大学生物化学课件氨基酸分解和尿素生成1. The surplus amino acids in animals can be completely oxidized or converted to other storable fuels Amino acids in excess (from diet, protein turnover) can neither be stored, nor excreted, but oxidized to release energy or converted to fatty acids or glucose.Animals also utilize amino acid for energy generation during starvation or in diabetes mellitus (糖尿病糖尿病).Microorganisms can also use amino acids as an energy source when the supply is in excess.Plants almost never use amino acids as an energy source (neither fatty acids).2. Dietary proteins are digested into amino acids in the gastrointestinal tractPepsin cleaves polypeptides into smaller peptides in stomach (N-terminal side of Phe, Trp and Tyr residues).Trypsin (C-terminal side of Arg and Lys) and chymotrypsin (C-terminal side of Phe, Trp and Tyr) further cleave the peptides in small intestine.Carboxypeptidase and aminopeptidase cleave the small peptides into amino acids, which are then absorbed and eventually delivered to liver.Part of the human digestive (gastrointestinal) tract3. The amino groups and the carbon skeletons of amino acids take separate but interconnected pathwaysThe amino group is reused or excreted, as ammonia, urea (via the urea cycle) or uric acid.The carbon skeletons (a a-keto acids) generally find their way to the citric acid cycle for further oxidation or conversion.The degradation of the carbon skeletons may be very complicated but similar to that of fatty acids in some cases.Overview of amino acid catabolism in mammals4. Liver is the major site of amino acid degradation in vertebrates Glutamate, a a-ketoglutarate and pyruvate collects amino groups (in forms of Gln, Glu and Ala) to liver mitochondria for further processing.The excess NH4+ is excreted directly in bony fishes, or as urea in most terrestrial vertebrates, or as uric acid in birds and terrestrial reptiles.The carbons in both urea and uric acid are highly oxidized (with most of the energy extracted).Overview of catabolism of amino groups in vertebrate liver*Excretory form of nitrogenDifferent aminotransferases catalyze the transfer of the amino group from an amino acid to a-a-ketoglutarate to form Glu and a a a-keto acid5. PLP facilitates the transamination and other transformations of amino acidsPyridoxal phosphate (PLP), being derived from vitamin B6 (i.e., pyridoxine) and the prosthetic group for all the aminotransferases, acts as a temporary carrier of the amino groups.PLP is bound covalently to the active sites of aminotransferases via structural determination.PLP accepts and then donates an amino group by forming a Schiff base with the amino-donating amino acid and amino-accepting a a-keto acid (being a a-ketoglutarate in many cases).PLP is bound covalently to the active sites of aminotransferases through Schiff-baselinkage.PLP bound to aspartate aminotransferaseActive site of aspartate aminotransferaseThe reaction occurs via a typical ping-pong mechanism: the first product leaves before the second substrate enters.An interconversion between an aldimine（醛亚胺（醛亚胺) and a ketimine（酮亚胺）（酮亚胺）is proposed to occur via a quinonoid（醌型的）（醌型的） intermediate during the transamination reaction.PLP act in a variety of other reactions at the a a, b b, and g g carbons of amino acids, including racemizations, decarboxylations at the a a carbon, elimination and replacement reactions at the b b and g g carbons.6. Glutamate collects and delivers free ammonia to the liver Free ammonia is produced in tissues (e.g., by the direct deamination of Ser and Thr, deamination of nucleotides) and is toxic to animals, thus need to be transported to the liver by first converting to a nontoxic compound, Gln.Glutamine synthetase catalyzes the two-step addition of ammonia to Glu to yield Gln, with ATP consumed to activate the g g-COOH.This reaction also represents how fixed nitrogen in bacteria enter biomolecules; Gln is the source of amino groups in a variety of biosynthetic reactions.Ammonia transport in the form of glutamine7. Alanine transports ammonia from muscle to the liverPyruvate is an abundant product from muscle glycolysis and can take an amino group (from Glu) to form Ala (alternatively, be reduced to lactate).Alanine, once gets to liver, will transfer its amino group to a a-ketoglutarate or oxaloacetate to reform pyruvate.Pyruvate is reconverted to glucose in liver via the gluconeogenesis pathway, which will be transported back to muscle for energy supply.This is called glucose-alanine cycle, complementing the Cori cycle for liver to continuously provide glucose to vigorously contracting skeletal muscles. Glucose-alanine cycleCori cycle8. Gln and Glu releases NH4+ in liver mitochondriaThe glutaminase in liver mitochondria catalyzes the conversion of Gln to Glu, releasing NH4+ (from the side chain amide of Gln).The glutamate dehydrogenase (a hexameric allosteric enzyme) there catalyzes the oxidative deamination of Glu, releasing NH4+, with released electrons collected by either NAD+ or NADP+.Glutamate dehydrogenase is allosterically activated by ADP and GDP, but inhibited by ATP and GTP, i.e., a lowering of the energy charge accelerates the oxidation of amino acids.Oxidative deaminationGlutamate dehydrogenase9. NH4+ in hepatocytes is converted into urea in most terrestrial vertebrates for excretionHans Krebs and Kurt Henseleit revealed in 1932 (five years before the citric acid cycle was elucidated) that this conversion is accomplished via a cyclic pathway, called the urea cycle.The two nitrogen atoms are derived from Asp and NH4+, with the carbon atom coming from CO2.Ornithine（鸟氨酸鸟氨酸),), acting as the carrier of the carbon and nitrogen atoms, has a role similar to that of oxaloacetate in the citric acid cycle.The urea cycle spans the mitochondria and cytosol.Four phosphoanhydride bonds (equivalent to four ATP molecules) are hydrolyzed for the production of each urea. 2NH4+ + HCO3- + 3ATP4- + H2O Urea + 2ADP3- + 4Pi2- + AMP2- + 5H+ The urea cycle takes place in the mitochondria and cytosol of liver cells10. The conversion of ammonia to urea takes five enzymatic stepsFirst a carbamoyl phosphate (氨基甲酰磷酸氨基甲酰磷酸, an activated carbamoyl group donor) is produced in the mitochondrial matrix using one NH4+, one HCO3-, and two ATP molecules, with the catalysis of carbamoyl phosphate synthetase I (isozyme II exists in the cytosol, acting in pyrimidine synthesis).The urea cycle begins in the mitochondrial matrix when a carbamoyl group is transferred to ornithine to form citrulline (瓜氨酸瓜氨酸), in a reaction catalyzed by ornithine transcarbamoylase.Citrulline then moves into the cytosol.The amino group of one Asp condenses with the ureido group of citrulline to form argininosuccinate, in an ATP-dependent reaction catalyzed by argininosuccinate synthetase, via a citrullyl-AMP intermediate.The argininosuccinate is then cleaved to form Arg and fumarate, in a reaction catalyzed by argininosuccinate lyase.Arg is then cleaved to form urea and regenerate ornithine at the same time, catalyzed by arginase.Fumarate enters mitochondria and is reconverted to Asp: converted to oxaloacetate first via the citric acid cycle (generating one NADH), then take an amino group from Glu via a transamination reaction.Urea cycle and reactions that feed amino groups into the cycle1.ornithine transcarbamoylase 2.argininosuccinate synthetase 3.argininosuccinate lyase4.arginaseThe urea cycle and the citric acid cycle are linked viathe aspartate-arginino-succinate shunt“Krebs bicycle”Links between the urea cycle and citric acid cycle11. The rate of urea synthesis is controlled at two levelsAllosteric regulation of enzyme activity (fast): N-acetylglutamate, synthesized from acetyl-CoA and glutamate by the catalysis of N-acetylglutamate synthase, positively regulates carbamoyl phosphate synthetase I activity.Gene regulation of enzyme amount (slow): syntheses of the five liver enzymes involved in urea synthesis are increased during starvation (when energy has to be obtained from muscle proteins!) or after high protein uptake. Carbamoyl phosphate synthetase I is positively regulated by the enigmatic N-acetylglutamate12. Genetic defects of the urea production enzymes lead to hyperammonemia and brain damageGenetic defects of all five urea cycle enzymes have been revealed.High levels of ammonia lead to mental disorder or even coma and death.Ingenious strategies for coping with the deficiencies have been devised based on a thorough understanding of the underlying biochemistry.Strategy I: diet control, provide the essential amino acids in their a a-keto acid forms.Strategy II: when argininosuccinate lyase is deficient, ingesting a surplus of Arg will help (ammonia will be carried out of the body in the form of argininosuccinate, instead of urea).Strategy III: when carbamoyl phosphate synthetase, ornithine transcarbamoylase, or argininosuccinate synthetase are deficient, the ammonia can be eliminated by ingesting compounds (e.g., benzoate or phenylacetate), which will be excreted after accepting ammonia.Treatment for deficiencies in urea cycle enzymes13. The carbon skeletons of the amino acids are converted (funneled) into seven major metabolic intermediates Intermediates include: acetoacetyl-CoA, acetyl-CoA (which can be converted to fatty acids and ketone bodies, these amino acids are thus ketogenic) Pyruvate, a a-ketoglutarate, succinyl-CoA, fumarate, oxaloacetate (all can be converted to glucose, these amino acids are thus glucogenic)Amino acids having long carbon chains often degrade in ways similar to fatty acid oxidation.Amino acids having short chains often degrade into pyruvate or citric acid intermediates directly.Some of the conversions are very complicated, using a variety of cofactors.The carbon skeletons of amino acids are oxidized via the citric acid cycle*14. Some amino acids are converted to intermediates of citric acid cycle by simple removal of the amino groups Ala pyruvate Asp oxaloacetate Glu a a-ketoglutarate Asn Asp (via a deamination reaction catalyzed by asparaginase) Gln Glu (via a deamination reaction catalyzed by glutaminase)15. Acetyl-CoA is formed from the degradation of many amino acids Trp, Ala, Ser, Gly, Thr and Cys are converted to pyruvate first before being converted to acetyl-CoA.Portions of the carbon skeletons of Trp, Phe, Try, Lys, Leu, and Ile are converted (via acetoacetyl-CoA or directly) to acetyl-CoA.Some of the final steps in the degradation of Leu, Lys, and Trp resemble steps in fatty acid oxidation.Tryptophan degradation is the most complex.Trp, Thr, Ala, Ser, Gly and Cys are converted to pyruvate, before being converted to acetyl-CoATrp, Phe, Tyr, Lys, Leu,and Ile are convertedto acetyl-CoAIntermediates of tryptophandegradation are precursors for synthesizing other biomolecules Arg, His, Glu, Gln and Pro are converted to a a-ketoglutarateMet, Ile, Thr and Val are converted to succinyl-CoAAsp and Asn are converted tooxaloacetate16. Leu, Ile, and Val are degraded via reactions similar to fatty acid oxidationThey are oxidized primarily in muscle, adipose, kidney and brain tissue, not in liver.The same branched-chain aminotransferase and branched-chain a a-keto acid dehydrogenase complex catalyze the first two degradative reactions (transamination and oxidative decarboxylation) of all these three amino acids in extrahepatic tissues.The a a-keto acid dehydrogenase complex has a similar structure and catalyzes essentially the same type of reaction as pyruvate dehydrogenase complex and the a a-ketoglutarate dehydrogenase complex.Catabolic pathways for Val, Ile and LeuAbsent in liver17. A few genetic diseases are related to defects in amino acid catabolism Defects in enzymes of amino acid degradation lead to accumulation of specific intermediates, many of which cause diseases.Deficiency of phenylalanine hydroxylase causes phenylketonuria (PKU, 苯丙酮尿症苯丙酮尿症), one of the earliest human genetic defects of metabolism (first revealed in 1934 in testing mentally retarded patients, whose urine turned olive-green on addition of FeCl3) .The accumulated Phe is converted to phenylpyruvate (via an aminotransferase) which caused the color change of urine.Phe and Tyr are eventually convertedto fumarate and acetoacetyl-CoA(PKU)Phenylalanine that isaccumulated in PKUpatients isconverted to other alternative products.Another disease related to Phe/Tyr catabolism and of historical interest is alkaptonuria (尿黑酸尿黑酸症症).Archibald Garrod discovered that the condition is transmitted as a single recessive inheritable trait and could be traced to the absence of a single enzyme (in early 1900s), thus hinted the direct relation between genes and enzymes. Homogentisate dioxygenase was found to be defective in such patients.Amino acids can be converted to glucose (glucogenic) or ketone bodies (ketogenic)KeywordsTransfer of NH4+-Ala, Glu, GlnUrea cycle-reaction and regulationPathways of amino acid degradation -as groups into TCAWords of the weekhyper vs. hypomacro vs. microglucogenic vs. ketogenicSummaryAmino acid in excess can neither be stored, nor excreted, but oxidized or converted.The amino groups and carbon skeletons of amino acids take separate but interconnected pathways.Liver is the major site of amino acid degradation in vertebrates.PLP facilitates the transamination and other transformations of amino acids.Glutamate collects and delivers free ammonia to the liver.Gln and Glu releases NH4+ in liver mitochondria.NH4+ in hepatocytes is converted to urea through the urea cycle in most terrestrial vertebrates for excretion.The conversion of ammonia to urea takes five enzymatic steps.The rate of urea synthesis is controlled at two levels.The carbon skeletons of the amino acids are first converted (funneled) into seven major metabolic intermediates.Some amino acids are converted to intermediates of citric acid cycle by simple removal of the amino groups.