Showing posts with label anthocyanin. Show all posts
Showing posts with label anthocyanin. Show all posts

Thursday, December 10, 2015

Anthocyanin content as a source of color in red wine

According to Jackson (Wine Science), the sources of color in red wine are: (i) its anthocyanin content; (ii)the polymerization of grape-and oak-derived flavonoids; and (iii) the oxidation of grape- and oak-derived flavonoids. Of the three, anthocyanins are the most important. In this post I will discuss anthocyanins as the source of color in red wine.

As discussed previously, anthocyanins exist in grapes as glycosides (a bonding of the flavonoid component -- called an anthcyanidin -- with a sugar), a situation which increases both the chemical stability and solubility of the anthocyanidin.

The figure at the top shows the anthocyanidins in native form while the bottom shows a glucosylated Malvidin, Malvidin-3-glucoside.

The anthocyanin can be further complexed through the bonding of the sugar with either acetic, coumaric, or caffeic acid (Jackson).

Malvidin-3O-coumaroylglucoside

In wine, spectral color is a function of anthocyanin concentration, the concentration of co-factors which bind with anthocyanin to cause co-pigmentation, and the number and quality of polymeric pigments (Enology Note #120).

In young red wines, anthocyanins occur predominantly as a dynamic equilibrium between one molecular state bonded to sulfur dioxide and four free-form states. Most of these forms are colorless within the range of of wine pH. The exception is a small portion that exists in the flavylium state (2-phenylchromenylium ion), that portion being dependent on pH and free-sulfur dioxide content. According to Jackson, low pH increases the concentration of the flavylium (thus increasing redness) while increases in pH will decrease the color density as the proportion of anthocyanin in the flavylium declines.

When sulfites bind to anthocyanins, the anthocyanins go from a colored to a colorless form (Practical Winery). Because of its effectiveness as an anthocyanin bleacher, sulfur dioxide is the most significant factor affecting the color density of young red wines (Jackson).

The free form of anthocyanin is rendered stable by a number of short- and long-term factors. The short-term factor that is most impactful is co-pigmentation, a process whereby anthocyanin complexes are held together by hydrophobic interaction with non-anthocyanin compounds (anthocyanin-anthocyanin aggregates combined similarly are referred to as self-associations). According to Jackson, the stacking of molecules in these complexes "physically limits water access to (and hydration of) red flavylium and bluish quinoidal base states to colorless carbinol forms." In the case of these co-pigmentation complexes "covalent bonds form between acyl groups of anthocyanin and co-pigments."


The principal compounds which act as co-pigments are epicatechin, procyanidins, cinnamic acids, and hydroxycinnamoyl esters but a wide array of compounds may be involved in this role (Jackson).

Co-pigmentation has the following effects on young red wines (Jackson; Boulton):
  • It significantly increases color density and may affect color tint
  • It accounts for over half of the observed color of young red wines
  • It is important to the purplish coloration of young wines
  • Color enhancement has been found to be between two and ten times that expected from the pigment alone
  • It also adds temporary stability towards oxidation and SO₂ bleaching.
During the color extraction phase of wine production, co-pigmentation co-factors seem to attain a maximum extraction after which the ability to absorb additional pigments is exhausted. The general consensus seems to be that extraction seems to peak after approximately six days. In a review of Boulton's article, Curtis Phillips points out Boulton's position that saignée and a host of other contact regimes have yet to "demonstrate any ability to modify this equilibrium other than by temperature effects." And those results are short term.

In the Northern Rhone, Syrah has normally been blended with a small amount of Viognier and the resulting wine is rich in color. Phillips notes the following Boulton comment: "The possibility exists in which red grapes that are deficient in certain cofactors might benefit from being fermented in the presence of others that might have an excess of them, especially if they are cofactors, such as flavones, with limited solubility."

Anthocyanins in polymeric relationships will be discussed in a subsequent post.


Bibliography
Boulton, The Copigmentation of Anthocyanins and its role in the color of Red Wines: A Critical Review, AJEV 52(2), 2001.
Curtis Phillips, Recent Research: Comments on a Critical Review, Wine Business Monthly, July 2003.
Robert S. Jackson, Wine Science.
Enology Note #120, Virginia Tech.

©Wine -- Mise en abyme

Wednesday, December 9, 2015

The biosynthesis of anthocyanins

The quantity and quality of phenolic compounds (especially tannins, anthocyanins, and co-factors) in the wine post-fermentation, and the interaction of those compounds, are critical elements in the postmodern winemaking process as laid out by Clark Smith. Before delving into these phenolic interactions, I sought to provide some background, beginning with tannins in a prior post and anthocyanins in the current.

The most important source of color in red wines is anthocyanin, a class of phenolic compound resident in grape skins. As is the case for all phenolic compounds, anthocyanin is synthesized from the amino acid phenylalanin through the phenylpropanol and flavonoid pathways (graphically illustrated below).


The flavonoid pathway. Abbreviations:
ANS -- anthocyanidine synthase;
CHI -- chalcone isomerase;
CHS -- chalcone synthase;
DFR -- Dihydroflavonol reductase;
F3H -- flavanone 3-hydroxylase;
GT -- glucoysltransferase;
Source: 
http://www.hindawi.com/

Grape anthocyanidins. Source: www.intechopen.com/books/

Anthocyanins are synthesized directly from anthocyanidins by glycosylation (adding of a sugar to a protein) at the 3 and 5 positions of the C ring and are accumulated in the berry skins from veraison until full maturity. After synthesis in the cytosol (fluid portion of the cell cytoplasm), anthocyanins are transported into the vacuole (cell organelle responsible for a number of functions including nutrient storage) where they are stored as colored coalescences called anthocyanic vascular inclusions (Flamini, et al.)

Environmental effects can influence anthocyanin content in the fruit but its composition is most closely associated with grape variety. In the fruit, anthocyanin has the following functions (Flamini, et al.):
  • Protection against solar exposure and and UV radiation
  • Protection against pathogen attacks
  • Protection against oxidation attacks
  • Protection against attacks by free radicals
  • Attracting animals for seed dispersal after the fruit has attained maturity
Each anthocyanin has a particular hue ranging from red to blue (shown below) and the combination of quantities and profiles will determine the color intensity of fruit and wine.

Grape anthocyanins. Source: gopixpic.com

In a follow-up post I will describe anthocyanin interactions and reactions in young wines.


Bibliography
Flamini, et al., Advanced knowledge of three important classes of grape phenolics: Anthocyanins, Stilbenes, and Flavonols, Int J Mol Sci. 2013, Oct; 14910). Accessed online at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821578/
Enology Note #120


©Wine -- Mise en abyme

Sunday, September 20, 2015

Sources and roles of phenolic compounds found in wine

Phenols are highly reactive chemical compounds of primary importance in the quality of red wines. Phenol, the basic building block, is an aromatic organic compound (formula C6H5OH) where the phenyl group (C6H5, where six bonded carbon atoms with alternating double bonds are connected to five hydrogen atoms) is bonded to a hydroxyl group (OH, where the oxygen atom is covalently bonded to an hydrogen atom). A graphical representation of a phenol is provided below.


Phenolic compounds are:
  • Responsible for the color of red grapes and wine
  • Involved in the oxidative browning of white wines
  • Contributors to taste and astringency through interactions with salivary proteins
  • Another measure of wine quality.
The two major classes of wine phenolic compounds are flavonoids (defined by a C6-C3-C6 skeleton consisting of two phenolic rings joined by a central, oxygen-containing ring -- Jackson) and nonflavonoids (possessing a C6-C1 or C6-C3 skeleton; all numbers following "C" are subscripts). The sources and roles of the phenolic compounds falling into these two classes are illustrated in the figure below and the relative concentrations of selected classes are provided in the table following.


Table 1. Generalized concentration of various phenolic compounds
present in wine
Phenolic White Wine (mg/L) Light Red Wine (mg/L) Full Red Wine (mg/L)
Volatile Trace
10
40
Hydroxycinnamic acids
150
200
200
Other nonflavonoids
25
40
60
Anthocyanins
0
200
400
Catechins
25
150
200
Polymeric catechins
0
600
900
  Totals
200
1200
1800
Source: Kennedy, et al., Grape and wine phenolics: History and perspective,
AJEV, 57(3), September 2006.


©Wine -- Mise en abyme