Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to lysine phenylpuruvate tyrosine fumarate lysine phenylpuruvate tyrosine fumarate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a glucogenic amino acid none of these ketogenic amino acid keto-gluco amino acid glucogenic amino acid none of these ketogenic amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Transaminase enzymes are present in liver pancreas intestine none of these liver pancreas intestine none of these ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate glutamate = hexanoic acid + NH3 aspartate + α ketoglutarate = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria will convert phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine phenylalanine to phenylpyruvate phenylpyruvate to phenylalanine phenylalanine to isoleucine tyrosine to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Glucose Aspartame Glycine containing foods Fat containing food Glucose Aspartame Glycine containing foods Fat containing food ANSWER DOWNLOAD EXAMIANS APP
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