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Download 26.9 Purines ond pyrimidines ,,,,,f sr`-c
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26.9 Purinesand Pyrimidines 805 26.9 Purinesond pyrimidines AIMS: To show the link betweenomino ocids ond nucleicocids in the body, Tonome the product of purine cotobolism ond nome the diseosethot resultsfrom excessive concentrotions of this substonce in the blood. Many of the ring atoms of pyrimidines and purines come from amino acids. Patients with high serum uric acid concentrations may have to take drugs for life to prevent development of hypertension or kidney disease.The drugs act either by preventing the formation of uric acid or by increasingits rate of excretion by the kidneys. Organisms need to synthesizepurine and pyrimidine basesfor incorporation into the nucleic acids RNA and DNA. Moreover, nucleosides such as adenosine are found as part of ATB cyclic AMf; CoA (coenzymeA), NAD+ (nicotinamide adenine dinucleotide), and FAD (flavin adenine dinucleotide). The atoms that constitute both pyrimidine and purine ring systems come from amino acids, ammonia, and carbon dioxide, as shovunfor uracil and adenine in Figure 26.6. The pathway of purine degradation is shorrrmin Figure 26.7. The end product of this pathway is uric acid. Uric acid does not have a carboxyl group, but it is an acidic compound because one of the hydrogens on its five-membered ring readily dissociates. Human beings normally excrete uric acid as a minor waste product in the urine. For reptiles and birds, uric acid is the major form of excreted waste nitrogen. The white part of the deposits that pigeons leave on statues in the park is almost pure uric acid. Some people, almost always male, make too much uric acid or fail to excreteit. Uric acid is quite insoluble, and it also readily forms an insoluble sodium salt, sodium urate. In gout, uric acid or sodium urate exceedsits solubility in plasma and forms needle-likecrystalsthat are depositedin joints, especiallyin the big toe. Gout attacks, which result in swelling and inflammation of the affected joint, are agonizinglypainful. Ralph, the accountant in the Casein Point earlier in this chapter, has gout. Lesch-Nyhan slmdrome, a genetic disease,is caused by the lack of an enzymeneededto catalyze the synthesisof purines. At about 2 or 3 years of /-\ 'NU" / ammonia{ o Ammonia\ ll \ -- C - ^ - 'H C H-N- carbon dioride Asparticacid li ^l /\ ro" n, - C - - , j H (a) Uncil n dioxide .,Carbon GlYcine \-rt \tzc'-a -N1 'c-H I ll sr'-c-*/ \ ,,,,,f "\ \s*,in" /'iH "I Serine/ V Glutamine (amidenitrogen) (b) Adenine Figure26.6 Theatomsthatcomprise pyrimidines andpurinescomefromaminoacids. The figureshowsthe pyrimidineuracil(a) andthe pu.rine adenine(b). 804 CHAPTER 26 Metabolismof NitrogenCompounds o NHr l- "T-Y\ Nz-)r-\ tlt =*^il ) trt\tAil' Adenine Guanine t'o H,o ['-"*,r.. t- o 'T-Y\ I 1."ruH,t J- o + Xanthine oxidase =^^[ Hlpoxanthine "T-Y\ o^il^il Xanthine ^ l*.n,.r" U r- l J oxroase o ilH HN/-\r-Nr lll on..At' ii Figure26.7 Purines aredegraded to uricacid. ,Fo H <-Acidic hydrogen Uric acid age, Lesch-Nyhan victims begin to show an uncontrollable urge to bite themselves.Unless they are forcibly restrained, some Lesch-Nyhan patients will literally bite offtheir flngers and lips. This diseaseis rare; about 60 cases are reported in the medical literature. Victims of the Lesch-Nyhan syndrome often show symptoms of gout. These s),Tnptomsare alleviated by allopurinol, but there is no alleviation of the tendency for self-destruction. Folrow-upro rHECnsrlt Poltr: A painful episode Ralph's painful symptoms indicated gout, and a blood test showed that he had elevated levels of uric acid in his blood. The symptoms of gout may often be relieved by a diet that restricts the intake of foods high in purines, such as shellfish, bacon, beef, and turkey. In severe cases, the drug allopurinoi ls sometimes effective. Allopurinol prevents the synthesis of uric acid by inhiblting xanthine oxidase, the enzyme that xanthine uric :: "o:y"r^tr. acid. A low-purine diet and oH I H il: ^,c._._l ""i3."lliri.-':$:il Ralph back on his feet. I ll HC\n'-b-^/ i\ \ 'r' H AJlopurinol