Literature DB >> 2579114

Reduction of acidurance of streptococcal growth and glycolysis by fluoride and gramicidin.

G R Bender, E A Thibodeau, R E Marquis.   

Abstract

The acidurance of glycolysis by intact cells of Streptococcus mutans GS-5, Streptococcus salivarius ATCC 25925, and Streptococcus sanguis NCTC 10904 was found to be highly dependent on membrane functions affected by gramicidin, which increases the proton permeability of cell membranes. Plots of % glucose utilized during two hours against suspension pH values for cells suspended in 100 mM phosphate buffer plus 1 mM MgCl2 plus 13.9 mM glucose indicated, for 50% glucose utilization, pH values of 5.0 for S. mutans, 5.7 for S. salivarius, and 6.2 for S. sanguis. Gramicidin treatment shifted these values to 6.0, 6.3, and 6.9, respectively. Growth of S. mutans and S. salivarius in complex media proved to be more acid-sensitive than was glycolysis, and in batch cultures, there was a well-defined, post-growth phase of glycolysis. Minimum pH values for growth and for glycolysis in medium with excess glucose were approximately 4.8 and 4.4, respectively, for S. mutans, and 4.9 and 4.3 for S. salivarius. S. sanguis was less aciduric and showed little differential acid sensitivity, with minimum pH values of about 5.2 for both growth and glycolysis. Fluoride acted to eliminate the differences in acidurance of growth and glycolysis for S. mutans or S. salivarius and to render both processes more acid-sensitive. Thus, glycolysis was more fluoride-sensitive than was growth. Growth was found to be acid-limited in media with initial glucose levels greater than 0.2, 0.3, and 0.5% (weight/volume) for S. sanguis, S. mutans, and S. salivarius, respectively, and to be glucose-limited at lower levels.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1985        PMID: 2579114     DOI: 10.1177/00220345850640021701

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  21 in total

1.  Characterization of the sat operon in Streptococcus mutans: evidence for a role of Ffh in acid tolerance.

Authors:  B H Kremer; M van der Kraan; P J Crowley; I R Hamilton; L J Brady; A S Bleiweis
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

2.  Evaluation of pH at the bacteria-dental cement interface.

Authors:  G Mayanagi; K Igarashi; J Washio; K Nakajo; H Domon-Tawaraya; N Takahashi
Journal:  J Dent Res       Date:  2011-09-20       Impact factor: 6.116

3.  Arginine deiminase system and bacterial adaptation to acid environments.

Authors:  R E Marquis; G R Bender; D R Murray; A Wong
Journal:  Appl Environ Microbiol       Date:  1987-01       Impact factor: 4.792

4.  Role of the arginine deiminase system in protecting oral bacteria and an enzymatic basis for acid tolerance.

Authors:  A Casiano-Colón; R E Marquis
Journal:  Appl Environ Microbiol       Date:  1988-06       Impact factor: 4.792

5.  Membrane ATPases and acid tolerance of Actinomyces viscosus and Lactobacillus casei.

Authors:  G R Bender; R E Marquis
Journal:  Appl Environ Microbiol       Date:  1987-09       Impact factor: 4.792

6.  β-Phosphoglucomutase contributes to aciduricity in Streptococcus mutans.

Authors:  Andrew A Buckley; Roberta C Faustoferri; Robert G Quivey
Journal:  Microbiology (Reading)       Date:  2014-02-07       Impact factor: 2.777

Review 7.  Role of Streptococcus mutans in human dental decay.

Authors:  W J Loesche
Journal:  Microbiol Rev       Date:  1986-12

Review 8.  Acid tolerance mechanisms utilized by Streptococcus mutans.

Authors:  Robert Matsui; Dennis Cvitkovitch
Journal:  Future Microbiol       Date:  2010-03       Impact factor: 3.165

9.  Spontaneously Arising Streptococcus mutans Variants with Reduced Susceptibility to Chlorhexidine Display Genetic Defects and Diminished Fitness.

Authors:  Justin R Kaspar; Matthew J Godwin; Irina M Velsko; Vincent P Richards; Robert A Burne
Journal:  Antimicrob Agents Chemother       Date:  2019-06-24       Impact factor: 5.191

Review 10.  Biology, ecology, and biotechnological applications of anaerobic bacteria adapted to environmental stresses in temperature, pH, salinity, or substrates.

Authors:  S E Lowe; M K Jain; J G Zeikus
Journal:  Microbiol Rev       Date:  1993-06
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