Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.

The ascomycetes Candida albicans, Saccharomyces cerevisiae and Scheffersomyces stipitis metabolize the pentose sugar xylose very differently. S. cerevisiae fails to grow on xylose, while C. albicans can grow, and S. stipitis can both grow and ferment xylose to ethanol. However, all three species con...

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Main Authors: Doreen Harcus, Daniel Dignard, Guylaine Lépine, Chris Askew, Martine Raymond, Malcolm Whiteway, Cunle Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3827475?pdf=render
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spelling doaj-9962905a715c4bef8d069f27889505c32020-11-24T21:59:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e8073310.1371/journal.pone.0080733Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.Doreen HarcusDaniel DignardGuylaine LépineChris AskewMartine RaymondMalcolm WhitewayCunle WuThe ascomycetes Candida albicans, Saccharomyces cerevisiae and Scheffersomyces stipitis metabolize the pentose sugar xylose very differently. S. cerevisiae fails to grow on xylose, while C. albicans can grow, and S. stipitis can both grow and ferment xylose to ethanol. However, all three species contain highly similar genes that encode potential xylose reductases and xylitol dehydrogenases required to convert xylose to xylulose, and xylulose supports the growth of all three fungi. We have created C. albicans strains deleted for the xylose reductase gene GRE3, the xylitol dehydrogenase gene XYL2, as well as the gre3 xyl2 double mutant. As expected, all the mutant strains cannot grow on xylose, while the single gre3 mutant can grow on xylitol. The gre3 and xyl2 mutants are efficiently complemented by the XYL1 and XYL2 from S. stipitis. Intriguingly, the S. cerevisiae GRE3 gene can complement the Cagre3 mutant, while the ScSOR1 gene can complement the Caxyl2 mutant, showing that S. cerevisiae contains the enzymatic capacity for converting xylose to xylulose. In addition, the gre3 xyl2 double mutant of C. albicans is effectively rescued by the xylose isomerase (XI) gene of either Piromyces or Orpinomyces, suggesting that the XI provides an alternative to the missing oxido-reductase functions in the mutant required for the xylose-xylulose conversion. Overall this work suggests that C. albicans strains engineered to lack essential steps for xylose metabolism can provide a platform for the analysis of xylose metabolism enzymes from a variety of species, and confirms that S. cerevisiae has the genetic potential to convert xylose to xylulose, although non-engineered strains cannot proliferate on xylose as the sole carbon source.http://europepmc.org/articles/PMC3827475?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Doreen Harcus
Daniel Dignard
Guylaine Lépine
Chris Askew
Martine Raymond
Malcolm Whiteway
Cunle Wu
spellingShingle Doreen Harcus
Daniel Dignard
Guylaine Lépine
Chris Askew
Martine Raymond
Malcolm Whiteway
Cunle Wu
Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
PLoS ONE
author_facet Doreen Harcus
Daniel Dignard
Guylaine Lépine
Chris Askew
Martine Raymond
Malcolm Whiteway
Cunle Wu
author_sort Doreen Harcus
title Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
title_short Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
title_full Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
title_fullStr Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
title_full_unstemmed Comparative xylose metabolism among the Ascomycetes C. albicans, S. stipitis and S. cerevisiae.
title_sort comparative xylose metabolism among the ascomycetes c. albicans, s. stipitis and s. cerevisiae.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description The ascomycetes Candida albicans, Saccharomyces cerevisiae and Scheffersomyces stipitis metabolize the pentose sugar xylose very differently. S. cerevisiae fails to grow on xylose, while C. albicans can grow, and S. stipitis can both grow and ferment xylose to ethanol. However, all three species contain highly similar genes that encode potential xylose reductases and xylitol dehydrogenases required to convert xylose to xylulose, and xylulose supports the growth of all three fungi. We have created C. albicans strains deleted for the xylose reductase gene GRE3, the xylitol dehydrogenase gene XYL2, as well as the gre3 xyl2 double mutant. As expected, all the mutant strains cannot grow on xylose, while the single gre3 mutant can grow on xylitol. The gre3 and xyl2 mutants are efficiently complemented by the XYL1 and XYL2 from S. stipitis. Intriguingly, the S. cerevisiae GRE3 gene can complement the Cagre3 mutant, while the ScSOR1 gene can complement the Caxyl2 mutant, showing that S. cerevisiae contains the enzymatic capacity for converting xylose to xylulose. In addition, the gre3 xyl2 double mutant of C. albicans is effectively rescued by the xylose isomerase (XI) gene of either Piromyces or Orpinomyces, suggesting that the XI provides an alternative to the missing oxido-reductase functions in the mutant required for the xylose-xylulose conversion. Overall this work suggests that C. albicans strains engineered to lack essential steps for xylose metabolism can provide a platform for the analysis of xylose metabolism enzymes from a variety of species, and confirms that S. cerevisiae has the genetic potential to convert xylose to xylulose, although non-engineered strains cannot proliferate on xylose as the sole carbon source.
url http://europepmc.org/articles/PMC3827475?pdf=render
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