Montandon P E, Nicolas P, Schürmann P, Stutz E
Nucleic Acids Res. 1985 Jun 25;13(12):4299-310. doi: 10.1093/nar/13.12.4299.
We sequenced the chloroplast 16S rRNA gene of two Euglena gracilis mutants which contain streptomycin-resistant chloroplasts (Smr 139.12/4 and Smr 139.20/2). These mutants are known to contain a single intact rrn operon per circular chloroplast genome. Nucleotide sequence comparison between a 16S rRNA gene of wild type Euglena gracilis, strain Z, with streptomycin-sensitive chloroplasts, and the 16S rRNA gene of both Smr-strains reveals a single base change (C to T) at position 876. This position is equivalent to the invariant position 912 of the E. coli 16S rRNA gene. The analogous position is also conserved in all chloroplast small subunit RNA genes from lower and higher plants sequenced so far. Light dependent protein synthesis with purified chloroplasts from streptomycin-resistant cells is not inhibited by streptomycin. Based on the results reported here we postulate linkage between the observed point mutation on the 16S rRNA gene and streptomycin-resistance of chloroplast 70S ribosomes.
我们对两种纤细裸藻突变体(Smr 139.12/4和Smr 139.20/2)的叶绿体16S rRNA基因进行了测序。已知这些突变体每个环状叶绿体基因组含有一个完整的rrn操纵子。对具有链霉素敏感叶绿体的野生型纤细裸藻Z株的16S rRNA基因与两种链霉素抗性株的16S rRNA基因进行核苷酸序列比较,发现在876位有一个单碱基变化(C到T)。该位置相当于大肠杆菌16S rRNA基因的不变位置912。到目前为止,在所有已测序的低等和高等植物的叶绿体小亚基RNA基因中,类似位置也保守。来自链霉素抗性细胞的纯化叶绿体的光依赖蛋白质合成不受链霉素抑制。基于此处报道的结果,我们推测16S rRNA基因上观察到的点突变与叶绿体70S核糖体的链霉素抗性之间存在联系。