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Applied and Environmental Microbiology, July 2007, p. 4326-4331, Vol. 73, No. 13
0099-2240/07/$08.00+0     doi:10.1128/AEM.03008-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Isolation of Key Methanogens for Global Methane Emission from Rice Paddy Fields: a Novel Isolate Affiliated with the Clone Cluster Rice Cluster I{triangledown}

Sanae Sakai,1 Hiroyuki Imachi,1,2* Yuji Sekiguchi,1,3 Akiyoshi Ohashi,1 Hideki Harada,4 and Yoichi Kamagata1,3,5

Department of Environmental Systems Engineering, Nagaoka University of Technology, Nagaoka, Niigata 940-2188, Japan,1 Subground Animalcule Retrieval (SUGAR) Program, Extremobiosphere Research Center, Japan Agency for Marine-Earth Science & Technology (JAMSTEC), Yokosuka, Kanagawa 237-0061, Japan,2 Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (AIST), Central 6, Tsukuba, Ibaraki 305-8566, Japan,3 Department of Civil Engineering, Tohoku University, Sendai 980-8579, Japan,4 Research Institute of Genome-Based Biofactory, National Institute of Advanced Industrial Science and Technology (AIST), Sapporo, Hokkaido 062-8517, Japan5

Received 29 December 2006/ Accepted 1 May 2007

Despite the fact that rice paddy fields (RPFs) are contributing 10 to 25% of global methane emissions, the organisms responsible for methane production in RPFs have remained uncultivated and thus uncharacterized. Here we report the isolation of a methanogen (strain SANAE) belonging to an abundant and ubiquitous group of methanogens called rice cluster I (RC-I) previously identified as an ecologically important microbial component via culture-independent analyses. To enrich the RC-I methanogens from rice paddy samples, we attempted to mimic the in situ conditions of RC-I on the basis of the idea that methanogens in such ecosystems should thrive by receiving low concentrations of substrate (H2) continuously provided by heterotrophic H2-producing bacteria. For this purpose, we developed a coculture method using an indirect substrate (propionate) in defined medium and a propionate-oxidizing, H2-producing syntroph, Syntrophobacter fumaroxidans, as the H2 supplier. By doing so, we significantly enriched the RC-I methanogens and eventually obtained a methanogen within the RC-I group in pure culture. This is the first report on the isolation of a methanogen within RC-I.


* Corresponding author. Mailing address: Subground Animalcule Retrieval (SUGAR) Program, Extremobiosphere Research Center, Japan Agency for Marine-Earth Science & Technology (JAMSTEC), 2-15 Natsushima-cho, Yokosuka, Kanagawa 237-0061, Japan. Phone: 81-46-867-9709. Fax: 81-46-867-9715. E-mail: imachi{at}jamstec.go.jp

{triangledown} Published ahead of print on 4 May 2007.


Applied and Environmental Microbiology, July 2007, p. 4326-4331, Vol. 73, No. 13
0099-2240/07/$08.00+0     doi:10.1128/AEM.03008-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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