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菊芋ISSR-PCR反应体系的建立与优化
引用本文:赵孟良,韩睿,李莉.菊芋ISSR-PCR反应体系的建立与优化[J].西南农业学报,2012,25(1):243-246.
作者姓名:赵孟良  韩睿  李莉
作者单位:青海省农林科学院菊芋研发中心,青海省蔬菜遗传与生理重点实验室,青海西宁810016
基金项目:国家大宗蔬菜产业技术体系西宁综合试验站(CARS-25-G-49);青海省蔬菜遗传与生理重点实验室创新基金(Sc-zdsys-2011-02)
摘    要:利用正交试验设计的方法,从Mg2+浓度、dNTPs浓度、引物浓度和Taq酶浓度4因素对菊芋ISSR-PCR反应体系进行优化分析,并在此基础上对模板DNA浓度及退火温度进行梯度检测。结果表明:菊芋20μl最佳反应体系包括10×PCR buffer,200μmol/L dNTP,0.5μmol/L引物,1.5 mmol/L Mg2+,1.0 U Taq DNA聚合酶和50 ng模板DNA。这一优化系统的建立,将为菊芋种质资源鉴定及遗传多样性的研究奠定基础。

关 键 词:菊芋  ISSR-PCR  优化

Establishment and Optimization of ISSR-PCR Reaction System for Helianthus tuberosus L.
ZHAO Meng-liang , HAN Rui , LI Li.Establishment and Optimization of ISSR-PCR Reaction System for Helianthus tuberosus L.[J].Southwest China Journal of Agricultural Sciences,2012,25(1):243-246.
Authors:ZHAO Meng-liang  HAN Rui  LI Li
Institution:(Qinghai Academy of Agriculture and Forestry Research and Development Center of the Helianthus tuberosus L. Qinghai Province Laboratory of Vegetable Genetics and Physiology,Qinghai Xining 810016,China)
Abstract:In order to optimizing ISSR-PCR reaction system in Helianthus tuberosus L.,the concentrations of Mg2+,dNTPs,primer DNA,and Taq DNA polymerase were optimized at three levels by orthogonal design.Then,based on the optimal ISSR-PCR amplification the concentration of DNA template and annealing temperature were selected.As a result,the optimal PCR(20 μl)mixture contained 10×PCR Buffer,200 μmol/L dNTP,0.5 μmol/L primer,1.5 mmol/L MgCl2,1.0 U Taq polymerase and 50 ng DNA template.This optimized system would play an important role in further research on germplasm identification and the genetic diversity of H. tuberosus by using ISSR molecular marker techniques.
Keywords:Helianthus tuberosus L    ISSR-PCR  Optimization
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