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FCH 532 Lecture 23

FCH 532 Lecture 23. Chapter 26: Amino acid metabolism. Alanine aminotransferase Serine dehydratase Glycine cleavage system 4, 5. Serine hydroxymethyl-transferase Threonine dehydrogenase  -amino-  -ketobutyrate lyase. Page 996. Serine dehydratase.

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FCH 532 Lecture 23

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  1. FCH 532 Lecture 23 Chapter 26: Amino acid metabolism

  2. Alanine aminotransferase • Serine dehydratase • Glycine cleavage system 4, 5. Serine hydroxymethyl-transferase • Threonine dehydrogenase • -amino--ketobutyrate lyase. Page 996

  3. Serine dehydratase • PLP-enzyme forms a PLP-amino acid Schiff base (like transamination) catalyzes removal of the amino-acid’s hydrogen. • Substrate loses the -OH group undergoing an  elimination of H2O rather than deamination. • Aminoacrylate, the product of this dehydration reaction, tautomerizes to the imine which hydrolyzes to pyruvate and ammonia.

  4. Figure 26-13 The serine dehydratase reaction. Page 997 1. Formation of Ser-PLP Schiff base, 2. Removal of the -H atom of serine, 3.  elimination of OH-, 4. Hydrolysis of Schiff base, 5. Nonenzymatic tautomerization to the imine, 6. Nonenzymatic hydrolysis to form pyruvate and ammonia.

  5. Alanine aminotransferase • Serine dehydratase • Glycine cleavage system 4, 5. Serine hydroxymethyl-transferase • Threonine dehydrogenase • -amino--ketobutyrate lyase. Page 996

  6. Glycine conversion to pyruvate • Gly is converted to Ser before it is transformed to pyruvate. • Gly to serine is catalyzed by serine hydroxymethyltransferase (another PLP) enzyme that also uses N5, N10-methylene-tetrahydrofolate (N5, N10-methylene-THF) cofactor to proved the C1 unit necessary for this conversion. • The methylene group is derived from another Gly and the remaining parts are released as CO2 and ammonia catalyzed by the glycine cleavage system

  7. Figure 26-14 The reactions catalyzed by the glycine cleavage system, a multienzyme complex. PLP-dependent glycine decarboxylase (P-protein) Lipoamide-containing protein (H-protein) THF requiring enzyme (T-protein) NAD+-dependent, FAD-requiring dihydrolipoyl dehydrogense (L-protein) Page 997

  8. B: O H H H3C-HC--C-COO- N H H C O- 2-O3PO + N CH3 H Serine hydroxymethyltransferase catalyzes PLP-dependent C-C cleavage • Catalyzes the conversion of Thr to Gly and acetaldehyde • Cleaves C-C bond by delocalizing electrons of the resulting carbanion into the conjugated PLP ring:

  9. Asn and Asp are degraded to OAA O H • Asp can be converted to Asp by L-asparaginase: O Asparagine C-CH2-C-C-O- H2N NH3+ H2O L-asparaginase NH4+ O H O Aspartate C-CH2-C-C-O- -O NH3+

  10. Asn and Asp are degraded to OAA O H • Transamination of aspartate to oxaloacetate: O Aspartate C-CH2-C-C-O- -O NH3+ -ketoglutarate aminotransferse glutamate O O Oxaloacetate C-CH2-C-C-O- -O O

  11. Arg, Glu, Gln, His, and Pro are degraded to -KG • Arg, Gln, His, and Pro are converted to Glu which is oxidized to -ketoglutarate by glutamate dehydrogenase. • Gln to Glu is catalyzed by glutaminase • His requires several reactions to get to Glu.

  12. Figure 26-17 Degradation pathways of arginine, glutamate, glutamine, histidine, and proline to -ketoglutarate. Page 1001

  13. Gln to Glu to -KG 2. Glutaminase 1. Glutamate dehydrogense Page 1001

  14. His to Glu His is nonoxidatively deaminated, hydrated, and the imidazole ring is cleaved to form N-formiminoglutamate 8. Histidine ammonia lyase Urocanate hydratase Imidazolone proponase Glutamate formiminotransferase Page 1001

  15. 3. Arginase 4. Ornithine--aminotransferase 5. Glutamate-5-semialdehyde dehydrogenase Proline oxidase Spontaneous Arg and Pro to Glu Page 1001

  16. Ile, Met and Val are degraded to succinyl-CoA • Ile, Met, and Val are degraded to propionyl-CoA • Propioyl-CoA is a product of odd-chain fatty acid degradation that is converted to succinyl-CoA via propionyl-CoA carboxylase (biotin cofactor), methylmalonyl-CoA racemase, and methylmalonyl-CoA mutase (B12 cofactor). • See Ch. 25-2E for review.

  17. Figure 25-18 Conversion of propionyl-CoA to succinyl-CoA. Page 922

  18. Met degradation • Met reacts with ATP to form S-adenosylmethionine (SAM). • SAM’s sulfonium ion is a highly reactive methyl group so this compound is involved in methylation reactions. • Methylation reactions catalyzed by SAM yield S-adenosylhomocysteine and a methylated acceptor molecule. • S-adenosylhomocysteine is hydrolyzed to homocysteine. • Homocysteine may be methylated to regenerate Met, in a B12 requiring reaction with N5-methyl-THF as the methyl donor. • Homocysteine can also combine with Ser to form cystathionine in a PLP catalyzed reaction and -ketobutyrate. • -ketobutyrate is oxidized and CO2 is released to yield propionyl-CoA. • Propionyl-CoA proceeds thorugh to succinyl-CoA.

  19. Methionine adenosyltransferase Methyltransferase Adenosylhomocysteinase Methionine synthase (B12) Cystathionine -synthase (PLP) Cystathionine -synthase (PLP) -ketoacid dehydrogenase Propionyl-CoA carboxylase (biotin) Methylmalonyl-CoA racemase Methylmalonyl-CoA mutase Glycine cleavage system or serine hydroxymethyltransferase N5,N10-methylene-tetrahydrofolate reductase (coenzyme B12 and FAD) Page 1002

  20. Page 987

  21. Figure 25-18 Conversion of propionyl-CoA to succinyl-CoA. Page 922

  22. Ile, Met and Val are degraded to succinyl-CoA • Ile, Met, and Val are degraded to propionyl-CoA • Propioyl-CoA is a product of odd-chain fatty acid degradation that is converted to succinyl-CoA via propionyl-CoA carboxylase (biotin cofactor), methylmalonyl-CoA racemase, and methylmalonyl-CoA mutase (B12 cofactor). • See Ch. 25-2E for review.

  23. Branched chain amino acid degradation • Degradation of Ile, Leu, and Val use common enzymes for the first three steps • Transamination to the corresponding -keto acid • Oxidative decarboxylation to the corresponding acyl-CoA • Dehydrogenation by FAD to form a double bond. First three enzymes • Branched-chain amino acid aminotransferase • Branched-chain keto acid dehydrogenase (BCKDH) • Acyl-CoA dehydrogeanse

  24. Figure 26-21 The degradation of the branched-chain amino acids (A) isoleucine, (B) valine, and (C) leucine. Page 1004

  25. Page 1004

  26. After the three steps, for Ile, the pathway continues similar to fatty acid oxidation (propionyl-CoA carboxylase, methylmalonyl-CoA racemase, methylmalonyl-CoA mutase). • Enoyl-CoA hydratase - double bond hydration • -hydroxyacyl-CoA dehydrogenase- dehydrognation by NAD+ • Acetyl-CoA acetyltransferase - thiolytic cleavage Page 1004

  27. For Valine: • Enoyl-CoA hydratase - double bond hydration • -hydroxy-isobutyryl-CoA hydrolase -hydrolysis of CoA • hydroxyisobutyrate dehydrogenase - second dehydration • Methylmalonate semialdehyde dehydrogenase - oxidative carboxylation Last 3 steps similar to fatty acid oxidation Page 1004

  28. For Leucine: • -methylcronyl-CoA carboxylase-carboxylation reaction (biotin) • -methylglutaconyl-CoA hydratase-hydration reaction • HMG-CoA lyase Acetoacetate can be converted to 2 acetyl-CoA Leucine is a ketogenic amino acid! Page 1004

  29. Lys is also ketogenic • Leu proceeds through a typical branched amino acid breakdown but the final products are acetyl-CoA and acetoacetate. • Most common Lys degradative pathway in liver goes through the formation of the -ketoglutarate-lysine adduct saccharopine. • 7 of 11 reactions are found in other pathways. • Reaction 4: PLP-dependent transamination • Reaction 5: oxidative decarboxylation of an a-keto acid by a multienzyme complex similar to pyruvate dehydragense and a-ketoglutarate dehydrogenase. • Reactions 6,8,9: fatty acyl-CoA oxidation. • Reactions 10 and 11 are standard ketone body formation reactions.

  30. Page 1007

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