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Lysine Iron Agar, LIA

For simultaneous detection of hydrogen sulfide production and lysine decarboxylase (LDC) to identify Enterobacteriaceae, especially Salmonella and Arizona.

Catalog Number: AS-1279

A differential media called lysine iron agar (LIA) is used to distinguish between Enterobacteriaceae strains based on their ability to produce hydrogen sulfide, lysine decarboxylate, and lysine deamination. Peptone, yeast extract, glucose, lysine, ferric ammonium citrate, sodium thiosulfate, and a pH indicator are all included in LIA, which was created by Edwards and Fife. To avoid masking lysine responses, lactose is excluded. Salmonella species, especially lactose-fermenting strains, can be distinguished from other intestinal bacteria because to the medium. A reddish-brown slant is produced by deamination of lysine, whereas an alkaline slant is produced by decarboxylation. The generation of hydrogen sulfide is indicated by a black precipitate.

Storage
Keep the container at 15-30 °C and prepared medium at 2-8 °C.

Composition (gr/L)
peptone from meat5
Yeast extract3
Glucose1
L-Lysine10
Sodium Thiosulphate0.04
Ferric Ammonium Citrate0.5
Bromocresol Purple0.02
Agar12.5
Final pH at 25°C6.7 ± 0.2
Dehydrated AppearanceBeige to greenish beige, free flowing, homogeneous.
Reaction of 3.2% Solution at 25°CpH 6.7 ± 0.2
Prepared AppearancePurple, slightly opalescent.
Incubate at 35±2 °C for 18 to 48 hours.
Organism (ATCC)GrowthButtSlant
Escherichia coli (25922)Good/ Very GoodYellowViolet
Salmonella typhimurium (14028)Good/ Very GoodViolet and BlackViolet
Citrobacter freundii (8090)Good/ Very GoodYellow and BlackViolet
Proteus mirabilis (29906)Good/ Very GoodYellow and BlackReddish-Brown

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