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25'9 Fates of the Carbon Atoms from

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... are intermediates or converted to intermediates for use in the citric acid cycle. ... from glycolysis or the citric acid cycle produces nonessential amino acids. ... – PowerPoint PPT presentation

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Title: 25'9 Fates of the Carbon Atoms from


1
Chapter 25 Metabolic Pathways for Lipids and
Amino Acids
  • 25.9 Fates of the Carbon Atoms from
  • Amino Acids
  • 25.10 Synthesis of Amino Acids

2
Carbon Atoms from Amino Acids
  • Carbon skeletons of amino acids are
    intermediates or converted to intermediates for
    use in the citric acid cycle.
  • Three-carbon skeletons
  • Alanine, serine, and cysteine Pyruvate
  • Four-carbon skeletons
  • Aspartate, asparagine Oxaloacetate
  • Five-carbon skeletons
  • Glutamine, glutamate, proline,
  • arginine, histidine Glutamate

3
Three carbon skeletons
4
Four carbon skeletons
5
Five-carbon skeletons
6
Glucogenic and Ketogenic Amino Acids
  • Amino acids are classified as
  • Glucogenic if they generate pyruvate or
    oxaloacete, which can be used to synthesize
    glucose.
  • Ketogenic if they generate acetoacetyl CoA or
    acetyl CoA, which can form ketone bodies or fatty
    acids.

7
Ketogenic Glucogenic
8
Sources of Amino Acids
  • Essential amino acids must be obtained in the
    diet.
  • Nonessential amino acids are synthesized in the
    body.

9
Synthesis of Amino Acids
  • In humans, transamination of compounds from
    glycolysis or the citric acid cycle produces
    nonessential amino acids.

10
Synthesis of Glutamine
  • Glutamine is synthesized by adding another amino
    group to glutamate.
  • NH3 Glutamine

  • synthetase
  • -OOCCHCH2CH2COO- NH3 ATP
  • Glutamate
  • NH3 O
  • -OOCCHCH2CH2CNH2 ADP Pi
  • Glutamine

11
Phenylketonurea (PKU)
  • In phenylketonurea (PKU)
  • The gene that converts phenylalanine to tyrosine
    is defective.
  • Phenylalanine forms phenylpyruvate
    (transamination), which goes to phenylacetate
    (decarboxylation).
  • High levels of phenylacetate cause severe mental
    retardation.
  • A diet low in phenylalanine and high in tyrosine
    is recommended.

12
Phenylketonurea (PKU)
13
Overview of Metabolism
  • In metabolism
  • Catabolic pathways degrade large molecules.
  • Anabolic pathway synthesize molecules.
  • Branch points determine which compounds are
    degraded to acetyl CoA to meet energy needs or
    converted to glycogen for storage.

14
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