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Dehydrated culture media

SIM Medium

For the identification and differentiation of Enterobacteriaceae and the confirmation of C. perfringens.

Cat. No.
LC-1514
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months
Standards
ISO 15213

SIM Medium is a semisolid medium used for the differentiation of enteric bacteria through sulfide production, indole formation and motility. The sulfur reduction test is useful in differentiating enteric organisms, especially Salmonella and Shigella. The indole test is used for differentiating the Enterobacteriaceae. The motility test is useful for testing a wide variety of organisms. The medium is also useful in the differentiation of Klebsiella from Enterobacter and Serratia species.

Supplement to be added: Kovac's Reagent LC-5205

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Cat. No.FormatPrice
LC-1514500 g

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Key features

Applications

Differentiation of enterobacteria.

Industry

Food, water.

Standards

ISO 15213.

Preparation

29.9 g in one liter of distilled water; boil for one minute, dispense and sterilize in autoclave at 121 °C for 15 minutes.

Principles and uses

Casein and meat peptones provide nitrogen, vitamins, minerals and amino acids essential for growth. Casein peptone is rich in tryptophan which is reduced and produces indole. Sodium thiosulfate provides sulphur and ferric ammonium citrate is the indicator for H₂S production under alkaline conditions. Bacteriological agar is the solidifying agent in a low concentration to enable the motility to be seen.

Technical specifications

SolubilityWithout residues
AppearanceFine powder
Color of the dehydrated mediumBeige
Color of the prepared mediumAmber, slightly opalescent
Final pH (25 °C)7.3 ± 0.2
Amount per litre29.9 g
Storage2 to 25 °C

Formula

Ingredientg/L
Bacteriological agar3.5
Meat peptone6
Sodium thiosulfate0.2
Ferric ammonium sulfate0.2
Enzymatic digest of soya20

Typical formula in g/L, adjusted and/or supplemented as required to meet performance criteria.

Preparation and use

Preparation

Suspend 29.9 grams of the medium in one liter of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. Dispense into appropriate containers and sterilize in autoclave at 121 °C for 15 minutes.

Instructions for use

  1. Inoculate the pure culture by stabbing to a depth of 3/4 of the tube.
  2. Incubate at 37 ± 1 °C for 18-24 hours and read the results.
  3. Darkening indicates the production of H₂S. Motility is indicated by a diffuse turbidity away from the line of inoculation. Growth only along the inoculation line indicates non-motility.
  4. The presence of indole is tested by adding Kovac's Reagent (LC-5205), giving a purple-red coloration to the reagent.

Quality control

Microbiological test

Incubation conditions: 37 ± 1 °C / 18-24 h.

MicroorganismSpecificationCharacteristic reaction
Shigella flexneriATCC 12022Good growthH₂S (-), indole (-), motility (-)
Clostridium perfringensATCC 13124Good growthH₂S (+), indole (-), motility (-)
Salmonella typhimuriumATCC 14028Good growthH₂S (+), indole (-), motility (+)
Escherichia coliATCC 25922Good growthH₂S (-), indole (+), motility (+)

Bibliography

  • S.A.B. Manual of Microbiological. McGraw-Hill Book Co. New York, 1957.
  • Greene, Bilum de Cora, Fairchail, Kaplan, Landau and Sharp. J. Bact. 63:347. 1951.
  • Harrigan W.F. and MacCarice M.E. (1966) Laboratory Methods in Microbiology. Academic Press, 53.

What you receive

The product

Shipped under controlled temperature when the product requires it.

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