Hottinger H, Ohgi T, Zwahlen M C, Dhamija S, Söll D
Nestlé Research Center, Nestec Ltd., Lausanne, Switzerland.
Gene. 1987;60(1):75-83. doi: 10.1016/0378-1119(87)90215-0.
A Lactobacillus bulgaricus gene encoding a serine tRNA with the anticodon CGA was isolated from a L. bulgaricus clone bank and characterized. This gene is expressed and active in Escherichia coli. The wild-type form of the gene allele specifically complements the E. coli leuB6 mutation. This process depends on gene copy number; high copy number restores leucine prototrophy, while low copy number does not. We suggest that restoration of activity of the mutant leuB6 allele occurs by missense suppression. The L. bulgaricus tRNA(CGASer) when overproduced in E. coli is misacylated at a low frequency, leading to the insertion of an amino acid other than serine in response to the presumed mutant codon UCG in the leuB6 gene. Nucleotide (nt) sequences flanking the tRNA coding region are present in the L. bulgaricus tRNA gene, closely resembling E. coli promoter and terminator elements. A noteworthy feature of this tRNA gene is the extreme length (22 nt) of its extra arm. The 3'-terminal CCA of the tRNA is not encoded in this tRNA gene and thus must be added posttranscriptionally.
从保加利亚乳杆菌克隆文库中分离并鉴定了一个编码反密码子为CGA的丝氨酸tRNA的保加利亚乳杆菌基因。该基因在大肠杆菌中表达且具有活性。该基因等位基因的野生型形式可特异性地互补大肠杆菌leuB6突变。这一过程取决于基因拷贝数;高拷贝数可恢复亮氨酸原养型,而低拷贝数则不能。我们认为,突变型leuB6等位基因活性的恢复是通过错义抑制实现的。当保加利亚乳杆菌tRNA(CGASer)在大肠杆菌中过量表达时,会以低频率发生错配酰化,导致在leuB6基因中对应假定的突变密码子UCG时插入丝氨酸以外的氨基酸。保加利亚乳杆菌tRNA基因中存在tRNA编码区两侧的核苷酸(nt)序列,与大肠杆菌启动子和终止子元件非常相似。该tRNA基因的一个显著特征是其额外臂的长度极长(22 nt)。该tRNA基因中未编码tRNA的3'-末端CCA,因此必须在转录后添加。