Rauch P J, de Vos W M
Department of Biophysical Chemistry, Netherlands Institute for Dairy Research, Ede.
J Bacteriol. 1994 Apr;176(8):2165-71. doi: 10.1128/jb.176.8.2165-2171.1994.
The 70-kb transposon Tn5276, originally detected in Lactococcus lactis NIZO R5 and carrying the genes for nisin production and sucrose fermentation, can be conjugally transferred to other L. lactis strains. Sequence analysis and complementation studies showed that the right end of Tn5276 contains two genes, designated xis and int, which are involved in excision. The 379-amino-acid int gene product shows high (up to 50%) similarity with various integrases, including that of the Tn916-related conjugative transposons. The xis gene product, like almost all known excisionase (Xis) proteins, is a small (68-residue), basic protein. Expression of both the Tn5276 int and xis genes is required for efficient excision of the ends of Tn5276 in Escherichia coli that appeared to be circularized in the excision process. Mutational analysis of the xis and int genes showed that excision efficiency is dependent on the integrity of the int gene but that an intact xis gene is also required for efficient excision.
最初在乳酸乳球菌NIZO R5中检测到的70kb转座子Tn5276,携带乳链菌肽产生基因和蔗糖发酵基因,可通过接合转移至其他乳酸乳球菌菌株。序列分析和互补研究表明,Tn5276的右端包含两个基因,分别命名为xis和int,它们参与转座子的切除。379个氨基酸的int基因产物与多种整合酶具有高度(高达50%)相似性,包括与Tn916相关的接合转座子的整合酶。xis基因产物与几乎所有已知的切除酶(Xis)蛋白一样,是一种小的(68个残基)碱性蛋白。Tn5276的int和xis基因的表达是在大肠杆菌中有效切除Tn5276末端所必需的,这些末端在切除过程中似乎被环化。xis和int基因的突变分析表明,切除效率取决于int基因的完整性,但完整的xis基因也是有效切除所必需的。