Peptone Water: Intended Use: Composition
Peptone Water: Intended Use: Composition
Peptone Water: Intended Use: Composition
Intended Use:
Peptone Water is used as a growth medium and as a base for carbohydrate fermentation media.
Composition**
Ingredients Gms / Litre
Peptone 10.000
Sodium chloride 5.000
Final pH ( at 25°C) 7.2±0.2
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 15.0 grams in 1000 ml distilled water. Add the test carbohydrate in desired quantity and dissolve completely.
Dispense in tubes with or without inverted Durhams tubes and sterilize by autoclaving at 15 lbs pressure (121°C) for 15
minutes.
Principle And Interpretation
Peptone Water is particularly suitable as a substrate in the study of indole production. Peptone used in Peptone Water is
rich in tryptophan content. Presence of indole can be demonstrated using either Kovacs or Ehlrich reagent. Peptone Water
is also utilized as a base for carbohydrate fermentation studies with the addition of sugar and indicators such as
bromocresol purple, phenol red or bromothymol blue.
Peptone Water is recommended (3,6,7) for studying the ability of an organism to ferment a specific carbohydrate which
aid in differentiation of genera and species. Peptone water is formulated as per Shread, Donovan and Lee (9). Peptone
Water with pH adjusted to 8.4 is suitable for the cultivation and enrichment of Vibrio species. Peptone
provides nitrogenous and carbonaceous compounds, long chain amino acids, vitamins provides essential nutrients.
Sodium chloride maintains the osmotic balance of the medium. To study the fermentation ability of
carbohydrates, saccharose, rhamnose, salicin are generally added in 0.5% amount separately to the basal medium before or
after sterilization. The acidity formed during fermentation can be detected by addition of phenol red indicator, which
shows a colour change of the medium from red to yellow under acidic conditions. If desired, Durham's tube may be used
to detect the gas production if produced.
Type of specimen
Isolated microrganism from clinical specimen , food, dairy and water samples
Specimen Collection and Handling
For clinical samples follow appropriate techniques for handling specimens as per established guidelines (4,5).
For food and dairy samples, follow appropriate techniques for sample collection and processing as per guidelines (1,8,10).
For water samples, follow appropriate techniques for sample collection, processing as per guidelines and local standards.(2)
After use, contaminated materials must be sterilized by autoclaving before discarding.
Limitations
1. Due to nutritional variations , some strains may show poor growth.
Quality Control
Appearance
Cream to yellow homogeneous free flowing powder
Colour and Clarity of prepared medium
Light amber coloured clear solution without any precipitate
Reaction
Reaction of 1.5% w/v aqueous solution at 25°C. pH : 7.2±0.2
pH
7.00-7.40
Cultural Response
Cultural characteristics observed after an incubation at 35-37°C for 18-24 hours.
Cultural Response
Organism Inoculum Growth Indole test
(CFU)
Escherichia coli ATCC 50-100 luxuriant positive reaction, red ring at the
25922 (00013*) interface of the medium on
addition of Kovac's reagent (R008)
Salmonella Typhimurium 50-100 luxuriant negative reaction, no red ring at the
ATCC 14028 (00031*) interface of the medium on
addition of Kovac's reagent (R008)
Disposal
User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product. Follow
established laboratory procedures in disposing of infectious materials and material that comes into contact with clinical
sample must be decontaminated and disposed of in accordance with current laboratory techniques (4,5).
References
1. American Public Health Association, Standard Methods for the Examination of Dairy Products, 1978, 14th Ed., Washington
D.C.
2. Baird R.B., Eaton A.D., and Rice E.W., (Eds.), 2015, Standard Methods for the Examination of Water and
Wastewater, 23rd ed., APHA, Washington, D.C.
3. Finegold and Baron, 1986, Bailey and Scotts Diagnostic Microbiology, 7th ed., The C.V. Mosby Co., St. Louis.
nd
4. Isenberg, H.D. Clinical Microbiology Procedures Handbook 2 Edition.
5. 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.
6. Lennette and others (Eds.), 1985, Manual of Clinical Microbiology, 4th ed, ASM, Washington, D.C.
7. MacFaddin J., 1980, Biochemical Tests for Identification of Medical Bacteria, 2nd ed., Williams and Wilkins, Baltimore.
8. Salfinger Y., and Tortorello M.L., 2015, Compendium of Methods for the Microbiological Examination of Foods, 5th
Ed., American Public Health Association, Washington, D.C.
9. Shread P., Donovan T.J, and Lee J.V, (1981), Soc. Gen, Microbiol. Q., 8, 184.
10. Wehr H. M. and Frank J. H., 2004, Standard Methods for the Microbiological Examination of Dairy Products, 17th Ed.,
APHA Inc., Washington, D.C.
Revision : 04 / 2019
CE Marking
10°C
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