Differentiate gram-negative enteric bacilli based on the enzymatic ability of an organism to decarboxylate ornithine using Thermo Scientific™ Remel™ Decarboxylase Broth (Moeller) Ornithine
In 1955, Moeller developed the amino acid decarboxylase media to detect production of lysine and ornithine decarboxylase and arginine dihydrolase 1
These media are used to differentiate bacterial groups within the Enterobacteriaceae 2
Ewing, Davis, and Edwards reported Moeller's formulation to be more reliable for differentiating Klebsiella and Enterobacter as compared to other media tested
3 The Moeller method is considered the standard or reference method for determining the decarboxylase reactions of the Enterobacteriaceae
This medium helps differentiate gram negative bacilli by their ability to decarboxylate ornithine
The ornithine decarboxylase test is especially important for separating members of the Klebsiella - Enterobacter - Serratia group and for identifying species of Proteus
Recommended as the standard or reference method for determining decarboxylase reactions of Enterobacteriaceae
Ready to Use: Convenience of prepared media
Ease of Identification: Visual detection of color change This liquid medium is recommended for use in qualitative procedures
This basal medium contains meat peptone and beef extract that provide the nitrogenous nutrients required for bacterial growth
Dextrose acts as a source of energy and fermentable carbohydrate
Bromcresol purple and cresol red are pH indicators
Pyridoxal is an enzyme cofactor which enhances decarboxylase activity 4
Ornithine is an amino acid that is added to the basal medium to detect the production of ornithine decarboxylase
When an organism ferments dextrose, acids are produced which lower the pH, resulting in a color change from purple to yellow
If decarboxylation of ornithine occurs in response to the acid pH, the alkaline end-product putrescine (amine) is formed which results in the medium reverting to its original color (purple)
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