Lee’s HiVeg™ Agar

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SKU:
MV602
Used for differential enumerations of yoghurt starter bacteria ( Lactobacillus bulgaricus and Streptococcus thermophilus ).


Lee's HiVeg™ Agar

Lee's HiVeg Agar is used for differential enumerations of yoghurt starter bacteria (Lactobacillus bulgaricus and Streptococcus thermophilus).

Product Profile

Vegetable based (Code MV) Animal based (Code M)
MV602 HiVeg hydrolysate M602 Casein enzymic hydrolysate
Recommended for Differential enumerations of yoghurt starter bacteria.
Reconstitution 51.52 g/l
Quantity on preparation (500g) 9.70 L
pH (25°C) 7.0 ± 0.2
Supplement None
Sterilization 121°C / 20 minutes.
Storage Dry Medium - Below 30°C, Prepared Medium 2 - 8°C.

Composition

Ingredients Grams/Litre
HiVeg hydrolysate 10.0
Yeast extract 10.0
Lactose 5.0
Sucrose 5.0
Calcium carbonate 3.0
Dipotassium phosphate 0.5
Bromo cresol purple 0.02
Agar 18.0

Final pH (at 25°C) 7.0 ± 0.2

** Formula adjusted, standardized to suit performance parameters.

Directions

Suspend 51.52 grams in 1000 ml distilled water. Heat just to boiling. Dispense and sterilize by autoclaving at 15 lbs pressure (121°C) for 20 minutes. While dispensing, mix carefully to suspend calcium carbonate evenly. Pour into sterile petri plates to obtain 4-5 mm thick gel.

NOTE : Due to the presence of calcium carbonate the prepared medium forms opalescent solution with white precipitate.

Principle and Interpretation

Lee's HiVeg Agar is prepared by using HiVeg hydrolysate which is a vegetable peptone instead of Casein enzymic hydrolysate and hence the medium is free from BSE/TSE risks. Lee's HiVeg Agar is the modification of Lee's Agar which is formulated as per APHA (1) for differential enumeration of yoghurt starter bacteria, homofermentative Lactobacillus bulgaricus and heterofermentative Streptococcus thermophilus. Yoghurt is made by the controlled fermentation of milk held at 43°C using a starter culture of Streptococcus thermophilus and Lactobacillus bulgaricus. Streptococci grow first and produce a creamy, buttery aroma from diacetyl and similar metabolites. Redox potential is also lowered by Streptococci which enables Lactobacilli to grow thereby growth stimulatory products for Streptococci are synthesized by Lactobacilli. Hence the typical sharp acetaldehyde flavour of mature yoghurt is formed (2). HiVeg hydrolysate and yeast extract provide the essential nitrogenous nutrients to the yoghurt (lactic) starter bacteria. Lactose and sucrose are the fermentable carbohydrates. Calcium carbonate is added to medium along with the dipotassium phosphate to buffer the medium and avoid the drastic drop in pH due to lactic acid formation. Bromo cresol purple is the pH indicator which turns yellow in acidic condition and imparts yellow colour to the colony. It is recommended to dry the media plates for 18-24 hours prior to use.

Quality Control

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

Gelling
Firm, comparable with 1.8% Agar gel.

Colour and Clarity
Purple coloured, opaque gel forms in petri plates.

Reaction
Reaction of 5.15% w/v aqueous solution is pH 7.0 ± 0.2 at 25°C.

Cultural Response

Cultural characteristics observed after an incubation at 35-37°C for 48 hours in presence of Carbon dioxide (COâ‚‚).

Organisms (ATCC) Inoculum (CFU) Growth Recovery Colour of colony
Lactobacillus bulgaricus (11842) 102-103 luxuriant >70% white
Streptococcus thermophilus (14486) 102-103 luxuriant >70% yellow

References

  1. Downes FP, Ito K (Eds.), 2001, Compendium of Methods For the Microbiological Examination of Foods, 4th ed., APHA, Washington, D.C.
  2. Davis J.G., Ashton T.F. and MaCaskill M., 1971, Dairy Ind., 36:569.
More Information
Product Name Lee’s HiVeg™ Agar
SKU MV602
Product Type HiVegâ„¢
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Lee S. Y., Vedamuthu E. R., Washam C. J. and Reinbold G. W., 1974, J . Milk Food Technol., 37: 272
2.Downes F. P. and Ito K., (Eds.), 2001, Compendium of Methods for the Microbiological Examination of Foods, 4th Ed.,APHA, Washington, D.C.
3.Davis J. G., Ashton T. F. and MaCaskill M., 1971, Dairy Ind., 36:569.
Customized Product Available No
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