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机构地区:[1]西北大学生命科学学院教育部西部资源与现代生物技术重点实验室,陕西西安710069
出 处:《生物技术》2006年第2期45-47,共3页Biotechnology
基 金:陕西省自然科学基金资助项目(99JK122);陕西省教育厅专项科研资金(04JK133)
摘 要:目的:从野生花生的新鲜根瘤中分离纯化花生慢生根瘤菌。方法:将野生型花生的新鲜根瘤灭菌后捣碎制成悬浮液,通过稀释涂布、划线和贴片三种方法,在YMA结晶紫和YMA刚果红选择培养基上逐步分离纯化得到单菌落。结果:三种方法均分离得到表面性状一致的单菌落,其中用稀释5^3-5^4倍的悬浮液划线分离的效果最好。所得菌株经理化性质和回接试验鉴定为慢生根瘤菌,从而为接着的花生根瘤菌及其结瘤基因的研究提供了基础。Objectives: To isolate the bradyrhizobium bacterium from peanut. Methods: Triturated fresh root nodules that were surface sterilized. Then, by spreading, streaking, and adhibiting, the bacterium was isolated from fresh suspend of wild peanut's root nodules. Results: Bacterium strains were isolated by all of three methods. And, the best result appeared when the fresh suspend was diluted by 5^3 -5^4 times sterilized water. Character and re- inoculation experiment indicated that the strains were Bradyrhizobium sp. (A rachis), which provide a base for the coming research of peanut's nodulation gene.
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