共查询到6条相似文献,搜索用时 15 毫秒
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During the processes of claiming land from the sea, river sediments are used to fill and transform the sea area along the margin of islands and lands into new lands. These activities would probably affect microbial ecosystems of the beach sediment. However, little is known about these effects. In this study, a simulation test was conducted to evaluate these effects. Pyrosequencing technique was employed to assess the effects of river sediment addition to the beach bacterial communities. The used river sediments were collected from different rivers. The results indicated that river sediment addition greatly impacted microbial ecosystems of the beach and caused a clear shift in the beach bacterial community composition. These processes remarkably increased toxic metals and decreased the bacterial diversity in the beach sediment, mainly including the phyla of Bacteroidetes, Cyanobacteria, Proteobacteria, and Spirochaetes. River sediment addition caused an increase in potentially pathogenic bacterial genera of the beach sediment. Bacterial phylotype richness in the beach without river sediment addition was higher than that in the beach with river sediment input. There were significant differences in bacterial communities between beach sediments with and without river sediment addition, and the most dominant classes were Gammaproteobacteria and Flavobacteria. 相似文献
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Shuting ZHANG Bo WEI Xin YU Bing LIU Zhuoying WU Li GU 《Frontiers of Environmental Science & Engineering》2010,4(4):459-465
The biologic activated carbon (BAC) process is widely used in drinking water treatments. A comprehensive molecular analysis of the microbial community structure provides very helpful data to improve the reactor performance. However, the bottleneck of deoxyribonucleic acid (DNA) extraction from BAC attached biofilm has to be solved since the conventional procedure was unsuccessful due to firm biomass attachment and adsorption capacity of the BAC granules. In this study, five pretreatments were compared, and adding skim milk followed by ultrasonic vibration was proven to be the optimal choice. This protocol was further tested using the vertical BAC samples from the full-scale biofilter of Pinghu Water Plant. The results showed the DNA yielded a range of 40 μg·g-1 BAC (dry weight) to over 100 μg·g-1 BAC (dry weight), which were consistent with the biomass distribution. All results suggested that the final protocol could produce qualified genomic DNA as a template from the BAC filter for downstream molecular biology researches. 相似文献
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一种经济、简单的微生物基因组DNA的提取方法 总被引:6,自引:0,他引:6
获得一定浓度和纯度的DNA是进行分子生物学研究的基础。破解细胞壁与细胞膜是获得基因组DNA的前提,而蛋白质和核酸物质的分离是获得高质量DNA产物的关键。目前,主要采用的破壁方法有:冷冻研磨法、溶菌酶法、EDTA测等,这些方法一般采用复杂的裂解液体系,并借助蛋白酶K和RNA酶的帮助来获得高质量的抽提产物。由于细胞裂解体系不仅配制十分麻烦,而日部分药品有毒操作危险性大,此外部分药品及相关酶试剂价格昂贵。本文充分利用DNA在不同温度下自身可变性与复性的特性和在高盐与高温条件下蛋白质能够变性并沉淀。以无菌的SDS(c/c=20%)和NaCl(c/c=8%)的混合液作裂解体系,在沸水浴中破壁膜并使得部分的蛋白质变性和DNA变性并得到初步分离;随后在60℃和72℃水浴中使变性的DNA复性和重新凝聚,同时让RNA、蛋白质和细胞壁碎片等杂质降解或沉淀,从而获得高质量的DNA产物。 相似文献
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A laboratory experiment was used to investigate the mobilization kinetics of heavy metals from the sediment of a contaminated river located in northern Taiwan with varied concentrations of NTA and EDTA. We found that there were two stages of desorption in the mobilization of heavy metals from the sediment. As the concentrations of NTA and EDTA ranged 0–3.9 x 10‐4M (0–100mg/l) and 0–2.7 x 10‐4M (0–100mg/l) respectively, the mobilization percentages of heavy metals were proportional to the logarithm values of the concentrations of NTA and EDTA. The physical meaning of the multiple first‐order reaction was significant for the actual condition, but occasionally, it had more errors for Cu and Zn in the initial phase. The two‐constant model was most appropriate for describing the rates of mobilization of Pb, Cu, Zn, and Cr. The agreement between the diffusion model and the experimental data was satisfactory for Pb, Cu, Zn, and Cr only in the initial 5 h. 相似文献
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Hefu Pu Aamir Khan Mastoi Xunlong Chen Dingbao Song Jinwei Qiu Peng Yang 《Frontiers of Environmental Science & Engineering》2021,15(4):67