Rapid Review of Amino Acid Metabolism

Amino acid pool

  • Describes all free amino acids in the body
  • Amino acids: body’s primary source of nitrogen

AMINO ACID STRUCTURE

  • Central carbon bound to: -H, -COOH, -NH3, R-group
  • R-group: acidic (-), basic (+), branched, etc.

AMINO ACID POOL: INPUTS AND OUTPUTS

Input

  • Dietary proteins: absorbed as amino acids/peptides in small intestine
    – Pass through hepatic portal vein and immediately enter liver
    – Liver plays central role in fates of free amino acids
  • De novo amino acid synthesis: use C-skeletons & alpha-amino group of other amino acids to synthesize new ones
  • Protein turnover: breakdown of cellular proteins

Output

  • Oxidation: excess amino acids degraded to alpha amino group & C-skeleton
    – Urea cycle: liver rids body of nitrogen waste
    – Energy production: C-skeletons enter glycolysis or citric acid cycle
    – Gluconeogenesis: occurs in liver
    – Storage: amino acids can’t be stored –> C-skeletons stored as glycogen/fats
  • Synthesis of nitrogen-containing molecules
    – Amino acids
    – Neurotransmitters
    – Nucleotides (purines and pyrimidines)
    – Creatine, etc.
  • Protein turnover: synthesis of new proteins

Protein turnover

Cyclic synthesis and breakdown of proteins in the body

  • Produces and consumes free amino acids
  • Protein synthesis: depletes pool of free amino acids
  • Protein breakdown: replenishes pool

ESSENTIAL AMINO ACIDS

Must be obtained from diet

  • “My Tall Vegan Friend Is Watering Kale Leaves” – M, T, V, F, I, W, K, L
  • Glucogenic: Methionine, threonine, valine
  • Glucogenic & ketogenic: Phenylalanine, isoleucine, tryptophan
  • Ketogenic: lysine & leucine

Branched chain amino acids (BCAA)

  • Valine, leucine, isoleucine
  • Immediately shunt from liver to circulation
  • Liver lacks an aminotransferase that muscle, adipose, kidney & brain have

Aminotransferases: family of enzymes involved in amino acid breakdown

NONESSENTIAL AMINO ACIDS

Synthesized endogenously (The rest of the amino acids)

  • Glucogenic: alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, histidine*, proline & serine
  • Glucogenic and ketogenic: tyrosine
  • Histidine is often considered essential because it is essential during the first 5 years of life but later becomes nonessential.

Note that there are many ways to categorize essential/nonessential amino acids

CLINICAL CORRELATION

Conditionally essential amino acids

  • Cannot be synthesized under certain physiologic conditions
  • Infants < 5 years old can’t synthesize: arginine, cysteine, histidine, tyrosine
  • Immunosuppressed patients/postoperative infections: treat w/ arginine & glutamine supplements

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