Amino Acid Metabolism Lysine is degraded to acetoacetyl CoA and is described as a ketogenic amino acid keto-gluco amino acid none of these glucogenic amino acid ketogenic amino acid keto-gluco amino acid none of these glucogenic amino acid ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism In the normal breakdown of phenylalanine, it is initially degraded to tyrosine lysine phenylpuruvate fumarate tyrosine lysine phenylpuruvate fumarate ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person with phenylketonuria is advised not to consume which of the following products? Glycine containing foods Fat containing food Glucose Aspartame Glycine containing foods Fat containing food Glucose Aspartame ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid keto-gluco amino acid ketogenic and glucogenic amino acid ketogenic amino acid glucogenic amino acid keto-gluco 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 aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 glutamate = hexanoic acid + NH3 aspartate + hexanoic acid = glutamate + oxaloacetate aspartate + α ketoglutarate = glutamate + oxaloacetate glutamate = α-ketoglutarate + NH3 ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of tyrosine phenylalanine isoleucine phenylpyruvate tyrosine phenylalanine isoleucine phenylpyruvate ANSWER DOWNLOAD EXAMIANS APP
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