Literature DB >> 4564783

Production of staphylococcal alpha toxin. II. Glucose repression of toxin formation.

J L Duncan, G J Cho.   

Abstract

The effect of glucose on alpha toxin production was studied in the Wood 46 strain of Staphylococcus aureus. Optimal toxin production occurred when 0.2% glucose was present in the medium. Omission of glucose gave lower yields of toxin, and concentrations of 0.5% and higher severely depressed toxin formation. Glucose affected the initiation of alpha toxin synthesis in growing cultures. As the glucose concentration increased, the time lag prior to the onset of toxin production also increased, and maximal rates of synthesis were not obtained until essentially all the glucose had been exhausted from the medium. The addition of glucose to toxin-producing cultures caused a temporary, almost complete repression of toxin formation which was not due to pH changes in the culture. The synthesis of most extracellular proteins was not inhibited during the period of repression. After recovery, toxin was produced at rates equal to those of untreated control cultures. The kinetics of toxin repression and the observation that the glucose analogues, 2-deoxy-d-glucose and alpha-methyl-glucoside, as well as other carbon sources, inhibit toxin production suggest that transient repression is responsible for the inhibition of toxin formation. No evidence for a regulatory role of adenosine 3', 5'-cyclc monophosphate in alpha toxin production was obtained.

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Year:  1972        PMID: 4564783      PMCID: PMC422594          DOI: 10.1128/iai.6.5.689-694.1972

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  8 in total

1.  A comparison of use of carbohydrate, cell structure, and toxin formation in naturally occurring and thymine-requiring Staphylococcus aureus strains.

Authors:  J de Repentigny; L G Mathieu
Journal:  Can J Microbiol       Date:  1971-11       Impact factor: 2.419

2.  Cyclic AMP regulates catabolite and transient repression in E. coli.

Authors:  R L Perlman; B De Crombrugghe; I Pastan
Journal:  Nature       Date:  1969-08-23       Impact factor: 49.962

Review 3.  Biochemistry and regulation of streptomycin and mannosidostreptomycinase (alpha-D-mannosidase) formation.

Authors:  A L Demain; E Inamine
Journal:  Bacteriol Rev       Date:  1970-03

4.  Physiological basis of transient repression of catabolic enzymes in Escherichia coli.

Authors:  B Tyler; B Magasanik
Journal:  J Bacteriol       Date:  1970-05       Impact factor: 3.490

5.  Transient repression of the lac operon.

Authors:  B Tyler; W F Loomis; B Magasanik
Journal:  J Bacteriol       Date:  1967-12       Impact factor: 3.490

6.  Regulation of staphylococcal enterotoxin B.

Authors:  S A Morse; R A Mah; W J Dobrogosz
Journal:  J Bacteriol       Date:  1969-04       Impact factor: 3.490

7.  Cyclic adenosine monophosphate in bacteria.

Authors:  I Pastan; R Perlman
Journal:  Science       Date:  1970-07-24       Impact factor: 47.728

8.  Production of staphylococcal alpha toxin. I. Relationship between cell growth and toxin formation.

Authors:  J L Duncan; G J Cho
Journal:  Infect Immun       Date:  1971-10       Impact factor: 3.441

  8 in total
  21 in total

Review 1.  The hemolysins of Staphylococcus aureus.

Authors:  G M Wiseman
Journal:  Bacteriol Rev       Date:  1975-12

2.  Production of Hemolysin and Bacteriolysin in a Synthetic Medium by Streptococcus faecalis var. zymogenes.

Authors:  B Appelbaum; L N Zimmerman
Journal:  Infect Immun       Date:  1974-11       Impact factor: 3.441

Review 3.  At the crossroads of bacterial metabolism and virulence factor synthesis in Staphylococci.

Authors:  Greg A Somerville; Richard A Proctor
Journal:  Microbiol Mol Biol Rev       Date:  2009-06       Impact factor: 11.056

4.  Steady-state staphylococcal enterotoxin type C mRNA is affected by a product of the accessory gene regulator (agr) and by glucose.

Authors:  L B Regassa; J L Couch; M J Betley
Journal:  Infect Immun       Date:  1991-03       Impact factor: 3.441

5.  Repression of heat-stable enterotoxin synthesis in enterotoxigenic Escherichia coli.

Authors:  J F Alderete; D C Robertson
Journal:  Infect Immun       Date:  1977-09       Impact factor: 3.441

6.  Temporal production of streptococcal erythrogenic toxin B (streptococcal cysteine proteinase) in response to nutrient depletion.

Authors:  M S Chaussee; E R Phillips; J J Ferretti
Journal:  Infect Immun       Date:  1997-05       Impact factor: 3.441

7.  Staphylococcus aureus enterotoxin B release (excretion) under controlled conditions of fermentation.

Authors:  J F Metzger; A D Johnson; W S Collins; V McGann
Journal:  Appl Microbiol       Date:  1973-05

8.  Factors affecting the regulation of staphylococcal enterotoxin B.

Authors:  S A Morse; J N Baldwin
Journal:  Infect Immun       Date:  1973-06       Impact factor: 3.441

9.  Dual Gene Expression Analysis Identifies Factors Associated with Staphylococcus aureus Virulence in Diabetic Mice.

Authors:  Rudy Jacquet; Annette E LaBauve; Lavoisier Akoolo; Shivani Patel; Abdulelah A Alqarzaee; Tania Wong Fok Lung; Kunal Poorey; Timothy P Stinear; Vinai C Thomas; Robert J Meagher; Dane Parker
Journal:  Infect Immun       Date:  2019-04-23       Impact factor: 3.441

10.  Glucose and nutrient concentrations affect the expression of a 104-kilodalton Listeria adhesion protein in Listeria monocytogenes.

Authors:  Ziad W Jaradat; Arun K Bhunia
Journal:  Appl Environ Microbiol       Date:  2002-10       Impact factor: 4.792

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