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