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Molecular Cloning of cDNAs and Genes for Three α-Glucosidases from European Honeybees, Apis mellifera L., and Heterologous Production of Recombinant Enzymes in Pichia pastoris

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Title: Molecular Cloning of cDNAs and Genes for Three α-Glucosidases from European Honeybees, Apis mellifera L., and Heterologous Production of Recombinant Enzymes in Pichia pastoris
Authors: NISHIMOTO, Mamoru Browse this author
MORI, Haruhide Browse this author
MOTEKI, Tsuneharu Browse this author
TAKAMURA, Yukiko Browse this author
IWAI, Gaku Browse this author
MIYAGUCHI, Yu Browse this author
OKUYAMA, Masayuki Browse this author →KAKEN DB
WONGCHAWALIT, Jintanart Browse this author
SURARIT, Rudee Browse this author
SVASTI, Jisnuson Browse this author
KIMURA, Atsuo Browse this author
CHIBA, Seiya Browse this author
Keywords: honeybee α-glucosidase
Apis mellifera
cloning of α-glucosidase
Pichia pastoris
Issue Date: Jul-2007
Publisher: Japan Society for Bioscience, Biotechnology, and Agrochemistry
Journal Title: Bioscience, Biotechnology, and Biochemistry
Volume: 71
Issue: 7
Start Page: 1703
End Page: 1716
Publisher DOI: 10.1271/bbb.70125
PMID: 17617712
Abstract: cDNAs encoding three α-glucosidases (HBGases I, II, and III) from European honeybees, Apis mellifera, were cloned and sequenced, two of which were expressed in Pichia pastoris. The cDNAs for HBGases I, II, and III were 1,986, 1,910, and 1,915 bp in length, and included ORFs of 1,767, 1,743, and 1,704 bp encoding polypeptides comprised of 588, 580, and 567 amino acid residues, respectively. The deduced proteins of HBGases I, II, and III contained 18, 14, and 8 putative N-linked glycosylation sites, respectively, but at least 2 sites in HBGase II were unmodified by N-linked oligosaccharide. In spite of remarkable differences in the substrate specificities of the three HBGases, high homologies (38–44% identity) were found in the deduced amino acid sequences. In addition, three genomic DNAs, of 13,325, 2,759, and 27,643 bp, encoding HBGases I, II, and III, respectively, were isolated from honeybees, and the sequences were analyzed. The gene of HBGase I was found to be composed of 8 exons and 7 introns. The gene of HBGase II was not divided by intron. The gene of HBGase III was confirmed to be made up of 9 exons and 8 introns, and to be located in the region upstream the gene of HBGase I.
Relation: http://www.jstage.jst.go.jp/
Type: article
URI: http://hdl.handle.net/2115/30119
Appears in Collections:農学院・農学研究院 (Graduate School of Agriculture / Faculty of Agriculture) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 木村 淳夫

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