The Impact of Yeast on Wine Aroma and Flavor: The Good, the Bad
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Transcript The Impact of Yeast on Wine Aroma and Flavor: The Good, the Bad
Sulfur Compounds in Wine
Linda Bisson
Department of Viticulture and
Enology
Introduction to S-Containing Faults
Why Are Sulfur Compounds a
Problem?
Low thresholds of detection
Negatively-associated aromas
Chemical reactivity
Difficulty in removal
Difficulty in masking
The Classic Sulfur Fault Descriptors
Rotten egg
Fecal
Rubber/Plastic tubing
Burnt match
Burnt molasses
Burnt rubber
Rotten vegetable: cauliflower, cabbage, potato,
asparagus, corn
Onion/Garlic
Clam/Tide pool
Butane/Fuel/Chemical
The Sulfur Taints
Hydrogen sulfide
Higher sulfides
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Mercaptans
•
Methyl (Ethyl) mercaptan
Thioesters
•
Dimethyl (Diethyl) sulfide
Dimethyl disulfide
Methyl (ethyl) thioacetate
Other S-amino acid metabolites
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Thioethers
Cyclic and heterocyclic compounds
Sources of Sulfur Compounds
Non-biological
• Elemental sulfur
• S-containing pesticides
Biological
• Sulfate/Sulfite reduction and reduced sulfide
reactions
• S-containing amino acid metabolism
• S-containing vitamins and cofactors degradation
• Glutathione metabolism and degradation
• S-containing pesticides degradation
• Elemental sulfur
Timing of Sulfur Fault Formation
Primary Fermentation Early: Hydrogen
Sulfide
Primary Fermentation Late: Hydrogen
Sulfide
Post Fermentation: Hydrogen Sulfide or
Sur Lie Faults
Bottling: S-fault development
Hypotheses to Explain S-Taint
Formation
Correlated with H2S formation during the primary
fermentation
Correlated with late H2S formation (peak 2) but not with
H2S formation during primary fermentation
Associated with S-containing amino acid levels during
primary fermentation
Due to degradation of S-containing metabolites during
yeast lees aging, but not related to levels of these
compounds present in the initial juice
Yeast strain most important
Juice composition most important
Problems with Previous Studies
Lack of control of all variables
Invalid comparisons (too many variables)
Confounding factors not considered to be
important
Differences in strains and conditions used
Driving reactions by having an excess of
precursors, beyond anything found in
juices or wines
HYDROGEN SULFIDE
Why is H2S formed?
Off-shoot of metabolism
Reductive environment
Signaling molecule
Hydrogen Sulfide Formation: OffShoot of Metabolism
Due to release of reduced sulfide from the enzyme
complex sulfite reductase
Reduction of sulfate decoupled from amino acid
synthesis
Sulfate reduction regulated by nitrogen availability
Lack of nitrogenous reduced sulfur acceptors leads
to excessive production of reduced sulfate and
release as H2S
Also a stress response
Strain variation
Stress Response: Reduction
Pathway Remains Operational
Need cysteine for glutathione (tripeptide
cytoplasmic redox (electron) buffer
Need methionine for Sadenosylmethionine and one carbon
transfers needed for ethanol tolerance
Sulfate Reduction Pathway
SO4
SUL1, SUL2
SO4
MET3
Adenylylsulfate
H2 S
MET14
Phosphoadenylylsulfate
Sulfite
Sulfide
Cysteine
CYS3
Cystathionine
CYS4
MET16 (1,8,20,22)
MET10 (1,5?,8,20)
MET17/25/15
Homocysteine
MET6
Methionine
Hydrogen Sulfide Formation:
Reductive Environment
Biological energy is obtained from recapture
of light (carbon bond) energy, from proton
movements and from electron movements
Cell is dealing with an excess of electrons
that exceeds buffering capacity
Many electrons can be used to reduce a
single sulfate molecule restoring the proper
balance of cytoplasmic electrons
Hydrogen Sulfide Formation:
Reductive Environment
Tank dimensions leading to stratification of
electron gradients
Settling of yeast cells
Chemical composition of juice
Oxygen level and content of juice
Hydrogen Sulfide Formation:
Signaling Molecule
Hydrogen sulfide coordinates population
metabolic activities: shuts down respiration
in favor of fermentation, coordinating
population of cells in fermentation
Hydrogen sulfide inhibits respiration of a
variety of organisms: allows more rapid
domination of fermentation
Explains selective pressure for high sulfide
producers in the wild
Current Understanding of H2S Formation
Nitrogen levels not well-correlated with H2S
formation, but generally see increased H2S
at lower nitrogen
Tremendous strain variation in H2S
production
Can get H2S with high nitrogen
Get more H2S with higher solids content
Get more H2S with unsound fruit
Factors Impacting H2S Formation
Level of total nitrogen
Level of methionine relative to total nitrogen
Fermentation rate
Use of SO2
Vitamin deficiency
Presence of metal ions
Inorganic sulfur in vineyard
Use of pesticides/fungicides
Strain genetic background
Timing of Formation of H2S
Brix
H2S
Time
Timing of Formation of H2S
•Early (first 2-4 days): due to N/vitamin
shortage, electron imbalance, signaling
•Late (end of fermentation): due to
degradation of S-containing compounds
•Sur lie (post-fermentation aging): due to
autolysis
•In Bottle: screw cap closures: return
from an altered chemical form
HIGHER SULFIDES
Higher Sulfides
Emerge late in fermentation and during sur lie
aging
Release of compounds during entry into
stationary phase by metabolically active yeast
Come from degradation of sulfur containing
amino acids
Biological
Chemical
From reaction of reduced sulfur intermediates with other
cellular metabolites?
Formed chemically due to reduced conditions?
Degradation of cellular components: autolysis
Volatile Sulfur Compounds
Methanethiol: CH3-SH
Ethanethiol: C2H5-SH
Dimethyl sulfide: CH3-S-CH3
Dimethyl disulfide: CH3-S-S-CH3
Dimethyl trisulfide: CH3-S-S-S-CH3
Diethyl sulfide: C2H5-S-C2H5
Diethyl disulfide: C2H5-S-S-C2H5
Sources of Higher Sulfides
S-Containing Amino Acids
S-Containing Vitamins and Co-factors
Glutathione (Cysteine-containing tripeptide
involved in redox buffering)
Defining Metabolic Behaviors Resulting
in Taint Formation
S-amino acid catabolism
Vitamin/Co-factor interactions and
metabolism
Glutathione turnover and reactions
Metabolic roles of sulfate reduction
Defining Metabolic Behaviors Resulting
in Taint Formation
S-amino acid catabolism
Degradation of methionine and cysteine: methional
and methionol
Chemical reaction products of methionine and
cysteine: stress resistance
Influence of wine composition and chemistry on
yeast behavior
Vitamin/Co-factor interactions and metabolism
Glutathione turnover and reactions
Metabolic roles of sulfate reduction
Defining Metabolic Behaviors Resulting in
Taint Formation
S-amino acid catabolism
Vitamin/Co-factor interactions and
metabolism
Role
of thiamin
Role of S-adenosylmethionine
Glutathione turnover and reactions
Metabolic roles of sulfate reduction
Defining Metabolic Behaviors Resulting in
Taint Formation
S-amino acid catabolism
Vitamin/Co-factor interactions and
metabolism
Glutathione turnover and reactions
Role
in stress response: prevention of
oxidative damage
Impact of nitrogen level on metabolism
Biological turnover of ‘reacted’ glutathione
Metabolic roles of sulfate reduction
Defining Metabolic Behaviors Resulting in
Taint Formation
S-amino acid catabolism
Vitamin/Co-factor interactions and
metabolism
Glutathione turnover and reactions
Metabolic roles of sulfate reduction
Stress response:
Prevention of oxidative damage
Role in ethanol tolerance
Environmental/metabolic detoxification
Banking on reactivity to inactivate a toxic substance
Metabolic demands
Understanding the Interface between Metabolite
Production and Wine Chemistry and Composition
What environmental conditions impact Scompound metabolic activities?
Separating a biological response from a
chemical one
Control the metabolites
Control the chemistry
Sulfur Compound Flight #1
Spiked Compounds
Glass 1: Control Wine (Cabernet Sauvignon)
Glass 2: Hydrogen sulfide H2S
Glass 3: Dimethyl sulfide CH3-S-CH3
Glass 4: Dimethyl trisulfide: CH3-S-S-CH3
Glass 5: Diethyl sulfide: C2H5-S-C2H5
Glass 6: Diethyl disulfide: C2H5-S-S-C2H5
Sulfur Compound Flight #1
Spiked Compounds
•
•
•
•
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•
G 1: Control Wine (Cabernet Sauvignon)
G2: Hydrogen sulfide: rotten egg
G 3: Dimethyl sulfide: cabbage, cooked corn,
asparagus, canned
vegetable
G 4: Dimethyl trisulfide: meaty, fishy, clams, green,
onion, garlic, cabbage
G 5: Diethyl sulfide:
garlic, onion
G 6: Diethyl disulfide: overripe onion, greasy,
garlic, burnt rubber,
manure
Sulfur Compound Flight #2:
Taints produced late in fermentation
Glass 1: Control Wine (Cabernet Sauvignon)
Glass 2: Ethanethiol
Glass 3: Mercapto -2- methyl propanol
(Methionol)
Glass 4: Methyl thiopropionaldehyde
(Methional)
Glass 5: Mercapto-3-methyl butanol
Glass 6: BM45 French Colombard
Sulfur Compound Flight #2
Spiked Compounds
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•
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G 1: Control Wine (Cabernet Sauvignon)
G 2: Ethanethiol: onion, rubber, natural gas
G 3: Methionol: cauliflower, cabbage, potato
G 4: Methional: musty, potato, onion, meaty
G 5: Mercapto-3-methyl butanol: meaty
G 6: French Colombard: reduced
BM 45:
Isolated in Montalcino
Produces high polyphenol reactive
polysaccharides = mouth feel
Has high nitrogen requirements and can
produce H2S
Aroma characteristics: fruit jam, rose,
cherry, spice, anise, cedar and earthy