• 제목/요약/키워드: Antifungal compounds

검색결과 353건 처리시간 0.025초

Bacillus subtilis가 생산하는 길항물질에 의한 아플라톡신 생성균의 억제 (Inhibition of Aflatoxin-producing Fungi with Antifungal Compound Produced by Bacillus subtilis)

  • 강길진;정지현;조정일
    • 한국식품위생안전성학회지
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    • 제15권2호
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    • pp.122-127
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    • 2000
  • 아플라톡신 생성균의 생육을 억제할 수 있는 미생물을 분리동정하고 진공동결 건조한 대사산물로부터 길항물질을 분리하였다. 대두로부터 아플라톡신 생육을 저해하는 길항균을 분리하였으며, 그 균은 Bacillus subtilis로 동정되었다. Bacillus subtilis는 아플라톡신 생성균에 대한 길항물질을 생산하였으며 MeOH추출, 실리카겔 흡착 크로마토그래피법, Sephadex LH-20 크로마토그래피법으로 길항물질을 분리하였다. 아플라톡신 생성균인 Asp. flavus와 Asp. parasiticus의 생육은 길항미생물인 Bacillus subtilis가 생산하는 길항물질에 의해 강하게 저해되었으며 이는 아플라톡신 오염방지를 위하여 효과적인 생물학적 방법일 것이라 기대된다.

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Large-Scale Screening of the Plant Extracts for Antifungal Activity against the Plant Pathogenic Fungi

  • Song Hee, Lee;Young Taek, Oh;Do-Yeon, Lee;Eunbyeol, Cho;Byung Su, Hwang;Junhyun, Jeon
    • The Plant Pathology Journal
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    • 제38권6호
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    • pp.685-691
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    • 2022
  • Plants produce chemicals of immense diversity that provide great opportunities for development of new antifungal compounds. In search for environment-friendly alternatives to the fungicide of current use, we screened plant extracts obtained from more than eight hundred plant materials collected in Korea for their antifungal activity against the model plant pathogenic fungus, Magnaporthe oryzae. This initial screening identified antifungal activities from the eleven plant extract samples, among which nine showed reproducibility in the follow-up screening. These nine samples were able to suppress not only M. oryzae but also other fungal pathogens. Interestingly, the plant extracts obtained from Actinostemma lobatum comprised five out of eight samples, and were the most effective in their antifungal activity. We found that butanol fraction of the A. lobatum extract is the most potent. Identification and characterization of antifungal substances in the A. lobatum extracts would provide the promising lead compounds for new fungicide.

수목추출물의 생리활성에 관한 연구(X) - 헛개나무 목부의 항균활성 물질 - (Studies on Biological Activity of Wood Extractives (X) - Antifungal Compounds of Hovenia dulcis -)

  • 최윤정;이학주;이성숙;최돈하
    • Journal of the Korean Wood Science and Technology
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    • 제31권1호
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    • pp.1-9
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    • 2003
  • 항균활성이 우수한 헛개나무 목부 에탄올 조추출물로부터 7종의 화합물을 단리하였으며, 기기분석 결과 flavonoid인 5-hydroxy-7-methoxyflavone를 비롯하여 5,7-dihydroxyflavone (chrysin), 5,7-dihydroxyflavanone (pinocembrin), 3,5,7-trihydroxyflavanone (pinobanksin), 3,4',5,7-tetrahydroxyflavanone (aromadendrin)과 stilbenoid인 3-hydroxy-5-methoxystilbene과 3,5-dihydroxystilbene (pinosylvin)으로 각각 동정되었다. 이들 단리물질에 대한 항균활성을 조사한 결과 stilbenoid인 3-hydroxy-5-methoxystilbene이 공시균주의 생장을 완전히 저해하여 단리물질 중 활성이 가장 높은 것으로 나타났다. 그 다음이 pinocembrin과 pinosylvin으로 Cryphonectria parasitica, Trametes versicolor, Tyromyces palustris 그리고 Trichoderma viride에 대해 높은 균사생장억제율을 나타내어 활성이 우수한 것으로 나타났다. 그러나, flavonoid인 pinobanksin, 5- hydroxy-7-methoxyflavone, chrysin, 그리고 aromadendrin은 항균활성이 낮은 것으로 나타났다. 이상의 결과, 헛개나무 목부 에탄올 조추출물의 높은 항균활성은 3-hydroxy-5-methoxystilbene과 pinocembrin, 그리고 pinosylvin에서 유래된 것으로 사료되었다.

점액세균 Myxococcus sp. JW154로 부터 항균물질의 분리 및 식물병원균에 대한 in vivo 활성 (Isolation and in vivo Activities of Antifungal Compounds from Myxococcus sp. JW154 (Myxobacteria).)

  • 안종웅;김병섭
    • 한국미생물·생명공학회지
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    • 제30권2호
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    • pp.162-166
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    • 2002
  • 제주도 서귀포의 해변에서 채집한 해양퇴적물로부터 Myxococcus속의 점액세균 JW154를 분리하여 그 대사산물로부터 강한 항균활성을 나타내는 두 개의 bithiazole계 화합물을 분리하고 각종 기기분석을 통하여 구조를 확인한 바, 이들은 각각 KR025와 melithiazole F로 보고된 화합물임을 밝혔다. 유묘 검정법으로 조사된 이 화합물의 주요 식물병원균에 대한 in vivo 항균활성은 토마토 역병과 밀 녹병 및 보리 흰가루병에 대해 높게 나타났는데, 20$\mu\textrm{g}$/m1 수준으로 처리하였을 때 80% 이상의 높은 방제가를 보였다.

Synthesis of Benzoxazole Amides as Novel Antifungal Agents against Malassezia Furfur

  • Kim, Beom-Joon;Kim, Jin-Ah;Kim, Young-Kook;Choi, Soon-Yong;ParkChoo, Hea-Young
    • Bulletin of the Korean Chemical Society
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    • 제31권5호
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    • pp.1270-1274
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    • 2010
  • Malassezia is a pathogenic fungus that causes skin diseases, such as tinea versicolor, atopic dermatitis and fatal sepsis. We report the synthesis of a series of benzoxazole amides and evaluation of their antifungal activity against Malassezia furfur. Twelve benzoxazole amides were prepared through the cyclization of the substituted 2-hydroxy aniline with N-(bis-methylsulfanylmethylene) amides. Among the prepared compounds, the compounds 4a, 8b, 8c and 8d showed in vitro antifungal activity.

Solvent Free Microwave Accelerated Synthesis of Heterocyclic Thiazolidin-4-ones as Antimicrobial and Antifungal Agents

  • Sekhar, Kondapalli Venkata Gowri Chandra;Rao, Vajja Sambasiva;Reddy, Aravalli Satish;Sunandini, Ravada;Satuluri, V S A Kumar
    • Bulletin of the Korean Chemical Society
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    • 제31권5호
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    • pp.1219-1222
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    • 2010
  • A simple and efficient method has been developed for conversion of arenecarbaldehyde-3-methylquinoxalin-2-ylhydrazones to 3-(2-methylquinoxalin-3-yl)-2-(substitutedphenyl)thiazolidin-4-ones in good yields using microwave irradiation technique on silica as solid support under solvent free conditions. The synthesized compounds were characterized by elemental microanalysis, infrared spectroscopy, $^1H$ NMR, and mass spectroscopy. All the synthesized thiazolidinones were investigated for their antimicrobial and antifungal activities. The results of the biological activities revealed that the compounds 3b, 3d, 3f and 3h exhibited excellent antibacterial activities while 3d and 3h exhibited good antifungal activity.

Design, Synthesis and Antifungal Activities of Novel Strobilurin Derivatives Containing Pyrimidine Moieties

  • Zhang, Xiang;Gao, Yong-Xin;Liu, Hui-Jun;Guo, Bao-Yuan;Wang, Hui-Li
    • Bulletin of the Korean Chemical Society
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    • 제33권8호
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    • pp.2627-2634
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    • 2012
  • Strobilurins are one of the most important classes of agricultural fungicides. To discover new strobilurin derivatives with high activity against resistant pathogens, a series of novel ${\beta}$-methoxyacrylate analogues were designed and synthesized by integrating substituted pyrimidine with a strobilurin pharmacophore. The compounds were confirmed and characterized by infrared, $^1H$ nuclear magnetic resonance, elemental analysis and mass spectroscopy. The bioassays indicated that most of the compounds (1a-1h) exhibited potent antifungal activities against Colletotrichum orbiculare, Botrytis cinerea Pers and Phytophthora capsici Leonian at the concentration of 50 ${\mu}g/mL$. Exhilaratingly, compound 1d (R=3-trifluoromethylphenyl) showed better antifungal activity against all the tested fungi than the commercial strobilurin fungicide azoxystrobin.

점액세균 KR025의 분리 동정 및 생리활성물질의 탐색 (Isolation and Identification of Myxobacteria KR025 and Searching of Their Bioactive Compounds)

  • 김병섭;안종웅;조광연
    • 한국식물병리학회지
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    • 제14권4호
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    • pp.345-349
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    • 1998
  • Fifty isolates of myxobacteria were isolated from soils from several areas in Korea during 1996-1997 and bioactivity against plant pathogenic fungi of these isolates was examined. A myxobacterial isolate KR025 showed good antifungal activities against Pyricularia oryzae, Cryphonectria parasitica, Colletotrichum lagenarium, and C. gloeosporioides but did not against Rhizoctonia solani, Fusarium oxysporum and Pythium ultimum. The bacterium was identified as Myxococcus fulvus based on morphological and physiological characteristics. Antifungal substances were extracted from culture broth and bacterial cell of Myxococcus fulvus KR025 by ethyl acetate. Antifungal substance of Myxothiazole (100 ${\mu}{\textrm}{m}$/ml) produced by Myxococcus fulvus KR 025 controlled 97.0% rice blast, tomato late blight, wheat leaf rust, and barley powdery mildew and showed 45.0 and 82.6% disease control of rice sheath blight and cucumber gray model, respectively.

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Synthesis and evaluation of antifungal activities of 5-arylamino-6-chloro-4. 7 -dioxoindazoles

  • You, Hea-Jung;Shim, Ju-Yeon;Shon, Eun-Ha;Choi, Ko-Un;Choi, Ik-Hwa;Chae, Mi-Jin;Ryu, Chung-Kyu
    • 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.353.2-353.2
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    • 2002
  • 5-Arylamino-6-chloro-4.7-dioxoindazoles (DZs) were newly synthesized for the evaluation of antifungal activities. The compounds DZs were prepared by regioselective nucleophilic substitution of 5.6-dichloro-4.7-dioxoindazoles with appropriate arylamines in high yield. DZs were tested for their growth inhibitory activities against Candida species and Aspergillus niger. The MIC values were determined by the two-fold dilution method. In general. DZs showed in vitro antifungal activities. Among the tested compounds, DZ1, 3, 6, 7 and 12 showed potent antifungal activities against Candida species and Aspergillus niger. DZ7 was the most effective in preventing the growth of Candida species.

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식물오일과 그 성분들의 살균활성 (Phytopathogenic Activities of Essential Oils and Their Main Compounds)

  • 최원식;김관영;장도연;엄대용;김태준;정봉진
    • 농약과학회지
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    • 제10권3호
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    • pp.201-209
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    • 2006
  • 43종의 식물오일들을 대상으로 잿빛곰팡이병균 (Botrytis cinerea) 외 9종의 식물병원균에 대한 살균 효과로 이들의 생리활성 검증을 실시하였다. 이 중 thyme 오일이 잿빛곰팡이병균(Botrytis cinerea), 잎집무늬 마름병균(Rhizoctonia solani), 고추역병균(Phytophthora capsici), 고추탄저병균(Glomerella cingulate), 사과점무늬 낙엽병균(Alternaria mali)과 벼도열병균(Magnaporthe grisea)에서 광범위하게 살균효과를 나타내었다. Thyme 오일의 주성분을 GC/MS로 분석한 결과 thymol, carvacrol, borneol, linalool과 p-cymene임을 확인하였다. 이 중 thymol과 carvacrol이 높은 살균활성을 나타내었다. 한편, 식물병원균에 대한 살균활성관련 작용기작을 실험한 결과, 잿빛곰팡이병균(Botrytis cinerea), 잎집무늬마름병균(Rhizoctonia solani)과 사과점무늬낙엽병균(Alternaria mali)의 포자발아를 억제하는 것으로 나타났다. Thymol과 carvacrol은 in vivo에서 잿빛곰팡이병균(Botrytis cinerea)과 잎집무늬마름병균(Rhizoctonia solani)에 대하여 높은 예방효과를 나타내었으며, thymol, carvacrol의 유사구조를 갖는 alkylphenol계 화합물들도 살균활성이 있음을 검정하였다.