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Diterbitkan olehRatna Santoso Telah diubah "6 tahun yang lalu
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METABOLISME PROTEIN Prasetyastuti Depart. Of Biochemistry
GADJAH MADA UNIVERSITY
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BIOSYNTHESIS NON-ESSENTIAL AMINO ACID
CATABOLISM N - AMINO ACID CATABOLISM C – AMINO ACID CONVERTION AMINO ACID TO SPECIALIZED PRODUCTS
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Naturally amino acids : 300 Amino acids in protein : 20
INTRODUCTION Naturally amino acids : 300 Amino acids in protein : 20 essential non-essential Arg* Ala His* Asp, Asn Ile Glu, Gln Leu Cys(*) Lys Gly Met Hyp Phe HyL(**) Thr Pro Trp Ser Val Tyr(**) (**) from essential AA
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Grains : poor essential amino acid
Animal : >> essential amino acid Egg = 1 (complete essential amino acids) Kwashiorkor : protein deficient Marasmus : protein & caloric deficients Essential amino acid : number enzyme to synthesize large relative than non-essential amino acids (manufacture “easy” amino acids)
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BIOSINTESIS ASAM AMINO NON ESSENSIAL
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1. Glutamat
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2. Glutamin
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3. Alanin
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4. Aspartat & Asparagin
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5. Serin
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6. Glisin a. dari kolin
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b. dari serin
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7. Prolin
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8. Sistein
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9. Tyrosin
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10. Hidroksi Prolin & Hidroksi Lisin
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KATABOLISME PROTEIN & NITROGEN ASAM AMINO
Kepentimgan Biomedis - dewasa normal : Intake Nitrogen sesuai dg N yg diekskresikan Balance N (-) : cancer, kwasiorkor,marasmus Balance N (+) : masa pertumbuhan, pregnansi Amonia berasal dr N α NH2 asam amino : toxic Dlm jar : nitrogen amide glutamin : non toxic
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Di hepar: glutamin , deaminasi amonia - urea (non toxic)
Fs hepar terganggu(sirosis/hepatitis)- [amonia ]darah meningkat Turn over protein 1-2% /hari dari protein tubuh total Dari % digunakan untuk sintesis protein baru 20-25% membentuk urea
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Degradasi protein dinyatakan dengan t1/2
: waktu yang diperlukan untuk mereduksi kadarnya menjadi 50% dari nilai awalnya. T1/2 protein hepar < 30 menit- > 150 jam Protein dg t1/2 pendek : prolin, glutamin, serin, treonin T ½ 100 jam : aldolase, laktat Dh, sitokrom Kelebihan asam amino tidak disimpan tp di degradasi Kebutuhan protein orang dewasa : g/hari
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Ikatan peptid --- melepas peptid---- as. am. Bebas
protease peptidase Ik. Internal ----- peptida yang lebih pendek endopeptidase Amino peptidase : mengeluarkan as. am. yg berasal dari amino terminal Karboksi peptidase : mengeluarkan as. am. yg berasal dari karbok sil terminal
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Nitrogen diekskresi sebagai amonia, asam urat, urea Ikan (hidup di air) : amonotelik mengekskresi amonia Burung : urikotelik : mengekskresi asam urat Hewan darat, manusia: ureotelik mengekskresi urea [urea] darah , pada penderita peny. Ginjal, suatu akibat bukan penyebab gangguan fs ginjal
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Biosintesis Urea 1. transaminasi 2. deaminasi oksidatif glutamat
3. transport amonia 4. siklus urea
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Transaminasi
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Alanin amino transferase I: & glutamat amino transferase II: mengkatalisis gugus amino ke piruvat membentuk alanin/α- ketoglutarat piruvat α as.amino α- KG α as. Amino I II alanin α as.keto glutamat α as.keto
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Oxidative deamination catalyzed by L-amino acid oxidase (L-α-amino acid:O2 oxidoreductase). The α-imino acid
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The glutamine synthase reaction strongly favors glutamine synthesis
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The glutaminase reaction proceeds essentially irreversibly in the direction of glutamate and NH4+ formation. Note that the amide nitrogen, not the α-amino nitrogen, is removed.
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Reaksi dan intermediet biosintesis urea
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KATABOLISME CARBON SKELETON ASAM AMINO
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Amphibolic intermediates formed from the carbon skeletons of amino acids.
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Catabolism of L-asparagine (top) and of L-glutamine (bottom) to amphibolic intermediates
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KATABOLISME PROLIN
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Katabolisme Histidin & alfa ketoglutarat
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Interconversion of serine and glycine catalyzed by serine hydroxymethyltransferase. (H4 folate,tetrahydrofolate.)
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Reversible cleavage of glycine by the mitochondrial glycine synthase complex. (PLP, pyridoxalphosphate.)
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Reaksi sistin reduktase
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Catabolism of L-cysteine via the cysteine sulfinate pathway (top) and by the 3-mercaptopyruvate pathway (bottom).
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Mixed disulfide of cysteine and homocysteine
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Perubahan treonin menjadi glisin & asetil KoA
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Intermediates in L-hydroxyproline catabolism
Intermediates in L-hydroxyproline catabolism. (α-KA, α-keto acid; α-AA, α-amino acid.) Numerals identify sites of metabolic defects in 1 hyperhydroxyprolinemia and 2 type II hyperprolinemia.
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Intermediet katabolisme tirosin
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Alternative pathways of phenylalanine catabolism in phenylketonuria
Alternative pathways of phenylalanine catabolism in phenylketonuria. The reactions also occur in normal liver tissue but are of minor significance
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Katabolisme lisin
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Katabolisme triptofan
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Pembentukan xanturenat pada defisiensi vitamin B6
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Formation of S-adenosylmethionine
Formation of S-adenosylmethionine. ~CH3 represents the high group transfer potential of “active methionine.”
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Perubahan metionin menjadi propionil KoA
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The analogous first three reactions in the catabolism of leucine, valine, and soleucine. Note also the analogy of reactions 2 and 3 to reactions of the catabolism of fatty acid
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Catabolism of the β-methylcrotonyl- CoA formed from L-leucine
Catabolism of the β-methylcrotonyl- CoA formed from L-leucine. Asterisks indicate carbon atoms derived from CO2.
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Subsequent catabolism of the tiglyl- CoA formed from L-isoleucine.
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Subsequent catabolism of the methacrylyl-CoA formed from L-valine (see Figure 30–19). (α-KA, α-keto acid; α-AA, α-amino acid.)
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PERUBAHAN ASAM AMINO MENJADI PRODUK KHUSUS
Glisin - metabolit & produk farmasi diekskresi sbg konjugat glisin larut air asam glikokolat asam hipurat : dibentuk dr bensoat (bhn mkn aditive) Obat2an, metabolit obat, seny lain dg gugus karboksil - diekskresi dlm urin sbg konjugat glisin PERUBAHAN ASAM AMINO MENJADI PRODUK KHUSUS
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Biosintesis hipurat
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Β-Alanin - metabolit sistein , terdapat dlm KoA
Sebagai - alanil (carnosin) Jar mamalia : membentuk - alanin drv sitosin, karnosin & anserin transaminasi - alanin - malonat semiald Gangguan metab hiperbeta-alaninemia -- [ - alanin, taurin, - NH2 isobutirat ] dlm jaringan & C tubuh meningkat
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- alanil dipeptid Carnosin, & anserin mengaktivasi miosin ATPase, mengkelat Cu & meningkatkan ambilan Cu Biosintesis carnosin dikatalisis oleh carnosin sintetase melalui 2 tahap - pembentukan asil –adenilat - alanin terikat enzim - transfer alanil ke histidin
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-alanil –AMP ATP + - alanin - -alanil –AMP + PPi
-alanil –AMP + histidin karnosin + AMP Hidrolisis carnosin ke -alanin & histidin dikatalisis oleh carnosinase Carnosinuria : def carnosin & turunannya -alanil –AMP
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Homocarnosin Kadarnya dlm otak manusia > [carnosin] Disintesis dlm jar otak oleh carnosin sintetase Dlm serum, tdk menghidrolisis homocarnosin Homocarnosinosis - kelainan genetik - dihub kan dg perkembangan paraplegia spastic & retardasi mental
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- fosforilasi & defosforilasi residu seril, treonil & tirosil mengatur aktivitas enzim tertentu metab KH & L
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* Metionin: S-adenosil metionin
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* Sistein - prekursor bag thioetanolamin CoA & taurin yg berkonjugasi dg asam empedu (as taurokolat)
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Histidin dekarboksilasi histidin ----- histamin Dikatalisis oleh dekarboksilase (antihipertensi -aktivitasnya dihambat oleh α CH3 asam amino -mengkatalisis de-CO2 DOPA,5OH trp,phe,tyr,trp Dlm tubuh sbg: - ergothionein - carnosin -anserin
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Ornithin & arginin - donor formimidin utk sintesis creatin
Melalui ornitin putresin, spermin & spermidin Arginin -prekursor NO yg bekerja sbg neurotransmiter relaxan otot polos vasodilator Sintesis NO dikatalisis oleh NO sintase , tgt NADPH dr arginin + O2 menghasilkan citrulin +NO
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Metabolisme arginin, ornitin & prolin
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Poliamin -spermidin & spermin berfungsi dlm:
- proliferasi & pertumbuhan - faktor pertumbuhan sel mamalia yg dikultur - menstabilkan sel utuh, organela sub seluler & membran Dosis farmakologis poliamin adalah hipotermik & hipotensif
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Triptophan Hidroksilasi trp 5-OH trp, dekarboksilasi --- serotonin
(vasokonstriktor, stimulator kontraksi otot polos Katab serotonin - 5-OH indolasetat Mrpk rks deaminasi oxidative oleh monoamin Oksidase Sel tumor produksi serotonin >>>
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Di ginjal, hepar, Trp --- triptamin -- indolasetat Katabolit utama trp dlm urin normal : - indol 3-asetat - 5-OH indolasetat
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CATABOLISM CARBON AMINO ACID
Glycogenic Ketogenic Glycogenic & Ketogenic Ala Gly His Arg Hyp Met Asp Pro Ser Cys Thr Val Glu Leu Ile Lys Phe Trp Tyr
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