Thermo Scientific™ Oxoid™ Lysine Iron Agar (Dehydrated)

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A diagnostic medium for salmonellae including Salmonella arizonae

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    Specifications:
    Application Microbiology
    Storage Temperature Room Temperature
    Product Type Culture Medium Forms Powder
    Product Brand Oxoid
    Product Grade Microbiology grade

    The Oxoid™ Lysine Iron Agar (LIA) is a differential diagnostic medium specifically formulated for detecting Salmonella spp., including Salmonella arizonae. This medium enables the identification of bacteria through lysine decarboxylase activity and hydrogen sulfide (H₂S) production, making it a vital tool for clinical, food safety, and research applications.

    Key Features

    1. Differential Medium:
      • Detects lysine decarboxylation, H₂S production, and other metabolic activities specific to Salmonella.
      • Differentiates Salmonella spp. from other Enterobacteriaceae.
    2. Sensitive to Lactose-Fermenting Salmonellae:
      • Allows detection of lactose-fermenting Salmonella arizonae, often missed by traditional media.
    3. Precise Identification:
      • Differentiates between Salmonella, Proteus, Citrobacter, and other enteric bacteria based on metabolic reactions.
    4. Versatile Usage:
      • Applicable in clinical microbiology for pathogen detection.
      • Supports foodborne pathogen investigations.
    5. Ready-to-Prepare Formula:
      • Dehydrated medium supplied for convenient preparation and storage.

    Typical Formula (per litre)

    IngredientConcentration (g/L)
    Bacteriological Peptone5.0
    Yeast Extract3.0
    Glucose1.0
    L-Lysine10.0
    Ferric Ammonium Citrate0.5
    Sodium Thiosulphate0.04
    Bromocresol Purple0.02
    Agar14.5
    pH6.7 ± 0.2 @ 25°C

    Preparation Instructions

    1. Suspend 34 g of dehydrated medium in 1 litre of distilled water.
    2. Heat to boiling to dissolve completely.
    3. Dispense into tubes.
    4. Sterilize by autoclaving at 121°C for 15 minutes.
    5. Cool tubes in an inclined position to form slants with deep butts.

    Interpretation of Results

    Reaction TypeSlantButtH₂S Production
    Salmonella spp.AlkalineAlkalinePositive
    Proteus spp.RedAcidNegative
    Citrobacter spp.AlkalineAcidPositive
    Escherichia spp.AlkalineAcid/NeutralNegative
    Shigella spp.AlkalineAcidNegative
    Klebsiella spp.AlkalineAlkalineNegative

    Note:

    • Salmonella paratyphi A does not produce lysine decarboxylase, resulting in an alkaline slant and acid butt.
    • Proteus species producing H₂S do not blacken this medium.

    Storage Conditions

    • Dehydrated Medium: Store at 10–30°C.
    • Prepared Medium: Store at 2–8°C.
    • Use before the expiry date indicated on the label.

    Quality Control

    Control OrganismExpected Result
    Enterobacter aerogenes ATCC 13048Slant: Alkaline; Butt: Alkaline; H₂S: Negative
    Proteus mirabilis ATCC 29906Slant: Red; Butt: Acid; H₂S: Positive
    Enterobacter cloacae ATCC 23355Slant: Alkaline; Butt: Acid; H₂S: Negative

    Applications

    1. Clinical Diagnostics:
      • Identification of Salmonella infections, including lactose-fermenting Salmonella arizonae.
    2. Food Safety Testing:
      • Detection of foodborne Salmonella spp. to ensure compliance with safety standards.
    3. Research:
      • Studies on bacterial metabolism, particularly lysine decarboxylation and H₂S production.

    Advantages

    1. Sensitive and Specific:
      • Detects lactose and non-lactose fermenting Salmonella with high accuracy.
    2. Comprehensive Results:
      • Differentiates multiple Enterobacteriaceae species in a single test.
    3. Ease of Preparation:
      • Simple preparation and storage make it convenient for routine use.

    The Oxoid™ Lysine Iron Agar (CM0381) is a reliable diagnostic medium designed for rapid detection and differentiation of Salmonella spp. and other Enterobacteriaceae based on metabolic characteristics. Its high sensitivity and specificity make it a valuable tool in clinical, food safety, and research laboratories.

    References

    1. Edwards, P.R., and Fife, M.A. (1961). Appl. Microbiol. 9:478-480.
    2. Moeller, V. (1954). Acta Pathol. Microbiol. Scand. 355:259-277.
    3. Ewing, W.H., Davis, B.R., and Edwards, P.R. (1960). Pub. Hlth Labs. 18:77-83.
    4. Thatcher, F.S., and Clark, D.S. (1968). University of Toronto Press, p.100.
    5. Timms, L. (1971). Med. Lab. Technol. 28:150-156.
    6. Finegold, S.M., and Martin, W.J. (1982). Bailey & Scott’s Diagnostic Microbiology, 6th Ed., C.V. Mosby.


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