Directed evolution as an approach to increase fructose utilization in synthetic grape juice by wine yeast AWRI 796

Author:

Walker Michelle E1,Watson Tommaso L1,Large Christopher R L23,Berkovich Yan1,Lang Tom A1,Dunham Maitreya J2,Formby Sean4,Jiranek Vladimir15

Affiliation:

1. Department of Wine Science, The University of Adelaide , PMB 1, Glen Osmond, SA 5064, Australia

2. Department of Genome Sciences, University of Washington , 3720 15th Ave NE , Seattle, WA 98195, United States

3. Molecular and Cellular Biology Program, University of Washington , Seattle, WA 98195, United States

4. Bioinformatics Graduate Program, University of British Columbia , Genome Sciences Centre, BCCA, 100-570 West 7th Avenue, Vancouver, BC, V5Z 4S6, Canada

5. Australian Research Council Training Centre for Innovative Wine Production , PMB 1, Glen Osmond, SA 5064, Australia

Abstract

AbstractIn winemaking, slow or stuck alcoholic fermentation can impact processing efficiency and wine quality. Residual fructose in the later stages of fermentation can leave the wine ‘out of specification’ unless removed, which requires reinoculation or use of a more fructophilic yeast. As such, robust, fermentation efficient strains are still highly desirable to reduce this risk. We report on a combined EMS mutagenesis and Directed Evolution (DE) approach as a ‘proof of concept’ to improve fructose utilization and decrease fermentation duration. One evolved isolate, Tee 9, was evaluated against the parent, AWRI 796 in defined medium (CDGJM) and Semillon juice. Interestingly, Tee 9 exhibited improved fermentation in CDGJM at several nitrogen contents, but not in juice. Genomic comparison between AWRI 796 and Tee 9 identified 371 mutations, but no chromosomal copy number variation. A total of 95 noncoding and 276 coding mutations were identified in 297 genes (180 of which encode proteins with one or more substitutions). Whilst introduction of two of these, Gid7 (E726K) or Fba1 (G135S), into AWRI 796 did not lead to the fermentation improvement seen in Tee 9, similar allelic swaps with the other mutations are needed to understand Tee 9’s adaption to CDGJM. Furthermore, the 378 isolates, potentially mutagenized but with the same genetic background, are likely a useful resource for future phenotyping and genome-wide association studies.

Funder

Wine Australia

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Microbiology

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