| PCR-DGGE研究处理垃圾渗滤液序批式生物膜反应器(SBBR)中的细菌多样性 |
| 摘要点击 2667 全文点击 2076 投稿时间：2006-07-13 修订日期：2006-08-24 |
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| 中文关键词 16S rDNA SBBR PCR DGGE 垃圾渗滤液 系统发育分析 |
| 英文关键词 16S rDNA SBBR PCR DGGE landfill leachate phylogenetic analysis |
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| 中文摘要 |
| 为了研究序批式生物膜反应器中的细菌多样性及其脱氮的微生物学机理，为工艺改进提供依据，从同步高效去除垃圾渗滤液中高氨氮和高COD的SBBR生物膜和渗滤液原水中采集微生物样品并提取微生物总DNA，使用细菌通用引物对（GC341F/907R）从总DNA中成功扩增出目标16S rDNA片段，然后对扩增的16S rDNA进行DGGE，对凝胶染色并进行条带统计分析和切胶测序，使用序列数据进行同源性分析并建立了系统发育树.结果表明，该驯化后的SBBR生物膜和渗滤液原水中都有比较丰富的细菌多样性，驯化的生物膜细菌主要来自渗滤液原水，而且生物膜细菌在反应器正常运行时不会出现明显的群落结构变化；在该SBBR中有多种硝化细菌与反硝化细菌、好氧反硝化细菌和厌氧氨氧化细菌共存，说明该反应器中可能同时存在全程硝化反硝化、同步硝化反硝化和厌氧氨氧化3种脱氮方式.研究结果为SBBR脱氮微生物机理研究提供了一些有价值的参考依据. |
| 英文摘要 |
| For studying the bacterial diversity and the mechanism of denitrification in sequencing bath biofilm reactor (SBBR) treating landfill leachate to provide microbial evidence for technique improvements, total microbial DNA was extracted from samples which were collected from natural landfill leachate and biofilm of a SBBR that could efficiently remove NH+4-N and COD of high concentration. 16S rDNA fragments were amplified from the total DNA successfully using a pair of universal bacterial 16S rDNA primer, GC341F and 907R, and then were used for denaturing gradient gel electrophoresis (DGGE) analysis. The bands in the gel were analyzed by statistical methods and excided from the gel for sequencing, and the sequences were used for homology analysis and then two phylogenetic trees were constructed using DNAStar software. Results indicated that the bacterial diversity of the biofilm in SBBR and the landfill leachate was abundant, and no obvious change of community structure happened during running in the biofilm, in which most bacteria came from the landfill leachate. There may be three different modes of denitrification in the reactor because several different nitrifying bacteria, denitrifying bacteria and anaerobic ammonia oxidation bacteria coexisted in it. The results provided some valuable references for studying microbiological mechanism of denitrification in SBBR. |
