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AMINO ACID METABOLISM

AMINO ACID METABOLISM

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AMINO ACID METABOLISM

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  1. AMINO ACID METABOLISM Jana Novotná Department of the Medical Chemistry and Biochemistry The 2nd Faculty of Medicine, Charles Univ.

  2. Amino acid structure

  3. The 20 common amino acids of proteins

  4. BODY PROTEINS 250 – 300 g/day Degradation Proteosynthesis NONPROTEIN DERIVATIVES Porphyrins Purines Pyrimidines Neurotransmitters Hormones Komplex lipids Aminosugars Digestion AMINO ACIDS DIETARY PROTEINS GLYCOLYSIS KREBS CYCLE Transamination Conversion (Carbon skeleton) UREA NH3 GLUCOSE ACETYL CoA CO2 KETONBODIES Metabolic relationship of amino acids

  5. Enzymes cleaving the peptide bond Endopeptidases – hydrolyse the peptide bond inside a chain: pepsin, trypsin, chymotrypsin Exopeptidases – split the peptide bond at the end of a protein molecule: aminopeptidase, carboxypeptidases Dipeptidases pepsin (pH 1.5 – 2.5) – peptide bond derived from Tyr, Phe, bonds between Leu and Glu trypsin (pH 7.5 – 8.5) – bonds between Lys a Arg chymotrypsin (pH 7.5 – 8.5) – bonds between Phe a Tyr

  6. Essential amino acids in humans Lysine Methionine Threonine Phenylalanine Tryptophan Arginine* Histidine* Isoleucine Leucine Valine *Required to some degree in young growing period and/or sometimes during illness.

  7. Non-essential and nonessential amino acids in humans Can be formed from a-keto acids by transamination and subsequent reactions. Alanine Asparagine Aspartate Glutamate Glutamine Glycine Proline Serine Cysteine (from Met*) Tyrosine (from Phe*) * Essential amino acids

  8. + NH4+ O O C C COO- COO- R R deamination transamination NH2 NH2 CH CH COO- COO- R R NH3+ oxidative decarboxylation CH2 R + CO2 General reactions of amino acid catabolism

  9. The fate of the amino group during amino acid catabolism

  10. Transamination reaction The first step in the catabolism of most amino acids is removal of a-amino groups by enzymes transaminases or aminotransferases All aminotransferases have the same prostethic group and the same reaction mechanism. The prostethic group is pyridoxal phosphate (PPL), the coenzyme form of pyridoxine (vitamin B6)

  11. Biosynthesis of amino acid: transamination reactions amino acid1+a-keto acid2 amino acid2 +a-keto acid1 Keto-acid + Glutamate Pyridoxal phosphate (PLP)- dependent aminotransferase Amino acid + a-Ketoglutarate

  12. Active metabolic form of vitamin B6

  13. Mechanism of transamination reaction: PPL complex with enzyme accept an amino group to form pyridoxamine phosphate, which can donate its amio group to an a-keto acid.

  14. Allamino acids except threonine, lysine, and proline can be transaminated Transaminases are differ in their specificity for L-amino acids. The enzymes are named for the amino group donor.

  15. Clinicaly important transaminases Alanine-a-ketoglutarate transferase ALT (also called glutamate-pyruvate transaminase – GPT) Aspartate-a-ketoglutarate transferase AST (also called glutamate-oxalacetate transferase – GOT) Important in the diagnosis of heart and liver damage caused by heart attack, drug toxicity, or infection. ALT

  16. Glucose-alanine cycle Alanine plays a special role in transporting aminogroups to liver. Ala is the carrier of ammonia and of the carbon skeleton of pyruvate from muscle to liver. The ammonia is excreted and the pyruvate is used to produce glucose, which is returned to the muscle. According to D. L. Nelson, M. M. Cox :LEHNINGER. PRINCIPLES OF BIOCHEMISTRY Fifth edition

  17. Glutamate releases its amino group as ammonia in the liver The amino groups from many of the a-amino acids are collected in the liver in the form of the amino group of L-glutamate molecules. • Glutamate undergoes oxidative deamination catalyzed by L-glutamate dehydrogenase. • Enzyme is present in mitochondrial matrix. • It is the only enzyme that can use either NAD+ or NADP+ as the acceptor of reducing equivalents. • Combine action of an aminotransferase and glutamate dehydrogenase referred to as transdeamination.

  18. Ammonia transport in the form of glutamine Excess ammonia is added to glutamate to form glutamine. Glutamine synthetase Glutamine enters the liver and NH4+ is liberated in mitochondria by the enzyme glutaminase. Ammonia is remove by urea synthesis.

  19. Relationship between glutamate, glutamine and a-ketoglutarate NH3 NH3 E E a-ketoglutarate glutamate glutamine NH3 NH3 E A. Glutamate dehydrogenase E + + + + H2O glutamate a-ketoglutarate NH3 NADH NAD+ To urea cycle From transamination reactions B. Glutamine synthetase (liver) ADP ATP E + glutamine glutamate NH3 C. Glutaminase (kidney) E + + H2O glutamate NH3 glutamine

  20. A. Oxidative deamination Amino acids + FMN + H2O E L-amino acid oxidase + a-keto acids FMNH2 + NH3 O2 catalse E H2O + O2 FMN H2O2 B. Nonoxidative deamination serine threonine E Serin-threonin dehydratase E pyruvate + NH3 a-ketoglutate + NH3 Oxidative deamination • L-amino acid oxidase produces ammonia and a-keto acid directly, using FMN as cofactor. • The reduced form of flavin must be regeneratedby O2 molecule. • This reaction produces H2O2 molecule which is decompensated by catalase. Is possible only for hydroxy amino acids

  21. Amino acid metabolism and central metabolic pathways • 20 amino acids are converted to 7 products: • pyruvate • acetyl-CoA • acetoacetate • a-ketoglutarate • succynyl-CoA • oxalacetate • fumarate

  22. Glucogenic Amino Acids formed:a-ketoglutarate, pyruvate,oxaloacetate, fumarate, or succinyl-CoA Alanine Serine Cysteine Glycine Threonine Tryptophan Methionine Valine Glutamine Glutamate Proline Histidine Aspartate Asparagine Arginine Phenylalanine Tyrosine Isoleucine

  23. Ketogenic Amino Acids formed acetyl CoA or acetoacetate Lysine Leucine

  24. Both glucogenic and ketogenic amino acids formed:a-ketoglutarate, pyruvate,oxaloacetate, fumarate, or succinyl-CoA in addition to acetyl CoA or acetoacetate Isoleucine Threonine Tryptophan Phenylalanine Tyrosine

  25. Alanine Serine Cysteine Threonine The C3 family: alanine, serine, cysteine and threonine are converted to pyruvate Pyruvate

  26. Asparagine Aspartic acid Oxalacetate The C4 family: aspartate and asparagine are converted into oxalacetate

  27. The C5 family: several amino acids are converted into a-ketoglutarate through glutamate Glutamine a-ketoglutarate Proline Arginine Histidine

  28. Interconversion of amino acids and intermediates of carbohydrate metabolism and Krebs cycle

  29. Metabolism of some selected amino acids

  30. Serine biosynthesis from glycolytic intermediate 3-phosphoglycerate Copy from:http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

  31. Glycine biosynthesis from serine Reaction involves the transfer of the hydroxymethyl group from serineto the cofactor tetrahydrofolate (THF), producing glycine and N5,N10-methylene-THF. Copy from:http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

  32. Glycine oxidation to CO2 Glycine produced from serine or from the diet can also be oxidized by glycine decarboxylase (also referred to as the glycine cleavage complex, GCC) to yield a second equivalent of N5,N10-methylene-tetrahydrofolate as well as ammonia and CO2. Copy from:http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

  33. Cysteine and methionine are metabolically related The sulfur for cysteine synthesis comes from the essential amino acid methionine. SAM Condensation of ATP and methionine yield S-adenosylmethionine (SAM) SAM serves as a precurosor for numerous methyl transfer reactions (e.g. the conversion of norepinephrine to epinenephrine).

  34. Cysteine synthesis * Conversion of homocysteine back to Met. N5-methyl-THF is donor of methyl group. *folate + vit B12 • Conversion of SAM to homocysteine. • Condensation of homocysteine with serine to cystathione. • Cystathione is cleavaged to cysteine. Copy from:http://themedicalbiochemistrypage.org/amino-acid-metabolism.html

  35. Homocystinuria Genetic defects for both the synthase and the lyase. Missing or impaired cystathionine synthase leads to homocystinuria. High concentration of homocysteine and methionine in the urine. Homocysteine is highly reactive molecule. Disease is often associated with mental retardation, multisystemic disorder of connective tissue, muscle, CNS, and cardiovascular system.

  36. Biosynthesis of Tyrosine from Phenylalanine Phenylalanine hydroxylase is a mixed-function oxygenase: one atom of oxygen is incorporated into water and the other into the hydroxyl of tyrosine. The reductant is the tetrahydrofolate-related cofactor tetrahydrobiopterin, which is maintained in the reduced state by the NADH-dependent enzyme dihydropteridine reductase

  37. Phenylketonuria Hyperphenylalaninemia- complete deficiency of phenylalanine hydroxylase (plasma level of Phe raises from normal 0.5 to 2 mg/dL to more than 20 mg/dL). The mental retardation is caused by the accumulation of phenylalanine, which becomes a major donor of amino groups in aminotransferase activity and depletes neural tissue of α-ketoglutarate. Absence of α-ketoglutarate in the brain shuts down the TCA cycle and the associated production of aerobic energy, which is essential to normal brain development. Newborns are routinelly tested for blood concentration of Phe. The diet with low-phenylalanine diet.

  38. Catabolism of branched amino acids valine isoleucine leucine a-ketoglutarate glutamate (transamination) a-ketoisovalerate a-keto-b-methylbutyrate a-ketoisokaproate NAD+ oxidative decarboxylation Dehydrogenase of a-keto acids* CO2 NADH + H+ isovaleryl CoA a-methylbutyryl CoA isobutyryl CoA Dehydrogenation etc., similar to fatty acid b-oxidation acetyl CoA acetyl CoA propionyl CoA + + propionyl CoA acetoacetate

  39. Branched-chain aminoaciduria Disease also called Maple Syrup Urine Disease(MSUD) (because of the characteristic odor of the urine in affected individuals). Deficiency in an enzyme, branched-chain α-keto acid dehydrogenase leads to an accumulation of three branched-chain amino acids and their corresponding branched-chain α-keto acids which are excreted in the urine. There is only one dehydrogenase enzyme for all three amino acids. Mental retardation in these cases is extensive.

  40. Histidine Metabolism: Histamine Formation Histidine decarboxylase Histidine CO2 Histamine • Histamine: • Synthesized in and released by mast cells • Mediator of allergic response: vasodilation, bronchoconstriction

  41. Tryptophan catabolism • Tryptophan has complex catabolic pathway: • the indol ring is ketogenic • the side chain forms the glucogenic products • Kynurenate and xanthurenate are excrete in the urine.

  42. Enzymes which metabolised amino acides containe vitamines as cofactors THIAMINE B1 (thiamine diphosphate) oxidative decarboxylation of a-ketoacids RIBOFLAVIN B2 (flavin mononucleotide FMN, flavin adenine dinucleotide FAD) oxidses ofa-aminoacids NIACIN B3 – nicotinic acid (nikotinamide adenine dinucleotide NAD+ nikotinamide adenine dinukleotide phosphate NADP+) dehydrogenases, reductase PYRIDOXIN B6 (pyridoxalphosphate) transamination reaction and decarboxylation FOLIC ACID (tetrahydropholate) Meny enzymes of amino acid metabolism

  43. Helpful website http://themedicalbiochemistrypage.org/amino-acid-metabolism.html