IMViC

In this test, the organism under consideration is grown in peptone water broth. It contains tryptophan, which under the action of enzyme tryptophanase is converted to an Indole molecule, pyruvate and ammonium. The indole is then extracted from the broth by means of xylene. The broth is sterilized for 15 minutes at around 121°c. To test the broth for indole production, Kovac's reagent . Kovac's reagent consist of amyl alcohol and para-dimethylaminobenzaldehyde and concentrated hydrochloric acid. Kovac's reagent is actually used to determine ability of an organism to separate indole from amino acid tryptophan and it is added after incubation. A positive result is indicated by a pink/red layer forming on top of the liquid.

These tests both use the same broth for bacterial growth. The broth is called MR-VP broth. After growth, the broth is separated into two different tubes, one for the methyl red (MR) test and one for the Voges-Proskauer (VP) test.

The methyl red test detects production of acids formed during metabolism using mixed acid fermentation pathway using pyruvate as a substrate. The pH indicator Methyl Red is added to one tube and a red color appears at pH's lower than 4.2, indicating a positive test (mixed acid fermentation is used). The solution remaining yellow (pH = 6.2 or above) indicates a negative test, meaning the butanediol fermentation is used.

The VP test uses alpha-naphthol and potassium hydroxide to test for the presence of acetylmethylcarbinol (acetoin), an intermediate of the 2,3-butanediol fermentation pathway. After adding both reagents, the tube is shaken vigorously then allowed to sit for 5-10 minutes. A pinkish-red color indicates a positive test, meaning the 2,3-butanediol fermentation pathway is used.

In the 1930's, S.A. Koser conducted experiments that were used to study bacterial catabolism of organic acids.[1] Koser found that citrate metabolism could be an indicator for bacteria found in natural environments. Additionally, citrate could be used to distinguish bacterial coilforms found in soil, and aquatic environments, such as Enterobacteiacea , and coilforms with fecal contamination. It was found that coilforms without fecal contamination grew, while the coilforms with fecal contamination did not grow.

This test uses Simmon's citrate agar to determine the ability of a microorganism to use citrate as its sole carbon and energy source. The agar contains citrate and ammonium ions (nitrogen source) and bromothymol blue (BTB) as a pH indicator.[2] Bromothymol blue was added in order to reduce false positives. The citrate agar is green before inoculation, and turns blue, because of BTB as a positive test indicator, meaning citrate is utilized. The test is also prepared on a slant to maximize bacterial growth for an even better indication of the use of citrate.

These IMViC tests are useful for differentiating the family Enterobacteriaceae, especially when used alongside the Urease test.

The IMViC results of some important species are shown below.[3]