3. Quality assurance (QA) and quality control (QC). Flashcards
(136 cards)
What are the components of wine?
- Alcohol.
- Acids.
- Esters.
- Residual sugars.
- Glycerol.
- Aldehydes/ketones.
- Phenolic compounds
Why are aromas hard to fully detect in wine.
- People sensitivity - there are 1000 volatile compounds/molecules, only a few have a threshold of perception, and people will have different threshold for each molecules.
- Aromas are not additive, but a sum of different chemicals interactions like:
A. Masking interaction - one compound masks another.
B. Synergistic interaction - combination of multiple compounds to form an aroma.
What are the compounds that are forming aromas?
- Wine aroma - 20 main different aromatic chemicals, the only one present in grapes is b-damascenone, the rest is all produced by yeast’s metabolism working on precursors in grape juice.
- Contributory compounds - low perception threshold compounds with high synergistic interactions.
- Impact compounds - low concentration but they contribute to varietal character, many wines lack these compounds.
- Nonvolatile wine matrix - wine constituents with no aromatic characteristics influence aromatic molecules perception.
Main wine aromas are coming from?
- Higher alcohols (e.g. butyric, isoamylic, hexylic, phenylethylic).
- Acids (acetic, butyric, hexanoic, octanoic, isovaerianic).
- Ethyl esters from fatty acids.
- Acetates and compounds (e.g. diacetyl).
- Ethanol.
Most common contributory compounds.
- Volatile phenols (e.g. guiaicol, eugenol, isoeutigenol, 2,6dimethoxyphenol, allyl-2,6-dimethoxyphenol).
- Ethyl esters.
- Fatty acids.
- Acetates of higher alcohols.
- Ethyl esters of branched fatty acids.
- Aliphatic aldehydes with 8 to 10 carbon atoms.
- Branched aldehydes (e.g. 2-methylpropanol, ketons)
- Vanillin and its derivatives.
Famous impact compounds.
- Methoxypyrazine - green, grassy aromas, is formed in grapes and is highly stable during fermentation/ageing.
- Monoterpenes - eg. linalool the floral compound of Muscat and rose-cis oxide, the rose of Gewurztraminer.
- Rotundone - pepper in Syrah.
- Polyfunctional thiols (mercaptans) - tropical fruit scent in Sauvignon Blanc (called 4MMP, 3MHA, 3MH).
Most famous volatile compounds for wine aromas.
- Esters - reaction of organic acids with alcohols during fermentation and ageing. (e.g. ethyl acetate = acetic acid + ethanol), mostly are fruity aromas also oily, herbaceous, buttery, nutty.
- Aldehydes - minor but important in Sherry for acetaldehyde.
- Vanillin - from oak barrels.
- Ketons - mainly diacetyl, buttery aromas (also from acetoin) or roses/floral in Chardonnay or bouquet in Riesling (b-damascenone) at low level, bad at high levels like bitter taint of benzoic (usually comes from bad application of epoxy resin in vat lining).
- Higher alcohols/fused oils - amyl alcohols pungent aromas that can be pleasurable in contained quantities (e.g. hexanol grassy aromas).
- Lactones - sweet spicy coconut in oak, or botrytised and oxidated wines for aromas of sweet spicy toast and nuts.
- Acetic acid (acetobacter) - sour and vinegar aromas.
- Volatile phenols - brettanomyces forms 4-ethylphenol and 4-ethylguaiacol has aromas of spiicy, gamey. animal.
- Terpenes - floral, grapey, linalool, geranium character in Muscat, Gewurz, Pinot Gris. There are around 40 different types in the grapes but only 24 can really pass the threshold.
- Methoxypyrazines - metabolism of amino acids, heterocyclic compounds that contain nitrogen, herbeceous aromas in Cab Franc, Sauv, and Sauvvy B.
- Volatile sulfut compounds - mercaptans (thiols) in controlled quantities are good, if too high is a fault.
What gives green aromas to wine?
- Compound group called alkyl-methoxypyrazines - present in green tissue of plants (e.g. green bell pepper). Most famous type is isobutyl (high threshold), also isopropyl and sec-butyl in low levels.
Methoxy can also be influence by other things:
A. Insect taint - e.g. ladybug has insane levels of methoxypyrazine and can taint a wine if found in the middle of the bunches, or falls into the vat.
B. Viruses - leafroll virus delays berry maturation so more methoxypyrazine are retained.
- Green leaf volatiles - oxyplin pathway chemical reaction, typical from plant defence.
- Eucalyptus taint - molecules are transferring from eucalyptus and pine trees.
How methoxypyrazine grows inside a grape and why?
Together with tannins they work as antifeedand for the birds - to keep them away to eat grapes when unripe.
They grow reaching a high level just before veraison, then they decrease with ripeness.
How can a winemaker lower the levels of methoxypyrazines?
Methoxypyrazine are a stable compound (also during and after fermentation) and don’t go away with simply more hang time.
- Expose grapes to the sun with leaf removal (reduce accumulation rather than increase degradation, so impact is minor).
- Slowing growth just before accumulation phase.
- Winemaking techniques such as oak ageing, gentle pressing, must clarification in must, thermovinification. Low level of impact. Most of the work needs to be done in the vineyard.
How alcohol impacts wine aromas?
- Alcohol and natural acids, coming in contact, form esters.
Usually esters are split apart again by water (hydrolysed) into acids and alcohol and then recombined in different ways creating more aromas.
Higher-alcohol wines have more fruity aromas (e.g. pineapple, bananas, strawberry, raspberry and others).
- Alcohol can also masks aromas as it modify solubility of aroma compounds and it doesn’t leave the solution making the wine less aromatic.
- Alcohol has a sweet tasting component to it. Infact low alcohol wines are drier. The problem if that when it’s too high it does have an effect of making the wine hot, astringent and bitter.
How alcohol is chemically formed?
Carbon chain (carbon C groups with hydrogen H) + OH (group that gives alcohol its characteristics)
The number of carbon chains present forms different types of alcohol.
Is ethanol the only form of alcohol produced during fermentation?
No, is just the dominant.
All the small quantities of other alcohol are playing a part in bouquet and flavour.
How can we divide types of alcohol in wine?
By relating them to ethanol in carbon chains.
- Less carbon chains than ethanol.
Methanol (CH3OH) - unpleasant and highly toxic (in high quantities can bring blind, madness and death). In wine has low quantities, while in spirit it is discarded as head (boils at low temperature).
- Ethanol (CH3CH2OH).
- Higher alcohols/fused oils - bigger carbon chains than ethanol.
Propanol (CH3CH2CH2OH) and Butanol (CH3CH2CH2CH2OH).
Less toxic but unpleasant (nausea, headaches). They are discarded in spirits as tails boiling at high temperatures.
How can you calculate alcohol by volume rather than weight?
17 grams of sugar = 1% alcohol volume.
In this way you can calculate alcohol and volume of enrichment.
E.g. if a must has 170 g/L it will be equal to 10% so if 2% more is required you will need 34 g/L.
To understand the total you can then multiply 34 for the mass of must e.g. 4000 litles X 34 = 136 kg.
It is a simplification, as fermentation is more complex than this but it is helpful.
What happens to alcohol when it oxidises? What it produces?
(all VA questions can be used into Va section later in this chapter)
- Acetic acid (the acid of vinegar) is produced through the influence of acetic bacteria (acetobacter). It is also called volatile acidity.
Ethanol (CH3CH2OH) + oxygen (O2) = acetic acid (CH3COOH) + water (H2O).
It is an aerobic process, VA needs oxygen to form.
- Aldehyde - ethanol oxidation specifically produces acetaldehyde (ethanal) which is the most important aldehyde (90% in wine).
Where are the bacteria for VA present?
In the skins of the grapes.
For this reason it is hard to find rose and white wines with high VA.
Is volatile acidity good for the wine? When it become noticeable? What does is smell of?
Every wine has a particular amount of it, it add complexity to the wine but needs to be kept in check as if high can become a fault.
Becomes noticeable at 0.8g/L. Limits on VA in EU is 1.2g/L for reds and 1.08g/L for whites and roses.
If too high it will smell like nail varnish removal or cellulose thinners.
Can you name two examples of rising VA and the causes?
- VA raises with time. Older wines will have a stronger VA.
- Esterification - similar to bottle maturing process. The acetic acid (CH3COOH) reacts with ethanol (HOCH2CH3) and produces (=) the ester ethyl acetate (CH3COOCH2CH3) and water (H2O) augmenting VA aromas.
- Hot climates and warm temperature fermentation will increase the rate of activity of the bacteria.
How can a winemaker get rid of VA?
- Filter the bacteria out.
- Gas blanket the vat (nitrogen, CO2 or a mixture of both).
- SO2 calm the bacteria.
What are the problems of acetaldehyde?
- Unpleasant flavours - yeasty, green apple (good in fino sherry though).
- Binds with sulphur dioxide producing bisulfite components and lowering SO2 protection.
These problems are rare thanks to modern equipment in the winery.
- Can cause headaches in certain people.
What is the third most abundant component of wine after alcohol and water?
Glycerol (4g/L to 10g/L).
Colourless liquid with a sweet taste - improves mouthfeel giving weight and smoothness to the wine.
You can see it as the legs in the wine glass are formed by the combination of alcohol and glycerol due to a surface tension effect.
How glycerol is formed?
- From the sugar of the grapes, during fermentation (the higher the sugars, the higher the glycerol levels).
- Yeast strain can affect levels.
- In botrytis cinerea wines glycerol is naturally formed by noble rot’s metabolism reaching up to 30g/L giving lush, smooth viscosity.
Can a winemaker influence esters formation?
Yes.
- Use specific commercial yeasts.
- Add specific malolactic bacteria.
- Lower temperatures (to retain aromas, high will destroy them).
- Acidification to increase esters formation.