Literature DB >> 8384621

Two glucose transport systems in Bacillus licheniformis.

M Tangney1, F G Priest, W J Mitchell.   

Abstract

Bacillus licheniformis NCIB 6346 showed active accumulation of glucose which was inhibited by agents which affect the transmembrane proton gradient. Phosphotransferase (PTS) activity, identified as phosphoenolpyruvate-dependent phosphorylation of glucose, was found in cell extracts but could not be demonstrated in cells permeabilized with toluene when assays were conducted at pH 6.6. The same was true for mannitol and fructose phosphotransferase activities. Cells grown on fructose accumulated glucose at a slower rate than glucose-grown cells, and extracts prepared from them did not contain glucose PTS activity. Examination of the effects of analogs on glucose uptake and phosphorylation showed that 2-deoxyglucose was not a PTS substrate, but did markedly inhibit glucose uptake, with stronger inhibition in cells grown on fructose. Glucose accumulation by whole cells grown on glucose became less sensitive to the uncoupler tetrachlorosalicylanilide (TCS) as the pH was raised from 6.6 to 8.0, while in fructose-grown cells TCS was equally effective across this pH range. PTS activity was exhibited by toluene-treated cells at pH 7.5 and above, although the system itself in extracts was not affected by pH in the range of 5.0 to 8.0. The results are consistent with the presence of two glucose transport systems, one a PTS and the other operating by an alternative mechanisms, and suggest that the PTS in B. licheniformis may be regulated in a pH-dependent manner.

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Year:  1993        PMID: 8384621      PMCID: PMC204328          DOI: 10.1128/jb.175.7.2137-2142.1993

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


  18 in total

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2.  Periplasmic space in Salmonella typhimurium and Escherichia coli.

Authors:  J B Stock; B Rauch; S Roseman
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3.  A new assay of the phosphotransferase system in Escherichia coli.

Authors:  G Gachelin
Journal:  Biochem Biophys Res Commun       Date:  1969-02-21       Impact factor: 3.575

4.  Effect of growth rate and glucose concentration on the activity of the phosphoenolpyruvate phosphotransferase system in Streptococcus mutans Ingbritt grown in continuous culture.

Authors:  D C Ellwood; P J Phipps; I R Hamilton
Journal:  Infect Immun       Date:  1979-02       Impact factor: 3.441

5.  Regulation of glycerol uptake by the phosphoenolpyruvate-sugar phosphotransferase system in Bacillus subtilis.

Authors:  J Reizer; M J Novotny; I Stuiver; M H Saier
Journal:  J Bacteriol       Date:  1984-07       Impact factor: 3.490

6.  Induction of the phosphoenolpyruvate: hexose phosphotransferase system associated with relative anaerobiosis in an obligate aerobe.

Authors:  N Pelliccione; B Jaffin; M E Sobel; T A Krulwich
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7.  Properties of ATP-dependent protein kinase from Streptococcus pyogenes that phosphorylates a seryl residue in HPr, a phosphocarrier protein of the phosphotransferase system.

Authors:  J Reizer; M J Novotny; W Hengstenberg; M H Saier
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

8.  Properties of Streptococcus mutans Ingbritt growing on limiting sucrose in a chemostat: repression of the phosphoenolpyruvate phosphotransferase transport system.

Authors:  D C Ellwood; I R Hamilton
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

9.  Quantitative measurements of the proton-motive force and its relation to steady state lactose accumulation in Escherichia coli.

Authors:  S Ahmed; I R Booth
Journal:  Biochem J       Date:  1981-12-15       Impact factor: 3.857

10.  Maltose uptake and its regulation in Bacillus subtilis.

Authors:  M Tangney; C J Buchanan; F G Priest; W J Mitchell
Journal:  FEMS Microbiol Lett       Date:  1992-10-01       Impact factor: 2.742

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  5 in total

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Authors:  C Parker; R W Hutkins
Journal:  Appl Environ Microbiol       Date:  1997-02       Impact factor: 4.792

2.  Catabolite repression of the Bacillus subtilis xyl operon involves a cis element functional in the context of an unrelated sequence, and glucose exerts additional xylR-dependent repression.

Authors:  A Kraus; C Hueck; D Gärtner; W Hillen
Journal:  J Bacteriol       Date:  1994-03       Impact factor: 3.490

3.  Characterization of a glucose transport system in Vibrio parahaemolyticus.

Authors:  R I Sarker; W Ogawa; M Tsuda; S Tanaka; T Tsuchiya
Journal:  J Bacteriol       Date:  1994-12       Impact factor: 3.490

4.  The glucose kinase of Bacillus subtilis.

Authors:  P Skarlatos; M K Dahl
Journal:  J Bacteriol       Date:  1998-06       Impact factor: 3.490

5.  Glucose Transport in Stationary-Phase Cultures of an Asporogenous Strain of Bacillus licheniformis.

Authors:  M Tangney; J E Tate; F G Priest; W J Mitchell
Journal:  Appl Environ Microbiol       Date:  1996-02       Impact factor: 4.792

  5 in total

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