Liu X L, Scopes R K
Centre for Protein and Enzyme Technology, La Trobe University, Bundoora, Australia.
Biochim Biophys Acta. 1993 Aug 19;1174(2):187-90. doi: 10.1016/0167-4781(93)90113-r.
The gene encoding the enzyme NADH oxidase from the extreme thermophile Thermoanaerobium brockii has been isolated from a recombinant library of genomic DNA and sequenced. An open reading frame corresponds to the 651 amino acids of the enzyme's subunit, which include characteristic FAD- and NADH-binding sequences, as well as cysteines which are involved in the FeS cluster present in the enzyme. The enzyme is expressed either from its own promoter or from vector promoters in Escherichia coli. After heat-treating the recombinant extracts at 70 degrees C, most of the host proteins are denatured, leaving the NADH oxidase 5- to 10-fold enriched.
编码嗜热厌氧菌布氏嗜热栖热菌中NADH氧化酶的基因已从基因组DNA重组文库中分离出来并进行了测序。一个开放阅读框对应于该酶亚基的651个氨基酸,其中包括特征性的FAD和NADH结合序列,以及参与该酶中存在的FeS簇的半胱氨酸。该酶可从其自身启动子或大肠杆菌中的载体启动子表达。在70℃对重组提取物进行热处理后,大多数宿主蛋白变性,使NADH氧化酶富集5至10倍。