Simmons Citrate Agar

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M099S
for differentiation between faecal coli and members of the aerogenes group on the basis of citrate utilization. It is recommended by BIS committee under the specifications IS:5887(Part I)-1976.


Simmons Citrate Agar is used for differentiation between faecal coli and members of the aerogenes group on the basis of citrate utilization.

Composition**

Ingredients Gms / Litre
Ammonium dihydrogen phosphate 1.000
Magnesium sulphate 0.200
Dipotassium phosphate 1.000
Sodium citrate 2.000
Sodium chloride 5.000
Bromo thymol blue 0.080
Agar 15.000

Final pH (at 25°C): 6.8±0.1

**Formula adjusted, standardized to suit performance parameters

Directions

Suspend 24.28 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Mix well and distribute in tubes. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool the tubes as slants.

Principle And Interpretation

These media are used for the differentiation between Enterobacteriaceae and the members of aerogenes group on the basis of citrate utilization as sole carbon source. Initially the citrate medium was developed by Koser (1) containing ammonium salt as the only nitrogen source and citrate as the only carbon source for differentiating Escherichia coli and Enterobacter aerogenes by IMViC tests. Later on Simmons (2) modified Kosers formulation by adding agar and bromothymol blue (3). It is recommended by APHA (4). It is also recommended by BIS (5) for isolation of Escherichia coli

Ammonium dihydrogen phosphate and sodium citrate serves as the sole nitrogen and carbon source respectively. Bromo thymol blue is the pH indicator. The organisms produce an alkaline reaction which is indicated by the change in colour from green to blue.

Quality Control

Appearance: Yellow coloured homogeneous free flowing powder

Gelling: Firm, comparable with 1.5% Agar gel

Colour and Clarity of prepared medium: Forest green coloured slightly opalescent gel forms as slants.

Reaction: Reaction of 2.43% w/v aqueous solution at 25°C. pH: 6.8±0.1

pH: 6.70-6.90

Cultural Response

Cultural characteristics observed after an incubation at 35-37°C for 18 - 24 hours.

Organism Inoculum (CFU) Growth Citrate Utilisation
Enterobacter aerogenes ATCC 13048 50-100 good-luxuriant Positive reaction, blue colour
Escherichia coli ATCC 25922 50-100 inhibited
Salmonella Enteritidis ATCC 13076 50-100 good-luxuriant Positive reaction, blue colour
Salmonella Typhimurium ATCC 14028 50-100 good-luxuriant Positive reaction, blue colour
Salmonella Typhi ATCC 6539 50-100 fair to good Negative reaction, green colour
Shigella dysenteriae ATCC 13313 50-100 inhibited Negative reaction, green colour

Storage and Shelf Life

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

Reference

  1. Koser, 1923, J. Bact., 8:493.
  2. Simmons, 1926, J. Infect. Dis., 39:209.
  3. MacFaddin J., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams and Wilkins, Baltimore.
  4. American Public Health Association, 1981, Standard Methods for the Examination of Water and Wastewater, 15th ed., APHA Inc., Washington, D.C.
  5. Bureau of Indian Standards, IS:5887 (Part II) 1976, reaffirmed 1986
More Information
Product Name Simmons Citrate Agar
SKU M099S
Product Type Regular
Physical Form Powder
Origin Chemically defined (HiCynth™)
Packaging type HDPE
References 1. Koser, 1923, J. Bact., 8:493.
2.Simmons, 1926, J. Infect. Dis., 39:209.
3.MacFaddin J., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams andWilkins, Baltimore.
4.Eaton A. D., Clesceri L. S., Rice E. W., and Greenberg A W., (Eds.), 2005, Standard Methods for the Examination of Waterand Wastewater, 21st Ed., APHA, Washington, D.C.
5.American Public Health Association, Standard Methods for the Examination of Dairy Products, 1978, 14th Ed., WashingtonD.C.
6.Salfinger Y., and Tortorello M.L. Fifth (Ed.), 2015, Compendium of Methods for the Microbiological Examination ofFoods, 5th Ed., American Public Health Association, Washington, D.C.
7.Baird R.B., Eaton A.D., and Rice E.W., (Eds.), 2015, Standard Methods for the Examination of Water andWastewater, 23rd ed., APHA, Washington, D.C.
8.Isenberg, H.D. Clinical Microbiology Procedures Handb0ook. 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.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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