Professional Documents
Culture Documents
MICROORGANISMS IN FOOD
PROCESSING
BY
JAIYESINMI ADEOLA PRAISE
19/57MB/01226
2
MICROORGANISMS AND FOOD
Microorganisms are a group of tiny (microscopic) organisms that live all around
us (and on us).
However, some bacteria and fungi are commonly used to make food; viruses
have no widespread use in food production.
3
HISTORY OF MICROORGANISM USE
IN FOODS
4
MICROORGANISMS IN FERMENTED
FOODS
1. Bacteria
Bacteria are the most dominant microorganisms in both naturally
fermented foods fermented by the use of starter cultures. Among
the bacteria, lactic acid bacteria are commonly associated with
acidic fermented foods, while non-LAB bacteria such as Bacillus,
micrococcaceae, Bifidobacterium, Brachybacterium,
Brevibacterium, and Propionibacterium etc., are also involved in
food fermentation, frequently as minor or secondary groups.
5
MICROORGANISMS IN FERMENTED
FOODS
2. Fungi
The major roles of fungi, mostly filamentous molds, in fermented
foods and alcoholic beverages are the production of intra- and
extracellular proteolytic and lipolytic enzymes that highly influence the
flavor and texture of the product, and also the degradation of
antinutritive factors improving bioavailability of minerals (Aidoo and
Nout, 2020). Species of Actinomucor, Amylomyces, Aspergillus,
Monascus, Mucor, Neurospora, Penicillium, Rhizopus, and Ustilago are
reported from many fermented foods, Asian nonfood amylolytic starters
and alcoholic beverages (Aidoo and Nout, 2020).
6
MICROORGANISMS IN FERMENTED
FOODS
2.1 Yeasts
The role of yeasts in food fermentation is to ferment sugar, produce secondary
metabolites, inhibit growth of mycotoxin-producing molds and display several
enzymatic activities such as lipolytic, proteolytic, pectinolytic, glycosidasic and urease
activities (Watanabe et al., 2019). Genera of yeasts reported from fermented foods,
alcoholic beverages and nonfood mixed amylolytic starters are Brettanomyces,
Candida, Cryptococcus, Galactomyces, Geotrichum, Kluyveromyces, Metschnikowia,
Pichia, Rhodotorula, Rhodosporidium, Saccharomyces Saccharomycodes,
Saccharomycopsis, Schizosaccharomyces, Torulaspora, Torulopsis, Trichosporon,
Yarrowia, and Zygosaccharomyces (Watanabe et al., 2020).
7
FACTORS THAT INFLUENCE THE
DEVELOPMENT OF FERMENTED FOODS
1. Salt Concentration
The lactic acid bacteria are known to tolerate high salt
concentration which gives them advantage to proliferate
over non-salt tolerant microorganisms. Leuconostoc sp
is known to majorly initiate lactic acid fermentations
because they have high salt tolerance levels (Prescott et
al., 2020).
1
8
FACTORS THAT INFLUENCE THE
DEVELOPMENT OF FERMENTED FOODS
2. Temperature
Different groups of bacteria function within certain temperature
range which is relevant to different fermentation processes (Lee
et al., 2019). Some bacteria have optimum temperature between
20 to 30 0C, higher temperatures of 50 – 55 0C and colder
temperatures of 15-20 0C while lactic acid bacteria and
Lactobacillus species function best at 18 – 22 0C (Lee et al.,
2019).
9
1
FACTORS THAT INFLUENCE THE
DEVELOPMENT OF FERMENTED FOODS
3. Hydrogen ion concentration (pH)
For most bacteria, their optimum pH is around 7.0
while some survive at low pH levels. Acid tolerant
bacteria such as Streptococcus sp and Lactobacillus sp
play significant roles in dairy and vegetable product
fermentations (Lee et al., 2019).
10
1
FACTORS THAT INFLUENCE THE
DEVELOPMENT OF FERMENTED FOODS
4. Water activity
Generally, bacteria require fairly high water activity of about 0.9 and
above to thrive. Only few species of bacteria could survive water
activities lower than the above as yeasts and fungi proliferate in foods
with low water activities (Prescott et al., 2020).
1 11
FACTORS THAT INFLUENCE THE
DEVELOPMENT OF FERMENTED FOODS
5. Oxygen availability
Fermentative bacteria could be anaerobes or aerobic depending on their
requirement for oxygen to undergo metabolism. Lactobacillus sp are
microaerophilic as they grow in reduced atmospheric oxygen. Insufficient
oxygen being available during aerobic fermentation becomes a limiting factor
since it is what determines the product, the energy released and the amount of
biological product obtained from the reaction (Lee et al., 2020).
1
12
ROLE OF MICROORGANISMS IN THE PRODUCTION OF SOME
INDIGENOUS FERMENTED FOODS IN NIGERIA
1. FUFU
Bacillus sp plays a major role by breaking down the pectin in the cell
walls of the cassava root (Adesulu and Awojobi, 2018). This was as a
result of the production of pectinase. After the pectinase activity, the
lactic acid bacterium (LAB) acts by the production of flavour. The soft
tubers are then sieved and allowed to sediment and dewatered with press
(Adesulu and Awojobi, 2018).
13
ROLE OF MICROORGANISMS IN THE PRODUCTION OF
SOME INDIGENOUS FERMENTED FOODS IN NIGERIA
2. GARI
Corynebacterium manihot played a significant role in the fermentation of Gari (Oyewole and Isah,
2020). It breaks down the starch to organic acids including lactic acid. This brings about a drop in the
pH value which encouraged the rapid breakdown of linamarin and this ushers in the second stage where
there is subsequent proliferation of the fungus Geotrichum candidum which produces the favouring
ketones, aldehydes and other compounds (Oyewole and Isah, 2020). Lactobacillus sp, Leuconostoc sp
and the yeast Candida sp are also present in the fermenting mash and they produce linamarse which
breaks down the linamarin and remove the cyanide in the gari (Oyewole and Isah, 2020).
14
1
ROLE OF MICROORGANISMS IN THE PRODUCTION OF
SOME INDIGENOUS FERMENTED FOODS IN NIGERIA
3. OGI
Initially, the fungi Cephalosporium and Fusarium which were
acquired from the field were involved in the fermentation of ogi
within the first 24 hours (Obire and Amadi, 2019). They were soon
replaced by lactic acid bacteria (Lactobacillus plantarum and
Lactobacillus mesenteroides) and yeast (Saccharomyces cerevisiae,
Rhodotorula spp and Candida mycoderma). These microbes are
predominant during the wet milling of the corn. The activities of
lactic acid bacteria and occasionally that of yeasts and acetic acid
bacteria are responsible for flavour production in the ogi (Oyewole
and Isah, 2020).
15
1
CONCLUSION
17
1
REFERENCES
Charpentier, E. and Doudna, J.A. (2018). Biotechnology: Rewriting a genome. Nature.
495(7439):50-51.
Chen, J.S., Ma, E., Harrington, L.B., Da Costa, M., Tian, X. and Palefsky, J.M., (2018). CRISPR-
Cas12a target binding unleashes indiscriminate singlestranded DNase activity. Science.
360(6387):436-439.
Chevalier, B.S., Kortemme, T., Chadsey, M.S., Baker, D., Monnat, R.J. and Stoddard, B.L.
(2022). "Design, activity, and structure of a highly specific artificial endonuclease". Molecular
Cell. 10 (4): 895–905.
Gaj, T., Gersbach, C.A. and Barbas, C.F. (2019). "ZFN, TALEN, and CRISPR/Cas-based methods
for genome engineering". Trends in Biotechnology. 31 (7): 397–405.
Saurabh, S. (2021). "Genome Editing: Revolutionizing the Crop Improvement". Plant Molecular
Biology Reporte. 39: 752–772.
Shi, J., Wang, E., Milazzo, J.P., Wang, Z., Kinney, J.B. and Vakoc, C.R. (2019). Discovery of
cancer drug targets by CRISPR-Cas9 screening of protein domains. Nature Biotechnology.
33(6):661-667.
Smith, J., Grizot, S., Arnould, S., Duclert, A., Epinat, J.C. and Chames, P. (2019). "A combinatorial
approach to create artificial homing endonucleases cleaving chosen sequences". Nucleic Acids
Research. 34 (22): 149-165.
18
1
THANK YOU
19
1