TRIPLE SUGAR IRON AGAR

Product Code TM 424

  • Description

    Triple Sugar Iron Agar was originally proposed by Sulkin and Willett and modified by Hajna for identifying Enterobacteriaceae. This medium complies with the recommendation of Indian Pharmacopoeia for the identification of Gram-negative bacilli. Peptone, yeast extract and beef extract provide nitrogenous compounds sulphur, trace elements and vitamin B complex etc. Sodium chloride maintains osmotic equilibrium. Lactose, sucrose and dextrose monohydrate are fermentable carbohydrates. Sodium thiosulphate and ferric or ferrous ions make an H2S indicator system. Sodium thiosulphate is also an inactivator of halogen and can minimize its toxicity in the testing sample, if any during microbial limit tests. Phenol red is the pH indicator. Organisms that ferment dextrose monohydrate produce a variety of acids, varying the colour of the medium from red to yellow. More amounts of acids are liberated in butt region (fermentation) than in the slant (respiration). Growing bacteria also form alkaline products from the oxidative decarboxylation of peptone and these alkaline products neutralize the large amounts of acid present in the butt. Thus the appearance of an alkaline (red) slant and an acid (yellow) butt after incubation indicates that the organism is a dextrose fermenter but is unable to ferment lactose and/or sucrose. Bacteria that ferment lactose or sucrose (or both), in addition to dextrose, produce large amounts of acid enabling no reversion of pH in that region and thus bacteria exhibit an acid slant and acid butt. Gas production (CO2) is detected by the presence of cracks or bubbles in the medium, when the accumulated gas escapes. Thiosulphate is reduced to hydrogen sulphide by several species of bacteria and H2S combines with ferric ions of ferric salts to produce the insoluble black precipitate of ferrous sulphide. Reduction of thiosulphate proceeds only in an acid environment and blackening usually occurs in the butt of the tube.

    Triple Sugar Iron Agar should be used in parallel with Urea Agar / Broth to distinguish between Salmonella and Proteus species. Some members of the Enterobacteriaceae and H2S producing Salmonella may not be H2S positive on Triple Sugar Iron Agar. Some bacteria may show H2S production on Kligler Iron Agar but not on TSI Agar. This can happen because utilization of sucrose in TSI Agar suppresses the enzymic pathway that results in H2S production.

  • Principle

    for con?rmation of gram negative enteric bacilli on basis of dextrose, lactose and sucrose fermentation and H2S production

  • Microorganism

    • Citrobacter freundii
    • Escherichia coli
    • Klebsiella aerogenes
    • Klebsiella pneumoniae
    • Proteus vulgaris
    • Salmonella Paratyphi A
    • Salmonella typhi
    • Salmonella Typhimurium
    • Shigella flexneri
  • Industry

    • Clinical Diagnostics
    • Water
  • Pack Size

    • 100 gm
    • 500 gm
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