FACTORS INFLUENCING TETRAZOLE REDUCTION BY REDUCED NICOTINAMIDE–ADENINE DINUCLEOTIDE IN PIGEON-HEART MITOCHONDRIA

1967 ◽  
Vol 45 (2) ◽  
pp. 299-307 ◽  
Author(s):  
C. L. Talesara ◽  
M. C. Blanchaer

The effect of adenosine triphosphate, adenosine diphosphate, adenosine monophosphate and inorganic phosphate on the reduction of 2-(p-iodophenyi)-3-p-nitrophenyl-5-phenyl tetrazolium chloride (INT) to its formazan by reduced nicotinamide-adenine dinucleotide (NADH) was studied in pigeon-heart mitochondria. Formazan production was followed at 540 mμ in 2.2 ml medium containing 0.4–0.5 mg mitochondrial protein, 0.22 M mannitol, 0.067 M sucrose, 0.02 M Tris–chloride, 0.02 mM EDTA, 0.5–3.0 mM INT, and 38 μM NADH at pH 7.2 and 28 °C. By means of the respiratory inhibitors Amytal, rotenone, antimycin A, and cyanide, it was shown that INT diverts electrons from the respiratory chain principally at the flavoprotein level. In contrast to its inhibitory effect on "the O2-linked oxidation of NADH, 10 mM adenosine triphosphate stimulated the reaction rate and formazan yield in the present system. Equimolar inorganic phosphate also increased the initial velocity but adenosine diphosphate and adenosine monophosphate did not. Preliminary kinetic studies suggest that NADH, but not INT, combines with the form of NADH dehydrogenase in the respiratory chain with which adenosine triphosphate reacts.

1978 ◽  
Vol 56 (4) ◽  
pp. 809-813 ◽  
Author(s):  
J. H. A. Fields ◽  
W. R. Driedzic ◽  
C. J. French ◽  
P. W. Hochachka

Glutamate dehydrogenase was isolated from the gills of Arapaima gigas and Osteoglossum bicirrhosum and kinetically characterized, in order to determine whether there was any alteration in the ability of the gills to generate ammonia associated with the development of an air-breathing life-style. The catalytic and regulatory properties of both enzymes were found to be very similar. They were activated by leucine, adenosine monophosphate, and adenosine diphosphate, and inhibited by guanosine triphosphate, guanosine diphosphate, and adenosine triphosphate. Inhibition by nicotinamide adenine dinucleotide and reduced nicotinamide adenine dinucleotide was strong in both cases. It was concluded that both enzymes were regulated by a combination of the energy charge of the cell and the redox potential. There is no evidence for any qualitative alteration of the gills to produce ammonia from amino acids in the air breather, Arapaima gigas, as compared with the water breather, Osteoglossum bicirrhosum.


1966 ◽  
Vol 44 (11) ◽  
pp. 1527-1537 ◽  
Author(s):  
M. C. Blanchaer ◽  
Thomas J. Griffith

The rate of oxidation of 10–35 μM reduced nicotinamide–adenine dinucleotide (NADH) by pigeon-heart mitochondria was increased not only by osmotic swelling and sonic disruption of the organelles but also by milder procedures such as washing or dilution, which had no deleterious effect on the P: O and respiratory control ratios when glutamate was the substrate. In all cases, the enhanced oxidation of 10 μM NADH was suppressed by 5 mM adenosine triphosphate (ATP). From these and other findings it was concluded that the access of extra-mitochondrial NADH to the respiratory chain is controlled at a minimum of two sites. Control of NADH flux through the first site is lost after treatment of the mitochondria by procedures which increase their permeability. A second level of NADH control survives sonic disruption of the mitochondria and is a site at which the oxidation of 10 μM NADH is stimulated by Pi and inhibited by ATP, adenosine diphosphate (ADP), and oxidized nicotinamide–adenine dinucleotide (NAD+). The ATP and ADP effects at this level are not blocked by oligomycin. Magnesium releases the adenine nucleotide inhibition of NADH oxidation under certain conditions, but its site and mode of action is not clear as yet. In these experiments, NADH oxidation was determined polarographically and photometrically at 28° in a medium containing 0.23 M mannitol, 0.07 M sucrose, 0.02 M Tris–chloride, and 0.02 mM ethylenediamine tetra-acetic acid (EDTA) at pH 7.2.


Sign in / Sign up

Export Citation Format

Share Document