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King’s Medium B Base, Granulated
Intended Use
Recommended for non-selective isolation, cultivation and pigment production of Pseudomonas species.
Composition
| Ingredients | g/L |
|---|---|
| Proteose peptone | 20.000 |
| Dipotassium hydrogen phosphate | 1.500 |
| Magnesium sulphate heptahydrate | 1.500 |
| Agar | 20.000 |
| Final pH (at 25°C) | 7.2±0.2 |
Formula adjusted, standardized to suit performance parameters
Directions
Suspend 42.23 grams of dehydrated medium in 1000 ml purified / distilled water containing 15 ml of glycerol. Heat to boiling to dissolve the medium completely. Mix well. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 45-50°C. Aseptically pour into sterile Petri plates.
Principle And Interpretation
Pseudomonas aeruginosa is known to produce two types of pigments, pyocyanin and fluorescein which is a characteristic property and aids in isolation of Pseudomonas from clinical material. An additional pigment called as pyorubin was reported by King. Pyocyanin is green while fluorescein is fluorescent yellow and pyorubin is reddish brown. Some strains produce all these pigments while the others produce one or two pigments. P.aeruginosa can be identified on Hugh Leifson Medium (M826). Kings Medium B Base is particularly suited for fluorescein.
Kings Medium B Base is based on the formulation of King et al (1,2). This medium can be used as a general medium for the non-selective isolation and pigment production of Pseudomonas species from foods, cosmetic samples etc. Agrobacterium have been traditionally identified as gram-negative bacteria that do not produce fluorescent pigment on Kings B medium and do produce tumors (or hairy roots) when inoculated onto test plants (3).
These media contain proteose peptone, which provides carbonaceous and nitrogenous compounds for the growth of bacteria. Glycerol serves as a source of energy and also enhances pigment production. Magnesium sulphate also enhances pigment production. Pigments and/or their derivatives produced by Pseudomonas species play a role as siderophores in the iron uptake systems of bacteria, and hence, their production is markedly enhanced under conditions of iron deficiency. The production of pigments especially non-fluorescent blue pigment, pyocyanin is readily demonstrated by culturing on Kings Medium B, which contains no added iron (4). The addition of dipotassium phosphate increases the phosphorus content of the medium thereby enhancing production of fluorescent pigment. For inoculation, use the organisms freshly cultured in Kings Medium A, incubate overnight at 37°C and then at room temperature for 6 days. With Kings Medium B, incubate at 37°C for 6 days.
Type of specimen
Food samples; Water samples.
Specimen Collection and Handling
For food samples, follow appropriate techniques for sample collection and processing as per guidelines (5).
For water samples, follow appropriate techniques for sample collection, processing as per guidelines and local standards.(6)
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
- Individual organisms differ in their growth requirement and may show variable growth patterns on the medium.
- Each lot of the medium has been tested for the organisms specified on the COA. It is recommended to users to validate the medium for any specific microorganism other than mentioned in the COA based on the user's unique requirement.
- Results should be noted after 18-24 hours. Else it might result in erroneous results.
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 granular powder
Gelling: Firm, comparable with 2.0% Agar gel
Colour and Clarity of prepared medium: Light yellow coloured, clear to slightly opalescent gel forms in Petri plates
Reaction: Reaction of 4.22% w/v aqueous solution (containing 1.5%v/v glycerol) at 25°C. pH: 7.2±0.2
pH: 7.00-7.40
Cultural Response
Cultural characteristics observed after an incubation at 35-37°C for 18-24 hours.
| Organism | Inoculum (CFU) |
Growth | Recovery | Pigment production |
|---|---|---|---|---|
| Pseudomonas aeruginosa ATCC 17934 | 50-100 | good-luxuriant | >=70% | greenish yellow |
| Pseudomonas aeruginosa ATCC 27853 (00025*) | 50-100 | good-luxuriant | >=70% | greenish yellow |
| ^Pseudomonas paraeruginosa ATCC 9027 (00026*) | 50-100 | good-luxuriant | >=70% | greenish yellow |
| Burkholderia cepacia ATCC 25609 | 50-100 | good-luxuriant | >=70% | no pigment |
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 (7,8).
| Product Name | King’s Medium B Base, Granulated |
|---|---|
| SKU | GM1544 |
| Product Type | Granulated |
| Physical Form | Granular |
| Origin | Animal |
| Packaging type | HDPE |
| References | 1.King E. O., Ward M. K. and Raney D. E., 1954, J. Lab and Clin. Med., 44:301-307.2.Murray P. R, Baron E, J., Jorgensen J. H., Pfaller M. A., Yolken R. H., (Eds.), 2007, Manual of Clinical Microbiology, 9th Ed., ASM, Washington, D.C.3.Ann G., Matthysse, 1998, The Genus Agraobacterium, Chapter 3.1. |
| Customized Product Available | No |








