• 한국미생물·생명공학회지
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• 제26권3호
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• pp.269-274
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• 1998

Triphenylmethane계 염료 탈색균인 E. cloacae MG 82를 이용한 crystal violet의 탈색 특성을 조사하였다. 배지내의 용존산소의 양이 많을수록 crystal violet의 탈색과 E. cloacae MG82의 균생장이 좋았다. 균생장 중기의 세포 군에서 crystal violet의 탈색능이 가장 활발하였고 염료의 농도가 높아짐에 따라 균생장과 탈색능이 억제되었으며, 균생장이 가능한 crystal violet의 최고 농도치는 375 $\mu$M이었다. E. cloacae MG82는 crystal violet을 유일한 탄소원으로 이용할 수 없었고, 균생장 및 염료의 탈색에 또 다른 에너지원을 필요로 하였다.

• 한국식품위생안전성학회지
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• 제16권2호
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• pp.89-95
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• 2001

한약재 중에서 항균성 물질을 찾고자하는 연구의 일환으로 실험균의 생육에 대한 항생제와 보존료의 영향을 조사하였고, 각종 한약재 물추출물의 항균성을 조사하였다. 오미자 물추출물은 모든 실험균에 대하여 공통적으로 생장 저해를 나타내었다. 오미자 추출물의 농도별 항세균능을 살펴본 결과, 0.2%이상 첨가할 경우 시간의 경과에 따른 Escherichia coli W3110과 Enterobactey cloacae MG82 및 Salmonella typhimurium의 증식을 크게 억제할 수 있었다. 오미자 추출물을 첨가하지 않은 대조구에 있어서 Escherichia coli W3110의 평균 비증식 생장속도는 0.514 (hr￣)이었고, Enterobacter cloacae MG82는 0.381(hr￣)이었고, Salmonella typhimurium은 0.489(hr￣)이었다. 오미자 추출물을 0.2% 첨가할 경우 Escherichia coli W3110과 Enterobacter cloacae MG82 및 Salmonella typhimurium의 평균 비증식 생장속도는 대조구에 비해 각각 1.26배, 2.23배, 1.50배 감소하였으며, 최소 저해 농도는 0.25%로 강한 항균활성을 보였다. 오미자 추출물은 Enterobacter cloacae MG82에 대해 가장 큰 증식 저해효과를 나타내었다.

• 한국미생물·생명공학회지
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• 제25권1호
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• pp.37-43
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• 1997

Triphenylmethane was decolorized rapidly by enterbacter cloacae MG 82 at initial reaction time. The spheroplast showed higher activity of triphenylmentane decolorization than that of intact cell suspension. The outer part of the bacterial cell envelope and the peptidoglycan are important for the function of transport barrier of triphenylmethane. In intact cell, decolorization activity was higher at 37$\circ $C than at $\circ $C, indicating that triphenylmethane decolorization is due to the enzyme reaction. Culture filtrate showed no decolorization activity, while cell-free extract appeared high activity of 1.45 units, clearly showing that decolorization activity was due to the cell-free extract. Comparing decolorization activities of cell fractions, it was found that decolorization activity was located at the compartment of cytoplasmic membrane. The enzyme activity was also shown to be Mg$^{++}$-dependent. The optimum pH and temperature of enzyme activity were 7.0 and 50$\circ $C, respectively. The thermostability of this enzyme at 35$\circ $C was kept to 58% for 3 hours.

• 약학회지
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• 제38권2호
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• pp.140-148
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• 1994

${\beta}-Lactamase$ stability, chemotherapeutic activity, and pharmacokinetics of 7-[(Z)-2-(2-aminothiazole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyridyl)piperazinyl]thiocarbonylthiomethyl-3-cephem-4-carboxylic acid(CEN1), 7-[(Z)-2-(2-aminothiazole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyrimidyl)piperazinyl]thiocarbonylthiomethyl-3-cephem-4-carboxylic acid(CEN2), pivaloyloxymethyl-7-[(Z)-2-(2-aminothizaole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyridyl)piperazinyl]thiocarbonyl-thiomethyl-3-cephem-4-carboxylate(CEN1P), and pivaloyloxymethyl-7-{(Z)--2-(2-aminothizaole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyridyl)piperazinyl]thiocarbonyl-thiomethyl-3-cephem-4-carboxylate(CEN2P) were examined. CEN1, CEN2, CEN1P, and CEN2P were very stable to the ${\beta}-lactamase$ obtained from three strains(Enterobacter cloacae P99, Escherichia coli TEM, and Citrobacter freundii). Chemotherapeutic activities$(ED_{50})$ of CEN2 and CEN2P against experimental systemic infections due to Streptococcus pyogenes 77A and Escherichia coli 078 were superior to those of CEN1 and CEN1P, respectively. The $ED_{50}$ values of CEN1, CEN2 were 5.82 mg/kg, 0.89 mg/kg(s.c., S. pyogenes 77A) while those of CEN1P, CEN2P were 14.56mg/kg, 6.40mg/kg(p.o., S. pyogenes 77A), respectively. The pharmacokinetics of CEN1, CEN2, CEN1P, and CEN2P were investigated in mice and rats. In mice, peak blood levels of $1.25\;{\mu}g/ml$ were recorded within 20 min after oral administration of a single dose equivalent to 40 mg/kg CEN1P. Cmax of CEN1P was much higher than that of CEN1 in mice and rats. Oral absorption of CEN2P was much higher than that of CEN2.