Effect of refrigerated storage temperature on the viability of probiotic micro-organisms in yogurt

Similar documents
Journal of Food Biosciences and Technology, Islamic Azad University, Science and Research Branch, 1, 63-69, 2011

Int.J.Curr.Microbiol.App.Sci (2018) 7(7):

The Effect of Homogenization Pressure and Stages on the Amounts of Lactic and Acetic Acids of Probiotic Yoghurt

Viability of Probiotic (Bifidobacterium, Lactobacillus acidophilus and Lactobacillus casei) and Nonprobiotic Microflora in Argentinian Fresco Cheese

Lactic acid bacteria fermentations in oat-based suspensions

Effect of adding inulin on microbial and physicochemical properties of low fat probiotic yogurt

Street, Galati, Romania * Corresponding author: Received 5 July 2011 Revised 29 September 2011

Mixtures of soy- and cow s milk as potential probiotic food carriers

[Type text] [Type text] [Type text]

Standardization of Technology for Preparation of Functional Frozen Misti Dahi

PROBIOTIC STARTERS VERSUS TRADITIONAL STARTER IN QUARG PRODUCTION

Journal of Food Biosciences and Technology, Islamic Azad University, Science and Research Branch, 3, 29-36, 2013

THE STUDY OF CARBOHYDRATES FERMENTATION ABILITY OF B.LACTIS IN MILK

THE ANNALS OF VALAHIA UNIVERSITY OF TÂRGOVIŞTE Fascicle VII 2006 GROWTH AND ACTIVITY OF BIFIDOBACTERIA IN MIXED CULTURE WITH LACTOBACILLUS HELVETICUS

Effect of Oregano on the Growth of Lactobacillus acidophilus and Bifidobacterium bifidum in Probiotic Dairy Products

Effect of Some Plant Supplements on the Number of Lactic Acid Bacteria in Bulgarian Fermented Milk

Journal of Food Biosciences and Technology, Islamic Azad University, Science and Research Branch, Vol. 4, No. 1, 57-64, 2014

Studies of the Microbial and Physical Properties of Oriental Style Dairy Product Kou Woan Lao with Probiotics

Hassan Pyar Kok-Khiang Peh *

Effect of Bioyogurt Consumption on Fatty Metabolites of Serum and Colonic Microflora in Healthy Subjects

Jamali et al. UJPBS 2014, 02 (02): Page UNIQUE JOURNAL OF PHARMACEUTICAL AND BIOLOGICAL SCIENCES

PRODUCTION OF PLAIN YOGHURT ADDING HAIRY BASIL MUCILAGE AS PREBIOTICS Piyanoot Noiduang, 1, * Areerat Ittakornpan 1, Vasinee Marukatat 1 1

Augmentation of Probiotic Viability in Ice Cream Using Microencapsulation Technique

Effect of High Pressure Homogenization on Viability and Physicochemical of Probiotic Stirred Yogurt

Viability of Probiotic Bacteria during Refrigerated Storage of Commercial Probiotic Fermented Dairy Products Marketed In Jordan

Effect of Lactulose and Inulin on Physicochemical and Microbial Properties of Synbiotic Yogurt

Survival of Free and Encapsulated Probiotic Bacteria and their effect on the Sensory Properties of Quarg Cheese

RAPID METHOD FOR SELECTIVE ENUMERATION OF BIFIDUS ESSENSIS IN ACTIVIA YOGURTS

Role of Food Matrix for Probiotic Effects

Asian Journal of Food and Agro-Industry ISSN Available online at

Asian Journal of Food and Agro-Industry ISSN Available online at

Production of Probiotic Fermented Mixture of Carrot, Beet and Apple Juices

Improve probiotic viability of probiotic yogurt in supermarket chain and consumer chain

Survival of free and microencapsulated human-derived oral probiotic Lactobacillus paracasei SD1 in orange and aloe vera juices

Probiotics : What we Know and Where we are Going Next

Songklanakarin Journal of Science and Technology SJST R1 Teanpaisan

Physicochemical, microbiological and sensory properties of probiotic drinking yoghurt developed with goat milk

Study summaries L. casei 431

Development of finger millet based probiotic beverage using Lactobacillus casei431

Survivability of Lb. Acidophilus and Bif. Bifidum after Enzymatic Treatment and Lyophilization

Growth of Lactic Acid Bacteria in Milk for the Preparation of Functional Frozen Misti Dahi (Sweet Curd)

EVALUATION OF VIABILITY OF CO-ENCAPSULATED PRE- AND CERTAIN PROBIOTICS IN ICE CREAM DURING FROZEN STORAGE

Assessing and Maintaining Probiotics in Food

Development of synbiotic beverage from beetroot juice using beneficial probiotic Lactobacillus Casei 431

Survival of new probiotic strains with anti-inflammatory & anti-obesity effects used in non-fat yogurt and low-fat Cheddar cheese making

PROFESSIONAL FORMULATION. ProBiotic & ProBiotic Multi. Probiotics: A Common Sense Discussion

Understanding Today s Probiotics Regulations in South East Asia. Wai Mun Poon Regulatory Affairs Consultant

ACID AND BILE TOLERANCE OF PROBIOTIC BACTERIA USED FOR LACTIC ACID FERMENTATION OF VEGETABLE JUICES

Quantification of lactic acid bacteria and bifidobacteria in goat milk based yoghurts with added water-soluble soy extract

Preparation of a Whey-Based Probiotic Product with Lactobacillus reuteri and Bifidobacterium bifidum

Understanding probiotics and health

Standardization and Evaluation of Probiotic Shrikhand

Factors that Affect the Adhesion of Probiotics Bacteria to Resist Rice Starch

Probiotic. Prebiotics:

Available online at Downloaded from pbr.mazums.ac.ir at 9: on Monday January 28th 2019 [ DOI: /pbr.v4i2.

השפעת חיידקים פרוביוטיים

EFFECTS OF ALETA IN PROMOTING THE GROWTH OF PROBIOTIC BACTERIA: IN VITRO STUDY

Lactobacillus bulgaricus

Enhancement of probiotic bioactivity by some prebiotics to produce bio-fermented milk. Amnah A. H. Rayes

Probiotic yoghurt and supplements: Retail sales in the EU Supplements and yoghurts to record 4%, and -1% growth over

Survival of probiotic bacteria during lactic acid fermentation of vegetable juices

Q What are Probiotics?

PRODUCTION OF PROBIOTIC ICE CREAM

ENHANCEMENT OF PROBIOTIC VIABILITY IN ICE CREAM BY MICROENCAPSULATION

Effect of L-cysteine and ascorbic acid on the propagation of Lactobacillus casei in milk

Journal of Chemical and Pharmaceutical Research

Research Article. The effects of hyaluronic acid on the morphological physiological differentiation of Lactobacillus

SUPER PROBIO OR... 1 capsule! 20 BILLION. 40 pots WORLDWIDE BACTERIA PER CAPSULE PRACTITIONER STRENGTH

Effect of culture medium and cryoprotectants on the growth and survival of probiotic lactobacilli during freeze drying

INFLUENCE OF STARTER CULTURES ON THE ACIDITY AND SENSORY CHARACTERISTICS IN PROBIOTIC YOGHURT

Survivability of probiotics in symbiotic low fat buffalo milk yogurt

Lavanya Nutankalva,MD Consultant: Infectious Diseases

Fermentation Kinetics and Sensory Attributes of Milk Fermented by Probiotic Bacteria

PROBIOTICS are live microorganisms which, when ingested, confer a health benefits.

Bile Salts and Acid Tolerance and Cholesterol Removal from Media by some Lactic Acid Bacteria and Bifidobacteria

SCREENING LACTIC ACID BACTERIA FOR ANTIMICROBIAL COMPOUND PRODUCTION K. KHALISANNI, K. LEE HUNG

VIABILITY OF ENCAPSULATED BIFIDOBACTERIUM LACTIS (BB-12) IN SYNBIOTIC UF CHEESE AND IT S SURVIVAL UNDER IN VITRO SIMULATED GASTROINTESTINAL CONDITIONS

Survival of Weissella confusa and Lactobacillus paracasei strains in. fermented milks under cold storage and after freeze-drying

More than a gut feeling: How the microbiota improves health

Evaluation of Fibre Enriched and Vitamin - C Fortified Sweetened Probiotic Dahi

Alpha Beta Microbes. Information Pack

Universidad Michoacana San Nicolas Hidalgo

Sensory, Chemical and Microbial Quality of Fermented Probiotic Cereal Based Health Drink

Spirulina enhances the viability of Lactobacillus rhamnosus E N after freeze-drying in a protective medium of sucrose and lactulose

ANTIBACTERIAL TOOTHPASTE: DO NOT SWALLOW

Feeding Lactobacilli as probiotic and proportion of Escherichia coli in the intestine of calves

Introduction ORIGINAL PAPER. Fu-Mei Lin Æ Chiu-Hsia Chiu Æ Tzu-Ming Pan

Materials and Methods UDC :

Fermented Milk Starch and Milk Inulin Products as Vehicles for Lactic Acid Bacteria

Effect of Prebiotic Inulin on the Fermentation and Growth Kinetics Pattern of Probiotic Yoghurt Bacteria

Viability of Probiotics in Frozen Yogurt Supplemented with Inulin and Glycerol

Cholic acid resistance and the adherence ability of Bifidobacterium pseudocaenulatum G4

Changes in the Microflora of Bovine Colostrum During Natural Fermentation

Studies on keeping quality of Shrikhand prepared from buffalo milk blended with soymilk

Effect of Encapsulation on some Probiotic Criteria

Selective enumeration of dairy based strains of probiotic and lactic acid bacteria

Probiotic properties of Lactobacillus plantarum BG24, isolated from naturally fermented cereal beverage

Disseminating Probiotic Yogurt Recipe and Educational Materials to Underserved People with Type II Diabetes in Albany County

!Microbiology Profile, stool

Assessment of increase in probiotic potential of Lactobacillus strains fortified with Aloe vera

Transcription:

ORIGINAL RESEARCH Blackwell Oxford, IDT International 1364-727X Society?? Original ORIGINAL of UK Article Dairy Publishing RESEARCH Journal Technology of LtdDairy 2007 Technology Effect of refrigerated storage temperature on the viability of probiotic micro-organisms in yogurt A M MORTAZAVIAN, 1 * M R EHSANI, 1 S M MOUSAVI, 1 K REZAEI, 1 S SOHRABVANDI 1 and J A REINHEIMER 2 1 Department of Food Science and Technology, Faculty of Agriculture, University of Tehran, P.O. Box 31587-78659, Karaj, Iran and 2 Programa de Lactologia Industrial, Faculted de Ingenieria, Quimica Universidad Nacional del Litoral, Santiago del Estero, 2829, 3000, Santa Fe, Argentina The effect of refrigerated storage temperature was studied at 2, 5 and 8 C on the viability of probiotics in ABY ( Lactobacillus acidophilus, Bifidobacterium lactis BB-12 and yogurt bacteria. Bulgaricus, i.e. Streptococcus thermophilus and Lactobacillus delbrueckii ssp. Bulgaricus) probiotic yogurt. The study was carried out during a 20-day refrigerated storage period to identify the best storage temperature(s). Also, the viability change of the probiotic micro-organisms was analysed at 5-day intervals throughout the refrigerated storage period. After 20 days, storage at 2 C resulted in the highest viability of L. acidophilus, whereas for Bifidobacterium lactis the highest viability was obtained when yogurt was stored at 8 C. Keywords Bifidobacterium lactis, L. acidophilus, Probiotic, temperature, Viability, Yogurt. *Author for correspondence. E-mail: mortazvn@ut.ac.ir 2007 Society of Dairy Technology INTRODUCTION As a general definition, probiotics can be described as live micro-organisms (bacteria or yeast) that bring health benefits to their host (human or animal) mainly by maintaining and/or improving the microbial balance of the intestinal medium (Fuller 1989; Gismondo et al. 1999; Holzaspfel and Schillinger 2001; Shah 2001). Several health benefits have been attributed to probiotics such as antimutagenic and anticarcinogenic effects, immune system stimulation or immunomodulation, antiinfection properties, reduction of serum cholesterol, alleviation of lactose intolerance/lactose maldigestion and nutritional enhancement (Sanders 1999; Saarela et al. 2000; Shah 2001). The species of lactobacilli and bifidobacteria are by far the most important probiotics used in probiotic products. Nowadays, many probiotic products are available for the consumption of humans, farm animals and pets (Hoier 1992; Sanders 1999; Shah 2001; Holzaspfel and Schillinger 2001). Probiotic products can be divided into nonfermented and fermented. Probiotic yogurts are categorized in the second group. As yogurt is the most popular fermented milk product, producing probiotic yogurt with optimum viability (as the critical value of the product) and suitable sensory, as well as economic properties is very important. The viability of probiotic micro-organisms in the final product until the moment of consumption has been proposed with the descriptor minimum of biovalue (MBV). This is the minimum of viable probiotic cells per gram or millilitre of probiotic product (Mortazavian and Sohrabvandi 2006a), and is the most important qualitative parameter of probiotic products as it determines their pharmaceutical effectiveness. Many kinds of probiotic yogurt with various types of culture composition are being produced worldwide. However, loss of viability of probiotics during the fermentation process and refrigerated storage is a major issue in the production of probiotic yogurt. Although the effect of cold storage on the viability of probiotics in fermented milks has been the subject of various studies (Centeno-de-Laro 1987; Shah et al. 1995; Nighswonger et al. 1996; Bolin et al. 1998; Schilliger 1999; Han-Seung et al. 2000; Vinderola et al. 2000), to the best of the authors knowledge, only a few have been carried out with the ABY culture. Also, in none of them the viability change of probiotic micro-organisms has been investigated throughout the refrigerated storage, as a function of different refrigeration temperatures. In our previous related study (Mortazavian et al. 2006b), the best conditions of two heat variables (heat treatment and incubation temperature) on the viability of probiotics in ABY probiotic yogurt were identified. Following the mentioned study, the effect of refrigerated storage temperature, as the third temperature variable, was investigated on the viability of probiotics in ABY (L. acidophilus, B. lactis, and Streptococcus *Author for correspondence. E-mail: mortazvn@ut.ac.ir Vol 60, No 2 May 2007 International Journal of Dairy Technology 123

thermophilus and Lactobacillus delbrueckii spp. Bulgaricus) probiotic yogurt in order to determine the viability change of probiotics during a 20-day refrigerated storage and identify the best refrigeration temperature(s). MATERIALS AND METHODS Starter culture Fifty-unit pouches of commercial lyophilized ABY culture (containing L. acidophilus, Bifidobacterium BB-12 and S. thermophilus and L. delbrueckii spp. Bulgaricus) that are known as FD-DVS ABY-1 were supplied by Chr-Hansen company (Horsholm, Denmark). This culture is currently used by the dairy industry to produce yogurt. The cultures were maintained according to the manufacturer s instructions at 18 C. Culture media for enumeration MRS-bile agar medium (MRS agar: Merck, Darmstadt, Germany and bile: Sigma Aldrich, Inc., Reyde, USA) was used for the selective enumeration of L. acidophilus and B. lactis in the ABY culture composition according to Mortazavian et al. (2006c), by applying the subtractive enumeration method (SEM). The plates were incubated at 37 C for 3 days under aerobiosis and anaerobiosis. Anaerobiotic conditions were produced using the GasPac system (Merck, Darmstadt, Germany). Yogurt preparation and viability analysis For each experimental stage, according to Chr- Hansen s recommended procedure, a 50-unit pouch of FD-DVS ABY-1 starter culture was dissolved in 1 L sterilized milk and then 12.0 ml of this inoculum was inoculated into 3 L of reconstituted heat-treated (95 C for 15 min) milk that had been cooled down to the fermentation temperature (37 C). The incubation was then carried out up to ph 4.50 ± 0.02. At the end of the fermentation stage, samples were cooled down and stored at different refrigeration temperatures (2, 5 or 8 C) for 20 days and their viable probiotic cell populations were enumerated throughout the refrigerated storage period, at 5-day intervals. Statistical analysis Experiments were performed in triplicate and ranked orders of the means were analysed using Duncan s test (on the basis of complete randomized design) from mstat software (Pussell D. Freed, Crop and Soil Science Department, Michigan State University, Version 2.10). RESULTS AND DISCUSSION The effect of refrigerated storage temperature on the viability of L. acidophilus Table 1 shows the variation in the microbial cell count during the refrigerated storage period at 5- day intervals. After 5 days, storage at 2 C resulted in significantly higher viability of L. acidophilus compared to the conditions of 5 and 8 C. This can be explained by the fact of one-way antagonistic effects of L. delbruecki ssp. bulgaricus against L. acidophilus (and also other probiotic bacteria), especially at higher temperatures (Shah et al. 1994; Dave and Shah 1997; Mortazavian and Sohrabvandi 2006a; Mortazavian et al. 2006b). At higher temperatures (5 and 8 C compared to 2 C) the L. delbruecki ssp. bulgaricus bacteria grow faster, therefore the amounts of produced lactic acid and hydrogen peroxide are increased. According to Dave and Shah (1996), hydrogen peroxide produced by L. delbruecki ssp. bulgaricus bacteria is the most important viability-reducing factor during refrigerated storage, which is in agreement with our results. Besides, in general, the increase in storage temperature resulted in the increase in metabolic activities of bacterial cells, thereby causing an increase in their death rate. As shown in Table 1, storing yogurt at 8 C for 10 days resulted in the lowest viability of L. acidophilus compared to that stored at 2 or 5 C. Table 1 Variation trend in the viable cell counts of probiotics (Lactobacillus acidophilus and Bifidobacterium lactis) during 20 days of refrigerated storage period, at 5-day intervals (log CFU/mL)* 0** 5 10 15 20 L. acidophilus 2 7.41 7.28 a 7.04 a 6.60 a 6.47 a 5 7.41 7.14 b 7.03 a 6.27 b 5.44 c 8 7.41 7.13 b 6.77 b 6.23 b 5.77 b B. lactis 2 7.53 7.41 a 6.87 b 6.38 b 5.80 b 5 7.53 7.42 a 6.97 b 6.15 c 5.65 b 8 7.53 7.44 a 7.17 a 6.62 a 6.15 a * The means shown with different letters are significantly different (P < 0.05). ** 0 days = immediately after fermentation. 124 2007 Society of Dairy Technology

Table 2 Viability loss of Lactobacillus acidophilus and Bifidobacterium lactis during 20 days of refrigerated storage period, at 5-day intervals (compared to the reference point of initial viable cell counts after fermentation) 5 10 15 20 L. acidophilus 2 25.0% 57.7% 84.6% 88.5% 5 46.2% 57.7% 92.7% 98.9% 8 48.1% 88.4% 92.7% 97.7% B. lactis 2 24.6% 78.3% 92.7% 98.1% 5 23.2% 72.5% 95.6% 98.7% 8 18.9% 56.5% 86.9% 95.6% Table 2 shows the variation trend of viability loss percentage and its stepwise increase for L. acidophilus and B. lactis, respectively. As shown in the Table, the maximum of viability loss percentage for 5 and 8 C is observed after 5 days of refrigerated storage; but for 2 C, it is observed after 10 days of storage. At 5 and 8 C, higher activity of L. delbruecki ssp. bulgaricus bacteria leads to considerable loss of L. acidophilus viability after 5 days of storage. Then, along with gradual loss of L. delbruecki ssp. bulgaricus activity and possibly relative rise in adaptation of L. acidophilus to detrimental environmental conditions, viability loss percentage is not increased as much as before. By storing yogurt at 2 C, all the mentioned phenomena occur at a slower rate and as a result, the maximum of viability loss percentage appears at a latter storage time (> 10 days). After 15 days of refrigerated storage, yogurt had the highest viability of L. acidophilus was recognized at 2 C compared to the two other temperatures (Table 1). The reason for such phenomenon is similar to what was mentioned for the first 5 days of storage. According to Table 2 except for the temperature of 8 C, a minimum increase in the viability loss percentage is observed after 20 days of refrigerated storage. This phenomenon can be attributed to the reduction in the activity of L. delbruecki ssp. bulgaricus bacteria and rising the adaptation of L. acidophilus to the harsh conditions of the product. After 20 days of refrigerated storage, the highest, intermediate and the lowest viabilities were obtained at 2, 8 and 5 C, respectively (Table 1). We could not think of any reason to explain why storage at 8 C led to a higher viability compared to that of 5 C. Therefore, among these three temperatures, 2 C can be selected as the best temperature to maintain the viability of L. acidophilus for a refrigerated storage of around 20 days. Effect of refrigerated storage temperature on the viability of B. lactis Table 1 shows the variation trend in the microbial cell counts of B. lactis during the refrigerated storage period at 5-day intervals. There is no significant difference between the refrigeration temperatures of 2, 5 and 8 C after 5 days of refrigerated storage. This may be because of the relatively high tolerance of the strain of B. lactis used in this starter culture against the stress factors such as molecular oxygen, acidity, hydrogen peroxide and antagonistic effects of L. delbruecki ssp. bulgaricus bacteria in comparison with other species/strains of bifidobacteria. Therefore, the adverse effects of environmental conditions on the B. lactis strain used must not have been severe enough to significantly affect the viability of the cells at different refrigeration temperatures. Table 3 shows the percentage viability loss of B. lactis and its stepwise increase, respectively. According to the Table, maximum increase in Table 3 Stepwise increase in viability loss of Lactobacillus acidophilus and Bifidobacterium lactis during 20 days of refrigerated storage period, at 5-day intervals 5 10 15 20 L. acidophilus 2 25.0% 32.7% 27.3% 3.5% 5 46.2% 11.5% 35.0% 6.2% 8 48.1% 40.4% 3.8% 5.4% B. lactis 2 24.6% 53.6% 14.5% 5.4% 5 23.2% 49.3% 23.2% 3.1% 8 18.9% 37.7% 30.4% 8.7% 2007 Society of Dairy Technology 125

viability loss percentage for all the refrigeration temperatures is observed after 10 days of refrigerated storage. This phenomenon can be associated with the sharp viability loss of B. lactis after 5 days of storage due to the decrease of its tolerance of the factors mentioned earlier. Table 1 shows that for B. lactis, storage at 8 C resulted in the highest viability compared with that of storage at 2 and 5 C over the 20-day storage. The reason that storage at 8 C in comparison with 5 C results in the higher viability can possibly be due to the early synergistic relationships between B. lactis, L. acidophilus and L. delbruecki ssp. bulgaricus that are enhanced at higher storage temperatures as previously reported by Gomes et al. (1998), Ishibashi and Shimamura (1993), and Klaver et al. (1993). temperatures of 2 and 5 C did not show significant differences in the viability of both probiotics. According to Table 3, at 10 days of refrigerated storage, the highest increase in viability loss is observed at the refrigeration temperature of 2 C, whereas after 15 days of storage, the highest increase occurs at a storage temperature of 8 C. We could not think of any feasible reason for this observation. The minimum increase in viability loss for all the refrigeration temperatures was observed after 20 days of refrigerated storage. This is possibly related to the adaptation of those B. lactis cells that survived the adverse environmental conditions; and also to the decrease in the antagonistic effect of L. delbruecki ssp. bulgaricus bacteria due to the reduction of their activity. In conclusion, of the storage temperatures of 2, 5 and 8 C used, obtaining the highest viability of B. lactis for a storage period of around 20 days requires a storage temperature of 8 C. CONCLUSIONS The main purpose of the present study was to observe the effect of different refrigerated storage temperatures on the viability change of L. acidophilus and B. lactis in ABY probiotic yogurt during 20 days of refrigerated storage, in order to identify the best refrigeration temperatures. The results demonstrated that a refrigeration temperature of 2 C led to the highest viability of L. acidophilus throughout the 20 days of refrigerated storage, whereas the highest viability for B. lactis throughout the 20 days of storage time occurred when yogurt was kept at 8 C. In order to select the best refrigeration temperature(s) for both of the probiotics, economic aspects of storage, the number of initial viable cells of both probiotics after fermentation (before refrigerated storage), and the viability loss patterns of probiotics according to Tables 2 and 3 needed to be considered. As viability losses for L. acidophilus and B. lactis are different from each other and can also vary during different days of storage (5, 10, 15 and 20 days), the best refrigeration temperature from both the viability and economic points of view can be identified by considering expected viable cell counts of each probiotic micro-organism and the average time needed for refrigerated storage of yogurt prior to sale and consumption. Furthermore, the sensory acceptability of yogurts stored at different refrigeration temperatures also needs to be studied. ACKNOWLEDGEMENTS This study was made possible by the collaborative support of Pak Dairy Co. (Tehran, Iran) and University of Tehran. Authors gratefully acknowledge Mr Venling-hilsen (technical sales manager, Chr-Hansen A/S- International Operations Dairy, Denmark) and Ms. Anne Soendergaard (development scientist, Chr-Hansen A/S, Denmark) for their useful and sincere guides and recommendations. REFERENCES Bolin Z, Libudzisz Z and Moneta J (1998) Viability of L. acidophilus in fermented milk products during refrigerated storage. Polish Journal of Food and Nutrition Science 7 465 472. Centeno-de-Laro R (1987) Effect of frozen and subsequent refrigerated storage on beta-galactosidase activity, viability and bile resistance of L. acidophilus. Dissertation Abstracts International B 48 1 13: Order No. DA8709692. Dave R I and Shah N P (1996) Viability of yoghurt and probiotic bacteria on yoghurts made from commercial starter cultures. International Dairy Journal 7 31 41. Dave R I and Shah N P (1997) Viability of yoghurt and probiotic bacteria in yoghurts made from commercial starter cultures. International Dairy Journal 7 31 34. Fuller R (1989) in man and animals. Journal of Applied Bacteriology 66 365 378. Gismondo M R, Drago L and Lombardi A (1999) Review of probiotics available to modify gastrointestinal flora. International Journal of Antimicrobial Agent 12 287 292. Gomes A M P, Malcata F X and Klaver F A M (1998) Growth enhancement of Bifidobacterium lactis Bo and L. acidophilus Ki by milk hydrolyzates. Journal of Dairy Science 81 1817 2825. Han-Seung J L, Pestka J J and Ustunol Z (2000) Viability of Bifidobacterium lactis in commercial dairy products during refrigerated storage. Journal of Food Protection 63 327 331. Hoier E (1992) Use of probiotic starter cultures in dairy products. Food Australia 44 418 420. Holzaspfel W H and Schillinger U (2001) Introduction to pre- and probiotics. Food Research International 35 109 116. Ishibashi N and Shimamura S (1993) Bifidobacterium lactis: research and development in Japan. Food Technology 47 129 134. Klaver F A M, Kingma F and Weerkamp A H (1993) Growth and survival of Bifidobacterium lactis in milk. Netherlands Milk Dairy Journal 47 151 164. 126 2007 Society of Dairy Technology

Mortazavian A M and Sohrabvandi (2006a) and Food Probiotic Products (Based on Dairy Probiotic Products). Iran: Eta Publication. Mortazavian A M, Ehsani M R, Mousavi S M, Reinheimer J A, Emamdjomeh Z, Sohrabvandi S and Rezaei K (2006b) Preliminary investigation of the combined effect of heat-treatment incubation temperature on the viability if the probiotic microorganisms in freshly made yoghurt. International Journal of Dairy Technology 59 8 11. Mortazavian A M, Sohrabvandi S and Reinheimer J A (2006c) MRS-bile agar: its suitability for the enumeration of mixed probiotic cultures in cultured dairy products. Milchwissenschaft. Accepted for publication. Nighswonger B D, Brashears M M and Gilliland S E (1996) Viability of L. acidophilus and L. casei in fermented milk products during refrigerated storage. Journal of Dairy Science 79 212 219. Saarela M, Mogensen G, Fonden R, Matto J and Mattila- Sandholm T (2000) Probiotic bacteria: safety, functional and technological properties. Journal of Biotechnology 84 197 215. Sanders M E (1999). Food Technology 53 67 75. Schilliger U (1999) Isolation and identification of lactobacilli from novel-type probiotic and mild yoghurts and their stability during refrigerated storage. Food Microbiology 47 79 87. Shah N P (2001) Functional foods from probiotics and prebiotics. Food Technology 55 46 53. Shah N P, Lankaputhra W E V, Britz M L and Kyle W S A (1994) Survival of L. acidophilus and Bifidobacterium bifidum in commercial yoghurt during refrigerated storage. International Dairy Journal 5 515 521. Vinderola G G, Bailo N and Reinheimer J A (2000) Survival of probiotic microflora in Argentinian yoghurt during refrigerated storage. Food Research International 33 97 102. 2007 Society of Dairy Technology 127