Answer:
- Glycine
- Ribulose 1,5-bisphosphate
- 3-phosphoglycerate
- Glyceraldehyde 3-phosphate.
- Glucose
- Sucrose
Explanation:
The glycine, among other amino acids, helps to improve chlorophyll production and promotes the process of photosynthesis.
<u>Calvin cycle</u>
During the carbon fixation phase, a CO² molecule combinate with a ribulose 1,5-bisphosphate to form 6-carbonated molecules, which will divide into two 3-phosphoglycerate molecules.
During the reduction phase, NADPH donates its electrons to reduce 3-phosphoglycerate molecules, and turn them into glyceraldehyde 3-phosphate.
During the regeneration phase, a glyceraldehyde 3-phosphate molecule leaves the cycle and goes to the cytosol to form glucose. This step can be done when three CO² enter the cycle and produce six glyceraldehyde 3-phosphate molecules. One of them leaves the cycle to form glucose, while the other five are recycled.
<u>Cytosol: </u>
Once in the cytosol, glyceraldehyde 3-phosphate molecules are used to form glucose and fructose. These two molecules are the monosaccharides that form the sucrose.
Once sucrose is formed, it is transported from the photosynthetic tissues to different parts of the plant by the phloem.
It is due to agitation of the heart. This is the result of a blow in the area directly over the heart.
<span>Are pollution can cause acid rain and the acid rain can hurt lots of living things. </span>
It is expected to see in the offspring of a woman who has DMD and a man who does not have the disease that all of their sons and none of their daughters will have the disease
Option A.
<h3><u>
Explanation:</u></h3>
Duchene muscular dystrophy, also known as DMD is a recessive, x-linked disease. It occurs when there is a mutation in the dystrophin gene. This mutation further affects the muscles of the body leading it to degenerate and ultimately death.
When a woman with DMD and a man without DMD have an offspring, their daughters and the sons will get the mutated gene signature from the mother as she is the carrier. But since the father has normal genes, the daughters will become the carriers and will not be afflicted by it. This is because the normal X chromosome from the father will be passed on to them. The sons on the other hand will have the disease as they will get one of their mother's X chromosome which would be carrying the mutated gene.
Hey There!
Basic units of all forms of life is D, the cell. Cells can be found in any living thing.
Have A Brainly Day :)
