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Solution: The main components of a universal indicator, in the form of a solution, are thymol blue, methyl red, bromothymol blue, and phenolphthalein. This mixture is important because each component loses or gains protons depending upon the acidity or alkalinity of the solution being tested. It is beneficial to use this type of universal ...
The protonated form of bromothymol blue has its peak absorption at 427 nm thus transmitting yellow light in acidic solutions, while the deprotonated form has its peak absorption at 602 nm thus transmitting blue light in more basic solutions. [3] In contrast, highly acidic bromothymol blue is magenta in color.
Bromothymol blue is the indicator used in the agar, it changes to yellow in case of acid production during fermentation of lactose or changes to deep blue in case of alkalinization. Lactose-positive bacteria build yellow colonies. Bacteria which decarboxylate L-cystine cause an alkaline reaction and build deep blue colonies. [1]
The increase in pH then causes color change in the bromothymol blue indicator, turning it blue. Under neutral conditions the medium remains a green color. The color change to blue is useful because growth on Simmons' citrate agar is often limited and would be hard to observe if it were not for the color change.
The observed spectrum (green) is the sum of the spectra of HA (gold) and of A − (blue), weighted for the concentration of the two species. When a single indicator is used, this method is limited to measurements in the pH range p K a ± 1, but this range can be extended by using mixtures of two or more indicators.
Sucrose fermentation produces acid, which converts the colour of bromothymol blue or thymol blue. Two dyes rather than one make the medium produce an array of yellow, green, or blue so that differentiating among various Vibrio species is possible.
Bacteria are inoculated on a medium containing sodium citrate and a pH indicator such as bromothymol blue. The medium also contains inorganic ammonium salts, which are utilized as sole source of nitrogen. Use of citrate involves the enzyme citrate lyase, which breaks down citrate to oxaloacetate and acetate.
Nessler tubes work on the same principle. There are also electronic automated colorimeters; before these machines are used, they must be calibrated with a cuvette containing the control solution. The concentration of a sample can be calculated from the intensity of light before and after it passes through the sample by using the Beer–Lambert ...
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