Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of tyrosine phenylpyruvate isoleucine phenylalanine tyrosine phenylpyruvate isoleucine phenylalanine ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Histidine is degraded to α-ketoglutarate and is described as a ketogenic amino acid gluco amino acid glucogenic amino acid keto-gluco amino acid ketogenic amino acid gluco amino acid glucogenic 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? Glucose Fat containing food Glycine containing foods Aspartame Glucose Fat containing food Glycine containing foods Aspartame ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a glucogenic amino acid none of these keto-gluco amino acid ketogenic amino acid glucogenic amino acid none of these keto-gluco amino acid ketogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to phenylpuruvate lysine tyrosine fumarate phenylpuruvate lysine tyrosine fumarate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism An example of the oxidative deamination is 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 glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + Oxaloacetate ANSWER DOWNLOAD EXAMIANS APP
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