Diversity and structure of the archaeal community in the leachate of a full-scale recirculating landfill as examined by direct 16S rRNA gene sequence retrieval

被引:41
作者
Huang, LN
Zhou, H
Chen, YQ
Luo, S
Lan, CY
Qu, LH [1 ]
机构
[1] Zhongshan Univ, Key Lab Gene Engn, Minist Educ, Sch Life Sci, Guangzhou 510275, Peoples R China
[2] Zhongshan Univ, Dept Environm Sci, Guangzhou 510275, Peoples R China
关键词
landfill; leachate recirculation; Archaea; molecular diversity; 16S rDNA;
D O I
10.1111/j.1574-6968.2002.tb11353.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The diversity and structure of the archaeal community in the effluent leachate from a full-scale recirculating landfill was characterized by direct 16S rRNA gene (16S rDNA) retrieval. Total-community DNA was extracted from the microbial assemblages in the landfill leachate, and archaeal 16S rDNAs were amplified with a universally conserved primer and an Archaea-specific primer. The amplification product was then used to construct a 16S rDNA clone library, and 70 randomly selected archaeal clones in the library were grouped by restriction fragment length polymorphism (RFLP) analysis. Sequencing and phylogenetic analysis of representatives from each unique RFLP type showed that the archaeal library was dominated by methanogen-like rDNAs. Represented in the kingdom of Euryarchaeota were phylotypes highly similar to the methanogenic genera Methanoculleus, Methanosarcina, Methanocorpusculum, Methanospirillum and Methanogenium, where the clone distribution was 48, 11, 3, 1 and 1, respectively. No sequences related to known Methanosaeta spp. were retrieved. Four rDNA clones were not affiliated with the known methanogenic Archaea, but instead, they were clustered with the uncultured archaeal sequences recently recovered from anaerobic habitats. Two chimeric sequences were identified among the clones analyzed. (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:235 / 240
页数:6
相关论文
共 26 条
[1]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[2]  
[Anonymous], MICROBIOL SOLID WAST
[3]  
[Anonymous], PROGR WATER TECHNOLO
[4]   METHANOGENS - RE-EVALUATION OF A UNIQUE BIOLOGICAL GROUP [J].
BALCH, WE ;
FOX, GE ;
MAGRUM, LJ ;
WOESE, CR ;
WOLFE, RS .
MICROBIOLOGICAL REVIEWS, 1979, 43 (02) :260-296
[5]   BACTERIAL COMMUNITY STRUCTURES OF PHOSPHATE-REMOVING AND NON-PHOSPHATE-REMOVING ACTIVATED SLUDGES FROM SEQUENCING BATCH REACTORS [J].
BOND, PL ;
HUGENHOLTZ, P ;
KELLER, J ;
BLACKALL, LL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (05) :1910-1916
[6]  
Dojka MA, 1998, APPL ENVIRON MICROB, V64, P3869
[7]   16S rRNA genes reveal stratified open ocean bacterioplankton populations related to the Green Non-Sulfur bacteria [J].
Giovannoni, SJ ;
Rappe, MS ;
Vergin, KL ;
Adair, NL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7979-7984
[8]   Molecular microbial diversity of an anaerobic digestor as determined by small-subunit rDNA sequence analysis [J].
Godon, JJ ;
Zumstein, E ;
Dabert, P ;
Habouzit, F ;
Moletta, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (07) :2802-2813
[9]  
Greenberg A. E., 1992, STANDARD METHODS EXA