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Nutrient Gelatin

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Nutrient Gelatin is prepared as per the formulation formerly used in the examination of water, sewage and other materials of sanitary importance (1). Gelatin liquefaction is one of the essential test for the differentiation of enteric bacilli (2). This medium can also be used for the microbial plate counts of water.

Peptic digest of animal tissue and beef extract supply nutrients for the growth of non-fastidious organisms. Gelatin is the substrate for the determination of the ability of an organism to produce gelatinase, a proteolytic enzyme active in the liquefaction of gelatin.

An 18-24 hours old pure culture from Triple Sugar Iron Agar (M021) or Kligler Iron Agar (M078) is stab-inoculated in Nutrient Gelatin with an inoculating needle directly down the centre of the medium to a depth of approximately one half an inches from the bottom of the tube. Incubate the tubes including an un-inoculated control at 35±2°C for 24-48 hours. Many species require prolonged incubation (3, 4) for gelatin liquefaction. Gelatin is solid at 20°C or less temperature and liquid at 35°C or higher temperature. Gelatin liquefies at about 28°C, so incubation is carried out at 35°C but kept in a refrigerator for about 2 hours before interpretation of the results (3). Liquefaction of gelatin occurs on the surface layer, so care should be taken not to shake the tubes (5). Control is run along with every testing as gelling ability of gelatin varies (3) and also the gelatin concentration should not exceed 12% as it may inhibit growth (6). For plate counts of water, the incubation is carried out at 20-22°C for upto 30 days.

Nutrient Gelatin Medium is not recommended for determination of gelatin liquefaction by fastidious species and obligate anaerobes. At various intervals during the incubation process, examine the tubes for growth and liquefaction. At each interval, tighten the caps and transfer the tubes to refrigerator for sufficient time period to determine whether liquefaction has occurred or not.

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

References:
1. American Public Health Association, 1975, Standard Methods for the Examination of Water and Wastewater, 14th Ed., APHA, Washington, D.C.
2. Ewing, 1986, Edwards and Ewings Identification of Enterobacteriaceae, 4th Ed., Elsevier Science Publishing Co., Inc. New York.
3. Cawan S. and Steel K., 1966, Manual for the Identification of Medical Bacteria, Cambridge University Press, Pg. 19, 27-28, 116 and 156.
4. Lautrop H., 1956, Acta. Pathol. Microbiol. Scand., 39:357.
5. Frobisher M., 1957, Fundamentals of Microbiology, 6th Ed., W.B. Saunders Co., Philadelphia, p. 239.
6. Branson D., 1972, Methods in Clinical Bacteriology, Springfield, III, pg. 21.

Quality Control
AppearanceCream to yellow homogeneous free flowing slightly coarse powder
GellingSemisolid, comparable with 12.0% Gelatin gel
Color and Clarity of Prepared MediumLight amber colored clear to slightly opalescent gel forms in tubes as butts
ReactionReaction of 12.8% w/v aqueous solution at 25°C. pH : 6.8±0.2
pH6.60-7.00
Cultural ResponseCultural characteristics observed after an incubation at 35-37°C for 1 to 7 days, (Incubated anaerobically for
Cl.perfringens). (For gelatinase test, cool below 20°C )
Composition**
IngredientsGms/Litre
Peptic digest of animal tissue5.000
Beef extract3.000
Gelatin120.000
Final pH ( at 25°C)6.8±0.2
**Formula adjusted, standardized to suit performance parameters

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Thomas No.
C979X90
Mfr. No.
M060-500G
Description
Nutrient Gelatin, 500 g
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Thomas No.
C979X91
Mfr. No.
M060-2.5KG
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Nutrient Gelatin, 2.5 kg
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Thomas No.
C979X92
Mfr. No.
M060-5KG
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Nutrient Gelatin, 5 kg
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