1 / 14

Chapter 25 Metabolic Pathways for Lipids and Amino Acids

Chapter 25 Metabolic Pathways for Lipids and Amino Acids. 25.6 Digestion of Proteins 25.7 Degradation of Amino Acids 25.8 Urea Cycle. Proteins in the Body. Proteins provide: Amino acids for protein synthesis. Nitrogen atoms for nitrogen-containing compounds.

brenna
Download Presentation

Chapter 25 Metabolic Pathways for Lipids and Amino Acids

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 25 Metabolic Pathways for Lipids and Amino Acids 25.6 Digestion of Proteins 25.7 Degradation of Amino Acids 25.8 Urea Cycle

  2. Proteins in the Body Proteins provide: • Amino acids for protein synthesis. • Nitrogen atoms for nitrogen-containing compounds. • Energy when carbohydrate and lipid resources are not available.

  3. Digestion of Proteins

  4. Transamination In transamination: • Amino acids are degraded in the liver. • An amino group is transferred from an amino acid to an -keto acid, usually -ketoglutarate. • The reaction is catalyzed by a transaminase or aminotransferase. • A new amino acid, usually glutamate, and a new -keto acid are formed.

  5. A Transamination Reaction NH3+O Alanine | || aminotransferase CH3—CH—COO- + -OOC—C—CH2—CH2—COO- Alanine -Ketoglutarate O NH3+ || | CH3—C—COO- + -OOC—CH—CH2—CH2—COO- Pyruvate Glutamate

  6. Oxidative Deamination Oxidative deamination: • Removes the amino group as an ammonium ion from glutamate. • Provides -ketoglutarate for transamination. NH3+ Glutamate | dehydrogenase -OOC—CH—CH2—CH2—COO- + NAD+ + H2O Glutamate O || -OOC—C—CH2—CH2—COO- +NH4++ NADH -Ketoglutarate

  7. Urea Cycle The urea cycle: • Detoxifies ammonium ion from amino acid degradation. • Converts ammonium ion to urea in the liver. O || H2N—C—NH2 urea • Provides 25-30 g urea daily for urine formation in the kidneys.

  8. Carbamoyl Phosphate • In the mitochondria, an ammonium ion reacts with CO2 from the citric acid cycle, 2 ATP, and water. NH4++ CO2 + 2ATP + H2O O O |||| H2N—C—O—P—O- + 2ADP + Pi | O- Carbamoyl phosphate

  9. Reaction 1 Transfer of Carbamoyl Group • The carbamoyl group is transferred to ornithine to form citrulline. • Citrulline moves across the mitochondrial membrane into the cytosol.

  10. Reaction 2 Condensation with Aspartate • In the cytosol, citrulline combines with aspartate. • Hydrolysis of ATP to AMP provides energy. • The N in aspartate is part of urea. Cytosol

  11. Reaction 3 Cleavage of Fumarate Fumarate: • Is cleaved from argininosuccinate. • Enters the citric acid cycle.

  12. Reaction 4 Hydrolysis Forms Urea Hydrolysis of arginine: • Forms urea. • Forms ornithine, which returns to the mitochondrion to pick up another carbamoyl group to repeat the urea cycle.

  13. Urea Cycle

  14. Summary of Urea Cycle The urea cycle converts: • Ammonium ion to urea • Aspartate to Fumarate • 3ATP to 2ADP, AMP, 4Pi NH4+ + CO2 + 3ATP + Aspartate + 2H2O Urea + 2ADP + AMP + 4Pi + Fumarate

More Related