Bilous P T, Weiner J H
Department of Biochemistry, University of Alberta, Edmonton, Canada.
J Bacteriol. 1988 Apr;170(4):1511-8. doi: 10.1128/jb.170.4.1511-1518.1988.
The dimethyl sulfoxide (DMSO) reductase operon coding for a membrane-bound iron-sulfur, molybdoenzyme, which functions as a terminal reductase in Escherichia coli, has been isolated and cloned from an E. coli gene bank. Two clones, MV12(pLC19-36) and MV12(pLC43-43), overexpressed both DMSO and trimethylamine N-oxide (TMAO) reductase activities 13- to 15-fold compared with wild-type cells. Amplification was highest in cells grown anaerobically on fumarate, while cells grown on DMSO or TMAO displayed reduced levels of enzyme amplification. Growth on nitrate or aerobic growth repressed expression of the enzyme. A 6.5-kilobase-pair DNA restriction endonuclease fragment was subcloned from pLC19-36 into the vector pBR322, yielding a recombinant DMSO reductase plasmid, pDMS159. Two polypeptides were amplified and identified on sodium dodecyl sulfate-polyacrylamide gels of proteins from E. coli HB101 harboring pDMS159: a membrane-bound protein with molecular weight 82,600 and a soluble polypeptide with molecular weight 23,600. Three plasmid-encoded polypeptides with molecular weights of 87,500, 23,300, and 22,600 were detected by in vivo transcription/translation studies. The smallest subunit was poorly defined and not detectable by Coomassie blue staining. The DMSO reductase operon was localized to the 20.0-min position on the E. coli linkage map.
编码一种膜结合铁硫钼酶的二甲基亚砜(DMSO)还原酶操纵子,该酶在大肠杆菌中作为末端还原酶发挥作用,已从大肠杆菌基因文库中分离并克隆出来。与野生型细胞相比,两个克隆MV12(pLC19 - 36)和MV12(pLC43 - 43)使DMSO和三甲胺N-氧化物(TMAO)还原酶活性过表达13至15倍。在以富马酸为厌氧生长底物的细胞中扩增最高,而在以DMSO或TMAO为生长底物的细胞中酶扩增水平降低。在硝酸盐上生长或有氧生长会抑制该酶的表达。一个6.5千碱基对的DNA限制性内切酶片段从pLC19 - 36亚克隆到载体pBR322中,产生了一个重组DMSO还原酶质粒pDMS159。在含有pDMS159的大肠杆菌HB101的蛋白质十二烷基硫酸钠-聚丙烯酰胺凝胶上扩增并鉴定出两种多肽:一种分子量为82,600的膜结合蛋白和一种分子量为23,600的可溶性多肽。通过体内转录/翻译研究检测到三种分子量分别为87,500、23,300和22,600的质粒编码多肽。最小的亚基定义不明确,考马斯亮蓝染色无法检测到。DMSO还原酶操纵子定位于大肠杆菌连锁图谱上的20.0分钟位置。