scholarly journals Ubiquinone reduction pattern in pigeon heart mitochondria. Identification of three distinct ubiquinone pools

1985 ◽  
Vol 229 (3) ◽  
pp. 621-629 ◽  
Author(s):  
B M Jørgensen ◽  
H N Rasmussen ◽  
U F Rasmussen

Intact pigeon heart mitochondria showed 10-30% ubiquinone reduction in the absence of substrates. This reduction could not be ascribed to endogenous substrates, as judged by lack of effect of inhibitors and uncouplers and by the very low endogenous respiratory rate. Addition of NADH in the presence of antimycin caused further reduction of about 10% ubiquinone, apparently coupled to the rotenone- and antimycin-sensitive exo-NADH oxidase system [Rasmussen (1969) FEBS Lett. 2, 157-162]. Citric acid cycle substrates reduced most of the remaining ubiquinone in the presence of antimycin; 15-20% of the total ubiquinone content was still in the oxidized form under the most reducing conditions. Three pools of ubiquinone therefore appeared to be present in heart mitochondria: a metabolically inactive pool consisting of reduced as well as oxidized ubiquinone, a pool coupled to oxidation of added (cytoplasmic) NADH, and the well-known pool coupled to citric acid cycle oxidations. Ferricyanide selectively oxidized the ubiquinol reduced by added NADH, indicating that this pool is situated on the outer surface of the mitochondrial inner membrane. Ubiquinone reduction levels were determined with a new method, which is described in detail.

1970 ◽  
Vol 245 (1) ◽  
pp. 102-111 ◽  
Author(s):  
Kathryn LaNoue ◽  
William J. Nicklas ◽  
John R. Williamson

1971 ◽  
Vol 17 (5) ◽  
pp. 617-624 ◽  
Author(s):  
A. Michael Charles

A quantitative study was conducted of enzymes involved in the citric acid cycle and associated systems of the facultative autotroph Thiobacillus novellus grown on five different substrates. Irrespective of the growth substrate the organism possessed complete citric and glyoxylic acid cycles and the specific activity of α-ketoglutarate dehydrogenase was always quite low. Also, the activities of the enzymes of both cycles were usually lowest in extracts from autotrophic cells, and highest in extracts from acetate-grown cells. The three remaining extracts had activities that were between the two extremes with those from glucose-grown cells generally lower than those from pyruvate and succinate. Several exceptions should be noted among these generalizations. For example, the activity of aconitate hydratase and malic dehydrogenase was lowest in extracts from glucose-grown cells while that of isocitric dehydrogenase was lowest in extracts from pyruvate-grown cells. Transhydrogenase activity was virtually absent from extracts of pyruvate- and succinate-grown cells while NADH oxidase, which was identical in these two extracts, was also relatively low. Of interest is the large amount of cytochrome c found in high-speed supernatants. In extracts from autotrophic cells this was about 2.3% of the soluble protein and is suggestive of a significant role being played by the electron-transport system during growth of the organism.


1963 ◽  
Vol 42 (4) ◽  
pp. 480-484 ◽  
Author(s):  
B. Eckstein ◽  
R. Landsberg

ABSTRACT The succinic, malic and isocitric dehydrogenases in the ovary of immature and mature, normal and serum gonadotrophin injected rats were examined. The Qo2 of these enzymes were markedly enhanced in the gonadotrophin injected rats of both age groups, except in the case of succinic dehydrogenase in the ovary of the immature rats, where a slight non-significant decrease was noted. It is concluded that in the mature rat ovary, gonadotrophin administration stimulates the activity of all the examined dehydrogenases of the citric acid cycle, whereas in the immature rat ovary, at least the isocitric- and malic dehydrogenases are thus stimulated.


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