Tributyrin HiVeg® Agar Base w/o Tributyrin

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SKU:
MV157
Recommended for detection of lipolytic microorganisms.


Composition

Ingredients Grams/Litre
HiVeg® peptone 5.0
Yeast extract 3.0
Agar 15.0

Final pH (at 25°C) 7.5± 0.2

** Formula adjusted, standardized to suit performance parameters.

Directions

Suspend 23 grams in 990 ml distilled water. Add 10 ml of Tributyrin. Mix and heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Shake the flask and pour plate so as to maintain uniform turbidity.

Principle and Interpretation

Tributyrin HiVeg® Agar Base is specially developed from HiVeg® peptone to avoid BSE/ TSE risks associated with animal origin Peptic digest of animal tissue. This medium is the modification of Tributyrin Agar Base, which was originally formulated by Anderson (1) for the detection and enumeration of lipolytic microorganisms such as Staphylococci (2), Clostridia (3), marine Flavobacteria and Pseudomonas (4) and moulds in foodstuffs and other materials.

HiVeg® peptone and yeast extract provide necessary nutrients for growth of the microorganisms. Tributyrin added in the medium on hydrolysis by esterase enzyme produces butyric acid which is water soluble therefore clearance is seen around the colony which produce the enzyme. Lipases hydrolysing low molecular weight or short chain triglycerides are refered as esterases. This is an invitro method followed to isolate lipolytic organisms and is used for screening lipase/ esterase producers. The medium should be properly mixed so that tributyrin substrate is distributed uniformly in the prepared plate.

Quality Control

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

Gelling
Firm, comparable with 1.5% Agar gel.

Colour and Clarity
Light yellow coloured, opalescent gel forms with oil droplets in petri plates.

Reaction
Reaction of 2.3% w/v aqueous solution containing 1% v/v Tributyrin is pH 7.5± 0.2 at 25°C

Product Profile

Vegetable based (Code MV) Animal based (Code M)
MV157 M157
HiVeg® peptone Peptic digest of animal tissue
Recommended for : Detection of lipolytic microorganisms.
Reconstitution : 23.0 g/l
Quantity on preparation (500g) : 21.73 L
(100g) : 4.34 L
pH (25°C) : 7.5± 0.2
Supplement : Tributyrin (FD081)
Sterilization : 121°C / 15 minutes
Storage : Dry Medium - Below 30°C, Prepared Medium 2 - 8°C.

Cultural Response

Cultural characteristics observed after an incubation at 35 - 37°C for 24-48 hours, in an appropriate atmosphere after addition of Tributyrin (FD081).

Organisms (ATCC)

Organisms (ATCC) Inoculum (CFU) Growth Lipase activity
*Clostridium perfringens (12924) 102-103 luxuriant -
*Clostridium sporogenes (11437) 102-103 luxuriant +
Bacillus subtilis (6633) 102-103 luxuriant +
Escherichia coli (25922) 102-103 luxuriant -
Staphylococcus aureus (25923) 102-103 luxuriant +

Key :

  • + = clear zone around colony
  • - = absence of zone
  • * = when incubated anaerobically
More Information
Product Name Tributyrin HiVeg® Agar Base w/o Tributyrin
SKU MV157
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Alford J. A., and Steinle E. E., 1967, J. Appl. Bacteriol., 30: 488
2.American Public Health Association, Standard Methods for the Examination of Dairy Products, 1978, 14th Ed.,Washington D.C.
3.Anderson J. A., 1939, Ber, IIIrd Int. Mikrobiol. Kongress, 3 : 726
4.Collee J. G., Fraser A. G., Marmion B. P., Simmons A., (Eds.), Mackie and McCartney, Practical Medical Microbiology, 1996, 14th Edition, Churchill Livingstone
5.Frayer T. T., Lawrence R. C., Reiter B, 1967, J. Dairy Sci., 50: 477.
6.Hayes P. R., 1963, J. Gen. Microbiol., 30: 17.Innes A. G., 1956, J. Appl. Bacteriol., 19: 398.Isenberg, H.D. Clinical Microbiology Procedures Handbook 2nd Edition.
9.Jorgensen, J.H., Pfaller, M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015) Manual of Clinical Microbiology, 11th Edition. Vol. 1.
10.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1,Williams and Wilkins, Baltimore11. Salfinger Y., and Tortorello M.L. Fifth (Ed.), 2015, Compendium of Methods for the Microbiological Examination of Foods, 5th Ed., American Public Health Association, Washington, D.C.1
2.Vanderzant C. and Splittstoesser D. F., (Eds.), 1992, Compendium of Methods for the Microbiological Examination of Foods, 3rd Ed., APHA, Washington, D.C.1
3.Willis A. T., 1960, J. Path. Bacteriol., 80 (2): 37914.Wehr H. M. and Frank J. H., 2004, Standard Methods for the Microbiological Examination of Dairy Products, 17th Ed.,APHA Inc., Washington, D.C
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