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Sellers Differential Agar
Sellers Differential Agar is used for differentiation and identification of gram-negative non-fermentative bacilli especially Pseudomonas aeruginosa and Acinetobacter calcoaceticus .
Composition**
| Ingredients | Gms / Litre |
|---|---|
| Yeast extract | 1.000 |
| Peptic digest of animal tissue | 20.000 |
| L-Arginine | 1.000 |
| D-Mannitol | 2.000 |
| Sodium chloride | 2.000 |
| Sodium nitrate | 1.000 |
| Sodium nitrite | 0.350 |
| Magnesium sulphate | 1.500 |
| Dipotassium phosphate | 1.000 |
| Bromo thymol blue | 0.040 |
| Phenol red | 0.008 |
| Agar | 15.000 |
Final pH ( at 25°C) 6.7±0.2
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 44.90 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Dispense in test tubes and sterilize by autoclaving at 15 lbs pressure (121°C) for 10 minutes. Cool the tubed medium in slanted position. Just before inoculation add 0.15 ml or 2 drops of 50% sterile dextrose solution to each slant by letting it run down the side of the tube opposite the slant.
Principle And Interpretation
Sellers Differential Agar is formulated as described by Sellers (1) for differentiation and identification of non-fermentative gram-negative bacilli especially Pseudomonas aeruginosa , Acinetobacter calcoaceticus and Alcaligenes faecalis . The medium is complex with differentiation ability based on oxidation of dextrose, fluorescence, production of nitrogen and pH changes.
Yeast extract and peptic digest of animal tissue are the sources of carbon and nitrogen compounds as well as vitamins and minerals. Oxidation of dextrose by the organisms is readily visible as a yellow band at the slant-butt junction. The dextrose added prior to inoculation diffuses into the medium during incubation period. P. aeruginosa exhibits acid reaction from dextrose. However, the reaction is masked by deamination of arginine and high peptone concentration. Most of Acinetobacter species produce a yellow band due to glucose oxidation. This band may disappear after 24 hours. D-Mannitol and magnesium sulphate stimulate fluorescence while nitrogen gas production is stimulated by dipotassium phosphate (1, 2). Sodium nitrate and nitrite serve as substrates for the production of nitrogen gas for denitrifying bacteria. Phenol red and bromothymol blue are the pH indicators. Arginine dihydrolase positive reaction is indicated by the formation of blue colour. Inoculation is done by stabbing deep into the butt and streaking the slant.
Quality Control
Appearance Light yellow to pink homogeneous free flowing powder
Gelling Firm, comparable with 1.5% Agar gel
Colour and Clarity of prepared medium Green coloured clear to slightly opalescent gel forms in tubes as slants with a butt.
Reaction Reaction of 4.5% w/v aqueous solution at 25°C. pH : 6.7±0.2
pH 6.50-6.90
Cultural Response M293: Cultural characteristics observed after an incubation at 35 - 37°C for 18 - 24 hours.
| Organism | Inoculum (CFU) | Growth | Slant | Butt | Band | Fluorescence(under uv) |
|---|---|---|---|---|---|---|
| Acinetobacter baumannii ATCC 19606 | 50-100 | good | blue | green | yellow | negative |
| Alcaligenes faecalis ATCC 8750 | 50-100 | good | blue | blue-green | none | positive |
| Pseudomonas aeruginosa ATCC 27853 | 50-100 | good | blue-green | blue-green | blue | positive |
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.
Reference
- Sellers W., 1964, J. Bacteriol., 87:46.
- MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams and Wilkins, Baltimore.
| Product Name | Sellers Differential Agar |
|---|---|
| SKU | M293 |
| Product Type | Regular |
| Physical Form | Powder |
| Origin | Animal |
| Packaging type | HDPE |
| References | 1. Schaedler R.W., Dubos R. and Castello R., 1965, J. Exp. Med., 122:59. 2.Mata L.J., Carrillo C. and Villatoro E., 1969, Appl. Microbiol, 17:596. 3.MacFaddin J., 1985, Media for Isolation-Cultivation-Identification- Maintenance of Medical Bacteria, Vol. I. Williams andWilkins, Baltimore. 4.Stalons D.R., Thornsberry C. and Dowel V.R., 1974, Appl. Microbiol, 27:1098. 5.Fass R.J., Prior R.B. and Rotilie C.A., 1975, Antimicrob. Agents Chemother., 8:444. 6.Rosner, 1968, Am. J. Clin. Pathol. 49:216. 7.Garrod, 1966, J. Pathol. Bacterial., 91:621. 8.Lowrence and Traub, 1969, Appl. Microbiol, 17:839. |
| Customized Product Available | No |



