Zhao Hengzhi, Dai Shikun, Sun Wei, Wang Guanghua, Guo Yatao, Guo Jun, Xu Meiying, Wu Houbo, Li Xiang
South China Sea Institute of Oceanology Chinese Academy of Sciences, CAS Key Laboratory of Marine Bio-resources Sustainable Utilization, Guangzhou 510301, China.
Wei Sheng Wu Xue Bao. 2011 Mar;51(3):377-85.
By using brominated flame retardant we compared the bacterial diversity of highly polluted river sediment with that of nearby unpolluted lake.
Total DNA was extracted from unpolluted and highly polluted sediment sample by brominated flame retardant in Guiyu of China. The 16S rRNA gene was amplified by PCR using bacterial primer 27F and 1500R. The plasmid libraries of the amplicons were constructed. The positive clones with insert were screened on plates with IPTG/X-gal/Ap. Amplified ribosmal DNA restriction analysis (ARDRA) was carried out with restriction enzymes Hha I and Hinf I. Representative clones of each operational taxonomic unit based on the ARDRA patterns were selected to be sequenced. After proof reading and careful comparison to remove the chimeric sequences, the partial sequence of 16S rRNA gene were used for construction of the phylogenetic tree.
The result of blast searching showed that clones from unpolluted sediment sample belonged to alpha-Proteobacteria, beta-Proteobacteria, gamma-Proteobacteria, delta-Proteobacteria, Planctomycetes, Acidobacteria, Actinobacteria, Chloroflexi, Verrucomicrobia, Firmicutes, the predominant bacteria (30.2% of total clones) is Acidobacteria; most clones from polluted sediment belonged to alpha-Proteobacteria, beta-Proteobacteria, epsilon-Proteobacteria, delta-Proteobacteria, Planctomycetes, Acidobacteria, Actinobacteria, Chloroflexi, Bacteroidetes, Firmicutes, candidate division 0P01, candidate division OP08, the predominant bacteria (44.9% of total clones) are epsilon-Proteobacteria and Chloroflexi.
Bacterial community structure of polluted sediment has distinguished feature and obviously different from the unpolluted sediment sample, which is mainly reflected in the dominant position of epsilon-Proteobacteria and Chloroflexi in the bacterial flora.
通过使用溴化阻燃剂,比较了高度污染的河流沉积物与附近未受污染湖泊的细菌多样性。
在中国贵屿,采用溴化阻燃剂从未受污染和高度污染的沉积物样本中提取总DNA。使用细菌引物27F和1500R通过PCR扩增16S rRNA基因。构建扩增子的质粒文库。在含有IPTG/X-gal/Ap的平板上筛选带有插入片段的阳性克隆。用限制性内切酶Hha I和Hinf I进行扩增核糖体DNA限制性分析(ARDRA)。根据ARDRA模式选择每个操作分类单元的代表性克隆进行测序。经过校对和仔细比较以去除嵌合序列后,使用16S rRNA基因的部分序列构建系统发育树。
Blast搜索结果表明,来自未受污染沉积物样本的克隆属于α-变形菌纲、β-变形菌纲、γ-变形菌纲、δ-变形菌纲、浮霉菌门、酸杆菌门、放线菌门、绿弯菌门、疣微菌门、厚壁菌门,其中优势菌(占总克隆数的30.2%)是酸杆菌门;来自污染沉积物的大多数克隆属于α-变形菌纲、β-变形菌纲、ε-变形菌纲、δ-变形菌纲、浮霉菌门、酸杆菌门、放线菌门、绿弯菌门、拟杆菌门、厚壁菌门、候选分类单元0P01、候选分类单元OP08,优势菌(占总克隆数的44.9%)是ε-变形菌纲和绿弯菌门。
污染沉积物的细菌群落结构具有显著特征,与未受污染的沉积物样本明显不同,这主要体现在ε-变形菌纲和绿弯菌门在细菌菌群中的优势地位。