Answer:
Please find what occurs in the single nucleotide-pair substitution below
Explanation:
Single nucleotide-pair substitution is a type of point mutation as stated in this question. Point mutation is when one nucleotide base (single) is affected in the sequence. In this single nucleotide-pair substitution, ONE nucleotide base is substituted by another base.
For example, in a DNA sequence that reads: TAA GTC GGG, a mutated sequence affected by single nucleotide-pair substitution will read as follows: TAA GTC TGG. Note that in the last codon (GGG), a single nucleotide G has been replaced by another nucleotide T. Therefore, single nucleotide-pair substitution is said to have occur.
A class of broad-spectrum bacteriostatic antibiotics that are produced by soil organisms and inhibit protein synthesis by binding to bacterial ribosomes is known as Chloramphenicol.
Chloramphenicol is a drug used to treat superficial eye infections such as bacterial conjunctivitis and otitis externa. It was also used to treat typhoid fever and cholera. Chloramphenicol is an antibiotic and belongs to the class of antibacterial agents that inhibit protein synthesis.
Chloramphenicol is used to treat serious infections in different parts of the body. It may also be given with other antibiotics. However, Chlorum phenicole should not be used to prevent colds, flu, other viral infections, sore throats, other mild infections, or infections.
Learn more about Chloramphenicol here: brainly.com/question/9670046
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I believe that is is replication, but I'm not 100%
Answer:
The cell membrane is semi-permeable. It allows some molecules to enter easily inside the cell whereas some molecules are blocked from entering the cell.
Small, polar molecules and hydrophobic molecules enter easily through the cell membrane. But large molecules and ions cannot easily move inside the cell membrane.
A hydrophilic substance like the substance L mentioned in the question enters the cell membrane through the help of carrier proteins. The substance attached to the large protein might enter through active or passive diffusion but it can only enter the cell by attaching to carrier proteins.
Answer: If this population were in equilibrium and if the sickle-cell allele is recessive, the proportion of the population susceptible to sickle-cell anemia under typical conditions should be 0.20
Explanation: Hardy-Weinberg law provides an equation to relate genotype frequencies and allele frequencies in a randomly mating population. The equation is;
p² + 2pq + q² = 1
For 2 alleles such as A and a, where
p² = homozygous dominant
q² = homozygous recessive and
2pq = heterozygous
From the question, it is said that the sickle-cell allele (SS) constitutes 20% (that is, 20/100) of the hemoglobin alleles in the human gene pool and it is also said to be the homozygous recessive allele.
Therefore, q² = 20/100 = 0.20
