日本地球惑星科学連合2015年大会

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セッション記号 B (地球生命科学) » B-GM 地下圏微生物学

[B-GM22] 地球惑星科学と微生物生態学の接点

2015年5月26日(火) 09:00 〜 10:45 105 (1F)

コンビーナ:*砂村 倫成(東京大学大学院理学系研究科地球惑星科学専攻)、高井 研(海洋研究開発機構極限環境生物圏研究センター)、木庭 啓介(東京農工大学大学院農学研究院)、濱村 奈津子(愛媛大学)、座長:布浦 拓郎(独立行政法人海洋研究開発機構海洋生命理工学研究開発センター)、砂村 倫成(東京大学大学院理学系研究科地球惑星科学専攻)

09:15 〜 09:30

[BGM22-02] 環境中には未知なる脱窒微生物が豊富に存在している

*磯部 一夫1Wei Wei1妹尾 啓史1 (1.東京大学大学院農学生命科学研究科)

キーワード:脱窒, 亜硝酸還元酵素遺伝子, nirS, nirK

Denitrification is an important process in the global nitrogen cycle. The genes encoding NirK and NirS (nirK and nirS), which catalyze the reduction of nitrite to nitric oxide, have been used as marker genes to study the ecological behavior of denitrifiers in environments. However, conventional polymerase chain reaction (PCR) primers can only detect a limited range of the phylogenetically diverse nirK and nirS. Thus, we developed new PCR primers covering the diverse nirK and nirS. Clone library and qPCR analysis using the primers showed that nirK and nirS in terrestrial environments are more phylogenetically diverse and 2-6 times more abundant than those revealed with the conventional primers. RNA- and culture-based analyses using a cropland soil also suggested that microorganisms with previously unconsidered nirK or nirS are responsible for denitrification in the soil. PCR techniques still have a greater capacity for the deep analysis of target genes than PCR-independent methods including metagenome analysis, although efforts are needed to minimize the PCR biases. The methodology and the insights obtained here should allow us to achieve a more precise understanding of the ecological behavior of denitrifiers and facilitate more precise estimate of denitrification in environments.