An activity transition from NADH dehydrogenase to NADH oxidase during protein denaturation

被引:1
作者
Huston, Scott [1 ]
Collins, John [1 ]
Sun, Fangfang [2 ]
Zhang, Ting [1 ]
Vaden, Timothy D. [3 ]
Zhang, Y. -H. Percival [2 ,4 ]
Fu, Jinglin [1 ,5 ]
机构
[1] Rutgers Univ Camden, Dept Chem, 315 Penn St, Camden, NJ 08102 USA
[2] Cell Free Bioinnovat Inc, Blacksburg, VA USA
[3] Rowan Univ, Dept Chem & Biochem, Glassboro, NJ USA
[4] Virginia Tech, Dept Biol Syst Engn, Blacksburg, VA USA
[5] Rutgers Univ Camden, Ctr Computat & Integrat Biol, Camden, NJ USA
基金
美国国家科学基金会;
关键词
protein denaturation; FMN diaphorase; NADH oxidase; NADH dehydrogenase; flavoproteins; IONIC LIQUIDS; CIRCULAR-DICHROISM; FLAVOPROTEIN OXIDASE; GLUCOSE; C4A-HYDROPEROXYFLAVIN; COMPONENTS;
D O I
10.1002/bab.1607
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A decrease in the specific activity of an enzyme is commonly observed when the enzyme is inappropriately handled or is stored over an extended period. Here, we reported a functional transition of an FMN-bound diaphorase (FMN-DI) that happened during the long-term storage process. It was found that FMN-DI did not simply lose its -nicotinamide adenine diphosphate (NADH) dehydrogenase activity after a long-time storage, but obtained a new enzyme activity of NADH oxidase. Further mechanistic studies suggested that the alteration of the binding strength of an FMN cofactor with a DI protein could be responsible for this functional switch of the enzyme.
引用
收藏
页码:286 / 293
页数:8
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