Welcome to visit Scientia Silvae Sinicae,Today is

Scientia Silvae Sinicae ›› 2008, Vol. 44 ›› Issue (5): 160-164.doi: 10.11707/j.1001-7488.20080529

Previous Articles     Next Articles

Establishment and Optimization of ISSR-PCR System in Macadamia

Guo Lingfei1.2,Zou Minghong1,Zeng Hui1,Du Liqing1,Lu Chaozhong1

  

  1. (1.South Subtropical Crops Research Institute,Chinese Academy of Tropical Agricultural Sciences Zhanjiang 524091; 2.College of Horticulture,South China University of Tropical Agriculture Danzhou 571737)
  • Received:2007-04-16 Revised:1900-01-01 Online:2008-05-25 Published:2015-04-22

Abstract:

An one factor test was used to optimize ISSR-PCR amplification system on macadamia in four levels of five factors (Taq DNA polymerase,template DNA,dNTPs,primer and Mg2+,respectively) in this study. The results showed that the 25 μL reaction system consisted of 1×PCR buffer,1 U Taq DNA polymerase,20 ng template DNA,0.15 mmol·L-1 dNTPs,0.25 μmol·L-1primer and 2.5 mmol·L-1 Mg2+. In addition,adding 0.4% formamide was able to reduce the background noise. The optimal PCR amplification process was as the following: 1 cycle initial denaturalization at 94 ℃ for 5 min,followed by 35 cycles,which included denaturalization at 94 ℃ for 30 s,annealing for 1 min,and extension at 72 ℃ for 2 min, and then extension at 72 ℃ for 7 min,and finally holding the samples at 4 ℃.

Key words: macadamia, ISSR, system optimization