AbstractMitochondria from beef heart and yeast catalyze the reduction of NAD to NADH at the expense of reduced methylviologen (MV+). Based on protein the specific activity of mitochondria for this reaction is about 10–20-times higher than the consumption of oxygen in the presence of succinate or NADH. In 2H2O buffer (4S)-[4-2H]NADH is formed in high enantiomeric excess if the reduced methylviologen is electrochemically regenerated
AbstractReverse electron transfer (RET) from succinate to NAD+ is known to be accompanied by high ge...
AbstractH+-transhydrogenase (H+-Thase) and NADP-linked isocitrate dehydrogenase (NADP—ICDH) are very...
AbstractThe oxidation of matrix and cytosolic NADH by isolated beetroot and wheat leaf mitochondria ...
AbstractTranshydrogenase from beef-heart mitochondria was solubilised with Triton X-100 and purified...
AbstractThe saturation kinetics of NADH and succinate oxidation for Coenzyme Q (CoQ) has been re-inv...
1. The ATP-dependent reduction of NAD+ by succinate catalysed by submitochondrial particles prepared...
drial outer membrane oxidizes exogenous NADH. The elec-trons contained in this exogenous nucleotide ...
AbstractCoupled rat heart mitochondria produce externally hydrogen peroxide at the rates which corre...
The mitochondrial NAD pool is particularly important for the maintenance of vital cellular functions...
AbstractThe rates of NADH-supported superoxide/hydrogen peroxide production by membrane-bound bovine...
AbstractConsiderable quantitative variations in the competitive inhibition of NADH oxidase activity ...
Using newer techniques of data collection that accumulate entire spectra at a series of discrete vol...
NAD plays essential redox and non-redox roles in cell biology. In mammals, its de novo and recycling...
Folate is required for the synthesis of nucleotides, the regeneration of methionine, and methylation...
Many metabolic engineering strategies rely on the manipulation of enzyme levels to achieve the ampl...
AbstractReverse electron transfer (RET) from succinate to NAD+ is known to be accompanied by high ge...
AbstractH+-transhydrogenase (H+-Thase) and NADP-linked isocitrate dehydrogenase (NADP—ICDH) are very...
AbstractThe oxidation of matrix and cytosolic NADH by isolated beetroot and wheat leaf mitochondria ...
AbstractTranshydrogenase from beef-heart mitochondria was solubilised with Triton X-100 and purified...
AbstractThe saturation kinetics of NADH and succinate oxidation for Coenzyme Q (CoQ) has been re-inv...
1. The ATP-dependent reduction of NAD+ by succinate catalysed by submitochondrial particles prepared...
drial outer membrane oxidizes exogenous NADH. The elec-trons contained in this exogenous nucleotide ...
AbstractCoupled rat heart mitochondria produce externally hydrogen peroxide at the rates which corre...
The mitochondrial NAD pool is particularly important for the maintenance of vital cellular functions...
AbstractThe rates of NADH-supported superoxide/hydrogen peroxide production by membrane-bound bovine...
AbstractConsiderable quantitative variations in the competitive inhibition of NADH oxidase activity ...
Using newer techniques of data collection that accumulate entire spectra at a series of discrete vol...
NAD plays essential redox and non-redox roles in cell biology. In mammals, its de novo and recycling...
Folate is required for the synthesis of nucleotides, the regeneration of methionine, and methylation...
Many metabolic engineering strategies rely on the manipulation of enzyme levels to achieve the ampl...
AbstractReverse electron transfer (RET) from succinate to NAD+ is known to be accompanied by high ge...
AbstractH+-transhydrogenase (H+-Thase) and NADP-linked isocitrate dehydrogenase (NADP—ICDH) are very...
AbstractThe oxidation of matrix and cytosolic NADH by isolated beetroot and wheat leaf mitochondria ...