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Dehydrated culture media

Lysine Decarboxylase Broth

For the identification of microorganisms, especially enteric bacilli, based on the decarboxylation of lysine.

Cat. No.
LC-1208
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months
Standards
ISO 10273

Lysine Decarboxylase Broth is used to detect and differentiate enterobacteria from other microorganisms, based on lysine decarboxylation.

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Cat. No.FormatPrice
LC-1208500 g

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Key features

Applications

Differentiation of enterobacteria.

Industry

Food, water.

Standards

ISO 10273.

Preparation

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

Principles and uses

Gelatin peptone provides nitrogen, vitamins, minerals and amino acids essential for growth. Yeast extract is a source of vitamins, particularly of the B-group. Dextrose is the fermentable carbohydrate. Bromocresol purple is the pH indicator. Lysine is added to detect the production of the specific enzyme.

When the medium is inoculated with a bacterium that is able to ferment dextrose, the acid produced lowers the pH of the medium and changes the color of the indicator from purple to yellow. The acidic condition also stimulates decarboxylase activity. The bacteria that decarboxylate the L-lysine to cadaverine are identified by the presence of a purple-red color. The production of these amines elevates the pH of the medium. A yellow color after 24 hours indicates a negative result.

By substituting L-lysine with arginine or ornithine, the new resulting medium (Falkow Broth Base) can be used to study the decarboxylation of these amino acids.

Technical specifications

SolubilityWithout residues
AppearanceFine powder
Color of the dehydrated mediumLight beige
Color of the prepared mediumViolet
Final pH (25 °C)6.8 ± 0.2
Amount per litre14 g
Storage2 to 25 °C

Formula

Ingredientg/L
Bromocresol purple0.02
Dextrose1
Gelatin peptone5
L-Lysine5
Yeast extract3

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

Preparation and use

Preparation

Suspend 14 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 quantities of 5 mL into screw-capped tubes. Sterilize in autoclave at 121 °C for 15 minutes. Leave caps loose to allow gas exchange. Close well after sterilization.

Instructions for use

  1. Gently insert the inoculation loop with the sample into the tube and move the loop back and forth several times to inoculate the medium.
  2. Incubate at 35 ± 2 °C for 24 hours.
  3. Color change to purple: positive decarboxylation reaction (Escherichia, Klebsiella, Salmonella except S. paratyphi, Arizona, Alkalescens-Dispar, Serratia).
  4. Yellow color: negative decarboxylation reaction (Proteus, Providencia, S. paratyphi A, Shigella, Aeromonas, Citrobacter).

Quality control

Microbiological test

Incubation conditions: 35 ± 2 °C / 18-48 h.

MicroorganismCharacteristic reaction
Proteus vulgarisATCC 13315Lysine decarboxylation (-)
Escherichia coliATCC 25922Lysine decarboxylation (+)
Serratia liquefaciensATCC 27592Lysine decarboxylation (+) slow
Salmonella paratyphiATCC 9150Lysine decarboxylation (-)

Bibliography

  • Falkow A. S. Clin. Path. 28:598, 1958.
  • Ewing, Davis and Deaves, Studies in the Serratia Group. U.S. Dept. H.E.W., C.D.C. Atlanta, 1972.
  • Edwards and Ewing. Identification of Enterobacteriaceae, Burgess Publ. Co. Minneapolis, Minn., 1961.

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Shipped under controlled temperature when the product requires it.

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Frequently asked questions

Can I ask for formats other than those listed?

Yes: custom formats and OEM packs are available on request. Tell us the quantities you need.

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