Literature DB >> 4959807

Utilization of arginine as an energy source for the growth of Streptococcus faecalis.

R H Deibel.   

Abstract

Deibel, R. H. (American Meat Institute Foundation, Chicago, Ill.). Utilization of arginine as an energy source for the growth of Streptococcus faecalis. J. Bacteriol. 87:988-992. 1964.-Although both Streptococcus faecalis and S. faecium (and its variety durans) hydrolyze arginine, the utilization of this amino acid as an energy source appears to have taxonomic utility, as only S. faecalis and its varieties can couple the resultant energy with growth processes. Utilization of arginine by S. faecalis in a semisynthetic, casein-hydrolysate medium requires small concentrations of a fermentable carbohydrate (0.05%), presumably for synthetic reactions. The arginine analogue, agmatine, is utilized as an energy source by S. faecalis but not by S. faecium, and only approxinately 50% of the latter strains hydrolyzed this compound. Other ureido- and guanido-containing compounds tested were neither utilized as an energy source nor deaminated.

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Year:  1964        PMID: 4959807      PMCID: PMC277135          DOI: 10.1128/jb.87.5.988-992.1964

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


  16 in total

1.  The growth of micro-organisms in relation to their energy supply.

Authors:  T BAUCHOP; S R ELSDEN
Journal:  J Gen Microbiol       Date:  1960-12

2.  Simplified tests for some amino acid decarboxylases and for the arginine dihydrolase system.

Authors:  V MØLLER
Journal:  Acta Pathol Microbiol Scand       Date:  1955

3.  Tetrazolium reduction as a means of differentiating Streptococcus faecalis from Streptococcus faecium.

Authors:  E M BARNES
Journal:  J Gen Microbiol       Date:  1956-02

4.  The arginine dihydrolase system of Streptococcus faecalis. III. The decomposition of citruline.

Authors:  E L OGINSKY; R F GEHRIG
Journal:  J Biol Chem       Date:  1953-10       Impact factor: 5.157

5.  Conversion of citrulline to ornithine by cell-free extracts of Streptococcus lactis.

Authors:  M KORZENOVSKY; C H WERKMAN
Journal:  Arch Biochem Biophys       Date:  1953-09       Impact factor: 4.013

6.  The formation of arginine dihydrolase by streptococci and some properties of the enzyme system.

Authors:  H D SLADE; W C SLAMP
Journal:  J Bacteriol       Date:  1952-10       Impact factor: 3.490

7.  Bacterial metabolism of arginine.

Authors:  M KORZENOVSKY; C H WERKMAN
Journal:  Arch Biochem Biophys       Date:  1952-11       Impact factor: 4.013

8.  Hydrolysis of arginine by soluble enzymes of Streptococcus faecalis.

Authors:  H D SLADE
Journal:  Arch Biochem Biophys       Date:  1953-01       Impact factor: 4.013

9.  Ammonia production by pathogenic bacteria.

Authors:  G M Hills
Journal:  Biochem J       Date:  1940-07       Impact factor: 3.857

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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  25 in total

Review 1.  THE GROUP D STREPTOCOCCI.

Authors:  R H DEIBEL
Journal:  Bacteriol Rev       Date:  1964-09

2.  Energy conservation in chemotrophic anaerobic bacteria.

Authors:  R K Thauer; K Jungermann; K Decker
Journal:  Bacteriol Rev       Date:  1977-03

3.  Numerical taxonomy of catalase-negative cocci isolated from frozen vegetables.

Authors:  D F Splittstoesser; M Mautz; R R Colwell
Journal:  Appl Microbiol       Date:  1968-07

Review 4.  Biosynthesis and metabolism of arginine in bacteria.

Authors:  R Cunin; N Glansdorff; A Piérard; V Stalon
Journal:  Microbiol Rev       Date:  1986-09

5.  The gene cluster for agmatine catabolism of Enterococcus faecalis: study of recombinant putrescine transcarbamylase and agmatine deiminase and a snapshot of agmatine deiminase catalyzing its reaction.

Authors:  José L Llácer; Luis Mariano Polo; Sandra Tavárez; Benito Alarcón; Rebeca Hilario; Vicente Rubio
Journal:  J Bacteriol       Date:  2006-10-06       Impact factor: 3.490

6.  Free Amino Acids in Serine-Antagonized Cells of Tetrahymena pyriformis.

Authors:  J B Wragg; H Reynolds; M J Pelczar
Journal:  J Bacteriol       Date:  1965-09       Impact factor: 3.490

Review 7.  Enterococcus infection biology: lessons from invertebrate host models.

Authors:  Grace J Yuen; Frederick M Ausubel
Journal:  J Microbiol       Date:  2014-03-01       Impact factor: 3.422

8.  Comparative genomic analysis of pathogenic and probiotic Enterococcus faecalis isolates, and their transcriptional responses to growth in human urine.

Authors:  Heidi C Vebø; Margrete Solheim; Lars Snipen; Ingolf F Nes; Dag A Brede
Journal:  PLoS One       Date:  2010-08-31       Impact factor: 3.240

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

Authors:  J P Simon; B Wargnies; V Stalon
Journal:  J Bacteriol       Date:  1982-06       Impact factor: 3.490

10.  Transport of diamines by Enterococcus faecalis is mediated by an agmatine-putrescine antiporter.

Authors:  A J Driessen; E J Smid; W N Konings
Journal:  J Bacteriol       Date:  1988-10       Impact factor: 3.490

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