Exploring the xylose paradox in Saccharomyces cerevisiae through in vivo sugar signalomics of targeted deletants
(2019) In Microbial Cell Factories 18(1).- Abstract
Background: There have been many successful strategies to implement xylose metabolism in Saccharomyces cerevisiae, but no effort has so far enabled xylose utilization at rates comparable to that of glucose (the preferred sugar of this yeast). Many studies have pointed towards the engineered yeast not sensing that xylose is a fermentable carbon source despite growing and fermenting on it, which is paradoxical. We have previously used fluorescent biosensor strains to in vivo monitor the sugar signalome in yeast engineered with xylose reductase and xylitol dehydrogenase (XR/XDH) and have established that S. cerevisiae senses high concentrations of xylose with the same signal as low concentration of glucose, which may explain the poor... (More)
Background: There have been many successful strategies to implement xylose metabolism in Saccharomyces cerevisiae, but no effort has so far enabled xylose utilization at rates comparable to that of glucose (the preferred sugar of this yeast). Many studies have pointed towards the engineered yeast not sensing that xylose is a fermentable carbon source despite growing and fermenting on it, which is paradoxical. We have previously used fluorescent biosensor strains to in vivo monitor the sugar signalome in yeast engineered with xylose reductase and xylitol dehydrogenase (XR/XDH) and have established that S. cerevisiae senses high concentrations of xylose with the same signal as low concentration of glucose, which may explain the poor utilization. Results: In the present study, we evaluated the effects of three deletions (ira2δ, isu1δ and hog1δ) that have recently been shown to display epistatic effects on a xylose isomerase (XI) strain. Through aerobic and anaerobic characterization, we showed that the proposed effects in XI strains were for the most part also applicable in the XR/XDH background. The ira2δisu1δ double deletion led to strains with the highest specific xylose consumption- and ethanol production rates but also the lowest biomass titre. The signalling response revealed that ira2δisu1δ changed the low glucose-signal in the background strain to a simultaneous signalling of high and low glucose, suggesting that engineering of the signalome can improve xylose utilization. Conclusions: The study was able to correlate the previously proposed beneficial effects of ira2δ, isu1δ and hog1δ on S. cerevisiae xylose uptake, with a change in the sugar signalome. This is in line with our previous hypothesis that the key to resolve the xylose paradox lies in the sugar sensing and signalling networks. These results indicate that the future engineering targets for improved xylose utilization should probably be sought not in the metabolic networks, but in the signalling ones.
(Less)
- author
- Osiro, Karen O. LU ; Borgström, Celina LU ; Brink, Daniel P. LU ; Fjölnisdóttir, Birta Líf and Gorwa-Grauslund, Marie F. LU
- organization
- publishing date
- 2019
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- cAMP/PKA, GFP biosensor, Saccharomyces cerevisiae, SNF1/Mig1p, Snf3p/Rgt2p, Sugar sensing/signalling, Xylose, δhog1, δira2, δisu1
- in
- Microbial Cell Factories
- volume
- 18
- issue
- 1
- article number
- 88
- publisher
- BioMed Central (BMC)
- external identifiers
-
- scopus:85066403980
- pmid:31122246
- ISSN
- 1475-2859
- DOI
- 10.1186/s12934-019-1141-x
- project
- Understanding and improving microbial cell factories through Large Scale Data-approaches
- language
- English
- LU publication?
- yes
- id
- 5585f05c-7213-4bc4-9bf0-dc9e99baac6d
- date added to LUP
- 2019-07-04 09:23:07
- date last changed
- 2024-04-02 10:44:03
@article{5585f05c-7213-4bc4-9bf0-dc9e99baac6d,
abstract = {{<p>Background: There have been many successful strategies to implement xylose metabolism in Saccharomyces cerevisiae, but no effort has so far enabled xylose utilization at rates comparable to that of glucose (the preferred sugar of this yeast). Many studies have pointed towards the engineered yeast not sensing that xylose is a fermentable carbon source despite growing and fermenting on it, which is paradoxical. We have previously used fluorescent biosensor strains to in vivo monitor the sugar signalome in yeast engineered with xylose reductase and xylitol dehydrogenase (XR/XDH) and have established that S. cerevisiae senses high concentrations of xylose with the same signal as low concentration of glucose, which may explain the poor utilization. Results: In the present study, we evaluated the effects of three deletions (ira2δ, isu1δ and hog1δ) that have recently been shown to display epistatic effects on a xylose isomerase (XI) strain. Through aerobic and anaerobic characterization, we showed that the proposed effects in XI strains were for the most part also applicable in the XR/XDH background. The ira2δisu1δ double deletion led to strains with the highest specific xylose consumption- and ethanol production rates but also the lowest biomass titre. The signalling response revealed that ira2δisu1δ changed the low glucose-signal in the background strain to a simultaneous signalling of high and low glucose, suggesting that engineering of the signalome can improve xylose utilization. Conclusions: The study was able to correlate the previously proposed beneficial effects of ira2δ, isu1δ and hog1δ on S. cerevisiae xylose uptake, with a change in the sugar signalome. This is in line with our previous hypothesis that the key to resolve the xylose paradox lies in the sugar sensing and signalling networks. These results indicate that the future engineering targets for improved xylose utilization should probably be sought not in the metabolic networks, but in the signalling ones.</p>}},
author = {{Osiro, Karen O. and Borgström, Celina and Brink, Daniel P. and Fjölnisdóttir, Birta Líf and Gorwa-Grauslund, Marie F.}},
issn = {{1475-2859}},
keywords = {{cAMP/PKA; GFP biosensor; Saccharomyces cerevisiae; SNF1/Mig1p; Snf3p/Rgt2p; Sugar sensing/signalling; Xylose; δhog1; δira2; δisu1}},
language = {{eng}},
number = {{1}},
publisher = {{BioMed Central (BMC)}},
series = {{Microbial Cell Factories}},
title = {{Exploring the xylose paradox in Saccharomyces cerevisiae through in vivo sugar signalomics of targeted deletants}},
url = {{http://dx.doi.org/10.1186/s12934-019-1141-x}},
doi = {{10.1186/s12934-019-1141-x}},
volume = {{18}},
year = {{2019}},
}