Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA.
Environ Microbiol. 2010 May;12(5):1282-92. doi: 10.1111/j.1462-2920.2010.02172.x. Epub 2010 Feb 18.
Marine Crenarchaeota are among the most abundant microbial groups in the ocean, and although relatively little is currently known about their biogeochemical roles in marine ecosystems, recognition that Crenarchaeota posses ammonia monooxygenase (amoA) genes and may act as ammonia-oxidizing archaea (AOA) offers another means of probing the ecology of these microorganisms. Here we use a time series approach combining quantification of archaeal and bacterial ammonia oxidizers with bacterial community fingerprints and biogeochemistry, to explore the population and community ecology of nitrification. At multiple depths (150, 500 and 890 m) in the Southern California Bight sampled monthly from 2003 to 2006, AOA were enumerated via quantitative PCR of archaeal amoA and marine group 1 Crenarchaeota 16S rRNA genes. Based on amoA genes, AOA were highly variable in time - a consistent feature of marine Crenarchaeota- however, average values were similar at different depths and ranged from 2.20 to 2.76 x 10(4) amoA copies ml(-1). Archaeal amoA genes were correlated with Crenarchaeota 16S rRNA genes (r(2) = 0.79) and the slope of this relationship was 1.02, demonstrating that the majority of marine group 1 Crenarchaeota present over the dates and depths sampled possessed amoA. Two AOA clades were specifically quantified and compared with betaproteobacterial ammonia-oxidizing bacteria (beta-AOB) amoA genes at 150 m; these AOA groups were found to strongly co-vary in time (r(2) = 0.70, P < 0.001) whereas AOA : beta-AOB ratios ranged from 13 to 5630. Increases in the AOA : beta-AOB ratio correlated with the accumulation of nitrite (r(2) = 0.87, P < 0.001), and may be indicative of differences in substrate affinities and activities leading to periodic decoupling between ammonia and nitrite oxidation. These data capture a dynamic nitrogen cycle in which multiple microbial groups appear to be active participants.
海洋泉古菌是海洋中最丰富的微生物群体之一,尽管目前人们对它们在海洋生态系统中的生物地球化学作用知之甚少,但认识到泉古菌拥有氨单加氧酶(amoA)基因,并可能充当氨氧化古菌(AOA),为研究这些微生物的生态学提供了另一种手段。在这里,我们采用时间序列方法,结合定量测定氨氧化古菌和细菌的氨氧化菌与细菌群落指纹图谱和生物地球化学,来探索硝化作用的种群和群落生态。在 2003 年至 2006 年期间,每月从南加州湾的多个深度(150、500 和 890 米)采集样本,通过定量 PCR 测定古菌 amoA 和海洋 1 组泉古菌 16S rRNA 基因来对 AOA 进行计数。基于 amoA 基因,AOA 在时间上具有高度的可变性-这是海洋泉古菌的一个一致特征-然而,不同深度的平均值相似,范围在 2.20 到 2.76 x 10(4)amoA 拷贝/ml(-1)。古菌 amoA 基因与泉古菌 16S rRNA 基因呈正相关(r(2) = 0.79),且该关系的斜率为 1.02,这表明在所采样的日期和深度上,大多数海洋 1 组泉古菌都具有 amoA。在 150 米处,我们具体量化了两个 AOA 分支,并与β变形菌氨氧化细菌(β-AOB)amoA 基因进行了比较;这些 AOA 组在时间上强烈共变(r(2) = 0.70,P < 0.001),而 AOA:β-AOB 比值范围从 13 到 5630。AOA:β-AOB 比值的增加与亚硝酸盐的积累相关(r(2) = 0.87,P < 0.001),这可能表明在底物亲和力和活性方面存在差异,导致氨和亚硝酸盐氧化之间出现周期性解偶联。这些数据捕捉到一个动态的氮循环,其中多个微生物群体似乎都是活跃的参与者。