Myers J M, Myers C R
Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.
Biochim Biophys Acta. 1998 Aug 14;1373(1):237-51. doi: 10.1016/s0005-2736(98)00111-4.
The sequence of the omcA gene, which encodes a decaheme cytochrome c that is localized to the outer membrane (OM) of Shewanella putrefaciens MR-1, was determined. The 2202 bp nucleotide sequence of omcA encodes for 734 amino acids with a predicted molecular protein mass of 78.6 kDa. Comparison with the amino-terminal sequence of the mature protein suggests the presence of a hydrophobic leader sequence which is cleaved during translocation of the protein to the OM. This leader sequence has a lipoprotein consensus sequence for signal peptidase II at the cleavage site. The predicted mature protein is comprised of 708 amino acids with a predicted molecular mass of 75.8 kDa, but the addition of ten covalently attached heme c groups and covalent lipid modification to the amino-terminal cysteine increases the predicted mass to 82.7 kDa. This is consistent with its apparent mass of 83 kDa in SDS-PAGE gels. The predicted amino acid sequence for the OmcA protein shows no significant homology to known proteins. A RNA of approx. 2300 bases that hybridizes to the omcA gene was detected in anaerobically grown MR-1 cells. The size of this transcript is similar to the coding region of the omcA gene, suggesting that it is not part of a multicistronic operon. Similar to MR-1, four other strains of S. putrefaciens were all found to localize a majority of their membrane-bound cytochromes to the OM when grown under anaerobic conditions, and all contained an OM cytochrome of similar size to OmcA. In two of these strains, MR-4 and MR-8, a homolog of omcA was identified by RT-PCR and Southern blotting using primers and probes specific for omcA of MR-1. Western blot analysis using a polyclonal antibody to OmcA was similarly positive in strains MR-4 and MR-8. Partial nucleotide sequence analysis of these homologs demonstrated 74-77% predicted amino acid homology with OmcA of MR-1. In contrast, strains MR-30 and MR-42 tested negative for omcA homologs by Southern and Northern blots, RT-PCR, and Western blots.
测定了omcA基因的序列,该基因编码一种定位于腐败希瓦氏菌MR-1外膜(OM)的十血红素细胞色素c。omcA的2202 bp核苷酸序列编码734个氨基酸,预测的分子蛋白质量为78.6 kDa。与成熟蛋白的氨基末端序列比较表明存在一个疏水前导序列,该序列在蛋白转运至外膜过程中被切割。这个前导序列在切割位点具有信号肽酶II的脂蛋白共有序列。预测的成熟蛋白由708个氨基酸组成,预测分子量为75.8 kDa,但十个共价连接的血红素c基团的添加以及氨基末端半胱氨酸的共价脂质修饰使预测质量增加到82.7 kDa。这与其在SDS-PAGE凝胶中83 kDa的表观质量一致。OmcA蛋白的预测氨基酸序列与已知蛋白无显著同源性。在厌氧生长的MR-1细胞中检测到一个约2300个碱基的RNA,它与omcA基因杂交。该转录本的大小与omcA基因的编码区相似,表明它不是多顺反子操纵子的一部分。与MR-1相似,另外四株腐败希瓦氏菌在厌氧条件下生长时,都发现其大部分膜结合细胞色素定位于外膜,并且都含有一个大小与OmcA相似的外膜细胞色素。在其中两株菌MR-4和MR-8中,使用针对MR-1的omcA的特异性引物和探针,通过RT-PCR和Southern印迹鉴定出omcA的同源物。使用针对OmcA的多克隆抗体进行的Western印迹分析在MR-4和MR-8菌株中同样呈阳性。这些同源物的部分核苷酸序列分析表明,与MR-1的OmcA预测氨基酸同源性为74 - 77%。相比之下,MR-30和MR-42菌株通过Southern和Northern印迹、RT-PCR以及Western印迹检测omcA同源物均为阴性。