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Journal of Bacteriology, November 1998, p. 5885-5890, Vol. 180, No. 22
Division of Applied Life Sciences, Graduate
School of Agriculture, Kyoto University, Kitashirakawa-Oiwake,
Sakyo-ku, Kyoto 606-8502, Japan
Received 10 June 1998/Accepted 15 September 1998
The physiological role of dihydroxyacetone synthase (DHAS) in
Candida boidinii was evaluated at the molecular level. The
DAS1 gene, encoding DHAS, was cloned from the host genome,
and regulation of its expression by various carbon and nitrogen sources
was analyzed. Western and Northern analyses revealed that
DAS1 expression was regulated mainly at the mRNA level. The
regulatory pattern of DHAS was similar to that of alcohol oxidase but
distinct from that of two other enzymes in the formaldehyde
dissimilation pathway, glutathione-dependent formaldehyde dehydrogenase
and formate dehydrogenase. The DAS1 gene was disrupted in
one step in the host genome (das1
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Regulation and Physiological Role of the
DAS1 Gene, Encoding Dihydroxyacetone Synthase, in
the Methylotrophic Yeast Candida boidinii
strain), and the
growth of the das1
strain in various carbon and nitrogen
sources was compared with that of the wild-type strain. The
das1
strain had completely lost the ability to grow on
methanol, while the strain with a disruption of the formate
dehydrogenase gene could survive (Y. Sakai et al., J. Bacteriol.
179:4480-4485, 1997). These and other experiments (e.g., those to
determine the expression of the gene and the growth ability of the
das1
strain on media containing methylamine or choline
as a nitrogen source) suggested that DAS1 is involved in
assimilation rather than dissimilation or detoxification of
formaldehyde in the cells.
*
Corresponding author. Mailing address: Division of
Applied Life Sciences, Graduate School of Agriculture, Kyoto
University, Kitashirakawa-Oiwake, Sakyo-ku, Kyoto 606-8502, Japan.
Phone: 81-75-753-6455. Fax: 81-75-753-6385. E-mail:
ysakai{at}kais.kyoto-u.ac.jp.
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