論文

査読有り
2010年7月

Molecular Characterization of Two Genes with High Similarity to the Dihydroxyacetone Synthase Gene in the Methylotrophic Yeast Pichia methanolica

BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
  • Tomoyuki Nakagawa
  • Shuki Fujimura
  • Takashi Ito
  • Yoshimi Matsufuji
  • Shotaro Ozawa
  • Tatsuro Miyaji
  • Junichi Nakagawa
  • Noboru Tomizuka
  • Hiroya Yurimoto
  • Yasuyoshi Sakai
  • Takashi Hayakawa
  • 全て表示

74
7
開始ページ
1491
終了ページ
1493
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1271/bbb.100153
出版者・発行元
TAYLOR & FRANCIS LTD

The methylotrophic yeast Pichia methanolica possesses two genes, PmDAS1 and PmDLP1, whose amino acid sequences show high similarity to dihydroxyacetone synthase (DAS), the formaldehyde-fixing enzyme for methanol metabolism within the peroxisome. The PmDAS1 and PmDLP1 genes encode 709 and 707 amino acid residues respectively, and PmDas1p contains a type-1 peroxisomal targeting signal (PTS1), while PmDlp1p does not. Upon phylogenetic analysis, PmDas1p fit into the DAS group with other DASs, while PmDlp1p was grouped with the DAS-like proteins (DLP) of non-methylotrophic yeasts and fungi, a branch of the phylogenetic tree independent of the DAS and transketolase (TK) groups. While expression of PmDAS1 restored the methylotrophic growth of the Candida boichnii das1 Delta strain, the PmDLP1 and PmDAS1-Delta PTS1 genes did not. Taken together, these results indicate that PmDAS1 encodes a functional DAS and has an indispensable role in methanol metabolism, and that PmDlp1p share a common, as yet uncharacterized function in P. methanolica as well as in non-methylotrophic yeasts and fungi.

リンク情報
DOI
https://doi.org/10.1271/bbb.100153
J-GLOBAL
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201002201533241660
CiNii Articles
http://ci.nii.ac.jp/naid/10027557611
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000280458200033&DestApp=WOS_CPL
ID情報
  • DOI : 10.1271/bbb.100153
  • ISSN : 0916-8451
  • eISSN : 1347-6947
  • J-Global ID : 201002201533241660
  • CiNii Articles ID : 10027557611
  • Web of Science ID : WOS:000280458200033

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