首页|BOX-PCR分子标记对补播紫花苜蓿共生根瘤菌田间竞争结瘤能力的研究

BOX-PCR分子标记对补播紫花苜蓿共生根瘤菌田间竞争结瘤能力的研究

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本研究利用SX01、HB02 两株根瘤菌菌株对山西右玉草地补植的紫花苜蓿中苜一号进行了田间接种试验.为了检验根瘤菌菌株的接种效果和筛选高效紫花苜蓿根瘤菌菌株,采用BOX-PCR分子标记方法对接种根瘤菌菌株的田间竞争结瘤能力进行了研究.通过对接种供试菌株及田间分离获得的根瘤菌菌株进行BOX-PCR及不同菌株之间的BOX分子指纹图谱比较,检测供试菌株的田间占瘤率.结果表明,紫花苜蓿接种供试菌株60 d后,SX01、HB02两株根瘤菌菌株的田间占瘤率分别达到46.7%,53.3%,说明这两株根瘤菌菌株均具有较强竞争结瘤能力,可以作为高效根瘤菌菌株进行田间推广应用;并阐明了BOX-PCR作为一种分子标记方法,可对根瘤菌菌株竞争结瘤能力进行研究.
Study on Competitive Nodulation Ability of Rhizobia in Symbiosis with Reseeding Medicago sativa in Field Test by Using BOX-PCR Molecular Marker Method
In this study,two rhizobial strains SX01 and HB02 were used to carry out the inoculation experiment with reseeding Medicago sativa Zhongmu no. 1 in You Yu county, Shanxi Province. In order to test the effect of rhizobial strains inoculation and screen high efficient rhizobia strains ,we used BOX-PCR Molecular Marker Method to Study the competitive nodulation ability of strain SXO1 and HB02 . The rhizobia strains reisolated from root nodules of alfalfa and inoculation stains were analyzed by BOX-PCR on meantime,the nodule occupancy of inoculation stains were detected by comparing BOX molecular fingerprint. The results showed that the nodule occupancy of two strains for SXO1 and HB02 were 46.7% ,53.3% respectively ,when the plant are harvest after the plant grew 60 days in the field ,this indicated that two rhizobia strains have high competitive abilities and can promote to use it in the field. In general ,the results suggested that BOX molecular marker method is an easy,rapid and accurate method for studying the competitive nodulation ability of inoculation of Rhizobia in soil.

BOX-PCRZhongmu no. 1RhizobiaNodule occupancy

肖猛、刘晓云、刘桂霞、戴燕燕、郭振国、郭晓叶、魏爽

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河北大学,生命科学学院,河北省微生物多样性研究与应用实验室,河北,保定,071002

BOX-PCR 中苜一号 根瘤菌 占瘤率

"十一五"国家科技支撑计划课题

2007BAD56B01

2011

华北农学报
河北,北京,天津,山西,河南,内蒙古六省市农科院农学会

华北农学报

CSTPCDCSCD北大核心
影响因子:1.067
ISSN:1000-7091
年,卷(期):2011.26(1)
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