Weber S, Stubner S, Conrad R
Max-Planck-Institut für Terrestrische Mikrobiologie, D-35043 Marburg, Germany.
Appl Environ Microbiol. 2001 Mar;67(3):1318-27. doi: 10.1128/AEM.67.3.1318-1327.2001.
Rice straw is a major substrate for the production of methane, a greenhouse gas, in flooded rice fields. The bacterial community degrading rice straw under anoxic conditions was investigated with molecular methods. Rice straw was incubated in paddy soil anaerobically for 71 days. Denaturing gradient gel electrophoresis (DGGE) of the amplified bacterial 16S rRNA genes showed that the composition of the bacterial community changed during the first 15 days but then was stable until the end of incubation. Fifteen DGGE bands with different signal intensities were excised, cloned, and sequenced. In addition, DNA was extracted from straw incubated for 1 and 29 days and the bacterial 16S rRNA genes were amplified and cloned. From these clone libraries 16 clones with different electrophoretic mobilities on a DGGE gel were sequenced. From a total of 31 clones, 20 belonged to different phylogenetic clusters of the clostridia, i.e., clostridial clusters I (14 clones), III (1 clone), IV (1 clone), and XIVa (4 clones). One clone fell also within the clostridia but could not be affiliated to one of the clostridial clusters. Ten clones grouped closely with the genera Bacillus (3 clones), Nitrosospira (1 clone), Fluoribacter (1 clones), and Acidobacterium (2 clones) and with clone sequences previously obtained from rice field soil (3 clones). The relative abundances of various phylogenetic groups in the rice straw-colonizing community were determined by fluorescence in situ hybridization (FISH). Bacteria were detached from the incubated rice straw with an efficiency of about 80 to 90%, as determined by dot blot hybridization of 16S rRNA in extract and residue. The number of active (i.e., a sufficient number of ribosomes) Bacteria detected with a general eubacterial probe (Eub338) after 8 days of incubation was 61% of the total cell counts. This percentage decreased to 17% after 29 days of incubation. Most (55%) of the active cells on day 8 belonged to the genus Clostridium, mainly to clostridial clusters I (24%), III (6%), and XIVa (24%). An additional 5% belonged to the Cytophaga-Flavobacterium cluster of the Cytophaga-Flavobacterium-Bacteroides phylum, 4% belonged to the alpha, beta, and gamma Proteobacteria, and 1.3% belonged to the Bacillus subbranch of the gram-positive bacteria with a low G+C content. The results show that the bacterial community colonizing and decomposing rice straw developed during the first 15 days of incubation and was dominated by members of different clostridial clusters, especially clusters I, III, and XIVa.
稻草是淹水稻田中产生甲烷(一种温室气体)的主要底物。采用分子方法研究了缺氧条件下分解稻草的细菌群落。将稻草在稻田土壤中厌氧培养71天。对扩增的细菌16S rRNA基因进行变性梯度凝胶电泳(DGGE)分析表明,细菌群落组成在培养的前15天发生了变化,但随后直至培养结束都保持稳定。切除了15条具有不同信号强度的DGGE条带,进行克隆和测序。此外,从培养1天和29天的稻草中提取DNA,对细菌16S rRNA基因进行扩增和克隆。从这些克隆文库中,对在DGGE凝胶上具有不同电泳迁移率的16个克隆进行了测序。在总共31个克隆中,20个属于梭菌的不同系统发育簇,即梭菌簇I(14个克隆)、III(1个克隆)、IV(1个克隆)和XIVa(4个克隆)。有一个克隆也属于梭菌,但无法归入任何一个梭菌簇。10个克隆与芽孢杆菌属(3个克隆)、亚硝化螺菌属(1个克隆)、噬氟菌属(1个克隆)、嗜酸菌属(2个克隆)以及先前从稻田土壤中获得的克隆序列(3个克隆)紧密聚类。通过荧光原位杂交(FISH)确定了稻草定殖群落中各种系统发育组的相对丰度。通过对提取物和残渣中16S rRNA的斑点杂交测定,从培养的稻草上分离细菌的效率约为80%至90%。培养8天后,用通用真细菌探针(Eub338)检测到的活性(即有足够数量核糖体)细菌数量占总细胞数的61%。培养29天后,这一百分比降至17%。培养第8天,大多数(55%)活性细胞属于梭菌属,主要属于梭菌簇I(24%)、III(6%)和XIVa(24%)。另外5%属于噬纤维菌 - 黄杆菌 - 拟杆菌门的噬纤维菌 - 黄杆菌簇,4%属于α、β和γ变形菌门,1.3%属于低G + C含量革兰氏阳性菌的芽孢杆菌亚分支。结果表明,定殖并分解稻草的细菌群落在培养的前15天形成,且以不同梭菌簇的成员为主,尤其是簇I、III和XIVa。