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Difference between revisions of "Azzone 1961 J Biol Chem"

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{{Publication
{{Publication
|title=Azzone GF, Ernster L (1961) Demonstration of a requirement of high energy phosphate for the aerobic oxidation of succinate in liver mitochondria. J Biol Chem 236:1518-1525.  
|title=Azzone GF, Ernster L (1961) Demonstration of a requirement of high energy phosphate for the aerobic oxidation of succinate in liver mitochondria. J Biol Chem 236:1518-1525.
|info=[http://www.jbc.org/content/236/5/1518.full.pdf+html PMID: 13685481 Open Access]
|info=[http://www.jbc.org/content/236/5/1518.full.pdf+html PMID: 13685481 Open Access]
|authors=Azzone GF, Ernster L
|authors=Azzone GF, Ernster L
|year=1961
|year=1961
|journal=J Biol Chem
|journal=J Biol Chem
|abstract=Preincubation  of  rat  liver  mitochondria  in  a  sucrose-KCl medium  in  the  presence  of  2  to  3 mM  arsenate  and  0.06  mM  Dicumarol  or  0.1  mM  2,4dinitrophenol  for  3  to  4  minutes  results  in  a  marked  depression  of  the  succinoxidase  capacity.  No  depression  is found  when  the  preincubation  is made  in  the  presence of  Amytal,  cysteine  sulfinate,  or  inorganic  phosphate.  Addition  of  adenosine  triphosphate  after  the  preincubation  stimulates succinate  oxidation  several-fold.  The  effect  of  adenosine  triphosphate  is  not  duplicated  by  cysteine  sulfinate,  inorganic phosphate,  ethylenediaminetetraacetate,  adenosine  5’-phosphate, cytidine triphosphate,  uridine  triphosphate,  inosine  triphosphate, or  guanidine  triphosphate.  Similar  results  are  obtained  with mitochondria  pretreated  with  dinitrophenol  and  adenosine  5’-phosphate.
The  data  are  consistent  with  the  conclusion  that  conditions leading  to  a  depletion  of  the  endogenous  content  of  mitochondrial  high  energy  phosphate  result  in  a  reversible  depression  of the  succinoxidase  capacity.
The  concept  is  developed  that  the  aerobic  oxidation  of  succinate  in  intact  liver  mitochondria  requires  an  activation  by high  energy  phosphate.  Some  implications  of  this  concept  regarding  the  enzymic  organization  of  mitochondrial  electron transport  and  oxidative  phosphorylation  are  discussed.
|keywords=succinate oxidation, high energy phosphate, ATP
}}
}}
{{Labeling
{{Labeling
|organism=Rat
|tissues=Hepatocyte; Liver
|preparations=Isolated Mitochondria
|enzymes=Complex II; Succinate Dehydrogenase
|topics=Respiration; OXPHOS; ETS Capacity, Substrate; Glucose; TCA Cycle, ATP; ADP; AMP; PCr
|additional=Made history
|additional=Made history
}}
}}

Revision as of 21:17, 12 June 2012

Publications in the MiPMap
Azzone GF, Ernster L (1961) Demonstration of a requirement of high energy phosphate for the aerobic oxidation of succinate in liver mitochondria. J Biol Chem 236:1518-1525.

» PMID: 13685481 Open Access

Azzone GF, Ernster L (1961) J Biol Chem

Abstract: Preincubation of rat liver mitochondria in a sucrose-KCl medium in the presence of 2 to 3 mM arsenate and 0.06 mM Dicumarol or 0.1 mM 2,4dinitrophenol for 3 to 4 minutes results in a marked depression of the succinoxidase capacity. No depression is found when the preincubation is made in the presence of Amytal, cysteine sulfinate, or inorganic phosphate. Addition of adenosine triphosphate after the preincubation stimulates succinate oxidation several-fold. The effect of adenosine triphosphate is not duplicated by cysteine sulfinate, inorganic phosphate, ethylenediaminetetraacetate, adenosine 5’-phosphate, cytidine triphosphate, uridine triphosphate, inosine triphosphate, or guanidine triphosphate. Similar results are obtained with mitochondria pretreated with dinitrophenol and adenosine 5’-phosphate.

The data are consistent with the conclusion that conditions leading to a depletion of the endogenous content of mitochondrial high energy phosphate result in a reversible depression of the succinoxidase capacity.

The concept is developed that the aerobic oxidation of succinate in intact liver mitochondria requires an activation by high energy phosphate. Some implications of this concept regarding the enzymic organization of mitochondrial electron transport and oxidative phosphorylation are discussed. Keywords: succinate oxidation, high energy phosphate, ATP


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Organism: Rat  Tissue;cell: Hepatocyte; Liver"Hepatocyte; Liver" is not in the list (Heart, Skeletal muscle, Nervous system, Liver, Kidney, Lung;gill, Islet cell;pancreas;thymus, Endothelial;epithelial;mesothelial cell, Blood cells, Fat, ...) of allowed values for the "Tissue and cell" property.  Preparation: Isolated Mitochondria"Isolated Mitochondria" is not in the list (Intact organism, Intact organ, Permeabilized cells, Permeabilized tissue, Homogenate, Isolated mitochondria, SMP, Chloroplasts, Enzyme, Oxidase;biochemical oxidation, ...) of allowed values for the "Preparation" property.  Enzyme: Complex II; Succinate Dehydrogenase"Complex II; Succinate Dehydrogenase" is not in the list (Adenine nucleotide translocase, Complex I, Complex II;succinate dehydrogenase, Complex III, Complex IV;cytochrome c oxidase, Complex V;ATP synthase, Inner mt-membrane transporter, Marker enzyme, Supercomplex, TCA cycle and matrix dehydrogenases, ...) of allowed values for the "Enzyme" property.  Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., Substrate; Glucose; TCA Cycle"Substrate; Glucose; TCA Cycle" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., ATP; ADP; AMP; PCr"ATP; ADP; AMP; PCr" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property. 



Made history