JCC0759

JOURNAL OF CULTURE COLLECTIONS

Volume 5, 2006-2007, pp. 64-7<= /span>2

= BACTERIOCIN-LIKE ACTIVITY FROM WEISSELLA CONFUSA

= AND PEDIOCOCCUS ACIDILACTICI ISOLATED = FROM

= TRADITIONAL THAI FERMENTED SAUSAGES

= Veerapon Chavasirikunton¹, Savitri Vatanyoopaisarn² and <= /o:p>

= Chantaraporn Phalakornkule^1*

¹Department of Chemical Engineering, Faculty of Engineering;
²Department of Agro-Industrial Technology, Faculty of Applied Science, King Mongkut’s Institute of Technology,

North Bangkok, 1518 Pibulsongkram road, Bangsue 10800, Thailand

*Corresponding author, e-mail: cpk@kmitnb.ac.th<= /o:p>

= Summary

Bacteriocin-like activity (B= LA) was screened in 133 strains of lactic acid bacteria (LAB) isolated from traditional Thai fermented sausages. The inhibition assay against the test organisms showed that eight out of 133 isolates (CP1-15, CP2-11, CP3-1, CP7= -3, CP10-3, CP11-6, CP14-1 and CP14-4) suppressed the growth of Bacillus cereus and four (CP1-1= 5, CP7-3, CP14-2 and CP14-3) suppressed the growth of Staphylococcus aureus but none could suppress the growth of= Escherichia coli and Salmonella sp. The isolates wit= h the highest activity against the two Gram positive test strains (CP3-1 for B. cereus and CP7-3 for S. aureus) were further investi= gated for the effect of heat treatment at different pH values and for combined effects of dual mixtures. The increase in heating temperature (between 65 a= nd 100 ^oC) and time (between 5 and 60 min) significantly decre= ased BLA, while the changes in pH (between 4 and 6) had little effect. When the filtrates of the two isolates were mixed, BLA seemed to be synergistic agai= nst each test strain. Regression equations were obtained by fitting the experimental percent inhibition data with second-order polynomial equations= . The simulated data agreed well with the experimental data within 10 % when= the filtrates were incubated at 65 ^oC for 5, 15, 30 and 60 min = and at 80 ^oC for 5, 15 and 30 min. The isolates CP3-1 and CP7-3, which had an antagonistic effect against the two strains of Gram positive foodborne bacteria, were formerly identified as Weissella confusa and Pediococcus acidilactici, respectively. It is the researcher’s belief that this is the first report on BLA from W. confusa against B. c= ereus.

Key words= : lactic acid bacteria, bacteriocin, antibacterial activity, inhibitory activity, Weissella confusa, Pediococcus acidilactici

Introduction

“Sai-krork-prieo” is a traditional Thai fermented sausage, consumed all around the country and produced from minced pork, sliced pork/beef liver, garlic, pepper, spices, = salt and sugar. “Mum” is a product similar to “Sai-krork-prieo” but can be made from beef as well as pork, an= d is popular only in the Northeast of Thailand. In a previous study [9], lactic = acid bacteria (LAB) from “Sai-krork-prieo” and “Mum” were isolated and characterized. It was found that Lactobacillus plant= arum and Pediococcus pentosaceus were the species most frequently identif= ied. On the other hand, Weissella sp., P. acidilactici, L.= fermentum, L. brevis, L. farciminis and L. sakei w= ere isolated from fewer samples. The study first reported the isolation of W= . cibaria/kimchii, W. confusa, L. brevis, and L. farcim= inis, from “Sai-krork-prieo”, and P. pentosaceus, P.&n= bsp;acidilactici, L. fermentum, L. brevis, and L. sakei <= /i>from “Mum”.

Information on bacteriocin-producing LAB isolated from traditional Thai fermented sausa= ges was rather limited. Some LAB isolated from tropical fermented sausages may produce new bacteriocins with properties suitable for adaptation to a tropi= cal niche. This study screened for bacteriocin-like activity (BLA) of 133 LAB strains previously isolated from “Sai-krork-prieo” and “Mum”. Representative test organisms included Bacillus cereu= s, Staphylococcus aureus, Escherichia coli and Salmonella sp. These organisms are foodborne bacteria which are known to cause food poison= ing worldwide [4]. In particular, the tropical climate is an optimum environment for cell multiplication leading to an awareness of food safety in the South= east Asian region. The effect of heat treatment at different pH values and the combined effect of selected bacteriocin-like activities were also described= .

=

Materials and methods

Bacterial strains and growth conditions. One hundred and thirty-three LAB isolated from “Sai-krok-prieo” and “Mum” were g= rown on tryptic soy agar (without glucose) with 2.0 % yeast extract (TSAYE) slant at 37 ^oC for two days be-fore use. The test organisms were B. cereus TISTR 037, S. aureus TISTR 029, E. col= i TISTR 073 and Salmonella sp. isolated from chicken intestine. The test str= ains were cultured on nutrient agar (NA) slant at 37 ^oC for one = day. All strains were maintained as frozen stocks at minus 20 ^oC= in their medium supplement with 30 % glycerol.

Cell suspension preparation. Each one-day old test strai= n on NA slant was suspended in normal saline solution (NSS) to an OD_{600
of 0.5 in
order to obtain a viable cell number =
of 10⁸ – 10⁹CFU/ml. Subsequently, the cell suspension was diluted to an initial c=
ell
number of 10⁵ – 10⁶ CFU/ml.}

Screening for BLA. The screening method was modified according to the lawn method from Ohmomo et al. [8]. The LAB cultures from TSAYE slant were streaked on TSAYE plates (without glucose) and incubated u= nder anaerobic conditions at 37 ^oC for one day. One ml of the suspended test bacteria was mixed with 15 ml of melted TSA at 50 ^=
oC and was overlaid on overnight-grown LAB plates. The plates were further incubated anaerobically at 37 ^oC for 1-2 days and were obse= rved for inhibition zones in parallel with the overlay plate without LAB serving= as a control.

Broth dilution method. The broth dilution method modified = from Waterworth [14] was employed to investigate BLA in broth medium. Each LAB strain was grown anaerobically in tryptic soy broth (glucose excluded) supplemented with 2.0 % yeast extract (TSBYE) at 37 ^oC= for 24 hours. The broth was centrifuged at 5000 rpm for 15 min and the supernat= ant was collected and filtered through a 0.45 µm of cellulose acetate membrane (no. 41334, Gelman). The filtrate was diluted with Mueller Hinton broth (MHB) to a concentration of 1/2-, 1/4-, 1/8-, 1/16- and 1/32 fold of = an undiluted filtrate. One volume of each test bacterial suspension, prepared = as described above, was added to an equal volume of each undiluted and diluted filtrate and the mixtures were incubated at 37 ^oC for 24 ho= urs. Optical density at 600 nm of each mixture was measured and compared with a control (the test bacterial suspension diluted by half with MHB) and the differences were reported as a percent inhibition according to equation (1)= [1, 6]. One bacteriocin unit (B.U.) was defined as the amount of bacteriocin th= at inhibited growth of the test microorganism by 50 %, when compared with= a control culture without bacteriocin [2].

=

Percent Inhibition =3D 100 ´ (OD_{600, control} –= OD_600,
test)/OD_{600, control} = ;           (1)

=

Heat treatment at different pH values and BLA of dual mixtures. Selected LAB strains were grown on TSBYE at 37 ^oC for two days. <= /b>Cell-free supernatants were harvested and filtered through 0.45 µm cellulose acetate membranes. The filtrate was adjusted to pH 4, 5 and 6 and heated at= 65, 80 and 100 ^oC for 5, 15, 30 and 60 min according to Yin et = al. [15]. One volume of each test bacterial suspension was added to one volume = of each filtrate and the mixtures were incubated at 37 ^oC for = 24 hours. Optical density at 600 nm of each mixture was measured and percent inhibition was calculated. To investigate the combined effect of BLA against the test organisms, one volume of dual filtrate mixture (1:1 ratio)= was added to one volume of each test bacterial suspension and the final mixtures were incubated at 37 ^oC for 24 hours. Optical densit= y at 600 nm of each mixture was measured and the percent inhibition was calculat= ed.

Statistical analysis and regression mo-del. Each treatment was repeated twice and the measurement of optical density of each sample was performed in triplicate. Average values were reported along with standard deviations. Te= sts of significant difference based on t-statistics were performed using MINITAB software (Minitab Inc., USA): non-significant difference if (probability; P > 0.05) and a significant difference if.(P <&n= bsp;0.05). Data were computed with MINITAB software for correlation coefficients and regression models.

=

Results and Discussion

BLA of the isolates

The screening method modified according to the lawn method showed that 8 out of= 133 (CP1-15, CP2-11, CP3-1, CP7-3, CP10-3, CP11-6, CP14-1 and CP14-4) suppressed the growth of B. cereus and 4 out of 133 isolates (CP1-15, CP7-= 3, CP14-2 and CP14-3) suppressed the growth of S. aureus. However, there was no antagonistic activity against E. coli and Salmonella= sp. The isolate CP3-1 was previously identified as Weissella confusa, whereas CP7-3 was Pediococcus acidilactici, and CP1-15, CP2-11 and CP10-3 were Lactobacillus plantarum [9]. The use of tryptic s= oy media without glucose limited the effect of organic acids produced from glu= cose catabolism. The exclusion of the effect of organic acids produced from gluc= ose catabolism was also ensured by the pH at the time of filtrate collection wh= ich was approximately 6.5. <= /o:p>

The inhibition activities against B. cereus = and S. aureus from the broth dilution test at various dilutions are shown in Fig. 1, A and B, respective= ly. There were 8 isolates with BLA against B. cereus. The degree of inhibition was reduced more than twice when the filtrate was two-fold dilut= ed. The isolate CP3-1 showed the highest BLA against B. cereus (94 %) at an undiluted concentration. Four isolates showed inhibitory = activities against S. aureus and the isolate CP7-3 showed the highest inhibition (48 %). Although the activity against S. aureus= at undiluted concentrations was less than 50 % inhibition, the inhibition activities could still be detected at the lowest concentration used in this study (diluted to 1/32 fold). Bacteriocin units at the highest concentratio= n of the filtrate (1 ml filtrate/ml total volume) of each isolate are reported in Table 1. It was also noted that the filtrates from two isolates, CP1-15 and= CP7-3, showed antibacterial activity against both B. cereus and S. = aureus with different percentages.

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= Fig. 1. Inhibitory activities in broth medium at various dilutions against B. cereus (A) and S. aureu= s (B).

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Table 1. Bacteriocin units at the highest concentration of filtrate (1 ml filtrat= e/ml total volume) of each isolate.

Is= olate

Bacteriocin Units

B. cereus

S. aureus

CP= 1-15

0.92

0.81

CP= 2-11

1.56

-

CP= 3-1

1.84

-

CP= 7-3

0.72

0.98

CP= 10-3

1.77

-

CP= 11-6

0.28

-

CP= 14-1

0.91

-

CP= 14-2

-

0.76

CP= 14-3

-

0.85

CP= 14-4

0.83

-

From the literature, BLA found in Lactobacillus sp. and Pediococcus sp. are common [7, 11, 12] but those from Weissella sp. are rare. This study showed a clear evidence for the detection of BLA from W= eissella sp.

=

Effect of heat treatment and pH of medium

W. confusa= CP3-1 with highest B.U. against B. cereus and P. acidilactici CP7-3 with highest B.U. against S. aureus were selected for fur= ther studies. Fig. 2 and Fig. 3 show the effect of heat treatment on the inhibit= ion activity of CP3-1 filtrate against B. cereus and that of CP7-3 filtrate against S. aureus at various pH, respectively. The data shows that the alteration of pH of the medium had little effect on the inhibitory activity and CP7-3 and CP3-1 reported in this work has the potential for application in a broader pH range since the inhibitory activities in acid and near neutral conditions we-re not significantly different.

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= Fig. 2. Effect of the heat treatment on the inhibition activity of CP3-1 filtrate against = B. cereus at pH 4, 5 and 6.

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= Fig. 3. Effect of the heat treatment on the inhibition activity of CP7-3 filtrate against = S. aureus at pH 4, 5 and 6.

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B. cereus, i.e., the percent inhibition of CP3-1 filtrate dropped from 92 % to 65 % when the filtrate was incubated at 65 ^oC for five minutes, while tha= t of CP7-3 filtrate dropped from 49 % to 46 %. For both cases of CP3-1 filtrate against B. cereus and CP7-3 filtrate against = S. aureus, the effect of time became more apparent with increasing temperature, i.e., when heated for the same period, the per-cent inhibition dropped faster at 80 ^oC than at 65 ^oC and heat treatment at 100 ^oC for long= er than five minutes completely destroyed BLA. The heating temperature of 65&n= bsp;^oC and 80 ^oC reflect the temperature in the pasteurization pro= cess applied in the food industry. This study suggests the tendency of where the= se bacteriocins could be exploited, provided that they must be used in conjunction with the other hurdles.

Combined effects of dual filtrate mixtures

By adding one volume of dual filtrate mixture (1:1 ratio) to an equal volume of the test bacteria, the working concentration of each filtrate was reduced by half. However, the activity only slightly decreased from that of the undilu= ted filtrate of each individual strain (Fig. 4, A and B). The results in Fig. 1, A and B show that when the individual filtrate was diluted to = half strength, the percent inhibition dropped from 94 % to 28 % in the case of CP3-1 filtrate against B. cereus and from 48 % to 36&nb= sp;% in the case of CP7-3 filtrate against S. aureus. This suggested that the combined effect of the BLA was synergistic. In the literature, the combination of Pediocin AcH and nisin was reported to have a greater bactericidal effect than their individual use [5]. The food ecosyst= em in reality may have more than one food borne disease involved, thus bacteriocins that possess synergistic activity or one bacteriocin that have functional duality are desirable for bio-preservation in the food industry. These synergistic effects and the BLA of W. confusa prompt attention for further investigation.

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Fig. 4. Effect of the heat treatment on the inhibitory activities of: dual filtrate mixture and CP3-1 filtrate against = B. cereus (A); dual filtrate mixture and CP7-3 filtrate against = S. aureus (B).

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Regression equations predicting the effect of heat treatment

Using regression analysis, model equations for the prediction of the effect of he= at treatment were given by Equations (2), (3), (4) and (5) for CP3-1 filtrate against B. cereus, CP7-3 filtrate against S. aureus, the mixture of CP3-1 and CP7-3 filtrates against B. cereus and the mixture of CP3-1 and CP7-3 filtrates against S. aureus, respectively= .

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Y =3D -7.0 + 2.89T – 5.89 x 10^-1t -2.47 x 10= ^-2T² + 1.07 x 10^-2t² – 7.09 x 10= ^-3Tt        &= nbsp;           &nbs= p;       (2)

Y =3D 40.0 + 8.90 x 10^-1T – 1.50 x 10-1t - 1.07 x 10^-2T² + 4.54 x 10^-=
2t² – 7.09 x 10^-3Tt&= nbsp;           &nbs= p;   (3)

Y =3D 30.0 + 1.89T – 7.41 x10^-1t -1.92 x 10-2T² + 6.93 x 10^-3t² – 1.80 x 10= ^-5Tt        &= nbsp;           &nbs= p;       (4)

Y =3D 120 – 1.09T – 5.79 x 10^-1t +1.10 x 10^-3T² + 5.01 x 10^-3=t² – 1.80 x 10^-5Tt&= nbsp;           &nbs= p;            &= nbsp; (5)

where Y is the output response (i.e. percent inhibition), T the temperature in oC and t the time in minutes.

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Regression equations were obtained by fitting the experimental data with second-order polynomial equations. Fig. 5, A and B show the model prediction of heat treatment effect on antibacterial a= ctivity of CP3-1 filtrate against B. cereus and of CP7-3 filtrate again= st S. aureus, respectively. Fig. 6, A= and B show the model prediction of heat treatment effect on antibacterial activity of the dual filtrate mixture against B. cereus and = S. aureus, respectively. The simulated data agreed well with the experimental data wit= hin 10 % when the filtrates we-re incubated at 65 ^oC for 5, 15, 30 and 60 min and at 80 ^oC for 5, 15 and 30 min. T= he effect of heat treatment at 80 ^oC for 60 min and at 100 ^oC for longer t= han five minutes was more severe than that predicte= d by the second-order polynomial equations.

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Fig. 5. Model prediction of the heat treatment effect on the antibacterial activity of CP3-1 filtrate against B. c= ereus (A) and CP7-3 filtrate against= S. aureus (B).

Fig. 6. Model prediction of the heat treatment effect on the antibacterial activity of the dual filtrate mixture against B. cereus (A) and S. aureus (B).

Conclusion

Bacteriocin-like activity was found in Weissella confusa CP3-1 providing a restrictio= n to the growth of B. cereus. Pediococcus acidilactici CP7-3 also showed antagonistic effects against S. aureus. Bacteriocins produced from both strains can be applied in a wide pH range (4–6). Though their stability decreased by increasing the temperature, the activity was found to withstand a pasteurization processing temperature. As the food industry does not alwa= ys employ purified bacteriocins due to the need of regulation approval, fermen= ted ingredients or bacteriocin-producing cultures become more appealing. Also, highlighted was the potential of exploiting the mixture of crude bacteriocins to gain greater effectiveness against two Gram positive food borne disease.

Acknowledgement. The study was sup-ported by a Research Grant for New Scholars (RGNS) from the Commission on Higher Education and the Thailand Research Fund (TRF). Suggestions from mentor Assoc. Prof. Somboon Tanasupaw= at are gratefully acknowledged.

References

1.&n= bsp; Charernjiratrakul, W., 2000. Songklanakarin J. Sci. Technol., 22 (2), 177-189 (In Thai).

2.&n= bsp; Cuozzo, S. A., J. M. S. Fernando, A. R. P. Aida, R. R. Rual, 2001. Methods for the detection and concentration of bacteriocins produced by lactic acid bacteri= a. In: Food Microbiology Prot-cols, J. F. T. Spencer, A. L Ragout de Spencer (Eds), Totowa: Himana Press, 141-146.

3.&n= bsp; Deegan, L. H., P. D. Cotter, C. Hill, P. Ross, 2006. Int. Da= iry Journal, 16, 1058-1071.

4.&n= bsp; Eley, A. R., 1996. Microbial Food Poisoni= ng, second edn, London= : Chapman & Hall.

5.&n= bsp; Hanlin, M. B., N. Dalchayanand, P. Ray, B. Ray, 1993. J. Food Protect., 5= 6, 252-255.

6.&n= bsp; Ibrahim, S. A., A. Bezkorovainy, 1993. J. Food Protect., 55, 713-715. =

7.&n= bsp; Kostinek, M., S. Ingrid, V.A. Edward, U. Schillinger, C. Hertel, W. H. Holzapfel, C. = M. A. P. Franz, 2005. Sys. Appl. Microbiol., 28 (6), 527-54= 0

8.&n= bsp; Ohmomo, S., M. Kobayashi, M. Yajima, P. Suyanandana, P. Budka, P. Somchai, 1999. Japan Agricultural Research Quarterly, 33, 125-131.

9.&n= bsp; Phalakornkule, C., S. Tanasupawat, 2006-2007. Character= ization of lactic acid bacteria from traditional Thai fermented sausages. J. Cul= t. Collections (Sofia), 5, 46-57.

10.&= nbsp; Rayman, K., N. Malik, A. Hurst, 1983. Appl. Environ. Microbiol., 46, 1450-1452.

11.&= nbsp; Rodríguez, J. M., M. I. Martínez, N. Horn, H. M. Dodd, 2003. Int. J. Food Microbiol., 80, 101-116.

12.&= nbsp; Ross, R. P., S. Morgan, C. Hill, 2002. Int. J. Food Microbiol., 79, 3-16.

13.&= nbsp; Scott, V., S. Taylor, 1981. J. Food Sci.= , 46, 121-126.

14.&= nbsp; Waterworth, P. M., 1978. Quantitative methods for bacterial sensitivity testing. In: Laboratory Methods in Antimicrobial Chemotherapy, D. S. Reeves, I. Phillips, J. D. Williams, R. Wise (Eds), Edinburgh: Churchill Livingstone, 35-37.

15.&= nbsp; Yin, L.-J., C.-W. Wu, S.-T. Jiang, 2003. J. Agric. Food Chem., 51, 1071-1076.

БАКТЕРИ = 54;ЦИНОПОДОБН&#= 1040; АКТИВНОСТ ПРИ

WEISSELLA CONF= USA И PEDIO= COCCUS ACIDILACTICI,

ИЗОЛИРА = 53;И ОТ ТРАДИЦИОННh= 8; ФЕРМЕНТИРАi= 1;И НАДЕНИЦИ THAI

&n= bsp;

Веерапо = 85; Чавасирикуl= 5;тон¹, Савитри Ватаниопаиl= 9;арн²,

Чантара = 87;орн Фалакорнкуl= 3;е¹*

Ре= зюме

133 щама млечнокисеl= 3;и бактерии, изолирани о = 90; традиционнl= 0; ферментираl= 3;и наденици Thai, сk= 2; скринирани за бактериоциl= 5;оподобна активност (БПА). Изследванеm= 0;о на инхибира = 97;ото действие срещу тест-органи = 79;ми показва, че осем от изолатите (CP1-15, CP2-11, CP3-1, CP7-3, CP10-3, CP11-6, CP14-1 и CP14-4) подтискат растежа на Bacillus cereus, а четири (CP1-15, CP7-3, CP14-2 и CP14-3) на S= taphylococcus aureus, но нито един не подтиска Escherichia coli и Salmonella sp. Изолатите с най-висока активност срещу двата Грам-положи = 90;елни тест-щама (CP3-1 з= 072; B. cereus и CP7-3 за S. aureus) са изследвани за ефекта на топлинната обработка при различн = 86; рН и за комбиниранl= 6; действие на двойните смеси. Повишаванеm= 0;о на температ = 91;рата на нагряван = 77; (между 65 и 100 ^oC) = 080; удължаванеm= 0;о на времето (между 5 и 60 мин) значително намаляват БПА, докато промените в рН (между 4 и 6) имат слаб ефект. При смесване на филратите н = 72; двата изолата БПА показва синергизъм срещу всеки тест-щам. Получени са уравнения н = 72; регресия чрез екстраполиl= 8;ане на експерим = 77;нталните данни за процента на = 080;нхибиране с полиномни уравнения о = 90; втори поряд = 98;к. Прогнозираl= 5;ите данни съответствk= 2;т добре на експерименm= 0;алните в рамките на 10 % при инкубиране на филтратите при 65 ^oC за 5, 15, 30 и= ; 60 мин, и при 80 ^oC за 5, 15 и 30 мин. Изолатите CP3-1 l= 0; CP7-3, които имат антагоностl= 0;чен ефект срещу двата щама Г= 088;ам-положите= лни бактерии, са идентифициl= 8;ани по-рано съответно като Wei= ssella confusa и Pediococc= us acidilactici. Авторите смятат, че това е първото съо = 73;щение за БПА от W. confusa срещу B. cereus.

&n= bsp;

Is= olate	Bacteriocin Units
B. cereus	S. aureus
CP= 1-15	0.92	0.81
CP= 2-11	1.56	-
CP= 3-1	1.84	-
CP= 7-3	0.72	0.98
CP= 10-3	1.77	-
CP= 11-6	0.28	-
CP= 14-1	0.91	-
CP= 14-2	-	0.76
CP= 14-3	-	0.85
CP= 14-4	0.83	-