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作 者:李俊[1,2] 刘信[3] 曹应龙[2] 武玉花[2] 厉建萌[3] 吴刚[2] 张丽[2] 卢长明[2]
机构地区:[1]中南民族大学生命科学学院,湖北武汉430074 [2]中国农业科学院油料作物研究所,湖北武汉430062 [3]农业部科技发展中心,北京100026
出 处:《作物学报》2012年第4期639-647,共9页Acta Agronomica Sinica
基 金:国家转基因生物新品种培育重大专项(2009ZX08012-009B)资助
摘 要:植酸酶基因在农业生产中具有很高的应用价值,正被广泛用于农作物的基因工程研究。为了满足转植酸酶基因作物安全监管的需要,通过优化PCR检测条件,建立了植酸酶基因特异性定性PCR检测方法。该方法具有良好的扩增特异性和检测灵敏度,可以满足我国植酸酶转基因作物监管需要。此外,我们将6种主要农作物(小麦、水稻、棉花、大豆、玉米和油菜)的内标准基因和植酸酶基因克隆到同一载体上,构建成了阳性质粒分子pBS Endogenous-phytase。该质粒分子适用于这6种作物中植酸酶基因的筛查检测。本研究为转植酸酶基因作物的安全监管提供了阳性材料和检测方法。Phytase gene is valuably applicated in agricultural production, especially in genetic engineering of crops. In order to meet the requirements of safety regulation of transgenic crops, the gene-specific qualitative PCR detection method targeting the fungal-originated phytase gene was developed. A primer pair Phytase-F5/R5 yielding a 389 bp amplicon was selected from 11 primer pairs, then the PCR reaction system was optimized by improving Mg^2+ concentration, primer concentration and primer anneal temperature. Twenty transgenic and nontransgenic lines from different crops we.re used as templates in PCR, showing that the PCR method had good amplification specificity. The results of sensitivity testing indicated that the phytase amplicon was still observed when the template concentration was down to 0.05%, which reaches the national standards for GMO (Genetically Modi- fied Organism) detection method. In addition, we Cointegrated the phytase gene and the endogenous reference genes from six major crops of wheat, rice, cotton, soybeans, corn, and rapeseed into a vector, yielding a positive plasmid molecule pBS Endoge- nous-phytase. The positive plasmid molecule was suitable for screening phytase gene in the six crops about wheat, soybeans, corn, cotton, rice, and rape. This study provides positive materials and detection method for safety regulation of genetically modified crops carrying phytase gene.
关 键 词:转基因检测 植酸酶基因 定性PCR 阳性质粒分子
分 类 号:S188[农业科学—农业基础科学]
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