• 대한미생물학회지
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• 제22권1호
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• pp.23-33
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• 1987

To detect lepotospiral strains which produce hemolysin and determine the optimal condition for assaying hemolysin, we screened reference strains and observed some property of hemolysin. Hemolysin activity was assayed with cell free culture liquids and erythrocyte suspension. The production of hemolysin by local strains isolated in Korea was assayed and compared with that of reference strains. The hemolysin was produced by 18 strains among 38 reference strains and 3 local strains isolated in Korea. The production of hemolysin began with growth of Leptospira cultured in EMJH medium and reached maximum at stationary phase. The optimum temperature for hemolytic activity was $37^{\circ}C$. At lower temperature the activity of hemolysin was decreased progressively. The hemolytic activity was completely inactivated after :30 minutes' exposure at $56^{\circ}C$. Hemolysis pattern was "hot-cold type" which showed increased hemolysis after cold incubation. The hemolysin was most active on sheep erythrocyte and less active on ox, goat, human and guinea pig erythrocyte with the decreasing order.

• 한국환경과학회지
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• 제6권3호
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• pp.225-229
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• 1997

호염기성 V. vulnificus는 연안에 존재하는 미생물로서 치명적인 상처 감염과 생명을 위협하는 패혈증과 관련이 있다. Hemolysin은 V. vulnificus를 포함하는 여러 가지 세균종에 의해 생성되는 독성 물질이다. 본 연구에서는 해양 V. vulnificus에서 hemolysin을 정제한 후 hemolysin의 활성에 미치는 pH, 온도 및 금속 이온의 영향을 조사하였다. Hemolysin은 sheep red blood cell을 용혈시켰으며 hemolysin의 최적 pH는 8.0, 최적 온도는 4$0^{\circ}C$이었으며 $K^+$ 이온은 homolysin의 활성을 증가시켰으나 $Mn^{2+}$는 감소시켰다. 그러나 hemolysin은 열에 불안정하였다.

• 한국수산과학회지
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• 제30권4호
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• pp.556-561
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• 1997

해수로부터 분리한 V. cholerae non-O1 FM-3 이 생산하는 hemolysin의 특성에 관하여 연구한 결과를 요약하면 다음과 같다. 1. V. cholerae non-O1 FM-3이 생산하는 hemolysin은 대수증식기일 때 가장 높은 활성을 나타내었으며, Sephadex G-100 gel column chromatography로 부분정제한 후 hemolysin의 특성을 실험한 결과, pH 7.0, $4^{\circ}C$에서 가장 안정하였으며, $60^{\circ}C$, 30분 가열에 의해 완전히 실활되었다. 2. 적혈구와 hemolysin이 반응할 때, $Na^+,\;K^+$과 같은 1가 양이온을 첨가하면 약간의 활성증가를 보였으며, $Ca^{2+},\;Mg^{2+},\;Mn^{2+}$과 같은 2가 양이온을 첨가하였을 때 급격한 활성증가를 보였고, 반면 $Zn^{2+}$ 첨가시에는 급격히 활성이 저하되었다. 3. 적혈구 현탁액과 hemolysin을 각각 다른 온도대에서 반응시킨 결과, $4^{\circ}C$에서도 온도와 관계없이 적혈구막과 hemolysin의 결합이 가능한 온도 비의존적인 제1단계와, 용혈황성의 최적온도대인 $37^{\circ}C$에서만 용혈작용이 일어나는 온도 의존적인 제2단계로 나누어졌다.

• 한국미생물·생명공학회지
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• 제19권3호
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• pp.303-307
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• 1991

B.thuringiensis subsp. darmstadiensis 73E10-2의 내독소에 존재하는 hemolysin이 Sephadex G-100 gel filtration과 DEAE-cellulose ion exchange column chromatography에 의해 정제되었으며, 그 순도는 SDS-PAGE와 Ouchterlony test로 확인하였다. 그 결과 정제된 hemolysin의 분자량은 64KDa 의 단백질 이었으며, in vivo 상태에서는 전혀 모기유충에 독작용을 나타내지 않았다는 점이 28KDa 단백질의 차이가 있었다. 또한 정제된 hemolysin과 B.thuringiensis subsp. israelensis의 내독소를 효소항체법으로 검토해 본 결과 양단백질 사이에는 면역학적으로 전혀 상관이 없었다.

• 생명과학회지
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• 제8권2호
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• pp.145-157
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• 1998

We isolated 100 Vobrio sp. from marine products and sea from July to September, 1997. We attemped on purification of hemolysin produced by Vibrio sp. The growth, hemolysin production patterns by the 100 strains of Vibrio sp. showed identical, in general. V. unlnificus ys-1 produced hemolysis as the higtest titer. The optimal culture conditions for the hemolysin production by the V. vunificus ys-1 are followings; 1. Hemolysin production was optimal dering the late exponetial phage. 2. Maximal growth, hemolysin production were in heart infusion broth. 3. Maximal yields of hemolysin was obtained when the heart infusion broth had an intial pH of 8.0, 3$0^{\circ}C$, 3% NaCL. Hemolysin was purified from culture filtrate of the strain by ammonium sulfate recipitation, ion exchange and hydrophobic interaction chromatography. The results were as follows; 1. Hemogeneity of the purified hemolysin was demonstrated by revealing single band on SDS-PAGE. The molecular weight of purified hemolysin was 45KDa. 2. The absorbance rattern in ultraviolet wsa typical of those seen with most proteinb with 280nm. 3. Purified hemolysin was atable at 5$0^{\circ}C$ but 7$0^{\circ}C$ of the acivity was lost by heating for 30 min at 6$0^{\circ}C$/ Optimal temperature of purified hemolysin was 35$^{\circ}C$. 4. Purified hemolysin was stable at the pH range of 6~9, but in the less the pH5.0. above the pH 9.0, the hemolysin activity was lost completely.

• 생명과학회지
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• 제12권4호
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• pp.490-495
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• 2002

병원성 미생물인 Vibrio fluvialis로부터 hemolysin을 분리정제 하였다. 즉, hemolysin의 정제는 균 배양액을 황산암모늄, ion exchange chromatography를 행하였으며 SDS-PAGE를 통해 그 단백질의 크기가 약 79kDa임을 알게되었다. 정제된 hemolysin (VFH)는 35$^{\circ}C$에서 최적활성을 나타내었고, 4$0^{\circ}C$에서는 그 활성이 감소되었다. RTG-2 어류유래 세포주에 hemolysin (VFH)의 처리로 세포독성을 측정한 결과 50$\mu\textrm{g}$의 VFH가 약 80%의 cell line을 사멸시켰다. 또한 현미경을 통한 관찰에서도 세포의 형태변화를 관찰할 수 있었다.

• 한국미생물·생명공학회지
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• 제15권6호
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• pp.425-429
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• 1987

B. thuringiensis subsp. israelensis 균주가 생성하는 $\delta$-endotoxin의 alkali 용해에서 생성되는 hemolysin fragment 와 extra-cellular hemolysin 의 상관관계를 조사하기 위한 기초자료로서 extra-cellular hemolysin을 분리 정제하여 그 성질을 조사하였다. 균체 배양액에 유안을 염석 및 투석시킨 후, Sephadex G-200 gel filtration 과 DEAE-cellulose column chromatography를 행하여 균체외 homely-sin을 정제하였다. 정제된 extra-cellular hemolysin 은 SDS-polyacrylamide gel 전기영동에서 47,000 dalton의 분자량을 가진 단일 단백질 band를 얻었다. 또한 정제된 hemolysin은 thiol agents에 의해 그 활성이 증가되었으나, cholesterol 및 protease 처리 또는 금속이온 즉, FeSO$_4$나 CuSO$_4$에 의해 그 활성 이 감소되었다.

• 한국수산과학회지
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• 제41권4호
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• pp.243-247
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• 2008

The hemolysin of Vibrio cholerae non-O1 CT isolated from sea water was purified and characterized. The purified hemolysin displayed an optimum at $37^{\circ}C$ and exhibited more than 70% of residual hemolytic activity after incubation at $45^{\circ}C$ for 120 min. However, the activity dropped dramatically at temperature above $55^{\circ}C$. The purified protein showed the highest hemolytic activity at pH 7.0, while the activity was completely lost outside of the pH ranges of 5.0 and 10.0. The activity of hemolysin was inactivated by addition of divalent cations, such as $Cu^{2+},\;Fe^{2+},\;Hg^{2+},\;Mn^{2+},\;and\;Zn^{2+}$, however, the activity was not completely inhibited by additions of $Ca^{2+},\;Mg^{2+},\;K^+,\;Na^+,\;and\;Li^+$.

• Journal of Microbiology and Biotechnology
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• 제13권6호
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• pp.1021-1026
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• 2003

Numerous secreted and cell-associated virulence factors have been proposed to account for the fulminating and destructive nature of Vibrio vulnificus infections. Among the putative virulence factors are an elastase, elastolytic protease, and a cytolytic hemolysin. Effects of the elastase on the hemolysin were assessed by evaluating changes of hemolytic activities either in the presence or absence of the protease. Although hemolytic activity in the culture supernatant was lowered by the purified elastase added in vitro, the cellular level of hemolytic activity was unaffected by the mutation of vvpE encoding the elastase. Growth kinetic studies revealed that hemolysin reached its maximum level in the exponential phase of growth, and the elastase appeared at the onset of the stationary phase. These results have provided insight into the regulation of virulence factors: temporally coordinate regulation of virulence factors is essential for the overall success of the pathogen during pathogenesis.

• Journal of Microbiology and Biotechnology
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• 제14권2호
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• pp.330-336
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• 2004

Fifty-two pathogenic Vibrio parahaemolyticus strains were isolated from the environments of Busan and Yeosu, Korea. Forty-three of these strains showed protease activities, whereas 4 strains showed $\alpha / \beta$ hemolysin activities and 6 strains had urease activities. Their pathogenic factors were not overlapping except one strain, which had both protease and hemolysin activities. The 6 urease-positive strains (V. parahaemolyticus YKB4, YKB14, S25, YFB20, YFO21, and YFO22) showed the same biochemical characteristics as a reference strain [V. parahaemolyticus KCTC 2471 (urease-negative)], except for urease production. The 6 urease-positive strains showed different urease activities in their culture supernatant during the growth. The urease activity of S25 increased sharply at the late exponential phase, and was the highest at the initial stationary phase and was kept until the late stationary phase. The other 5 isolates, except C25, showed urease activities at the mid-stationary phase and increased steadily until the late stationary phase, when the urease activity was maximal. To compare the degree of virulence of V. parahaemolyticus with different pathogenic factors, hemolysin, protease, or urease-positive strains were injected into groups of 10 each of ICR mice (7- to l0-week-old males). The lethal rates of urease-positive V. parahaemolyticus, YKB14, YKB4, and S25, were significantly high, being 50, 70, and 80%, respectively. Protease-positive V. parahaemolyticus strains FM39 and FM50 showed 40% and 60% of lethal rate, respectively. Hemolysin-positive V. parahaemolyticus strains S34 and S72 had no mortality, similar to nonpathogenic V. parahaemolyticus FM12.