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
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: 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.