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Chill haze is
the most common type in beer; it is temporary in the sense that the haze appears on cooling the
beer, but disappears on warming. The greater the haze stability, the closer to 0 C the beer can be
brought before chill haze appears. Chill haze is formed by interactions between proteins and
polyphenols; the former are derived mostly from malt, whereas the latter come from both malt
and hops. Polyphenols (catechin family) and various oligomers are particularly active in forming
colloidal complexes with proteins from malted cereals, especially hordein (barley) and gliadin
(wheat). These proteins are rich in proline residues, which are disruptors thus forming random
coils in the proteins. Although these proteins are denatured during the early parts of the brewing
process, they will refold to some extent; never retrieving their native structures. The bonding
holding the complexes together is probably mostly weak hydrogen bonding that can be broken
at higher temperatures (25 C), thus explaining the disappearance of chill haze on raising the
temperature. However, chill haze appears to be a frequent precursor of permanent haze, the
polyphenols, occurs to give o-benzoquinone units which can then react with amino acid residues
of proteins to give much stronger covalent bonds that cannot be broken by raising the
temperature by 20 C. Beers produced by low oxygen regimes suffer least from this problem.
Permanent hazes are essentially caused by brewing fault. All the haze types displayed here can
be avoided in the brewery by using hygienic brewing techniques, along with good quality
materials and in the absence of market abuse (rough handling, storage at high temperatures,
etc.).
(B) Adjuncts in beer- 2 kinds of adjuncts are used in brewing; in the sense that they can be solid
(mashable adjuncts) or liquid (kettle) adjuncts. Solid (mashable) adjuncts must firstly be
starch hence it must be converted to sugar, providing substrate for yeast. This is accomplished by
gelatinization where - amylase can gain access to the granular starch molecules. A slurry
consisting of the adjunct and water is cooked (cooker), the starch granules start to adsorb water
and swell. They gradually lose their crystalline structure until they become large, gelfilled sacs
that tend to fill all of the available space and break with agitation and abrasion. Different
adjuncts have different gelatinization temperatures. It is impeccable (in some distilleries) that an
indirect proportionality exist between the slurry temperature of the adjunct (must be below
gelatinized temperature) and gelatinization temperature. This is done as to avoid frivolous belief
that the adjunct has been gelatinized which creates an impeccable layer of coating thereby
preventing penetration of enzymes to starch hence affecting conversion. Kettle adjuncts consist
of fermentable sugars (maltose). They contain the enzyme amylase and hence can convert their
own starch to sugar. These don not need to undergo mashing.Beta and alpha amylases directly
breaks down sugar hence kettle adjuncts do not need to be gelatinized; saccharification ensuses.
Some mashable adjuncts lack enzymes (eg. Rice and corn) whereas malted barley contains a
surplus of enzymes; stemming from malting process. Many distillers, however, go to the other
extreme and slurry at temperatures as high as 90C (190F). At these temperatures starch
gelatinizes almost immediately and with adequate agitation there is no increase in viscosity and
no loss of yield.
(C) Beer head- The foam in beer is generally considered to be the head on the top of the glass.
Beer head is formed from wort proteins, residual hops and yeast. Proteins consist of amino
groups which subsequently contain nitrogen which forms a constituent of beer heads.Mash ph
and temperature becomes important as these encoyage hydrophobic proteins. These aid in beer
terms of conferring stability to beer (head retention). In breweries 50% of bittering agent in hops
can be lost from boiling wort. Beers rich in bittering agents have good beer stability and hence
good head retention. This stems from iso acids in hops. The loss of hops from boiling sees many
breweries buying a pre isomerized hop product which stabilizes beer (3.5-5 ppm). Beers brewed
at high gravity tend to have poor foam performance. There are also other important visual effects
from the foam adhering to the side of the glass called Cling or Lacing. This effect is
particularly noticeable in beers, which form larger heads and have better foam performance. Beer
is a supersaturated solution of gas. In the case of lager this is carbon dioxide, but in the case of
ales may be a mixture of carbon dioxide and nitrogen gas. Bottle conditioned beers are
sometimes injected with nitrogen gas to influence beer head formation. When the beer is poured
out (either from a bottle or draught) the gas bubbles break out from solution and rise to the top of
the glass. As it pertains beer foam; 2 important parameters are considered, that is head formation
and head retention. The head formation is the ability of beer to form a head when poured. The
head retention is the ability of beer to retain a head once it has formed, after dispense. It is
necessary to have adequate head formation in order to ensure sufficient foam remains during the
(D) Diacetyl in beers- Diacetyl is a compound responsible for butterscotch flavours that
sometimes arise in beers. An understanding of its mechanism, leading to its production can
control diacetyl levels in beer. Diacetyl and other vicinal diketones (VDK) are important
contributors to beer flavor and aroma. Its threshold in breweries ranges from 0.03mg/L-1.0mg/L.
Diacetyl is unstable in beers. For some beer styles diacetyl can be a desired flavor constituent;
eg. Belgian ales. Originally it was believed that diacetyl formed in beers was attributed to
compound oftentimes arose. J Owades pioneered a technique which highlighted yeast a being the
major frontrunner in diacetyl formation and reduction. Research later discovered aceotolactic
acid as being the precursor for diacetyl. Enzymatic reduction by yeast produces acetoin and
subsequently butanediol which does not impart added flavor or aroma to the beer. Some yeast
strains are not good reducers; hence high levels of diacetyl remains in beer (non-flocculent
yeast). Yeast cropping and subsequent reuse can trigger high levels of diacetyl. This is because
yeast becomes respiratory deficient and mutations arise which compromises yeast reduction.
Gram positive bacteria (Pediococci) and gram negative lactobacilli can elevate diacetyl levels.
Temperature also affects diacetyl production and reduction. Hence ales and lagers which have
different fermenting temperatures are affected. This leads to diacetyl rest in breweries. Diacetyl
reduction is high in ales than lagers. Wort deficient in valine and leucine leads to accelerated
diacetyl levels. Wort must have sufficient free amino nitrogen (FAN) for reduction of diacetyl
(ideally; 300-325mg/L).
(E) Malolactic fermentation of wines- preceding alcohol fermentation, some wines undergoes
secondary fermentation in the form of malolactic fermentation. The mechanism converts malic
acid to lactic acid. This process is de-acidifies wines. This is true for grapes produced in cooler
climates where due to soil terroir; wines in such regions are often acidic. Malolactic fermentation
is carried out by Oenococcuc oeni, Lactobacillus, Leuconostoc and Pediococci sp. These bacteria
impart stability to wine, enriching composition of wine aroma. Bacteria influence aroma through
metabolic activity and modification of aromas derived from grape (fruity aroma-esters, buttery
note and reduction of vegetative aroma). Enzymes hydrolyze flavor precursors thus attributing
aroma. Besides aroma, malolactic fermentation affects wine body and mouthfeel. For warmer
for malolactic fermentation of wine. Vanillin derived from oak is often used by lactic acid
bacteria to sub sequential aroma compounds. Acetaldehyde present in wine affects the
metabolism of lactic acid bacteria. O. oeni is responsible for reducing vegetative aromas and
conversely produces ethanol and acetate. The most significant feature of malolactic fermentation
is its capability to produce butter flavours in wine. These are VDK (vicinal diketones) such as
diacetyl, acetoin etc. Unlike beers, diacetyl formation is ideal. This is imparted from the
conglomerate of lactic acid bacteria. Pediococci and yeast present during fermentation. Such
actions of diacetyl provide wines with mouth feel. It was also highlighted from recent studies the
modal action of O. oeni to reduce methionine, hence contributing to beer flavor impacting
sulphur compounds.
(F) Maturation of rums- Ageing in wood is generally carried out in ex-Bourbon casks, their
singed interiors imparting both flavor congeners and an amber or dark brown color, depending
on the severity of singeing and on the resting time in cask. Most rum aged this way remains in
the casks for no more than five years, but a few (particularly some Demerara, Jamaica and
Martinique rums) are aged for longer periods up to around 20 years. Rum aged in stainless
steel vats (colourless) can impart colour by added caramel or dark rum.While the rums are
maturing in oak barrels, natural tannins in the wood are extracted yielding a rich brown cast
following aging. The alcohol in the rum acts as a solvent and attracts the tannins due to porosity
of the wood as well as esters imparting rich rum flavours; depending on the age of the spirit. This
is referred to as a cycle and depending on how long rum is aged, it can undergo many cycles
under maturation. On the other hand, any color acquired by a light rum during wood ageing can
be removed by filtration through charcoal. In general, casked spirits age more rapidly in
10% per annum (angels share), as opposed to the 2% lost by Scotch whisky maturing in cask
in the cool, damp climate of Scotland. There are many differences in the concentrations of
certain components in the unaged white spirit and the cask-aged rums. In general, the aged rums
had higher levels of ethyl acetate, ethyl butanoate, ethyl isobutanoate, a number of other esters,
benzaldehyde and some terpenoids. On the other hand, sugar cane spirit have higher levels of
certain esters, some hydrocarbons, phenols and some edulans. Compounds normally associated
with wood ageing (e.g. acetals, certain lactones, phenols and terpenoids) are only present in the
aged rums.
(G) Blending rums- Distilleries with both pot and column stills have the advantage of
generating a number of rum marks. These are specific flavor profiles of rum. Due to pot stills
having high congers and esters generated from natural fermentation (heavy rum), different rum
marks are generated through blending. Column stills are pure hence lacking unwanted congeners
and hence flavours. Thus is becomes vital for blending different marks to achieve a desired rum.
Marks can be determined by GC or the natural sense of smell denoted Noses. Most aged rum is
destined for blends that are mostly medium bodied, consistent and whose bottles do not carry any
indication of age. However, there is a growing market for premium rums. Premium rums are
generally blends of spirits of different cask ages, whereupon the age of the youngest component
is stated on the bottle label, as for Scotch whisky. Premium rums, like fine Cognacs and malt
whiskies are meant to be sipped; they are usually medium to full bodied dark rums from Guyana,
Hati, Jamaica and the French West Indies, but premium rum is made elsewhere, notably
Barbados, Bermuda and the US Virgin Islands. A few rums from the French West Indies are even
vintage dated, like some Scotch malt whiskies. For rum, like most distilled beverages, the art of
year. The blenders job is to ensure that consistency, which depends on the union of several
distillates (or marks) to strike the best balance in the final product. This depends on the age and
congener profile of the distillates available for blending. After ageing and blending, but before
bottling, cask-aged rum is chilled and then filtered to remove flocs formed by the precipitation of
fatty acids.
References-
T.W.G. Solomons. (1984). Organic Chemistry: John Wiley and Sons, New York.
Zalacain A, Marin J, Alonso G, Salinas M .(2007). Analysis of wine primary aroma
compounds by stir bar sorptive extraction. Talanta 71:16101615