Thirteen strains of L. plantarum exhibited antimicrobic activity against Escherichia coli O157: H7 DMST 12743 with zone suppression ranged between 11.5-12.5 millimeter. All trial strains were evaluated for their ability to last under GI piece of land conditions with and without cereals ; soya bean, benne and Job? s Tears. Sing stomachic tolerance, seven strains of PKWB6-12, PKWB7-1, PKWB7-2, PKWC6-1, PKWC6-9, PKWC7-1 and PKWD7-1 were more tolerant with more than 4.6 log CFU/ml while the viability of other six strains decreased to undetectable degree after 180 min exposure. However, all trial strains exhibitied high opposition to imitate little enteric juice pH 8.0 with 0.45 % gall salt. The consequence showed that cereal exerted a protective consequence on the endurance of all trial strains. Interestingly, the add-on of cereals particularly soybean exhibited a significantly improved the viability of all trial strains in fake stomachic juices pH 2.0. Whereas, Job? s Tears showed a greater positive influence on viability of most trial strains. These consequences indicated that soya bean, benne and Job? s Tears could be used as nutrient bearers to bringing probiotic lactic acid bacteriums through the GI piece of land system.
Keywords soya bean ; sesame Job? s Tears GI piece of land conditions
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Probiotics are unrecorded microbic nutrient addendums which play an of import function in advancing and keeping human wellness. Probiotics propose many wellness benefits such as cut downing GI jobs like diarrhoea, commanding inflammatory diseases and exciting the immune system, bettering enteric microbic balance ( Prado et al. , 2008 ) . In Asiatic states, a figure of new probiotic strains isolated from fermented veggie and meat merchandises have been developed. Many researches have been focused on developing new probiotic nondairy nutrients to run into the increased demand from consumers for alternate to probiotic milk-based merchandise. Probiotics can today be found in non-fermented milk, fruit juices and cereal-based merchandises ( Saarela et al. , 2006 ) . In order to exercise probiotic good consequence after ingestion, probiotics need to last transition through the GI piece of land conditions chiefly attributed to their acid and gall tolerance which are important belongingss of probiotics. Cereal merchandises have been shown to be suited substrates for the growing of possible probiotics ( Valerio et al. , 2006 ) . In old surveies, malt, wheat and barley were found to heighten acerb tolerance of L. plantarum NCIMB 8826 ( Michida et al. , 2006 ) and bile tolerance of L. reuteri NCIMB 1195 and L. acidophilus NCIMB 8821 and L. plantarum NCIMB 8826 ( Patel et al. , 2004 ) . The endurance of L. plantarum ITM21B and L. paracasei IMPC2.1 was improved during exposure to simulated GI digestion when Cynara scolymuss were used as nutrient bearers ( Valerio et al. , 2006 ) . Cereals including soya bean ( Glycine soap ( L. ) Merr. ) , benne ( Sesamum orientale L. ) and Job? s Tears ( Coix lacryma-jobi Linn. ) are considerable economic harvest in eastern Asia used as nutrients, ingredients and constituent of drugs. They are high in nutrition value and contain important sums of dietetic fibre, protein, saccharides, energy, minerals and vitamins required for human wellness. Therefore, the purpose of this survey was to measure counter activity of L. plantarum L. plantarum against Escherichai coli O157: H7 DMST 12743 and the consequence of these cereals on the stableness of L. plantarum under GI piece of land conditions.
Materials and methods
Thirteen strains of Lactobacillus plantarum isolated from fermented veggie with high acid production were used in this survey. The trial strains were preserved in MRS stock ( Merck, Darmstadt, Germany ) incorporating 20 % ( v/v ) glycerin at -20 oC. For everyday analysis, the trial strains were subcultured twice in MRS stock to keep freshness. Escherichia coli O157: H7 DMST 12743 was purchased from Department of Medical Science, Ministry of Public Health, Thailand. The civilization was grown in Tryptic Soy Broth ( TSB ) ( Difco Laboratories, Detroit, MI, USA ) supplemented with 0.6 % Yeast infusion ( TSBYE ) at 37 oC.
Determination of counter activity of L. plantarum
L. plantarum were investigated for their antimicrobic activity against E. coli O157: H7 DMST 12743 by agar diffusion method and topographic point on lawn method. For the inhibitory activity by agar good diffusion method, index strains was adult overnight in TSBYE. 20 milliliter of TSAYE home bases ( 1.5 % agar ) were inoculated with 50? cubic decimeter nightlong civilization of the index micro-organism ( 106 CFU/ml concluding concentration ) . The Wellss ( 6 mm-diameter ) were formed by pluging out of the solid agar utilizing unfertile cork bore bit, and 50? fifty volume of L. plantarum civilization was added to the holes and incubate at 37 oC for 24 H ( Domrongpokkaphan and Wanchaitanawong, 2006 ) . The diameters of the suppression zones were measured in millimetres ( millimeter ) .
To finding of the inhibitory activity by topographic point on lawn method, the index home bases were prepared by covering 5 milliliter of soft TSA ( with 0.75 % agar ) with 10? cubic decimeter of index strain at the concentration of about 106 CFU/ml. Cell-free supernatant was obtained from nightlong lactobacilli MRS civilization. The supernatant were collected by centrifugation at 10,000 revolutions per minute for 15 min, adjusted to pH 5.0 and 6.0 with 5 M NaOH and filtered through a 0.2? m pore size unfertile filter ( Minisarts? , satorius ) . Consecutive dilutions of cell-free supernatant was spotted ( 10? cubic decimeter ) on the surface of the agar. The home bases were so incubated at 37? C. Inhibition country was revealed by the formation of clear zone in the index bacterial lawn. Antimicrobial activity is expressed in arbitrary units ( AU ) per milliliter of the original civilizations calculated as follows: AU/ml is the highest dilution exhibition suppression zone per volume of descrying supernatant ( Hamsupo, 2005 ) .
Preparation of cereals pulverization and chemical analysis
Soy, benne and Job? s Tears grains were land and separated with a sieve size of 0.5 millimeter. Samples of 5 g the ensuing pulverization were assorted with 45 milliliter of distilled H2O and sterilise at 121oC for 15 min earlier used as 10 % ( w/v ) cereals.
Entire sugar concentration was determined by the phenol-sulphuric acid method ( Dubois et al. , 1956 ) . The analysis of the samples was conducted based on a standardization curve ( R2=0.993 ) utilizing an array of glucose standard solution ( 400 mg/l ) . Reducing sugar concentration was determined by the 3, 5-dinitrosalicylic acid method ( Miller, 1959 ) . The analysis of the samples was conducted on the footing of a standardization curve ( R2=0.993 ) utilizing an array of glucose standard solutions ( 1 g/l ) . The buffering capacity of samples was determined by titrating 100 milliliter of the medium with HCl ( 1N ) . The value was expressed as the sum of HCl ( mmole ) required dropping 1 pH unit per unit volume ( cubic decimeter ) .
Preparation of fake stomachic juices and little enteric juices
Fake gastric and little enteric juices were prepared fresh day-to-day following to method of Michida et Al. ( 2006 ) and Huang and Adam ( 2004 ) . Briefly, Simulated gastric juice was prepared by suspending pepsin ( 1:10,000, ICN ) in unfertile saline ( 0.5 % , w/v ) to a concluding concentration of 3 g/l and seting to pH 2.0 with concentrated HCl utilizing a pH metre ( Mettler Toledo, FiveEasy ) . Simulated little enteric juice was prepared by suspending pancreatin USP ( P-1500, Sigma, Basingstoke, Hampshire, UK ) in the unfertile saline to a concluding concentration of 1 g/l with 0.45 % gall salt ( Oxoid, Basingstoke, Hampshire, UK ) and seting to pH 8.0 with unfertile 0.1 mol/l NaOH utilizing a pH metre.
Determination of fake GI piece of land tolerance of L. plantarum
Washed bacterial cell suspension was prepared. Bacterial cell of 20 h civilization was centrifuged at 5,000 revolutions per minute for 10 min, washed twice with unfertile saline ( 0.5 % , w/v ) and resuspended in unfertile saline utilizing as washed cell suspension. The feasible cell count was determined prior to assay of theodolite tolerance.
The tolerance of a washed cell of L. plantarum to the simulated gastric and little enteric juices was determined utilizing Michida et Al. ( 2006 ) method with a small alteration. Aliquots ( 0.2 milliliter ) of the free-cell suspension were transferred to a 2.0 milliliter Eppendorf tubing, assorted with 0.3 milliliters unfertile saline ( 0.5 % , w/v ) or cereal ( 10 % , w/w ) and eventually blend with 1.0 milliliters of fake gastric ( pH 2.0 ) or little enteric juices ( pH 8.0 ) . The concluding concentration of cereals was 2 % and so the mixture was incubated at 37? C. For fake stomachic juices tolerance finding, feasible cell counts were measured after 30, 60, 90, and 180 min. For fake little enteric juices tolerance finding, feasible cell counts were measured after 240 min. Feasible cell counts were determined by the standard home base count method with Lactobacilli MRS medium. The home bases were incubated at 37? C for 36 h. Viable cell counts were expressed as log10 values. The per centum of cells endurance was calculated as follows: % survival = ( log N/log N0 ) ? 100, where N0 figure of feasible cells ( CFU/ml ) before exposure to simulated gastric and little enteric juices and N is figure of feasible cells ( CFU/ml ) after exposure to simulated gastric and little enteric juices.
Scaning negatron microscopy
After exposure to simulated stomachic juice ( pH 2.0 ) added with soya bean, benne and Job? s Tear, L.plantalum PKWB6-12 was monitored by scanning negatron microscopy. The cells were first fixed with a 2.5 % glutaraldehyde in Na phosphate buffer pH 7.2 for 12 hours. After three times wash with phosphate buffer, the samples were fixed with 1 % Os tetroxide for 1 hr and washed with distilled H2O for three times. The samples were so dehydrated through a ranked series of ethanol soaks ( 30, 50, 70, 90 and 100 % ethyl alcohol, utilizing 100 % ethyl alcohol three times ) and drying with liquid carbondioxide. The dried samples were coated with Au and determined in a scanning negatron microscope JSM 5600 LV ( JEOL Ltd, Tokyo, Japan ) .
Consequences and Discussion
Antimicrobial activity of 13 strains of L. plantarum
Thirteen strains of L. plantarum isolated from fermentated veggie were evaluated for their ability to suppress the growing of E. coli O157: H7 DMST 12743 utilizing agar good diffusion method. It was found that all trial strains had an antimicrobic belongings against the index strain with the suppression zone runing from 11.5? 0.10 to 12.5? 0.10 millimeter. The cell-free supernatant ( pH 3.5-3.6 ) from all trial strains besides exhibited antimicrobic activity of about 100 – 300 AU/ml. The repressive consequence observed for all trial strains may be attributed to the lowered pH, the undissociated acids and production of other primary and secondary antimicrobic metabolites produced by lactic acid bacteriums ( H? terrestrial time et al. , 2006 ) . Furthermore, it was found that the neutralised pH 6.0 supernatant of PKWA6-1, PKWA7-1, PKWB 6-3 and PKWB6-12 inhibited the growing of index strain with the antimicrobic activity of 200 – 300 AU/ml. Based on these consequences, four strains were capable of synthesising repressive substances including bacteriocin-like compounds ( Albano et al. , 2007 ; Con et al. , 2001 ; Con et al. , 2000 ) .
3.2 Effect of soya bean, benne and Job? s Tears on viability of L. plantarum under simulated stomachic juice pH 2.0
The acerb tolerance of 13strains of L. plantarum was tested at pH 2.0 ( Figure 1 ) . It was observed that all trial strains exhibited certain opposition ability to gastric juice for 180 min. Among the 13 strains tested, 7 strains ( PKWB6-12, PKWB7-1, PKWB7-2, PKWC6-1, PKWC6-9, PKWC7-1 and PKWD7-1 ) appered to be more capable to last higher than 4.5 log CFU/ml. After incubation for 180 min, PKWB6-12 was found to be the most tolerant with the decrease rate of 28.80? 8.43 % ( from 9.73? 0.28 to 6.93? 0.82 log CFU/ml ) . Meanwhile, other six strains ( PKWA6-1, PKWA7-1, PKWB6-3, PKWC8-1, PKWD6-10 and PKWD7-2 ) were susceptible to stomachic status and the figure of feasible cell decreased to undetectable degree after exposure for 180 min.
Furthermore, the consequence of cereals on the endurance of all trial strains during 180 min exposure to acid juice was shown in Figure 2. The add-on of soya bean, benne and Job? s Tears increasingly improved the stomachic tolerance. All trial strains were able to keep feasible cell degree of 4.93? 0.09 to 9.64? 0.06 log CFU/ml for 180 min exposure depending on cereal type. Unusually, sensitive strains ( PKWA6-1, PKWA7-1, PKWB6-3, PKWC8-1, PKWD6-10 and PKWD7-2 ) displayed high endurance after 180 min exposure compared with control group. Results besides showed that acerb tolerance depended on type of strain and cereal. Soy was found to be the most protective compound followed by benne and Job? s Tear. Compared with control, the viability of all trial strains was considerable improved by about 2.13 – 9.45, 2.08 – 9.27 and 2.10 – 9.17 log CFU/ml in the nowadays of soya bean, benne and Job? s Tear, severally. Among these lactic acid bacteriums, add-on of soya bean and benne enhanced acerb tolerance of PKWD7-1 with the highest survival rate of 97.67? 0.56 % and 94.57? 1.61 % , severally. Further, the add-on of Job? s Tears resulted in the highest viability of 95.72 % for PKWC7-1.
There have been reported that proteins, polyoses, and free amino acids have a good protective consequence on lactic acid bacteriums and heighten their viability in the GI conditions ( Michida et al, 2006 ; Charalampopoulos et al. , 2003 ) . In this present survey, the add-on of cereals particularly soybean displayed a significantly improved the viability of all trial strains in fake stomachic juices pH 2.0. Their viability were higher than 8 log CFU/ml at the terminal of incubation. This indicated that soya bean protein played an of import function in the sweetening of endurance of lactic acid bacteriums ( Wang et al. , 2008 ) . In add-on, higher concentration of entire sugar, cut downing sugar and buffering capacity in soya bean ( Table 2 ) may hold a interactive consequence on the GI tolerance ( Michida et al, 2006 ) . By and large, L. plantarum exhibited high cell population owing to its alone ability to digest low pH values by keeping pH homeostasis ( Giraud et al. , 1998 ) . Under acidic status, F1F0-ATPase proton pump is an of import mechanism responsible for the endurance of some Gram-positive micro-organisms ( Cotter and Hill, 2003 ) . The F0F1-ATPase could increase interior pH by bring forthing a proton motivation force, via proton ejection. This reaction requires energy in signifier of ATP obtained from sugar use as carbon-source of L. plantarum. ( Sheng and Marquis, 2006 ; Corcoran et al. , 2005 ; McDonald et al. , 1990 ) .
From SEM consequences, it was clear that high cell denseness of L. plantalum PKWB6-12 were entrapped on the fibre construction of soya bean, benne and Job? s Tears. The raggedness construction may offer protection to the cell in the acerb status ( Valerio et al. , 2006 ) . Therefore, the cereals could be used as nutrient vehicles for probiotic so as to heighten their stableness during exposure to gastric digestion.
3.3 Effect of soya bean, benne and Job? s Tears on endurance of L. plantarum under simulated little enteric juices pH 8.0
Bile tolerance of 13 trial strains of L. plantarum was presented in Table 3. As a general inclination, all trial strains appeared to be most capable to last during exposure to imitate little enteric juice ( pH 8.0 ) with 0.45 % gall salt for 240 min and decrease of feasible cell count ranged 0.26 – 2.64 log CFU/ml. Of 13 strains, a somewhat decreased in viability was observed in PKWD6-10 and PKWA6-1 and their cell population somewhat decreased from 9.95 to 9.69 log CFU/ml ( 97.28? 0.11 % endurance ) and 9.27 to 8.86 log CFU/ml ( 95.42? 2.20 % endurance ) , severally. For other 10 strains, endurance ranged between 73.14 – 89.86 % ( Figure 4 ) .
Futhermore, the influence of soya bean, benne and Job? s Tears on the endurance of all trial strains under simulated little enteric juice with 0.45 % gall salt for 240 min was examined. Although these cereals may work as buffering agents ( Table 2 ) , merely PKWD7-1 and PKWB7-1 were significantly ( P & lt ; 0.01 ) improved in viability of & gt ; 1 log CFU/ml as compared to command after 240 min incubation retained at the degree of 109 and 108 CFU/ml and their survival rate of 94.80 % -99.65 % for PKWD7-1and 83.11 % -87.39 % for PKWB7-1 were obtained, severally ( Figure 4 ) . After 240 min incubation clip, significantly ( P & lt ; 0.01 ) decreased in viability of PKWA6-1, PKW D6-10 and PKWD7-2 with add-on of benne and PKWA7-1, PKWB6-3, PKWB6-12 and PKWC6-9 with add-on of soya bean was obtained. Furthermore, it was observed that most of trial strains could last better in the nowadays of Job? s Tears.
The present survey has shown that our possible probiotic L. plantarum exhibited antimicrobic activity against E. coli O157: H7. The consequences indicated that soya bean, benne and Job? s Tears could better the tolerance of L. plantarum to simulated GI piece of land conditions depending on the composing of cereals. Specially, soya bean enhanced the acerb tolerance while Job? s Tears improved the bile tolerance.
Consequences indicated that the cereals could be used as vehicle for bringing of lactic acid bacteriums as probiotic to the human GI piece of land. This determination could farther take to the development of new probiotic functional nutrient with the combination of LAB and cereal which reffered to as symbiotic.
Feasible cell counts ( log CFU/ml ) of each strain in the presence of cereals in system were compared with control ( no cereal ) , *p & lt ; 0.05, **p & lt ; 0.01 ( pupil? s t-test, two tailed )
Figure 4 Consequence of soya bean, benne and Job? s Tears on viability of L. plantarum during exposure to imitate little enteric juices pH 8.0 with 0.45 % gall salt for 240 min
This work was granted by the Commission on Higher Education allowing. Miss Wanticha Lapsiri was supported for CHE-PhD-SW from the Commission on Higher Education. Thailand.
- Albano, H. , M. Oliveira, R. Aroso, N. Cubero, T. Hogg and P. Teixeira. 2007. Antilisterial activity of lactic acid bacteriums isolated from? Alheiras? ( traditional Protuguese fermented sausages ) : In situ checks. Meat Sci. 76: 796-800.
- Begley, M. , C.G.M. Gahan and C. Hill. 2005. The interaction between bacteriums and gall. FEMS Microbiol. Rev. 29: 625-651.
- Charalampopoulos, D. , S.S. Pandiella. and C. Webb. 2003. Evaluation of the consequence of malt, wheat and barley infusions on the viability of potentially probiotic lactic acid bacteriums under acidic conditions. Int. J. Food Microbiol. 82: 133-141.
- Charalampopoulos, D. , R. Wang. , S.S. Pandiella and C. Webb. 2002. Application of cereals and cereal constituents in functional nutrients: a reappraisal. Int. J. Food Microbiol. 79: 131-141.
- Charteris, W.P. , P.M. Kelly, L. Morelli and J.K. Collins. 1998. Development and application of an In vitro methodological analysis to find the theodolite tolerance of potentially probiotic Lactobacillus and Bifidobacterium species in the upper human GI piece of land. J. Appl. Microbiol. 84: 759-768.
- Con, A. H. and H. Y. G? kalp. 2000. Production of bacteriocin-like metabolites by lactic acid civilizations isolated from sucuk samples. Meat Sci. 55: 89-96.
- Con, A. H. , H. Y. G? kalp and M. Kaya. 2001. Antagonistic consequence on Listeria monocytogenes and L. innocua of a bacteriocin-like metabolite produced by lactic acid bacteriums isolated from sucuk. Meat Sci. 59: 437-441.
- Corcoran, B.M. , C. Stanton, G.F. Fitzgerald and R.P. Ross. 2005. Survival of probiotic Lactobacilli in acidic environments is enhanced in the presence of metabolizable sugars. Appl. Environ. Microbiol. 3060-3067.
- Cotter, P.D. and C. Hill. 2003. Surviving the acerb trial: responses of Gram-positive bacteriums to low pH. Microbiol. Mol. Biol. Rev. 429-453.
- Del Piano, M. , L. Morelli, GP. Strozzi, S. Allesina, M. Barba, F. Deidda, P. Lorenzini, M. Ballare, F. Montino, M. Orsello, M. Sartori, E. Garello, S. Carmagnola, M. Pagliarulo and L. Capurso. 2006. Probiotics: from research to consumer. Digest. Liver Dis. S248-S255.
- Gibson, G.R. , H.M. Probert, J.V. Loo. , R.A. Rastall and M.B. Roberfroid. 2004. Dietary transition of the human colonic microbiota: updating the construct of prebiotics. Nutri. Res. Rev. 17: 259-275.
- Giraud, E. , Chanpailler, A. , Moulard, S. , Raimbault, M. , 1998. Development of a miniaturized selevtive numbering stratergy of lactic acid bacteriums for rating of assorted starting motor in a theoretical account manioc agitation. J. Appl. Microbiol. 84: 444-450. ? ? ? ? ? ? paper reappraisal application of cereals and cereals constituents in map.
- Hamsupo, K. 2005. Production and preparation of lactic acid bacteriums bring forthing antimicrobic substances as poulet probiotic adjuncts. Dortor of Philosophy Thesis. Kasetsart University, Bangkok.
- Huang, Y. and M.C. Adams. 2004. In vitro appraisal of the upper GI tolerance of possible probiotic dairy propionibacteria. Int. J. Food Microbiol. 91: 253-260
- Mattila-Sandholm, T. M. Blaut, C. Daly, L. De Vuyst, J. Dore, G. Gibson, H. Goossens, D. Knorr, J. Lucas, L. Lahteenmaki, A. Mercenier, M. Saarela, F. Shanahan and W.M. de Vos. 2002. Food, GI-tract functionality and human wellness bunch: PROEUHEALTH. Microb Ecol Health Dis. 14: 65-74.
- McDonald, L.C. , H.P. Fleming and H.M. Hassan. 1990. Acid tolerance of Leuconostoc mesenteroides and Lactobacillus plantarum. Appl. Environ. Microbiol. 2120-2124.
- Michida, H. , S. Tamalampudi. , S.S. Pandiella. , C.Webb. , H. Fukada and A. Kondo. 2006. Consequence of cereal infusions and cereal fibre on viability of Lactobacillus plantarum under GI piece of land conditions. Biochem. Eng. J. 28: 73-78.
- Miller 1959
- Patel, H.M. , S.S. Pandiella. , R.H. Wang. And C. Webb. 2004. Influence of malt, wheat, and barley infusions on the bile tolerance of selected strains of lactobacilli. Food Microbiol. 21: 83-89.
- Prado, F.C. , J.L. Parada, A. Pandey and C.R. Soccol. 2008. Tendencies in non-dairy probiotic drinks. Food Res. Int. 41: 111-123.
- Saarela, M. , I. Virkajarvi, H. Alakomi, P. Sigvart-Mattila and J. Matto. 2006. Stability and functionality of lyophilized probiotic Bifidobacterium cells during storage in juice and milk. Int. Dairy J. 16: 1477-1482.
- Saarela, M. , I. Virkajarvi, L. Nohynek, A. Vaari and J. Matto. 2006. Fibers as bearers for Lactobacillus rhamnosus during freeze-drying and storage in apple juice and chocolate-coated breakfast cereals. Int. J. Food Microbiol. 112: 171-178.
- Sheng, J. and R.E. Marquis. 2006. Enhanced acerb opposition of unwritten streptococcus at deadly pH values associated with acid-tolerant katabolism and with ATP synthase activity. FEMS Microbiol. Lett. 93-98.
- Shima, M. , T. Matsuo, M. Yamashita and S. Adachi. 2009. Protection of Lactobacillus acidophilus from bile salts in a theoretical account enteric juice by incorporation into the inner-water stage of a W/O/W emulsion. Food Hydrocolloids. 23: 281-285.
- Valerio F. , P. De Bellis, S. L. Longigro, L. Morelli, A. Visconti and P. Lavermicocca. 2006. In vitro and In vivo endurance and theodolite tolerance of potentially probiotic strains carried by Artichokes in the GI piece of land. Appl. Environ. Microbiol. 3042-3045.
- Wang, N.-F. , Y.-H. Shi, J. Sun and G.-W. Le. 2007. Evaluation of peanut flour fermented with lactic acid bacteriums as a probiotic nutrient. Food Sci. Tech. Int. 13 ( 6 ) : 469-475.
- Wang, J. , Z. Guo, Q. Zhang, L. Yan, W. Chen, X.-M. Liu and H.-P. Zhang. 2009. Agitation features and theodolite tolerant of probiotic Lactobacillus casei Zhang in soya milk and bovine milk during storage. J. Dairy. Sci. 92: 2468-2476.
- H? terrestrial time, P. , J.Shchepetova, K. L? ivukene, T. Kullisaar and M. Mikelsaar. 2006. Antagonistic activity of probiotic lactobacilli and bifidobacteria against entero- and uropathogens. J. Appl. Microbiol. 100: 1324-1332.
Therefore, these six strain was considered as per se tolerant to gastric theodolite pH 2.0 for 180 min.