Amino Acid Metabolism A ketogenic amino acid is one which degrades to pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA either acetyl CoA or acetoacetyl CoA keto-sugars pyruvate or citric acid cycle intermediates multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA either acetyl CoA or acetoacetyl CoA keto-sugars ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism A glucogenic amino acid is one which is degraded to keto-sugars either acetyl CoA or acetoacetyl CoA None of these pyruvate or citric acid cycle intermediates keto-sugars either acetyl CoA or acetoacetyl CoA None of these pyruvate or citric acid cycle intermediates ANSWER DOWNLOAD EXAMIANS APP
Amino Acid Metabolism The most toxic compounds is tyrosine phenylalanine lysine phenylpyruvate tyrosine phenylalanine lysine phenylpyruvate 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 An example of the oxidative deamination 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 tyrosine to phenylalanine phenylalanine to isoleucine phenylpyruvate to phenylalanine phenylalanine to phenylpyruvate tyrosine to phenylalanine phenylalanine to isoleucine phenylpyruvate to phenylalanine ANSWER DOWNLOAD EXAMIANS APP
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