• Title/Summary/Keyword: /beta-galactosidase

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Comparison of Cultured Soymilk by Bifidobacterium and Various Human Intestinal Bacteria (Bifidobacterium과 기타 장내 세균에 의한 두유 배양 비교)

  • Lee, Se-Kyung;Son, Heon-Soo;Ji, Geun-Eog
    • Korean Journal of Food Science and Technology
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    • v.25 no.6
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    • pp.694-697
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    • 1993
  • Soymilk was cultured by various human large intestinal bacteria and lactic acid bacteria; Bifidobacterium longum, Lactobacillus acidophilus, Baeteroides fragilis, Eubacterium limosum, Clostridium perfringens and Escherichia coli. Among them, only B. longum utilized raffinose and stachyose actively which are major oligosaccharides present in soymilk by producing active ${\alpha}-galactosidase$ and produced greatest acid. Number of colony forming unit of B. longum reached $1.5{\times}10^{8}$ after 16 hr culture in soymilk. Also Bifidobacterium longum produced the highest level of ${\alpha}-galactosidase,\;{\beta}-galactosidase\;and\;{\alpha}-galactosidase$, in soymilk during culture.

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Enzymatic Synthesis of 2-Phenoxyethanol Galactoside by Whole Cells of ${\beta}$-Galactosidase-Containing Escherichia coli

  • Lee, Hyang-Yeol;Jung, Kyung-Hwan
    • Journal of Microbiology and Biotechnology
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    • v.24 no.9
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    • pp.1254-1259
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    • 2014
  • We investigated whether ${\beta}$-galactosidase (${\beta}$-gal)-containing Escherichia coli cells could transfer a galactose to 2-phenoxyethanol, resulting in 2-phenoxyethanol galactoside (PE-Gal). PE-Gal was confirmed by liquid chromatography-mass spectrometry. In addition, we also confirmed that a galactose molecule was covalently bonded with PE during thin-layer chromatography analysis of the ${\beta}$-gal hydrolysate of PE-Gal. The yield for PE-Gal synthesis was about 37.5% (weight basis), which was about 7-8 times greater than that of a previous report. In addition, the concentration of ${\beta}$-gal (0.96 U/ml) used in this PE-Gal synthesis was about 20 times less than that in a previous report.

Characteristics of $\beta$-Galactosidase with High Transgalactosylation Activity Produced by Penicillium sp. KFCC 10888. (Penicillium sp. KFCC 10888이 생산하는 갈락토스 전이활성이 우수한 $\beta$-Galactosidase의 특성)

  • 인만진;채희정
    • Microbiology and Biotechnology Letters
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    • v.26 no.1
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    • pp.40-44
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    • 1998
  • A Penicillium strain which produces $eta$-galactosidase with high transgalactosylation activity, was isolated from soil and registered as Penicillium sp, KFCC 10888. When $eta$-galactosidase from Penicillium sp. KFCC 10855 reacted with 40% lactose, transgalactosylation ratio reached up to 70% at the 73% conversion of initial lactose. The biosynthesis of the enzyme in Penicillium sp. KFCC 10888 was not induced by lactose. The soybean meal was an effective component of the culture medium. The optimum pH and temperature for transgalactosylation were 4.0 and 55$^{\circ}C$, respectively. The production of galactooligosaccharides was in proportion to the initial lactose concentration. When the enzyme reacted with 40% lactose (pH 4.0) at 55$^{\circ}C$, the concentration of galactooligosaccharides increased up to 40% of total solid concentration.

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QUANTIFICATION OF β-GALACTOSIDASE TO MEASURE INTESTINAL DAMAGE IN ROTAVIRUS INFECTED CALVES

  • Agrawal, D.K.;Singh, N.P.
    • Asian-Australasian Journal of Animal Sciences
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    • v.6 no.3
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    • pp.373-375
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    • 1993
  • Quantitative ${\beta}$-galactosidase estimation in the intestinal mucosal cells of calves with diarrhea under experimental conditions due to rotavirus were undertaken. A quantitative decrease of 40-70% in ${\beta}$-galactosidase activity was observed in proximal and middle segments of the small intestine of the infected calves, more so in the middle segments. The decrease in the distal part of the intestine, however, was lesser (5 to 30%). The decrease in the activity was more marked on the day 2 to 6 post infection indicating the degree of the damage of the villi of the small intestine.

Effect of ginseng saponins on the induction of $\beta$-galactosidase in yeast

  • Lee, Hee-Bong;Kim, Kyung-Hoon;Han, Byoung-Dong
    • Journal of Ginseng Research
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    • v.22 no.4
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    • pp.310-315
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    • 1998
  • The effect of red ginseng saponins (total saponins, Rbl- and Rgl- fraction of saponins) on the induction of $\beta$-galactosidase in yeast, hccharomyces cereuisiae, was investigated to see that ginseng saponins would penetrate the cell membrane and have a function in a nucleus as steroid hormones do. To attain such a kind of purpose, a DNA fragment (685bp) containing GALI promoter was inserted into the sites of EcoRl and BamHl of polylinker region, upstream of lace gene of the plasmid YEp356 (7.966 Kb), and thus the resulting plasmid pGALl-lacZ is supposed to express $\beta$- galactosidase only in the presence of galactose. The plasmid pGALl -lacZ was introduced into yeast, Ky106 (a leu2 ura3 his3 trp 1 Iys2), and the growth of the transformed cells was much slower in the presence of galactose than glucose. The effects of saponins on the specific activity of P-galactosidase from transformed yeast cells were detected. No significant increase was observed in case of total saponins, but the Rbl- or Rgl- fraction of saponins gave much higher increase in the activity. Maximum increase was observed as 35% in 10-3% of Rbl and as 75% in 10-1% of Rgl. These data suggest that ginseng saponins might be able to enter the nucleus and stimulate transcription. However, further studies to find out the putative saponin receptor are needed to confirm this possibility. Key words : Red ginseng saponin, $\beta$-galactosidase induction, Saccharomyces cerevisiae.

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Mannanolytic Enzyme Activity of Paenibacillus woosongensis (Paenibacillus woosongensis의 만난분해 효소활성)

  • Yoon, Ki-Hong
    • Korean Journal of Microbiology
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    • v.46 no.4
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    • pp.397-400
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    • 2010
  • The activities of mannanase, ${\beta}$-mannosidase, and ${\alpha}$-galactosidase were detected in culture filtrate of Paenibacillus woosongensis showing mannanolytic activity for locust bean gum. Optimal conditions occurred at pH 5.5 and $60^{\circ}C$ for mannanase toward locust bean gum, pH 6.5 and $50^{\circ}C$ for ${\beta}$-mannosidase toward para-nitrophenyl-${\beta}$-D-mannopyranoside, and pH 6.0-6.5 and $50^{\circ}C$ for ${\alpha}$-galactosidase toward para-nitrophenyl-${\alpha}$-D-galactopyranoside in the culture filtrate, respectively. The mannanolytic enzyme of culture filtrate hydrolyzed mannobiose as well as manno-oligosaccharides including mannotriose, mannotetraose, mannopentaose and mannohexaose. It could also hydrolyze ${\alpha}$-1,6 linked galacto-oligosaccharides such as melibiose, raffinose and stachyose to liberate galactose residue. From these results, it is assumed that P. woosongensis produces three enzymes required for the complete decomposition of galactomannan.

Studies on the Production of $\beta$-Galactosidase by Lactobacillus sporogenes - Properties and Application of $\beta$-Glactosidase- (Lactobacillus sporogenes에 의한 $\beta$-Galactosidase 생산에 관한 연구 -$\beta$-Galactosidase의 효소학적 성질 및 응용-)

  • 김영만;이정치;최용진;양한철
    • Microbiology and Biotechnology Letters
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    • v.13 no.4
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    • pp.355-359
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    • 1985
  • The purified $\beta$-galactosidase from L. sporogenes was most active at pH 7.0 and 6$0^{\circ}C$ with O-nitrophenyl-$\beta$-D-galactopyranoside (ONPG) in 0.05 M phosphate buffer. It was stable over a pH range from 5.0 to 9.0 and lost less than 10% of its activity after heating for 30 minutes at 6$0^{\circ}C$ and pH 7.0. All the mineral ions examined in this work showed no significant activating effect, whereas L-cysteine exerted a great stimnlatory effect on the enzyme activity at the concentration of 10 mM. The Km values were 1.2 mM for ONPG and 33.3 mM for lactose. Approximately 85% of lactose in cow's milk, in 10% skim milk and in 5% lactose solution was hydrolyzed after 4 hours incubation at 6$0^{\circ}C$ with 2 units of the purified $\beta$-galactosidase per $m\ell$ of the substrate solutions. The $\beta$-galactosidase from L. sporogenes, therefore, is considered to be suitable for hydrolysis of lactose in milk and other dairy products.

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(${\beta}-Galactosidase$를 이용한 Isofalvone 배당체의 비배당체화 연구)

  • Kim, Nam-Cheol;Jeon, Byeong-Ju;Gwak, Hae-Su
    • Proceedings of the Korean Society for Food Science of Animal Resources Conference
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    • 2004.10a
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    • pp.371-374
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    • 2004
  • 본 연구는 식물성 에스트로겐인 isoflavone 배당체의 ${\beta}-1,4\;glycoside$ 결합을 ${\beta}-galactosidase$로 분해하여 그 생리적 작용이 더욱 효과적인 aglycone화 하기 위한 조건을 연구하여 기능성식품개발에 응용토록 하는데 목적이 있다. 실험 결과, 모든 ${\beta}-galactosidase$${\beta}-1,4\;glycoside$ 결합의 분해력이 인정되지는 않았으며, 분해 가능성이 인정된 효소를 선택하여 실험한 결과 효소의 함량이 증가함에 따라 aglycone의 성분비율이 증대된 반면, 그 손실률 또한 증대되었고 배양시간이 길수록 aglycone의 성분비율이 증가하였으나 배양초기에 급격한 증가율을 보였으며, pH6과 7, 8에서 유사한 정도의 증가율을 보였고, 온도가 증가함에 따라 aglycone 성분비율이 증가되었지만 $40^{\circ}C$이상에서는 그 손실률이 크게 증가하였다. 결과적으로 판단해 볼 때, isoflavone을 aglycone화 하는데 있어 인체 내 유사조건에서 aglycone의 증가율이 높았으며 최적의 조건과 많은 차이를 나타내지 않았고 그 손실률 또한 최소화된 결과를 나타내어 isofalvone을 적용한 기능성 유제품을 연구하는데 있어 긍정적인 가능성을 보였다.

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각 미생물의 ${\beta}-galactosidase$와 Phytase의 활성비교

  • Jo, Jin-Guk;Jang, U-Jin;Choe, Jin-Yeong;Heo, Gang-Chil;Lee, Jong-Ik
    • Proceedings of the Korean Society for Food Science of Animal Resources Conference
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    • 2005.05a
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    • pp.375-379
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    • 2005
  • 본 연구는 ${\beta}-galactosidase$와 phytase활성이 높은 균주의 선발을 목적으로 수각 미생물들을 Kefir와 자연환경에서 분리하여 효소활성을 측정하였다. 배양한 유산균과 효모 균체액을 French pressure cell press로 세포를 파쇄하였을 때, 각 미생물의 단백질농도는 효모보다 유산균이 높은 것으로 나타났다. ${\beta}-galcactosidase$의 비활성은 Kluyveromyces maxiranus와 Candida utilis를 제외하고는 대부분 $0.80{\sim}0.89\;umol/min/mg$ 사이였다. 체적활성의 경우는 Lactobacillus paracasei 및 Lactobacillus rahmnosus, Enterococcus faecium이 각각 15.9 및 14.5, 14.5 umol/ml를 기록하여 ${\beta}-galcactosidase$의 추출재료로 우수하였다. phytase의 비활성은 Lactobacillus paracasei 와 Enterococcus faecium이 0.032와 0.038 umol/min/mg로 가장 높았다. 체적활성의 경우는 Lactobacillus paracasei가 35.12 umol/ml로 가장 높았다. 결론적으로 ${\beta}-galactosidase$와 phytase의 생산측면에서 이용한 미생물중에서는 Lactobacillus paracasei가 가장 우수한 것으로 사료되었다.

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Changes in the Enzyme Activities, Pectins and Structure of Persimmon Fruit during Softening (감과실의 연화중 효소활성, 펙틴 및 조직의 변화)

  • 신승렬;문광덕;이광희;김광수
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.22 no.5
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    • pp.611-616
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    • 1993
  • This study was carried out to investigate change in the polygalacturonase and ${\beta}-galactosidase$ activities, pectins, cell wall structure of persimmon fruit during ripening and softening. Polygalacturonase and ${\beta}-galactosidase$ activities were not detected at turning stage. However polygalacturonase activities of mature and soft persimmon fruits were 55.01 and 206.70units/100g-fresh weight(fr. wt.), respectively. ${\beta}-Galactosidase$ activities of mature and soft persimmon fruits were 21.79 and 380.23unit/100g-fr. wt. respectively. The contents of total and insoluble pectins increased during maturation but decreased during softening. The content of water-soluble pectin increased during maturation and softening. The intercellular space was in larged during ripening, and middle lamella was degraded in mature persimmon fruit, and the cells of soft persimmon fruit were separated each other.

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