Identification and structure of a novel flavin prosthetic group associated with reduced nicotinamide adenine dinucleotide dehydrogenase from Peptostreptococcus elsdenii.
نویسندگان
چکیده
A novel prosthetic group, which is present in NADH dehydrogenase (EC 1.6.99.3) from Pepfosfrejfococcus etsdenii, has been purified and its physicochemical properties investigated. The chemical structure of this species has been established as the FAD analogue of 7-methyl-B-hydroxyisoalloxazine. The proposed structure is confirmed by: (a) chemical synthesis of 7-methyl-S-hydroxy-isoahoxazine models and comparison of their spectral and physical properties with those of the natural chromophore, and (b) photochemical degradation of the N(lO)-polyhydroxy side chain of the FMN portion of the isolated coenzyme to yield 7methyl-S-hydroxy-alloxazine. The synthesis of these models is outlined.
منابع مشابه
Evidence for a Novel Flavin Prosthetic Group Associated with Nadh Dehydrogenase From
I. NADH dehydrogenase (EC 1.6.99.3) has been purified from the strictly anaerobic rumen bacterium Peptostreptococcus elsdenii. The purified protein is specific for NADH as electron donor; it can use 2,6-dichlorophenolindophenol (DCIP), cytochrome c, KzFe(CN)6 or flavodoxin as electron acceptor. It has a molecular weight of about 63 ooo. The absorption spectrum shows maxima at 475, 375, 356, 318...
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عنوان ژورنال:
- The Journal of biological chemistry
دوره 248 18 شماره
صفحات -
تاریخ انتشار 1973