Devi Selvaraju Gayathri, Fathima Anwar Aliya, Radha Sudhakar, Arunraj Rex, Curtis Wayne R, Ramya Mohandass
Department of Genetic Engineering, SRM University, Kattankulathur, Tamilnadu, India.
Department of Chemical Engineering, Pennsylvania State University, University Park, Pennsylvania, United States of America.
PLoS One. 2015 Jul 13;10(7):e0132441. doi: 10.1371/journal.pone.0132441. eCollection 2015.
A rapid, cost effective method of metagenomic DNA extraction from soil is a useful tool for environmental microbiology. The present work describes an improved method of DNA extraction namely "powdered glass method" from diverse soils. The method involves the use of sterile glass powder for cell lysis followed by addition of 1% powdered activated charcoal (PAC) as purifying agent to remove humic substances. The method yielded substantial DNA (5.87 ± 0.04 μg/g of soil) with high purity (A260/280: 1.76 ± 0.05) and reduced humic substances (A340: 0.047 ± 0.03). The quality of the extracted DNA was compared against five different methods based on 16S rDNA PCR amplification, BamHI digestion and validated using quantitative PCR. The digested DNA was used for a metagenomic library construction with the transformation efficiency of 4 X 106 CFU mL-1. Besides providing rapid, efficient and economical extraction of metgenomic DNA from diverse soils, this method's applicability is also demonstrated for cultivated organisms (Gram positive B. subtilis NRRL-B-201, Gram negative E. coli MTCC40, and a microalgae C. sorokiniana UTEX#1666).
一种从土壤中快速、经济高效地提取宏基因组DNA的方法是环境微生物学的有用工具。目前的工作描述了一种改进的DNA提取方法,即从不同土壤中提取DNA的“玻璃粉末法”。该方法包括使用无菌玻璃粉末进行细胞裂解,然后添加1%的粉末状活性炭(PAC)作为净化剂以去除腐殖质。该方法产生了大量的DNA(5.87±0.04μg/g土壤),纯度高(A260/280:1.76±0.05),腐殖质减少(A340:0.047±0.03)。基于16S rDNA PCR扩增、BamHI消化,将提取的DNA质量与五种不同方法进行比较,并使用定量PCR进行验证。消化后的DNA用于构建宏基因组文库,转化效率为4×106 CFU mL-1。除了能从不同土壤中快速、高效且经济地提取宏基因组DNA外,该方法对培养的生物体(革兰氏阳性枯草芽孢杆菌NRRL-B-201、革兰氏阴性大肠杆菌MTCC40和微藻索氏梭菌UTEX#1666)的适用性也得到了证明。