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Inoculating two organisms when testing for motility helps to establish a comparison between a motile and a non-motile organism. This allows for a clearer interpretation of results, as the motility of the test organism can be evaluated relative to the control organism. It enhances the reliability of the test by providing a point of reference, making it easier to identify true motility versus other factors that might influence movement. Overall, this approach improves the accuracy of the motility assessment.

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1mo ago

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What is an inoculation?

Inoculating needle is used like a pen. Hold it like you hold a pen. Inoculating loop and a needle is mainly used to pick a single colony(pure) so u need to be gentle on the agar. practice using an inoculating needle on a paper with pen.


Why is important to inoculate o ly a single tube per organism when performing a MRVP test?

Inoculating only a single tube per organism helps to ensure that the results obtained are accurate and specific to that particular organism. It also helps to prevent contamination and confusion that may arise from testing multiple organisms in the same tube. Additionally, it allows for easier interpretation of results and reduces the risk of errors in the testing process.


Microbiology - what is SIM test?

Its a test where a semisolid agar called Sulfide-Indole-Motility medium (or SIM medium) is inoculated with a bacteria to test for hydrogen Sulfide, Indole, and Motility of the organism. The medium is inoculated by a swab and stab type method (rub some bacteria on the surface of the medium and stab a straight hole through the medium using a straight wire with the bacteria on it). Incubate the bacteria for about 24 hours and then begin testing.... If hydrogen sulfide is present, it will react with the sodium thiosulfate in the medium and the indicator, ferric ammonium citrate, to produce ferrous sulfide which falls out of solution as a blackish precipitate. The presence of hydrogen sulfide typically means that the bacteria produces the enzyme cysteine desulfanase which breaks up the cysteine in the medium into, among other components, hydrogen sulfide. The Indole portion of the test is performed by adding Kovac's reagent to the inoculated medium. The Kovac's reagent reacts with the indole(if indole is present) to produce a pinkish-red or redish-purple ring around the top of the test tube. If indole isn't present, there will be no color change. The presence of indole means that the bacteria produces tryptophanase, an enzyme which breaks down tryptophan into smaller components, one of which being indole. The Motility aspect of the test is done by checking the medium for turbidity, or "fuzziness". If the medium has become fairly turbid throughout the medium, then the bacteria is motile. If the medium is clear and the only turbid appearance is in the stab line, then the bacteria is non-motile. Unfortunately, the motility aspect of this test typically gives false negative results. Sometimes the temperature that the bacteria was incubated at wasn't optimum for the species, sometimes the bacteria only have weak motility, sometimes the bacteria's flagella can get damaged which would impair motility, etc... The point is, this test is good if you want to know whether or not the bacteria you're testing produces tryptophanase or cysteine desulfanase. The motility aspect of the test is suspect to question, at least if the test result was negative for motility(a large amount of turbidity in the medium is a definite sign of motility and is hard to refute though).


How is agar media used for motility testing differ from the used for plate cultures?

Agar media used for motility testing typically contains a lower concentration of agar (around 0.3-0.5%) compared to standard plate culture media (usually 1.5-2% agar). This reduced viscosity allows for the movement of motile bacteria away from the inoculation point, creating a diffuse growth pattern. In contrast, plate cultures are designed to provide a solid surface for bacteria to grow in isolated colonies, making it easier to identify and characterize individual species. Therefore, the primary difference lies in the agar concentration and its impact on bacterial movement.


What is the purpose of aliquot?

The purpose of aliquoting is to divide a sample into smaller, equal parts for testing or storage. This process helps ensure accuracy and consistency in experiments by using the same sample for multiple analyses. It also reduces the risk of contamination or degradation of the original sample.

Related Questions

What ingredient or step could be eliminated in the SIM medium were used strictly for testing motility among sulfur reducers?

You could first verify that you have sulfur reducers in your culture by inoculating the SIM medium and checking for the formation of the black FeS precipitate. Then, you could re-make the SIM medium excluding the ferric ammonium citrate (Fe source) and re-inoculate. There will be no black precipitate formation and you could see growth along the stab line and possibly emanating from it.


What is an inoculation?

Inoculating needle is used like a pen. Hold it like you hold a pen. Inoculating loop and a needle is mainly used to pick a single colony(pure) so u need to be gentle on the agar. practice using an inoculating needle on a paper with pen.


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