Nonenzymatic tight binding of radioactivity to macromolecular fractions as a source of error in labeling experiments

A highly sensitive recording method is developed for determining the activity of the CoB-12-dependent enzyme, bacterial glycerol dehydratase. The method is based on the ability of alcohol dehydrogenase, in the presence of NADH₂, to reduce aldehydes formed from glycols by glycerol dehydratase. The rate of the coupled reaction is measured spectrophotometrically by the decrease in optical density at 340 nm or by measuring the decrease of H⁺ concentration with a sensitive pH-metric method. The conditions for coupling these two reactions, method of application, and its advantages and limitations are discussed. The method is highly sensitive and makes it possible to detect 0.5–2.5 × 10^?3 glycerol dehydratase units.