Malic
and tartaric acid are the primary acids in wine grapes.
The acids
in wine are an important component in both winemaking and
the finished product of wine. They are present in both grapes
and wine, having direct influences on the color, balance and
taste of the wine as well as the growth and vitality of yeasts
during fermentation and protecting the wine from bacteria. The
measure of the amount of acidity in wine is known as the “Titratable
Acidity†or “Total acidityâ€, which refers to the test
that yields the total of all acids present, while strength of
acidity is measured according to pH with most wines having a
pH between 2.9–3.9. Generally, the lower the pH, the higher
the acidity in the wine. However, there is no direct connection
between total acidity and pH (it is possible to find wines with
a high pH for wine and high acidity).[1] In wine tasting,
the term “acidity†refers to the fresh, tart and sour attributes
of the wine which is evaluated in relation to how well the acidity
balances out the sweetness and bitter components of the wine
such as tannins. There are three primary acids found in wine
grapes: tartaric, malic and citric. During the course of winemaking
and in the finished wines, acetic, butyric, lactic and succinic
acid can play significant roles. Most of the acids involved
with wine are fixed acids with the notable exception of acetic
acid, mostly found in vinegar, which is volatile and can contribute
to the wine fault known as volatile acidity. Sometimes additional
acids are used in winemaking such as ascorbic, sorbic and sulfurous
acids.[2]
Tartaric
acid
Tartaric
acid is, from a winemaking perspective, the most important in
wine due to the prominent role it plays in maintaining the chemical
stability of the wine and its color and finally in influencing
the taste of the finished wine. In most plants, this organic
acid is rare but it is found in significant concentrations in
grape vines. Along with malic acid, and to a lesser extent citric
acid, tartaric is one of the fixed acids found in wine grapes.
The concentration varies depending on grape variety and the
soil content of the vineyard. Some varieties, such as Palomino,
are naturally deposed to having high levels of tartaric acids
while Malbec and Pinot noir generally have lower levels. During
flowering, there are high levels of tartaric acid concentrated
in the grape flowers and then young berries. As the vine progresses
through ripening, tartaric does not get metabolized through
respiration like malic acid so that the levels of tartaric acid
in the grape vines remains relatively consistent throughout
the ripening process.[3]
Less than
half of the tartaric acid found in grapes is free standing,
with the majority of the concentration present as potassium
acid salt. During fermentation, these tartrates bind with the
lees, pulp debris and precipitated tannins and pigments. While
there is some variance among grape varieties and wine regions,
generally about half of the deposits are soluble in the alcoholic
mixture of wine. The crystallization of these tartrates can
happen at unpredictable times and in a wine bottle appear like
broken glass though they are in fact harmless. Winemakers will
often put the wine through cold stabilization where it is exposed
temperatures below freezing to encourage the tartrates to crystallize
and precipitate out of the wine.[3]
Malic
acid
Riesling
from cool climate wine regions, such as the Rheingau in
Germany will have more malic acid and green apple notes
than wines from warmer regions.
Malic acid,
along with tartaric acid, is one of the principal organic acids
found in wine grapes. It is found in nearly every fruit and
berry plant but its most often associated with green apples
from which flavor it most readily projects in wine. Its name
comes from the Latin malum. In the grape vine, malic
acid is involved in several processes which are essential for
the health and sustainability of the vine. Its chemical structure
allows it to participate in enzymatic reactions that transport
energy throughout the vine. The concentration of malic acids
varies depending on the grape variety with some varieties, like
Barbera, Carignan and Sylvaner being naturally deposed to high
levels. The levels of malic acid in grape berries are at their
peak just before veraison when they can be found in concentrations
as high as 20 g/L. As the vine progresses through the ripening
stage, malic acid is metabolized in the process of respiration
and by harvest could be as low as 1 to 9 g/L. The respiratory
loss of malic acid is more pronounced in warmer climates. When
all the malic acid is used up in the grape it is considered
“over-ripe†or senescent. Winemakers must compensate for
this loss by manually adding acid at the winery in a process
known as acidification.[4]
Malic acid
can be further reduced during the winemaking process through
malolactic fermentation or MLF. In this process bacteria convert
the stronger malic acid into the softer lactic acid: formally,
malic acid is polyprotic (contributes multiple protons, here
2), while lactic acid is monoprotic (contributes 1 proton),
and thus has only half the effect on acidity (pH); also, the
first acidity constant (pKa) of malic acid
(3.4 at room temperature) is lower than the (single) acidity
constant of lactic acid (3.86 at room temperature), indicating
stronger acidity. Thus after MLF, wine has higher pH (less acidic),
and different mouthfeel.
The bacteria
behind this process can be found naturally in the winery, in
cooperages which make oak wine barrels that will house a population
of the bacteria or it can be manually introduced by the winemaker
with a cultured specimen. For some wines, the conversion of
malic into lactic acid can be beneficial, especially if the
wine has excessive levels of malic. For other wines, such as
Chenin blanc and Riesling, it produce off flavors in the wine
(such as the buttery smell of diacetyl) that would not be appealing
for that variety. In general, red wines are more often put through
MLF than whites which means that there is a higher likelihood
of finding malic acid in white wines (though there are notable
exceptions like oaked Chardonnay which is often put through
MLF).[4]
Lactic
acid
Chardonnay
is often put through malolactic fermentation when it is
being oaked. The softer, milky lactic helps contribute to
a creamier mouthfeel in the wine.
A much milder
acid than tartaric and malic, lactic acid is often associated
with milky flavors in wine and is the primary acid of yogurt
and sauerkraut. It is produced during winemaking by lactic acid
bacteria (known as LAB) which includes three genera: Oenococcus,
Pediococcus and Lactobacillus. These bacterium convert
both sugar and malic acid into lactic acid, the later through
a process known as malolactic fermentation or MLF. The process
of converting malic into lactic acid can be beneficial for some
wines, adding complexity and softening the harshness of malic
acidity but it can generate off flavors and turbidity in others.
Some strains of LAB can produce biogenic amines like histamine,
tyramine and putrescine which may be a cause of red wine headaches
in some wine drinkers. Winemakers wishing to control or prevent
MLF can use sulfur dioxide to stun the bacteria. Racking the
wine quickly off its lees will also help control the bacteria
since lees are a vital food source for them. They must also
be very careful of what wine barrels and winemaking equipment
that the wine is exposed to because of the bacteria's ability
to deeply embed themselves within wood fibers. A wine barrel
that has completed one successful malolactic fermentation will
almost always induce MLF in every wine that gets stored in it
from then on.[5]
Citric
acid
While very
common in citrus fruits, such as limes, citric acid is found
only in very minute quantities in wine grapes. It often has
a concentration about 1/20 that of tartaric acid. The citric
acid most commonly found in wine are commercially produced acid
supplements derived from fermenting sucrose solutions. These
inexpensive supplements can be used by winemakers in acidification
to boost the total acidity of the wine. It is used less frequently
than tartaric and malic due to aggressive citric flavors that
it can add to the wine. When citric acid is added, it is always
done after primary alcohol fermentation has been completed due
to the tendency of yeast to convert citric into acetic acid.
In the European Union, use of citric acid for acidification
is prohibited but limited use of citric acid is permitted for
removing excess iron and copper from the wine if potassium ferrocyanide
is not available.[6]
Other
acids
Acetic
acid is a two-carbon fatty acid produced in wine during
or after the fermentation period. It is the most volatile of
the primary acids associated with wine and is responsible for
the sour taste of vinegar. During fermentation, activity by
yeast cells naturally produce a small amount of acetic acid.
If the wine is exposed to oxygen, acetobacter bacteria will
convert the ethanol alcohol into acetic acid. This process is
known as the “acetification†of wine and is the primary
process behind wine degradation into vinegar. Excessive amounts
of acetic acid is also considered a wine fault. A taster's sensitivity
to acetic acid will vary but most people can detect excessive
amounts at around 600 mg/L.[2]
Ascorbic
acid, also known as vitamin C, is found in young wine grapes
prior to veraison but is rapidly lost throughout the
ripening process. In winemaking it is used with sulfur dioxide
as an anti-oxidant to prevent oxidation, often added during
the bottling process for white wines. In the European Union,
use of ascorbic acid as an additive is limited to 150 mg/L.[7]
Butyric
acid is a bacteria-induced wine fault that can cause a wine
to smell of spoiled Camembert or rancid butter.[8]
Sorbic
acid is a winemaking additive used often in sweet wines
as a preservative against fungi, bacteria and yeast growth.
Unlike sulfur dioxide, it does not hinder the growth of the
lactic acid bacteria. In the European Union there is a limitation
on the amount of sorbic acid that can be added no more than
200 mg/L. Most humans have a detection threshold of 135 mg/L,
with some having a sensitivity to detect its presence at 50 mg/L.
Sorbic acid can produce off-flavors and aromas which can be
described as “rancidâ€. When lactic acid bacteria metabolizes
sorbates in the wine, it creates a wine fault that is most recognizable
by an aroma of crushed Pelargonium geranium leaves.[9]
Succinic
acid is most commonly found in wine but can also be present
in trace amounts in ripened grapes. While concentration varies
amount grape varieties, it is usually found in higher levels
with red wine grapes. The acid is created as a by-product of
the metabolization of nitrogen by yeast cells during fermentation.
The combination of succinic acid with one molecule of ethanol
will create the ester mono-ethyl succinate that is responsible
for a mild, fruit aroma in wines.[10]
In
winemaking
A wine
with high pH and low acidity like Carménère
will have more bluish color notes than a wine with
high acidity.
Acidity
is highest in wine grapes just before the start of veraison,
which ushers in the ripening period of the annual cycle of grape
vines. As the grapes ripen, their sugars level increase and
their acidity decreases. Through the process of respiration,
malic acid is metabolized by the grape vine. Grapes from cooler
climate wine regions, generally have a higher level of acidity
due to the slower ripening process which is accelerated by warmer
temperatures. The levels of acidity still present in the grape
is an important consideration for winemakers in deciding when
to begin harvest. For wines, like Champagne and other sparklers,
having high levels of acidity is even more vital to the winemaking
process and so grapes are often picked under-ripe and at higher
acid levels.[2]
In the winemaking
process, acids aid in enhancing the effectiveness of sulfur
dioxide to protect the wines from spoilage and can also protect
the wine from bacteria due to the inability of most bacteria
to survive in an acidic solution. Two notable exceptions to
this are acetobacter and the lactic acid bacteria. In red wines,
acidity helps preserve and stabilize the color of the wine.
The ionization of anthocyanins is affected by pH so wines with
lower pH (such as Sangiovese based wines) have redder colors
that are more stable. Wines with higher pH (such as Syrah based
wines) have more blue pigments that are less stable, eventually
taking on a muddy grey hue. These wines can also develop a brownish
tinge. In white wines, higher pH (and such lower acidity) cause
the phenolics in the wine to darken and eventually polymerize
as brown deposits.[2]
Winemakers
will sometimes add additional acids to the wine, known as acidification,
in order to increase the acidity level of the wine. This is
most common in warm climate regions where grapes are often harvested
at advanced stages of ripeness with high levels of sugars but
very low levels of acid. Tartaric acid is most often added but
winemakers will sometimes add citric or malic acid. Acids can
be added either before or after primary fermentation. It can
be added during blending or aging but the increase acidity will
become more noticeable to wine tasters if added at this point.[2]
In
wine tasting
The acidity
in wine is an important component in the quality and taste of
the wine. It adds a sharpness to the flavors and is detected
most readily by a prickling sensation on the sides of the tongue
and a mouth watering after taste. Of particular importance is
the balance of acidity versus the sweetness of the wine (the
left over residual sugar) and the more bitter components of
the wine (most notably tannins but also includes other phenolics).
A wine with too much acidity will taste excessive sour and sharp.
A wine with too little acidity will taste flabby, flat and with
less defined flavors.[2]
See Also:
Home
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Science of Wine Aroma
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(Tannins) in Wine
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in Wines
The Basic Wine Pairing Rules
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in Wine
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a Wine Sommelier
References
- Bellman, R. B.; Gallander, J. F. (1979). [Deacidification
in Wine "Wine Deacidification"]. In Chichester, C. O.;
Mrak, Emil Marcel; Stewart, George Franklin. Advances in Food Research Vol. 25. Academic Press. pp. 3.
. Deacidification in Wine. Retrieved 2009-08-04.
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J. Robinson (ed) The Oxford Companion to Wine
Third Edition pg 2-3 Oxford University Press 2006
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J. Robinson (ed) The Oxford Companion to Wine Third
Edition pg 681 Oxford University Press 2006
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J. Robinson (ed) The Oxford Companion to Wine Third
Edition pg 421–422 Oxford University Press 2006
- J.
Robinson (ed) the Oxford Companion to Wine Third
Edition pg 387 Oxford University Press 2006
- J.
Robinson (ed) The Oxford Companion to Wine Third
Edition pg 171 Oxford University Press 2006
-
J. Robinson (ed) The Oxford Companion to Wine Third
Edition pg 35-36 Oxford University Press 2006
-
International Sommelier October, 2003, pg 10. Accessed 10/4/2008
-
J. Robinson (ed) The Oxford Companion to Wine Third
Edition pg 644 Oxford University Press 2006
-
J. Robinson (ed) The Oxford Companion to Wine
Third Edition pg 665 Oxford University Press 2006