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have been described (2). NADPH and reduced nicotinamide adenine dinucleotide (NADH) oxidases were determined by following the decrease in absorbancy at 340 nm. The assays were made in 0.05 M tris(hydroxymethyl)aminomethane (Tris) buffer (pH 7.5) or in 0.05 M cacodylate buffer (pH 6.0). Pyridine nucleotide transhydrogenase was assayed by following the reduction of acetylpyridinenicotinamide adenine dinucleotide (NAD) by the method of Stein et al. (9) . All kinetic experiments were conducted in adoi:10.1128/jb.97.3.1362-1373.1969 fatcat:tbgrza2uvbhjfdiarywkrdjowa