Literature DB >> 669789

Molar growth yields and enterotoxin B production of Staphylococcus aureus S-6 with amino acids as energy sources.

G M Keller, R S Hanson, M S Bergdoll.   

Abstract

Staphylococcus aureus S-6 was able to utilize glutamate, proline, histidine, aspartate, alanine, threonine, serine, or glycine as a major energy source, when these were added singly at a concentration of 2.5 g/liter to a base medium containing salts, vitamins, and 30 mg of each of 18 amino acids per liter. Molar growth yields (Y) for each of the eight amino acids were determined in aerobic batch cultures. Except with aspartate and serine, all molar growth yields decreased with increasing concentration of the energy source, whether or not it was present in excess. The average molar growth yields for both aspartate and serine were Y = 35 g/mol. The highest Y values obtained with the other amino acids were 79, 78, 56, 46, 58, and 21 g/mol for glutamate, proline, histidine, alanine, threonine, and glycine, respectively. Histidine was not utilized as an energy source at concentrations of less than 2 mM. Enterotoxin yields (mg of toxin per g [dry wt] of cells) higher than in the basal medium were obtained when proline, histidine, alanine, serine, and glycine were the major energy sources. When proline and alanine were the major energy sources, enterotoxin yields were not affected by the concentration, whereas toxin yields were reduced at high concentrations of the other six amino acids. The highest cell yields and Y values were obtained with glutamate, but its utilization as an energy source markedly reduced enterotoxin yields.

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Year:  1978        PMID: 669789      PMCID: PMC421565          DOI: 10.1128/iai.20.1.151-157.1978

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


  17 in total

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Review 2.  Membrane transport.

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Review 3.  Utilization of energy for growth and maintenance in continuous and batch cultures of microorganisms. A reevaluation of the method for the determination of ATP production by measuring molar growth yields.

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4.  Regulation of staphylococcal enterotoxin B: effect of anaerobic shock.

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5.  Amino acid transport and staphylococcal membrane vesicles.

Authors:  S A Short; H R Kaback
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6.  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

7.  Amino acid requirements for the production of enterotoxin B by Staphylococcus aureus S-6 in a chemically defined medium.

Authors:  R D Miller; D Y Fung
Journal:  Appl Microbiol       Date:  1973-05

Review 8.  The generation and utilization of energy during growth.

Authors:  W W Forrest; D J Walker
Journal:  Adv Microb Physiol       Date:  1971       Impact factor: 3.517

9.  Staphylococcal enterotoxin B and nuclease production under controlled dissolved oxygen conditions.

Authors:  D F Carpenter; G J Silverman
Journal:  Appl Microbiol       Date:  1974-10

10.  Stimulation of Enterotoxin B Production II. Synthetic Medium for Staphylococcal Growth and Enterotoxin B Production.

Authors:  C H Wu; M S Bergdoll
Journal:  Infect Immun       Date:  1971-06       Impact factor: 3.441

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4.  Investigation of associations of Yarrowia lipolytica, Staphylococcus xylosus, and Lactococcus lactis in culture as a first step in microbial interaction analysis.

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