Literature DB >> 14219047

FUMARATE REDUCTION AND ITS ROLE IN THE DIVERSION OF GLUCOSE FERMENTATION BY STREPTOCOCCUS FAECALIS.

R H DEIBEL, M J KVETKAS.   

Abstract

Deibel, R. H. (American Meat Institute Foundation, Chicago, Ill.), and M. J. Kvetkas. Fumarate reduction and its role in the diversion of glucose fermentation by Streptococcus faecalis. J. Bacteriol. 88:858-864. 1964.-Fumarate diverts the normal fermentation of glucose by Streptococcus faecalis FB82, as shown by the production of increased amounts of CO(2), formate, acetate, and acetoin, and decreased formation of lactate and ethanol. Experiments with d-glucose-1-C(14), in which low levels of labeled CO(2) were recovered, indicated that C-1 cleavage of the glucose molecule was not involved. The presence of fumarate afforded consistently larger cell crops in growth studies with glucose and other energy sources. On a molar growth-yield basis, anaerobically grown, glucose-fumarate cultures were equivalent to aerobically grown, glucose cultures. The reduction of fumarate by cell suspensions indicated that glucose, gluconate, and, to a lesser extent, glycerol and mannitol could serve as hydrogen donors. Several common metabolic inhibitors had no effect upon the fumarate reductase system in cell suspensions, although some sensitivity to acidic pH was noted. Significant levels of succinate oxidation activity were not detected. Fumarate reductase activity was demonstrated in all five S. faecalis strains tested. Distribution of this ability in S. faecium strains was variable, ranging from activity comparable with that of S. faecalis to total inactivity. The observations support the conclusion that fumarate functions as an alternate hydrogen acceptor, thus allowing pyruvate to participate in the energy-yielding phosphoroclastic and dismutation pathways.

Entities:  

Keywords:  EXPERIMENTAL LAB STUDY; FERMENTATION; FUMARATES; GLUCONATES; GLUCOSE METABOLISM; GLYCERIN; MANNITOL; OXIDOREDUCTASES; PYRUVATES; STREPTOCOCCUS FAECALIS

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Substances:

Year:  1964        PMID: 14219047      PMCID: PMC314825          DOI: 10.1128/jb.88.4.858-864.1964

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


  14 in total

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6.  Pathways of carbohydrate metabolism in microorganisms.

Authors:  I C GUNSALUS; B L HORECKER; W A WOOD
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7.  Products of Anaerobic Glycerol Fermentation by Streptococci faecalis.

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Authors:  H W SEELEY; P J VANDEMARK
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9.  PYRUVATE FERMENTATION BY STREPTOCOCCUS FAECALIS.

Authors:  R H DEIBEL; C F NIVEN
Journal:  J Bacteriol       Date:  1964-07       Impact factor: 3.490

10.  PHYSIOLOGY OF THE ENTEROCOCCI AS RELATED TO THEIR TAXONOMY.

Authors:  R H DEIBEL; D E LAKE; C F NIVEN
Journal:  J Bacteriol       Date:  1963-12       Impact factor: 3.490

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  11 in total

1.  Energy conservation in chemotrophic anaerobic bacteria.

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4.  Isolation and properties of fumarate reductase mutants of Escherichia coli.

Authors:  M E Spencer; J R Guest
Journal:  J Bacteriol       Date:  1973-05       Impact factor: 3.490

5.  Control of enzyme synthesis in the arginine deiminase pathway of Streptococcus faecalis.

Authors:  J P Simon; B Wargnies; V Stalon
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6.  Metabolome variations in the Porphyromonas gingivalis vimA mutant during hydrogen peroxide-induced oxidative stress.

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7.  Molar growth yields as evidence for oxidative phosphorylation in Streptococcus faecalis strain 10Cl.

Authors:  A J Smalley; P Jahrling; P J Van Demark
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8.  Fumarate reductase activity of Streptococcus faecalis.

Authors:  B J Aue; R H Deiel
Journal:  J Bacteriol       Date:  1967-06       Impact factor: 3.490

9.  Fumarate reduction and product formation by the Reiter strain of Treponema phagedenis.

Authors:  H A George; R M Smibert
Journal:  J Bacteriol       Date:  1982-12       Impact factor: 3.490

10.  Fermentation of fumarate and L-malate by Clostridium formicoaceticum.

Authors:  M Dorn; J R Andreesen; G Gottschalk
Journal:  J Bacteriol       Date:  1978-01       Impact factor: 3.490

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