A Short Review of Multifunctional
Roles of Bacteriocins
Abdul Wahab1, Alina
binti Abdul Rahim2, Muhammad Abdullah
Qadri3
1Institute of Home and
Food Sciences, Faculty of Life Sciences, Malaysia
2Faculty of Science and
Technology, University Sains Islam Malaysia, 71800,
Malaysia
3Depatment of Botany,
Faculty of Life Sciences, University of the Punjab, Lahore, 54000, Pakistan
|
METADATA Paper history Received: 01 May 2025 Revised: 12 April 2025 Accepted: 30 April 2025 Published online: 20 May 2025 Corresponding author Email: abdul.wahab14670@gmail.com (Abdul Wahab) Keywords Bacteriocins Innovative Industrial Perspective Multidimensional Citation Wahab A, Rahim AbA, Qadir MA (2025) A short review on multifunctional roles of bacteriocins. Innovations in STEAM: Research &
Education 3: 25030101. https://doi.org/10.63793/ISRE/0021 |
ABSTRACT Background: Rising demand for healthy food products has created
the need for more innovative food preservation methods. One such method
involves the use of bacteriocins, which are natural
antimicrobial peptides with potential application in the food industry. Objective: The purpose of this review is to highlight the
purification processes of bacteriocins and discuss
their multidimensional roles, particularly in controlling harmful pathogens. Methodology: Information was compiled from relevant scientific literature
focusing on the purification methods, properties, and applications of bacteriocins. Emphasis was given to their potential
mechanisms of action against foodborne pathogens and their prospective role
in food preservation. Results: Current findings indicate that bacteriocins
exhibit promising antimicrobial activity against a wide range of harmful
microorganisms and enhance meat shelf-life, improve plant growth, and control
skin-related diseases. However, further industrial-scale studies are still
needed to fully validate their commercial applications. Conclusion: Bacteriocins hold
significant potential as innovative tools for food preservation and can
potentially improve meat shelf-life, enhance plant growth, and control
skin-related disease infestation. Their purification and demonstrated
antimicrobial roles provide a foundation for future research aimed at
integrating them into industrial applications for safer and healthier food
production. |
INTRODUCTION
Foodborne diseases remain one of the biggest threats to the food
industry, and when outbreaks occur, they cause significant losses to a country,
as a large portion of the national budget is spent on managing such disasters.
To address this, the food industry has upgraded its safety systems to ensure
consumer protection. This continuous improvement has also created healthy
competition among food industries, driving technological advancements. Nature
has blessed us with a wide variety of foods, and food lovers always expect
these to be nutritious, wholesome, and safe for consumption. According to Obafemi et al. (2025), microbial spoilage is a major
factor affecting food quality and safety. When microbes enter food products,
they can cause discoloration, destroy flavour compounds, and lead to food
toxicity. This not only damages public perception but may also contribute to
food scarcity. Preservation is therefore essential to control spoilage-causing
pathogens. Bacteriocins, the native antimicrobial
peptides of bacteria, are becoming increasingly important tools in contemporary
food protection. They inhibit pathogenic and spoilage bacteria quite
effectively, providing a biological alternative to conventional preservatives
(Le et al. 2016; Obafemi et al. 2025).
In the quest for safe, natural,
and effective antimicrobial agents, bacteriocins have
become a cornerstone of modern biotechnology. These ribosomally
synthesized peptides, which are secreted by various strains of bacteria, have
strong inhibitory action against other microorganisms, such as foodborne
pathogens and spoilage bacteria. Their use includes antimicrobial function to
preserve foods, promote animal health, and treat diseases (Ali et al.
2020). Food technologists and scientists have increasingly turned to biopreservatives, among which bacteriocins
produced through biotechnology are of particular interest. Bacteriocins
show promising antimicrobial effects against food spoilage organisms and are
widely considered natural food biopreservatives
(Mahindra et al. 2015). Bacteriocins play a
vital role in overcoming food safety issues, lowering the dependence on
chemical preservatives, and minimizing threats of foodborne illness. In the
food sector, they provide a reliable solution for shelf-life extension and
product safety. Outside of the food sector, they are investigated for their
therapeutic applications, such as fighting antibiotic-resistant infections and
influencing the gut microbiome (Gu 2023). This review highlights bacteriocins,
their classifications, and their importance in the meat sector, plant growth,
and skin care products.
BACTERIOCINS
The extensive use of conventional medicines in the
treatment of human and animal diseases has become a concern in recent years
(Roy 1997; Yoneyama and Katsumata 2006). The emergence
of resistant strains has complicated the treatment of many diseases, making the
development of new antimicrobial agents an important goal (Kumar and Schweiser 2005; Fisher et al. 2005). Bacteriocins have gained attention as alternatives to
antibiotics because they are non-toxic, active at nanomolar
concentrations, and produced naturally by lactic acid bacteria (Parada et al. 2007). They are proteinaceous
compounds with antimicrobial activity, produced by bacteria to inhibit or kill
other bacterial strains (Parada et al. 2007).
Although they are bacterial products, they are not classified as antibiotics to
avoid confusion with therapeutic drugs (Deraz et
al. 2005). For the food industry, bacteriocin
production is highly beneficial, as it helps inhibit and eliminate pathogens.
Many bacteriocins are effective against closely
related bacteria, often displaying a narrow host range (Deegan
et al. 2006). It is used predominantly in canned foods and dairy
products and is especially effective when utilized in the production of
processed cheese and cheese spreads, where it protects against heat-resistant
spore-forming organisms such as those belonging to
the genera Bacillus and Clostridium (Tarelli et al. 1994).
CLASSES OF BACTERIOCINS
Bacteriocins are broadly divided into four main classes. Class I
includes lantibiotics, which are small peptides of
less than 5 kDa in size and are heat-stable. They act
mainly by disrupting bacterial membranes, and nisin is
the most well-known example (Broadbent et al. 1989). Within this class, subclass-Ia- Ia consists of positively
charged, elongated, and flexible peptides, while subclass-Ib
includes peptides that are more rigid, globular in shape, and either uncharged
or negatively charged (Parada et al. 2007). Class
II bacteriocins, often referred to as non-lantibiotics, are heat-stable peptides composed of amino
acids and show variability in molecular weight. This class is further divided
into three groups: Class-IIa, which contains peptides
active against Listeria species and is represented by pediocin PA-1; Class-IIb, which
includes bacteriocins that require two different
peptides to achieve antimicrobial activity; and Class-IIc,
which is characterized by small, heat-stable peptides transported by leader
sequences (Venema et al. 1997; Holo et al. 2002; Mauriello
et al. 1999; Parada et al. 2007). Class-III
bacteriocins are larger in size, with molecular
weights exceeding 30 kDa, while Class-IV bacteriocins are complex molecules containing carbohydrate
or lipid moieties in addition to protein components (Parada
et al. 2007; Holo et al. 2002; Mauriello et al. 1999).
EFFECT OF PURIFICATION METHODS, pH AND TEMPERATURE ON BACTERIOCIN
PRODUCTION
Different purification methods have been developed
depending on the class of bacteriocin (Table 1).
These include protein precipitation, chromatography, and electrophoretic
techniques, which allow isolation and characterization of bacteriocins
for food and pharmaceutical applications. The production and activity of bacteriocins vary with environmental conditions. Studies
have shown that each bacterial strain has an optimum pH range and temperature
at which bacteriocin production is maximized (Table 2
and 3).
BENEFITS OF BACTERIOCINS
The application of bacteriocins
in the food industry is valuable for extending shelf life and protecting
against harmful pathogens. Their use reduces the risk of disease transmission
and economic losses associated with food spoilage. Growing consumer demand for
natural, minimally processed foods further supports the role of bacteriocins as natural antimicrobial agents (Soltani et al. 2021). When tested individually or in
combination, bacteriocins show promising results
against foodborne pathogens (Rendueles et al.
2022). In the dairy and poultry sectors, they have been applied successfully to
control Clostridium spp. (Arqués et al.
2015; Le et al. 2016). However, bacteriocins that
are applied commercially as biopreservatives must
fulfill specific requirements (Holo et al.
2002; Mauriello et al. 1999), such as being
non-toxic, accepted by recognized authorities, remaining sufficiently stable
during storage, and not negatively affecting the quality of the product to
which they are applied.
APPLICATIONS OF BACTERIOCINS
Metal
industry
Several
bacteriocins have been applied in the meat sector to control
pathogens, thereby improving food safety and Table
1: Purification of bacteriocins according to their classes Class Purification Method Procedure Result Reference Class I Bacteriocins Expanded bed ion exchange
chromatography Through processing of the Lactococcus lactis
subsp diluted culture broth of A164
obtained, and further, this broth was processed by using this method 31-fold purification was
achieved with a yield of 90% Cheigh et al. 2004 Ion exchange, Hydrophobic
Interaction 20%
of ammonium sulphate was used with the
precipitate of the cell-free supernatant Through the use of Lactobacillus
sake L45, its strain Lactocin S, a 3,7 kDa bacteriocin, was
created and then refined to uniformity Mřrtvedt et al. 1991 Combinations of different
chromatographic methods Hydrophobic and Cation exchange principles were applied during the use
of these methods Purification of Acidocin CH5 manufactured by using L. acidophilus in lab Chumchalova et al. 2004 Class II Bacteriocins Ethanol precipitation In the first step, ampholytes, Tween 20, and glycine were mixed,
followed by ultrafiltration to achieve a pure sample. Lastly, the sample was
moved to tricine SDS-PAGE Pediococcus acidilactici was used to produce purified pediocin PA-1, with a yield between 30 and 40% Venema etal. 2004 Saturation with ammonium
sulfate (35%) In an FPLC system, purification
includes Gel filtration chromatography, and then is moved to
methanol-chloroform extraction, followed by three methods. Firstly by
ion-exchange, then by hydrophobic interaction, and lastly through
reverse-phase chromatography Lactobin A,
produced by L. amylovorus, was purified Contreras et al. 1997 ion-exchange chromatography,
ultrafiltration, and successive gel filtrations One of these methods can be
used in the presence of two experimental consituents,
8 M urea followed by sodium dodecyl sulfate 0,1% sodium dodecyl sulfate Lactacin B
produced from L. acidophilus was purified Barefoot et al. 1984 Class III Bacteriocins Ammonium sulfate precipitation In sodium acetate buffer, the
pellet was placed and then dialysed against
sodium acetate buffer. Lactobacillus helveticus 481 produced Helveticin J, a peptide was purified Joerger and Klaenhammer 1986 Table
2: Effect of pH on bacteriocin Bacteriocin
producing strain Optimum pH Reference Leuconostoc
MF215B pH 6.0 Blom
et al. 1999 L. gelidin pH 6.5 Stiles and
Hasting 1991 amylovorin
L471 pH 6.5 Callewaert
et al. 1999) C. piscicola 7.0 Herbin
et al. 1997 Table
3: Effect of temperature on bacteriocin Bacteriocin
/Strain Suitable Temperature
for Bacteriocin Production Observation Reference Strain D53 10°C to
37°C -------- Uhlman
et al. 1992 Brevibacterium
linens 25°C No growth found at 37°C Diep et al.
2000 Diep
et al. 2000 L. sake 25–30°C At 33.5°C decline in production occurs, and
zero production is observed at 34.5°C L. plantarumY21 30°C At 37°C, especially in milk products, bacteriocin was produced during incubation Tarelli
et al. 1994
Veterinary use
Nisin has been investigated for the prevention of
bovine mastitis caused by Staphylococcus aureus
and Streptococcus agalactiae. Injectable formulations
containing nisin have shown up to 99.9% effectiveness
in controlling these Table 4: Role of different bacteriocins against different
pathogens in meat sector Type of
meat Meat
product Strains
of bacteriocin Action
against pathogens Other
changes References Meat Salami Ostrich
meat salami Lactobacillus
curvatus DF126 Anti-Listeria
activity ----- Dicks et al. 2004 Salami
from ostrich, beef, mutton Lactobacillus
plantarum 423 ---- Dicks et al. 2004; Todorov et al. 2007 Lactobacillus
curvatus DF38 ---- Todorov et al. 2007 Fermented Meat Fermented pork
sausage Pediococcus
pentosaceus BCC 3772 Anti-Listeria
activity No
changes in sensory properties, as well as in consumer
acceptability of the product Kingcha et al. 2012 Fermented
pork sausage Lactobacillus
sakei C2 nti-Listeria
and Anti-Enterobacteriacae activity, Both the
ratio of malondialdehyde and The
nitrite content in the product was reduced Gao et al. 2014 Raw Meat Raw beef Lactobacillus
curvatus CWBI-B28 Anti-Listeria
activity -------- Dortu et al. 2008 Packed Meat Vacuum-packed
fresh beef Lactobacillus
curvatus CRL705 Anti-Listeria
activity ------- Castellano
et al. 2010; Castellano and
Vignolo et al. 2006
Skincare
Scientific
evidence suggests that certain probiotics help maintain the skin’s lipid
barrier and microflora, supporting skin immunity and
homeostasis (Munir et al. 2025). In one study,
a lotion containing ESL5, a bacteriocin from Enterococcus
faecalis SL-5, significantly reduced pimples and
inflammatory acne lesions caused by Propionibacterium
acnes (Kang et al. 2009), suggesting their potential role in skin
care products.
Plant growth promotion
Bacteriocins such as thuricin 17, bacthuricin F4, and bacteriocin C85 have been shown to enhance plant growth.
When applied with their producing bacteria on tomato, soybean, and corn, they
improved leaf area, increased photosynthesis rates by up to 6%, and raised
plant dry weight by 15%. Additionally, root nodulation increased by 21%
compared to control plants (Smith et al. 2008).
CONCLUSIONS
In the 21st century,
the preparation of various food products requires knowledge and integration of
multiple scientific fields, with the primary objective of ensuring food safety.
Bacteriocins are associated with the control of
harmful pathogens in the food and pharmaceutical industries, although further
research is needed to fully understand their hidden roles in food safety. At
present, consumers are paying greater attention to food safety, and to address
their concerns, so industries are developing strong research-based models that
ensure food safety. However, more research is needed to explore the use of bacteriocins in food and other industries.
AUTHOR CONTRIBUTIONS
Conceptualization and data collection were carried out by AW;
manuscript drafting was performed by AbAR; review and
editing were undertaken by MAQ. All authors read and approved the final version
of the manuscript.
CONFLICT OF INTEREST
The authors affirm that they possess no conflicts of interest.
DATA AVAILABILITY
The data will be made available on a fair request to the corresponding
author
ETHICS APPROVAL
Not applicable to this paper
FUNDING SOURCE
This project is not funded by any agency.
REFERENCES
Ali A, Parisi A, Conversano MC, Iannacci A, D’Emilio F, Mercurio V, Normanno G (2020)
Food-borne bacteria associated with seafoods: A brief
review. Journal of Food Quality and Hazards Control 7: 4–10. https://doi.org/10.18502/jfqhc.7.1.2446.
Arqués JL, Rodríguez
E, Langa S, Landete JM,
Medina M (2015) Antimicrobial activity of lactic acid bacteria in dairy
products and gut: Effect on pathogens. BioMed
Research International 2015: 584183. https://10.1155/2015/584183.
Broadbent JR,
Chou C, Guillies K, Kondo JK (1989) Nisin inhibits several gram-positive, mastitis-causing
pathogens. Journal of Dairy Science 72: 3342–3345. https://10.3168/jds.S0022-0302(89)79496-0.
Barefoot SF, Klaenhammer TR (1984) Purification and characterization of
the Lactobacillus acidophilus bacteriocin lactacin B. Antimicrobial Agents and Chemotherapy
26: 328–334. https://doi.org/10.1128/aac.26.3.328.
Blom H, Katla T, Holck A, Sletten K, Axelsson L, Holo H (1999) Characterization, production and purification
of leucocin H, a two-peptide bacteriocin
from Leuconostoc MF215B. Current Microbiology
39: 43–48. https://doi.org/10.1007/pl00006825.
Cheigh C, Kook M, Kim
S, Hong Y, Pyun Y (2004). Simple
one-step purification of nisin Z from unclarified culture broth of Lactococcus
lactis subsp. lactis A164
using expanded bed ion exchange chromatography. Biotechnology Letters
26: 1341–1345. https://10.1023/B:BILE.0000045630.29494.45.
Chumchalova J, Stiles J, Josephsen J, Plocková M (2004)
Characterization and purification of acidocin CH5, a bacteriocin produced by Lactobacillus acidophilus
CH5. Applied Microbiology
96: 1082–1089. https://doi.org/10.1111/j.1365-2672.2004.02237.x.
Contreras BGL,
De Vuyst L, Devreese B, Busanyova K, Raymaeckers J, Bosman F, Sablon E, Vandamme EJ (1997) Isolation, purification, and amino acid
sequence of lactobin A, one
of the two bacteriocins produced by Lactobacillus amylovorus LMG P-13139. Applied and Environmental
Microbiology 63: 13–20. https://doi.org/10.1128/aem.63.1.13-20.1997.
Callewaert R, Holo H, Devresse B, Beeumen JV, Nes I, Vuyst LD (1999) Characterization and production of amylovorin L471, a bacteriocin
purified from Lactobacillus amylovorus DCE 471
by a novel three-step method. Microbiology 145: 2559–2568. https://10.1099/00221287-145-9-2559.
Castellano P, Vignolo G (2006) Inhibition of Listeria innocua
and Brochothrix thermosphacta
in vacuum-packaged meat by addition of bacteriocinogenic
Lactobacillus curvatus
CRL705 and its bacteriocins. Letters in Applied
Microbiology 43: 194–199. https://10.1111/j.1472-765X.2006.01933.x.
Castellano P, González C,
Carduza F, Vignolo G (2010)
Protective action of Lactobacillus curvatus
CRL705 on vacuum-packaged raw beef: Effect on sensory and structural
characteristics. Meat Science 85: 394–401. https://doi.org/10.1016/j.meatsci.2010.02.007.
Deraz SF, Karlsson EN, Hedstrom M, Andersson MM, Mattiasson B (2005)
Purification and characterisation of acidocin D20079, a bacteriocin
produced by Lactobacillus acidophilus DSM 20079. Biotechnology 117:
343–354. https://doi.org/10.1016/j.jbiotec.2005.02.005.
Deegan LH, Cotter PD,
Hill C, Ross P (2006) Bacteriocins: Biological tools
for biopreservation and shelf-life extension. International
Dairy Journal 16: 1058–1071. https://doi.org/10.1016/j.idairyj.2005.10.026.
Diep BD, Axelsson L, Grefsli C, Nes IF (2000) The synthesis of bacteriocin sakasin A is a
temperature-sensitive process regulated by a pheromone peptide through a
three-component regulatory system. Microbiology 146: 2155–2160. https://doi.org/10.1099/00221287-146-9-2155.
Dicks LMT, Mellett FD, Hoffman LC (2004) Use of bacteriocin-producing
starter cultures of Lactobacillus plantarum
and Lactobacillus curvatus in production of
ostrich meat salami. Meat Science 66: 703–708. https://doi.org/10.1016/j.meatsci.2003.07.002.
Dortu C, Huch M, Holzapfel WH, Franz CMAP,
Thonart P (2008) Anti-listerial
activity of bacteriocin-producing Lactobacillus curvatus CWBI-B28 and Lactobacillus sakei CWBI-B1365 on raw beef and poultry meat. Letters
in Applied Microbiology 47: 581–586. https://doi.org/10.1111/j.1472-765X.2008.02468.x.
Fisher JF, Meroueh SO, Mobashery S (2005)
Bacterial resistance to beta-lactam antibiotics: Compelling opportunism,
compelling opportunity. Chemical Reviews 105: 395–424. https://doi.org/10.1021/cr030102i.
Gao Y, Li B, Liu X
(2014) Bacteriocin-producing Lactobacillus sakei C2 as starter culture in fermented sausages. Food Control 35: 1–6. https://doi.org/10.3390/foods11050736.
Gu Q (2023)
Application of bacteriocins in the food industry. Bacteriocins 26: 63–83. https://doi.org/10.1007/978-981-99-2661-9_4.
Holo H, Fye T, Brede DA, Nilsen T, Odegard I, Langsrud T, Brendehaug J, Nes IF (2002) Bacteriocin of propionic acid bacteria. Institut
National de la Recherche Agronomique
82: 59–68. https://doi.10.1051/lait
: 2001005.
Herbin S, Mathien F, Brule F, Branlant C,
Lefebvre G, Lebrihi A (1997) Characteristics and
genetic determinants of bacteriocin activities
produced by C. piscicola CP5 isolated from
cheese. Current Microbiology 35: 319–326. https://doi.org/10.1007/s002849900262.
Joerger MC, Klaenhammer TR (1986) Characterization and purification of helveticin J and evidence for a chromosomally determined bacteriocin produced by Lactobacillus helveticus 481. Journal of Bacteriology 167:
439–446. https://doi.org/10.1128/jb.167.2.439-446.1986.
Kumar A, Schweiser HP (2005) Bacterial resistance to antibiotics:
Active efflux and reduced uptake. Advanced Drug Delivery Reviews 57:
1486–1513. https://doi.org/10.1016/j.addr.2005.04.004.
Kingcha Y, Tosukhowong A, Zendo T, Roytrakul S, Luxananil P, Chareonpornsook K, Visessanguan W
(2012) Anti-listeria activity of Pediococcus
pentosaceus BCC 3772 and application as
starter culture for Nham, a traditional fermented
pork sausage. Food Control 25: 190–196.
Kang BS, Seo JG, Lee GS et al. (2009) Antimicrobial activity of enterocins from Enterococcus faecalis
SL-5 against Propionibacterium acnes, the causative
agent in acne vulgaris, and its therapeutic effect. The Journal of
Microbiology 47: 101–109. https://doi.org/10.1007/s12275-008-0179-y.
Le LC, Dridi L, Bergeron MG, Ouellette M, Fliss
I (2016) Nisin is an effective inhibitor of Clostridium
difficile vegetative cells and spore
germination. Journal of Medical Microbiology 65: 169–175. https://doi.org/10.1099/jmm.0.000202.
Mauriello G, Aponte M, Andolfi R, Moschetti G, Villani F (1999) Spray drying of bacteriocin-producing
lactic acid bacteria. Food Protection 62: 773–777. https://doi.org/10.4315/0362-028x-62.7.773.
Mřrtvedt CI, Nissen-Meyer J, Sletten K, Nes IF (1991) Purification and amino acid sequence of lactocin S, a bacteriocin
produced by Lactobacillus sake L45. Applied and Environmental
Microbiology 57: 1829–1834. https://doi.org/10.1128/aem.57.6.1829-1834.1991.
Munir A, Janbey A, Sajjad B et al. (2025)
Bioinformatics-driven discovery of skin microbiota bacteriocins as potential antibiotics and probiotics. Journal
of Antibiotics 1–15. https://doi.org/10.1038/s41429-025-00847-2.
Obafemi YD, Obiukwu AC, Oranusi SU (2025)
Revisiting the application, current trends, and prospect of bacteriocins
in food preservation. Discover Food 5: 165. https://doi.org/10.1007/s44187-025-00472-w.
Parada JL, Caron CR, Mediros ABP, Soccol CR (2007) Bacteriocin from lactic acid bacteria: Purification,
properties and use as biopreservatives. Brazilian
Archives of Biology and Technology 50: 521–542. https://doi.org/10.1590/S1516-89132007000300018.
Perez RH, Zendo T, Sonomoto K (2014) Novel bacteriocins from lactic acid bacteria (LAB): Various
structures and applications. Microbial Cell Factories 13: 1. https://doi.org/10.1186/1475-2859-13-s1-s3.
Roy PH (1997)
Dissemination of antibiotic resistance. Medical Science 13: 927–933. https://doi.org/10.1086/321877.
Rendueles C, Duarte AC,
Escobedo S, Fernández L, Rodríguez A, García P, Martínez B (2022)
Combined use of bacteriocins and bacteriophages as
food biopreservatives: A review. International
Journal of Food Microbiology 368: 109611. https://doi.org/10.1016/j.ijfoodmicro.2022.109611.
Stiles ME,
Hasting JW (1991) Bacteriocin production by lactic
acid bacteria: Potential for use in meat preservation. Trends in Food
Science and Technology 2: 247–251. https://doi.org/10.1016/0924-2244(91)90706-O.
Soltani S, Hammami R, Cotter PD, Rebuffat S,
Said LB, Gaudreau H, Bédard
F, Biron E, Drider D, Fliss I (2021) Bacteriocins as a
new generation of antimicrobials: Toxicity aspects and regulations. FEMS
Microbiology Reviews 45: fuaa039. https://doi.org/10.1093/femsre/fuaa039.
Smith D, Lee
KD, Gray E, Souleimanov A, Zhou X (2008) Use of bacteriocins for promoting plant growth and disease
resistance. US Patent 20080248953.
Tarelli TG, Carminati D, Giraffa G (1994)
Production of bacteriocin active against Listeria monocytogenes and Listeria innocua
from dairy enterococci. Food Microbiology 11: 243–252. https://doi.10.1006/fmic.1994.1027.
Todorov SD, Koep KSC, Van Reenen CA, Hoffman
LC, Slinde E, Dicks LMT (2007) Production of salami
from beef, horse, mutton, blesbok (Damaliscus dorcas phillipsi) and springbok (Antidorcas
marsupialis) with bacteriocinogenic
strains of Lactobacillus plantarum and Lactobacillus
curvatus. Meat Science 77: 405–412. https://doi.org/10.1016/j.meatsci.2007.04.007.
Uhlman L, Schrillinger U, Rupnew J, Holzapfel WH (1992) Identification and characterization of
two bacteriocin-producing strains of Lactococcus lactis
isolated from vegetables. International Journal of Food Microbiology 2:
141–151. https://doi.org/10.1016/0168-1605(92)90007-p.
Venema K, Chikindas
ML, Seegers JFMI, Haandrikman
AJ, Leenhouts KJ, Venema G,
Kok J (1997) Rapid and efficient purification method
for small, hydrophobic, cationic bacteriocins:
Purification of lactococcin B and pediocin
PA-1. Applied and Environmental Microbiology 63: 305–309. https://doi.org/10.1128/aem.63.1.305-309.1997.
Yoneyama H, Katsumata R
(2006) Antibiotic resistance in bacteria and its future for novel antibiotic
development. Bioscience, Biotechnology and Biochemistry 70:
1060–1075. https://doi.org/10.1271/bbb.70.1060.