Lysine Iron Agar

SKU:
M377
Availability: In stock
Only %1 left
As low as $36.00
For the differentiation of enteric organisms especially Salmonella Arizonae based on their ability to decarboxylate or deaminate lysine and to form hydrogen sulphide (H2S).


Intended Use

Recommended for the differentiation of enteric organisms especially Salmonella Arizonae based on their ability to decarboxylate or deaminate lysine and to form hydrogen sulphide (H2S). The composition of this medium is in accordance with FDA BAM and APHA.

Composition**

Ingredients Gms/Litre
Peptone 5.000
Yeast extract 3.000
Dextrose (Glucose) 1.000
L-Lysine 10.000
Ferric ammonium citrate 0.500
Sodium thiosulphate 0.040
Bromocresol purple 0.020
Agar 15.000
Final pH (at 25°C) 6.7±0.2

**Formula adjusted, standardized to suit performance parameters

Directions

Suspend 34.56 grams in 1000 ml purified/distilled water. Heat to boiling to dissolve the medium completely. Dispense into tubes and sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool the tubes in slanted position to form slants with deep butts.

Principle And Interpretation

Lysine Iron Agar was developed by Edwards and Fife (1) to detect lactose fermenting Salmonellae. Salmonellae are known to decarboxylate lysine rapidly and produce large amounts of hydrogen sulphide (2,3). This medium is a sensitive medium for the detection of lactose fermenting and lactose non-fermenting Salmonella species. Many strains of this group ferment lactose very rapidly thus suppressing H2S production on Triple Sugar Iron Agar (M021). So there is a possibility that the organisms frequently found in food poisoning outbreaks could be overlooked. Thatcher and Clark described the isolation of Salmonella species from foods from selective agar and to inoculate it on Lysine Iron Agar and Triple Sugar Iron (M021) together. Using these two media greater discrimination can be made between coliform organisms e.g. Escherichia coli and Shigella species (4,5). This medium is recommended by FDA BAM (6) and APHA (7) for biochemical testing of Salmonella from food samples.

Peptone and yeast extract provide essential nutrients. Dextrose is a source of fermentable carbohydrate. Ferric ammonium citrate and sodium thiosulphate are indicators of H2Sformation. Cultures that produce hydrogen sulphide cause blackening of the medium due to ferrous sulphide production. Lysine decarboxylation causes an alkaline reaction (purple colour) to give the amine cadaverine and the organisms which do not decarboxylate lysine, produce acid butt (yellow colour). Organisms that deaminate lysine, form alpha - ketocarboxylic acid, which reacts with iron salt near the surface of the medium under the influence of oxygen to form reddish-brown compound. The medium is stabbed to the base of the butt and streaked on slant.

Type of specimen

Isolated Microorganisms

Specimen Collection and Handling:

For food and dairy samples, follow appropriate techniques for sample collection and processing as per guidelines (6,7). 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. Individual organisms differ in their growth requirement and may show variable growth patterns on the medium.
  2. 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.

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 Light yellow to greyish yellow homogeneous free flowing powder
Gelling Firm, comparable with 1.5% Agar gel
Colour and Clarity of prepared medium Purple coloured, clear to slightly opalescent gel forms in tubes as slants
Reaction Reaction of 3.45% w/v aqueous solution at 25°C. pH: 6.7±0.2
pH 6.50-6.90

Cultural Response

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

Organism Inoculum (CFU) Growth Butt Slant H2S
Citrobacter freundii ATCC 8090 50-100 luxuriant acidic reaction, yellowing of the medium alkaline reaction, purple or no colour change positive blackening of medium
Escherichia coli ATCC 25922 (00013*) 50-100 luxuriant alkaline reaction, purple or no colour change alkaline reaction, purple or no colour change negative
Proteus mirabilis ATCC 25933 50-100 luxuriant acidic reaction, yellowing of the medium deep red, lysine deamination positive blackening of medium
Salmonella Arizonae ATCC 13314 50-100 luxuriant alkaline reaction, purple or no colour change alkaline reaction, purple or no colour change positive blackening of medium
Salmonella Enteritidis ATCC 13076 (00030*) 50-100 luxuriant alkaline reaction, purple or no colour change alkaline reaction, purple or no colour change positive blackening of medium
Salmonella Typhimurium ATCC 14028 (00031*) 50-100 luxuriant alkaline reaction, purple or no colour change alkaline reaction, purple or no colour change positive blackening of medium
Shigella flexneri ATCC 12022 (00126*) 50-100 luxuriant acidic reaction, yellowing of the medium alkaline reaction, purple or no colour change negative

Key: *Corresponding WDCM numbers.

Storage and Shelf Life

Store between 10-30°C in a tightly closed container and the prepared medium at 2-8°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.

More Information
Product Name Lysine Iron Agar
SKU M377
Product Type Regular
Physical Form Powder
Origin Animal
Packaging type HDPE
References 1. Moeller V., 1954, Acta. Pathol. Microbiol. Scand., 34:102.
2.Moeller V., 1954, Acta. Pathol. Microbiol. Scand., 34:259.
3.Moeller V., 1955, Acta. Pathol. Microbiol. Scand., 36:158.
4.Falkow, 1958, Am. J. Clin. Pathol., 29:598.
5.Eaton A. D., Clesceri L. S., Rice E. W. and Greenberg A. W., (Eds.), 2005, Standard Methods for the Examination of Water and Wastewater, 21st Ed., APHA, Washington, D.C.
6.Downes F. P. and Ito K., (Eds.), 2001, Compendium of Methods for the Microbiological Examination of Foods, 4th Ed., American Public Health Association, Washington, D.C.
7.Isenberg (Ed.), 1992, Clinical Microbiology Procedures Handbook, Vol. 1. American Society for Microbiology, Washington, D.C.
8.FDA Bacteriological Analytical Manual, 2005, 18th Ed., AOAC, Washington, DC.
Write Your Own Review
Only registered users can write reviews. Please Sign in or create an account

What is Lysine Iron Agar used for?

Lysine Iron Agar (LIA) tests for: (1) Lysine decarboxylase, (2) Lysine deaminase, (3) H2S production. Used with TSI for Enterobacteriaceae identification. Inoculate by stabbing butt and streaking slant. Results: Purple butt = lysine decarboxylase (Salmonella, most E. coli). Red slant = lysine deaminase (Proteus, Providencia). Black = H2S production (Salmonella, Citrobacter). Yellow = glucose fermentation only (Klebsiella). Critical for differentiating Salmonella (purple/purple or purple/red with black) from other enterics. Used in conjunction with TSI in identification schemes.