Beom-Suk Kim
Korea University · 医学
研究室紹介
Professor Beom-Suk Kim's research lab specializes in the discovery and characterization of bioactive microbial metabolites with potent antifungal properties, particularly targeting plant-pathogenic fungi. The lab focuses on identifying novel natural products from actinobacteria and other microorganisms that act on fungal cell envelopes or cellular components, with an emphasis on mechanisms such as zoospore lysis and membrane disruption. Key research directions include the biosynthesis and enzymatic editing roles of thioesterase enzymes in polyketide pathways, as well as the structural elucidation and mode-of-action studies of macrolide and glutarimide antibiotics. The ultimate goal is to develop environmentally sustainable, microbiologically derived fungicides for agricultural applications.
Research Overview
Research Output Trend
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Selected Papers
15The glycolipid antibiotic rhamnolipid B isolated from Pseudomonas aeruginosa strain B5 was evaluated for in vitro antifungal activity and in vivo control against phytophthora blight and anthracnose under glasshouse conditions. Rhamnolipid B showed antifungal activity against Cercospora kikuchii, Cladosporium cucumerinum, Colletotrichum orbiculare, Cylindrocarpon destructans, Magnaporthe grisea and Phytophthora capsici. Microscopic observation revealed that the high level of antifungal activity (
Abstract As environmental and commercial requirements for new fungicides are increasingly demanding, antifungal compounds of microbial origin attract tremendous interest as a starting point in the development of environmentally sound agricultural fungicides. As seen in fenpiclonil, fludioxonil and synthetic derivatives of the strobilurins such as azoxystrobin and krexosim‐methyl, this approach for the development of microbial fungicides has proven to be a promising and effective strategy for dev
The pikromycin biosynthetic gene cluster contains the pikAV gene encoding a type II thioesterase (TEII). TEII is not responsible for polyketide termination and cyclization, and its biosynthetic role has been unclear. During polyketide biosynthesis, extender units such as methylmalonyl acyl carrier protein (ACP) may prematurely decarboxylate to generate the corresponding acyl-ACP, which cannot be used as a substrate in the condensing reaction by the corresponding ketosynthase domain, rendering th
The antibiotic As1A, strongly inhibitory to Phytophthora capsici Leonian in vitro and in vivo, was isolated from the broth culture of Streptomyces libani Baldacci & Grein using various chromatographic procedures. The molecular formula of the antibiotic As1A was deduced to be C 45 H 74 O 11 (M+H, m/z 791.5307) by high resolution fast atom bombardment - mass spectroscopy. The analysis of 1 H-NMR (nuclear magnetic resonance) and 13 C-NMR spectroscopy, DEPT experiment, and two-dimensional NMR sp
AIMS: The objective of this study was to explore antifungal metabolites targeting fungal cell envelope and to evaluate the control efficacy against anthracnose development in pepper plants. METHODS AND RESULTS: A natural product library comprising 3000 microbial culture extracts was screened via an adenylate kinase (AK)-based cell lysis assay to detect antifungal metabolites targeting the cell envelope of plant-pathogenic fungi. The culture extract of Streptomyces mauvecolor strain BU16 displaye
The antibiotic Ao58A,which showed strong antifungal activity against some plant pathogenic fungi, was purified from the culture broth and mycelial mats of Micromonospora coerulea strain Ao58 using various chromatographic procedures. The molecular formula of the antibiotic Ao58A was deduced to be C(16)H(23)NO(4) (M + H, m/z 294.1707) by high-resolution FAB mass spectroscopy. Analyses of (1)H NMR, (13)C NMR, and 2D NMR spectral data revealed that the antibiotic Ao58A is the glutarimide antibiotic
The actinomycete strain Ao108 producing antifungal metabolites active against some plant pathogenic fungi was identified as Actinomadura roseola, based on the analyses of morphological and physiological characteristics. The antibiotic Da2B that showed a strong antifungal activity was isolated from the culture broth and mycelial mats of A. roseola strain Ao108 using various chromatographic procedures. On the basis of (1)H NMR, (13)C NMR, and 2-D NMR correlation data, the antibiotic Da2B was confi
During screening of microorganisms producing antifungal metabolites, Streptomyces psammoticus strain KP1404 was isolated. The culture extract of this strain showed potent disease control efficacy against Fusarium wilt on tomato plants. The antifungal metabolites ST-1 and ST-2 were isolated from the culture extract using a variety of chromatographic procedures. On the basis of MS and NMR spectrometric analysis, the structures of the antifungal active compounds ST-1 and ST-2 were determined to be
BACKGROUND: Microbial secondary metabolites are a rich source of antifungal agents and have merit as alternatives to synthetic fungicides. To develop disease control agents against powdery mildew, the lipopeptide antibiotic neopeptins were identified from the culture broth of a Streptomyces sp., and in vivo control efficacy of the compounds was evaluated on cucumber plants under glasshouse conditions. RESULTS: The Streptomyces sp. KNF2047 antagonistic against powdery mildew development in cucumb
AIMS: Cytochrome P450 monooxygenases (CYPs) are useful catalysts for oxidation reactions. Self-sufficient CYPs harbour a reductive domain covalently connected to a P450 domain and are known for their robust catalytic activity with great potential as biocatalysts. In an effort to expand genetic sources of self-sufficient CYPs, we devised a sequence-based screening system to identify them in a soil metagenome. METHODS AND RESULTS: We constructed a soil metagenome library and performed sequence-bas