Histidine is degraded to α-ketoglutarate and is described as a keto-gluco amino acid glucogenic amino acid ketogenic amino acid gluco amino acid TRUE ANSWER : ? YOUR ANSWER : ?
In the normal breakdown of phenylalanine, it is initially degraded to fumarate phenylpuruvate lysine tyrosine TRUE ANSWER : ? YOUR ANSWER : ?
An example of a transamination process is glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate aspartate + hexanoic acid = glutamate + oxaloacetate TRUE ANSWER : ? YOUR ANSWER : ?
A ketogenic amino acid is one which degrades to keto-sugars either acetyl CoA or acetoacetyl CoA multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates TRUE ANSWER : ? YOUR ANSWER : ?
A person with phenylketonuria cannot convert phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones TRUE ANSWER : ? YOUR ANSWER : ?
Lysine is degraded to acetoacetyl CoA and is described as a glucogenic amino acid ketogenic amino acid keto-gluco amino acid none of these TRUE ANSWER : ? YOUR ANSWER : ?
A best described ketogenic amino acid is valine tryptophan lysine none of these TRUE ANSWER : ? YOUR ANSWER : ?
A glucogenic amino acid is one which is degraded to None of these either acetyl CoA or acetoacetyl CoA pyruvate or citric acid cycle intermediates keto-sugars TRUE ANSWER : ? YOUR ANSWER : ?
Which of the following is the best described glucogenic amino acid? Valine None of these Lysine Tryptophan TRUE ANSWER : ? YOUR ANSWER : ?
A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of tyrosine phenylpyruvate isoleucine phenylalanine TRUE ANSWER : ? YOUR ANSWER : ?