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首页> 外文期刊>Applied and Environmental Microbiology >Transposition in Lactobacillus sake and its abolition of lactocin S production by insertion of IS1163, a new member of the IS3 family.
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Transposition in Lactobacillus sake and its abolition of lactocin S production by insertion of IS1163, a new member of the IS3 family.

机译:通过插入IS3家族的新成员IS1163,在日本乳杆菌中进行转座,并废除乳酸菌素S的产生。

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摘要

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.
机译:该报告介绍了IS1163的核苷酸序列和插入活性,它是IS3可转座元件家族的新成员。对产生内毒素S的乳酸杆菌L45菌株的自发突变体的分析表明,细菌素阴性表型是由于生产质粒的丢失或IS1163插入内毒素S操纵子(las operon)所致。数据进一步表明,内毒素S操纵子的插入失活是涉及IS1163的染色体供体拷贝的转座事件的结果。尽管描述的插入集中在las操纵子的250 bp区域内,但是没有插入位点的特征提示IS1163的靶标特异性插入。 IS1163中发现的两个主要的开放阅读框的重叠,移码组织是IS3系列的典型特征,但是推定移码区的结构具有将IS1163与该组其他成员区分开的特征。 IS1163在清酒乳杆菌L45中的插入活性已帮助鉴定了对于产乳球菌S必不可少的pCIM1区域,并且可能作为清酒乳杆菌中的突变工具具有进一步的实际应用。

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