<span>The apoplast and symplast are two locales of the plant that fill in as pathways for water and solute transport over both short and long separations. These pathways are spoken to by the bolts in the graph beneath, which indicates three adjoining cells in a leaf or root.</span>
Answer:
The genes are linked, and the arrangement is coupled (one homolog has both dominant alleles; the other homolog has both recessive alleles).
RY
/
ry
Explanation:
R_= colored aleurone
rr= colorless aeurone
Y_= green plant
yy= yellow plant
They do a testcross between a plant of unknown genotype and phenotype and a plant that is homozygous recessive for both traits (yr/yr) the following F1 is obtained:
- 88 Colored, green (RY/ry)
- 92 colorless, yellow (ry/ry)
- 8 colorless, green (rY/ry)
- 12 colored, yellow (Ry/ry)
If the genes assorted independently, all of the possible offspring phenotypes would appear in the same frequency. However, they obtained 2 phenotypes much more abundant that the other two. Since recombination is a rare event during crossing over, when two genes are linked the recombinant gametes are produced less frequently than the parentals.
We can propose that the phenotypes Colored, green (RY) and colorless yellow (ry) are the parental gametes, and the unknown plant has the arrangement RY/ry, with both genes linked.
<span>Neither. You need a nutritionist. Biochemist and food scientists could peripherally be involved by seeing that food is processed in such a way as to preserve the nutritional value of the food. (e.g., seeing that the vitamins are not degraded by processing) and contaminates and bacteria are not introduced.</span>
In complementary base pairing, the G pairs with C, and A pairs with T. Given that this be the rule, the complementary nucleotides for your sequence would be as follows: CGATTAACGTAGGCA.
With regards to proofreading, mutations in cell division occur once in around every 100,000 base pairs. If this happens, the enzyme that pairs the nucleotides to form DNA, called DNA polymerase, detects the error and moves back along the strand, it then cuts the incorrect nucleotide and replaces it with the correct one, fixing the error and continuing with the DNA synthesis.
This process corrects the majority of errors in DNA synthesis, but some errors can still be missed by the DNA polymerase, this is then rectified by a protein complex which binds to the incorrect pairing until anther complex, comes along and cuts that particular section of DNA out, which is then replaced by a new section of correct nucleotides synthesized by the polymerase enzyme, the two sections at either end that were cut is then sealed by ligase, an enzyme which essentially "glues" the DNA stands back together.
My apologies for the long answer, I hope I answered your question and that you understand it well enough.
Active site is the answer, i hope this helps:)
