Purohit M K, Singh S P
Department of Biosciences, Saurashtra University, Rajkot, Gujarat, India.
Lett Appl Microbiol. 2009 Sep;49(3):338-44. doi: 10.1111/j.1472-765X.2009.02663.x.
To develop total DNA extraction protocol from saline soil for further metagenomic applications.
The protocols combine the application of mechanical (Beads and Sonicator) and Soft Lysis (SDS and enzymes) method for the isolation of total DNA from saline soil of coastal Gujarat followed by its quantification and purity assessment. The quality and purity of metagenomic DNA was quite consistent and reliable, although it contained residual concentartions of humic acid. The extracted DNA was used to successfully amplify 16S rRNA region. The amplicons were suitable for further applications such as diversity-based analysis by denaturing gradient gel electrophoresis (DGGE).
The methods appear to have wide applicability in investigating molecular diversity and exploring functional genes from the total DNA.
The protocol is simple, short and facilitates rapid isolation of PCR amplifiable total genomic DNA from saline soil. The method yielded good quality of the DNA suitable for metagenomic studies. The results are also significant as only few extreme environments, particularly saline habitats, are explored for their metagenomic potential.
开发从盐渍土中提取总DNA的方法,以用于进一步的宏基因组学研究。
该方法结合了机械(珠磨法和超声破碎法)和温和裂解(SDS和酶)方法,从古吉拉特邦沿海地区的盐渍土中分离总DNA,随后对其进行定量和纯度评估。尽管宏基因组DNA中含有残留的腐殖酸,但质量和纯度相当稳定可靠。提取的DNA成功扩增出16S rRNA区域。扩增产物适用于进一步的应用,如通过变性梯度凝胶电泳(DGGE)进行基于多样性的分析。
这些方法在研究分子多样性和从总DNA中探索功能基因方面似乎具有广泛的适用性。
该方法简单、耗时短,便于从盐渍土中快速分离出可用于PCR扩增的总基因组DNA。该方法获得了质量良好的DNA,适用于宏基因组学研究。该研究结果也具有重要意义,因为目前仅对少数极端环境,特别是盐渍生境的宏基因组潜力进行了探索。