Answer:
Reduce or stop the production of energy molecule i.e ATP
Explanation:
Proton is an essential ingredient to carry out light reactions successfully and the proton requirement is fulfilled through the proton gradient formed along the membrane. A chemical that blocks the flow of electrons thereby hindering the flow of proton will adversely affect the electron transport chain reactions thereby causing reduced/no conversion of ADP to ATP.
B is the answer hopefully is accurate
As per the given scenario, the chances of an offspring as a male or female is 50% each.
<h3>What are chromosomes?</h3>
The thread like structure resides inside the nucleus is referred to as chromosomes.
As there are 23 pair of chromosomes present in the organisms, they transfer their equal numbers in the future generation with some variations.
As per the given image, it is clearly shown that there is 50% possibility of being male or female offspring.
Thus, the chances of an offspring of this pairing being born male or female are 50%.
For more details regarding chromosomes, visit:
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Answer:
No, there are multiple ways in which different mutations in the same gene can cause the same phenotype
Explanation:
Several different mechanisms of mutation can lead to the same phenotype. For example, lets say our phenotype is that flies have white eyes, and we know that this occurs in one particular gene that normally makes the eye colour red. (the red gene)
These mutations likely rendered the red gene ineffective (as the eyes are not red). However, this could happen in a variety of ways.
- There could be a single base deletion in the first exon of the mRNA, changing the reading frame of the protein and messing up the entire sequence (a frame shift mutations)
- The entire gene could be deleted
- A single base could be substituted in an important site of the gene, for example, one which translates into a catalytic residue or binding site in the protein
- There could be an inversion at the promoter region of the gene, such that a transcription factor can no longer bind to transcribe the gene.
There are countless other ways in which a mutation could have been caused. Therefore, just because we know the same gene is affected does not mean that we can assume the mutations are identical.