Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of phenylpyruvate isoleucine tyrosine phenylalanine phenylpyruvate isoleucine tyrosine phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria cannot convert phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones phenylalanine to isoleucine phenylalanine to lysine phenylalanine to tyrosine phenol into ketones ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of a transamination process is 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 glutamate = α-ketoglutarate + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a none of these ketogenic amino acid glucogenic amino acid keto-gluco amino acid none of these ketogenic amino acid glucogenic amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a ketogenic amino acid glucogenic amino acid gluco amino acid keto-gluco amino acid ketogenic amino acid glucogenic amino acid gluco amino acid keto-gluco amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Fat containing food Aspartame Glucose Glycine containing foods Fat containing food Aspartame Glucose Glycine containing foods ANSWER DOWNLOAD EXAMIANS APP
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