Kindaichi Tomonori, Ito Tsukasa, Okabe Satoshi
Department of Urban and Environmental Engineering, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan.
Appl Environ Microbiol. 2004 Mar;70(3):1641-50. doi: 10.1128/AEM.70.3.1641-1650.2004.
Ecophysiological interactions between the community members (i.e., nitrifiers and heterotrophic bacteria) in a carbon-limited autotrophic nitrifying biofilm fed only NH(4)(+) as an energy source were investigated by using a full-cycle 16S rRNA approach followed by microautoradiography (MAR)-fluorescence in situ hybridization (FISH). Phylogenetic differentiation (identification) of heterotrophic bacteria was performed by 16S rRNA gene sequence analysis, and FISH probes were designed to determine the community structure and the spatial organization (i.e., niche differentiation) in the biofilm. FISH analysis showed that this autotrophic nitrifying biofilm was composed of 50% nitrifying bacteria (ammonia-oxidizing bacteria [AOB] and nitrite-oxidizing bacteria [NOB]) and 50% heterotrophic bacteria, and the distribution was as follows: members of the alpha subclass of the class Proteobacteria (alpha-Proteobacteria), 23%; gamma-Proteobacteria, 13%; green nonsulfur bacteria (GNSB), 9%; Cytophaga-Flavobacterium-Bacteroides (CFB) division, 2%; and unidentified (organisms that could not be hybridized with any probe except EUB338), 3%. These results indicated that a pair of nitrifiers (AOB and NOB) supported a heterotrophic bacterium via production of soluble microbial products (SMP). MAR-FISH revealed that the heterotrophic bacterial community was composed of bacteria that were phylogenetically and metabolically diverse and to some extent metabolically redundant, which ensured the stability of the ecosystem as a biofilm. alpha- and gamma-Proteobacteria dominated the utilization of [(14)C]acetic acid and (14)C-amino acids in this biofilm. Despite their low abundance (ca. 2%) in the biofilm community, members of the CFB cluster accounted for the largest fraction (ca. 64%) of the bacterial community consuming N-acetyl-D-[1-(14)C]glucosamine (NAG). The GNSB accounted for 9% of the (14)C-amino acid-consuming bacteria and 27% of the [(14)C]NAG-consuming bacteria but did not utilize [(14)C]acetic acid. Bacteria classified in the unidentified group accounted for 6% of the total heterotrophic bacteria and could utilize all organic substrates, including NAG. This showed that there was an efficient food web (carbon metabolism) in the autotrophic nitrifying biofilm community, which ensured maximum utilization of SMP produced by nitrifiers and prevented buildup of metabolites or waste materials of nitrifiers to significant levels.
通过全周期16S rRNA方法结合微自显影(MAR)-荧光原位杂交(FISH),研究了仅以NH(4)(+)作为能源的碳限制自养硝化生物膜中群落成员(即硝化细菌和异养细菌)之间的生态生理相互作用。通过16S rRNA基因序列分析对异养细菌进行系统发育分化(鉴定),并设计FISH探针来确定生物膜中的群落结构和空间组织(即生态位分化)。FISH分析表明,这种自养硝化生物膜由50%的硝化细菌(氨氧化细菌[AOB]和亚硝酸盐氧化细菌[NOB])和50%的异养细菌组成,其分布如下:变形菌纲α亚类(α-变形菌)成员占23%;γ-变形菌占13%;绿色非硫细菌(GNSB)占9%;噬纤维菌-黄杆菌-拟杆菌(CFB)类群占2%;未鉴定的(除EUB338外不能与任何探针杂交的生物)占3%。这些结果表明,一对硝化细菌(AOB和NOB)通过产生可溶性微生物产物(SMP)来支持一种异养细菌。MAR-FISH显示,异养细菌群落由系统发育和代谢多样且在一定程度上代谢冗余的细菌组成,这确保了作为生物膜的生态系统的稳定性。α-和γ-变形菌在该生物膜中对[(14)C]乙酸和(14)C-氨基酸的利用中占主导地位。尽管CFB类群在生物膜群落中的丰度较低(约2%),但其成员在消耗N-乙酰-D-[1-(14)C]葡糖胺(NAG)的细菌群落中占最大比例(约64%)。GNSB占消耗(14)C-氨基酸细菌的9%和消耗[(14)C]NAG细菌的27%,但不利用[(14)C]乙酸。分类在未鉴定组中的细菌占异养细菌总数的6%,并且可以利用包括NAG在内的所有有机底物。这表明在自养硝化生物膜群落中存在一个有效的食物网(碳代谢),它确保了硝化细菌产生SMP的最大利用,并防止硝化细菌的代谢产物或废料积累到显著水平。