Answer:
D
Explanation:
A robin building a nest is not learned or taught like the others. It is just instinctive for robins to build nests.
Answer:
The fate of glucose-6-phosphate,glycolytic intermediates and pentose phosphate pathways are described below
Explanation:
Fate of Glucose -6-phosphate
Glucose-6-phosphate undergo dephosphorylation to form glucose when there is an increase demand of glucose in the body.
Glucose-6-phosphate enters into pentose phosphate pathway to synthesize ribose-5-phosphate which is used during denovo pathway of purine nucleotide biosynthesis.
Fate of glycolytic intermediates
Glyceraldehyde-3-phosphate is an important intermediate of glycolysis.The glyceraldehyde-3-phosphate act as a precursor during lipogenesis that deals with the biosynthesis of triacylglycerol.
Fate of pentose phosphate pathway intermediates
Ribose-5-phosphate and NADPH are the important intermediates of pentone phosphate pathway.
Ribose-5-phosphate act as a substrate molecule during the denovo biosynthesis pathway of purine nucleotides.
NADPH act as a reducing agent during fatty acid biosynthesis process.
Answer:
an energy source during cellular respiration
Answer:
Lactase
Explanation:
Lactaid is a medication that contains the milk protein digesting enzyme Lactase. It is an enzyme supplement for those people who have trouble in digesting milk and other dairy products. Such condition occurs in Crohn's disease and termed as lactose intolerance. Lactase specifically acts on the lactose containing substrates and digests them by enzymatic activity. So people with lactose intolerance can be able to take dairy products with the help of Lactaid.
Answer:
Human males much more likely than human females to inherit the recessive condition hemophilia because it follows X-linked recessive pattern.
Explanation:
Actually hemophilia is an X-linked recessive disorder i-e the defective genes are located on the X chromosome (sex chromosome) and are transmitted through it. As males have only one X chromosome (inherited from mother), one altered copy of the gene in every cell cause this disease.On the other hand females have 2 X chromosomes thus this disease is rare in females.
