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Pseudomonas Agar Medium For Detection of Fluorescein
Pseudomonas#CC293D
Intended Use
Recommended for detection of fluorescein production by Pseudomonas species in accordance with USP
Composition**
| Ingredients | g/L |
|---|---|
| Tryptone | 10.000 |
| Peptone | 10.000 |
| Anhydrous dibasic potassium phosphate | 1.500 |
| Magnesium sulphate heptahydrate | 1.500 |
| Agar | 15.000 |
| pH after sterilization (at 25°C) | 7.2±0.2 |
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 37.23 grams of (the equivalent weight of dehydrated medium per litre) in 1000 ml purified/distilled water, containing 10 ml glycerin. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 45-50°C. Mix well and pour into sterile Petri plates.
Principle And Interpretation
Pseudomonas Agar (For Fluorescein) is based on the formula described by King et al (1) and as modified in the U.S. Pharmacopeia (2) for the detection of fluorescein production a water soluble, chloroform insoluble fluorescent pigment by Pseudomonas species (3). Pseudomonas is ubiquitous in environment and is a common causative agent of burn, skin and nosocomial infections. They are also common contaminant of pharmaceutical and cosmetics related preparations. Pseudomonas strains are reported to produce phenazine pigments like Pyocyanin-blue green redox-active secondary metabolite pigment, pyorubin-rust brown pigment, -oxyphenzine- a breakdown product of Pyocyanin, pyoverdin-a water soluble yellow green pigments also known as fluorescein.
This medium enhances the elaboration of fluorescein by Pseudomonas and inhibits the pyocyanin formation. The fluorescein pigment diffuses from the colonies of Pseudomonas into the agar and shows yellow fluorescent colouration. Some Pseudomonas strains produce small amounts of pyocyanin resulting in a yellow-green colouration. Tryptone provides the essential nitrogenous nutrients, carbon, sulfur and trace elements for the growth of Pseudomonas. These nutrients are also conducive to the production of fluroescein. Peptone and phosphorous in the medium enhance the production of pyoverdin/fluorescein pigment. Dipotassium phosphate buffers the medium while magnesium sulphate provides necessary cations for the activation of fluorescein production. Salt concentration exceeding 2% affects pigment production. UV illumination may be bactericidal, so make sure that there is good growth before placing culture under UV light (1).
Type of specimen
Pharmaceutical samples
Specimen Collection and Handling:
For pharmaceutical samples follow appropriate techniques for handling specimens as per established guidelines (2). After use, contaminated materials must be sterilized by autoclaving before discarding.
Warning and Precautions :
Read the label before opening the container. Wear protective gloves/protective clothing/eye protection/face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling specimens. Safety guidelines may be referred in individual safety data sheets.
Limitations :
- UV illumination may be bactericidal, so make sure that there is good growth before placing culture under UV light (3).
Performance and Evaluation
Performance of the medium is expected when used as per the direction on the label within the expiry period when stored at recommended temperature.
Quality Control
Appearance
Cream to yellow homogeneous free flowing powder
Gelling
Firm, comparable with 1.5% Agar gel
Colour and Clarity of prepared medium
Yellow coloured clear to slightly opalescent gel forms in Petri plates
pH
7.00-7.40
Growth Promotion Test
Growth Promotion is carried out in accordance with the harmonized method of USP. Cultural response was observed after an incubation at 33-37°C for not less than 3 days. Recovery rate is considered as 100% for bacteria growth on Soyabean Casein Digest Agar.
Cultural Response
Cultural characteristics observed after incubation at 33-37°C for 18-48 hours. Recovery rate is considered as 100% for bacteria growth on Soyabean Casein Digest Agar.
| Organism | Inoculum (CFU) | Observed Lot Recovery value (CFU) | Characteristic colonial morphology | Fluorescence in UV light | Oxidase | |
|---|---|---|---|---|---|---|
| Test for Pseudomonas aeruginosa | ||||||
| ^Pseudomonas paraeruginosa ATCC 9027 (00026*) | 50-100 | 35-100 | >=70% | Generally colourless to yellowish | positive | positive |
Key: *Corresponding WDCM numbers.
^ Formerly known as Pseudomonas aeruginosa
Storage and Shelf Life
Store between 10-30°C in a tightly closed container and the prepared medium at 20-30°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle in order to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition. Seal the container tightly after use. Product performance is best if used within stated expiry period.
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 sample must be decontaminated and disposed of in accordance with current laboratory techniques (4,5).
| Product Name | Pseudomonas Agar Medium For Detection of Fluorescein |
|---|---|
| SKU | MU120 |
| Product Type | Regular |
| Physical Form | Powder |
| Origin | Animal |
| Packaging type | HDPE |
| References | 1. King, Ward and Raney, 1954, J. Lab. Clin. Med., 44 : 301. 2.The United States Pharmacopoeia, 2006, USP29/NF24, The United States Pharmacopeial Convention, Rockville, MD. 3.MacFaddin J., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. I, Williams andWilkins, Baltimore. |
| Customized Product Available | No |










