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Updated: Sep 3, 2026

Precise, High-throughput Analysis of Bacterial Growth
Published on: September 19, 2017
CHEMICALLY DEFINED MEDIUM FOR GROWTH STREPTOCOCCUS PYOGENES
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.
Insights
Researchers developed a chemically defined medium for Streptococcus pyogenes growth. This peptide-free and protein-free medium supports luxuriant bacterial growth, crucial for studying this pathogen.
Area of Science:
- Microbiology
- Bacteriology
Background:
- Streptococcus pyogenes, a significant human pathogen, requires specific growth conditions for laboratory study.
- Previous culture media often contained undefined peptides and proteins, complicating nutritional analyses.
Purpose of the Study:
- To develop a chemically defined, peptide-free, and protein-free culture medium for Streptococcus pyogenes.
- To identify essential nutrients and growth factors for optimal growth of group A hemolytic streptococci.
Main Methods:
- Serial subculturing of three group A hemolytic streptococci strains (>100 transfers).
- Utilizing a modified amino acid assay medium with specific additions (glutamine, ammonium acetate, phosphate).
- Assessing the impact of glutamic acid, glutamine, biotin, NaHCO(3), aspartic acid, and asparagine on bacterial growth.
Main Results:
- High concentrations of glutamic acid or glutamine were essential for growth.
- Biotin significantly stimulated growth and could be partially replaced by NaHCO(3).
- Maximal growth was achieved with NaHCO(3) and biotin, omitting aspartic acid and asparagine, yielding luxuriant growth in 24-48 hours.
Conclusions:
- A chemically defined medium supporting luxuriant Streptococcus pyogenes growth was successfully developed.
- This defined medium allows for precise nutritional studies of Streptococcus pyogenes.
- The findings provide a foundation for further research into the metabolic requirements of this pathogen.
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