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    King Agar

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    Dip Majumder
    King Agar B is a selective and differential growth medium used for the detection and enumeration of fluorescing bacteria, particularly Pseudomonas fluorescens, in water samples. The medium enhances fluorescein production and inhibits pyocyanin formation. It contains peptone, dipotassium phosphate, magnesium sulfate, and agar. Glycerol is added after autoclaving. Pseudomonas species will produce yellow-green pigment colonies that fluoresce under UV light. The medium allows differentiation of Pseudomonas species based on pigment production and growth characteristics.

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    King Agar

    Uploaded by

    Dip Majumder
    131 views2 pages
    King Agar B is a selective and differential growth medium used for the detection and enumeration of fluorescing bacteria, particularly Pseudomonas fluorescens, in water samples. The medium enhances fluorescein production and inhibits pyocyanin formation. It contains peptone, dipotassium phosphate, magnesium sulfate, and agar. Glycerol is added after autoclaving. Pseudomonas species will produce yellow-green pigment colonies that fluoresce under UV light. The medium allows differentiation of Pseudomonas species based on pigment production and growth characteristics.

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    King Agar B is a selective and differential growth medium used for the detection and enumeration of fluorescing bacteria, particularly Pseudomonas fluorescens, in water samples. The medium enhances fluorescein production and inhibits pyocyanin formation. It contains peptone, dipotassium phosphate, magnesium sulfate, and agar. Glycerol is added after autoclaving. Pseudomonas species will produce yellow-green pigment colonies that fluoresce under UV light. The medium allows differentiation of Pseudomonas species based on pigment production and growth characteristics.

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    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    131 views2 pages

    King Agar

    Uploaded by

    Dip Majumder
    King Agar B is a selective and differential growth medium used for the detection and enumeration of fluorescing bacteria, particularly Pseudomonas fluorescens, in water samples. The medium enhances fluorescein production and inhibits pyocyanin formation. It contains peptone, dipotassium phosphate, magnesium sulfate, and agar. Glycerol is added after autoclaving. Pseudomonas species will produce yellow-green pigment colonies that fluoresce under UV light. The medium allows differentiation of Pseudomonas species based on pigment production and growth characteristics.

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    60786 King Agar B (Pseudomonas Agar; F Agar; Pseudomonas Agar (for Fluorescein))

    For the detection and enumeration of fluorescing bacteria in water, in particular Pseudomonas fluorescens in drinking water acc. to King et al. (1954). Composition: Ingredients Mixed peptone Dipotassium hydrogen phosphate Magnesium sulfate Agar Final pH 7.2 +/- 0.2 (at 25 C) Store prepared media below 8 C, protected from direct light. Store dehydrated powder, in a dry place, in tightly-sealed containers at 2-25 C. Directions : Dissolve 33 g in 990 ml distilled water and add 10 ml glycerol (Fluka 49769). Sterilize by autoclaving at 121 C for 15 minutes. Optional CFC Selective Supplement (Fluka 53477) can be added to make the media selective. According to the Dansk Standard, prepare dilution series of the sample material (dilution factor 10). Pipet two 1 ml aliquots from each dilution step and inoculate the plate using pour plate method. Incubate the plates up to 72 hours at 20-25 C. Determine the count of the fluorescing bacteria under the UV lamp and the total microbial count. Principle and Interpretation: King Agar B enhances the elaboration of fluorescein and inhibits the pyocyanin formation. Mixed peptone provide the essential nitrogenous nutrients, carbon, sulphur and trace elements. Glycerol serves as a C-source and Dipotassium hydrogen phosphate buffers the medium. Magnesium sulfate is necessary for the activation of fluorescein production [8]. Ps. aeruginosa build colonies surrounded by a yellow to greenish-yellow zone due to fluorescein production which fluoresces under UV light. If pyocyanin is also synthesized, a bright green colour is produced. For the confirmation of pyocyanin the coloured pigments can be extracted with chloroform. Most pyocyanin-producing Pseudomonas strain synthesize also fluorescein and others produce just one pigments. The temperature can be a determinig factor as most fluorescent strains will not grow at 35 C. Rather, they grow 25-35 C. Atypical pyocyanin-negative, fluoresceinpositive Ps. aeruginosa strains can also be differentiated from Ps. fluorescens and Ps. putida (6). Ps. aeruginosa can be differentiated by following cultivation on Mac Conkey Agar (Fluka 70143, because Ps. putida and Ps. fluorescence do not fluorescens under UV light and grow poorly [7]. CFC Selective Supplement is an antibiotic supplement for the selective isolation of Pseudomonas species. Grams/Litre 20.0 1.5 1.5 10.0

    Cultural characteristics after up to 72 hours at 20-25 C. Organisms (ATCC) Pseudomonas fluorescens (17397) Pseudomonas aeruginosa (27853) Pseudomonas aeruginosa (9027) Pseudomonas aeruginosa (17397) Pseudomonas cepacia (25609) Aeromonas hydrophila (7966) Escherichia coli (25922) Enterobacter cloacae (13047) Growth +++ +++ +++ +++ (48 h) +++ +++ +++ +++ Yellow-green pigment in daylight + + + +/Fluorescense at 366 nm + + + +/-

    References: 1. E.O. King, et al., Media for the demonstration of pyocyanin and fluorescein, J. Lab. Clin. Med. 44, 301 (1954) 2. G.J. Bonde, Bacterial Indicators of Water Pollution, (1962) 3. G.J. Bonde, resunds-Vandkomiteens undersgelser, 288 (1965-70). 4. G.J. Bonde, Medlemsblad for Den danske Dyrlaegeforening, 55, 671 (1972). 5. L.C.D Formiga, New possibilies for the laboratory diagnosis of diphtheria, Brazilian J. Med. Biol. Res., 18, 401 (1985) 6. D.J. Blazevic, M.H. Kpcke, J.M. Matsen, Incidence and identification of Pseudomonas fluorescens and Pseudomonas putida in the clinical laboratory, Appl. Microbiol., 25, 107 (1973) 7. M.H. Brodsky, M.C. Nixon, Rapid method for detection of Pseudomonas aeruginosa on Mac Conkey-Agar under ultraviolet light. - Appl. Microbiol., 26, 219 (1973) 8. MacFaddin, Media for isolation-cultivation-identification-maintenance of medical bacteria, vol. 1. Williams & Wilkins, Baltimore, Md. (1985.)

    Precautions and Disclaimer This product is for R&D use only, not for drug, household, or other uses. Please consult the Material Safety Data Sheet for information regarding hazards and safe handling practices.

    Sigma brand products are sold through Sigma-Aldrich, Inc. Sigma-Aldrich, Inc. warrants that its products conform to the information contained in this and other Sigma-Aldrich publications. Purchaser must determine the suitability of the product(s) for their particular use. Additional terms and conditions may apply. Please see reverse side of the invoice or packing slip.

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