sequencing (TraDIS).

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