Fabrication of a Partial Genome Microarray of the Methylotrophic Yeast Hansenula polymorpha: Optimization and Evaluation of Transcript Profiling

The methylotrophic yeast Hansenula polymorpha has been extensively studied as a model organism for methanol metabolism and peroxisome biogenesis. Recently, this yeast has also attracted attention as a promising host organism for recombinant protein production. Here, we describe the fabrication and e...

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Veröffentlicht in:Journal of microbiology and biotechnology 2004-12, Vol.14 (6), p.1239-1248
Hauptverfasser: Oh, K.S. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Gellissen, Gerd (Rhein Biotech GmbH, Dusseldorf, Germany), Kwon, O.S. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Oh, Y.W. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Sohn, M.J. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Jung, S.H. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Kim, Y.K. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Kim, M.G. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Rhee, S.K. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), Kang, H.A. (Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea), E-mail: hyunkang@kribb.re.kr
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Sprache:eng
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Zusammenfassung:The methylotrophic yeast Hansenula polymorpha has been extensively studied as a model organism for methanol metabolism and peroxisome biogenesis. Recently, this yeast has also attracted attention as a promising host organism for recombinant protein production. Here, we describe the fabrication and evaluation of a DNA chip spotted with 382 open reading frames (ORFs) of H. polymorpha. Each ORF was PCR-amplified using gene-specific primer sets, of which the forward primers had 5'-aminolink. The PCR products were printed in duplicate onto the aldehyde-coated slide glasses to link only the coding strands to the surface of the slide via covalent coupling between amine and aldehyde groups.
ISSN:1017-7825