Sequential cleavage from the non-reducing terminals of glucose molecules is required for both glycogen degradation and polysaccharides hydrolysis.
Why non-reducing end is selected for digestion?
A polysaccharide's non-reducing end is the one where an anomeric carbon participates in the glycosidic connection. The elimination of carbohydrate remnants one at a time out from the non-reducing terminal occurs during glycogenolysis and polysaccharides hydrolysis.
- For example, several enzymes are involved in glycogenolysis in the liver and muscle.
- An example of such an enzyme is glycogen phosphorylase, which catalyzes the successive dissociation of the alpha 1->4 glycosidic bond that connects two glucose molecules at a non-reducing terminal of glycogen. The last glucose residue is eliminated as alpha-D-glucose 1-phosphate.
That is why non-reducing end of glucose is chosen for digestion or breakdown of the carbohydrate polymer.
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The relative time of divergence from a common ancestor can be estimated by comparing the nucleotide/protein sequence.
<h3>What is sequence homo-logy?</h3>
In molecular biology, sequence homo-logy means the degree of similarity between sequences due to a common ancestor.
A sequence is a given fragment of a single DNA strand where nucleotides are arranged in a specific linear order.
Divergence or separation between lineages is directly proportional to the level of sequence homo-logy.
In conclusion, the relative time of divergence from a common ancestor can be estimated by comparing the nucleotide/protein sequence.
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Answer:
The DNA strand breaks apart (splits in half, if you will) in order for the translation process to begin.
Nuclear envelope is the answer
<span>They have various isomer structures often either open chain or cyclic isomers that readily interchange structures. </span>
