McCarver Addison C, Lessner Faith H, Soroeta Jose M, Lessner Daniel J
Department of Biological Sciences, University of Arkansas-Fayetteville, Fayetteville, AR 72701, USA.
Microbiology (Reading). 2017 Jan;163(1):62-74. doi: 10.1099/mic.0.000406. Epub 2017 Feb 8.
The thioredoxin system plays a central role in the intracellular redox maintenance in the majority of cells. The canonical system consists of an NADPH-dependent thioredoxin reductase (TrxR) and thioredoxin (Trx), a disulfide reductase. Although Trx is encoded in almost all sequenced genomes of methanogens, its incorporation into their unique physiology is not well understood. Methanosarcina acetivorans contains a single TrxR (MaTrxR) and seven Trx (MaTrx1-MaTrx7) homologues. We previously showed that MaTrxR and at least MaTrx7 compose a functional NADPH-dependent thioredoxin system. Here, we report the characterization of all seven recombinant MaTrxs. MaTrx1, MaTrx3, MaTrx4 and MaTrx5 lack appreciable disulfide reductase activity, unlike previously characterized MaTrx2, MaTrx6 and MaTrx7. Enzyme assays demonstrated that, of the MaTrxs, only the reduction of disulfide-containing MaTrx7 is linked to the oxidation of reduced coenzymes. NADPH is shown to be supplied to the MaTrxR-MaTrx7 system through the oxidation of the primary methanogen electron carriers F420H2 and ferredoxin, indicating that it serves as a primary intracellular reducing system in M. acetivorans. Bioinformatic analyses also indicate that the majority of methanogens likely utilize an NADPH-dependent thioredoxin system. The remaining MaTrxs may have specialized functions. MaTrx1 and MaTrx3 exhibited thiol oxidase activity. MaTrx3 and MaTrx6 are targeted to the membrane of M. acetivorans and likely function in the formation and the reduction of disulfides in membrane and/or extracellular proteins, respectively. This work provides insight into the incorporation of Trx into the metabolism of methanogens, and this reveals that methanogens contain Trx homologues with alternative properties and activities.
硫氧还蛋白系统在大多数细胞的细胞内氧化还原维持中起着核心作用。经典系统由一种依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的硫氧还蛋白还原酶(TrxR)和硫氧还蛋白(Trx,一种二硫键还原酶)组成。尽管Trx在几乎所有已测序的产甲烷菌基因组中都有编码,但其在产甲烷菌独特生理过程中的作用尚未得到充分了解。嗜乙酰甲烷八叠球菌含有一种单一的TrxR(MaTrxR)和七个Trx(MaTrx1 - MaTrx7)同源物。我们之前表明MaTrxR和至少MaTrx7组成了一个功能性的依赖NADPH的硫氧还蛋白系统。在此,我们报告了所有七种重组MaTrxs的特性。与之前表征的MaTrx2、MaTrx6和MaTrx7不同,MaTrx1、MaTrx3、MaTrx4和MaTrx5缺乏明显的二硫键还原酶活性。酶活性测定表明,在MaTrxs中,只有含二硫键的MaTrx7的还原与还原型辅酶的氧化相关。研究表明,NADPH通过产甲烷菌主要电子载体F420H2和铁氧化还原蛋白的氧化被供应到MaTrxR - MaTrx7系统,这表明它在嗜乙酰甲烷八叠球菌中作为主要的细胞内还原系统发挥作用。生物信息学分析还表明,大多数产甲烷菌可能利用依赖NADPH的硫氧还蛋白系统。其余的MaTrxs可能具有特殊功能。MaTrx1和MaTrx3表现出硫醇氧化酶活性。MaTrx3和MaTrx6分别定位于嗜乙酰甲烷八叠球菌的膜上,可能分别在膜和/或细胞外蛋白质中二硫键的形成和还原中发挥作用。这项工作为Trx纳入产甲烷菌的代谢提供了见解,并且揭示了产甲烷菌含有具有不同特性和活性的Trx同源物。