Answer:
The first stage of cellular respiration, called glycolysis, takes place in the cytoplasm. In this step, enzymes split a molecule of glucose into two molecules of pyruvate, which releases energy that is transferred to ATP
Explanation:
C cause they won’t be identical to the parent since they are reproducing sexually
Mutations and natural selection cause adaptations. Mutations can cause instant adaptations, while natural selection is the process by which adaptations occurs over a series of generations.
Adaptations are changes or processes of changes by which an organism or species becomes better suited for its environment.
A mutation is an alteration of the DNA sequence. Sometimes such alterations code for the same amino acid sequence as the unaltered DNA strand during protein synthesis. In such a circumstance, the mutation is not detectable. However, other mutations alter the genetic code in such a way that a noticeable change in the trait that is associated with that gene is visible. Sometimes such mutations are advantageous and improve the organism's ability to survive in its environment.
Natural selection is the process by which organisms with more advantageous traits (being camouflaged, being covered with the correct outer covering for the temperatures of that environment, stronger/ larger/ or faster to fight off or run from predators, etc.) are more likely to survive in a particular environment. Likewise, organisms less advantageous traits are more likely to die due to the pressures exerted by the environment (such as temperature, predators, illness, etc.). Therefore, the organisms with the advantageous traits that survive are more likely to survive to find a mate and reproduce. Thus, the advantageous traits are passed down to future generations.
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<u><em>Soruces that might help: </em></u>
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Examples
High respiration rates from mass global population
Deforestation
Answer:
1. The difference between the normal hemoglobin protein DNA sequence and the sickle cell hemoglobin DNA sequence is a base to base shift, in this case adenine (GAG) to thymine (GTG).
2. The difference affects the amino acid sequence of the protein by replacing glutamic acid (Glu) with valine (Val).
Explanation:
In sickle cell anemia, a change in the DNA nucleotide sequence is observed, where adenine is substituted by thymine, whose expression is the change in the amino acid sequence of globine β, incorporating valine instead of glutamic acid. This represents a molecular mutation - point mutation - by subtitution, which corresponds to missense mutation.
<u>Normal hemoglobin protein in a RBC</u>
DNA CTG ACT CCT GAG GAG AAG TCT
Amino acids Leu Thr Pro Glu Glu Lys Ser
<u>Sickle cell hemoglobin protein in a RBC</u>
DNA CTG ACT CCT <em>GTG</em> GAG AAG TCT
Amino acids Leu Thr Pro <em>Val</em> Glu Lys Ser
When GAG is transcribed to mRNA, the CUC codon is obtained, which codes for glutamic acid. Thymine substitution causes the DNA sequence to change to GTG, which is transcribed as CAC, the codon that encodes the amino acid valine. The <u>change from glutamic acid to valine in β-globin causes an altered hemoglobin, giving the abnormal erythrocytes observed in sickle cell disease</u>.
