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Disruption of the cell wall integrity gene ECM33 results in improved fermentation by wine yeast

Disruption of the cell wall integrity gene ECM33 results in improved fermentation by wine yeast
Disruption of the cell wall integrity gene ECM33 results in improved fermentation by wine yeast

Severe oenological conditions, such as limited assimilable nitrogen and high sugar contents restrict yeast's ability to successfully complete fermentation. In the absence of a comprehensive commercially available deletion collection in a wine yeast background, a screening approach was applied to a transposon library in a wine yeast derivative to identify clones with superior fermentation performance. Five candidate genes, when disrupted by Ty insertion, were identified as enabling yeast to efficiently complete a model oenological fermentation with limited nitrogen availability. Analogous single gene disruptions were subsequently constructed in the haploid wine yeast strain C911D, and the performance of these during fermentation was analysed. Deletion of ECM33 resulted in the shortest fermentation (up to 31% reduction) in both synthetic medium and grape juice. Interestingly, no significant differences were found in nitrogen utilization, cell viability or biomass yield between ∆ecm33 and the wild type. ∆ecm33 did, however, display growth hypersensitivity to the dyes Calcofluor White and Congo Red, suggesting a link to cell wall integrity. Transcriptional profiling of ∆ecm33 during fermentation demonstrated the up-regulation of SLT2 and HOG1, encoding mitogen activated protein kinases involved in the cell wall integrity (CWI) and high osmolarity glycerol (HOG) pathways, respectively. CHS3 a major chitin synthase gene was also found to be upregulated, and the transcript abundance of key genes of central nitrogen metabolism, GLN1, GLT1, GDH1 and GDH2 in mutant ∆ecm33 were also altered. The findings highlight the complexity of the robust fermentation phenotype and provide clues for further improvement of industrial strains.

Fermentation efficiency, Gene expression, Industrial biotechnology, Wine yeast
1096-7176
255-264
Zhang, Jin
5694f8d3-3068-4272-a652-22fdad9e5740
Astorga, Maria A.
515d3fa2-de10-4b74-85d9-d1bbeccd206b
Gardner, Jennifer M.
0d95188b-206d-4817-8437-e163351f6e7f
Walker, Michelle E.
5e8a98ce-9e08-409a-99e4-a0b96a490940
Grbin, Paul R.
e1cce428-cbfc-4cd2-aef0-c0e3a076a955
Jiranek, Vladimir
8e5a8dfd-f5b2-43e3-928b-11dff324abc7
Zhang, Jin
5694f8d3-3068-4272-a652-22fdad9e5740
Astorga, Maria A.
515d3fa2-de10-4b74-85d9-d1bbeccd206b
Gardner, Jennifer M.
0d95188b-206d-4817-8437-e163351f6e7f
Walker, Michelle E.
5e8a98ce-9e08-409a-99e4-a0b96a490940
Grbin, Paul R.
e1cce428-cbfc-4cd2-aef0-c0e3a076a955
Jiranek, Vladimir
8e5a8dfd-f5b2-43e3-928b-11dff324abc7

Zhang, Jin, Astorga, Maria A., Gardner, Jennifer M., Walker, Michelle E., Grbin, Paul R. and Jiranek, Vladimir (2018) Disruption of the cell wall integrity gene ECM33 results in improved fermentation by wine yeast. Metabolic Engineering, 45, 255-264. (doi:10.1016/j.ymben.2017.12.012).

Record type: Article

Abstract

Severe oenological conditions, such as limited assimilable nitrogen and high sugar contents restrict yeast's ability to successfully complete fermentation. In the absence of a comprehensive commercially available deletion collection in a wine yeast background, a screening approach was applied to a transposon library in a wine yeast derivative to identify clones with superior fermentation performance. Five candidate genes, when disrupted by Ty insertion, were identified as enabling yeast to efficiently complete a model oenological fermentation with limited nitrogen availability. Analogous single gene disruptions were subsequently constructed in the haploid wine yeast strain C911D, and the performance of these during fermentation was analysed. Deletion of ECM33 resulted in the shortest fermentation (up to 31% reduction) in both synthetic medium and grape juice. Interestingly, no significant differences were found in nitrogen utilization, cell viability or biomass yield between ∆ecm33 and the wild type. ∆ecm33 did, however, display growth hypersensitivity to the dyes Calcofluor White and Congo Red, suggesting a link to cell wall integrity. Transcriptional profiling of ∆ecm33 during fermentation demonstrated the up-regulation of SLT2 and HOG1, encoding mitogen activated protein kinases involved in the cell wall integrity (CWI) and high osmolarity glycerol (HOG) pathways, respectively. CHS3 a major chitin synthase gene was also found to be upregulated, and the transcript abundance of key genes of central nitrogen metabolism, GLN1, GLT1, GDH1 and GDH2 in mutant ∆ecm33 were also altered. The findings highlight the complexity of the robust fermentation phenotype and provide clues for further improvement of industrial strains.

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More information

Published date: January 2018
Additional Information: Funding Information: This project was funded by the University of Adelaide and Wine Australia (Project No: GWR Ph1106 ). The University of Adelaide is a member of the Wine Innovation Cluster. We thank Dr Tommaso Liccioli Watson, Dr Joanna Sundstrom and Dr Bo Xu for technical support. Dr Jin Zhang is a holder of a China Scholarship Council Award and an Adelaide University China Fee Scholarship (AUCFS). Part of Professor Jiranek’s contribution to this work was made via ARC project IC130100005 . Funding Information: This project was funded by the University of Adelaide and Wine Australia (Project No: GWR Ph1106). The University of Adelaide is a member of the Wine Innovation Cluster. We thank Dr Tommaso Liccioli Watson, Dr Joanna Sundstrom and Dr Bo Xu for technical support. Dr Jin Zhang is a holder of a China Scholarship Council Award and an Adelaide University China Fee Scholarship (AUCFS). Part of Professor Jiranek's contribution to this work was made via ARC project IC130100005. Publisher Copyright: © 2018 International Metabolic Engineering Society
Keywords: Fermentation efficiency, Gene expression, Industrial biotechnology, Wine yeast

Identifiers

Local EPrints ID: 482651
URI: http://eprints.soton.ac.uk/id/eprint/482651
ISSN: 1096-7176
PURE UUID: 80f5e7fd-834b-4ac4-98c0-957a4142e832
ORCID for Vladimir Jiranek: ORCID iD orcid.org/0000-0002-9775-8963

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Date deposited: 11 Oct 2023 16:48
Last modified: 18 Mar 2024 04:12

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Contributors

Author: Jin Zhang
Author: Maria A. Astorga
Author: Jennifer M. Gardner
Author: Michelle E. Walker
Author: Paul R. Grbin
Author: Vladimir Jiranek ORCID iD

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