Spoilage and preservation of meat: a general appraisal and potential of lactic acid bacteria as biological preservatives

Abstract

Spoilage of meat has remained a serious challenge in developing countries, including Nigeria, for decades. This has been due to poor storage systems in such countries where necessary facilities that could help promote preservation are unavailable. Where available, unsteady power supply necessary to maintain such facilities has constituted a serious problem, thereby rendering them to function below their maximum capacity. Furthermore, the ambient temperature in developing countries that are in tropical regions is usually about 30 o C or above; most spoilage organisms have been found to have their optimum growth temperature within such temperature range. In the present review, a general appraisal of meat spoilage and the potential of lactic acid bacteria in its biopreservation are discussed, with the view to suggesting a way to reduce wastage normally associated with meat due to spoilage. This could be of tremendous importance in developing countries, such as Nigeria, where procurement and maintenance of storage facilities have remained a matter of serious concern for many meat processors till date.

Full text

International Research Journal of Biotechnology (ISSN: 2141-5153) Vol. 2(1) pp.033-046, February, 2011
Available online http://www.interesjournals.org/IRJOB
Copyright © 2011 International Research Journals
Review Paper
Spoilage and preservation of meat: a general appraisal
and potential of lactic acid bacteria as biological
preservatives
*Olusegun A. Olaoye and Iniobong G. Ntuen
Food Technology Department, The Federal Polytechnic, PMB 420, Offa, Kwara State, Nigeria
Accepted 20 January, 2011
Spoilage of meat has remained a serious challenge in developing countries, including Nigeria, for
decades. This has been due to poor storage systems in such countries where necessary facilities that
could help promote preservation are unavailable. Where available, unsteady power supply necessary to
maintain such facilities has constituted a serious problem, thereby rendering them to function below
their maximum capacity. Furthermore, the ambient temperature in developing countries that are in
tropical regions is usually about 30oC or above; most spoilage organisms have been found to have their
optimum growth temperature within such temperature range. In the present review, a general appraisal
of meat spoilage and the potential of lactic acid bacteria in its biopreservation are discussed, with the
view to suggesting a way to reduce wastage normally associated with meat due to spoilage. This could
be of tremendous importance in developing countries, such as Nigeria, where procurement and
maintenance of storage facilities have remained a matter of serious concern for many meat processors
till date.
Keywords: challenge, storage systems, unsteady power supply, spoilage organisms, biopreservation, meat
processors
INTRODUCTION
Meat is a nutritious, protein-rich food which is highly
perishable and has a short shelf-life unless preservation
methods are used (Olaoye and Onilude, 2010). Shelf life
and maintenance of the meat quality are influenced by a
number of interrelated factors including holding
temperature, which can result in detrimental changes in
the quality attributes of meat. Spoilage by microbial
growth is the most important factor in relation to the
keeping quality of meat (Lambert et al. 1991).
In most developing countries, including Nigeria, fresh
meat forms a significant proportion of meat intake
(Olaoye and Onilude, 2010). It is either eaten cooked or
processed into other forms to avoid associated spoilage.
The main causative factor of such spoilage has been
linked to unavailability of necessary storage facilities and
favourable ambient temperature that usually prevail in
developing countries that are in tropical regions (Olaoye
*Corresponding author Email: olaayosegun@yahoo.com
et al., 2010). Research findings have suggested that
there is increasing attention on the use of naturally
occurring metabolites produced by selected lactic acid
bacteria (LAB) to inhibit the growth of spoilage
microorganisms (Onilude et al. 2002; Olaoye and
Onilude, 2010; Olaoye et al., 2010; Olaoye and Dodd,
2010). These authors have demonstrated the potential of
LAB cultures as biopreservatives during processing and
preservation of many forms of meat products. Lactic acid
bacteria growing naturally in foods produce antimicrobial
substances such as lactic and acetic acids, diacetyl,
hydrogen peroxide and bacteriocins (Olaoye et al. 2008).
A general appraisal on the spoilage of meat and possible
preservation by the application of LAB as biological
preservatives are presented in this review.

034 Int.Res.J.Biotechnol.
Spoilage and preservation of meats
Factors affecting meat spoilage
Meat has long been considered a highly desirable and
nutritious food, but unfortunately it is also highly
perishable because it provides the nutrients needed to
support the growth of many types of microorganisms
(Kolalou et al., 2004). Due to its unique biological and
chemical nature, meat undergoes progressive
deterioration from the time of slaughter until consumption.
In general, the metabolic activity of the ephemeral
microbial association which prevails in a meat ecosystem
under certain aerobic conditions, or generally introduced
during processing, leads to the manifestation of changes
or spoilage of meat (Nychas et al., 2008). These changes
or spoilage are related to the (i) type, composition and
population of the microbial association and, (ii) the type
and the availability of energy substrates in meat. Indeed
the type and the extent of spoilage is governed by the
availability of low-molecular weight compounds (e.g.,
glucose, lactate) existing in meat (Nychas et al., 1998;
Nychas and Skandamis, 2005). By the end of the phase
changes and subsequently, overt spoilage is due to
catabolism of nitrogenous compounds and amino acids
as well as secondary metabolic reactions
The post-mortem glycolysis, caused by indigenous
enzymes, ceases after the death of the animal when the
ultimate pH reaches a value of 5.4–5.5 (Olaoye, 2010).
Afterwards, the contribution of meat indigenous enzymes
in its spoilage is negligible compared to the microbial
action of the microbial flora (Tsigarida and Nychas,
2001). A number of interrelated factors influence the shelf
life and keeping quality of meat, specifically holding
temperature, atmospheric oxygen (O2), indigenous
enzymes, moisture (dehydration), light and, most
importantly, micro-organisms. All of these factors, either
alone or in combination, can result in detrimental
changes in the colour, odour, texture and flavour of meat.
Fresh meat has a shelf life of 1 day or less at ambient
storage temperatures, 20-30°C (Lambert et al., 1991).
Spoilage is said to be a state of a particular food in which
it is offensive to consumers' senses, usually caused by
metabolites of contaminant microorganisms (Paulsen and
Smulders, 2003). Meat spoilage is not always evident
and consumers would agree that gross discoloration,
strong off-odours, and the development of slime would
constitute the main qualitative criteria for meat rejection.
In general, spoilage is a subjective judgment by the
consumer, which may be influenced by cultural and
economic considerations and background as well as by
the sensory acuity of the individual and the intensity of
the change (Nychas et al., 2008). Spoilage of meat can
be considered as an ecological phenomenon that
encompasses the changes of the available substrata,
such as low molecular weight compounds, du
ring the proliferation of bacteria that constitute the
microbial association of the stored meat (Nychas et al.,
2007). The prevailing of a particular microbial community
of meat depends on the factors that persist during
processing, transportation and storage in the market.
Such may vary widely from one country to another as a
result of differences in climatic conditions, coupled with
possible varying levels in knowledge of food hygiene
practices of the handlers.
The microbiological quality of meat depends on the
physiological status of the animal at slaughter, the spread
of contamination during slaughter and processing, the
temperature and other conditions of storage and
distribution. In fact, some of the microorganisms originate
from the animal’s intestinal tract as well as from the
environment with which the animal had contact at some
time before or during slaughter (Koutsoumanis and
Sofos, 2004). Other organisms, including psychrotrophic
bacteria, are recovered from hides and work surfaces
within an abattoir as well as from carcasses and
butchered meat at all stages of processing (Gill, 2005).
A wide range of micro-organisms coming from different
sources are introduced onto carcass surfaces, which
contain abundant nutrients and which have high water
availability. Only a few of the contaminants will be able to
initiate growth, and only some of these will eventually
spoil the meat by means of their biochemical attributes.
Predominance of different groups of microorganisms on
meat depends on the characteristics of the meat, the
environment in which meat is stored as well as the
processing that meat may undergo (Gill and Molin, 1991).
As earlier noted, a vast number of studies in meat
microbiology have established that spoilage is caused by
only a fraction of the initial microbial association that
comes to dominate (Nychas et al., 2007). The range of
microbial taxa found on meat is given in Table 1. A
consortium of bacteria, commonly dominated by
Pseudomonas spp., is in most cases responsible for
spoilage of meat stored aerobically at different
temperatures (-1 to 25oC); the Pseudomonas spp. can
grow under refrigeration temperatures (Stanbridge and
Davis, 1998; Koutsoumanis et al., 2006). It is established
that under aerobic storage three species of
Pseudomonas, Ps. fragi, Ps. fluorescens and Ps.
Lundensis, are the most important spoilage organisms.
The population of pseudomonads to the level of 107-8
CFU/g, has been attributed to slime and off-odours
formation (Table 2 and 3). However, in practice both
these characteristics become evident when the
pseudomonads have exhausted the glucose and lactate
present in meat and begin to metabolise nitrogenous
compounds such as amino acids. This is significant in dry
firm dark meat (produced due to exercise preslaughter;
Olaoye, 2010) where there is no carbohydrate and
therefore spoilage occurs earlier at lower populations
(106). Brochothrix thermosphacta and lactic acid bacteria
(LAB) have been detected in the aerobic spoilage flora of

Olaoye and Ntuen. 035
Table 1 Genera of spoilage bacteria commonly found on meats and poultry
Microorganisms Gram reaction Fresh Processed
Achromobacter - X
Acinetobacter - XX X
Aeromonas - XX X
Alcaligenes - X
Bacillus + X X
Brochothrix + X X
Campylobacter - X
Carnobacterium + X
Chromobacterium - X
Citrobacter - X
Clostridium + X
Corynebactenum + X X
Enterobacter - X X
Enterococcus + XX X
Escherichia - X
Flavobacterium - X
Hafnia - X X
Janthinobacterium - X
Klebsiella - X
Lactobacillus + X XX
Lactococcus + X
Leuconostoc + X X
Listeria + X X
Microbacterium + X X
Micrococcus + X X
Moraxella - XX
Proteus - X
Providencia - X X
Pseudomonas - XX X
Shewanella - X X
Staphylococcus + X X
Streptococcus + X X
Weissella + X X
Yersinia - X
Source: Nychas et al. (2007)
X, known to occur; XX, most frequently isolated
Table 2 Common defects in meat products and causal bacteria
Defect Meat product Bacteria
Slime Meats Pseudomonas, Lactobacillus,
Enterococcus, Weissella, Brochothrix
H
2
O
2
greening Meats Weisella, Leuconostoc, Enterococcus,
Lactobacillus
H
2
S greening Vacuum Shewanella
packaged meat
H
2
S production Cured meats Vibrio, Enterobacteriaceae
Sulfide odour Vacuum Clostridium, Hafnia
Packaged meat
Cabbage odour Bacon Providencia
Putrefaction Ham Enterobacteriaceae, Proteus
Bone taint Whole meats Clostridium, Enterococcus
Souring Ham Lactic acid bacteria, Enterococcus,
Micrococcus, Bacillus, Clostridium
Source: Nychas et al. (2008)

036 Int.Res.J.Biotechnol.
Table 3. Factors and precursors affecting the production of odour end-products of
Gram-negative bacteria, such as Pseudomonas spp., Shewanella putrefaciens and
Moraxella
End product Factors Precursors
Sulfur compounds
Sulfides Temperature and Cysteine,
substrate (glucose) cystine, methionine
limitation
Dimethylsulfide Methanethiol,
methionine
Dimethyldisulfite Methionine
Methyl mercaptan nad
Methanethiol Methionine
Hydrogen sulfide High pH Cystine, cysteine
Dimethyltrisulfide nad
a
Methionine, methanothiol
Esters Methyl esters Glucose (l)
b
nad
Ethyl esters Glucose (l) nad
Aldehydes
2-Methylbutanal nad iso-Leucine
Alcohols
Methanol nad nad
Ethanol nad nad
2-Methylpropanol nad Valine
2-Methylbutanol nad iso-Leucine
Other compounds
Ammonia Glucose (l) Amino acids
Adapted from Nychas et al. (2007)
a nad, no available data
b (l) low concentration of glucose
chilled meat (Holzapfel, 1998). These organisms have
been isolated from beef carcasses during boning,
dressing and chilling. Moreover, lairage slurry, cattle hair,
rumen contents, walls of slaughter houses, the hands of
workers, air in the chill room, neck and skin of the animal
as well as the cut muscle surfaces have been shown to
be contaminated with these organisms (Holzapfel, 1998;
Nychas et al., 2008). Both LAB and Br. thermosphacta
are the main, if not the most important, cause of spoilage,
which can be recognized as souring rather than
putrefaction (Table 2). Br. thermosphacta has been
reported to be responsible for spoilage of meat products
under refrigeration conditions (Lawrie and Ledward,
2006).
Need and forms of meat preservation in developing
countries
Owning to the spoilage potential of meat, many varieties
of preservation techniques are employed in improving its
keeping quality and shelf life. In good hygienic conditions,
after slaughter and evisceration, the optimal way to
preserve meat is under refrigeration at temperatures
around 4oC. However, in Nigeria and most African
countries, because of lack of refrigeration facilities in the
slaughter house, ambient temperatures above 20oC and
lack of suitable transportation between the production
and marketing areas, meat can be exposed to conditions
of high risk with respect to increased contamination
resulting from growth of pathogens and spoilage
microorganism. Although most regulations recommend
meat to be kept under refrigeration, the fact is that in
many areas of most developing countries this does not
occur (Guerrero et al., 1995).
In Nigeria, the majority of meat produced in abattoirs is
sold for immediate consumption through retailers who
buy from butchers and resell to consumers who usually
subject it to cooking and consume within days. However,
for various reasons, there are left-overs that are not sold.
Since proper storage facilities are lacking, the left-over
meat is processed into various forms in order to avoid

spoilage. This involves improvising traditional techniques
of preservation. In cases where modern storage methods
(such as refrigerators and freezers), are available, they
are either expensive to maintain or means for their
maintenance (electricity) are lacking. As an alternative,
meat is preserved by processing to semi-dry and dry
forms. A typical example is kundi, a dry meat product
produced by cutting raw meat into pieces which is then
parboiled and sundried in an open container, made of
materials that can conduct heat. This method of
preparation makes the meat product prone to microbial
and other sources of contamination. However, the
product, being an intermediate moisture meat (IMM), is
low in moisture content and is shelf stable under tropical
climates without refrigeration (Egbunike and Okubanjo,
1999).
Another product that meat is processed into is Suya. This
is a popular, traditionally processed meat which is served
or sold along streets, in club houses, on picnics and in
restaurants. There are three main forms of suya, namely
tsire, kilishi and balangu, but of these, tsire is the most
commonly preferred (Alonge and Hiko, 1981). Therefore,
to most consumers, tsire is synonymous with suya (Igene
and Abulu, 1984). Tsire is a roasted, boneless meat of
beef, goat or mutton that is cooked around a glowing
charcoal fire in which the meat pieces are staked on
wood sticks, spiced with peanut cake, spices, vegetable
oil, salt or other flavourings. It is a delicatessen item since
it does not receive any treatments designed to extend its
shelf life (Harris et al., 1975). Indeed, most sales-points
hardly exhaust their sales and leftovers are often carried
over to the second day or beyond. To this extent,
rancidity often sets in, leading to the spoilage of this
product. Suya products can become contaminated
microbiologically from raw materials, handlers and/or
equipment. Igene and Abulu (1984) reported the isolation
of Bacillus, Streptococcus, Staphylococcus, Escherichia,
Proteus, Pseudomonas and Klebsiella from raw and
freshly roasted tsire subjected to different storage
treatments. Uzeh et al. (2006) also reported the
confirmation of some of these organisms in the stick
meat, specifically Ps. aeruginosa, B. cereus, Staph.
aureus, and E. coli.
As earlier noted, Bacillus cereus is one of the organisms
that could cause food borne disease associated with
consumption of contaminated meat. The genus, Bacillus,
is also known to cause souring in meat (Table 1), while B.
anthracis can cause disease in man, though regarded as
a relatively low risk from meat and meat products
(McClure, 2002). B. cereus is a ubiquitous organism and
has been found in raw beef and milk, and the organism is
directly linked to dairy cows. Therefore, contamination of
carcasses of dairy cows is possible but is not thought to
constitute a significant risk in foods of animal origin.
Foodborne illness caused by B. cereus generally results
from improper handling of foods (McClure, 2002).
Proteus spp. have been found in small numbers in the
Olaoye and Ntuen. 037
flora on beef and pork carcases and in a variety of ready-
to-eat processed meats (Nychas et al., 2007). They have
also been associated with the spoilage of beef; Proteus is
known to be associated with putrefaction of meat
(Nychas et al., 2008).
Meat or meat products are not thought to be a major
source of Staph. aureus as causative agent of food borne
disease in man, even though the organism is an
important pathogen in animals. The principal source of
transmission between animals and man is unpasteurised
milk and cheese made from unpasteurised milk (McClure,
2002). Outbreaks of staphylococcal food poisoning in
man are frequently associated with improper food
handling and temperature abuse of foods of animal
origin, but it is generally believed that the main source of
contamination is food handlers (Sofos, 2008).
Nevertheless, strains of Staph. aureus can become
endemic in food processing plants and meat can be
contaminated from animal or human sources. Staph.
aureus has been isolated from cattle carcasses and is
also found in raw beef. The organism can become a
major problem in cured meats as it is very salt tolerant
and grows well when other flora are removed by the
preservation methods.
Preservation using lactic acid bacteria
A general overview
The lactic acid bacteria comprise a group of Gram
positive, non-sporulating, cocci or rods, and are catalase-
lacking organisms. LAB produce lactic acid as the major
end product during the fermentation of carbohydrates.
They only grow in complex media where fermentable
carbohydrates and higher alcohols are used as an energy
source, mainly to form lactic acid. Homofermentative LAB
degrade hexoses to lactate, whereas heterofermentative
LAB degrade hexoses to lactate and additional products
such as acetate, ethanol, CO2, formate, or succinate.
LAB are widespread in most ecosystems and are found
in soil, water, plants, and animals. They are responsible
for many food fermentation processes, but they are also
commonly found on non-fermented foods such as dairy
products, meat products, seafood, fruits, vegetables,
cereals, sewage, and in the genital, intestinal, and
respiratory tracts of humans and animals. LAB are widely
used as protective cultures in the food industry for the
production of fermented foods, including dairy (yogurt,
cheese), meat (sausages), fish, cereals (bread and
beverages such as beer), fruit (malolactic fermentation
processes in wine production), and vegetables
(sauerkraut, kimchi, silage).
Most LAB are considered as ‘generally recognized as
safe’, GRAS (Silva et al. 2002). They are used to ensure
safety, preserve food quality, develop characteristic new

038 Int.Res.J.Biotechnol.
flavours, and improve the nutritional qualities of food.
LAB exert strong antagonistic activity against many
related and unrelated microorganisms, including food
spoilage organisms and pathogenic bacteria such as
Listeria, Clostridium, Staphylococcus and Bacillus spp.
The antagonistic effect of LAB is mainly due to a lowering
of the pH of the food, to competition for nutrients, and to
the production of inhibitory metabolites (Stiles, 1996).
LAB are able to grow at refrigeration temperatures. They
tolerate modified atmosphere packaging, low pH, high
salt concentrations, and the presence of additives such
as lactic acid, ethanol, or acetic acid.
The classification of LAB is based on morphological,
metabolic and physiological criteria. As described earlier,
LAB are related by a number of typical metabolic and
physiological features. In the past few decades, DNA-
based methods targeting genes such as 16S rRNA,
applied to determine the relatedness of food-associated
LAB, have resulted in significant changes in their
taxonomic classification. The genera comprising LAB are
Lactobacillus, Leuconostoc, Pediococcus, Lactococcus,
and Streptococcus, as well as Aerococcus,
Carnobacterium, Enterococcus, Oenococcus,
Teragenococcus, Vagococcus, and Weisella (Stiles and
Holzapfel, 1997). Members of the LAB typically have a
G+C content below 50% (Stiles and Holzapfel 1997).
LAB in meat
In meats, LAB constitute a part of the initial microflora
which develops easily after meat is processed to
fermented sausages, chill stored or packed under
vacuum or modified atmosphere. The strains of LAB
generally considered as being found naturally in meats
and meat products are: Carnobacterium piscicola and C.
divergens; Lactobacillus sakei, Lb. curvatus and Lb.
plantarum; Leuconostoc mesenteroides subsp.
mesenteroides, Leuc. gelidum and Leuc. carnosum. LAB
in fresh meat bring about a mild fermentation process
without producing any changes in the sensory
characteristics because of the low carbohydrate content
and the strong buffering capacity of meat. In the same
way the growth of LAB in naturally fermented meats, after
the addition of sugar, transforms the products through the
production of lactic acid by the LAB. The subsequent
decrease in pH denatures the meat proteins favouring the
decrease of water activity (aw), which ends up in a
microbial stabilisation of the transformed product (Hugas,
1998).
In addition to the fermentable carbohydrates, glucose,
glycogen, glucose-6-phosphate and small amounts of
ribose, meat and meat products provide a number of vital
growth factors such as available amino acids and
vitamins that support the growth of the fastidious LAB.
Some species of the genera Lactobacillus,
Carnobacterium, Leuconostoc spp. and Weissella are
especially well adapted to this ecosystem (Holzapfel,
1998). Several representatives of the genus Lactobacillus
may typically dominate the microbial population
especially of vacuum packaged and processed meat
products. The facultative heteroferemtative species of Lb.
sake and Lb. curvatus are found in most meat systems
and are probably the most frequently encountered
species of the genus. These two species have been
shown to be of major economic importance in meat
products, or acting as main and desirable fermentative
organisms in dry sausages (Holzapfel, 1998; Conter et
al., 2005).
Persistence and competitive ability of Lactobacillus and
several other species of the genera Leuconostoc (Leuc.
amelibiosum, Leuc. carnosum, Leuc. gelidum), Weissella
(W. viridescens, W. halotolerans) and Carnobacterium
(Cb. divergens, Cb. piscicola) in processed meat systems
are explained by their ability to ferment the carbohydrates
in meat and their adaptation to the meat substrate. While
the leuconostocs appear to grow most rapidly on chilled
fresh meat (Borch and Agerhem, 1992), Lb. curvatus and
Lb. sake, on account of their higher tolerance of elevated
salt concentrations and nitrite, typically dominate raw
fermented sausage and pasteurized emulsified meat
products (Holzapfel, 1998). Some of these features also
apply to two species of the genus Pediococcus, Ped.
pentosaceus, and Ped. acidilactici, which are associated
with fermented meat products (Albano et al., 2007).
Enterococcus and Lactococcus are other genera of LAB
that are of some commercial significance. Enterococcus
spp. use the homolactic pathway for energy production,
yielding mainly L(+) lactic acid from glucose at pH values
less than 5. At pH values above 7, ethanol, acetic acid
and formic acid are the main products of glucose
fermentation. In the absence of heme and under aerobic
conditions, glucose is converted to acetic acid, acetoin
and carbon dioxide. The genus Enterococcus differs from
the lactococci by their resistance to 40% bile and growth
of most species at 6.5% salt. E. faecium and E. faecalis
are associated with the gastro-intestinal tract of man and
warm-blooded animals and have been suggested as
indicators of faecal contamination of meat (Franz et al.,
1999).
The association of pediococci with proteinaceous foods
such as fresh and cured meat, and raw sausages, has
frequently been reported and particularly for Ped.
acidilactici and Ped. pentosaceus in fermented sausages
(Porubcan and Sellars, 1979; Onilude et al., 2002; Conter
et al., 2005; Albano et al., 2007; Olaoye et al., 2008;
Olaoye and Onilude, 2009). The association of
pediococci with meat fermentations has been a topic of
intensive study (Holzapfel, 1998; Albano et al., 2007).
Meat and meat products provide a favourable growth
substrate for strains of Ped. acidilactici and Ped.
pentosaceus, and particularly in the fermentation of semi-
dry sausages or other cured products, such strains
appear to play some role during fermentation and

maturation (Parente et al., 2001). Pediococci are also
frequently found in vacuum or modified-atmosphere-
packaged meat and meat products, in which the LAB
population is, however, most often dominated by species
of the genera Lactobacillus, Leuconostoc,
Carnobacterium, Weissella and Enterococcus (Jones,
2004).
Use of LAB as biological preservatives
Biopreservation, preservation by the use of biological
agents, refers to the extension of the shelf-life and
improvement of the safety of foods using microorganisms
and/or their metabolites (Ross et al., 2002). Antagonistic
cultures which are added to meat products to inhibit
pathogens and/or prolong the shelf life, while changing
the sensory properties as little as possible, are termed
protective cultures (Lucke, 2000). Their antagonism
refers to inhibition through competition for nutrients
and/or production of one or more antimicrobially active
metabolites (Table 4; Holzapfel et al., 1995). In a recent
study by Olaoye and Onilude (2010), the potential of
selected species of Pediococcus as biological
preservatives in the extension of shelf life of fresh beef in
Nigeria was investigated. The authors reported that the
LAB strains used were able to effect preservation of the
meat product, for few days before spoilage was started to
set in. In a similar study, Olaoye and Dodd (2010) also
reported the extension in shelf life of tsire, a traditional
Nigerian stick meat, after treatment with bacteriocinogeic
cultures of Pediococcus.
Nowadays, the consumer pays a lot of attention to the
relation between food and health. As a consequence, the
market for foods with health-promoting properties, so
called functional foods, has shown a remarkable growth
over the past few years (Leroy and De-Vuyst, 2004).
Also, the use of food additives is regarded as unnatural
and unsafe (Ray, 1992). Yet, additives are needed to
preserve food products from spoilage and to improve the
organoleptic properties; hence the use of functional
protective cultures in the food fermentation industry is
being explored. Functional protective cultures are
microorganisms that possess at least one inherent
functional property. The latter can contribute to food
safety and/or offer one or more organoleptic,
technological, nutritional, or health advantages. The
implementation of carefully selected strains as microbial
cultures or co-cultures in fermentation processes can
help to achieve in situ expression of the desired property,
maintaining a perfectly natural and healthy product.
Examples are LAB that are able to produce antimicrobial
substances, sugar polymers, sweeteners, aromatic
compounds, useful enzymes, or nutraceuticals, or LAB
with health-promoting properties, so called probiotic
strains. This represents a way of replacing chemical
additives by natural compounds, at the same time
Olaoye and Ntuen. 039
providing the consumer with new, attractive food products
and it also leads to a wider application area and higher
flexibility of cultures (Jahreis et al., 2002; Pidcock et al.,
2002).
Production of antimicrobials by LAB for food
preservation
In meat, production of one or more antagonistic
metabolites may be part of the complex mechanism by
which a micro-organism becomes established in the
presence of other competing organisms (Holzapfel,
1998). The understanding of such mechanisms provides
a valuable key to our understanding the complexity of
microbial interactions in a meat system and hence the
basis of 'biological' approaches to food preservation. One
of the main roles of LAB in biopreservation is to improve
safety by inactivating pathogens and spoilage
microorganisms via acid production and bacteriocins.
Furthermore, it is essential that potential biopreservative
cultures show no pathogenic or toxic activities (Hammes
and Hertel, 1996; Ammor and Mayo, 2007). The food
industry is expected to produce safe, healthy and
nutritious products of high quality. For many food
products, fermentation with starter cultures containing
lactic acid bacteria (LAB) is an essential part of the
production process.
Organic acid production
An important role of meat LAB starter cultures is the rapid
production of organic acids; this inhibits the growth of
unwanted flora and enhances product safety and shelf-
life. The antimicrobial effect of organic acids lies in the
reduction of pH, and in the action of undissociated acid
molecules (Podolak et al., 1996). It has been proposed
that low external pH causes acidification of the
cytoplasm. The lipophilic nature of the undissociated acid
allows it to diffuse across the cell membrane collapsing
the electrochemical proton gradient. Alternatively, cell
membrane permeability may be affected, disrupting
substrate transport systems (Snijders et al., 1985). The
types and levels of organic acids produced during the
fermentation process depend on the LAB strains present,
the culture composition, and the growth conditions
(Lindgren and Dobrogosz, 1990).
Fermentation of the carbohydrates, glucose, glycogen,
glucose-6-phosphate and small amounts of ribose, in
meat and meat products, produces organic acids by
glycolysis (Embden-Meyerhof Parnas pathway, EMP-
pathway; Figure 1) or the Hexose Monophosphate, HMP-
pathway. L (+) lactic acid is more inhibitory than its D(-)
counterpart (Benthin and Villadsen, 1995). Lactic acid is
a major fermentation end product of LAB and a number
of other genera (e.g Brochothrix). The LAB in particular

040 Int.Res.J.Biotechnol.
Table 4 Metabolic products of lactic acid bacteria with antimicrobial properties
Product Main target organisms
Organic acids
Lactic acid Putrefactive and Gram-negative bacteria, some fungi
Acetic acid Putrefactive bacteria, clostridia. some yeasts and fungi
Hydrogen peroxide Pathogens and spoilage organisms. especially in
protein-rich foods
Low-molecular-weight
metabolites
Reuterin Wide spectrum of bacteria, moulds and yeasts
(3-OH-propionaldehyde)
Diacetyl Gram-negative bacteria
Fatty acids A range of different bacteria
Bacteriocins
Nisin Some LAB and Gram-positive bacteria, notably endospore-formers
Others Gram-positive bacteria, inhibitory spectrum according to producer
strain and bacteriocin type
Source: Holzapfel et al. (1995).
Table 5 Classification of bacteriocins from lactic acid bacteria
Category Subcategory
Class I—lantibiotics Type A: elongated molecules
Subtype A1: leader peptides are
cleaved by a dedicated serin proteinase
Subtype A2: leader peptides are
cleaved by a dedicated ABC- transporter
Type B: globular molecules
Class II—nonmodified, heat-stable bacteriocins Class IIa: pediocin-like bacteriocins Class IIb:
two-peptide bacteriocins
Class IIc: sec-dependent bacteriocins
Class IId: other bacteriocins
Class III—large, heat-labile bacteriocins
Source : Nes et al. (1996) and Moll et al. (1999)
are able to reduce the pH to levels where putrefactive
(e.g. clostridia and pseudomonads), pathogenic (e.g.
salmonellas and Listeria spp.) and toxinogenic bacteria
(Staphylococcus aureus. Bacillus cereus, Clostridium
botulinum) will be either inhibited or killed (Holzapfel et
al., 1995; Holzapfel, 1998). Also, the undissociated acid,
on account of its fat solubility, will diffuse into the
bacterial cell, thereby reducing the intracellular pH and
slowing down metabolic activities, and in the case of
Enterobacteriaceae such as E. coli inhibiting growth at
around pH 5.1. The rapid reduction of the pH below 5.3
during sausage fermentation is sufficient to inhibit growth
of salmonellas and Staph. aureus (Holzapfel, 1998).
Bacteriocin production by LAB
The bacteriocins of LAB possess common traits that
justify their classification on a sound scientific basis into
three well defined classes (Nes et al., 1996; Moll et al.,
1999) (Table 5):
Class I, the lantibiotics, small heat-stable polycyclic
peptides (<5 kDa) containing small, membrane active

Olaoye and Ntuen. 041
G l uc o se
(C
6
)
G lu cos e 6 -ph osphate (C 6)
n
F ruc tos e 6 – ph os p h a te ( C6)
Fr uct o s e 1,6 - b iph osp h a te ( C6)
D ihydroxy ac et o ne + G lyc eral deh yd e
pho sp hat e (C 3 ) 3 -p h o spha te (C3)
2 x g lyc e ra ldeh y de 3 - pho sph at e ( C 3 )
2 x 1,3 - bip h osp ho g lyce rate (C3 )
2 x 3 -p ho s p h og lyc erat e (C3 )
2 x 2 -p ho s p h og lyc erat e (C3 )
2H 2O
2 x ph osphoe nolp yru v a te ( C 3 )
2 x p y r uva te ( C 3 )
A T P
A DP
H ex o k in a se
A T P
A DP
Ph os p ho fr u ct ok in as e
A l do n as e
2 N
A
D
2 N AD H + 2 H
+
2
A
DP
2 A TP
2 A DP
2 A TP
Py r uva te k in ase
Figure 1. Embden Meyerhof Parnas pathway
Source: Adam and Moss, 2008
peptides;
Class II, the small (<10 kDa) heat-stable non-lantibiotics
such as pediocin-like bacteriocins with a strong anti-
Listeria activity;
Class III, large (>30 kDa) heat-labile bacteriocins.
Due to their abundance and possible application in
industrial processes, bacteriocins belonging to the first
two classes are the most thoroughly studied (Nes et al.,
1996; Moll et al., 1999). The most prominent Class I
bacteriocin is nisin, which is produced by strains of
Lactococcus lactis subsp. lactis isolated from milk and
vegetable-based products (Harris et al., 1992) and by Lc.
lactis BB24 isolated from Spanish-dry fermented
sausages (Rodríguez et al., 1995; Cintas et al., 1998).
Nisin is a broad spectrum bacteriocin with bactericidal
activity towards a wide range of Gram-positive bacteria,
including Staphylococcus aureus and Lis.
monocytogenes (Cintas et al., 1998). In addition, nisin
prevents spore outgrowth and inhibits vegetative cells of
Bacillus spp. and Clostridium spp. (Abee et al., 1995). To

042 Int.Res.J.Biotechnol.
date, nisin is the most thoroughly studied and
characterized bacteriocin of LAB and the only one
internationally accepted as a food biopreservative in
certain foods (Delves-Broughton et al., 1996).
Class II bacteriocins (non-lantibiotics) comprise a
heterogeneous group of bacteriocins. Despite differences
in their primary structures, most Class II bacteriocins are
small (<10 kDa) and heat-stable peptides with a high
content of small amino acids such as glycine.
They are usually cationic and often amphiphilic, reflecting
their ability to kill target cells by permeabilizing the cell
membrane (Nes et al., 1996; Moll et al., 1999). Class IIa
bacteriocins are the most thoroughly studied LAB
bacteriocins and possess interesting technological
properties and a strong antimicrobial activity against a
broad range of Gram-positive spoilage and food-borne
pathogens, especially Lis. monocytogenes. The search
for LAB producing antilisterial bacteriocins has lead to the
description and characterization of a large number of
Class IIa bacteriocins, produced by a wide variety of
Pediococcus, Leuconostoc, Enterococcus, Lactobacillus
and Carnobacterium strains. Class IIa is also referred to
as the pediocin family, which is named from pediocin PA-
1, the first and most thoroughly characterized bacteriocin
within the group (Marugg et al., 1992; Nieto-Lozano et al.,
1992). Pediocin-like bacteriocins, members of the class II
bacteriocins, are of considerable commercial interest
owing to their characteristics of being small, heat-
resistant peptides that are not modified post-
translationally. All the pediocin-like bacteriocins share
certain features, including a seven amino acid conserved
region in the N-terminal of the active peptide (–Tyr–Gly–
Asn–Gly–Val–Xaa–Cys–; Ennahar et al., 2000). They are
active against other LAB but are particularly effective
against Lis. monocytogenes (Calo-Mata et al., 2008).
Pediocin PA-1 is, perhaps, the best known, produced by
Pediococcus acidilactici isolated from American-style
sausages and Ped. pentosaceus Z102 from Spanish
style sausages (Castellano et al., 2008; Calo-Mata et al.,
2008). In the past, several pediocin PA-1-producing LAB
strains were independently isolated in different
laboratories (Bennik et al., 1997; Rodríguez et al., 1997).
However, in many cases the bacteriocin produced
received different names (pediocins PA-1, AcH, JD, Bac
and 347, mesentericin 5) before identification and
realization that all were the same molecule (Rodríguez et
al., 2007). The pediocin PA-1-containing fermentate
AltaTM 2341 is a commercial food ingredient reported to
extend the shelf life of a variety of foods and, particularly,
to inhibit the growth of Lis. monocytogenes in ready-to-
eat meat products (Rodríguez et al., 2007). The
determination of the pediocin PA-1 amino acid sequence,
the application of improved protocols for its purification,
and the identification of the pediocin PA-1 operon have
been reported (Nieto-Lozano et al., 1992; Marugg et al.,
1992).
The high molecular weight Class III bacteriocins have
been identified within the genera Lactobacillus and
Enterococcus (Fremaux and Klaenhammer, 1993). These
bacteriocins, in contrast to Class I and II bacteriocins, are
inactivated upon heat treatment (e.g., 60 - 100 ºC for 10 -
15 min) and, similar to type B lantibiotics, do not act on
sensitive cells by membrane-disruption.
Interest in the bacteriocins produced by meat LAB has
increased dramatically, reflecting their growing
importance with respect to the functional properties of
starter cultures (Abee et al., 1995). A number of
bacteriocins are produced by most LAB species involved
in meat fermentation, including Lb. sakei, Lb. curvatus,
Lb. plantarum, and Ped. acidilactici (Enan et al., 1996).
Meat-borne LAB produce a range of bacteriocins that are
generally active towards other LAB (contributing to the
competitiveness of the producing strain) and food borne
Gram–positive pathogens such as Lis. monocytogenes,
Staph. aureus, C. perfringens and B. cereus
(Noonpakdee et al., 2003). Bacteriocins exert their
inhibitory action via the formation of pores in the
cytoplasmic membrane of sensitive cells as well as
interrupting DNA and protein syntheses (Calo-Mata et al.,
2008). Generally, bacteriocins target the cell envelope
and, with the exception of the larger proteins (>20 kDa)
that degrade the murein layer (e.g. lysins and
muramidases), use non-enzymatic mechanisms to cause
the depolarization of the target cell membrane and/or
inhibit cell wall synthesis (Settanni and Corsetti, 2008).
Bacteriocins have generally a cationic character and
easily interact with Gram-positive bacteria that have a
high content of anionic lipids in the membrane
determining the formation of pores (Chen and Hoover,
2003). Pores in the cytoplasmic membrane clearly affect
the energetic status of the cell, i.e. dissipation of proton
motive force (PMF) causing an arrest of ∆pH and ∆ψ
(transmembrane electrical potential) dependent
processes (such as transport) while certain bacteriocins
cause ATP efflux (Settanni and Corsetti, 2008). A
bacteriocin producer protects itself against its own
antimicrobial compound by means of a system referred to
as immunity, which is expressed concomitantly with the
antimicrobial peptide (Nes et al., 1996; Settanni and
Corsetti, 2008). The mode of action of bacteriocins can
be bactericidal or bacteriostatic, determining death or
extension of lag phase respectively. In Gram-positive
bacteria, the bacteriocin nisin produced by Lc. lactis has
been shown to act on energized membrane vesicles to
disrupt PMF, inhibit uptake of amino acids, and cause
release of accumulated amino acids (Jack and Tagg,
1991). Studies on the mode of action of bacteriocins have
indicated that bactericidal activity was confined to pH
values of 6 and lower (Abee et al., 1995). This is possibly
due to the influence of two positively-charged (lysine) and
two negatively-charged (glutamate and aspartate) amino
acids and two histidine residues with a positive charge at
pH 6 or lower (pKa = 6 for His) and having a major role in
determining the effective charge of the peptide which is

crucial for activity (Abee et al., 1995). Gram-negative
bacteria are protected by their outer membrane, which
prevents bacteriocins from reaching the plasma
membrane (Abee et al., 1995).
It is generally accepted that bacteriocin activity is less
effective in meat products than in in vitro systems.
Activity may be reduced by the binding of the bacteriocin
molecules to food components (mainly the fat matrix),
and by the destabilizing action of proteases and other
enzymes (O’Keeffe and Hill, 2000). Further limitations of
bacteriocin effectiveness are uneven distribution in the
food matrix and their inhibition by salt and curing agents
(Leroy and de Vuyst, 1999; O’Keeffe and Hill, 2000; Calo-
Mata et al., 2008). Even so, several authors report that
certain bacteriocinogenic meat LAB could be used as
bioprotective cultures to prevent the growth of pathogens
in sausage. Indeed, the use of bacteriocin-producing
Lactobacillus sakei as a starter culture decreases the
numbers of Listeria in fermented sausage (De Martinis
and Franco, 1998). Antilisterial effects have also been
demonstrated with bacteriocinogenic Lb. curvatus, Lb.
plantarum and Ped. acidilactici (Luchansky et al., 1992;
Dicks et al., 2004). The production of bacteriocins with a
broad inhibition range, especially towards food-borne
pathogens is therefore highly desirable since this would
ensure the competitiveness of the starter strain while
reducing the numbers of harmful flora.
Other antimicrobials of LAB
Hydrogen peroxide is produced from lactate by LAB in
the presence of oxygen as a result of the action of
flavoprotein oxidases or nicotinamide adenine
dinucleotide (NADH) peroxidise (Ammor and Mayo,
2007). The antimicrobial effect of H2O2 may result from
the oxidation of sulfhydryl groups causing denaturing of a
number of enzymes, and from the peroxidation of
membrane lipids thus increasing membrane permeability
(Kong and Davison, 1980). H2O2 may also be a precursor
for the production of bactericidal free radicals such as
superoxide (O-2) and hydroxyl (OH-) radicals which can
damage DNA (Byczkowski and Gessner, 1988). The
enzyme catalase hydrolyses hydrogen peroxide. Some
LAB strains involved in meat fermentation, such as Lb.
sakei, Lb. plantarum, Lb. pentosus and Ped. acidilactici,
possess heme-dependent catalase activity which is
active in meat products since these substrates contain
heamin in abundance (Abriouel et al., 2004; Ammor et
al., 2005). Most undesirable bacteria such as
Pseudomonas spp. and Staph. aureus are many times
more sensitive than the LAB to H202.
Carbon dioxide is mainly produced by heterofermentative
LAB. The precise mechanism of its antimicrobial action is
still unknown. However, CO2 may play a role in
creating an anaerobic environment which inhibits
Olaoye and Ntuen. 043
enzymatic decarboxylations, and the accumulation of
CO2 in the membrane lipid bilayer may cause a
dysfunction in permeability (Eklund, 1984). CO2 can
effectively inhibit the growth of many food spoilage
microorganisms, especially Gram-negative
psychrotrophic bacteria (Farber, 1991). The degree of
inhibition by CO2 varies considerably between the
organisms. CO2 at 10% (v/v) could lower the total
bacterial counts by 50% (v/v) (Wagner and Moberg,
1989), and at 20–50% it had a strong antifungal activity
(Lindgren and Dobrogosz, 1990). Pathogens (e.g
Enterobacteriaceae and Listeria) could also be inhibited
due to reduced pH effects as CO2 dissolves to produce a
weak acid.
Diacetyl, an aroma component, is produced by strains
within all genera of LAB by citrate fermentation. It is
produced by heterofermentative lactic acid bacteria as a
by-product along with lactate as the main product.
Diacetyl is a high value product and is extensively used in
the dairy industry as a preferred flavour compound. Lb.
rhamnosus gives a high yield for diacetyl, 64 mg of
diacetyl per g of glucose consumed (Anuradha et al.,
1999). The physiological reason for the production of
diacetyl is not clearly understood. It is hypothesized that
diacetyl is synthesized to reduce the toxicity of pyruvate.
Diacetyl also has antimicrobial properties. It inhibits the
growth of Gram-negative bacteria by reacting with
arginine utilization (Jay, 1986). Jay (1982) showed that
Gram-negative bacteria were more sensitive to diacetyl
than Gram-positive bacteria; the former were inhibited by
diacetyl at 200 µg/ml. The antimicrobial activity of diacetyl
was evaluated against E. coli, Lis. monocytogenes and
Staph. aureus in a study by Lanciotti et al. (2003); the
authors concluded that the organisms were sensitive to
diacetyl with Lis. monocytogenes having the least
susceptibility. Generally varying concentrations of
diacetyl are required to bring about inhibitions of different
pathogenic and spoilage organism (Lanciotti et al., 2003).
Beneficial effects of LAB on meat
As noted earlier in this report, strains of LAB to be used
in the biopreservation must be carefully selected in order
to achieve the desired beneficial effect. This is because
not all LAB cultures can be used to achieve the purpose.
The use of LAB as biological preservatives on meat
products could confer health benefits to the consumers. A
comprehensive note has been reported by Olaoye and
Idowu (2010) on the various features and properties of
LAB used as biological preservatives of meat processing.
According to the authors, LAB cultures could function as
probiotics which are non-pathogenic microorganisms that
when ingested in certain numbers exert a positive
influence on host physiology and health beyond inherent
general nutrition.

044 Int.Res.J.Biotechnol.
CONCLUSION
In conclusion, spoilage of meat is inevitable, especially in
developing countries where storage systems have been
very epileptic. Although, in such countries, meat is being
processed into other forms to avoid the associated
spoilage, the potential of lactic acid bacteria as biological
preservatives could be exploited in complementing the
existing traditional preservation techniques.
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