Methanogenic populations involved in the degradation of rice straw in anoxic paddy soil

被引:61
作者
Weber, S [1 ]
Lueders, T [1 ]
Friedrich, MW [1 ]
Conrad, R [1 ]
机构
[1] Max Planck Inst Terr Mikrobiol, D-35043 Marburg, Germany
关键词
methanogen; small subunit ribosomal RNA gene; terminal restriction fragment length polymorphism analysis; rice cluster I; slot blot hybridization; Archaea;
D O I
10.1111/j.1574-6941.2001.tb00877.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Addition of straw to anoxic rice field soil stimulates production of CH4, an important greenhouse gas. The archaeal community colonizing rice straw was investigated by molecular methods targeting the small subunit ribosomal RNA gene. Cloning and sequencing of 60 clones detected predominantly relatives of Methanobacterium spp. (38 clones) and Methanosarcina spp. (16 clones). Terminal restriction fragment length polymorphisin (T-RFLP) analysis confirmed the dominance of Methanobacteriaceae and Methanosarcinaceae, and in addition showed restriction fragments characteristic for Rice cluster I (RC-I) methanogens. A new oligonucleotide probe specific for RC-I was designed. Quantitative slot blot hybridization of extracted rRNA with this probe indicated the presence of an active population of RC-I methanogens. Other methanogenic groups (e.g. Methanomicrobiaceae, Methanosaetaceae), although present and active in soil, could not be conclusively detected on rice straw. The methanogenic community pattern on straw, as revealed by T-RFLP and quantitative rRNA probing, was fairly constant with incubation time (8-57 days), but the total activity of methanogenic Archaea almost doubled. Our results indicate that the methanogens colonizing rice straw are less diverse than those inhabiting the soil. (C) 2001 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 20
页数:10
相关论文
共 52 条
[1]   The oligonucleotide probe database [J].
Alm, EW ;
Oerther, DB ;
Larsen, N ;
Stahl, DA ;
Raskin, L .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (10) :3557-3559
[2]   FLUORESCENT-OLIGONUCLEOTIDE PROBING OF WHOLE CELLS FOR DETERMINATIVE, PHYLOGENETIC, AND ENVIRONMENTAL-STUDIES IN MICROBIOLOGY [J].
AMANN, RI ;
KRUMHOLZ, L ;
STAHL, DA .
JOURNAL OF BACTERIOLOGY, 1990, 172 (02) :762-770
[3]   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
[4]  
[Anonymous], 1996, MICROBES ENVIRON, DOI DOI 10.1264/JSME2.11.73
[5]   GENE ORGANIZATION AND PRIMARY STRUCTURE OF A RIBOSOMAL-RNA OPERON FROM ESCHERICHIA-COLI [J].
BROSIUS, J ;
DULL, TJ ;
SLEETER, DD ;
NOLLER, HF .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 148 (02) :107-127
[6]  
Buckley DH, 1998, APPL ENVIRON MICROB, V64, P4333
[7]  
Chin KJ, 1999, APPL ENVIRON MICROB, V65, P5042
[8]  
Chin KJ, 1999, APPL ENVIRON MICROB, V65, P2341
[9]   BIOGEOCHEMICAL ASPECTS OF ATMOSPHERIC METHANE [J].
Cicerone, R. ;
Oremland, R. .
GLOBAL BIOGEOCHEMICAL CYCLES, 1988, 2 (04) :299-327
[10]   ARCHAEA IN COASTAL MARINE ENVIRONMENTS [J].
DELONG, EF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5685-5689