WINE PRODUCTION. Microbial. Wine yeast development. wine. spoilage. Molecular response to. Molecular response to Icewine fermentation

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Transcription:

WINE PRODUCTION Wine yeast development Microbial wine spoilage Molecular response to wine fermentation Molecular response to Icewine fermentation Molecular response to sparkling wine (secondary) fermentation Brettanomyces

EtOH; flavour compounds Nutrients & precursors Product Enzymes Substrate Biomass Proteins DNA Gene expression RNA

Parameter Optimal growth Temperature 25-30 C ph 5.0 5.5 Ethanol concentration < 1.4 % v/v Nitrogen Ammonia/Glutamine Oxygen Aerobic Water activity 0.998

Parameter Optimal growth Vinification Temperature 25-30 C Variable ph 5.0 < 3.4 Ethanol concentration < 1.4 % v/v Increasing to 11-16 % v/v Nitrogen Ammonia/Glutamine Nitrogen depletion Oxygen Aerobic Anaerobic Water activity 0.998 Low (0.982-0.939)

Log of Absorbance = yeast cell density In Boulton et al. (1998)

Temperature High acidity Growth, protection & survival Osmotic pressure Anaerobiosis Nutrient changes Ethanol tolerance Physiological & metabolic adaptation

Temperature High acidity Osmotic pressure Stimulus Sensing & Signal Transduction Anaerobiosis Nutrient changes Ethanol tolerance Cellular adaptation Transcriptional regulation Protein regulation Metabolic adaptation

Slow start Increased lag phase Wine, Icewine & Sparkling wine production Inefficient fermentations (stuck/sluggish) Delay in sugar utilization and nutrient uptake; affects product quality Off-flavour production Spoilage organisms Winery efficiency Cellar operations suffer; decreased/delayed production Impacts bottom line $$$

EtOH; flavour compounds Nutrients & precursors Product Enzymes Substrate Biomass Proteins DNA Gene expression RNA

HXT3 Yeast Chromosome Tagging cassette Green Fluorescent Protein HXT3 Green Fluorescent Protein Yeast Chromosome

Glucose/Fructose Environment Cytoplasm Glucose/Fructose GFP

VID/GID genes Vid30 complex (Vid30c) Participate in adaptation to changing nutrient conditions Involved in turnover of Hxt3 and Hxt7 Vid30c Vid30 Chris Snowdon

Nitrogen starvation (h) 0 6 12 24 Parent HXT7-GFP vid30c HXT7-GFP Snowdon et al. (2008) FEMS Yeast Res 8:204-216

Vid30c participates in Hxt3 turnover Shift from glucose to EtOH (h) 0 1.5 3 4.5 6 Parent HXT3-GFP vid30c HXT3-GFP Snowdon and van der Merwe (2012) PLoS ONE 7(12): e50458

VID/GID genes Vid30 complex (Vid30c) Participate in adaptation to changing nutrient conditions Involved in turnover of Hxt3 and Hxt7 Etp1 complex Etp1 needed for ethanol tolerance Vid30c Vid30 Moh1 Moh1 Etp1 Ubiquitin

7.5% (w/v) ethanol considered ethanol stress Impacts membrane fluidity Denatures proteins Greatly decreases cell viability Yeast s response Adjusts membrane fluidity Increase expression of chaperone proteins Induces transcription of HSP genes

Snowdon et al. (2009)

Parent HXT3-GFP etp1 HXT3-GFP Snowdon et al. (2009)

Construct homo- and heterozygous mutants of ETP1 in M2 Chardonnay fermentations Hypothesis: Needed for ethanol tolerance Expects homozygous mutant to ferment well until high levels of ethanol is produced before mutant stops fermenting Function when ethanol levels are high (around 7.5%) Impact HSP gene expression later in fermentation

Daily Weight Loss (g) 4.00 3.50 3.00 2.50 2.00 1.50 1.00 0.50 0.00 Ashley Hillier 1 2 3 4 5 6 7 8 9 10 11 12 13 14 Days M2 ETP1/etp1 etp1/etp1 Hillier and GvdM (unpublished)

n = 3 Hillier and GvdM (in preparation)

* p-value 0.05 Hillier and GvdM (in preparation)

* p-value 0.05 Hillier and GvdM (in preparation)

144h 10h 48h 24h Biological triplicates; n = 3 Hillier and GvdM (in preparation)

# genes compared to parent: 10 hours 24 hours 48 hours 144 hours Higher in etp1/etp1 101 376 493 870 Lower in etp1/etp1 142 227 374 635 Total genes 243 603 867 1505 All genes: p-value 0.05; fold-change > 2

# genes in etp1/etp1 compared to parent: Amino acid & Nitrogen metabolism 10 hours 24 hours 48 hours 144 hours Up Down Up Down Up Down Up Down 2 13 17 15 35 19 58 31 Cold & anaerobiosis 0 5 3 17 1 19 2 11 Cell wall 6 1 20 1 30 2 15 8

Mannoprotein β-glucan & Chitin Cell wall Periplasmic space Baba et al. (1989) Plasma membrane Integral membrane protein Cytoplasm

Temperature High acidity Osmotic pressure Stimulus Sensing & Signal Transduction Anaerobiosis Nutrient changes Ethanol tolerance Cellular adaptation Transcriptional regulation Protein regulation Metabolic adaptation

Temperature of grape must during fall harvest Cold soak Colder fermentations for white wines Oxygen as major threat to wine production Oxidation of flavour compounds Low levels of dissolved oxygen at start of fermentation quickly scavenged by yeast following inoculation Oxygenation during wine production Pump-overs; micro-oxygenation; yeast RAPIDLY consumes oxygen during fermentation

Impact on plasma membrane Decrease in fluidity; decreased membrane function Inability to produce new membrane lipids in absence of oxygen Alteration to existing lipid composition to increase fluidity and membrane function Remodeling of cell wall Alteration of cell wall components and proteins Induced transcription of cell wall mannoprotein genes DAN/TIR/PAU

Hillier and GvdM (in preparation)

Hillier and GvdM (in preparation)

Hillier and GvdM (in preparation)

Hillier and GvdM (in preparation)

ETP1 is needed for a normal fermentation to occur Significant impact on transcriptional adaptation process ETP1 deletion affects protein levels of Hog1 and Mpk1 early in fermentation Leads to significant down-regulation in PAU gene transcription early in fermentation Cell remodelling genes are mis-regulated Etp1 is most likely involved in the ubiquitin-dependent turnover of proteins Specific target(s)?

GvdM lab members Helena Morales Johansson Chris Hlynialuk Ryan Schierholtz Chris Snowdon Angus Ross Kirill Bessonov Stephen Le Roux Ashley Hillier Stephanie Hughes Erik Nielson Stephanie Hallows Peter Poliszczuk Nate Ferguson Collaborators Debbie Inglis (CCOVI) Barry Shelp (U. of Guelph) Hennie van Vuuren (UBC) Terence van Rooyen (NCTW) Hung Lee (U. of Guelph) Funding Support University of Guelph CFI NSERC OMAFRA Genome Canada ORF-RE

Hillier and GvdM (in preparation)