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机构地区:[1]武汉工业学院生物与制药工程系,湖北武汉430023
出 处:《微生物学杂志》2009年第4期62-66,共5页Journal of Microbiology
基 金:湖北省自然科学基金资助项目(2005ABA094)
摘 要:用RNA随机起始PCR(RAP-PCR)技术分析了盐杆菌NRC-1(Halobacterium NRC-1)不同NaCl盐度下基因表达的差异。81条引物用于比较17%、30%两种盐度下基因表达的差异,每条引物平均可以产生10条以上扩增条带,共得到15条在2种盐度下差异表达的条带,这些差异扩增条带的获得将有助从分子水平上了解Halobacterium NRC-1在高盐环境下的适应机制。The RNA arbitrarily primed PCR (RAP-PCR) approach was used to identify those genes that are differentially expressed in response to changing salinity in Halobacterium NRC-1. 81 primers were used to scan two different RNA pools derived from cultures of 17% and 30% NaC1 concentrations. On average, each RT-PCR reaction yielded more than ten bands on the agrose gel. Of the approximately 900 bands that were generated by 81 RT-PCR reaction pairs, 15 differentially-expressed bands were obtained. The results would be useful to understand the adaptation raeehanism of Halobacterium NRC-1 to high salinity conditions.
关 键 词:差异表达 盐杆菌NRC-1 RNA随机起始PCR
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