Zwahlen M C, Mollet B
Nestlé Research Center, Nestec Ltd., Lausanne, Switzerland.
Mol Gen Genet. 1994 Nov 1;245(3):334-8. doi: 10.1007/BF00290113.
Spontaneous, phenotypically stable mutations at the beta-galactosidase locus (lacL-lacM) in Lactobacillus helveticus were identified and analyzed. We found that a significant number of mutations were caused by integration of a new IS element, ISL2, into these lac genes. ISL2 is 858 bp long, flanked by 16-bp perfect inverted repeats and generates 3-bp target duplications upon insertion. It contains one open reading frame, which shows significant homology (40.1% identity) to the putative transposase of IS702 from Cyanobacterium calothrix. ISL2 is present in 4-21 copies in the L. helveticus genome, but it is not found in other lactic acid bacteria. Its divergence in copy number and genomic locations in different L. helveticus strains makes it useful as a tool for strain identification by genetic fingerprinting.
对瑞士乳杆菌中β-半乳糖苷酶基因座(lacL-lacM)的自发、表型稳定突变进行了鉴定和分析。我们发现,大量突变是由一种新的IS元件ISL2整合到这些lac基因中引起的。ISL2长858 bp,两侧是16 bp的完美反向重复序列,插入时会产生3 bp的靶标重复序列。它包含一个开放阅读框,与来自鞘丝藻的IS702的推定转座酶具有显著同源性(40.1%的同一性)。ISL2在瑞士乳杆菌基因组中以4 - 21个拷贝存在,但在其他乳酸菌中未发现。其在不同瑞士乳杆菌菌株中的拷贝数和基因组位置的差异使其成为通过基因指纹识别菌株的有用工具。