Phenol Red Adonitol Broth

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SKU:
M1200
Used for detection of adonitol fermenting bacteria.


Phenol Red Adonitol Broth is used for detection of adonitol fermenting bacteria.

Composition**

Ingredients Gms / Litre
Proteose peptone 10.000
Meat extract B # 1.000
Sodium chloride 5.000
Adonitol 5.000
Phenol red 0.018

Final pH (at 25°C): 7.4±0.2

**Formula adjusted, standardized to suit performance parameters

# Equivalent to Beef extract B

Directions

Suspend 21.02 grams in 1000 ml distilled water and mix well. Heat if necessary to ensure complete solution. Distribute in fermentation tubes (tubes containing inverted Durham's tubes). Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes.

Principle And Interpretation

Phenol Red Broth Medium is formulated as per Vera (2) and is recommended to determine the fermentation reaction of carbohydrates for the differentiation of microorganisms (3, 4, 5). Phenol Red Broth Medium with various carbohydrates serves as a differential medium by aiding in differentiation of various species and genera by their ability to ferment the specific carbohydrate, with the production of acid or acid and gas (6). Phenol Red Adonitol Broth is used to study adonitol fermentation in various bacteria.

Proteose peptone and meat extract B serve as sources for carbon and nitrogen. Sodium chloride is the osmotic stabilizer. Phenol red is the pH indicator, which turns yellow at acidic pH i.e. on fermentation of adonitol. Gas formation is seen in Durhams tubes. All of the Enterobacteriaceae grow well in this medium. In addition to producing a pH colour shift, the production of mixed acids, notably butyric acids, often results in a pungent, foul odour from the culture medium (1).

Quality Control

Appearance: Light yellow to pink coloured homogeneous free flowing powder

Colour and Clarity of prepared medium: Red coloured clear solution without any precipitate

Reaction: Reaction of 2.1% w/v aqueous solution at 25°C. 7.4±0.2 pH : 7.4±0.2

pH: 7.20-7.60

Cultural Response

M1200: Cultural characteristics observed after an incubation at 35-37°C for 18-24 hours.

Organism Inoculum (CFU) Growth Acid production Gas
Citrobacter freundii ATCC 8090 50-100 luxuriant Negative reaction, no colour change Negative reaction
Escherichia coli ATCC 25922 50-100 luxuriant Negative reaction, no colour change Negative reaction
Enterobacter aerogenes ATCC 13048 50-100 luxuriant Positive reaction, yellow colour Positive reaction
Klebsiella pneumoniae ATCC 13883 50-100 luxuriant Positive reaction, yellow colour Positive reaction
Proteus vulgaris ATCC 13315 50-100 luxuriant Negative reaction, no colour change Negative reaction
Serratia marcescens ATCC 8100 50-00 luxuriant Negative reaction, no colour change Negative reaction
Salmonella Typhi ATCC 6539 50-100 luxuriant Negative reaction, no colour change Negative reaction
Salmonella Typhimurium ATCC 14028 50-100 luxuriant Negative reaction, no colour change Negative reaction
Shigella flexneri ATCC 12022 50-100 luxuriant Negative reaction, no colour change Negative reaction

Storage and Shelf Life

Store below 30°C in tightly closed container and prepared medium at 2-8°C. Use before expiry date on the label.

Reference

  1. Koneman E. W., Allen S. D., Janda W.M., Schreckenberger P.C., Winn W.C. Jr., 1992, Colour Atlas and Textbook of Diagnostic Microbiology, 4th Ed., J. B. Lippinccott Company
  2. Vera H. D., 1950, Am. J. Public Health, 40, 1267
  3. MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification -Maintenanceof Medical Bacteria, Vol. I, Williams and Wilkins, Baltimore.
  4. Finegold S. M. and Baron E. J., 1986, Bailey and Scotts Diagnostic Microbiology, 7th Ed., The C.V. Mosby Co., St. Louis.
  5. Ewing W. H., 1986, Edwards and Ewings Identification of Enterobacteriaceae, 4th ed., Elsevier Science Publishing Co., Inc., New York.
  6. MacFaddin J. F., 2000, Biochemical tests for Identification of Medical Bacteria, 3rd edi., Lippincott, Williams and Wilkins, Baltimore.
More Information
Product Name Phenol Red Adonitol Broth
SKU M1200
Product Type Regular
Physical Form Powder
Origin Animal
Packaging type HDPE
References 1. Koneman E. W., Allen S. D., Janda W.M., Schreckenberger P.C., Winn W.C. Jr., 1992, Colour Atlas and Textbook of Diagnostic Microbiology, 4th Ed., J. B. Lippinccott Company2.Vera H. D., 1950, Am. J. Public Health, 40, 12673.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification -Maintenanceof Medical Bacteria, Vol. I, Williams and Wilkins, Baltimore.4.Finegold S. M. and Baron E. J., 1986, Bailey and Scotts Diagnostic Microbiology, 7th Ed., The C.V. Mosby Co., St. Louis.5.Ewing W. H., 1986, Edwards and Ewings Identification of Enterobacteriaceae, 4th ed.,Elsevier Science Publishing Co.,Inc., New York.6.MacFaddin J. F., 2000, Biochemical tests for Identification of Medical Bacteria, 3rd edi., Lippincott, Williams and Wilkins,Baltimore.
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