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DNA Research Advance Access originally published online on January 9, 2006
DNA Research 2005 12(5):291-299; doi:10.1093/dnares/dsi012
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© The Author 2006. Kazusa DNA Research Institute
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org

Complete set of ORF clones of Escherichia coli ASKA library (A Complete Set of E. coli K-12 ORF Archive): Unique Resources for Biological Research

Masanari Kitagawa1 4, Takeshi Ara2, Mohammad Arifuzzaman1, Tomoko Ioka-Nakamichi3, Eiji Inamoto3, Hiromi Toyonaga3 and Hirotada Mori1,2,3,*

1Graduate School of Biological Sciences, Nara Institute of Science and Technology 8916-5 Takayama, Ikoma, Nara 630-0101, Japan
2Institute for Advanced Biosciences, Keio University Tsuruoka, Yamagata 997-0035, Japan
3CREST, JST (Japan Science and Technology)

Based on the genomic sequence data of Escherichia coli K-12 strain, we have constructed a complete set of cloned individual genes encoding Histidine-tagged proteins with or without GFP fused for functional genomic analysis. Each clone encodes a protein of predicted ORF attached by Histidines and seven spacer amino acids at the N-terminal end, and five spacer amino acids and GFP at the C-terminal end. SfiI restriction sites are generated at both the N- and C-terminal boundaries of ORF upon cloning, which enables easy transfer of ORF to other vector systems by cutting with SfiI. Expression of cloned ORF is under the control of an IPTG-inducible promoter, which is strictly repressed by lacIq repressor gene product. The set of cloned ORFs described here should provide unique resources for systematic functional genomic approaches including (i) construction of DNA microarray, (ii) production and purification of proteins, (iii) analysis of protein localization by monitoring GFP fluorescence and (iv) analysis of protein–protein interaction.

Key words: Escherichia coli; bacterial functional genomics; ORF clone; resource


*To whom correspondence should be addressed. Tel. +81-743-72-5660, Fax. +81-743-72-5669, E-mail: hmori{at}gtc.naist.jp

4Present address: Dragon Genomics Center, Takara Bio Inc. 7870-15, Sakura-cho, Yokkaichi, Mie 512-1211, Japan

Communicated by Michio Oishi


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