論文

査読有り
2004年3月

Alcohol dehydrogenases that catalyse methyl formate synthesis participate in formaldehyde detoxification in the methylotrophic yeast Candida boidinii

YEAST
  • H Yurimoto
  • ,
  • B Lee
  • ,
  • F Yasuda
  • ,
  • Y Sakai
  • ,
  • N Kato

21
4
開始ページ
341
終了ページ
350
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/yea.1101
出版者・発行元
JOHN WILEY & SONS LTD

Methyl formate synthesis during growth on methanol by methylotrophic yeasts has been considered to play a role in formaldehyde detoxification. An enzyme that catalyses methyl formate synthesis was purified from methylotrophic yeasts, and was suggested to belong to a family of alcohol dehydrogenases (ADHs). In this study we report the gene cloning and gene disruption analysis of three ADH-encoding genes in the methylotrophic yeast Candida boidinii (CbADH1, CbADH2 and CbADH3) in order to clarify the physiological role of methyl formate synthesis. From the primary structures of these three genes, CbAdh1 was shown to be cytosolic and CbAdh2 and CbAdh3 were mitochondrial enzymes. Gene products of CbADH1, CbADH2 and CbADH3 expressed in Escherichia coli showed both ADH- and methyl formate-synthesizing activities. The results of gene-disruption analyses suggested that methyl formate synthesis was mainly catalysed by a cytosolic ADH (CbAdh1), and this enzyme contributed to formaldehyde detoxitication through glutathione-independent formaldehyde oxidation during growth on methanol by methylotrophic yeasts. The GenBank/EMBL/DDBJ Accession Nos for CbADH1, CbADH2 and CbADH3 are AB125900, AB125901 and AB125902, respectively. Copyright (C) 2004 John Wiley Sons, Ltd.

リンク情報
DOI
https://doi.org/10.1002/yea.1101
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/15042594
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000220600300006&DestApp=WOS_CPL
ID情報
  • DOI : 10.1002/yea.1101
  • ISSN : 0749-503X
  • PubMed ID : 15042594
  • Web of Science ID : WOS:000220600300006

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