Yanagisawa Tatsuo, Kawakami Makoto
Department of Biological Science, Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.
J Biol Chem. 2003 Jul 11;278(28):25887-94. doi: 10.1074/jbc.M302633200. Epub 2003 Apr 2.
Two isoleucyl-tRNA synthetases (IleRSs) encoded by two distinct genes (ileS1 and ileS2) were identified in pseudomonic acid (mupirocin)-producing Pseudomonas fluorescens. The most striking difference between the two IleRSs (IleRS-R1 and IleRS-R2) is the difference in their abilities to resist pseudomonic acid. Purified IleRS-R2 showed no sensitivity to pseudomonic acid even at a concentration of 5 mm, 105 times higher than the Ki value of IleRS-R1. The amino acid sequence of IleRS-R2 exhibits eukaryotic features that are originally found in eukaryotic proteins. Escherichia coli cells transformed with the ileS2 gene exerted pseudomonic acid resistance more than did those transformed with ileS1. Cells transformed with both genes became almost as resistant as P. fluorescens. These results suggest that the presence of IleRS-R2 could be the major reason why P. fluorescens is intrinsically resistant to the antibiotic. Here we suggest that the evolutionary scenario of the eukaryotic ileS2 gene can be explained by gene acquisition and that the pseudomonic acid producer may have maintained the ileS2 gene to protect itself from pseudomonic acid.
在产生假单胞菌酸(莫匹罗星)的荧光假单胞菌中,鉴定出由两个不同基因(ileS1和ileS2)编码的两种异亮氨酰 - tRNA合成酶(IleRSs)。这两种IleRSs(IleRS - R1和IleRS - R2)之间最显著的差异在于它们抵抗假单胞菌酸的能力不同。纯化的IleRS - R2即使在浓度为5 mM时也对假单胞菌酸不敏感,该浓度比IleRS - R1的Ki值高105倍。IleRS - R2的氨基酸序列呈现出最初在真核蛋白质中发现的真核特征。用ileS2基因转化的大肠杆菌细胞比用ileS1基因转化的细胞表现出更强的对假单胞菌酸的抗性。用这两个基因都转化的细胞几乎与荧光假单胞菌一样具有抗性。这些结果表明,IleRS - R2的存在可能是荧光假单胞菌对该抗生素具有固有抗性的主要原因。在此我们认为,真核ileS2基因的进化情况可以通过基因获得来解释,并且假单胞菌酸产生菌可能保留了ileS2基因以保护自身免受假单胞菌酸的影响。