scholarly journals Evidence for the Metabolism of Glycerol by Skeletal Muscle and the Presence of a Muscle Nicotinamide-Adenine Dinucleotide Phosphate-Dependent Glycerol Dehydrogenase

1966 ◽  
Vol 98 (3) ◽  
pp. 27C-29C ◽  
Author(s):  
C. J. Toews
1967 ◽  
Vol 105 (3) ◽  
pp. 1067-1073 ◽  
Author(s):  
C. J. Toews

The NADP-specific glycerol dehydrogenase of rat skeletal muscle has been partially purified by ammonium sulphate fractionation. The enzyme has been studied kinetically by initial-velocity analysis, product inhibition and inhibition by fluoride. The experimental results indicate that the reaction mechanism for the enzyme is ordered such that the first product leaves the enzyme before the addition of the second substrate.


1965 ◽  
Vol 43 (10) ◽  
pp. 1653-1659 ◽  
Author(s):  
A. M. Katz ◽  
W. Kalow

Several isoenzymes of lactate, malate, and isocitrate dehydrogenases have been demonstrated in human skeletal muscle, heart, and liver. Single zones of activity were shown for glucose-6-phosphate and glutamate dehydrogenases. A zone possessing a marked reducing capacity towards nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate was visualized in the absence of any substrate, using the tetrazolium-coupled histochemical method. This zone represents the so-called "nothing dehydrogenase".


2019 ◽  
Vol 31 (18) ◽  
pp. 1371-1410 ◽  
Author(s):  
Carlos Henríquez-Olguín ◽  
Susanna Boronat ◽  
Claudio Cabello-Verrugio ◽  
Enrique Jaimovich ◽  
Elena Hidalgo ◽  
...  

Author(s):  
M. Arif Hayat

Although it is recognized that niacin (pyridine-3-carboxylic acid), incorporated as the amide in nicotinamide adenine dinucleotide (NAD) or in nicotinamide adenine dinucleotide phosphate (NADP), is a cofactor in hydrogen transfer in numerous enzyme reactions in all organisms studied, virtually no information is available on the effect of this vitamin on a cell at the submicroscopic level. Since mitochondria act as sites for many hydrogen transfer processes, the possible response of mitochondria to niacin treatment is, therefore, of critical interest.Onion bulbs were placed on vials filled with double distilled water in the dark at 25°C. After two days the bulbs and newly developed root system were transferred to vials containing 0.1% niacin. Root tips were collected at ¼, ½, 1, 2, 4, and 8 hr. intervals after treatment. The tissues were fixed in glutaraldehyde-OsO4 as well as in 2% KMnO4 according to standard procedures. In both cases, the tissues were dehydrated in an acetone series and embedded in Reynolds' lead citrate for 3-10 minutes.


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