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Dehydrated culture media

Phenol Red Dextrose Agar

For the differentiation and confirmation of bacteria based on dextrose fermentation.

Cat. No.
LC-1023
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months

Phenol Red Dextrose Agar is similar to Dextrose Agar (LC-1021) with the addition of phenol red as a pH indicator. It is recommended to determine the ability of various organisms to ferment dextrose. Being a solid medium, it has the advantage of allowing fermentation reactions under aerobic and anaerobic conditions.

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Cat. No.FormatPrice
LC-1023500 g

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Key features

Applications

Confirmation and differentiation of dextrose fermenters.

Industry

Food.

Preparation

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

Principles and uses

Peptone mixture provides nitrogen, vitamins, minerals and amino acids essential for growth, and allows the abundant growth of a wide variety of fastidious microorganisms. Sodium chloride supplies essential electrolytes for transport and osmotic balance. Dextrose is the fermentable carbohydrate providing carbon and energy. Phenol red is the pH indicator. Bacteriological agar is the solidifying agent.

Phenol Red Dextrose Agar is an excellent substrate for streptococci, as well as for other less fastidious bacteria. A yellow color indicates fermentation, as the acid production reacts with the phenol red pH indicator. The formation of gas causes bubbles to appear at the base of the medium, which can lead to agar fragmentation. A control of Phenol Red Agar without carbohydrates should be used to control false positives.

Technical specifications

SolubilitySlightly opalescent
AppearanceFine powder
Color of the dehydrated mediumPink
Color of the prepared mediumRed
Final pH (25 °C)7.4 ± 0.2
Amount per litre40 g
Storage2 to 25 °C

Formula

Ingredientg/L
Dextrose10
Bacteriological agar15
Peptone mixture10
Phenol red0.025
Sodium chloride5

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

Preparation and use

Preparation

Suspend 40 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 medium by stabbing into the butt. If desired, inoculate obligate anaerobic bacteria into melted medium that has been cooled to 45 °C. Allow the agar to solidify prior to incubation.
  2. Incubate at 37 °C for 18-48 hours (or anaerobically for 24-72 hours).
  3. Examine periodically for growth, acid production and gas formation.

Quality control

Microbiological test

Incubation conditions: 37 ± 1 °C / 18-48 h.

MicroorganismCharacteristic reaction
Proteus vulgarisATCC 13315Acid (+) / Gas (+)
Salmonella typhimuriumATCC 14028Acid (+) / Gas (+)
Escherichia coliATCC 25922Acid (+) / Gas (+)
Alcaligenes faecalisATCC 8750Acid (-) / Gas (-)

Bibliography

  • Diagnostic Procedures and Reagents 3rd Edition p. 107. 1950.
  • Association of Official Analytical Chemists. 1995 official methods of analysis of AOAC Arlington, VA.
  • Baron EJ LR Peterson and S.M. Finegold 1994. Bailey & Scott's diagnostic microbiology, 9th edition. Mosby-Year Book, Inc. St. Louis, MO.
  • Murray, PR., E.J. Baron M.A. Pfaller F.C. Tenover and R.H. Yolken (ed) 1995. Manual of clinical microbiology, 6th edition. American Society for Microbiology, Washington DC.

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Shipped under controlled temperature when the product requires it.

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Other products in the same category

Dehydrated culture mediaDextrose AgarCat. No. LC-1021Formats 1 format

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Frequently asked questions

Can I ask for formats other than those listed?

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