PCR-DGGE方法分析原油储层微生物群落结构及种群多样性

使用基于 16 S r DNA的 PCR- DGGE(变性梯度凝胶电泳 )图谱分析结合条带割胶回收 DNA进行序列分析 ,对新疆克拉玛依油田一中区注水井 (12 # 9- 11)和与该注水井相应的两个采油井 (12 # 9- 9S、13# 11- 8)井口样品微生物群落的多样性进行了比较并鉴定了部分群落成员。 DGGE图谱聚类分析表明注水井与两油井微生物群落的相似性分别为 30 %和 2 0 % ,而两油井间微生物群落结构的相似性为 5 4 %。DGGE图谱中优势条带序列分析表明注水井样品和油井样品中的优势菌群为未培养的环境微生物 ,它们与数据库中 α、γ、δ、ε变形杆菌 (Proteobacteria)和拟杆菌 (Bacteroidetes)有很近的亲缘关系。 DGGE与分子克隆相结合的分子生物学方法在研究微生物提高原油采收率 (MEOR)机理 ,以及指导 MEOR在油田生产中的应用有着重要的意义     

PCR-DGGE技术在农田土壤微生物多样性研究中的应用

变性梯度凝胶电泳技术(DGGE)在微生物生态学领域有着广泛的应用。研究采用化学裂解法直接提取出不同农田土壤微生物基因组DNA,并以此基因组DNA为模板,选择特异性引物F357GC和R515对16S rRNA基因的V3区进行扩增,长约230bp的PCR产物经变性梯度凝胶电泳(DGGE)进行分离后,得到不同数目且分离效果较好的电泳条带。结果说明,DGGE能够对土壤样品中的不同微生物的16S rRNA基因的V3区的DNA扩增片断进行分离,为这些DNA片断的定性和鉴定提供了条件。与传统的平板培养方法相比,变性梯度凝胶电泳(DGGE)技术能够更精确的反映出土壤微生物多样性,它是一种有效的微生物多样性研究技术。     

PCR-DGGE技术分析染整废水微生物群落多样性

旨在揭示水解酸化-生物接触氧化工艺处理染整废水过程中的微生物多样性.取初级沉淀池,水解酸化池,生物接触氧化池和二沉池的活性污泥,通过细胞裂解直接提取基因组DNA,以细菌通用引物进行16S rRNA基因V3区域PCR扩增,将PCR产物进行变性梯度凝胶电泳,获得微生物群落的DNA特征指纹图谱,并对条带进行统计分析和切胶测序,进行了同源性分析并建立了系统发育树.研究表明,整个水处理过程中含有丰富的微生物群落,其中初级沉淀池、水解酸化池、二沉池和生物接触氧化池的污泥样品分别测出36条带、42条带、30条带和29条带.不同区段微生物群落间相似度最高达68％,最低达42.4％,说明群落间演替明显,不同工艺区段既存在共同的微生物种属也存在特异微生物种属.     

PCR-DGGE指纹图谱技术分析2型糖尿病模型小鼠胃微生物菌群结构

糖尿病患者多出现胃肠道功能紊乱,如急性胃炎、胃溃疡,以及胃动力低下,胃排空延迟、胃内细菌过度滋长等,进一步导致肠道疾病。研究糖尿病胃内容物菌群结构变化对研究糖尿病发病机理及并发症治疗具有重要意义。该项研究采用变性梯度凝胶电泳技术,对10只2型糖尿病模型小鼠及10只正常对照小鼠进行胃内容物和粘膜样本菌群结构研究。结果表明,实验组小鼠与对照组小鼠胃内容物和粘膜菌群条带数、多样性指数、丰富度指数、均匀度指数与优势度指数均无显著差异,且相似度系数差异不明显。而特异条带测序结果显示正常小鼠胃内含乳杆菌,实验组小鼠胃内乳杆菌含量很低甚至检测不到。提示胃内乳杆菌与2型糖尿病密切相关。     

乌梁素海湖滨湿地细菌群落结构多样性

【目的】了解乌梁素海湖滨湿地水陆过渡带细菌群落结构及多样性变化,探讨富营养化湖泊湿地基质条件对细菌群落结构的影响。【方法】应用变性梯度凝胶电泳(PCR-DGGE)技术,分析和比较了依陆向分布的4个水陆过渡带样点的湿地细菌群落结构多样性,采用典型对应分析(CCA)探讨了湿地基质因子对细菌多样性的影响。【结果】DGGE图谱显示依湖泊水体沉积物(S-1)→湖滨芦苇沼泽沉积物(S-2)→湖滨碱蓬盐化草甸土壤(S-3)→岸上白刺荒漠土壤(S-4),4个样点的条带数依次减少,对应菌群结构及多样性变化显著;多样性指数分析结果显示,Shannon-Wiener指数(H)、均匀度(E)、丰富度(S)以及Simpson指数(DS)均显示依陆向分布逐步下降的规律,即:S-1S-2S-3S-4。序列比对结果显示,沉积物及土壤细菌分属于变形菌门(78.6%)、酸杆菌门(7.1%)、拟杆菌门(14.3%)这3个细菌类群,优势菌门为变形菌门,而变形菌门又分为5个亚群,其中ε变形菌纲为优势亚群;CCA结果表明,图中各条带对应物种的分布受铵态氮、总氮、有机碳、水溶盐总量、氯离子以及钾离子影响最大。【结论】乌梁素海富营养化湖泊的水陆过渡带湿地细菌群落结构存在较大差异,富营养化相关基质因子对细菌多样性影响较大。这为研究富营养化湖泊湿地水陆过渡带的细菌结构多样性及空间异质性提供了科学依据。     

利用PCR-DGGE方法分析不同鸡群的盲肠微生物菌群结构变化

研究不同品种、饲养阶段的健康和不良鸡群对盲肠细菌种群结构和多样性的影响。使用基于16S rDNA的PCR-DGGE技术,结合割胶回收DNA进行克隆和测序,分别以4、6、10、16、20、40周龄蛋鸡及1、2、4、6、7、8周龄肉鸡健康、不良鸡群盲肠内容物为样本,研究其中特定细菌类群的16S rDNA序列片段指纹图谱,并进行聚类分析,鉴定特异性和共性种群。在两品种健康鸡群盲肠内容物的细菌群落中,Lactobacillus属菌株的相似性均高于不良鸡群,并且在不同饲养阶段的健康、不良鸡群间指纹图谱平均条带数差异显著(P<0.05);而Bacteroides属菌株在健康鸡群盲肠内容物细菌的相似性与不良鸡群较为相近,健康、不良鸡群间平均条带数差异显著(P<0.05);Clostridium属菌株在蛋鸡20、40周龄的平均条带数差异不显著(P>0.05),但肉鸡各周龄健康、不良鸡群间的平均条带数差异显著(P<0.05)。序列测序结果,在蛋鸡产蛋期健康、不良鸡群样本中均检测到能动乳杆菌(Lactobacillus agilis),而育雏和育成期中均检测到鸟乳杆菌(Lactobacillus aviaries)和不可培养细菌;两品种的健康、不良鸡群样本中均检测到Bacteroides属的生酸拟杆菌(Bacteroides acidifaciens)、不可培养物细菌(Uncultured bacterium);而健康、不良蛋鸡群样本中均检测到Clostridium属不可培养的变形菌(Uncultured proteobacterium),健康肉鸡群中检测到索氏志贺菌(Shigella sonnei),而两品种不良鸡群中均缺乏此类菌种。结果显示,不同品种、饲养阶段的鸡群,其盲肠细菌群落的组成差异显著,并且细菌种群结构对鸡群的生长发育影响较大。     

洪湖沉积物中真菌群落结构的垂直分布

湖泊沉积物中真菌的类群及其作用所知甚少。以长江中上游代表性湖泊洪湖为研究对象,从湖心截取了一个72cm长的沉积柱,通过rDNA内转录间隔区（ITS）的变性梯度凝胶电泳（DGGE）,对洪湖沉积物中真菌群落结构的垂直变化进行了分析。结果显示,DGGE条带以14－18cm层次为过渡,在2－14cm和14－72cm之间存在一定差异。Shannon-Weaver index（H′）在上下层之间有波动。聚类分析上层2－18cm和中下层18－72cm分别以不同的小类聚在一起。表明14－18cm以上和以下的类群存在差异,     

乡村沼气池污泥微生物多样性的研究

为了优化沼气池产气效率和开展污泥微生物多样性研究,通过对PCR-DGGE条件的优化,建立了农村户用沼气池污泥微生物16S r DNA V3区DGGE分析技术,通过DGGE技术分析了沼气池污泥中细菌和古细菌微生物多样性随沼气池深度的变化规律。同时通过构建污泥样品mcr A功能基因克隆文库,应用RFLP技术,开展了农村户用沼气池污泥样品中与次级代谢产物相关基因的功能基因多样性研究。结果显示,农村户用沼气池污泥中含有丰富的微生物资源,其中细菌群落受污泥深度因素影响小,而浅层污泥中古细菌群落与深层污泥中古菌群落却存在明显差异。所采集的沼气池污泥中含有较为丰富的产甲烷菌资源,其中可能存在类似功能或产生类似代谢物质的产甲烷菌。该结果为进一步优化群落结构、筛选功能基因提供了科学依据。     

DG-DGGE分析产氢发酵系统微生物群落动态及种群多样性

应用双梯度-变性梯度凝胶电泳(DG-DGGE)对生物制氢反应器微生物种群的动态变化及多样性进行监测。间隔7d从反应器取厌氧活性污泥,以细菌16SrDNA通用引物进行V2～V3区域PCR扩增,长约450bp的PCR产物经DGGE分离后,获得污泥微生物群落的16SrDNA指纹图谱。污泥接种到反应器后微生物群落中既有原始种群的消亡和增长,也有次级种群的强化和演变。反应器在运行初期群落演替迅速,15d时微生物群落结构变化最大。群落结构的相似性随着演替时间的增加而逐渐升高,种群动态变化后形成稳定的群落结构。29d时微生物多样性基本保持不变,微生物优势种属达到19个OTU。在细菌竞争和协同作用制约下,种群多样性降低后趋于稳定,形成顶级群落。有些种群在群落结构中一直存在,是群落建成的原始种群,原始种群与次级种群在代谢过程中具有协同作用,表现出群落的综合生态特征。     

新疆石油污染土壤苯并(a)芘降解微生物多样性研究

为研究新疆石油开采区污染土壤中苯并(a)芘降解微生物的群落结构特点,采集克拉玛依石油开采区受污染程度不同的土壤样品, 以苯并(a)芘为唯一碳源、氮源的无机盐培养基五代富集培养, 采用PCR-DGGE 技术对第五代富集培养物的微生物群落结构开展研究, 根据DGGE 指纹图谱分析它们的遗传多样性。研究显示: 三个不同污染样品微生物多样性指数(H) 丰度(S)和均匀度(EH)均有所不同, 重度污染土样降解苯并(a)芘的微生物类群最为丰富, 其次是中度污染土样, 最少的是轻度污染土样; 并且三个样品微生物类群种类差异较大, 菌落相似性低。对 DGGE 的优势条带序列分析, 同源性最高的微生物分别属于变形菌门(Proteobacteria)、拟杆菌门(Bacteroidetes)、放线菌门(Actinobacteria)和厚壁菌门(Firmicutes)。研究表明新疆石油开采区污染程度不同土壤中降解苯并(a)芘的微生物群落结构不同, 提示污染严重的环境里可能蕴藏着高效降解苯并(a)芘的微生物资源。     

Microbial diversity in lake sediments detected by PCR-DGGE

In this study, PCR-denaturing gradient gel electrophoresis (DGGE) was applied to analyze the microbial communities in lake sediments from Lake Xuanwu, Lake Mochou in Nanjing and Lake Taihu in Wuxi. Sediment samples from seven locations in three lakes were collected and their genomic DNAs were extracted. The DNA yields of the sediments of Lake Xuanwu and Lake Mochou were high (10 μg/g), while that of sediments in Lake Taihu was relatively low. After DNA purification, the 16S rDNA genes (V3 to V5 region) were amplified and the amplified DNA fragments were separated by parallel DGGE. The DGGE profiles showed that there were five common bands in all the lake sediment samples indicating that there were similarities among the populations of microorganisms in all the lake sediments. The DGGE profiles of Lake Xuanwu and Lake Mochou were similar and about 20 types of microorganisms were identified in the sediment samples of both lakes. These results suggest that the sediment samples of these two city lakes (Xuanwu, Mochou) have similar microbial communities. However, the DGGE profiles of sediment samples in Lake Taihu were significantly different from these two lakes. Furthermore, the DGGE profiles of sediment samples in different locations in Lake Taihu were also different, suggesting that the microbial communities in Lake Taihu are more diversified than those in Lake Xuanwu and Lake Mochou. The differences in microbial diversity may be caused by the different environmental conditions, such as redox potential, pH, and the concentrations of organic matters. Seven major bands of 16S rDNA genes fragments from the DGGE profiles of sediment samples were further re-amplified and sequenced. The results of sequencing analysis indicate that five sequences shared 99%–100% homology with known sequences (Bacillus and Brevibacillus, uncultured bacteria), while the other two sequences shared 93%–96% homology with known sequences (Acinetobacter, and Bacillus). The study shows that the PCR-DGGE technique combined with sequence analysis is a feasible and efficient method for the determination of microbial communities in sediment samples. __________ Translated from Acta Ecologica Sinica, 2006, 26(11): 3610–3616 [译自: 生态学报]     

Microbial diversity in lake sediments detected by PCR-DGGE

In this study,PCR-denaturing gradient gel electrophoresis (DGGE) was applied to analyze the microbial communities in lake sediments from Lake Xuanwu,Lake Mochou in Nanjing and Lake Taihu in Wuxi.Sediment samples from seven locations in three lakes were collected and their genomic DNAs were extracted.The DNA yields of the sediments of Lake Xuanwu and Lake Mochou were high (10 μg/g),while that of sediments in Lake Taihu was relatively low.After DNA purification,the 16S rDNA genes (V3 to V5 region) were amplified and the amplified DNA fragments were separated by parallel DGGE.The DGGE profiles showed that there were five common bands in all the lake sediment samples indicating that there were similarities among the populations of microorganisms in all the lake sediments.The DGGE profiles of Lake Xuanwu and Lake Mochou were similar and about 20 types of micro-organisms were identified in the sediment samples of both lakes.These results suggest that the sediment samples of these two city lakes (Xuanwu,Mochou) have similar microbial communities.However,the DGGE profiles of sediment samples in Lake Taihu were significantly differ-ent from these two lakes.Furthermore,the DGGE pro-files of sediment samples in different locations in Lake Taihu were also different,suggesting that the microbial communities in Lake Taihu are more diversified than those in Lake Xuanwu and Lake Mochou.The differences in microbial diversity may be caused by the different environmental conditions,such as redox potential,pH,and the concentrations of organic matters.Seven major bands of 16S rDNA genes fragments from the DGGE profiles of sediment samples were further re-amplified and sequenced.The results of sequencing analysis indicate that five sequences shared 99%-100% homology with known sequences (Bacillus and Brevibacillus,uncultured bacteria),while the other two sequences shared 93%-96% homology with known sequences (Acinetobacter,and Bacillus).The study shows that the PCR-DGGE tech-nique combined with sequence analysis is a feasible and efficient method for the determination of microbial com-munities in sediment samples.     

西北黄土高原柠条种植区土壤微生物多样性分析

柠条锦鸡儿(Caragana korshinskii)是我国黄土高原区重要的饲用豆科灌木植物。为揭示土壤微生物与柠条种植之间的关系,采用未培养技术提取样品宏基因组DNA,分别构建柠条根表、根际和自然土16SrDNA文库,分析各文库微生物群落的变化。结果显示,随距离柠条根部渐远,微生物数量呈现递减趋势。聚类分析发现,变形杆菌纲是根表土壤区系中的优势微生物种群(70.3%),尤其存在大量α-Proteobacteria类的能诱使植物形成根瘤的根瘤菌和对植物有促生作用的γ-Proteobacteria类微生物;而在根际和自然土中,酸杆菌属(Acidobacteria)和古菌(Archaea)数量较多。柠条根际的多样性指数最高,而根表和自然土微生物类群具有较高的优势度,表现出从根表、根际植物相关微生物到自然土单一简单微生物类群的过渡。说明植物根系和土壤环境与微生物类群具有相互选择性。     

茶园土壤微生物群落基因多样性

应用PCR技术,直接从土壤中抽提总DNA,扩增16S rDNA V3 片段,采用变性梯度凝胶电泳(DGGE)分析16S rDNA V3 片段的多态性,研究了杭州西湖梅家坞不同植茶年龄(8、50和90年)、不同利用方式(茶园、荒地和林地)的土壤微生物群落基因多样性.结果表明：不同植茶年龄和不同土地利用方式影响土壤微生物群落的基因多样性.荒地、茶园和林地土壤微生物群落基因多样性指数明显不同(P<0.05),其排列顺序为荒地>茶园>林地.不同植茶年龄的土壤中,50年茶园土壤的微生物群落基因多样性指数、微生物量碳和基础呼吸明显高于8年和90年茶园土壤(P<0.05).     

PCR-DGGE法在慢性胃炎病人舌苔菌群结构研究中的应用

在早间未刷牙和进食的情况下,刮取胃炎病人与正常人舌苔,去除杂质,分离菌体,采用酚/氯仿法抽提细菌基因组DNA,并对其中16S rDNA V3可变区进行聚合酶链式反应(PCR)扩增和变性梯度凝胶电泳(DGGE)测定.用Bionumerics软件对DGGE分子指纹图谱进行舌苔菌群结构相似性分析.实验结果表明,采用该方法成功地扩增出16S rDNA V3区片段,为230 bp.DGGE分子指纹图谱结果表明,正常人的舌苔菌群最高相似性为0.74,胃炎病人的舌苔菌群的最高相似性为0.52,正常人的舌苔菌群与胃炎病人的舌苔菌群相似性最高为0.38,即胃炎病人舌苔菌群结构发生了变化.     

海绵共附生细菌种群组成的PCR-DGGE基因指纹分析

采用不依赖于分离培养的16S rDNA的PCR-DGGE基因指纹技术对我国南海的细薄星芒海绵、皱皮软海绵、贪婪倔海绵、澳大利亚厚皮海绵体内的优势细菌的种群组成进行了比较分析。结果显示:每种海绵体内都含有丰富多样的细菌;通过DGGE指纹图的聚类分析发现来自同一海域的不同海绵的共附生细菌的种群组成具有明显不同,即共附生细菌具海绵宿主特异性;同时也发现有相同的细菌存在于不同的海绵体内。     

基于PCR-DGGE指纹图谱川纹笛鲷及圆白鲳消化道壁优势菌群结构比较分析

本文采用免培养的16S rDNA梯度凝胶电泳技术(DGGE)对集约化海水网箱养殖川纹笛鲷Lutjanus sebae及圆白鲳Ephippus orbis消化道壁优势菌群结构进行了比较分析。研究结果显示川纹笛鲷及圆白鲳消化道壁存在着大量细菌群落,对DGGE指纹图谱聚类分析表明两种鱼肠道壁及胃壁菌群组成相似度高于50%,其中二者肠道壁细菌组成相似性最高(67%),这些可能与两种鱼养殖在同一水域、摄食相同饵料相关,另外通过软件对DGGE指纹带谱相对丰度分析表明同种鱼肠道壁及胃壁具有相同最大优势菌群。同时,两种鱼消化道壁之间在细菌多样性及相对丰度上亦存在明显区别,圆白鲳消化道壁细菌多样性要高于川纹笛鲷,这可能归因于川纹笛鲷与圆白鲳在天然环境中栖息地的差异性。本研究通过首次建立不同海水鱼消化道壁16S rDNA-DGGE指纹图谱及比较分析,为澄清海水鱼消化道壁微生物区系奠定基础。     

内蒙古典型草原细菌群落结构的PCR-DGGE检测

用液氮冻融法和蛋白珠法对内蒙古典型草原土壤基因组DNA进行提取,用PCR—DGGE对细菌群落结构进行分析,并对主要的条带进行测序。发现蛋白珠法比液氮冻融法更能反应出实际的微生物群落结构和组成。内蒙古典型草原土壤细菌主要有5个分支：放线菌门（Actinobacteria）,变形菌门（Proteobacteria）的α、β及γ类群,拟杆纲门（Bacteriodetes）,芽单胞菌门（Gemmatimonadetes）和酸杆菌门（Acidobacteria）。与基因库中进行比较后发现有4个序列和已知的细菌种类相似达到了99％以上。     

Bacterial diversity in surface sediments from the Pacific Arctic Ocean

In order to assess bacterial diversity within four surface sediment samples (0–5 cm) collected from the Pacific Arctic Ocean, 16S ribosomal DNA clone library analysis was performed. Near full length 16S rDNA sequences were obtained for 463 clones from four libraries and 13 distinct major lineages of Bacteria were identified (α, β, γ, δ and ε-Proteobacteria, Acidobacteria, Bacteroidetes, Chloroflexi, Actinobacteria, Firmicutes, Planctomycetes, Spirochetes, and Verrucomicrobia). α, γ, and δ-Proteobacteria, Acidobacteria, Bacteroidetes, Actinobacteria were common phylogenetic groups from all the sediments. The γ-Proteobacteria were the dominant bacterial lineage, representing near or over 50% of the clones. Over 35% of γ-Proteobacteria clones of four clone library were closely related to cultured bacterial isolates with similarity values ranging from 94 to 100%. The community composition was different among sampling sites, which potentially was related to geochemical differences.