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Laboratory Report 1 Group 7 3H1
Laboratory Report 1 Group 7 3H1
Production of Beer
Babida, Niña Grace
Casiño, Jean Pearl
Gamay, Kresley
Jabunan, Eloida Jean
Pahuyo, Helms Christian
OBJECTIVES
The aim of this experiment is to determine and review the production of beer. The
experiment also addresses the following objectives:
• To monitor the viability of yeast during different stages of craft beer production
and to describe their role along with other ingredients, malt extract and hops;
• To learn about the different stages of the brewing process and to apply the
scientific method to the brewing process;
• And learning appropriate preventive food processing practices to apply to beer
production.
THEORY
Beers have been one of the go-to alcoholic beverages in occasions or events
ever since. With this, there have been different of types of beer depending on the place
it is produced and from what ingredient it is made. Examples of these types of beers
are sake in Japan from rice, pulque in Mexico from agave, bouza in Africa from corn,
etc (Young, 2021). Having these various beers in different locations, the process in
making these alcoholic beverage does not really differ from each other.
Furthermore, the brewing process has many stages. This process starts with
mashing, in which barley malt and brewing water are mixed, and heating of the slurry.
In this process, the enzymes that are found in the malt break down starch and proteins,
and formation of mixture of sugars, peptides, and amino acids takes place. A malt has
a variety of carbohydrates. It is composed of cellulose and soluble hemicellulose,
dextrin, starch, and sugars. About 50-60% of the weight of the malt is attributed to
starch, which is composed of amylose. Amylose decomposes into maltose,
maltotriose, and amylopectins during mashing. These saccharide units decompose
into glucose molecules. It is important to note that during mashing, the conversion of
starch into low-molecular weight fermentable sugars and unfermentable higher
molecular weight dextrin plays an important role. In addition to that, there are important
factors that need to be considered as they influence the enzymatic breakdown of the
starch molecules. These factors are time, temperature, and pH. Also, alpha- and beta-
amylase, the principal enzymes, have different pH and temperature operating range.
During the brewing process, the composition of the mash and the ratio of fermentable
and non-fermentable sugars are controlled by the difference in temperature optimum.
In the course of the mashing process, high operating temperature results to greater
proportion of unfermentable dextrins in the liquor. In contrast, during mashing, lower
operating temperatures result to formation of more fermentable sugars that leads to a
higher alcohol production during fermentation (Beddows, 2015).
PROCESS
A. Malting
Barley strains are sometimes better suited for fodder than for brewing. In
malting, the process begins with cleaning the barley grains; broken barley grains as
well as foreign grains, sand, metal parts, and so on, are removed. The grains are then
soaked in water at 10-15ºC. Because the grain absorbs water and eventually
increased in volume by about 4%, respiration of the embryo started as soon as water
is absorbed. To prevent grain spoilage, the spring water where micro-organisms
mostly evolved, is changed about every 12 hours for two to three days until the
moisture content of the grain is about 45%.
The grains are then dehumidified and transferred to either a malting floor or
rotary drum for germination. The heat generated by the sprouts further accelerated the
germination. At intervals, warm, moist air is blown through beds about 30 cm deep
with germinating seedlings or by sprinkling. The plant hormone gibberellic acid, which
is supplied to the grains to speed up germination, prompted the aleurone layer at the
grain periphery to produce multiple hydrolytic enzymes, which were then diffused into
the endosperm of the grain center where the synthesis of hemicellulose and alpha-
amylase enzymes took, and the existent of beta-amylase bound to proteins and
released by proteolytic enzymes took place.
C. Mashing
In this process, the enzymes are reactivated and were used to hydrolyze starch
and proteins, releasing nutrients for yeast nutrition. The soluble part of the malt is
utmost extracted, while the insoluble parts of the malt and additives are enzymatically
hydrolyzed. Mashing is done with three broad methods- decoction, infusion, and
double-mashing.
In the case of decoctions, the temperature of the mash is gradually increased
from 35-37°C to 70-75°C. About a third of the initial mash is removed, transferred to
the mash tun and slowly heated to boiling. Another portion is removed, boiled and
returned to the mash tun while the mash temperature is raised during the process.
While the starch granules are being cooked, gelatinized and exposed, the enzymes
have already been destroyed. Another portion is then removed, boiled and returned.
In this way, the process can be a one, two or three mash process, with the initial
temperature of 35-40°C favoring proteolysis; the mash is kept at 50°C for about half
an hour for complete proteolysis, at 60-65°C for about an hour for saccharification and
production of maltose, and at 70-75°C for two or three hours for dextrin production.
For the production of top-fermented beers, the infusion process is carried out
in a mash tun. The process involves milling malt and a smaller amount of unmalted
grain. The ground material or grist is thoroughly mixed with hot water in a 2:1 weight
ratio to produce a thick, mushy mash and the temperature is carefully raised and
maintained at about 65 for a period of time which varies from 30 minutes to °C held
for a few hours. On average, the holding time is 1-2 hours. More hot water at 75-78C
is sprayed onto the mash to preserve as much extract as possible and stop the enzyme
action.
In the double mashing process, the ground malt is mashed with hot water at
35°C. It is then held during protein rest for one hour for proteolysis. The supplements
are then cooked in a supplemental cooker for 60-90 minutes. Sometimes about 10%
malt is added during cooking. Hot cooked additive is then added to the ground malt
mash to raise the temperature to 65-68°C for starch hydrolysis and held at this level
for about half an hour. The temperature is then raised to 75°C-80°C, after which the
mashing is stopped. During the starch hydrolysis, the completion of the process is
checked with the iodine test.
D. Mash Separation
At the end of mashing, husks and other insoluble materials are removed from
the wort in two steps. First, the wort is separated from the solids. Second, the solids
themselves are freed from any further extractable material by washing or rinsing with
hot water. The skins and other solids from the mash are sieved into a lauter tub, which
is a vessel with a perforated false bottom about 10mm above the bottom proper, on
which the skins themselves form a bed through which filtration takes place. The Nooter
Strain Master, a tool commonly used in large breweries, is also used when filtration is
through a bed formed by the trays through a series of triangular perforated tubes
placed at different heights of the bed. Cloth filters placed in betwen plate filters and
screen centrifuges are also used. The sparging or hot water rinsing of the mash solids
is done with water at about 80°C and is continued until the extraction is considered
complete.,
E. Wort Boiling
Once a brewer has wort, it is sterilized by a lengthy boiling process in a kettle;
this stopped the enzyme activity and the liquid is then condensed. During the boiling,
which lasted 60-90 minutes, the hops are added after using the corn syrup or sucrose
as an additive at the beginning of the boiling process. Agitation and circulation of the
wort was also performed during boiling to increase the amount of precipitation and
flaking.
The hot wort is then prepared for pre-fermentation where it was not directly
passed into the fermentation tanks and the added dried hops are removed in a hop
sieve. During boiling, proteins and tannins are precipitated while the liquid is still warm.
The warm precipitation known as trub, which consists of 50-60% protein, 16-20% hop
resins, 20-30% polyphenols and around 3% ash, is then removed either with a
centrifuge or a vortex separator. The separated wort is cooled in a heat exchanger
and is ready for fermentation.
F. Fermentation
When transferring the fermenter, the wort was oxygenated at about 8 mg/liter
wort to provide the yeasts with the oxygen they need for initial growth; Fermentation
took place in a stainless-steel vat. The chilled wort is then pumped or gravity fed into
fermentation tanks and yeast is inoculated or added at a rate of 7-15 x 106 yeast cells
per milliliter collected from the previous brew.
CONCLUSIONS
In conclusion, making alcoholic beverages such as beer with the use of grains
and malt sauces from barley farm is a good way to get a gluten-free beer. In this sense,
sorghum malt was used in the experiment though it didn’t receive much recognition as
a brewing material it is somewhat ideal for beer-making for it is cheap, safe, and
available year-round in multiple countries. Sorghum malt’s abundance of alpha-
amylase is a critical concern for brewers because it digests large polymer of glucose
into small units which need further digestion by beta-amylase. The above process
makes it possible to produce beer from sorghum and sorghum malt with acceptable
sensory properties, a color suitable for commercial beer, and without the need for
additional carbon dioxide.
REFERENCES
Beddows, C. (2015, July 31). The Chemistry Behind Beer Flavor. Retrieved from
Elsevier SciTechConnect: https://scitechconnect.elsevier.com/chemistry-
behind-beer-
flavor/#:~:text=Brewing%20is%20a%20multistage%20process,and%20amino
%20acids%20are%20formed.