• 제목/요약/키워드: inhibition spectrum

검색결과 169건 처리시간 0.028초

CPC-222, A New Fluoroquinolone

  • Lee, Younha
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1997년도 춘계학술대회
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    • pp.12-12
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    • 1997
  • CFC-222 is a novel fluoroqinolone antibacterial agent synthesized and under development by the Cheil Jedang Corporation, Korea. CFC-222 exerts the antibacterial activity by inhibition of bacterial DNA gyrase leading to bactericidal action. In in vitro and in vivo preclinical testing, CFC-222 has been shown to possess a broad spectrum of antibacterial activity. In particular CFC-222 is very potent against Gram-positive bacteria such as Staphylococcus spp., Streptocuccus spp. (in particular penicillin G-resistant and -susceptible S. pneumoniae) and Enterococcus spp. when compared to other quinolones (ciprofloxacin, ofloxacin or lomefloxacin). CFC-222 also showed potent activity against the methicillin resistant clinical isolates of S. aureus (MRSA). Against Gram-negative bacteria (E. coli, Pseudomonas and Sarcina) the activity of CFC-222 was slightly weaker than that of ciprofloxacin, but was more potent than that of ofloxacin or lomefloxacin. In urinary systemic infections caused by both Gram-positive and -negative bacteria, CFC-222 demonstrated a potent therapeutic efficacy in particular against Cram-positive bacteria S. aureus, S. pyrogen 203 and S. pneumonia TypeIII.

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Use of Bacteriocinogenic Pediococcus acidilactici in Sausage Fermentation

  • Kim, Wang-June;Hong, Seok-San;Cha, Seong-Kwan;Koo, Young-Jo
    • Journal of Microbiology and Biotechnology
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    • 제3권3호
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    • pp.199-203
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    • 1993
  • The bacteriocin produced by Pediococcus acidilactici KFRI 168 exhibited a wide antimicrobial spectrum including many strains of lactic acid bacteria, Listeria monocytogenes, Staphylococcus aureus, and Enterococcus faecium by both disk and deferred assay methods. Inhibition of Lis. monocytogenes and Stph. aureus were observed only from deferred assay. Gram-negative bacteria were not inhibited. Bacteriocin production was observed at 10 h, and was maximized at 16 h in MRS broth incubated at $37^{\circ}C$. In a beaker sausage fermented with P. acidilactici KFRI 168, viable counts of Stph. aureus, Salmonella, Escherichia coli, Clostridium perfringens, and Lis. monocytogenes were reduced by 2.8, 2.3, 2.4, 0.7, and 0.5 log CFU/g, respectively. Inoculated P. acidilactici KFRI 168 maintained its viable count of more than $10^8$ CFU/g during the whole fermentation period, and it took less than 8 h to reduce sausage pH below 5.

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Preliminary antioxidant, antibacterial and cytotoxic activities of Momordica charantia Linn leaf

  • Rahman, Shafiur;Iqbal, Asif
    • Advances in Traditional Medicine
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    • 제7권4호
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    • pp.385-389
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    • 2007
  • We undertook the present study to evaluate different pharmacological as antioxidant, antibacterial and cytotoxic activities of the crude ethanolic extract of Momordica charantia (Family: Cucurbitaceae) leaves. The antioxidant property of the extract was assessed by 1, 1-diphenyl-2-picryl hydrazyl free radical scavenging assay. The extract showed antioxidant activity where $IC_{50}$ was about ${\sim}500{\mu}g/ml\;and\;IC_{50}$ was about ${\sim}10{\mu}g/ml$ for standard drug ascorbic acid. The extract showed a broad spectrum of antibacterial activity against all the tested gram positive and gram-negative bacteria where Staphylococcus epidermidis, Staphylococcus aureus, Salmonella typhi and Shigella dysenteriae were prominent. And the zones of inhibition were ranging from 8-15 mm for all the tested bacteria. Its cytotoxic property was evaluated by brine shrimp lethality bioassay. The extract showed significant lethality and the $LC_{50}$ value was $20{\mu}g/ml$.

김치 발효에 관여하는 젖산균에서의 Bacteriocin의 검색 (Dectection of the Bacteriocin from Lactic Acid Bacteria Involved in Kimchi Fermentation)

  • 조재선;정성제;김영목;전억한
    • 한국미생물·생명공학회지
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    • 제22권6호
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    • pp.700-706
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    • 1994
  • Lactic acid bacteria in Kimchi fermentation were tested for inhibitory activity against Gram positive bacteria and Gram negative bacteria. The Lactobacillus brevis (KCCM 35464) was found to produce a antimicrobial substance. It showed relatively wide range of inhibition spectrum against gram positive and gram negative bacteria and maintained the inhibitory activity between pH 4.0 and pH 9.0. The antimicrobial substance was obtained in the stationary growth phase and was purified by gel chromatography. The inhibitory effect of the antimicrobial substance on sensitive bacterial strains was determined by filter paper test. The activity of antimicrobial substa- nce was stable at 75$\circ$C. On the basis of its electrophoretic pattern is SDS-PAGE, antimicrobial substance appeared as a single band of 59 KDalton.

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초피추출물의 항균특성 (Antimicrobial Activities of Chopi(Zanthoxylum piperitum DC.) Extract)

  • 정순경;정재두;조성환
    • 한국식품영양과학회지
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    • 제28권2호
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    • pp.371-377
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    • 1999
  • In order to evaluate the antimicrobial function of natural herb extracts as antimicrobial agent or packaging material for the preservation of foods and greenhouse produce, the water extract of chopi (Zanthoxylum piperitum DC.) was prepared and its antimicobial activity was determined. In the paper disk test its antimicrobial activity was increased in proportion to its concentraion. The growth of microorganisms was completely inhibited above 500ppm of its concentration. It showed wide spectrum of thermal(40 to 180oC) and pH(4 to 10) stabilities. In the electronic microscopic observation(TEM and SEM) of microbial morphological change it showed to decrease the activation of physiological enzymes and to lose the function of cell membranes. Even in the activation test of galactosidase, it seemed to weaken the osmotic function of cell membranes remarkably in comparison with chloroform and its activation corresponded to 40~50% of toluene. Zanthoxylum piperitum DC. extract seemed to be an excellent antimicrobial for the inhibition of food borne microorganisms as well as the pre servation of greenhouse produces.

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SYNTHESIS OF HALOGENATED 9-(DIHYDROXYCYCLOPENT -4′-ENYL) ADENINES AND THEIR INHIBITORY ACTIVITIES AGAINST S-ADENOSYLHOMOCYSTEINE HYDROLASE

  • Choi, Won-Jun;Park, Jae-Gyu;Moon, Hyung-Ryong;Gunaga Prashantha;Lee, Kang-Man;Kim, Hea-Ok;Jeong, Lak-Shin
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.365.2-365.2
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    • 2002
  • S-Adenosylhomocysteine hydrolase (SAH) catalyzes the hydrolysis of S-adenosylhomocysteine to adenosine and L -homocysteine and has been an attractive target for the development of broad spectrum antiviral agents. Neplanocin A and 9-(dihydroxycyclopent-4' -enyl)adenine (DHCeA) have been known to inhibit SAH by cofactor (NAD+) depletion mechanism and their inhibition is reversed by the addition of NAD+ or dialysis. (omitted)

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Synthesis of new apicidin derivatives as Histone deacetylase(HDAC) inhibitors

  • H.O. Kang;C.H. Jin;J.W. Han;Lee, H.W.;Lee, Y.W.;Park, H.J.;O.P. Zee;Y.H. Jung
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 2001년도 추계학술대회 및 정기총회
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    • pp.110-110
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    • 2001
  • Histone deacetylase(HDAC), a neuclear enzyme that regulates gene trascription and the assembly of newly synthesized chromatin, has received much attention in recent literature. The explosion of activity in this field has yielded the cloning of a mammalian gene which encodes a complementary histone acetyl trasferases. Several cyclic tetrapeptide inhibitors of HDAC has been reported to affect the hyperacetylation of mammalian and plant histones. Apicidin, a natural product HDAC inhibitor recently isolated at Merck Research Laboratories, induces therapeutic applications as a broad spectrum antiprotozoal agent to multi-drug resistant malaria and a potential antitumor agnet. The biological activity of apicidin appears to be attributable to inhibition of apicocomplexan HDAC at low nanomolar concentrations.

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환경 방사능 처리기술에서의 Compton suppression 및 Unsuppression system을 이용한 토양시료의 MDA 측정 (Measurement of MDA of Soil Samples Using Unsuppression System and Compton Suppression of Environmental Radioactivity in Processing Technology)

  • 강수만;임인철;이재승;장은성;이미현;권경태;김창태
    • 한국방사선학회논문지
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    • 제8권6호
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    • pp.293-299
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    • 2014
  • Compton suppression 장치는 Compton 산란 반응을 이용하여, 스펙트럼의 Compton continuum 부분을 억제함으로써 Compton continuum 영역 내에서의 감마선 피크들의 분석을 보다 명확하게 할 수 있게 해주는 장치이다. 표층토양 시료에서 검출된 인공 방사능인 $^{137}Cs$과 자연 방사능인 $^{40}K$핵종의 방사능 농도 값들에 대한 방사능 계수치가 백그라운드를 상회하는 측정값이 발생되거나, 불필요한 방해피크나 비해석 대상 피크에 대하여 검출된 표준선원의 방사능 농도 값들의 실측치에 대한 background를 비억제 스펙트럼(Compton Unsuppression)과 억제 스펙트럼(Compton suppression)을 적용시켜 측정 에너지에 대한 교정을 알고자 점선원인 $^{137}Cs$을 거리별에 따라 측정하여, 몬테칼로 시뮬레이션과 비교 분석함으로서 효율적인 검출 능력을 얻고자 함이며, Compton 억제 인자를 보면 거리가 멀어짐에 따라 CSF 값이 클수록 더 많은 Compton suppression가 이루어졌음을 알 수 있고, $^{137}Cs$을 이용한 컴프턴 비억제 모드와 억제모드로 측정된 스펙트럼에서 컴프턴 연속에 의한 백그라운드가 감소함을 알 수 있었다.

젓갈유래 박테리오신 Lacticin NK24에 의한 식품부패 및 병원성 세균의 생육저해 (Inhibition of Spoilage and Pathogenic Bacteria by Lacticin NK24, a Bacteriocin Produced by Lactococcus lactis NK24 from Fermented Fish Food)

  • 김혜정;이나경;조상문;김기태;백현동
    • 한국식품과학회지
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    • 제31권4호
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    • pp.1035-1043
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    • 1999
  • 김치, 젓갈 등 전통 발효식품에서 분리한 유용 박테리오신 생산균주 및 이 균주가 생산하는 박테리오신에 의한 식품에서 발생하기 쉬운 주요 부패 및 병원성 세균에 대한 항균효과를 검정하여, 무독성 천연방부제로서의 향후 식품 및 생물산업에서의 활용 가능성을 검토하였다. 젓갈에서 분리한 LAB NK24는 Lactococcus lactis NK24로 잠정적으로 동정되었으며, 이 박테리오신 생산균주는 deferred method에서는 모든 대상균주에 대해서 항균활성을 보였으며, 김치에서 분리한 L. lactis BH5, L. lactis A164 균주에 비해 대체적으로 높은 항균활성을 나타내었다. 젓갈유래 박테리오신인 lacticin NK24는 75%황산암모늄침전법으로 부분정제되었으며, 부분정제된 lacticin NK24는 E. faecalis ATCC 19433 등 그람양성균 10균주, 그람음성균은 E. coli KCCM 32396, P. aeruginosa ATCC 15442 및 S. paucimobilis BNJ 9664 등 3균주에 대하여 항균활성을 보였으며, 효모와 곰팡이에는 활성을 보이지 않았다. 따라서 전통 발효식품인 젓갈에서 분리한 본 박테리오신은 비교적 항균범위가 넓고 식품에서 발생하기 쉬운 주요 부패 및 병원성 세균에 대해 뚜렷한 항균효과를 보이고 있으므로 향후 무독성 천연방부제로서 활용이 가능하리라 판단된다.

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Similar Pattern of Fourier-Transformed Infrared Spectrum of Bond Shift Shown in Human Cervical Cancer Cells and Rat Splenocytes Exposed to Colchicine and Methomyl

  • Sindhuphak, Ratana;Sinhaseni, Palarp;Suramana, Teerayut;Issaravanich, Somchai;Udomprasertkul, Venus;Dusitsin, Nikorn
    • Toxicological Research
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    • 제17권
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    • pp.329-333
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    • 2001
  • Apoptosis is the normal physiological process of cell death essential for the maintenance of homeostasis. The function of nicotinamide adenine dinucleotide (NAD) and adenine diphosphate (ADP) ribosylation (transfer of ADP-ribose to proteins) reactions in modifying apoptosis have recently been of great interest. Recently. CD38. a type 2 transmembrane glycoprotein expressed in hematopoietic and non hematopoietic cell lines. has been reported to possess NAD glycohydrolase activity (Han. 1999) and PC-1 and CD38 NADase regulates T cells by inhibition of phosphodiesterase/pyrophosphatase activity of PC-1 by its association with glycosaminoglycan (Hozada et al., 1999). Sindhuphak et al. (2000) has reported that cervical cancer cells can be differentiated from normal cells by using FTIR (Fourier-Transformed Infrared) technique. which has characterized shifts to be due to the phosphodiester bond in nucleic acid. protein amide I&II. carbohydrate and glycogen bands. Mechanisms how phosphodiester bond shift in cervical cancer cells as compared to control cells remain to be elucidated. Suramana et al. (2000) as well as Lohitnavy and Sinhaseni (1998) have studied methomyl and colchicine effects in rat splenocytes. Lactate Dehydroge-nase Isozymes 3 (LDH3) and LDH4 were observed to increase transiently and subsided in plasma of rats exposed to 6~8 mg/kg methomyl after 48 hours. Phosphodiester bond shift of nucleic acid. detected by FTIR. was also reported (Suramana et al., 2000). We report here, after analysis of bond shift patterns. a similar bond shifts detected by FTIR spectrum observed in human cervical cells and splenocytes of rats exposed orally to 2~8 mg/kg methomyl as well as rats exposed to colchicine 2~6 mg/kg orally.

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