Ujiiye T, Yamamoto I, Satoh T
Department of Biological Science, Faculty of Science, Hiroshima University, Higashi, Japan.
Biochim Biophys Acta. 1997 Jul 17;1353(1):84-92. doi: 10.1016/s0167-4781(97)00062-6.
Upstream of the dmsCBA genes encoding dimethyl sulfoxide (DMSO) reductase in the phototrophic bacterium Rhodobacter sphaeroides f. sp. denitrificans, there was found one gene (referred to dmsR) which encoded a protein composed of 232 amino acid residues and was divergently transcribed from the dmsCBA genes. The deduced amino acid sequence was homologous to the OmpR subfamily of response regulators in two-component systems for transcriptional regulation. The encoded protein DmsR was shown to bind to a DNA fragment containing the four direct repeats of a decameric nucleotide motif located between the dmsR and dmsCBA genes. The DNA-binding activity of DmsR was observed when the organism was grown anaerobically in the presence of DMSO. A dmsR-defected mutant strain showed no synthesis of DMSO reductase. These results indicate that the dmsR gene product acts as a positive regulator for expression of the dmsCBA genes in response to DMSO under anaerobic growth conditions.
在光合细菌球形红杆菌反硝化亚种中,编码二甲基亚砜(DMSO)还原酶的dmsCBA基因上游,发现了一个基因(称为dmsR),它编码一种由232个氨基酸残基组成的蛋白质,并且与dmsCBA基因呈反向转录。推导的氨基酸序列与用于转录调控的双组分系统中应答调节因子的OmpR亚家族同源。已证明编码的蛋白质DmsR与一个DNA片段结合,该片段包含位于dmsR和dmsCBA基因之间的一个十聚体核苷酸基序的四个直接重复序列。当该生物体在DMSO存在下厌氧生长时,观察到DmsR的DNA结合活性。一个dmsR缺陷突变株不合成DMSO还原酶。这些结果表明,在厌氧生长条件下,dmsR基因产物作为一种正调节因子,响应DMSO调节dmsCBA基因的表达。