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Glucose effects on denitrifier abundance, denitrification gene mrna levels, and denitrification activity in an anoxic soil microcosm

机译:葡萄糖对缺氧土壤微观分解,脱氮基因mRNA水平和反硝化活性的影响

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Organic carbon availability influences nitrous oxide (N_2O) emissions but its effect on denitrifier communities is not understood. Changes in denitrifier abundance, denitrification gene mRNA levels and denitrification activity were followed in anoxicsoil microcosms in the presence and absence of glucose with non-limiting nitrate concentration for 48 h. nosZ and nirS_p (Pseudomonas mandelii and closely-related spp.) genes (qPCR) and mRNA levels (qRT-PCR) were quantified. Abundance of nosZ and nirS_pwere unaffected by glucose addition and were stable over the duration of the incubation with average values of 4.3 X10~8 and 8.1 X10~8 gene number/g dry soil, respectively. nirS_p mRNA levels were increased by glucose addition. Glucose addition resultedin induction of nirS_p mRNA levels after 4 h, with a 2.5 fold increase in transcripts compared with 0 h, to 2.4 X10~4 transcripts /g dry soil. In contrast, nosZ mRNA levels were not affected by glucose addition and averaged 2.3 X10~6 transcripts /g dry soil. Glucose addition increased cumulative N_2O emissions, with final values of 4.9 and 0.9 mg N_2O-N /kg dry soil for the glucose amended and non-amended soils, respectively, at 48 hr. The increase in N_2O emissions resulting from glucose addition in this study were not clearly accompanied by significant changes in abundance or denitrification gene mRNA levels for the targeted bacterial communities.
机译:有机碳的可用性影响氧化二氮(N_2O)排放,但不明白其对解氮化器社区的影响。在存在和不存在具有非限制性硝酸盐浓度的葡萄糖中,在氧昔单机微观中遵循反硝化基因mRNA水平和反硝化活性的变化,脱氧基因mRNA水平和反硝化活性。 NOSZ和NIRS_P(假单胞菌_PSMBERELII和密切相关的SPP。)基因(QPCR)和mRNA水平(QRT-PCR)。 NoSz和Nirs_Pwere的丰富不受葡萄糖的影响,并且在孵育的持续时间内稳定,平均值为4.3×10〜8和8.1×10〜8基因数/ g干燥土壤。通过葡萄糖添加增加NIRS_P mRNA水平。葡萄糖添加结果诱导4小时后NiRS_P mRNA水平,转录物增加2.5倍,与0h,至2.4×10〜4转录物/ g干燥土壤。相比之下,NoSz mRNA水平不受葡萄糖添加和平均的2.3×10〜6转录物/ g干燥土壤。葡萄糖添加增加的累积N_2O排放,最终值为4.9和0.9mg N_2O-N / kg干燥土壤,用于葡萄糖修正和未修正的土壤,在48小时内。本研究中葡萄糖添加引起的N_2O排放的增加并不明显伴随着靶向细菌社区的丰富或脱氮基因mRNA水平的显着变化。

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