Jain Devendra, Sunda Sita D, Sanadhya Suman, Nath Dhruba Jyoti, Khandelwal Sunil K
Department of Molecular Biology and Biotechnology, RCA, Maharana Pratap University of Agriculture and Technology, Udaipur, 313001, India.
Department of Soil Science, Assam Agricultural University, Jorhat, 785013, India.
3 Biotech. 2017 May;7(1):4. doi: 10.1007/s13205-016-0583-7. Epub 2017 Apr 8.
Novel cry genes are potential candidates for resistance management strategies, due to their different structures and modes of action. Therefore, it is desirable to clone and express novel cry genes from several new isolates of Bacillus thuringiensis (Bt). In the present study, 28 Bt strains were characterized at morphological and molecular level. All these strains are Gram positive, endospore forming and had shown different crystal morphologies when viewed under the microscope. The ARDRA (16S rDNA PCR-RFLP technique) with AluI, HaeIII, HinfI and TaqI produced unique and distinguishable restriction patterns used for the molecular characterization of these isolates. Based on UPGMA clustering analysis, Bt strains showed significant molecular diversity and the dendrogram obtained differentiated 28 Bt strains into 1 major cluster at a similarity coefficient 0.56. PCR analysis demonstrated that the Bt strains showed diverse cry gene profiles with several genes per strain. The Bt strain G3C1 showed the presence of maximum cry-type genes by PCR. The toxicological characterization of these cry genes will have huge importance in transgenic technology and will be useful in transgenesis of crop plants for better resistance management.
由于其不同的结构和作用方式,新型cry基因是抗性管理策略的潜在候选基因。因此,从苏云金芽孢杆菌(Bt)的几个新分离株中克隆和表达新型cry基因是很有必要的。在本研究中,对28株Bt菌株进行了形态学和分子水平的鉴定。所有这些菌株都是革兰氏阳性、产芽孢的,在显微镜下观察时呈现出不同的晶体形态。使用AluI、HaeIII、HinfI和TaqI进行的ARDRA(16S rDNA PCR-RFLP技术)产生了独特且可区分的限制性图谱,用于这些分离株的分子鉴定。基于UPGMA聚类分析,Bt菌株显示出显著的分子多样性,得到的树状图在相似系数为0.56时将28株Bt菌株分为1个主要聚类。PCR分析表明,Bt菌株呈现出多样的cry基因谱,每个菌株含有多个基因。通过PCR检测,Bt菌株G3C1显示存在最多的cry型基因。这些cry基因的毒理学鉴定在转基因技术中将具有重要意义,并且将有助于作物植物的转基因操作以实现更好的抗性管理。