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Difference between revisions of "Slater 1953 Biochem J"

From Bioblast
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|journal=Biochem J
|journal=Biochem J
|abstract=See Free Text
|abstract=See Free Text
|keywords=tonicity of medium, oxidative phosphorylation, α-ketoglutaric oxidase
}}
}}
{{Labeling
{{Labeling
|organism=Other Mammal
|tissues=Cardiac muscle
|preparations=Isolated Mitochondria
|topics=Respiration; OXPHOS; ETS Capacity
|additional=Made history
|additional=Made history
}}
}}

Revision as of 12:42, 10 June 2012

Publications in the MiPMap
Slater EC, Cleland KW (1953) The effect of tonicity of the medium on the respiratory and phosphorylative activity of heart-muscle sarcosomes. Biochem J 53: 557-567.

» PMID: 13032109; Open Access

Slater EC, Cleland KW (1953) Biochem J

Abstract: See Free Text Keywords: tonicity of medium, oxidative phosphorylation, α-ketoglutaric oxidase


Labels:


Organism: Other Mammal"Other Mammal" is not in the list (Human, Pig, Mouse, Rat, Guinea pig, Bovines, Horse, Dog, Rabbit, Cat, ...) of allowed values for the "Mammal and model" property.  Tissue;cell: Cardiac muscle"Cardiac muscle" 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. 

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. 



Made history 

SUMMARY

  1. The α-ketoglutaric oxidase system of heartmuscle sarcosomes has a pH optimum at 74. The yield of oxidative phosphorylation (P:O ratio) is unchanged between pH 6*2 and 7.7.
  2. Hypertonic sucrose (0.88M) is an inhibitor of the succinic oxidase system in the Keilin & Hartree preparation. Its major effect appears to be on the accessibility of both the endogenous and added cytochrome c to the other components of the system.
  3. Maximum activity of the α-ketoglutaric oxidase system of heart-muscle sarcosomes is obtained under the most highly hypotonic conditions studied, equivalent to about one-third isotonic. Under these conditions, sarcosomes are swollen, but shrink again when placed in isotonic medium. The effect of tonicity on the activity of the α-ketoglutaric oxidase system is also reversible.
  4. As the tonicity is increased by saline, sucrose or phosphate, the activity of the α-ketoglutaric oxidase system decreases.
  5. The P: O ratio is not affected over a wide range of sucrose concentrations which have a marked effect on the activity of the α-ketoglutaric oxidase system. This and other examples where the oxidase system is more sensitive than the P: O ratio to variations of the conditions indicates that the phosphorylative enzymes are normally in excess of the purely oxidative enzymes and increases the likelihood that measurements of the yield of oxidative phosphorylation on isolated tissue preparations represent the state of affairs in the cell.
  6. Phosphate, in high concentration, decreases the P:O ratio; the optimal concentration is 0.03M.
  7. Hypertonic sucrose is unsuitable for the isolation of sarcosomes. There is, however, no significant difference between sarcosomes isolated with isotonic sucrose and isotonic saline, except that the latter are deficient in cytochrome c.