This question is incomplete because the options are not given; here is the complete question:
Which one of the following processes does not occur to excess neurotransmitters in the synapse?
A. Break down or digested into inactive fragments.
B. Collection by scavenger vesicles left over from the neurotransmitter release.
C. Drifting away from the synapse via diffusion.
D. Reuptake within the pre-synaptic neuron.
The answer to this question is B. Collection by scavenger vesicles left over from the neurotransmitter release.
Explanation:
The word synapse refers to the neurological structure that allows the transmission of signals or information between neurons. This process occurs through neurotransmitters, which are the molecules or substances with the messages.
Moreover, in this process, there can be in some cases excess. In this situation, the body reacts to this excess by degrading or breaking down the extra neurotransmitters, eliminating it through diffusion, or even reabsorbing it (reuptake). In this context, all are processes that occur due to excess neurotransmitters except collection by scavenger vesicles because in most cases neurotransmitters are simply absorbed or eliminated but there are not specialized scavenger vesicles that collect them.
Answer:
Homology is a study of similar characters found in two species because of common ancestry.
Explanation:
1.Morphological homology: Species placed under same taxonomic category exhibit similar anatomical structures.
2.Ontogenetic homology: Species belongs to same taxonomic category embryological similarities
3.Molecular homology: Species show molecular similarities such as DNA,RNA and protein
An example of homology is seen in the skeletal strycture of vertebrates. That is arm of a human,leg of a cat,fin of a whale and wing of a bat.
The answer is <span>root hairs</span>
There are a variety of points in the transcriptional chain at which it is possible to disrupt protein synthesis in bacteria. Let’s enumerate just a few:
<span>There’s the initial point where DNA is transcribed into mRNA;<span>there’s the point where mRNA binds to the Ribosome complex;</span>there’s the point where tRNA-aminoacyl pair binds to the Ribosome according to the current codon being “read out” in the mRNA;there’s the point where the aminoacid transported by the tRNA is transferred to the growing protein chain; andthere’s the point where the protein synthesis is determined complete, and the Ribosome disengages and releases the newly-synthesized peptide chain.</span>
In each of these stages (and in some other, more subtle phases) there are possible points of disruption and there are specific disruptors; some of which are indicated in the aboveProtein synthesis inhibitor article.
Note, by the way, that the Ribosomes of Prokaryotes (bacteria) and Eukaryotes (cells with nuclei) aren’t identical, and therefore the inhibitors/disruptors that work for one type of cell may not (and usually don’t) work on the other type. That’s why we can take antibiotics targeted at bacteria with little to no fear of them interfering with our eukaryotic cells’ functions.
(This is a simplified, somewhat hand-wavy response. There is a lot more to say, mainly because biological systems are anything but simple. Nevertheless this should be enough to get you started in the general direction.)
Answer:
Yes, it is
Explanation:
It is polysaccharide type of carbohydrates which are macromolecules.
