Skaugen M, Nes I F
Laboratory of Microbial Gene Technology, Agricultural University of Norway, As.
Appl Environ Microbiol. 1994 Aug;60(8):2818-25. doi: 10.1128/aem.60.8.2818-2825.1994.
This report presents the nucleotide sequence and insertional activity of IS1163, which is a new member of the IS3 family of transposable elements. Analysis of spontaneous mutants of the lactocin S-producing Lactobacillus sake strain L45 show that the bacteriocin-negative phenotype is due to either loss of the producer plasmid or the insertion of IS1163 into the lactocin S operon (las operon). The data further show that insertional inactivation of the lactocin S operon is the result of a transposition event involving a chromosomally located donor copy of IS1163. Although the insertions described are clustered within a 250-bp region of the las operon, there are no features of the insertion sites to suggest target-specific insertion of IS1163. The overlapping, frameshifted organization of the two major open reading frames found in IS1163 is typical for the IS3 family, but the structure of the putative frameshift region includes features which distinguish IS1163 from the other members of the group. The insertional activity of IS1163 in L. sake L45 has aided in identifying regions of pCIM1 essential for lactocin S production and may have further practical applications as a mutational tool in L. sake.
本报告介绍了转座元件IS3家族新成员IS1163的核苷酸序列和插入活性。对产乳酸乳球菌素S的清酒乳杆菌L45自发突变体的分析表明,细菌素阴性表型是由于产生菌质粒的丢失或IS1163插入到乳酸乳球菌素S操纵子(las操纵子)中所致。数据进一步表明,乳酸乳球菌素S操纵子的插入失活是涉及位于染色体上的IS1163供体拷贝的转座事件的结果。虽然所描述的插入集中在las操纵子的250 bp区域内,但插入位点没有特征表明IS1163存在靶标特异性插入。在IS1163中发现的两个主要开放阅读框的重叠、移码组织是IS3家族的典型特征,但推定的移码区域的结构包含一些将IS1163与该组其他成员区分开来的特征。IS1163在清酒乳杆菌L45中的插入活性有助于确定pCIM1中对乳酸乳球菌素S产生至关重要的区域,并且作为清酒乳杆菌中的一种突变工具可能具有进一步的实际应用。