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International Journal of Polymer Science
Volume 2017 (2017), Article ID 3072582, 7 pages
https://doi.org/10.1155/2017/3072582
Research Article

Isolation and Thermal Stabilization of Bacteriocin Nisin Derived from Whey for Antimicrobial Modifications of Polymers

1Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Tr. T. Bati 5678, 76001 Zlin, Czech Republic
2Dairy Research Institute, Ke Dvoru 12a, 16000 Prague 6, Czech Republic

Correspondence should be addressed to Vladimir Sedlarik; zc.btu.tf@kiraldes

Received 19 July 2017; Revised 7 October 2017; Accepted 23 October 2017; Published 14 November 2017

Academic Editor: Marc Behl

Copyright © 2017 Pavlina Holcapkova et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

This work describes novel alternative for extraction of bacteriocin nisin from a whey fermentation media and its stabilization by using polyethylene glycol as matrix with high practical applicability. This product was compared with commercially available nisin product stabilized by sodium chloride and nisin extracted and stabilized by using ammonium sulfate and polysorbate 80. The stability of samples was tested by means of long-term storage at −18, 4, 25, and 55°C up to 165 days. The nisin content in the samples was determined by high-performance liquid chromatography and electrophoresis. In addition, effect of whey fortification with lactose on nisin production and antibacterial activity studied against Staphylococcus aureus was tested. Results show that stabilization by polyethylene glycol provides enhanced nisin activity at 55°C after 14 days and long-term stability at 25°C with keeping antibacterial activity.

1. Introduction

Nisin is a water-soluble polycyclic aromatic peptide possessing excellent antibacterial properties against Gram-positive bacterial strains [1]. The bacteriocin that belongs to the group of lantibiotics, in several variants differing in amino acid sequence in their structures, is produced by bacterial strains possessing specific genome. The bacteriocins are designated nisin A, nisin Z, nisin Q, F nisin (Lactococcus lactis), and nisin U (Streptococcus uberis) [26]. Recently, nisin H variant produced by Streptococcus hyointestinalis was described by O’Connor et al. [7].

Nisin belongs to the first described bacteriocins and it was recognized as a biological safe food preservative by Food and Agriculture Organization of the United Nations and World Health Organization already in 1968 [8]. It is produced biotechnologically through fermentation of a substrate such as whey or milk by the bacterial strains mentioned above [9].

Since there has been growing scientific and industrial interest in naturally occurring antimicrobial compounds that can be used for effective antimicrobial modifications of polymers, nisin is the ideal modifier showing antimicrobial activity at low concentrations that predetermine its application in food packaging, cosmetics and/or medical devices production. In addition, legislative requirements for introduction of nisin modified polymer system on the market could be significantly lower since it is considered to be a safe compound [8].

Since the nisin stability is limited, utilization of stabilizers is necessary to prolong its activity. Further additives improving its stability are used. The commercially available nisin is usually produced, concentrated, and processed into a powder containing over 90% of the stabilizer salt, especially sodium chloride (NaCl) [10]. Besides chlorides, sulfates [11] and/or surfactants [12] could be used. However, high concentration of the stabilizing salts is limiting for most of the applications dealing with incorporation into polymer systems due to their incompatibility with most of the matrices.

Several works dealing with antimicrobial modification of polymers with nisin have been published. However, most of the works describe nisin application on plasma activated polymer surface modifier [13] or in matrix of water-soluble polymers [14, 15]. The thermoplastic incorporation into thermoplastic starch matrix has been also reported [16]. On the other hand, nisin incorporation into the cosmetic compositions is rarely described in the relevant literature.

One of the possibilities for the salt-free nisin stabilization is its attachment via both covalent and noncovalent bonds to polymer chains. PEGylation is typical example involving polyethylene glycol (PEG) [17] that is fully biocompatible polymer from the group of polyethers [18]. PEG is commonly used in medicine, pharmaceutics, and cosmetics [19]. Thus combination of nisin as antibacterial agent and PEG as compatible stabilizer can be suitable for most of the applications introduced above.

Despite the fact that the nisin PEGylation has been known, the detailed study describing the PEGylation effect on nisin time-temperature stability and its comparison with the conventional salt stabilization has not been reported.

This work is focused on comparative study of the long-term stability (up to 165 days) and temperature (−4 to 55°C) activity of nisin stabilized by both salt and polymer based compounds. In this study, the nisin was experimentally prepared by fermentation of dairy by-product whey and subsequently stabilized sodium chloride, ammonium sulfate, nonionic surfactant (Tween), and PEG. Its long-term stability under various temperatures was studied by means of high-performance liquid chromatography (HPLC), electrophoresis, and microbiological analysis.

2. Experimental Part

2.1. Materials

Sweet milk whey was kindly provided by the local dairy research institute (KROMILK, Kromeriz, Czech Republic). Ammonium sulfate ((NH4)2SO4), sodium chloride (NaCl), sodium hydroxide (NaOH), sodium thiosulfate (Na2S2O3), copper(II) sulfate pentahydrate (CuSO4·5H2O), potassium sodium tartrate tetrahydrate (C4H4O6KNa·4H2O), formaldehyde solution, acetic acid, formic acid (85%), and methanol were purchased from PENTA (Prague, Czech Republic). Tween 80, TRIS Pufferan, Tricine Pufferan, tetramethylethylenediamine (TEMED), sodium dodecyl sulfate (SDS), mercaptoethanol, bromophenol blue Na-salt, and ammonium persulfate (APS) were supplied from P-Lab (Prague, Czech Republic). Polyethylene glycol (PEG) 2050, lactose, trifluoroacetic acid (TFAA), ammonium bicarbonate (NH4HCO3), acrylamide, N,N′-methylene bisacrylamide, Pharmalyte, Coomassie Brilliant Blue R250, glutaraldehyde, molecular weight (MW) and isoelectric focusing (IEF) markers, nisin standard (2.5%, balance sodium chloride and denatured milk solids), and bovine serum albumin (BSA) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Hydrochloric acid (HCl), monosodium phosphate (NaH2PO4), dipotassium phosphate (K2HPO4), boric acid (H3BO3), phosphoric acid (H3PO4), silver nitrate (AgNO3), ethanol (96%), and glycerol were supplied from IPL (Uhersky Brod, Czech Republic). HPLC gradient grade acetonitrile (ACN) was obtained from Chem-Lab (Zedelgem, Belgium). Lactobacillus MRS Broth (M369) and Mueller Hinton agar (MHA) were purchased from HiMedia (Mumbai, India). All chemicals were of analytical grade and used as received.

A bacteriocin-producing strain Lactococcus lactis subsp. lactis (CCDM 731) was obtained from collection of dairy microorganisms, Laktoflora, Dairy Research Institute, Prague, Czech Republic. A nisin-sensitive strain Staphylococcus aureus (CCM 4516) was acquired from Czech Collection of Microorganisms, Masaryk University in Brno, Czech Republic.

2.2. Sample Preparation

An aliquot (one inoculation loop) of L. lactis subsp. lactis was cultured in 50 ml of MRS broth (media recommended for cultivation of all Lactobacillus species) under anaerobic conditions at 30°C for 48 h. This preculture was transferred to milk whey fortified with lactose (0–200 g/l) in a 1 : 50 ratio (i.e., 1 ml of preculture to 50 ml of fortified whey) and the medium pH was raised to 5.5–6.0 with 0.1 M-NaOH. The inoculated medium was incubated for 48 h at 36°C with constant shaking (245 rpm) in laboratory incubator (Incucell 404, BMT a.s., Brno, Czech Republic). The fermentation product was centrifuged (Heraeus Multifuge X1R, Thermo Fisher Scientific Inc., Waltham, MA, USA) for 25 min at 10°C and 15,000 rpm and the supernatant was collected and processed by three different methods. A designation of prepared samples is shown in Table 1.

Table 1: Designation of standard and prepared samples.

Method 1: Precipitation with Ammonium Sulfate (AS). A quantity of (NH4)2SO4 (35% (w/v)) was added to the supernatant and continuously shaken at 4°C in conditioned chamber (Climacell 404, BMT a.s., Brno, Czech Republic) for 18 h. Then the mixture was centrifuged for 25 min at 10°C and 15,000 rpm. After that the upper phase was separated and dried using a freeze dryer (ScanVac CoolSafe 110-4 PRO, Lynge, Denmark).

Method 2: Two-Phase Extraction with Tween. The system was prepared by dissolving 1% (w/v) Tween 80 and 20% (w/v) (NH4)2SO4 in the obtained supernatant. Then the mixture was shaken for 30 min and left to stand for 16 hour. After phase separation the upper phase was separated and lyophilized.

Method 3: Two-Phase Extraction with PEG. First the medium pH was adjusted to 5.4–6.5 with 0.1 M-NaOH and 15% (w/v) PEG 2050 and 13% (w/v) (NH4)2SO4 were added. The extraction time was 40 min. After that, the mixture was kept for 1 h at 4°C and then the upper phase was separated and lyophilized.

2.3. Determination of Total Protein Concentration

The total amount of proteins and peptides was evaluated in the liquid phase after fermentation and centrifugation by using the colorimetric method proposed by Bradford [20], with BSA as the standard. The protein contents were determined spectrophotometrically (INFINITE M200Pro NanoQuant, with ELISA reader, Männedorf, Switzerland) at 595 nm.

2.4. Tris-Tricine-Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis (Tris-Tricine-SDS-PAGE)

The polyacrylamide (PAA) gel (10% T/3% C) as a uniform separating gel and stock solutions (buffers) for Tris-Tricine-SDS-PAGE were prepared according to Schägger and von Jagow [21]. The protein samples were combined with the buffer solution and the mixture was denatured for 5 min at 80°C prior to being loaded to the gel. Electrophoresis was carried out with a constant voltage of 190 V by using devices Bluestar (Blirt S.A., Dantsic, Poland) and Mini Vertical Dual (Carl Roth GmbH, Karlsruhe, Germany), power supply Consort EV 202 (Consort bvba, Turnhout, Belgium). Finally, the proteins were fixed and stained with Coomassie Brilliant Blue R250 [22] or with AgNO3 (when the protein content in a band was less than 0.5 μg).

The assumption was that the band corresponding with molecular weight of about 3.5 kDa according to MW marker contains a mixture of nisin A and nisin Z. After electrophoresis, these bands were excised and extracted. A destaining solution consisted of NH4HCO3 and ACN (1 : 1) and an extraction mixture was composed of 5% formic acid and ACN (1 : 2). The nisin concentration was then determined according to Bradford [20] and by HPLC. In the case of Bradford method, the calibration curves were constructed by using commercial nisin in the presence of corresponding stabilizing agents (PBS (phosphate buffered saline) for NIS-AS, Tween 80 for NIS-Tween, and PEG2050 for NIS-PEG samples).

2.5. Reverse Phase High-Performance Liquid Chromatography (RP-HPLC)

The nisin concentrations were measured using a HPLC Waters 717 plus Autosampler (Waters GmbH, Praha, Czech Republic) equipped with a dual wavelength UV/Vis detector. A XSelect, C18 CS column (5 μm, 4.6 × 250 mm, Waters, Milford, MA, USA) with precolumn Reprosil 100 C18 (5 μm, 50 × 4 mm, Watrex, Prague, Czech Republic) was used. The calibration solutions and samples were prepared by using 0.2 M HCl and filtered through the syringe filter with pore size 0.45 μm. The mobile phase was organized as gradient and composed of 0.05% (v/v) TFAA in HPLC gradient grade ACN (solvent A) and 0.05% (v/v) TFAA in distilled water (solvent B). The gradient consisted of 20% solvent (A) and 80% solvent (B) in 0–5 min, of 80% solvent (A) and 20% solvent (B) in 6–20 min, and of 80% solvent (A) and 20% solvent (B) again in 21–40 min. The injection volume was 25 μl and the flow rate was of 0.6 ml/min. The measurement was performed at wavelengths of 200 and 220 nm (the nisin concentration was calculated from the results of 200 nm).

2.6. Agar Diffusion Testing of Antimicrobial Activity

Nisin activity was determined by agar-well diffusion method, using S. aureus as the indicator microorganism. An aliquot of bacterial culture (108 CFU) was applied with a sterile swab on the surface of the Mueller Hinton agar plate. The test samples were prepared in deionized water so that the starting concentration of nisin corresponded to 25 μg/ml. Afterwards, the solutions were transferred into the bored wells of 8 mm in diameter (250 μl/well) and incubated for 24 h at 35°C. After incubation, the diameter of inhibition zones was determined as the average of four independent measurements.

2.7. Stability Testing

Prepared samples were assessed for stability during storage for 165 days at −18°C, 4°C, 25°C, and 55°C. The samples were continuously collected and tested by using the Bradford method, RP-HPLC, and agar diffusion assay for determination of nisin activity, as described above. The thermal stability (TS) of the prepared samples was calculated as follows:where is nisin concentration at particular time; is starting concentration of nisin.

3. Results and Discussion

3.1. Effect of Lactose Content on Nisin Production

An adequate content of carbon substrate is necessary for optimal production of bacteriocin nisin by lactic acid bacteria. Lactose is one of the possible carbon sources in the by-product, whey, comprising a major part of the fermentation media used in this work. In whey, the lactose content usually varies from 4.5 to 6.0% [23, 24].

The effect of fermentation media fortification by lactose on nisin production has been evaluated in many studies. The optimal nisin production was reported when the medium contained 30 g/l lactose [25, 26]. However, the yield of the reaction depends on many factors such as bacterial strains used, fermentation conditions (i.e., temperature, pH, and time), and composition of the media.

In this study, nisin production was examined at various levels of lactose fortification 0–20% (w/v). The results are depicted in Figure 1 as dependence of nisin production effectivity, expressed as concentration determined after 48 hours of fermentation. The nisin production was determined by RP-HPLC technique.

Figure 1: Effect of fermentation media fortification with lactose on nisin production after 48 hours of fermentation. Data points are average values of three independent analyses by RP-HPLC. Standard errors were less than 10%.

It can be seen that nisin intensity production increases with the rising level of fortification up to 4% of lactose addition. Further lactose addition led to reduction of the nisin biosynthesis due to possible occurrence of competitive processes and elevated osmotic pressure in the fermentation media [27]. Although the lactose concentration of 4% was found to be the best for nisin production, due to technological and economical aspects (high viscosity of the fermentation media at 4 wt.% additional lactose content), the whey fortified with 2 wt.% of lactose was chosen for further nisin experimental preparation.

3.2. Quantitative Analysis of Nisin Content in the Lyophilisates

The lyophilized samples prepared by the methods 1–3 were analysed by HPLC and electrophoresis as indicated above. The results presented in Table 2 show that both methods used in this study (HPLC and electrophoresis) bring comparable results. The nisin content determined by the latter method is about 15% higher than in the case of HPLC determination that is caused by the different principles of the both techniques. It is caused by the selectivity of both techniques. While HPLC considers only nisin in its A form (due to calibration on commercially available nisin), electrophoresis and subsequent analysis according to Bradford method cover the protein with molecular weight around 3.5 kDa, which includes also nisin Z form [3]. The nisin content in samples stabilized in ammonium sulfate (NIS-AS) and Tween (NIS-Tween) was found to be the same (2.3 mg/g, HPLC). On the other hand, the sample stabilized by using polyethylene glycol (NIS-PEG) had significantly higher nisin content, 5.3 mg/g (determined by HPLC). It was more than 2.3 times higher than in the case of NIS-AS and NIS-Tween.

Table 2: Determination of nisin concentration in prepared lyophilisates.

Since the initial material for nisin extraction was the same for all methods used (i.e., nisin content in the fermentation media was constant), it is clear that extraction step efficiency is the crucial for the nisin content in the resultant samples. The results show that PEG interacts with nisin, which leads to noticeable bacteriocin separation from the fermentation media. The principles of PEG-nisin interactions has been described referring to the ability of formation of protein-polymer conjugates that can display unique combination of protein and synthetic polymer based material properties [28].

3.3. Testing of Thermal Long-Term Stability

It is known that proteins are sensitive to heat treatment, especially in relation to long-term stability and activity [29]. In this study, thermal stability of nisin products was observed during storage (up to 165 days) at four different temperatures representing conditions of production (−18°C, lyophilization), storing (4 and 25°C), and processing (55°C). The nisin content change in the tested samples stored at various temperatures up to 55 days is shown in Figure 2. It can be noticed that the nisin concentration in all powder samples stored at −18°C changed only negligibly. The storage at 4°C caused slight reduction of the nisin content and TS subsequently (9% NIS-NaCl, 33% NIS-AS, 18% NIS-Tween, and 25% NIS-PEG). On the contrary, storage at 25°C led to significant drop in TS values after 55 days. The lowest nisin stability was observed in case of NIS-Tween (87% reduction) followed by NIS-PEG (71%), NIS-NaCl (85%), and NIS-AS (51%). Nevertheless, TS of the samples NIS-NaCl, NIS-AS, and NIS-PEG is relatively high within the first 15 days of the experiment. All samples stored at 55°C underwent steep drop in TS values. In all cases, the reduction of nisin concentration was above 90% after 55 days. TS of NIS-AS was detected up to 11 days due to low nisin stability in the sample leading to unreproducible results of analysis. In addition, it is worth mentioning that despite the TS of NIS-PEG systems is comparable to other investigated samples, the absolute values of nisin concentration are at least 2.3 times higher (see Table 2) (i.e., absolute concentration of nisin is higher).

Figure 2: Thermal stability of nisin (TS) versus storage time at –18°C (a), 4°C (b), 25°C (c), and 55°C (d). Nisin was determined by HPLC. Data points are average values of three independent analyses. Standard errors were less than 10%. Commercial product.

In Figure 3, TS values of nisin products determined after electrophoresis-Bradford method (A) and by HPLC (B) after 165 days were compared. Stability loss after 165 days of storage at −18°C was about 5–10% for all tested samples and at storage at 4°C it was about 20% for samples except for NIS-AS, where TS was about 40%. Significant changes of stability were observed at storage at 25°C and 55°C, where the highest stability was noticed at NIS-PEG (28% at 25°C and 4% at 55°C) in comparison with other samples including a commercial nisin (NIS-NaCl).

Figure 3: Thermal stability (TS) after 165 days of storage at various temperatures determined by electrophoresis-Bradford method (a) and by HPLC (b). Data points are average values of three independent analyses. Standard errors were less than 10%. Commercial product.

These results are principally in agreement with the work published by Rollema et al. [30] who reported chemical stability of nisin A at 20, 37, and 75°C in various buffers at pH range from 2 to 8. The nisin stability after 3 months of storage at 20°C resulted in 50–70% reduction in the bacteriocin content.

3.4. Testing of Nisin Antibacterial Activity in the Lyophilisates

It is known that nisin possesses strong antibacterial activity against Gram-positive bacterial strains [15]. There are two killing mechanisms aiming at the properties of bacterial cell membrane [31]. At lower concentrations, nisin molecule is binding to lipid II, which has a role in correct cell wall synthesis and its blocking that causes the cell death. Moreover, at higher concentrations, nisin-lipid II complex initiates membrane pore formation causing the dissipation of membrane potential and rapid efflux of ions and cytosolic solutes (especially amino acids and nucleosides), leading also to destruction of the cells.

The antibacterial activity of nisin lyophilisates stored at various temperatures (−18, 4, 25, and 55°C) immediately after preparation and after storing for 14 and 165 days by means of inhibition of Staphylococcus aureus bacterial strain is presented in the Table 3. It can be seen that freshly prepared NIS-AS and NIS-Tween showed results comparable with NIS-NaCl. On the other hand, inhibition zone diameter of NIS-PEG was slightly smaller than the others. This result is related to the limited mobility of nisin due to interactions with PEG (discussed above) causing lower diffusion of active substance trough agar media.

Table 3: Determination of nisin antibacterial activity on the growth of S. aureus by agar-well diffusion method. Data points are average values of three independent analyses.

The nisin activity of lyophilisates stored at −18°C was not changed even after 165 days. On the contrary, the reduction of antibacterial activity expressed as inhibition zone diameter was observed at temperature above 0°C. Although changes in the size of the inhibition zones were not observed after 14 days of storage at 4°C, this temperature after 165 days of treatment caused reduction of antibacterial activity by 31% at NIS-AS and about 10% for the other samples. Storage at 25°C led to significant drop in antibacterial activity. The lowest antimicrobial stability after 14 days was observed in case of NIS-NaCl (94% reduction) followed by NIS-AS (68%), NIS-Tween (29%), and NIS-PEG (18%). Storage at the same temperature after 165 days caused reduction of antibacterial activity above 90% at NIS-PEG and NIS-Tween and complete loss of activity in the case of NIS-NaCl and NIS-AS samples.

Finally, antibacterial activity of samples stored at 55°C was noticed only at NIS-Tween and NIS-PEG after 14 days. In the case of NIS-PEG it was even more than 70%. This result is related to nisin interactions with PEG, that is, interactions with uncommon unsaturated amino acids (dehydroalanine, dehydrobutyrine) or amino and carboxylic groups of amino acids [17].

4. Conclusions

Novel method for extraction and stabilization of bacteriocin nisin by using polyethylene glycol (PEG) was described in this study. The product NIS-PEG was compared with commercially available nisin product stabilized by NaCl and nisin extracted and stabilized by using (NH4)2SO4 and polysorbate 80 (Tween).

The results reveal that (i) fortification of whey with lactose is optimal at 4 wt.% of added lactose; however, 2 wt.% is convenient due to technological reasons; (ii) quantitative determination of nisin by both analytic techniques used in this work (HPLC, electrophoresis) corresponds to each other; (iii) thermal stability testing of NIS-PEG is comparable with other tested samples; (iv) NIS-PEG product possesses noticeably enhanced long-term stability when stored for 165 days at 25°C; (v) PEG stabilization is more efficient even for samples stored for 14 days at 55°C in comparison with the commercially available product (NIS-NaCl).

The newly introduced method significantly widens application possibilities of nisin as antimicrobial modifier for both hydrophobic and hydrophilic polymer systems.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was cofinanced by the Ministry of Agriculture of the Czech Republic (Grant no. QJ1310254) and the Ministry of Education, Youth and Sports of the Czech Republic (Grant no. LO1504). Pavlina Holcapkova is grateful to the Internal Grant Agency of Tomas Bata University in Zlin (IGA/CPS/2017/005).

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