A new cycling assay for NAD that uses thiazolyl blue as a terminal electron acceptor has been found to offer significant advantages over the more established procedure that employs 2,6dichlorophenolindophenol. With thiazolyl blue, the cycling assay is linear with NAD at picomole levels, and with tim
An improved enzymatic cycle for nicotinamide-adenine dinucleotide phosphate
โ Scribed by Maggie M.-Y. Chi; Charles V. Lowry; Oliver H. Lowry
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 704 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
โฆ Synopsis
An enzymatic cycling reagent for NADP is described which is capable of amplifying lOO,OOO-fold in 4 hr at 38ยฐC or 350,000-fold in 3 days at 15ยฐC. The improvement over a previously described reagent results from several changes, the most important of which is substitution of glucose-6-P dehydrogenase from Leuconostoc mesenteroides
for the baker's yeast enzyme. Tests of the same enzyme from Torula yeast showed it not to be well suited for this purpose. Procedures are given for final reading in either the fluorometer or spectrophotometer. The sensitivity limit for good precision would be about 50 fmol in the spectrophotometer and 0.5 fmol in the fluorometer (each with a I-ml final volume). This sensitivity is available for measuring any metabohte or enzyme which can be induced to react directly or indirectly with an NADP enzyme. The cycle is also effective for NAD, although the rate is much slower than with NADP. Therefore, it would not in general be suitable for measuring tissue NADP.
๐ SIMILAR VOLUMES
A method for measuring nicotinamide-adenine dinucleotide by enzymatic cycling is described which uses malic and alcohol dehydrogenases (EC 1.1.1.37, .and EC 1.1.1.1) for the enzyme couple. After cycling, malate is measured with either malic dehydrogenaze or malic enzyme (EC 1.1.1.40). The method has
## Abstract Uniformly labeled (U) ^14^C nicotinamide adenine dinucleotide phosphate (NADP^+^) was synthesized by phosphorylating [Uโ^14^C]nicotinamide adenine dinucleotide (NAD^+^) in the presence of immobilized NAD^+^ kinase. The 15 ฮผCi (600 ฮผL) synthesis consistently achieved yields between 80% a