2014
DOI: 10.1016/j.lwt.2013.11.003
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Effect of palmitoylated alginate microencapsulation on viability of Bifidobacterium longum during freeze-drying

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Cited by 62 publications
(35 citation statements)
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“…Bacteria were kept at −80 • C in glycerol stock solutions. The bacterial suspensions were thawed, and the bacteria were reactivated in De Man-Rogosa-Sharpe (MRS) broth with 0.05% L-cysteine hydrochloride for 24 h at 37 • C and subcultured in Bifidus selective medium (BSM) broth for 24 h at 37 • C. All cultures were incubated under anaerobic conditions using an anaerobic GasPak ® jar containing a generator envelope (Oxoid Ltd., Basingtoke, UK) [12]. In addition, 100 µL of Oxyrase (Oxyrase Inc., Mansfield, OH, USA) were added to the broth to remove oxygen from the microenvironment [13].…”
Section: Strains and Culture Conditionsmentioning
confidence: 99%
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“…Bacteria were kept at −80 • C in glycerol stock solutions. The bacterial suspensions were thawed, and the bacteria were reactivated in De Man-Rogosa-Sharpe (MRS) broth with 0.05% L-cysteine hydrochloride for 24 h at 37 • C and subcultured in Bifidus selective medium (BSM) broth for 24 h at 37 • C. All cultures were incubated under anaerobic conditions using an anaerobic GasPak ® jar containing a generator envelope (Oxoid Ltd., Basingtoke, UK) [12]. In addition, 100 µL of Oxyrase (Oxyrase Inc., Mansfield, OH, USA) were added to the broth to remove oxygen from the microenvironment [13].…”
Section: Strains and Culture Conditionsmentioning
confidence: 99%
“…In addition, 100 µL of Oxyrase (Oxyrase Inc., Mansfield, OH, USA) were added to the broth to remove oxygen from the microenvironment [13]. Bacterial biomass was harvested via centrifugation at 2000 g for 10 min at 4 • C, washed twice in a sterile saline solution (NaCl 0.85% w/v) under the same centrifugation conditions, and resuspended in 1 mL of a sterile saline solution [12,13]. These suspensions were incorporated in MWAX solutions and homogenized, and the gel was then prepared as previously reported [11].…”
Section: Strains and Culture Conditionsmentioning
confidence: 99%
“…The nature of this technique is packaging cells in small capsules by using some coating materials which provide the living cells with physical barrier (Chavarri et al, 2010). Studies have reported that the application of encapsulation resulted in improved viability and stability as well as functionality of B. longum cultures during freeze-drying and storage as well as gastro-intestinal conditions (Amine et al, 2014; Chavarri et al, 2010). Alginate is among the most commonly used coating materials for encapsulating probiotic microorganisms due to its non-toxic nature (Amine et al, 2014; Chavarri et al, 2010); however, it still shows limitations such as not always improving the probiotic microorganism’s survival (Chandramouli et al, 2004).…”
Section: Introductionmentioning
confidence: 99%
“…Studies have reported that the application of encapsulation resulted in improved viability and stability as well as functionality of B. longum cultures during freeze-drying and storage as well as gastro-intestinal conditions (Amine et al, 2014; Chavarri et al, 2010). Alginate is among the most commonly used coating materials for encapsulating probiotic microorganisms due to its non-toxic nature (Amine et al, 2014; Chavarri et al, 2010); however, it still shows limitations such as not always improving the probiotic microorganism’s survival (Chandramouli et al, 2004). In order to overcome the problem with alginate encapsulation, researchers have recently used fatty acids, glycerol or chitosan as the cryoprotectants to improve the survival of probiotic bacteria by reducing acid diffusion (Amine et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
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