http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
우이음 ( E-eum Woo ),이강선 ( Gang-seon Lee ),이인경 ( In-kyoung Lee ),최재을 ( Jae-eul Choi ),윤봉식 ( Bong-sik Yun ) 한국균학회 2016 韓國菌學會誌 Vol.44 No.3
한국의 인삼(Panax ginseng)은 다양한 생리학적, 약리학적 활성을 지닌 것으로 입증되어 왔다. 인삼 잘록병은 Rhizoctonia solani와 Pythium sp.과 같은 식물 병원균에 의해 발생하며 인삼 종자에 치명적이다. 잘록병은 일반적으로 화학농약을 이용하여 방제하고 있다. 또한 생물학적 방제는 인삼 잘록병을 방제하는데 효과적이며 환경친화적인 방법으로 알려져 있다. 본 연구진은 인삼 잘록병 방제를 위한 생물 방제제로서 잠재성을 지닌 토양 세균을 탐색하였으며, 그 결과 항균물질 guanidylfungin과 methylguanidylfungin을 생산하는 방선균 A3265 균주를 선발하였다. 본 연구는 방선균 A3265 균주의 인삼 잘록병 방제 활성을 포장에서 조사한 것이다. 그 결과 인삼종자를 방선균 A3265균주의 배양액에 침지한 후 파종하였을 때 잘록병의 발병률이 유의적으로 감소함을 확인하였다. 이는 방선균 A3265균주가 잘록병 방제에 효과적으로 활용될 수 있음을 나타낸다. Korean ginseng (Panax ginseng) possesses various biological and pharmacological properties. Damping-off is a critical disease on ginseng seedlings, which is caused by the fungal pathogens Rhizoctonia solani and Pythium sp.. This disease is generally controlled by the application of fungicides, but also biological control is an efficient and environmentally friendly way to prevent ginseng damping-off. In a previous study, we screened soil-borne bacteria with potential applications as biological control agents for ginseng damping-off and selected the bacterial strain Streptomyces sp. A3265, producing antifungal substances guanidylfungin and methylguanidylfungin. In this study, we investigated control efficacy of Streptomyces sp. A3265 against ginseng damping-off in the field. As a result, the incidence of damping-off was significantly reduced when soaking ginseng seeds in the culture broth of Streptomyces sp. A3265.
( Swarnalee Dutta ),( E-eum Woo ),( Sang-mi Yu ),( Rajalingam Nagendran ),( Bong-sik Yun ),( Yong Hoon Lee ) 한국균학회 2019 Mycobiology Vol.47 No.1
Fungi produce various secondary metabolites that have beneficial and harmful effects on other organisms. Those bioactive metabolites have been explored as potential medicinal and antimicrobial resources. However, the activities of the culture filtrate (CF) and metabolites of whiterot fungus (Schizophyllum commune) have been underexplored. In this study, we assayed the antimicrobial activities of CF obtained from white-rot fungus against various plant pathogens and evaluated its efficacy for controlling anthracnose and gray mold in pepper plants. The CF inhibited the mycelial growth of various fungal plant pathogens, but not of bacterial pathogens. Diluted concentrations of CF significantly suppressed the severity of anthracnose and gray mold in pepper fruits. Furthermore, the incidence of anthracnose in field conditions was reduced by treatment with a 12.5% dilution of CF. The active compound responsible for the antifungal and disease control activity was identified and verified as schizostatin. Our results indicate that the CF of white-rot fungus can be used as an eco-friendly natural product against fungal plant pathogens. Moreover, the compound, schizostatin could be used as a biochemical resource or precursor for development as a pesticide. To the best of our knowledge, this is the first report on the control of plant diseases using CF and active compound from white-rot fungus. We discussed the controversial antagonistic activity of schizostatin and believe that the CF of white-rot fungus or its active compound, schizostatin, could be used as a biochemical pesticide against fungal diseases such as anthracnose and gray mold in many vegetables.
( Nguyen Van Minh ),( E Eum Woo ),( Ji Yul Kim ),( Dae Won Kim ),( Byung Soon Hwang ),( Yoon Ju Lee ),( In Kyoung Lee ),( Bong Sik Yun ) 한국균학회 2015 Mycobiology Vol.43 No.3
In a previous study, we identified a Streptomyces sp., A3265, as exhibiting potent antifungal activity against various plant pathogenic fungi, including Botrytis cinerea, Colletotrichum gloeosporioides, and Rhizoctonia solani. This strain also exhibited a biocontrolling effect against ginseng root rot and damping-off disease, common diseases of ginseng and other crops. In this study, we isolated two antifungal substances responsible for this biocontrolling effect via Diaion HP-20 and Sephadex LH-20 column chromatography, medium pressure liquid chromatography, and high-performance liquid chromatography. These compounds were identified as guanidylfungin A and methyl guanidylfungin A by spectroscopic methods. These compounds exhibited potent antimicrobial activity against various plant pathogenic fungi as well as against bacteria.
Control Efficacy of Streptomyces sp. A501 against Ginseng Damping-off and Its Antifungal Substance
( Nguyen Van Minh ),( E-eum Woo ),( Gang-seon Lee ),( Dae-won Ki ),( In-kyoung Lee ),( Sang-yeob Lee ),( Kyeonghun Park ),( Jaekyeong Song ),( Jae Eul Choi ),( Bong-sik Yun ) 한국균학회 2017 Mycobiology Vol.45 No.1
Ginseng damping-off, caused by the fungal pathogens Rhizoctonia solani and Pythium sp., is a critical disease in ginseng seedling. In a continuing effort to find microorganisms with the potential of acting as a biocontrol agent against Rhizoctonia damping-off, we found that a Streptomyces sp. A501 showed significant antifungal activity against Rhizoctonia solani. In field experiment to test the efficacy of Streptomyces sp. A501 in controlling ginseng damping-off, the incidence of damping-off disease was meaningfully reduced when ginseng seeds were soaked in the culture broth of Streptomyces sp. A501 before sowing. To perform characterization of the antifungal compound, we isolated it from the culture broth of strain A501 through Diaion HP- 20 and silica gel column chromatographies and preparative high-performance liquid chromatography. The structure of the antifungal compound was assigned as fungichromin by spectroscopic methods, mainly nuclear magnetic resonance and electrospray ionization-mass analysis.
Neuraminidase Inhibitors from the Fruiting Body of Glaziella splendens
( Ji-yul Kim ),( E-eum Woo ),( Lee Su Ha ),( Dae-won Ki ),( In-kyoung Lee ),( Bong-sik Yun ) 한국균학회 2019 Mycobiology Vol.47 No.2
Neuraminidase (NA) cleaves the glycosidic bond linkages of sialic acids to release the mature virions from infected cells and has been an attractive therapeutic target for anti-influenza agents. In our ongoing investigation of NA inhibitors in mushroom extracts, we found that the extract the fruiting body of Glaziella splendens potently inhibited neuraminidase. The fruiting bodies of G. splendens were extracted and partitioned successively with hexane, ethyl acetate, and butanol. The ethyl acetate soluble-layer was subjected to silica gel and Sephadex LH-20 column chromatographies, and MPLC to obtain five compounds (1-5). Their structures were determined by spectroscopic methods. NA inhibitory activity of these compounds was evaluated using NAs from recombinant rvH1N1, H3N2, and H5N1 influenza A viruses. One compound (1) was elucidated as a new azaphilone derivative, and four compounds (2-5) were identified as entonaemin A, comazaphilone D, rubiginosin A, and entonaemin B, respectively. Compounds 3 and 4 showed considerable inhibitory activity against three types of neuraminidases with the IC<sub>50</sub> values of 30.9, 41.8, and 35.7 μM for 3 and 46.5, 50.4, and 29.9 μM for 4, respectively. This study reveals that the fruiting bodies of G. splendens possess azaphilone derivatives with the NA inhibitory activity. This is the first report on the isolation of neuraminidase inhibitors from the fruiting bodies of G. splendens.
Neuraminidase Inhibitors from the Fruiting Body of Phellinus igniarius
( Ji-yul Kim ),( Dae-won Kim ),( Byung Soon Hwang ),( E-eum Woo ),( Yoon-ju Lee ),( Kyeong-woon Jeong ),( In-kyoung Lee ),( Bong-sik Yun ) 한국균학회 2016 Mycobiology Vol.44 No.2
During our ongoing investigation of neuraminidase inhibitors from medicinal fungi, we found that the fruiting bodies of Phellinus igniarius exhibited significant inhibitory activity against neuraminidase from recombinant H3N2 influenza viruses. Two active compounds were isolated from the methanolic extract of P. igniarius through solvent partitioning and Sephadex LH-20 column chromatography. The active compounds were identified as phelligridins E and G on proton nuclear magnetic resonance (1H NMR) and electrospray ionization mass measurements. These compounds inhibited neuraminidases from recombinant rvH1N1, H3N2, and H5N1 influenza viruses, with IC50 values in the range of 0.7~8.1 μM.
Consoramides A-C, New Zwitterionic Alkaloids from the Fungus Irpex consors
( Ji-yul Kim ),( Dae-won Ki ),( Yoon-ju Lee ),( Lee Su Ha ),( E-eum Woo ),( In-kyoung Lee ),( Bong-sik Yun ) 한국균학회 2021 Mycobiology Vol.49 No.4
In our ongoing search for new secondary metabolites from fungi, a basidiomycete fungus Irpex consors was selected for mycochemical investigation, and three new zwitterionic alkaloids (1-3) and five known compounds (4-8) were isolated from the culture broth (16 l) of I. consors. The culture filtrate was fractionated by a series of column chromatography including Diaion HP-20, silica gel, and Sephadex LH-20, Sep-Pak C<sub>18</sub> cartridge, medium pressure liquid chromatography (MPLC), and high pressure liquid chromatography (HPLC) to yield eight compounds (1-8). The structures of the isolated compounds were elucidated by the interpretation of nuclear magnetic resonance (NMR) spectra and high-resolution mass spectrometry (HR-MS). Their antioxidant and antibacterial activities were examined. The zwitterionic structures of three new sesquiterpene alkaloids (1-3) were determined together with five known compounds identified as stereumamide E (4), stereumamide G (5), stereumamide H (6), stereumamide D (7), and sterostrein H (8). This is the first report of the zwitterionic alkaloids in the culture broth of I. consors. Three new zwitterionic alkaloids were named as consoramides A-C (1-3).