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细胞色素P450还原酶的黄素腺嘌呤二核苷酸结合结构域的表征

Characterization of the FAD binding domain of cytochrome P450 reductase.

作者信息

Hodgson A V, Strobel H W

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Medical School at Houston 77225, USA.

出版信息

Arch Biochem Biophys. 1996 Jan 1;325(1):99-106. doi: 10.1006/abbi.1996.0012.

Abstract

The redox potentials of FAD and FMN of Cytochrome P450 reductase (reductase) are equivalent in solution but differ by 138 mV when bound to reductase. The interaction of each flavin with its flavin binding domain confers the unique electron transferring abilities to each flavin. In order to determine flavin binding properties and activity of the FAD binding domain, we have expressed in pTrcHis three fragments (1161, 1244, and 1556 bp) of rat liver reductase cDNA encompassing the proposed FAD and NADPH binding domain. The FAD binding fragments from cells harboring the 1161- and 1556-bp-containing vectors were stable and bound 0.66 and 0.71 mol FAD/mol enzyme, respectively. Both fragments reduce ferricyanide (54 and 104% of FMN-less reductase/mol bound flavin, respectively) and participate in the transhydrogenation reaction of 3-AcPy-ADP (41 and 65% of FMN-less reductase/mol bound flavin, respectively). FAD-less fragments were purified and reconstituted with 8-amino-FAD and 8-chloro-FAD to determine binding efficiencies.

摘要

细胞色素P450还原酶(还原酶)的黄素腺嘌呤二核苷酸(FAD)和黄素单核苷酸(FMN)的氧化还原电位在溶液中相当,但与还原酶结合时相差138毫伏。每个黄素与它的黄素结合结构域的相互作用赋予了每个黄素独特的电子转移能力。为了确定FAD结合结构域的黄素结合特性和活性,我们在pTrcHis中表达了大鼠肝脏还原酶cDNA的三个片段(1161、1244和1556碱基对),这些片段包含了推测的FAD和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)结合结构域。含有1161和1556碱基对载体的细胞中的FAD结合片段是稳定的,分别结合0.66和0.71摩尔FAD/摩尔酶。两个片段都能还原铁氰化物(分别为无FMN还原酶/摩尔结合黄素的54%和104%),并参与3-乙酰吡啶-ADP的转氢反应(分别为无FMN还原酶/摩尔结合黄素的41%和65%)。纯化不含FAD的片段,并用8-氨基-FAD和8-氯-FAD进行重组,以确定结合效率。

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