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Cloning and sequence analysis of gene oipA encoding an outer membrane protein of human Helicobacter pylori

机译:幽门螺杆菌外膜蛋白编码oipA基因的克隆与序列分析

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摘要

AIM: To construct a recombinant E. coli strain that would highly express the proinflammatory outer membrane protein of human Helicobacter pylori (H pylori).METHODS: The oipA DNA was amplified by PCR, inserted into pET-32a, and transformed into Top10 E. coli strain. This recombinant plasmid of Top10 was sent out for nucleotide sequence analysis. Finally this sequence was compared with HP0638 and JHP0581.RESULTS: The sequence of the aim gene was obtained. It had 924 base pairs. The identity was 95.32% against HP0638, 95.02% against JHP0581, which was higher than the identity between HP0638 and JHP0581.CONCLUSION: Although the aim gene was obtained, but it was different from the published sequence of GenBank. It is not clear what makes this difference. Maybe it is because different strain was used or because there were some variations. So more researches are required to prove it.
机译:目的:构建高表达人幽门螺杆菌促炎性外膜蛋白的重组大肠杆菌。方法:通过PCR扩增oipA DNA,插入pET-32a,并转化入Top10E。大肠杆菌菌株。将该Top10的重组质粒送出进行核苷酸序列分析。最后将该序列与HP0638和JHP0581进行了比较。结果:获得了目的基因序列。它具有924个碱基对。与HP0638的同源性为95.32%,与JHP0581的同源性为95.02%,高于HP0638和JHP0581的同源性。结论:虽然获得了目的基因,但与GenBank公开的序列不同。目前尚不清楚是什么造成了这种差异。可能是因为使用了不同的应变,或者是因为有些差异。因此,需要更多的研究来证明这一点。

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