Zaniewski R, Deutscher M P
Mol Gen Genet. 1982;185(1):142-7. doi: 10.1007/BF00333804.
In order to determine the metabolic role of RNase D in Escherichia coli, we have attempted to isolate strains deficient in this enzyme. One strain containing a temperature-sensitive RNase D was found among a heavily mutagenized stock of strain temperature-sensitive for growth. Genetic mapping of the mutation responsible for the altered RNAse D enabled us to define the rnd locus, at 39.5-40.0 min on the E. coli map, which apparently specifies the RNase D structural gene. Using a Tn10 insertion near the rnd locus, we constructed isogenic strains containing RNase D and Rnase II mutations, alone or in combination. Although the original mutant isolate displayed temperature-sensitive growth. no growth phenotype was associated with the rnd mutation in wild type background, possibly because a substantial amount of RNase D remained in cells grown at 45 degrees C. However, elucidation of the map position of the rnd locus should prove useful for the isolation of other mutant strains with lower levels of RNase D.
为了确定核糖核酸酶D在大肠杆菌中的代谢作用,我们试图分离出缺乏这种酶的菌株。在对生长温度敏感的菌株进行大量诱变的菌株库中,发现了一株含有温度敏感型核糖核酸酶D的菌株。对导致核糖核酸酶D改变的突变进行遗传定位,使我们能够确定rnd位点,该位点在大肠杆菌图谱上位于39.5 - 40.0分钟处,显然它指定了核糖核酸酶D的结构基因。利用在rnd位点附近的Tn10插入,我们构建了单独或组合含有核糖核酸酶D和核糖核酸酶II突变的同基因菌株。尽管最初分离出的突变体表现出温度敏感型生长。但在野生型背景下,rnd突变与生长表型无关,这可能是因为在45摄氏度下生长的细胞中仍保留了大量的核糖核酸酶D。然而,阐明rnd位点的图谱位置对于分离其他核糖核酸酶D水平较低的突变菌株应该是有用的。