期刊文献+

污水处理活性污泥微生物群落多样性研究 被引量:25

Microbial Population Diversity of Activated Sludge for Wastewater Treatment
下载PDF
导出
摘要 为研究污水处理活性污泥微生物多样性,提取了活性污泥宏基因组DNA,并采用细菌通用引物27F和1492R扩增了上海污泥厂活性污泥细菌16S rDNA片段,构建了细菌16S rDNA克隆文库,并对该文库中的微生物群落进行了分析。共获得200条高质量序列并建立系统发育树,结果显示活性污泥主要的细菌类群为变形菌门(Proteobacteria)(91.9%)、厚壁菌门(Firmicures)(4.6%)、拟杆菌门(Bacteroidetes)(2%)、绿弯菌门(Chloroflexi)(0.5%)、硝化螺菌门(Nitrospirae)(1%)。其中,明显的优势菌群为Alcaligenes feacalis(55%)、Pseudomonas aeruginosa(12.8%)和Stenotrophomonas(12.8%),优势菌的产酶能力在活性污泥中显示生态修复功能菌的作用。 In order to study the microbial diversity of activated sludge (AS) for wastewater treatment, the macro-ge- notate DNA of the AS was extracted from a wastewater factory in Shanghai. The 16S rDNA of the AS bacteria was am- plified using bacteria general primers 27F and 1492R to construct the bacterial 16S rDNA clone library, and analyzed the microbial population of the library. All together 200 bands of high quality sequences were obtained and established a phylogenetie tree. The results showed that the main bacterial population of the AS was the phyla of Proteobacteria (91.9%) , Firmicutes (4.6%) , Baeteroidetes (2%) , Chloroflexi (0.5%), Nitrospirae (1%). Among them Al- caligenesfeacalis (55%) , Pseudomonas aeruginosa ( 12.8% ) , and Stenotrophomonas ( 12.8% ) were noticeably dominant bacterial population, enzyme production capacity of the dominant bacteria showed the ecological restoration function in the AS.
出处 《微生物学杂志》 CAS CSCD 2012年第4期1-5,共5页 Journal of Microbiology
基金 上海市科学技术委员会项目(09320503600)
关键词 活性污泥 宏基因组DNA 16S rDNA克隆文库 微生物多样性 activated sludge macro-gcnomic DNA 16S rDNA clone library microbial diversity
  • 相关文献

参考文献15

  • 1Britt-Marie Wil6n, Motoharu Onuki, Malte Hermansson,et a]. Microbial community structure in activated sludge floc analysed by fluorescence in situ hybridization and its relation to floc sta- bility [ J ]. Water Research,2008,42 ( 8-9 ) :2300 -2308.
  • 2Jiang CJ, Hao ZY, Zeng R, et al. Characterization of a novel serine protease inhibiter gene from a marine metagenome [J ] Mar Drugs,2011,9(9) :1487-1501.
  • 3Zhou J, Bruns MA, Tiedje JM. DNA Recovery from soils of di- verse composition [J]. App| Environ Microbio], 1996,62 ( 2 ) : 316-322.
  • 4Annamalai N, Kumar A, Saravanakumar A, et al. Character-ization of protease from Alcaliger faecali and its antibacterial activity on fish pathogens[J]. J Environ Biol, 2011,32 ( 6 ) : 781-786.
  • 5Annamalai N, Veeramuthu Rajeswari M, Vijayalakshmi S,et al. Purification and characterization of chitinase from Alcallgenes faeealis AU02 by utilizing marine wastes and its antioxidant ac- tivit[ J]. Ann Microhiol, 201 ! ,61 (4) :801-807.
  • 6Liu ZQ, Dong LZ, Cheng F,et al. Gene cloning, expression, and characterization of a nitrilase from Alcallgenes faecalis 7_jUTBI0[J]. J Agfic Food Chem,2011,59(21): 11560- 1 1570.
  • 7Zhao B, An Q, He YL, ct al. N(2)O and N(2) production during hetcrotrophic nitrification by Alcaligenes faecalis strain NR[ J]. Bioresour Technol,2012 ,116 :379-385.
  • 8Ye RW, Thomas SM. Microbial nitrogen cycles: physiology, genomics and applications[J]. Current Opinion in Microbiolo- gy,2001,4(3) :307-312.
  • 9Mahanta N, Gupta A, Khare SK. Production of protease and lipase by solvent tolerant Pseudomonas aeruginosa PseA in sol- id-state fermentation using Jatropha curcas seed cake as sub- strate [ J ]. Bioresource Technology,2008,99 ( 6 ) : 1729 -1735.
  • 10De Azeredo LA, De Lima MB, Coelho RR, et al. Thermophilic protease production by Streptomyces sp. 594 in submerged and solid-state fermentations using feather meal[ J]. Journal of Ap- plied microbiology,2006,100(4) :641-647.

同被引文献366

引证文献25

二级引证文献107

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部