Oxidase test

From Wikipedia, the free encyclopedia
Jump to: navigation, search

The oxidase test is a test used in microbiology to determine if a bacterium produces certain cytochrome c oxidases.[1] It uses disks impregnated with a reagent such as N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD) or N,N-dimethyl-p-phenylenediamine (DMPD), which is also a redox indicator. The reagent is a dark-blue to maroon color when oxidized, and colorless when reduced. Oxidase-positive bacteria possess cytochrome oxidase or indophenol oxidase (an iron-containing hemoprotein).[2] These both catalyze the transport of electrons from donor compounds (NADH) to electron acceptors (usually oxygen). The test reagent, TMPD dihydrochloride acts as an artificial electron donor for the enzyme oxidase. The oxidized reagent forms the colored compound indophenol blue. The cytochrome system is usually only present in aerobic organisms that are capable of using oxygen as the terminal electron acceptor. The end-product of this metabolism is either water or hydrogen peroxide (broken down by catalase).[3]

Classification[edit]

Strains may be either oxidase-positive (OX+) or oxidase-negative (OX-).

OX+[edit]

OX+ normally means the bacterium contains cytochrome c oxidase and can therefore use oxygen for energy production with an electron transfer chain.

The Pseudomonadaceae are typically OX+[citation needed]

Another example is the preliminary identification of Neisseria versus Moraxella genera. Neisseria is oxidase-positive, Gram-negative diplococci and Moraxella is also oxidase-positive.

Many Gram-negative, spiral curved rods are also oxidase-positive, which includes Helicobacter pylori, Vibrio cholerae, and Campylobacter jejuni.

Also Legionella pneumophila is oxidase-positive.

OX-[edit]

OX- normally means the bacterium does not contain cytochrome c oxidase and, therefore, either cannot use oxygen for energy production with an electron transfer chain or employs a different cytochrome for transferring electrons to oxygen.

Enterobacteriaceae are typically OX-.[4]

Procedures[edit]

  1. Wet each disk with about four inoculating loops of deionized water.
  2. Use a loop to aseptically transfer a large mass of pure bacteria to the disk.
  3. Observe the disk for up to three minutes. If the area of inoculation turns dark-blue to maroon to almost black, then the result is positive. If a color change does not occur within three minutes, the result is negative.

In alternative manner, live bacteria cultivated on trypticase soy agar plates may be prepared using sterile technique with a single-line streak inoculation. The inoculated plates are incubated at 37°C for 24–48 hours to establish colonies. Fresh bacterial preparations should be used. After colonies have grown on the medium, 2-3 drops of the reagent DMPD are added to the surface of each organism to be tested.

  • A positive test (OX+) will result in a color change violet to purple, within 10–30 seconds.
  • A negative test (OX-) will result in a light-pink or absence of coloration.

References[edit]

  1. ^ "Oxidase Test and Modified Oxidase Test". Retrieved 2008-11-07. 
  2. ^ . Isenberg HD, editor. Clinical Microbiology Procedures Handbook. American Society for Microbiology; 2004. p. 3.3.2-3.3.2.13
  3. ^ MacFaddin JF, editor. Biochemical Tests for Identification of Medical Bacteria. 3rd ed. Philadelphia:Lippincott Williams and Wilkins; 2000. p. 363-7
  4. ^ Farmer JJ, Fanning GR, Huntley-Carter GP, et al. (May 1981). "Kluyvera, a new (redefined) genus in the family Enterobacteriaceae: identification of Kluyvera ascorbata sp. nov. and Kluyvera cryocrescens sp. nov. in clinical specimens". J. Clin. Microbiol. 13 (5): 919–33. PMC 273917. PMID 7240403. 

External links[edit]