Download - Biology Oxidation.ppt
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BIOLOGIC OXIDATIONBIOLOGIC OXIDATION
BIOLOGIC OXIDATIONBIOLOGIC OXIDATION
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ENERGI (ATP)
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Source of ATP :1. Oxidative Phosphorylation.2. Glycolysis.
3. Krebs Cycle.
Ox-red reactions O2 accept single electron
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Oxidation-reduction potential
• Oxidation : the removal of electrons• Reduction : the gain of electrons• Redox potential (E0
’) : the free energy change is proportionate to the tendency of reactants to donate or accept electrons
• Redox potential of a system (Eo) is compared with the potential of the hidrogen electrode
• Biologic systems E0’ expressed at PH 7
and electrode potential of H : – 0,42 volts
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System E’O volts
H+/H 2NAD+/ NADHLipoate; ox / redAcetoacetate/ 3 – hydroxybutyratePyruvate/ lactateOxaloacetate/ malateFumarate/ succcinateCytochrome b; Fe3+/Fe2+
Ubiquinone; ox/redCytocrome c1; Fe3+/Fe2+
Cytocrome a; Fe3+/Fe2+
Oxygen/ water
-0.42-0.32-0.29-0.27-0.19-0.17+0.03+0.08+0.10+0.22+0.29+0.82
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Enzymes in ox-red
• Called oxidoreductases (class I), classified into 4 groups:
- oxidases- dehydrogenases- hydroperoxidases- oxygenases
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Oxidases
• Catalyzing the removal hydrogen and using oxygen as a acceptor form water or hydrogen peroxide
• Some oxidases contain copper and others are flavoproteins
• Cytochrome oxidase ( cyt.a.a3 ) :heme protein contain Cuterminal component of respiratory chaincontain two molecules of heme as
prosthetic group and Cu
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• Flavoprotein enzyms contain FMN or FAD as prosthetic groups
• FMN and FAD are formed in body from riboflavin
• They are tightly bound to their apoenzymes but not covalently
• Exampels: L-amino acid oxidase (in kidney), xanthine oxidase (in intestinal, kidney, liver), aldehyde oxidase (in liver) and glucose oxidase (in fungus)
Oxidases
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AH2
A H2O
1/2 O2
OXIDASE
O2
H2O
2
AH2
A
OXIDASE
(Red)
(Ox)
Oxidation of a metabolite catalyzed by an oxidase (A) forming H2O, (B) forming H2O2
A B
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Dehydrogenases
• Can not use oxygen as a hydrogen acceptor• Performing two main functions:
1. transfer hydrogen in a coupled oxidation reduction reaction
specific for their substrates, but utilize common coenzymesuseful in enabling oxidative process to occur in the absence of oxygen
2. components in respiratory chain transfer electron from substrate to
oxygen
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Dehydrogenases link NAD
• Using NAD+ or NADP+ as a coenzyme• These coenzyme are formed in body from
niacin
- freely and reversibly dissociate from their apoenzymes
- NAD linked D-ase: oxidative pathways of metabolism (glycolysis, kreb’s cycle, respiratory chain)
- NADP linked D-ase: characteristically in reductive synthesis (fatty acid synthesis, steroid synthesis and PMP-shunt)
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Dehydrogenases link riboflavin• Using FMN and FAD as a coenzyme
- more tightly bound to their apoenzymes
- most of them are concerned with electron transport in / to resp chain
- NADH D-ase carrier of electrons between NADH and components of higher redox potential
- succinate D-ase, acyl Co-A D-ase, glycerol 3 P D-ase transfer electrons directly from substrate to resp. chain
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Cytochromes as dehydrogenase
• Classified as dehydrogenases, except for cytochrome oxidase
- as carriers of electrons from flavoproteins to cytochrome oxidase in the resp chain
- exampels: cyt b, c1, c, a, a3 (resp chain) and cyt P 450, b5 (endoplasmic reticulum)
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AH2
A
Carrier(Red)
(Ox)
Oxidation of a metabolite catalyzed by coupled dehydrogenases
(Ox)
Carrier-H2
(Red)
B
BH2
(Red)
(Ox)
DEHYDROGENASESPECIFIC FOR A
DEHYDROGENASESPECIFIC FOR B
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Hydroperoxidases
• Using hydrogen peroxide or an organic peroxide as substrate
• Two type : - peroxidase
- catalase• Protecting against harmful peroxides
• Peroxides generate free radicals disrupt membranes and cause cancer and atherosclerosis
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• PeroxidasesReducing peroxides using various electron
acceptors (ascorbate, quinones, cyt c):
H2O2 + AH2 2H2O + A
Founding in milk, leukocytes, platelets, erythrocytes and other tissues involved in eicosanoid metabolism
Glutathione peroxidase, containing selenium destruction of H2O2 and lipid
hydroperoxidases protecting membrane lipids and Hb
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• Catalase
Using hydrogen peroxide as electron donor and electron acceptor:
2 H2O2 2H2O + O2
In addition to possessing peroxidase activity, it is able to use one of H2O2 as a substrate (electron donor) and another of H2O2 as an oxidant (electron acceptor)
Founding in blood, bone marrow, mucous membranes, kidney and liver
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Role of catalase in the destruction of hydrogen peroxie
O2 2H2
OOXIDASE
CATALASE
H2O
2
O2H2O
2
A’H2 A’
AH2 A
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Oxygenases
• Catalyzing the direct transfer and incorporation of oxygen into a substrate
• Divided into two subgroups:
1. Dioxygenases / oxygen transferase
Incorporating both atoms of oxygen into substrate: A + O2 AO2
2. Monooxygenases
Mixed function oxidases and hydroxylases incorporate only 1 atom of oxygen into substrate, the other oxygen is reduced to water
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MONOOXYGENASES
• Need an additional electron donor / cosubstrate ( Z ):A-H + O2 + ZH2 A-OH + H2O + Z
• Cytochromes P450 are monooxygenases (as cosubstrate ) important for detoxification of many drugs and for hydroxylation of steroids
• NADH and NADPH donate reducing equivalents for the reduction of cyt P450
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Cytochrome P 450• Mitochondrial cyt P450 systems in
steroidogenic tissues biosynthesis of steroid hormones from cholesterol
• Mitochondrial cyt P450 systems in kidney metabolism of vitamin D
• Mitochondrial cyt P450 systems in liver biosynthesis of bile acid
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Superoxide free radicals (O2-)
• Generated from transfer of a single electron to O2
• It is formed reduced flavin, are reoxidized univalently by molecular oxygen
• Superoxide dismutase in aerobic organisms removal O2
- , the reaction:
O2- + O2
- + 2H+ H2O2 + O2
• Superoxide can reduce oxidized cyt c:
O2- + cyt c (Fe3+) O2 + cyt c (Fe2+)
• Exposure to an atmosphere of 100% oxygen causes an adaptive increase in superoxide dismutase
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OXIDATIVE OXIDATIVE PHOSPHORYLATIONPHOSPHORYLATION
OXIDATIVE OXIDATIVE PHOSPHORYLATIONPHOSPHORYLATION
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Oxidative phosphorylation
• Oxidative reaction Coupled by phosphorylation to the generation of high energy intermediate (ATP or other high phosphagen)
• Oxidative phosphorylation at resp chain level via NAD D-ases form 3 mol ATP and via flavoprotein D-ases form 2 mol ATP
• Phosphorylations at the substrate level captured smaller energy eg:a) High energy phosphates are captured in kreb’s cycle during the conversion of succinyl Co-A to succinate. And b) in glycolytic reactions on cytoplasmic.
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Respiratory chain• Enzyme complexes in mitochondria
collects and transports reducing equivalents directing them to final reaction with oxygen form water and ATP
• Reducing equivalents flow through from redox potential negative to positive
• There are 4 enzyme complexes:- NADH-Q dehydrogenase / I- Succinate-Q dehydrogenase / II- Cytochromes dehydrogenase / III- Cytochrome oxidase / IV
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Transport of reducing equivalents through the respiratory chain
NAD+
FpH2
NADH Fp
AH2
A
2Fe3
+
2Fe2
+
H2O
1/2O
2
Substrate Cytochromes
Flavoprotein
H+ H+ 2H+ 2H+
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Mitochondrial • Powerhouses of the cell most of energy
captured takes place inside it• Outer membrane permeable to most
metabolites, contain various enzym (acyl Co-A synthetase, glycerolphosphate acyltransferase )
• Inner membrane selectively permeable• Matrix contain phospholipid cardiolipin
together with enzymes of resp chain• Intermembrane space has similar
composition with cytoplasmic and contain adenylyl kinase and creatine
kinase
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Phosphorylatingcomplexes
OUTER MEMBRANE
INNERMEMBRAN
E
MATRIX
Cristae
B
A
OUTERMEMBRANE
INNERMEMBRANE
MATRIXF1 subunitsF0 subunits
Submitochondrial particel
Formed from fragments of the inner membrance
Sonication
B
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Respiratory chain
• Not all substrates are linked to resp chain through NAD-D-ase
• Co-Q (ubiquinone) mobile component, collects reducing equivalents from flavoprotein complexes and passes them on to cytochrome b (the lowest redox pot)
• Cytochrome oxidase has a very high affinity for oxygen resp chain to function at maximum rate until tissue depleted of O2 irreversible reaction
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Glycerol 3-phosphate
Pyruvate
- Ketoglutarate
Cyt aa3Cu
O2
FeS : Iron-sulfur protein
ETF : Electron- transferring
flavoproteinFp : FlavoproteinQ : UbiquinoneCyt : Cytochrome
Proline3-Hydroxyacyl-
CoA3-Hydroxybutyrate
GlutamateMalate
Isocitrate
Acyl-CoASarcosine
Dimethylglycin
Fp(FAD)FeS
Lipoate Fp(FAD) NAD
Fp(FMN)FeS
Succinate
Choline
Fp(FAD)FeS
FeSETF
(FAD)
Fp(FAD)
Q Cyt bFeS
Cyt c1 Cyt c
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Resp chain & oxd phos inhibitors• Inhibitors of resp chain1. Blocking electrons transfer from Fe-S to
co-Q , ie: barbiturates , pierisidin-A , rotenon , carboxine ,succinate D’ase competitive inhibitor: malonate
2. Blocking electrons transfer from cty b to cyt c, ie: dimercaprol , antimycin A
3. Inhibitors of cytochrome oxidase: H2S , CO and CN
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Resp chain & oxd phos inhibitors
• Inhibitors of oxidative phosphorylation, ie:oligomycine, atractyloside
• Un-couplers (dissociate oxidation in resp chain from phosphorylation) respiration to become uncontrolled, ie: dinitrophenol, dinitrochressol, pentachlorophenol, chloro carbonyl cyanide phenilhydrazon (cccp)
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Oligomycin
O2
SuccinateFADFeS
FMN, FeSNADH
BALAntimycin
A
Complex III
Cyt b, FeS, Cyt C1
Cyt c Cyt a Cyt a3
Cu CuQ
Uncouplers
ADP + P1
ADP + P1
ATPATP ADP + P1
Uncouplers
ATP
Piericidin A
Amobarbital
Rotenone
Complex I
Complex IV
H2SCOCN -
Oligomycin
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Mechanism of oxidative phosphorylation
• Mitchell’s chemiosmotic theory:- energy from oxidation in resp chain translocation of H+ (protons) electrochemical potential difference in matrix and intermembrane space drive the mechanism of responsible for the formation of ATP (ATP synthase)
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Mechanism of oxidative phosphorylation
• Complexes I, III and IV of resp chain is a proton pump
• Pi + ADP ATP, by ATP synthase
• ATP synthase is a complex enzyme consist of several protein subunits (F1), which attached to membrane protein complex (F0)
• F1 project into matrix and contain the phosphorylation mechanism
F0 spans the membrane and forms the proton channel
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Exchange metabolites at inner mitochondrial membrane
- Exchange of anions against OH- ions and cations against H+ ions for transport of ionized metabolites
- Freely permeable to uncharged small molecules O2 , H2O , CO2 , NH3 monocarboxylic acids (3 hydroxy butyric, acetoacetic, acetic)
- Long chain fatty acids need carnitine system
- Symport pyruvate - H+
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Exchange metabolites at inner mitochondrial
membrane
• Dicarboxylate and tricarboxylate anions require specific carrier linked to inorganic phosphate (H2PO4
- )
• Exchange ATP / ADP by adenine nucleotide transporter
• Transport of oxaloacetate need transamination process
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Oxidation of extramitochondrial NADH
- NADH cannot penetrate mitochondrial membrane produced continuously in cytosol by 3 phosphoglyceraldehyde D-ase
- Aerobic conditions: not accumulated be oxidized by resp chain
- Transfer of reducing equivalents from cytosol to mitochondrial require substrate pairs, linked by suitable D-ase
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Oxidation of extramitochondrial NADH- The mechanism:
1. Glycerophosphate shuttle only 2 mol ATP are formed per atom oxygen consumed present in brain, muscle, adipose, liver but deficient in heart muscle2. Malate shuttle more universal utility more complex, due to the impermeability of mitochondrial membrane to oxaloacetate
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INNERMEMBRANE
FAD
FDH2
Respiratory Chain
GLYCEROL-3-PHOSPHATE
DEHYDROGENASE(MITHOCONDRIAL)
GLYCEROL-3-PHOSPHATE
DEHYDROGENASE(CYTOSOLIC)
NAD+
NADH + H+
Dehydroxyacetone
phosphate
Dehydroxyacetone
phosphate
Glycerol 3-phosphate
Glycerol 3-phosphate
CYTOSOLMITOCHONDRION
OUTER MEMBRAN
E
Glycerophosphate shuttle for transfer of reducing equivalents from the cytosol into the mitochondrion
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MALATE DEHYDROGENASE
MALATE DEHYDROGENASE
TRANSAMINASE
TRANSAMINASE
INNER MAMBRA
NE MITHOCONDRION
Malate
Oxaloacetate
Glutamate
-KG
Asp
NAD+
NADH+H+
H+H+
Glutamate
-KG
Asp
Malate
Oxaloacetate
NAD+
NADH
+H+
CYTOSOL
1
2
Malate shuttle for transfer of reducing equivalents from the cytosol into the mitocondrion. 1. Ketoglutarate transporter, 2. glutamate-aspartate transporter (note the proton symport with glutamate)
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Creatine phosphate shuttle• Facilitating transport of high energy
phosphat from mitochondria in active tissues
• Isoenzyme of creatine kinase (CKM), in intermembrane space catalyzing transfer ~ P (ATP) to creatine:~ P(ATP) + creatine creatine-P , transported into cytosol via protein pores available for generation of
extramitochondrial ATP
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CREATINEKINASE
NH
H2N
C
NH3C
COO-
NH
H
N
C
N
COO-
P
Creatinephosphate Creatine
ΔGO’ = 12.6 kJ/mol
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Clinical aspects
• Fatal infantile mitochondrial myopathy and renal dysfunction due to severe diminution / absence of most oxidoreductase
• MELAS (mitochondrial encephalopathy, lactic acidosis and stroke) due to complex I or complex IV deficiency mutation in mt DNA