The answer is primary structure. The protein's primary structure pertains to the amino acids' linear sequence in the chain. Usually, the protein's structure is combined together with a covalent bond that is produced while the process of biosynthesis is present.
Many autotrophs make food through the
process of photosynthesis, in which light energy from the sun is changed
to chemical energy that is stored in glucose. All organisms use cellular respiration to break down glucose, release its energy, and make ATP. Autotrophs are also called producers. They produce food not only for themselves but for all other living things as well (which are known as consumers). This is why autotrophs form the basis of food chains.
Yes, autotrophs need to perform cellular respiration.
Answer:
No, Giardia is a protozoan that does not cause eosinophilia.
Explanation:
Eosinophilia refers to an increase in the number of eosinophils in the blood. The eosinophil is one of the white blood cells. When this occurs, the circulating eosinophils might be over 400 or 500.
Many factors might cause. One of them is parasite infections, in which helminths trigger the IgE generation, producing eosinophilia.
In the presence of the parasite antigen, eosinophils have a shorter medullar generation time, and they express a higher number of receptors for IgE and IgG. Their function is to damage the parasite, directly or indirectly, and to decrease the damages caused by their presence.
Giardia, among other protozoans, does not cause eosinophilia. Yet some other protozoans and parasites might induce it.
Pleiotropy refers to the phenomenon of a single gene affecting multiple traits. Phenylketonuria is an example of Pleiotropy.
<h3>What is Pleiotropy?</h3>
The production of diverse effects, especially the production by a single gene of several distinct and seemingly unrelated phenotypic effects known as pleiotropy.
Phenylketonuria, generally known as PKU, is a rare hereditary condition that results in an accumulation of the amino acid phenylalanine in the body. The phenylalanine hydroxylase (PAH) gene is altered in PKU. The enzyme required to degrade phenylalanine is produced in part because of this gene. PKU can be seen to behave as a 'complex' trait.
Only 11.1 percent of MHP patients were homozygous, compared to 58.4 percent of individuals with classic PKU. Individuals with mild PKU had a compound heterozygous rate of 72.5% compared to only 35.1% in patients with classic PKU.
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