Pseudomonas Agar Medium For Detection of Fluorescein

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MU120
For detection of fluorescein production by Pseudomonas species in accordance with US Pharmacopoeia.


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 :

  1. 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).

More Information
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
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