• 제목/요약/키워드: 항진균

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방선균 분리주 No. 1882-5로부터 Phorbol Ester에 의해 유도되는 K562 Cell의 소포형성을 억제하는 물질의 분리와 동정 (Purification and Chemical Identification of the Inhibitor on Bleb Formation of K562 Cell Induced by Phorbol Ester from Actinornycetes Isolate No. 1882-5)

  • 안종석;안순철;박문수;김보연;민태익;이현선;오원근
    • 한국미생물·생명공학회지
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    • 제20권5호
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    • pp.565-573
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    • 1992
  • Phorbol ester에 의해 유도되는 K562 cell의 소포 형성을 저해하는 물질을 생산하는 방선균 분리주 No.1882-5를 토양으로부터 분리하였다. 분리주 No. 1882-5로부터 용매추출, Amberlite XAD-4, silica, Lobar low pressure LC를 거쳐 항진균 활성물질 MT-1882-I과 K562 cell의 소포형성을 억제하는 활성물질 MT 1882-II를 분리하였다. 이 물질들에 대한 이화학적 성질의 조사와 UV, $^1H-NMR$, $^13C-NMR$, mass spectrum의 분석에 의하여 MT 1882-II은 piericidin $A_{1}$($C_{25}H_{37}0_4N$, MW 415), MT 1882-II는 glucopiericidin A($C_{31}H_{47}0_9N$, MW 577)로 동정하였다.

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북극유래 박테리아, Pseudomonas aeruginosa로 부터 대사산물들의 분리 및 항진균 활성 (Isolation of secondary metabolites from an Arctic bacterium, Pseudomonas aeruginosa and their antimicrobial activities)

  • 윤의중;김민주;한세종;임정한
    • 미생물학회지
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    • 제52권4호
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    • pp.415-420
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    • 2016
  • 북극 유래 박테리아인 Pseudomonas aeruginosa 균주의 대사산물에 대한 화학적 연구는 벤조산 유도체 6번을 포함하여, 두 개의 diketopiperazine 1과 2, 두 개의 phenazine alkaloid 3과 4, indole carbaldehyde 5번을 분리하였다. 화합물들의 구조는 1D 과 2D NMR, 및 MS 기법들과 기존 보고된 문헌 값 과의 비교에 의하여 동정되었다. 분리된 화합물들 중 5번과 6번은 북극 척지해 해수의 P. aeruginosa로 부터 처음으로 보고 되었다. 대사산물들 1-6의 항균 활성은 Staphylococcus aureus과 and Candida albicans에 대하여 측정하였다.

인체 병원성 진균에 대한 Bacillus sp. BCNU 2002의 항진균 효과 (Antifungal Activity of Bacillus sp. BCNU 2002 against the Human Pathogens)

  • 최혜정;안철수;정영기;김동완;주우홍
    • KSBB Journal
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    • 제25권2호
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    • pp.123-129
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    • 2010
  • An endospore-forming, rod-shaped bacterium was isolated from forest soil samples collected at the Taebaek mountain of Gangwon province, Korea, and taxonomically characterized by physiological, biochemical and phylogenetic methods. Its 16S rRNA sequences showed the maximum similarity of 97% with B. amyloliquefaciens. In addition, the isolate BCNU 2002 was determined to have the ability to produce enzymes such as amylase, protease, gelatinase and catalase. The in vitro antifungal activity of Bacillus sp. BCNU 2002 was also examined against human pathogenic fungi such as Aspergillus niger, Candida albicans, Epidermophyton floccosum, Saccharomyces cerevisiae, Trichophyton mentagrophytes and Trichophyton rubrum. A maximum production level of antifungal substances of Bacillus sp. BCNU 2002 was achieved under aerobic incubation at $28^{\circ}C$ for 7 days in LB broth. BCNU 2002 showed strong antifungal activities against T. mentagrophytes and T. rubrum with the range of percentage inhibition from 56.25 to 63.23%. It was also confirmed that ethylacetate extract of cultured broth showed a strong antifungal activity against A. niger, C. albicans, S. cerevisiae and T. rubrum by agar diffusion method. The peptide fraction also exhibited broad antifungal spectrum against various pathogenic fungi. The minimum inhibitory concentration values for active extracts ranged between 125 ${\mu}g$/mL and 1000 ${\mu}g$/mL.

황토로부터 분리한 Bacillus licheniformis의 항진균 chitinase 생산과 효소 특성 (Production and Characterization of Antifungal Chitinase of Bacillus licheniformis Isolated from Yellow Loess)

  • 한귀환;봉기문;김종민;김평일;김시욱
    • KSBB Journal
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    • 제29권3호
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    • pp.131-138
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    • 2014
  • In this study, we isolated two novel chitinase producing bacterial strains from yellow loess samples collected from Jullanamdo province. The chitinase producing bacteria were isolated based on the zone size of clearance in the chitin agar plates. Both of them were gram positive, rod ($2{\sim}3{\times}0.3{\sim}0.4{\mu}m$), spore-forming, and motility positive. They were facultative anaerobic, catalase positive and hydrolyzed starch, gelatin, and casein. From the 16s rRNA gene sequence analysis, the isolates were labeled as Bacillus licheniformis KYLS-CU01 and B. licheniformis KYLS-CU02. The isolates showed higher extracellular chitinase activities than B. licheniformis ATCC 14580 as a control. The optimum temperature and pH for chitinase production were $40^{\circ}C$ and pH 7.0, respectively. Response Surface Methodology (RSM) was used to optimize the culture medium for efficient production of the chitinase. Under this optimal condition, 1.5 times higher chitinase activity of B. licheniformis KYLS-CU02 was obtained. Extracellular chitinases of the two isolates were purified through ammonium sulfate precipitation and anion-exchange DEAE-cellulose column chromatography. The specific activities of purified chitinase from B. licheniformis KYLS-CU01 and B. licheniformis KYLS-CU02 were 7.65 and 5.21 U/mg protein, respectively. The molecular weights of the two purified chitinases were 59 kDa. Further, the purified chitinase of B. licheniformis KYLS-CU01 showed high antifungal activity against Fusarium sp.. In conclusion, these two bacterial isolates can be used as a biopesticide to control pathogenic fungi.

개 외이도에서 분리된 Malassezia pachydermatis에 대한 키토산의 항진균 효과 (Antifungal Effect of Chitosan against Malassezia pachydermatis Isolated from the Dog with Otitis Externa)

  • 오현호;김영인;서정아;최성원;배슬기;오태호
    • 한국임상수의학회지
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    • 제29권4호
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    • pp.323-327
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    • 2012
  • The effect of pH of chitosan solution (w/v) on antifungal activity against Malassezia pachydermatis isolated from a dog with otitis externa was evaluated. This study was investigated to find out the optimal pH of chitosan solution that could be able to eliminate yeast cells. For comparison of antifungal activity of chitosan solution 2% chlorhexidine that have been already proved the antifungal effect against M. pachydermatis was used as positive control. The chitosan solution at different pH (2.5, 3.0, 3.5, 4.0, 4.5, 5.0) were involved this experiment. The chitosan solutions at each pH could eliminate a number of yeast cells when they were compared to other antifungal agents. In chitosan solution's antifungal effect of varying degrees according to the pH M. pachydermatis was inhibited at pH of < 5.0. Especially it has been proved an effective antifungal effect at pH 3.5. Therefore, the pH of chitosan solution had a effect on antifungal activity and the optimal pH was 3.5 in vitro. The possibility of topical therapy with acidific solution of chitosan has a potential in skin infection against M. pachydermatis.

소아 급성골수성백혈병에서 관해유도 요법 중 Posaconazole의 예방적 항진균 치료 (Posaconazole for Prophylaxis of Fungal Infection in Pediatric Patients with Acute Myeloid Leukemia undergoing Induction Chemotherapy)

  • 김승민;이윤선;김재송;김수현;손은선;유철주
    • 한국임상약학회지
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    • 제28권3호
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    • pp.181-187
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    • 2018
  • Background: Posaconazole is a broad-spectrum triazole antifungal agent and the most recommended prophylactic antifungal agent for patients with acute myeloid leukemia (AML) undergoing induction chemotherapy. In this study, we evaluated the status and effectiveness of posaconazole as a prophylactic antifungal agent in pediatric patients receiving induction chemotherapy for AML. Methods: We retrospectively reviewed the electronic medical records of 36 pediatric patients with AML (between January 2013 and September 2017) at the Yonsei University Health System. Invasive fungal disease (IFD) was assessed as the primary endpoint of prophylactic antifungal effect. The secondary endpoints were incidence of fever, persistent fever despite the use of broad-spectrum antibiotics for 72 h, alteration of antifungal agent, intensive care unit admission, and death within 100 days. Results: Among the 36 patients, 18 patients used posaconazole, 12 were treated with suspension formula, and 6 of them were treated with tablets. Eighteen patients did not use antifungal agents prophylactically. The mean number of days of posaconazole administration was $26.8{\pm}16days$. IFD occurred in 2/18 (11.1%) patients in the no prophylaxis group and in 1/18 (5.6%) patients in the posaconazole group (p=0.49). Conclusion: Posaconazole is expected to be useful for the prevention of IFD in pediatric patients with AML undergoing induction chemotherapy. Prospective studies of the effectiveness of posaconazole prophylaxis should be conducted in more pediatric patients in the future.

Corallococcus와 Myxococcus 속 점액세균 균주들에 의한 항균 물질의 생산 (Production of Antimicrobial Substances by Strains of Myxobacteria Corallococcus and Myxococcus)

  • 신혜진;윤진권;안동주;조경연
    • 한국미생물·생명공학회지
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    • 제41권1호
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    • pp.44-51
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    • 2013
  • 국내 토양시료에서 분리한 174 Corallococcus 속 균주와 207 Myxococcus 속 균주들의 배양추출물을 제조하고 Candida albicans, Pseudomonas aeruginosa, Staphylococcus aureus에 대한 항균 활성을 비교하였다. 항진균 활성을 보이는 균주의 비율은 Corallococcus가 7.5%(174균주 중 13균주)로 51.7%(207균주 중 107균주)를 보인 Myxococcus에 비해 낮았다. 하지만, 항세균 활성을 보인 균주의 비율은 Corallococcus가 12.1%(21균주)로 1%(2균주)를 보인 Myxococcus에 비해 상대적으로 높았다. Corallococcus 균주 중 P. aeruginosa, S. aureus에 모두 활성을 보이는 6 C. coralloides 균주들은 자실체 형성에서는 차이를 보였지만 항세균 활성을 나타내는 배양추출물의 HPLC 크로마토그램은 유사하였는데, 이들이 생산하는 항세균 물질의 생산은 CYS 배지에서 6일 이상 배양할 때 가장 높았다.

Uridine Nucleoside 유도체의 합성과 생물 활성 (Syntheses and Biological Activities of Uridine Nucleoside Derivatives)

  • Bong-Hun Lee;Jang-Su Park;Shin-Won Kang
    • 생명과학회지
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    • 제9권1호
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    • pp.63-68
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    • 1999
  • 5-halogen substituted uridine, amino acid, peptide 및 penicillin G의 5'-amino -5' -deoxyuridine con-jugates, 5'-monophosphate uridine 유도체, 5'-monophosphate uridine -fat쇼 acid 유도체와 같은 nu-cleoside 화합물들을 화학적으로 합성한 후 이들의 항진균, 항균 및 항암 활성을 측정하였다. 5-Bromo-2',3'-O-isopropylideneuridine(6)은 Trichophyton rubrum의 성장을 억제하였다(MIC: $0.2{\mu}$g/ml). 5'-Amino-5' -deoxyuridine -penicillin G(19), 5'-amino-5'-deoxyuridine-cyclo(Phe -Asp)(20), 5-iodo-5'-amino -5' -deoxyuridine-penicillin G(22)는 항균적이었고(S. aureus에 대해 MIC가 $6.25{\mu}$g/ml) 뒤의 두 nucleoside 화합물은 항암 작용이 가장 강한 유도체이었다(L5178Y murine lymphoma cell에 대한 $IC_{50}$$6.5{\mu}$g/ml).

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비타민 B1 유도체(Thiamine Di-lauryl Sulfate:TDS)의 나노입자화를 통한 고추탄저병균의 항진균 활성 증진 (Enhancement of Antifungal Activity of Anthracnose in Pepper by Nanopaticles of Thiamine Di-lauryl Sulfate)

  • 서용창;조정섭;정해윤;임태빈;조경숙;이태우;정명훈;이강형;김성일;윤원병;이현용
    • 한국약용작물학회지
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    • 제19권3호
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    • pp.198-204
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    • 2011
  • This study was performed to enhance antifungal activity of anthracnose in chili pepper by nanopaticles of thiamine di-lauryl sulfate (TDS) through high pressure homogenization process. Yield of TDS was 79.14% by reaction of thiamine hydrochloride and sodium lauryl sulfate. TDS nanopaticle solution was manufactured through high pressure homogenization process. The turbidity of nanoparticles solution was increased with increasing the concentration of TDS, and nanoparticles solution of 100 ppm was showed the highest turbidity with absorbance of 3.212. The size of nanoparticles solution was measured as average 258.6 nm by DLS. Nanoparticles solution of 100 ppm showed growth inhibition activity with higher than about 80% compared to the control group against Colletotrichum gloeosporioides. Finally, nanoparticles solution was increased effectively the penetration of the TDS nanopaticles on attached cell membrane of hyphae and started to destruct the cells under microscope observation. Consequently, we suggested that the TDS nanoparticle solution by high pressure homogenization process might be suitable biochemical pesticides for improving the antifungal activities against anthracnose in pepper.

우루시올 및 우루시올 유도체의 항균 활성 (Antimicrobial Activities of Urushiol and Urushiol Derivatives)

  • 김진철;안정근;고수영;최영훈;김도현;이태용
    • 청정기술
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    • 제13권1호
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    • pp.22-27
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    • 2007
  • 옻은 전통적으로 옻칠로서 사용되었으며, 최근 많은 연구를 통하여 과학적으로 그 내구성, 항균성들이 밝혀졌기 때문에 본 연구진은 옻이 최근 대두되고 있는 친환경적 방오도료의 문제를 해결할 수 있을 것으로 예상하고 있다. 따라서 본 실험에서는 옻의 주성분인 urushiol을 화학적으로 합성하고, 그 유도체들과 함께 어느 정도의 항균효과가 있는지 알아보았다. 그 결과, 본 연구진은 합성된 urushiol이 뛰어난 항진균효과를 가짐을 알 수 있었고, 항균효과 측면에서는 그람양성균에는 좋은 효과를 보인 반면 그람음성균에서는 큰 효과를 보이지 않음을 알 수 있었다. 또한 urushiol과 그 유도체들의 항균력은 균주에 따라 서로 다른 특이적 항균성을 보이는 것을 알 수 있었다.

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