Answer:
c. FADH2
Explanation:
FADH2 is an electron carrier that is generated in the reaction catalyzed by malic enzyme.
Answer:
Sickle cell anemia is an inherited condition in which there aren't enough healthy red blood cells to carry oxygen through an individual's body. The red blood cells of a healthy individual are flexible and round, and they move through blood vessels with no problem, transporting oxygen successfully. However, a person with sickle cell anemia has rigid, sticky red blood shaped like sickles or crescent moons. These cells often get stuck in small blood vessels, which can slow or block blood flow and oxygen delivery to different parts of the body.
The sickle cell anemia trait is found on a recessive allele of the hemoglobin gene, while the regular red blood cell trait is found on the dominant allele. This means that a person must have two copies of the recessive allele (one from their mother and the other from their father) to be born with this condition. People who have one dominant and one recessive allele or both dominant alleles will have healthy red blood cells.
Answer:
The best answer to the question: What is the most likely explanation for this observation, would be, B: RNA processing removes the different segments from the mRNA molecules of each person prior to translation.
Explanation:
In order for cells to work, they depend on one of the four major macromolecules; proteins. These proteins are the messengers that carry out genetic commands from the DNA and they will ensure that all processes, including transcription and translation of new proteins, are carried out correctly. In order to produce proteins, the first step is for the DNA to be transcribed into mRNA, a nucleic acid that carries out the information on the DNA for protein generation. Once transcription stops, mRNA undergoes a series of clipping and reorganizing steps that will ensure that when it is decoded for protein formation, the process will be successful. These control steps are all part of the RNA processing mechanism that enures mRNA will successfully be translated into working proteins.
The reason why from genes of different people, a very similiar protein chain may result, is also explained from the fact that codons (a grouping of three nucleotides present in mRNA), when read by ribosomes, and coupled by tRNA, can pair these codons with similar amino acids. Thus, one codon, or similar codons, may code for a singular amino acid. However, mechanisms in the cells prevent these kinds of anomalies, by repairing the mRNA sequence before it is translated into protein.
