Tersteegen A, Hedderich R
Max-Planck-Institut für Mikrobiologie, Marburg, Germany.
Eur J Biochem. 1999 Sep;264(3):930-43. doi: 10.1046/j.1432-1327.1999.00692.x.
Two gene groups, designated energy converting hydrogenase A (eha) and energy converting hydrogenase B (ehb), each encoding a putative multisubunit membrane-bound [NiFe] hydrogenase, were identified in the genome of Methanobacterium thermoautotrophicum. The length of the transcription units was determined using reverse transcription (RT)-PCR. The eha operon (12.5 kb) and the ehb operon (9.6 kb) were found to be composed of 20 and 17 open reading frames, respectively. Competitive RT-PCR was used to compare the amounts of eha and ehb transcripts with the amounts of transcripts of genes encoding the M. thermoautotrophicum catabolic enzymes cyclohydrolase (mch) and a subunit of heterodisulfide reductase (hdrC). In cells grown under conditions in which H2 was nonlimiting, the eha transcripts were 250-fold and 125-fold less abundant and the ehb transcripts were approximately sixfold and threefold less abundant than the hdrC and mch transcripts, respectively. In cells grown under H2 limitation, the amounts of eha and ehb transcripts were about threefold higher than in cells grown with sufficient H2 when compared to the amounts of hdrC and mch transcripts. Sequence analysis of the deduced proteins indicated that the eha and ehb operons each encode a [NiFe] hydrogenase large subunit, a [NiFe] hydrogenase small subunit, and two conserved integral membrane proteins. These proteins show high sequence similarity to subunits of the Ech hydrogenase from Methanosarcina barkeri, Escherichia coli hydrogenases 3 and 4, and CO-induced hydrogenase from Rhodospirillum rubrum, all of which form a distinct group of multisubunit membrane-bound [NiFe] hydrogenases and show high sequence similarity to the energy-conserving NADH:quinone oxidoreductase (complex I) from various organisms. In addition to these four subunits, the eha operon encodes a 6[4Fe-4S] polyferredoxin, a 10[4F-4S] polyferredoxin, four nonconserved hydrophilic subunits, and 10 nonconserved integral membrane proteins; the ehb operon encodes a 2[4Fe-4S] ferredoxin, a 14[4Fe-4S] polyferredoxin, two nonconserved hydrophilic subunits, and nine nonconserved integral membrane proteins. A function of these putative membrane-bound [NiFe] hydrogenases as proton pumps involved in endergonic reactions, such as the synthesis of formylmethanofuran from CO2, H2 and methanofuran, is discussed.
在嗜热自养甲烷杆菌的基因组中鉴定出两个基因簇,分别命名为能量转换氢化酶A(eha)和能量转换氢化酶B(ehb),每个基因簇都编码一种假定的多亚基膜结合[NiFe]氢化酶。使用逆转录(RT)-PCR确定转录单位的长度。发现eha操纵子(12.5 kb)和ehb操纵子(9.6 kb)分别由20个和17个开放阅读框组成。竞争性RT-PCR用于比较eha和ehb转录本的量与编码嗜热自养甲烷杆菌分解代谢酶环水解酶(mch)和异二硫还原酶一个亚基(hdrC)的基因转录本的量。在氢气不限制生长的条件下培养的细胞中,eha转录本的丰度分别比hdrC和mch转录本低250倍和125倍,ehb转录本的丰度分别比hdrC和mch转录本低约6倍和3倍。在氢气限制条件下培养的细胞中,与hdrC和mch转录本的量相比,eha和ehb转录本的量比在有充足氢气条件下培养的细胞中高约3倍。推导蛋白质的序列分析表明,eha和ehb操纵子各自编码一个[NiFe]氢化酶大亚基、一个[NiFe]氢化酶小亚基和两个保守的整合膜蛋白。这些蛋白质与巴氏甲烷八叠球菌的Ech氢化酶、大肠杆菌氢化酶3和4以及红螺菌的CO诱导氢化酶的亚基具有高度序列相似性,所有这些都形成了一组独特的多亚基膜结合[NiFe]氢化酶,并且与来自各种生物体的能量保守型NADH:醌氧化还原酶(复合体I)具有高度序列相似性。除了这四个亚基外,eha操纵子还编码一个6[4Fe-4S]多铁氧还蛋白、一个10[4F-4S]多铁氧还蛋白、四个非保守的亲水性亚基和10个非保守的整合膜蛋白;ehb操纵子编码一个2[4Fe-4S]铁氧还蛋白、一个14[4Fe-4S]多铁氧还蛋白、两个非保守的亲水性亚基和九个非保守的整合膜蛋白。讨论了这些假定的膜结合[NiFe]氢化酶作为质子泵参与吸能反应(如由二氧化碳、氢气和甲呋喃合成甲酰甲呋喃)的功能。