Hatchikian E C, Zeikus J G
J Bacteriol. 1983 Mar;153(3):1211-20. doi: 10.1128/jb.153.3.1211-1220.1983.
A new type of dissimilatory bisulfite reductase, desulfofuscidin, was isolated from the nonsporeforming thermophilic sulfate-reducing microorganism Thermodesulfobacterium commune. The molecular weight of the enzyme was estimated at 167,000 by sedimentation equilibrium, and the protein was pure by both disc electrophoresis and ultracentrifugation. The bisulfite reductase was a tetramer and had two types of subunits with an alpha(2)beta(2) structure and an individual molecular weight of 47,000. The enzyme exhibited absorption maxima at 576, 389, and 279 nm, with a weak band at 693 nm. Upon the addition of dithionite, the absorption maxima at 576 and 693 nm were weakened, and a new band appeared at 605 nm. The protein reacted with CO in the presence of dithionite to give a complex with absorption peaks at 593, 548, and 395 nm. The extinction coefficients of the purified enzyme at 576, 389, and 279 nm were 89,000, 310,000, and 663,000 M(-1) cm(-1), respectively. Siroheme was detected as the prosthetic group. The protein contains 20 to 21 nonheme iron atoms and 16 to 17 acid-labile sulfur groups per molecule. The data suggest the presence of four sirohemes and probably four (4Fe-4S) centers per molecule by comparison with desulfoviridin, the dissimilatory sulfite reductase from Desulfovibrio species. The protein contains 36 cysteine residues and is high in acidic and aromatic amino acids. The N-terminal amino acids of the alpha and beta subunits were threonine and serine, respectively. With reduced methyl viologen as electron donor, the major product of sulfite reduction was trithionate, and the pH optimum for activity was 6.0. The enzyme was stable to 70 degrees C and denatured rapidly above this temperature. The dependence of T. commune bisulfite reductase activity on temperature was linear between 35 and 65 degrees C, and the Q(10) values observed were above 3. The presence of this new type of dissimilatory bisulfite reductase in T. commune is discussed in terms of taxonomic significance.
从非芽孢形成嗜热硫酸盐还原微生物普通嗜热脱硫杆菌中分离出一种新型异化型亚硫酸氢盐还原酶——脱硫褐菌素。通过沉降平衡法估计该酶的分子量为167,000,通过圆盘电泳和超速离心法鉴定该蛋白质是纯的。该亚硫酸氢盐还原酶是一种四聚体,具有两种类型的亚基,呈α(2)β(2)结构,单个分子量为47,000。该酶在576、389和279nm处有吸收最大值,在693nm处有一条弱带。加入连二亚硫酸盐后,576和693nm处的吸收最大值减弱,在605nm处出现一条新带。该蛋白质在连二亚硫酸盐存在下与CO反应,形成在593、548和395nm处有吸收峰的复合物。纯化后的酶在576、389和279nm处的消光系数分别为89,000、310,000和663,000M⁻¹cm⁻¹。检测到该酶的辅基为丝氨酸亚铁血红素。该蛋白质每分子含有20至21个非血红素铁原子和16至17个酸不稳定硫基团。与来自脱硫弧菌属的异化型亚硫酸盐还原酶脱硫绿菌素相比,数据表明每分子存在四个丝氨酸亚铁血红素,可能还有四个(4Fe-4S)中心。该蛋白质含有36个半胱氨酸残基,酸性和芳香族氨基酸含量较高。α和β亚基的N端氨基酸分别为苏氨酸和丝氨酸。以还原型甲基紫精作为电子供体时,亚硫酸盐还原的主要产物是连三硫酸盐,活性的最适pH为6.0。该酶在70℃下稳定,高于此温度则迅速变性。在35至65℃之间,普通嗜热脱硫杆菌亚硫酸氢盐还原酶活性与温度的关系呈线性,观察到的Q(10)值高于3。本文从分类学意义的角度讨论了普通嗜热脱硫杆菌中这种新型异化型亚硫酸氢盐还原酶的存在情况。