Klein A R, Thauer R K
Max-Planck-Institut für terrestrische Mikrobiologie and Laboratorium für Mikrobiologie des Fachbereichs Biologie der Philipps-Universität,Marburg, Germany.
Eur J Biochem. 1997 Apr 15;245(2):386-91. doi: 10.1111/j.1432-1033.1997.t01-1-00386.x.
The mtd gene encoding coenzyme-F420-dependent N5,N10-methylenetetrahydromethanopterin dehydrogenase (Mtd) in the hyperthermophilic Methanopyrus kandleri has been cloned, sequenced and functionally overexpressed in Escherichia coli. The overproduced enzyme was purified in a 90% yield to apparent homogeneity by means of only one chromatographic step. Its thermostability properties and most of its catalytic properties were the same as those of the native enzyme purified directly from M. kandleri. Only the dependence of the activity on the concentration of lyotropic salts differed slightly. Northern blot analysis revealed that in M. kandleri the mtd gene is monocistronically transcribed.
编码嗜热甲烷嗜热菌中依赖辅酶F420的N5,N10-亚甲基四氢甲蝶呤脱氢酶(Mtd)的mtd基因已在大肠杆菌中克隆、测序并实现功能过表达。过量表达的酶仅通过一步色谱步骤就以90%的产率纯化至表观纯一。其热稳定性特性和大部分催化特性与直接从嗜热甲烷嗜热菌中纯化的天然酶相同。只有活性对离液盐浓度的依赖性略有不同。Northern印迹分析表明,在嗜热甲烷嗜热菌中,mtd基因是单顺反子转录的。