Literature DB >> 6575744

Control of sugar utilization in the oral bacteria Streptococcus salivarius and Streptococcus sanguis by the phosphoenolpyruvate: glucose phosphotransferase system.

C Vadeboncoeur, G Bourgeau, D Mayrand, L Trahan.   

Abstract

Three different Strep. salivarius (G2, G5 and G29) and two Strep. sanguis (GS3 and GS12) mutants affected in the phosphoenolpyruvate: glucose phosphotransferase system were selected on agar plates containing lactose and 2-deoxyglucose. All 5 were defective in a membrane-bound component of the transport system and grew less rapidly than the parent strain in 5 mM glucose-containing medium. Mutants G2 and G29 grew poorly in the presence of 5 mM mannose. Growth on mixed substrates revealed that the mutants and wild-type parents behaved differently. Wild-type strains in medium containing glucose plus another sugar (lactose, galactose, melibiose, raffinose or trehalose for Strep. salivarius and lactose, galactose or trehalose for Strep. sanguis) always exhausted most of the glucose before utilizing the other sugar. The mutants used the second sugar concurrently or preferentially to glucose. In medium containing glucose plus fructose or mannose, the wild types consumed both sugars concurrently whereas the mutants utilized the second sugar before glucose. Mutants G2 and G5 were insensitive to repression by fructose and released glucose into the medium when grown in the presence of 0.4 per cent lactose. Mutant G5 also released galactose. Sugar release was not detected with the wild types. The Strep. salivarius mutants contained normal levels of glucokinase and beta-galactosidase but G5 was almost totally devoid of galactokinase activity after growth on lactose. On galactose, the activity was restored. It seems that the phosphoenolpyruvate: glucose phosphotransferase system is involved in the regulation of sugar utilization in these two streptococci.

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Year:  1983        PMID: 6575744     DOI: 10.1016/0003-9969(83)90119-x

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  7 in total

1.  Galactose and lactose genes from the galactose-positive bacterium Streptococcus salivarius and the phylogenetically related galactose-negative bacterium Streptococcus thermophilus: organization, sequence, transcription, and activity of the gal gene products.

Authors:  Katy Vaillancourt; Sylvain Moineau; Michel Frenette; Christian Lessard; Christian Vadeboncoeur
Journal:  J Bacteriol       Date:  2002-02       Impact factor: 3.490

2.  Phenotypic consequences resulting from a methionine-to-valine substitution at position 48 in the HPr protein of Streptococcus salivarius.

Authors:  P Plamondon; D Brochu; S Thomas; J Fradette; L Gauthier; K Vaillancourt; N Buckley; M Frenette; C Vadeboncoeur
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

3.  Diversity of Streptococcus salivarius ptsH mutants that can be isolated in the presence of 2-deoxyglucose and galactose and characterization of two mutants synthesizing reduced levels of HPr, a phosphocarrier of the phosphoenolpyruvate:sugar phosphotransferase system.

Authors:  S Thomas; D Brochu; C Vadeboncoeur
Journal:  J Bacteriol       Date:  2001-09       Impact factor: 3.490

4.  Phosphoenolpyruvate-sugar phosphotransferase transport system of Streptococcus mutans: purification of HPr and enzyme I and determination of their intracellular concentrations by rocket immunoelectrophoresis.

Authors:  L Thibault; C Vadeboncoeur
Journal:  Infect Immun       Date:  1985-12       Impact factor: 3.441

5.  Multiple sugar: phosphotransferase system permeases participate in catabolite modification of gene expression in Streptococcus mutans.

Authors:  Lin Zeng; Robert A Burne
Journal:  Mol Microbiol       Date:  2008-08-11       Impact factor: 3.501

6.  Lactose transport in Streptococcus mutans: isolation and characterization of factor IIIlac, a specific protein component of the phosphoenolpyruvate-lactose phosphotransferase system.

Authors:  C Vadeboncoeur; M Proulx
Journal:  Infect Immun       Date:  1984-10       Impact factor: 3.441

7.  ManLMN is a glucose transporter and central metabolic regulator in Streptococcus pneumoniae.

Authors:  Eleanor Fleming; Andrew Camilli
Journal:  Mol Microbiol       Date:  2016-08-18       Impact factor: 3.501

  7 in total

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