Answer:
A) A single base pair change.
Explanation:
Point mutation is a change in a single base pair of a nucleotide. This comes as a results of mistakes made during DNA replication, induced by ultravoilet radiations, extreme heat and X-rays. There are three types of point or substitution mutations; change, deletion and insertion. The nucleotide bases are either mistakenly inserted, changed or deleted, thus changing the resulting protein or amino acid being coded for.
The process is called denaturation.
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Answer:
C. THE CONVERSION OF FRUCTOSE 1,6-BISPHOSPHATE to fructose- 6- phosphate is not catalyzed by phosphofructokinase -1, the enzyme involved in glycolysis.
Explanation:
This statement is true as the enzyme involved in this step is FRUCTOSE-1,6-BISPHOSPHATASE.
Gluconeogenesis is the coversion of non-carbohydrate molecules (lactic acid, amino acids, glycerol) through the pyruvic acid into glucose in the cells.
This process takes place mainly in the liver and occurs during periods of fasting, starvation, low carbohydrate diets.
The pathway of gluconeogenesis involves eleven steps of enzymatic catalyzed reactions.
In the conversion of fructose 1,6- bisphosphate to fructose-6-phosphate is catalyzed by fructose 1,6-bisphosphatase and not by phosphofructokinase -1 which is involved in glycolysis. This step is a rate-limiting step of the pathway.
The conversion of glucose-6-phospahte to glucose is not catalyzes by hexokinase but glucose -6- phosphatase.
your answer would be c) iron deficiency
