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首页|期刊导航|农业科学研究|基于PCR-DGGE和16S rDNA克隆技术研究土壤细菌多样性的实验技术

基于PCR-DGGE和16S rDNA克隆技术研究土壤细菌多样性的实验技术

刘秉儒

农业科学研究Issue(3):34-38,5.
农业科学研究Issue(3):34-38,5.

基于PCR-DGGE和16S rDNA克隆技术研究土壤细菌多样性的实验技术

Experiment technology of soil bacterial diversity by using PCR-DGGE and 16S rDNA clone technique

刘秉儒1

作者信息

  • 1. 宁夏大学 西北土地退化与生态恢复国家重点实验室培育基地,宁夏 银川 750021
  • 折叠

摘要

Abstract

PCR-DGGE has been widely used for measuring soil microbial diversity, but microbial diversity information is limited for identification of microbial communities. If experiment method could completely combined with16S rDNA clone technique, its limitations could reduce, and conclusions also are accurate, reliable and with good repeatability. But the technology is technical process is more complex, and technical requirements is higher. In order to afford alutary experience or lessons to many new operators, experiment technology from the extraction of DNA, PCR amplification, DGGE experiment technology, dyeing and clone technique were described respectively.

关键词

PCR-DGGE/16S rDNA/克隆技术/土壤细菌多样性/实验技术

Key words

PCR-DGGE/16S rDNA/clone technique/soil bacterial diversity/experiment technology

分类

农业科技

引用本文复制引用

刘秉儒..基于PCR-DGGE和16S rDNA克隆技术研究土壤细菌多样性的实验技术[J].农业科学研究,2014,(3):34-38,5.

基金项目

国家自然科学基金项目“贺兰山土壤微生物多样性对植被垂直分异的响应机制”(41061003);宁夏大学博士科研启动基金项目 (41061003)

农业科学研究

1673-0747

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