Lee Jae Ho, Park Dong Oh, Park Sae Woong, Hwang Eun Ha, Oh Jeong Il, Kim Young Min
Department of Biology, Yonsei University, Seoul 120-749, Republic of Korea.
J Microbiol. 2009 Jun;47(3):297-307. doi: 10.1007/s12275-008-0210-3. Epub 2009 Jun 26.
Ribulose 1,5-bisphosphate carboxylase/oxygenase (RubisCO) is the key enzyme of the Calvin reductive pentose phosphate cycle. Two sets of structural genes (cbbLS-1 and -2) for form I RubisCO have been previously identified in the Mycobacterium sp. strain JC1, which is able to grow on carbon monoxide (CO) or methanol as sole sources of carbon and energy. Northern blot and reverse transcriptase PCR showed that the cbbLS-1 and -2 genes are expressed in cells grown on either carbon monoxide (CO) or methanol, but not in cells grown in nutrient broth. A promoter assay revealed that the cbbLS-2 promoter has a higher activity than the cbbLS-1 promoter in both CO- and methanol-grown cells, and that the activities of both promoters were higher in CO-grown cells than in methanol-grown cells. A gel mobility shift assay and footprinting assays showed that CbbR expressed in Escherichia coli from a cbbR gene, which is located downstream of cbbLS-1 and transcribed in the same orientation as that of the cbbLS genes, specifically bound to the promoter regions of the cbbLS-1 and -2 genes containing inverted repeat sequence. A DNase I footprinting assay revealed that CbbR protected positions -59 to -3 and -119 to -78 of the cbbLS-1 and -2 promoters, respectively. Overexpression of CbbR induced the transcription of RubisCO genes in Mycobacterium sp. strain JC1 grown in nutrient broth. Our results suggest that the CbbR product from a single cbbR gene may positively regulate two cbbLS operons in the Mycobacterium sp. strain JC1 as is the case for Rhodobacter sphaeroides and Cupriavidus necator.
1,5-二磷酸核酮糖羧化酶/加氧酶(RubisCO)是卡尔文还原戊糖磷酸循环的关键酶。先前已在分枝杆菌属菌株JC1中鉴定出两组用于I型RubisCO的结构基因(cbbLS-1和-2),该菌株能够以一氧化碳(CO)或甲醇作为唯一的碳源和能源生长。Northern印迹和逆转录酶PCR表明,cbbLS-1和-2基因在以一氧化碳(CO)或甲醇生长的细胞中表达,但在营养肉汤中生长的细胞中不表达。启动子分析表明,在以CO和甲醇生长的细胞中,cbbLS-2启动子的活性均高于cbbLS-1启动子,并且在以CO生长的细胞中,两个启动子的活性均高于以甲醇生长的细胞。凝胶迁移率变动分析和足迹分析表明,从位于cbbLS-1下游并与cbbLS基因同向转录的cbbR基因在大肠杆菌中表达的CbbR特异性结合到含有反向重复序列的cbbLS-1和-2基因的启动子区域。DNase I足迹分析表明,CbbR分别保护cbbLS-1和-2启动子的-59至-3位和-119至-78位。CbbR的过表达诱导了在营养肉汤中生长的分枝杆菌属菌株JC1中RubisCO基因的转录。我们的结果表明,单个cbbR基因的CbbR产物可能像球形红杆菌和食酸铜绿假单胞菌那样对分枝杆菌属菌株JC1中的两个cbbLS操纵子起正向调节作用。