Xin Yufeng, Liu Honglei, Cui Feifei, Liu Huaiwei, Xun Luying
State Key Laboratory of Microbial Technology, Shandong University, Jinan, 250100, People's Republic of China.
School of Molecular Biosciences, Washington State University, Pullman, WA, 991647520, USA.
Environ Microbiol. 2016 Dec;18(12):5123-5136. doi: 10.1111/1462-2920.13511. Epub 2016 Sep 23.
Many heterotrophic bacteria contain sulfide:quinone oxidoreductase (SQR) and persulfide dioxygenase (PDO) genes. It is unclear how these enzymes cooperate to oxidise sulfide in bacteria. Cupriavidus pinatubonensis JMP134 contains a gene cluster of sqr and pdo, and their functions were analysed in Escherichia coli. Recombinant E. coli cells with SQR and PDO rapidly oxidised sulfide to thiosulfate and sulfite. The SQR also contains a DUF442 domain that was shown to have rhodanese activities. E. coli cells with PDO and SQR-C94S, an active site mutant of the rhodanese domain, oxidised sulfide to thiosulfate with transitory accumulation of polysulfides. Cellular and enzymatic evidence showed that DUF442 speeds up the reaction of polysulfides with glutathione to produce glutathione persulfide (GSSH). Thus, SQR oxidises sulfide to polysulfides; rhodanese enhances the reaction of polysulfides with glutathione to produce GSSH; PDO oxidises GSSH to sulfite; sulfite spontaneously reacts with polysulfides to generate thiosulfate. The pathway is different from the proposed mitochondrial pathway because it has polysulfides, that is, disulfide and trisulfide, as intermediates. The data demonstrated that heterotrophic bacteria with SQR and PDO can rapidly oxidise sulfide to thiosulfate and sulfite, providing the foundation for using heterotrophic bacteria with SQR and PDO for sulfide bioremediation.
醌氧化还原酶(SQR)和过硫化物双加氧酶(PDO)基因。目前尚不清楚这些酶如何在细菌中协同氧化硫化物。皮纳图博戈氏菌JMP134含有一个sqr和pdo基因簇,并在大肠杆菌中分析了它们的功能。携带SQR和PDO的重组大肠杆菌细胞能迅速将硫化物氧化为硫代硫酸盐和亚硫酸盐。SQR还包含一个被证明具有硫氰酸酶活性的DUF442结构域。携带PDO和SQR-C94S(硫氰酸酶结构域的活性位点突变体)的大肠杆菌细胞将硫化物氧化为硫代硫酸盐,同时多硫化物会短暂积累。细胞和酶学证据表明,DUF442加速了多硫化物与谷胱甘肽反应生成过硫化谷胱甘肽(GSSH)。因此,SQR将硫化物氧化为多硫化物;硫氰酸酶增强多硫化物与谷胱甘肽反应生成GSSH;PDO将GSSH氧化为亚硫酸盐;亚硫酸盐与多硫化物自发反应生成硫代硫酸盐。该途径与提出的线粒体途径不同,因为它以多硫化物(即二硫化物和三硫化物)作为中间体。数据表明,携带SQR和PDO的异养细菌能够迅速将硫化物氧化为硫代硫酸盐和亚硫酸盐,为利用携带SQR和PDO的异养细菌进行硫化物生物修复提供了基础。