• Applied Biological Chemistry
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• 제50권4호
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• pp.316-320
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• 2007

Chaetomium sp.배양체를 acetone에 침지하여 추출한 후 n-hexane, $CHCl_3$, EtOAc, n-BuOH 및 물로 분획하였다. 이중 EtOAc 분획을 silica gel 및 HPLC(ODS)를 이용하여 3종의 활성물질 A.C-3, A.C-4 및 A.C-5를 분리하였다. 각 화합물의 화학구조를 NMR 및 MS등의 스펙트럼 데이터와 문헌검색을 통하여 chaetoglobosin 유도체인 chaetoglobosin F, chaetoglobosin C 및 chaetoglobosin E로 동정하였다. A.C-3, A.C-4 및 A.C-5의 논피에 대한 유근신장 저해활성 검정 결과, $IC_{50}$값은 각각 66, 65, $67{\mu}g/ml$이었다.

• Journal of Applied Biological Chemistry
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• 제42권3호
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• pp.146-150
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• 1999

As a part of the integrated disease system in greenhouse, an antifungal fungus(AF1) was isolated from greenhouse soil. It exhibited strong inhibitory activites against Pythium ultimum, Phytophtora capsici, Rhizoctonia solani, Botrytis cinerea, and Fusarium oxysporum based on dual culture on 1/5 strength of potato dextrose agar between antagonistic fungus and several plant pathogens. The antagonistic fungus was identified as Chaetomium cochliodes, based on morphological characteristics; the body of the perithecium bears straight or slightly wavy, unbranched hairs, whilst the apex bears a group of spirally coiled hairs. To investigate antagonistic principles, antifungal compound was extracted and fractionated by different solvent systems. An antifungal compound was isolated as pure crystal from is culture filtrate using organic solvent extraction and column chromatography, followed by preparative thin layer chromatography. The chemical structure of the purified antifungal compound was identified as chaetoglobosin A based on the data obtained form $^1H-NMR$, $^{13}C-NMR$, DEPT 90, 135, $^1H-^1H$ COSY, $^1H-^{13}C$ COSY and EI/MS. $ED_{50}$ values of the chaetoglobosin A against P. ultimum, P. capsici, R. solani, B. cinerea and F. oxysporum were 1.98, 4.01, 4.16, 2.67 and 35.14 ppm, respectively.