Zhao Genshi, Meier Timothy I, Peery Robert B, Matsushima Patti, Skatrud Paul L
Microbiology (Reading). 1999 Apr;145 ( Pt 4):791-800. doi: 10.1099/13500872-145-4-791.
Era, an essential GTPase, is present in many bacteria and Mycoplasma spp. and appears to play a major role in the cell cycle and other cellular processes. To further understand its function, an era gene from Streptococcus pneumoniae was identified and cloned, and a mutant era gene with a deletion of 68 codons from its 3'-terminus was constructed. The truncated Era protein was then purified and characterized, and the ability of the truncated era gene to complement an Escherichia coli mutant strain defective in Era production was examined. Like the full-length Era protein, the truncated Era protein was able to bind and hydrolyse GTP, but its binding activity was increased twofold and its hydrolytic activity was reduced sevenfold when compared with those of the full-length Era protein. Unlike the full-length Era protein, the truncated Era protein lost its ability to bind to the E. coli cytoplasmic membrane. The full-length era gene was able to complement the E. coli mutant deficient in Era production when carried on pACYC184, while the truncated era gene failed to do so when carried on pACYC184, pBR322 or pUC18. The cellular amounts of the truncated Era and the full-length Era proteins in E. coli and S. pneumoniae, respectively, were then determined by Western blot analysis. In addition, the minimal amount of the S. pneumoniae Era protein needed for complementation of the E. coli mutant was also measured. Taken together, these results suggest that the C-terminus of the Era protein might be responsible for the binding of the protein to the cytoplasmic membrane and be essential for function.
Era是一种必需的GTP酶,存在于许多细菌和支原体属中,似乎在细胞周期和其他细胞过程中起主要作用。为了进一步了解其功能,从肺炎链球菌中鉴定并克隆了era基因,并构建了一个从其3'末端缺失68个密码子的突变era基因。然后对截短的Era蛋白进行纯化和表征,并检测截短的era基因对Era产生缺陷的大肠杆菌突变株的互补能力。与全长Era蛋白一样,截短的Era蛋白能够结合并水解GTP,但与全长Era蛋白相比,其结合活性提高了两倍,水解活性降低了七倍。与全长Era蛋白不同,截短的Era蛋白失去了与大肠杆菌细胞质膜结合的能力。当携带在pACYC184上时,全长era基因能够互补Era产生缺陷的大肠杆菌突变体,而当携带在pACYC184、pBR322或pUC18上时,截短的era基因则不能。然后通过蛋白质免疫印迹分析分别测定了大肠杆菌和肺炎链球菌中截短的Era蛋白和全长Era蛋白的细胞含量。此外,还测定了互补大肠杆菌突变体所需的肺炎链球菌Era蛋白的最小量。综上所述,这些结果表明Era蛋白的C末端可能负责该蛋白与细胞质膜的结合,并且对其功能至关重要。