Chénier M R, Beaumier D, Fortin N, Roy R, Driscoll B T, Lawrence J R, Greer C W
Biotechnology Research Institute, National Research Council of Canada, 6100 Royalmount Avenue, Montreal, Quebec, Canada H4P 2R2.
Appl Environ Microbiol. 2006 Jan;72(1):575-84. doi: 10.1128/AEM.72.1.575-584.2006.
Biofilms were cultivated on polycarbonate strips in rotating annular reactors using South Saskatchewan River water during the fall of 1999 and the fall of 2001, supplemented with carbon (glucose), nitrogen (NH4Cl), phosphorus (KH2PO4), or combined nutrients (CNP), with or without hexadecane, a model compound representing aliphatic hydrocarbons used to simulate a pollutant. In fall 1999 and fall 2001, comparable denitrification activities and catabolic potentials were observed in the biofilms, implying that denitrifying populations showed similar activity patterns and catabolic potentials during the fall from year to year in this river ecosystem, when environmental conditions were similar. Both nirS and nirK denitrification genes were detected by PCR amplification, suggesting that both denitrifying bacterial subpopulations can potentially contribute to total denitrification. Between 91.7 and 99.8% of the consumed N was emitted in the form of N2, suggesting that emission of N2O, a major potent greenhouse gas, by South Saskatchewan River biofilms is low. Denitrification was markedly stimulated by the addition of CNP, and nirS and nirK genes were predominant only in the presence of CNP. In contrast, individual nutrients had no impact on denitrification and on the occurrence of nirS and nirK genes detected by PCR amplification. Similarly, only CNP resulted in significant increases in algal and bacterial biomass relative to control biofilms. Biomass measurements indicated a linkage between autotrophic and heterotrophic populations in the fall 1999 biofilms. Correlation analyses demonstrated a significant relationship (P < or = 0.05) between the denitrification rate and the biomass of algae and heterotrophic bacteria but not cyanobacteria. At the concentration assessed (1 ppb), hexadecane partially inhibited denitrification in both years, slightly more in the fall of 2001. This study suggested that the response of the anaerobic heterotrophic biofilm community may be cyclic and predictable from year to year and that there are interactive effects between nutrients and the contaminant hexadecane.
1999年秋季和2001年秋季,在旋转环形反应器中的聚碳酸酯条上利用南萨斯喀彻温河水培养生物膜,添加碳(葡萄糖)、氮(氯化铵)、磷(磷酸二氢钾)或组合营养素(CNP),添加或不添加十六烷(一种代表脂肪烃的模型化合物,用于模拟污染物)。在1999年秋季和2001年秋季,生物膜中观察到了相当的反硝化活性和分解代谢潜力,这意味着在该河流生态系统中,当环境条件相似时,每年秋季反硝化菌群表现出相似的活性模式和分解代谢潜力。通过PCR扩增检测到了nirS和nirK反硝化基因,表明这两个反硝化细菌亚群都可能对总反硝化有贡献。消耗的氮中有91.7%至99.8%以N2的形式排放,这表明南萨斯喀彻温河生物膜排放主要强效温室气体N2O的量很低。添加CNP显著刺激了反硝化作用,并且nirS和nirK基因仅在存在CNP时占主导地位。相比之下,单一营养素对反硝化以及通过PCR扩增检测到的nirS和nirK基因的出现没有影响。同样,只有CNP相对于对照生物膜导致藻类和细菌生物量显著增加。生物量测量表明1999年秋季生物膜中自养和异养菌群之间存在联系。相关性分析表明反硝化速率与藻类和异养细菌的生物量之间存在显著关系(P≤0.05),但与蓝细菌无关。在所评估的浓度(1 ppb)下,十六烷在这两年中都部分抑制了反硝化作用,在2001年秋季抑制作用稍强。这项研究表明,厌氧异养生物膜群落的反应可能是周期性的且每年可预测,并且营养素与污染物十六烷之间存在相互作用。