Vibrio Parahaemolyticus Sucrose HiVeg™ Agar

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MV1153
For isolation and enumeration of Vibrio parahaemolyticus from seafood samples in accordance with APHA.


Intended Use

Vibrio Parahaemolyticus Sucrose HiVeg Agar is used for isolation and enumeration of Vibrio parahaemolyticus from sea foods.

Composition

Ingredients Grams/Litre
HiVeg hydrolysate No. 1 5.0
HiVeg hydrolysate 5.0
Yeast extract 7.0
Sucrose 10.0
Sodium chloride 30.0
Synthetic detergent No. I 1.5
Bromo thymol blue 0.025
Agar 15.0

Final pH (at 25°C) 8.6 ± 0.2

** Formula adjusted, standardized to suit performance parameters.

Product Profile

Vegetable based (Code MV)©

  • MV1153
  • HiVeg hydrolysate No. 1
  • HiVeg hydrolysate
  • Synthetic detergent No. I

Animal based (Code M)

  • M1153
  • Tryptose
  • Casein enzymic hydrolysate
  • Bile salts mixture
Recommended for Isolation and enumeration of Vibrio parahaemolyticus from sea foods.
Reconstitution 73.52 g/l
Quantity on preparation (500g) 6.80 L
pH (25°C) 8.6 ± 0.2
Supplement None
Sterilization 121°C / 15 minutes
Storage Dry Medium-Below 30°C, Prepared Medium 2-8°C.

Directions

Suspend 73.52 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Dispense in sterile petri plates.

Principle and Interpretation

This medium is prepared by using vegetable peptones in place of animal based peptones which makes the medium free of BSE/TSE risks. Vibrio Parahaemolyticus Sucrose HiVeg Agar is the modification of Vibrio Parahaemolyticus Sucrose Agar (VPSA) which is recommended by APHA (1) for isolating and enumerating Vibrio parahaemolyticus from sea foods. It is a differential medium (and also selective to some extent) which distinguishes Vibrio parahaemolyticus from other marine Vibrios species.

Suspected seafood sample when diluted and blended with sterile HiVeg Peptone Tween Salt Diluent (prepared by dissolving 1.0gm of HiVeg Peptone and 10.0gm of Tween 80 in 1 litre of distilled water and autoclaved at 121°C for 15 mins), is filtered through HGMF using sterile diluent as a carrier. HGMF is then aseptically transferred to the Tryptone Soya HiVeg Agar w/ Magnesium Sulphate (TSAMS) plates and incubated for 4 hours at 35°C. HGMF is then transferred from TSAMS to the dry VPS HiVeg Agar plate and incubated for 18 - 20 hours at 42°C.

HiVeg hydrolysate No. 1, HiVeg hydrolysate and yeast extract provide the necessary nitrogen compounds, growth factors and vitamin B complex for the growth of Vibrio parahaemolyticus. Sucrose is the fermentable carbohydrate. Bromo thymol blue is the pH indicator. Synthetic detergent No. 1 inhibits the contaminating gram-positive bacteria. High salt content and alkaline pH of the medium meet the requirement of marine Vibrio and facilitates easy recovery of the organism respectively. Vibrio parahaemolyticus ferment sucrose and forms green to blue colonies.

Quality Control

Appearance of powder
Yellow coloured, may have slightly greenish tinge, homogeneous, free flowing powder.

Gelling
Firm, comparable with 1.5% Agar gel.

Colour and Clarity
Blue coloured, clear to slightly opalescent gel forms in petri plates.

Reaction
Reaction of 7.35% w/v aqueous solution is pH 8.6 ± 0.2 at 25°C.

Cultural Response
Cultural characteristics observed after an incubation at 42°C for 18-24 hours.

Organisms (ATCC) Inoculum (CFU) Growth Recovery Colour of colony
Staphylococcus aureus (25923) 102-103 inhibited 0% -
Vibrio parahaemolyticus (17802) 102-103 luxuriant >50% blue-green
More Information
Product Name Vibrio Parahaemolyticus Sucrose HiVeg™ Agar
SKU MV1153
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Downes F. P. and Ito K., (Eds.), 2001, Compendium of Methods for the Microbiological Examination of Foods, 4th Ed.,APHA, Washington, D.C.2.Entis P. and Boleszczuk P., 1983, J. Food Prot., 46:783.
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