摘要
采用灭菌的水稻田土壤为基质,分别投加细菌基因组DNA和细菌活体,应用该方法提取细胞内和细胞外DNA。结果表明,DNA提取效率平均在75.4%-82.3%,DNA纯度OD260/280在1.75-1.85之间。用细菌16S rDNA通用引物PCR表明,DNA纯度能满足PCR要求,细胞内DNA与细胞外DNA互不污染。
This article provides a method of simultaneous recovery of extracellular and intracellular DNA suitable for molecular studies from paddy soil. With sterile paddy soil as a substrate,dosing bacterial genomic DNA and bacteria in vivo,we applied this method to recover the extracellular and intracellular DNA. The results showed that the DNA extraction efficiency of an average is 75.4%-82.3%,and DNA purity OD260/280 is between 1.75-1.85.A 16S rDNA based PCR technique was evaluated using universal bacterial primers to detect the sample.We obtained evidence that the DNA purity can meet the requirements for PCR.Extracellular and intracellular DNA can avoid any contamination with DNA released by each other.
出处
《生物技术通报》
CAS
CSCD
北大核心
2012年第1期65-69,共5页
Biotechnology Bulletin
基金
转基因专项(2009ZX08011-010B)
海南研究生创新科研课题(Hys2010-8)