Differential test
Explanation:
A differential test helps to distinguish that which species lack or have the particular biochemical process,the three differential test media are:
1) Blood agar: Blood Agar is an enriched medium which is used to culture those bacteria or microbes that do not grow easily
It is also required to detect and differentiate haemolytic bacteria, especially Streptococcus speciesIt is also a differential media in allowing the detection of hemolysis (destroying the RBC) by cytolytic toxins secreted by some bacteria, such as certain strains of Bacillus, Streptococcus, Enterococcus and Staphylococcus
2) Eosin methylene blue agar (EMB): It is a selective and differential medium used to isolate fecal coliforms
Eosin methylene blue are pH indicator dyes which combine to form a dark purple precipitate at low pH; they also serve to inhibit the growth of most Gram positive organismsSucrose and lactose serve as fermentable carbohydrate sources which encourage the growth of fecal coliforms and provide a means of differentiating them
3) Mannitol Salt Agar (MSA): It is a selective and differential medium
The high concentration of salt (7.5%) selects for members of the genus Staphylococcus, since they can tolerate high saline levelsOrganisms from other genera may grow, but they typically grow very weakly
Three examples of tests which are done on colonies are:
1) Catalase test: Catalase is an enzyme that breaks hydrogen peroxide (H2O2) into H2O and O2
Hydrogen peroxide is often used as a topical disinfectant in wounds, and the bubbling that is seen is due to the evolution of O2 gasA small amount of growth from the culture is placed onto a clean microscope slide Few drops of H2O2 onto the smear is addedA positive result is the rapid evolution of O2 as evidenced by bubblingA negative result is no bubbles or only a few scattered bubbles
2) Indole test: The main requirement for a suitable indole test medium is that it contain
s a sufficient amount of tryptophan
Tryptone broth is commonly usedThe tube of tryptone broth with a small amount of a pure culture is inoculatedIncubation is done at 35°C (+/- 2°C) for 24 to 48 hoursTo test for indole production, 5 drops of Kovács reagent is directly added to the tubeA positive indole test is indicated by the formation of a pink to red color in the reagent layer on top of the medium within seconds of adding the reagent If a culture is indole negative, the reagent layer will remain yellow or be slightly cloudy
3) Urease test: Urease is a constitutively expressed enzyme that hydrolyzes urea to carbon dioxide and ammonia
The urease test identifies those organisms that are capable of hydrolyzing urea to produce ammonia and carbon dioxideUrease test media contain 2% urea and phenol red as a pH indicatorAn increase in pH due to the production of ammonia results in a color change from yellow (pH 6.8) to bright pink (pH 8.2)Urea broth is a highly buffered medium requiring large quantities of ammonia to raise the pH above 8.0 resulting in a color change
