Phenol Red Tartrate HiVeg™ Agar

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MV872
Used for identification and differentiation of Salmonellae on the basis of tartarate utilization.


Phenol Red Tartrate HiVeg™ Agar

Intended Use

Phenol Red Tartrate HiVeg Agar is recommended for identification and differentiation of Enterobactericeae especially Salmonella species.

Composition

Ingredients Grams/Litre
HiVeg peptone 10.0
Sodium potassium tartrate 10.0
Sodium chloride 5.0
Phenol red 0.024
Agar 15.0
Final pH (at 25°C) 7.6 ± 0.2

Formula adjusted, standardized to suit performance parameters.

Directions

Suspend 40 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense into tubes and sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Allow the medium to cool in a upright position.

Principle and Interpretation

Phenol Red Tartrate HiVeg Agar is prepared by using HiVeg peptone which is free of BSE/TSE risks associated with animal based peptones. This medium is the modification of Phenol Red Tartrate Agar which was originally formulated by Brown et al (1) and further modified by Jordon and Harmon (2) for the differentiation of Enterobacteriaceae especially Salmonella species. This medium, like the conventional medium can be used to differentiate Vibrio parahaemolyticus (positive) from Aeromonas species (negative) (3) and also with addition of sodium chloride (25.0 g/l) can differentiate halophilic Vibrio species e.g. Vibrio parahaemolyticus, Vibrio vulnificus, Vibrio aglinolyticus and Vibrio metschnikovii. On this medium, an acidic reaction is produced by Salmonella serotype Enteritidis, Salmonella serotype Cholerasuis, Salmonella serotype Typhi, Salmonella serotype Typhimurium, Escherichia coli, and Proteus vulgaris strains. However the organisms like Salmonella serotype Paratyphi and Salmonella serotype Schottmuelleri produce an alkaline reaction. HiVeg peptone provides the essential growth nutrients like nitrogenous compounds to the organisms. D-Tartaric acid is used most frequently because it is easy to be utilized by the organism. Sodium potassium tartrate corresponds to it in this medium. Tartrate utilization (fermentation) yields an acidic reaction which is indicated by the yellow colour formation at the bottom of the tube. Phenol red acts as the pH indicator while sodium chloride maintains the osmotic balance of the medium. Inoculate cultures isolated on solid medium. Do not take the inoculum from liquid or broth suspension (3).

Technical Data

Field Value
Vegetable based (Code MV) MV872 HiVeg peptone
Animal based (Code M) M872 Peptic digest of animal tissue
Recommended for Identification and differentiation of Enterobacteriaceae especially Salmonella species.
Reconstitution 40.0 g/l
Quantity on preparation (100g) 2.50 L
pH (25°C) 7.6 ± 0.2
Supplement None
Sterilization 121°C / 15 minutes.
Storage Dry Medium - Below 30°C, Prepared Medium 2 - 8°C.

Quality Control

Appearance of powder: Pinkish yellow coloured, homogeneous, free flowing powder.

Gelling: Firm, comparable with 1.5% Agar gel.

Colour and Clarity: Light pink coloured clear to slightly opalescent gel forms in tubes as butts.

Reaction: Reaction of 4.0% w/v aqueous solution is pH 7.6 ± 0.2 at 25°C

Cultural Response: Cultural characteristics observed after an incubation at 35-37° for 18-24 hours.

Organisms (ATCC) Growth Reaction
Escherichia coli (25922) luxuriant +
Salmonella serotype Enteritidis (13076) luxuriant +
Salmonella serotype Schottmuelleri luxuriant -
Salmonella serotype Typhimurium (14028) luxuriant +

Key: + = acid yellow, - = no acid, pink

References

  1. Brown H.C., Duncan J.T. and Henry T.A., 1924, J.Hyg. (Camb.), 23:1.
  2. Jordon E.O.and Harmon, P.H., 1928, J. Infect. Dis., 42:238.
  3. MacFaddin J.F., 1985, Media for Isolation-Cultivation-Identification - Maintenance of Medical Bacteria, Vol.1, Williams and Wilkins, Baltimore.
More Information
Product Name Phenol Red Tartrate HiVeg™ Agar
SKU MV872
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Brown H.C., Duncan J.T. and Henry T.A., 1924, J.Hyg. (Camb.), 23:1.2.Jordon E.O. and Harmon, P.H., 1928, J. Infect. Dis., 42:238.3.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol.1, Williamsand Wilkins, Baltimore.
Customized Product Available No
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