CHEMICALLY DEFINED MEDIUM FOR GROWTH OF STREPTOCOCCUS PYOGENES

Author:

Mickelson M. N.1

Affiliation:

1. National Animal Disease Laboratory, U.S. Department of Agriculture, Agricultural Research Service, Ames, Iowa

Abstract

Mickelson , M. N. (National Animal Disease Laboratory, Ames, Iowa). Chemically defined medium for growth of Streptococcus pyogenes . J. Bacteriol. 88: 158–164. 1964.—Three strains of group A hemolytic streptococci representing three serological types were serially subcultured for an extended period (100 or more transfers) in a peptide-free and protein-free culture medium. An amino acid assay medium, modified by addition of small amounts of glutamine, ammonium acetate, and 0.1 m phosphate (pH 7), was used. In this medium, high concentrations of glutamic acid or glutamine were required, and biotin was stimulatory to growth. Biotin could be partially replaced with NaHCO 3 . Maximal growth was obtained with NaHCO 3 when biotin was present, and aspartic acid and asparagine were omitted from the medium. In 24 to 48 hr of incubation at 37 C, luxuriant growth was obtained with complete removal and quantitative fermentation of 1% glucose to lactic acid. Optical densities of cultures were equivalent to those obtained with the best infusion media.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference13 articles.

1. Peptide requirements for the synthesis of streptococcal proteins;N.;J. Biol. Chem.,1961

2. Metabolic functions of biotin. I. The role of biotin in NaHCO3 utilization by Lactobacillus arabinosus studied with C14;LARDY H. A.;J. Biol. Chem.,1949

3. Ammonia formation from glutamine by hemolytic streptococci; its reciprocal relationship with glycolysis;MCILLWAIN H.;Biochem. J.,1946

4. Absence of type-specific M antigen from group A streptococci grown in a chemically defined medium;MICKELSON M. N.;J. Bacteriol.,1964

5. Biotin enzymes;OCHOA S.;Federation Proc.,1961

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