Answer:
is the process of making the number of each kind of atom on the reactant side and product side equal
Given what we know, we can confirm that the fact that Mannitol salt agar can determine which species of Staphylococcus is present makes it an example of a selective differential medium.
<h3>What is a selective differential medium?</h3>
- This type of medium is very similar to that of a differential medium in that it also allows more than one type of microbe to grow.
- It also allows the user to continue to distinguish between the microbe colonies based on biochemical differences.
- However, in contrast to that of a basic differential medium, this differential medium is also selective in that it controls which type of microbe specifically is allowed to grow.
Therefore, we can confirm that since Mannitol salt agar can determine which species of Staphylococcus is present, it can be considered a differential selective medium because it allows multiple microbes to grow while controlling which types are allowed to grow.
To learn more about microbes visit:
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<span>Archaeas and Bacterias are both Prokaryotes. Both used to be classified in Monera kingdom, but later genetists found that they have actually very different genes, despite they both have a similar metabolism. So they think they have a totally different evolutionary origin and they decided to classify them in 2 different domains. The other domain, Eukarya, includes every other organism (all the ones who are not Prokaryots), which are: plants, animals, fungi and protists.</span>
Answer:
Gelation is the analytical signal used for the qualitative and quantitative detection of lipopolysaccharides. Bacterial endotoxins are lipopolysaccharides (LPS) located exclusively on the outer membrane of gram-negative bacteria; Their presence in injectable pharmaceutical products may be associated with problems during production, there are established endotoxin limits for this type of product. When the reagent is faced with solutions containing endotoxins, it produces gelling.
Explanation:
The LAL (Limulus Amebocyte Lysate) test is used to detect and quantify endotoxins associated with gram-negative bacteria. It is based on the amebocytes from the blood of the Limulus polifemus crab gel in the presence of minimal concentrations of endotoxin (ng / ml of blood ). It is positive in 60% of bacilli due to gram-negative enteric bacilli. The presence of endotoxins is determined by the formation of an insoluble gel or clot. The reaction requires the presence of divalent cations. The speed of the reaction depends on the endotoxin concentration, the pH and the temperature. The lysate contains a cascade enzyme system that is progressively activated in the presence of endotoxins. As a final result, the coagulable protein (coagulogen) is transformed into a gel (coagulin), which is the basis of the tube gel method.
Answer:
See explanation
Explanation:
In a situation whereby a plant is in an environment where light is not totally absent, the plant continues to photosynthesize at a slower rate.
Recall that photosynthesis is the process by which green plants make their own food in the presence of sunlight, chlorophyll, carbon dioxide and water.
In a low light, plants are forced to stretch towards the low light source. This is known as etiolation of plants.
