• Journal of Microbiology and Biotechnology
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• 제4권2호
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• pp.151-154
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• 1994

Lactobacillus acidophilus KFRI 233, a strain isolated from human, was selected as a candidate for probiotics due to its excellent growth in MRS broth where no special anaerobic condition is required. Both simultaneous and deferred agar diffusion assays exhibited Lb. acidophilus KFRI 233 to possess an antagonistic effect against Clostridium perfringens. Its antagonistic effect was pH dependent Associative culture of KFRI 233 and Cl. perfringens in broth resulted in maximum 94.04% inhibition of Cl. perfringens. $\beta$-Galactosidase activity of KFRI 233 was higher than other tested strains that are sold as commercial probiotics. Survival of KFRI 233 in pasteurized skim milk (4$^{\circ}C$) and Sherbet mix (-15$^{\circ}C$) after 7 days of storage were 71.9 and 105.5%, respectively.

• 한국식품과학회지
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• 제25권6호
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• pp.694-697
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• 1993

Bifidobacterium과 기타 장내 세균을 두유에 배양하여 배양특성을 살펴보았다. 균주들은 다음과 같이 Bifidobacterium longum, Lactobacillus acidophilus, Bacteroides fragilis, Eubacterium limosum, Clostridium perfringens, E. coli.를 사용하였다. 이들중 B. longum만이 높은 활성의 ${\alpha}-galactosidase$를 생산해 두유의 주요 당인 raffinose와 stachyose를 이용하였고 가장 높은 산 생성을 보여주었다. 16시간 배양후에 B. longum은 $1.5{\times}10^{8}\;CFU$에 이르렀다. 또한 B. longum은 ${\alpha}-galactosidase$이외에 ${\alpha}-galactosidase$와 ${\beta}-galactosidase$의 활성도 다른 균주에 비하여 가장 높았다.

• Journal of Microbiology and Biotechnology
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• 제5권3호
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• pp.149-153
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• 1995

A simple and low-cost medium was developed for the growth of Bifidobacterium longum KFRI 977. Of three bifidobacterial strains, B. longum KFRI 977 (ATCC 15707) showed the best growth in MRSC broth containing 0.3% oxgall, grew well in partially anaerobic condition, exhibited highest $\beta$-galactosidase activity, and was inhibitory against Clostridium perfringens KFRI 434. Of three developed media, the population of B. longum KFRI 977 was highest (1.9$\times$$10^9$/ml) in ISP based medium. The composition of ISP based medium is ISP (5%), glucose (1%), L-cysteine HCI (0.05%), Trypticase peptone (0.5%), yeast extract (0.5%), $MgSO_4$ (0.05%), Tween-80 (0.1%), and phosphate buffer (pH 7.0). Hydrolysis of ISP by Protease A was unnecessary, and the use of phosphate buffer (pH 7.0) prevented the formation of protein precipitate. Associative culture of B. longum KFRI 977 with Lactobacillus acidophilus KFRI 233 was proven to be deleterous to the growth of B. longum KFRI 977.