Related Experiment Video
Updated: Jun 19, 2026

11:10
Respirometric Oxidative Phosphorylation Assessment in Saponin-permeabilized Cardiac Fibers
Published on: February 28, 2011
CORRELATION OF OXIDATION AND PHOSPHORYLATION IN HEMOLYZED BLOOD IN PRESENCE OF METHYLENE BLUE AND PYOCYANINE
1Laboratories of The Rockefeller Institute for Medical Research.
The Journal of General Physiology
|October 30, 2009
Summary
This study explores glucose metabolism in hemolyzed blood, finding that oxidation and phosphate ester synthesis can be coupled using specific chemical agents like methylene blue or pyocyanine.
Area of Science:
- Biochemistry
- Cellular Metabolism
Background:
- Glycolysis and glucose oxidation are fundamental cellular processes.
- Understanding the factors influencing these pathways is crucial for metabolic research.
Purpose of the Study:
- To investigate the conditions under which glucose oxidation and phosphate ester synthesis occur in hemolyzed blood.
- To identify chemical agents that can couple these two metabolic processes.
Main Methods:
- Experiments using hemolyzed blood with glucose or hexosephosphate esters.
- Addition of chemical agents like methylene blue, pyocyanine, cozymase, iodoacetate, and cyanide.
- Monitoring of glucose oxidation and phosphate ester synthesis.
Main Results:
- Hemolyzed blood with glucose does not show glycolysis or glucose oxidation.
- Hexosephosphate ester oxidation is induced by methylene blue or pyocyanine.
- Cozymase enhances oxidation with methylene blue and is necessary for phosphate ester synthesis.
- Pyocyanine facilitates phosphate ester synthesis without cozymase.
- Phosphate ester synthesis is always coupled with oxidation, but not vice versa.
- Iodoacetate inhibits synthesis, while cyanide has no effect.
Conclusions:
- Specific chemical mediators like methylene blue and pyocyanine can initiate and couple glucose oxidation with phosphate ester synthesis in hemolyzed blood.
- The requirement for cozymase differs depending on the oxidizing agent used.
- These findings provide insights into the mechanisms regulating coupled oxidation-phosphorylation processes.
More Related Videos
Related Concept Videos
Oxidation of Phenols to Quinones
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Pyruvate Oxidation
After glycolysis, the charged pyruvate molecules enter the mitochondria via active transport and undergo three enzymatic reactions. These reactions ensure that pyruvate can enter the next metabolic pathway so that energy stored in the pyruvate molecules can be harnessed by the cells.
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...

