Zinder S H, Brock T D
J Gen Microbiol. 1978 Apr;105(2):335-42. doi: 10.1099/00221287-105-2-335.
Dimethyl sulphoxide (DMSO) was reduced to dimethyl sulphide by a wide variety of micro-organism, including prokaryotes and eukaryotes, aerobes and anaerobes. Dimethyl sulphone was not reduced by any of the organisms tested. Cell-free extracts of Escherichia coli reduced DMSO using reduced pyridine nucleotides as electron donors. Activity was greater in anaerobically grown cells than in those grown aerobically. Two other sulphoxides, methionine sulphoxide and tetramethylene sulphoxide, substantially inhibited DMSO reduction by extracts. Mutants of E. coli, which were unable to reduce biotin sulphoxide to biotin, were tested for their ability to reduce DMSO in whole cells and extracts. These mutants were in four different gene loci, bisA to bisD. DMSO reductase activity of the mutants was generally less than that of the wild-type strain, and activity depended upon the gene locus involved, the growth medium and the growth conditions. Only the bisA mutant had very low activity under all conditions. All of the bis mutants were able to grow using methionine sulphoxide as a sulphur source, indicating that biotin sulphoxide and methionine sulphoxide are reduced by different enzyme systems. DMSO may be reduced by both of these enzyme systems.
二甲基亚砜(DMSO)可被多种微生物还原为二甲基硫醚,这些微生物包括原核生物和真核生物、需氧菌和厌氧菌。所测试的任何一种生物均不能还原二甲基砜。大肠杆菌的无细胞提取物以还原型吡啶核苷酸作为电子供体来还原DMSO。厌氧生长的细胞中的活性高于需氧生长的细胞。另外两种亚砜,即甲硫氨酸亚砜和四亚甲基亚砜,可显著抑制提取物对DMSO的还原。对无法将生物素亚砜还原为生物素的大肠杆菌突变体进行了全细胞和提取物中还原DMSO能力的测试。这些突变体位于四个不同的基因位点,即bisA至bisD。突变体的DMSO还原酶活性通常低于野生型菌株,其活性取决于所涉及的基因位点、生长培养基和生长条件。只有bisA突变体在所有条件下活性都非常低。所有的bis突变体都能够利用甲硫氨酸亚砜作为硫源生长,这表明生物素亚砜和甲硫氨酸亚砜是由不同的酶系统还原的。DMSO可能由这两种酶系统共同还原。