Pseudomonas HiVeg™ Agar (For Fluorescein)

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SKU:
MV120
For detection of fluorescein production by Pseudomonas species.


Intended Use

Recommended for the detection of fluorescein production by Pseudomonas species.

Composition

Ingredients Grams/Litre
HiVeg hydrolysate 10.0
HiVeg peptone No. 3 10.0
Dipotassium phosphate 1.5
Magnesium sulphate 1.5
Agar 15.0
Final pH (at 25°C) 7.0 ± 0.2

Formula adjusted, standardized to suit performance parameters.

Product Profile

Vegetable based (Code MV) Animal based (Code M)
MV120 M120
HiVeg hydrolysate Casein enzymic hydrolysate
HiVeg peptone No. 3 Proteose peptone

Recommended for: Detection of fluorescein production by Pseudomonas aeruginosa.

Reconstitution: 38.0 g/l

Quantity on preparation (500g): 13.15 L

(100g): 2.63 L

pH (25°C): 7.0 ± 0.2

Supplement: Glycerol

Sterilization: 121°C / 15 minutes.

Storage: Dry Medium - Below 30°C, Prepared Medium 2 - 8°C.

Directions

Suspend 38 grams in 1000 ml distilled water containing 10 ml glycerol. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes.

Principle and Interpretation

Pseudomonas HiVeg Agar (For Fluorescein) is prepared with the replacement of animal peptone by HiVeg peptone to avoid BSE/ TSE risks. Pseudomonas HiVeg Agar (For Fluorescein) is the modification of Pseudomonas Agar (For Fluorescein) which is based on the formula described by King et al (1) for the detection of fluorescein production, a water soluble, chloroform insoluble fluorescent pigment by Pseudomonas species (2). The 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.

HiVeg hydrolysate and HiVeg peptone No.3 provide the essential nitrogenous nutrients, carbon, sulphur and trace elements for the growth of Pseudomonas. Glycerol acts as a source of energy and enhances pigment production. Dipotassium phosphate buffers the medium as well as increases the phosphorus content of the medium, thereby enhancing production of fluorescein pigment. 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 (2). The formation of non pigmented colonies does not completely rule out a Pseudomonas aeruginosa isolate.

Quality Control

Appearance of powder: Yellow coloured, may have slightly greenish tinge, homogeneous, free flowing powder.

Gelling: Firm, comparable with 1.5% Agar gel.

Colour and Clarity: Yellow coloured, clear to slightly opalescent gel forms in petri plates.

Reaction: Reaction of 3.8% w/v aqueous solution (containing 1% v/v glycerol) is pH 7.0 ± 0.2 at 25°C.

Cultural Response

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

Organisms (ATCC) Inoculum (CFU) Growth Colour of Colony
Pseudomonas aeruginosa (17934) 30-300 luxuriant greenish yellow
Pseudomonas aeruginosa (27853) 30-300 luxuriant greenish yellow

References

  1. King, Ward and Raney, 1954, J. Lab. Clin. Med., 44: 301.
  2. MacFaddin J., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Volume I, Williams and Wilkins, Baltimore.
More Information
Product Name Pseudomonas HiVeg™ Agar (For Fluorescein)
SKU MV120
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
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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