Howeler Michael, Ghiorse William C, Walker Larry P
Department of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14853, USA.
J Microbiol Methods. 2003 Jul;54(1):37-45. doi: 10.1016/s0167-7012(03)00006-x.
We quantified both DNA and humic acid concentrations during the extraction and purification of DNA from compost. The DNA extraction method consisted of bead-beating with SDS for cell lysis, poly(ethylene glycol)-8000 precipitation for preliminary DNA purification, and chromatography on a 10-ml Sephadex G-200 column for final DNA purification. Direct microscopic observation of pre- and post-lysis samples revealed that 95.3+/-2.3% of native cells was lysed. Sixty-three percent of the original DNA was lost during purification, resulting in a final DNA yield of 18.2+/-3.8 microg DNA/g of wet compost. The humic acid content was reduced by 97% during the purification steps resulting in a final humic acid concentration of 27+/-4.7 ng humic acid/microl. The purified DNA fragments were up to 14 kbp in size and were sufficiently free of contaminants to allow both restriction enzyme digestion by four different enzymes and PCR amplification of 16S rDNA.
在从堆肥中提取和纯化DNA的过程中,我们对DNA和腐殖酸的浓度进行了量化。DNA提取方法包括用SDS进行珠磨以裂解细胞,用聚乙二醇-8000沉淀进行初步DNA纯化,以及在10毫升葡聚糖G-200柱上进行色谱分析以进行最终DNA纯化。对裂解前后样品的直接显微镜观察表明,95.3±2.3%的天然细胞被裂解。在纯化过程中,63%的原始DNA损失,最终DNA产量为18.2±3.8微克DNA/克湿堆肥。在纯化步骤中,腐殖酸含量降低了97%,最终腐殖酸浓度为27±4.7纳克腐殖酸/微升。纯化后的DNA片段大小可达14千碱基对,且足够不含污染物,能够进行四种不同酶的限制性内切酶消化和16S rDNA的PCR扩增。