Chakravarty L, Kittle J D, Tuovinen O H
Environmental Science Graduate Program, Ohio State University, Columbus 43210-1086, USA.
Can J Microbiol. 1997 Jun;43(6):503-8. doi: 10.1139/m97-072.
An insertion sequence, designated as IST3091, was located adjacent to the putative origin of replication region of plasmid pTFI91 of Thiobacillus ferrooxidans TFI-91. The DNA sequence of the transposase gene of IST3091 revealed similarity with that of IS30, IS1086, IS4351, and the integrase gene of SpV1-R8A2 B (a bacteriophage of Spiroplasma citri). The sequence of IST3091 is 1063 bp long with partially matched 30-bp terminal inverted repeats. Several restriction fragments of plasmid pTFI91 of T. ferrooxidans containing the IST3091 element were cloned into the vector pHSG398. The hybrid plasmids (pBTL) were transformed into Escherichia coli NK7379 containing a miniF plasmid, which was devoid of transposable elements. The transposition function of the IST3091 element was confirmed by mobilizing hybrid plasmids via conjugation from transformed E. coli NK7379 (donor) to E. coli M8820 (recipient). The presence of the transposed element in transconjugants was detected by polymerase chain reaction amplification.
一个名为IST3091的插入序列位于氧化亚铁硫杆菌TFI-91的质粒pTFI91假定复制起点区域附近。IST3091转座酶基因的DNA序列与IS30、IS1086、IS4351以及螺旋体噬菌体SpV1-R8A2 B的整合酶基因序列相似。IST3091序列长1063 bp,具有部分匹配的30 bp末端反向重复序列。将含有IST3091元件的氧化亚铁硫杆菌质粒pTFI91的几个限制性片段克隆到载体pHSG398中。将杂交质粒(pBTL)转化到含有miniF质粒且无转座元件的大肠杆菌NK7379中。通过从转化的大肠杆菌NK7379(供体)向大肠杆菌M8820(受体)进行接合转移杂交质粒,证实了IST3091元件的转座功能。通过聚合酶链反应扩增检测转接合子中转座元件的存在。