Department of Biotechnology, University of Szeged, Közép fasor 52, Szeged, 6726, Hungary.
Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Temesvári krt 62, Szeged, 6726, Hungary.
Appl Microbiol Biotechnol. 2018 Jun;102(12):5133-5147. doi: 10.1007/s00253-018-8973-x. Epub 2018 Apr 21.
Sulfide detoxification can be catalyzed by ancient membrane-bound flavoproteins, sulfide:quinone oxidoreductases (Sqr), which have important roles in sulfide homeostasis and sulfide-dependent energy conservation processes by transferring electrons from sulfide to respiratory or photosynthetic membrane electron flow. Sqr enzymes have been categorized into six groups. Several members of the groups I, II, III, and V are well-known, but type IV and VI Sqrs are, as yet, uncharacterized or hardly characterized at all. Here, we report detailed characterization of a type VI sulfide:quinone oxidoreductase (TrSqrF) from a purple sulfur bacterium, Thiocapsa roseopersicina. Phylogenetic analysis classified this enzyme in a special group composed of SqrFs of endosymbionts, while a weaker relationship could be observed with SqrF of Chlorobaculum tepidum which is the only type VI enzyme characterized so far. Directed mutagenesis experiments showed that TrSqrF contributed substantially to the sulfide:quinone oxidoreductase activity of the membranes. Expression of the sqrF gene could be induced by sulfide. Homologous recombinant TrSqrF protein was expressed and purified from the membranes of a SqrF-deleted T. roseopersicina strain. The purified protein contains redox-active covalently bound FAD cofactor. The recombinant TrSqrF enzyme catalyzes sulfur-dependent quinone reduction and prefers ubiquinone-type quinone compounds. Kinetic parameters of TrSqrF show that the affinity of the enzyme is similar to duroquinone and decylubiquinone, but the reaction has substantially lower activation energy with decylubiquinone, indicating that the quinone structure has an effect on the catalytic process. TrSqrF enzyme affinity for sulfide is low, therefore, in agreement with the gene expressional analyis, SqrF could play a role in energy-conserving sulfide oxidation at high sulfide concentrations. TrSqrF is a good model enzyme for the subgroup of type VI Sqrs of endosymbionts and its characterization might provide deeper insight into the molecular details of the ancient, anoxic, energy-gaining processes using sulfide as an electron donor.
硫解毒可以被古老的膜结合黄素蛋白、硫醌氧化还原酶(Sqr)催化,它在硫稳态和硫依赖的能量守恒过程中起着重要作用,通过将电子从硫转移到呼吸或光合膜电子流。Sqr 酶已被分为六组。I、II、III 和 V 组的几个成员是众所周知的,但 IV 型和 VI 型 Sqrs 至今尚未被描述或几乎没有被描述。在这里,我们报道了一种来自紫色硫细菌 Thiocapsa roseopersicina 的 VI 型硫醌氧化还原酶(TrSqrF)的详细特征。系统发育分析将该酶归类为由内共生体 SqrsF 组成的特殊组,而与迄今为止唯一被描述的 Chlorobaculum tepidum 的 SqrF 则存在较弱的关系。定点突变实验表明,TrSqrF 对膜的硫醌氧化还原酶活性有很大贡献。硫的存在可以诱导 sqrF 基因的表达。从 SqrF 缺失的 T. roseopersicina 菌株的膜中表达和纯化了 SqrF 的同源重组 TrSqrF 蛋白。纯化的蛋白含有氧化还原活性的共价结合 FAD 辅因子。重组 TrSqrF 酶催化硫依赖的醌还原,并且更喜欢泛醌型醌化合物。TrSqrF 的动力学参数表明,该酶的亲和力与二氢醌和癸基泛醌相似,但与癸基泛醌的反应具有显著较低的活化能,表明醌结构对催化过程有影响。TrSqrF 对硫的亲和力较低,因此与基因表达分析一致,SqrF 可能在高硫浓度下发挥作用,以保持能量守恒的硫氧化作用。TrSqrF 是内共生体 VI 型 Sqrs 亚组的良好模型酶,其特性可能为利用硫作为电子供体的古老、缺氧、获取能量的过程提供更深入的分子细节。