• 식물병연구
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• 제17권1호
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• pp.13-18
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• 2011

Fusarium oxysporum f. sp. conglutinans에 의해 발생하는 양배추 시들음병에 대한 효율적인 저항성 검정법을 확립하기 위하여, 시판 중인 9종 양배추 품종의 시들음병에 대한 저항성을 실험하고 이로부터 저항성 정도가 다른 5종 품종(YR호남, 오가네, 그린핫, 레드마트, 꼬꼬마)을 선발하여 뿌리 상처 유무, 포자현탁액에 침지하는 시간, 접종원 농도 및 재배 온도에 따라 이들 품종의 시들음병에 대한 저항성 반응의 변화를 조사하였다. YR호남과 오가네와 같은 고도의 저항성 품종들은 뿌리 상처 유무, 접종원 농도 및 포자현탁액 침지 시간에 따라 시들음병 발생에 큰 차이를 보이지 않았다. 그러나 이들은 재배 온도에 따라 시들음병 발병도에 큰 변화를 나타냈으며, $25^{\circ}C$에서 재배하였을 때 저항성과 감수성의 차이가 가장 컸다. 따라서 양배추 시들음병에 대한 저항성을 효과적으로 검정하는 방법으로 양배추 종자를 파종하여 14일 동안 재배한 양배추 유묘의 뿌리로부터 흙을 제거하고, 이들을 F. oxysporum f. sp. conglutinans의 포자가 ml 당 $1{\times}10^7$개 농도의 포자현탁액에 30분 동안 침지한 후 원예용 상토에 이식하고, $25^{\circ}C$ 생육상에서 3주 동안 재배하는 방법을 제안한다.

• 한국응용곤충학회지
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• 제23권2호
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• pp.89-95
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• 1984

딸기${\cdot}$겹무늬 Dendrophoma obscurans에 현저한 효과를 나타내는 thiophanate-methyl과 iprodione 제에 대하여 D. obscurans의 저항성균이 포장과 실험실에서 발생 및 저항성균에 의한 이들 약제의 방제효과 저하 여부등에 대하여 검토하였다. 1. 전국 주요 딸기 산지에서 분리한 본 균의 60개균주에 대하여 저항성검정을 실시한 결과 포장에서 thiophanate-methyl 저항성균의 발생율은 약 $43\%$로서 고도저항성균 SU1과 SU2외는 저도저항성균이었다. 이에 반하여 iprodione 저항성균의 발생율은 $10\%$이었고 모두 저도저항성균이었다. 2. in vitro에서 thiophanate-methyl 저항성균은 균계 단대배양 또는 자외선 처리에 의해서도 전현 분리되지 않았으나 iprodione 저항성균은 자외선 처리 없이도 iprodione $1{\mu}g/ml$ 또는 $10{\mu}g/ml$ 첨가 PDA 배지에서 용이하게 분리되었으며 모두 고도저항성균이었다. 3 딸기 잎에서 저항성균의 접종에 의한 thiophanate-methyl과 iprodione의 방제가는 저항성균 모두 저하되었으며 고도저항성균이 저도저항성균에 비하여 현저히 불량하였다. 4. thiophanate-methyl 저항성균은 benomyl에도 저항성을 보였으나 iprodione 저항성균은 thiophanate-methyl, benomyl, captan 및 zineb 등 공시약제에 모두 교차저항성을 보이지 않았으며, captan이 감성균은 물론 thiophanate-methyl 저항성균과 iprodione 저항성균을 효과적으로 방제하였다.

• The Plant Pathology Journal
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• 제33권2호
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• pp.125-132
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• 2017

Tan spot (TS), caused by the fungus Pyrenophora tritici-repentis (Died) Drechs, is an important foliar disease of wheat and has become a threat to world wheat production since the 1970s. In this study a globally diverse pre-1940s collection of 247 wheat genotypes was evaluated against Ptr ToxA, P. tritici-repentis race 1, and stem rust to determine if; (i) acquisition of Ptr ToxA by the P. tritici-repentis from Stagonospora nodorum led to increased pathogen virulence or (ii) incorporation of TS susceptibility during development stem rust resistant cultivars led to an increase in TS epidemics globally. Most genotypes were susceptible to stem rust; however, a range of reactions to TS and Ptr ToxA were observed. Four combinations of diseasetoxin reactions were observed among the genotypes; TS susceptible-Ptr ToxA sensitive, TS susceptible-Ptr ToxA insensitive, TS resistant-Ptr ToxA insensitive, and TS resistant-Ptr ToxA toxin sensitive. A weak correlation (r = 0.14 for bread wheat and -0.082 for durum) was observed between stem rust susceptibility and TS resistance. Even though there were no reported epidemics in the pre-1940s, TS sensitive genotypes were widely grown in that period, suggesting that Ptr ToxA may not be an important factor responsible for enhanced prevalence of TS.

• 한국식물병리학회지
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• 제14권4호
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• pp.339-344
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• 1998

Since the leaf inoculation procedures are time-consuming and require considerable growth chamber space, a rapid dioassay method for screening of pathogenicity of Didymella bryoniae, a casual agent of gummy stem blight in watermelon, was established in this paper. The method produced reliable results within 8 days ( 5 days for growing seedlings and 3 days for rapid disease response in the seedlings). After contaminants in the root of 4~5 day-old seedlings had been washed using sterilized water, 5 seedlings were dipped into a vial containing 12 ml of conidial suspension (106 cells/ml). After the vials were placed in a growth chamber (22$^{\circ}C$, RH 50%, 14hr light/10hr darkness) for 3 days, susceptibility and resistance of cultivars were determined by the degree of disease response on cotyledon. The result of obtained by the dip-inoculation method was well coincided with the results by the leaf inoculation procedures and the result that had been observed for several years in the field. Screening of collected watermelon cultivars by the dip-inoculation method revealed that all the 21 domestic cultivars collected were susceptible and only 3 foreign cultivars (PI 189225, PI 482322 and IT 188207) were resistant among 18 cultivars A cucumber cultivar (Marketer) and bitter cucumber were proven to be resistant against the D. bryoniae among 8 other different cucurbits tested. The SDS-PAGE patterns of total proteins from a susceptible (Keumcheon) and a resistant (PI 189225) watermelon cultivars were compared 0, 12, 24 and 36 hrs after inoculation. The amounts of two distinct protein bands (24 kDa and 70 kDa) were gradually increased after inoculation in both cultivars.

• International Journal of Industrial Entomology and Biomaterials
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• 제11권1호
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• pp.37-42
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• 2005

We cloned the $\beta$-tubulin genes from the wild type strain and two benomyl-resistant mutants of Metahizium anisopliae and determined their nucleotide sequences. A $\beta$-tubulin encoding 448-residue protein from wild type M. anisopliae shows strong homology to other $\beta$-tubulins. The coding region is interrupted by four introns. Comparisons of intron position between the M. anisopliae gene and other fungal $\beta$-tubulin genes show considerable positional conservation. The mutations responsible for benomyl resistance were determined in two spontaneous mutants, 8-18 and 8­19. One mutant 8-18 substituted glutamate for aspar­agine at position 33 and lysine for glutamine at position 134. The other mutant 8-19 showed alterations at three positions of $\beta$-tubulin arginine for tryptophan at position 21, lysine for asparagine at position 33, and phenylalanine for leucine at position 240. These data suggest that regions of $\beta$-tubulin containing amino acids 21, 33,134, and 240 interact to form the binding site of benomyl.

• Journal of Microbiology and Biotechnology
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• 제29권11호
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• pp.1806-1816
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• 2019

Candida albicans is an opportunistic fungus possessing multiple virulence factors controlling pathogenicity. Cell wall proteins are the most important among these factors, being the first elements contacting the host. Ddr48 is a cell wall protein consisting of 212 amino acids. A DDR48 haploinsufficient mutant strain was previously found necessary for proper oxidative stress response and drug resistance. In this study, we aimed to further elucidate the role of Ddr48 by performing additional phenotypic characterization assays. A combinatory proteomic and bioinformatics approach was also undertaken to determine differentially expressed cell wall proteins. Results showed that the mutant strain exhibited a 10% decrease in adhesion mirrored by a 20% decrease in biofilm formation, and slight sensitivity to menadione, diamide, and SDS. Both strains showed similar hyphae formation, virulence, temperature tolerance, and calcofluor white and Congo red sensitivities. Furthermore, a total of 8 and 10 proteins were identified exclusively in the wild-type strain grown under filamentous and non-filamentous conditions respectively. Results included proteins responsible for superoxide stress resistance (Sod4 and Sod6), adhesion (Als3, Hyr4, Pmt1, and Utr2), biofilm formation (Hsp90, Ece1, Rim9, Ipp1, and Pra1) and cell wall integrity (Utr2 and Pga4). The lack of detection of these proteins in the mutant strain correlates with the observed phenotypes.

• 약학회지
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• 제43권6호
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• pp.716-728
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• 1999

Whole oil and ketonic fraction (KF) of Leptospermum scoparium have been tested for their antimicrobial activity and combination effect with several antibiotics against various bacterial strains and fungi by using microbiological assay methods. Antibacterial activities of KF against a number of test strains were 2-3 fold stronger than those of whole oil. MICs of the KF were $65~125{\;}{\mu\textrm{g}}/ml$ against seven gram positive bacterial strains, $65~250{\;}{\mu\textrm{g}}/ml$ against 19 methicillin resistance Staphylococcus aureus strains, and $65~50{\;}{\mu\textrm{g}}/ml$ against 14 quinolone resistance strains. However, KF showed little or no activity against gram negative bacteria. MICs of the KF were $16~250{\;}{\mu\textrm{g}}/ml$ against more than 50% of the anaerobic bacterial strains tested. KF showed the higher antibacterial activity than bacitracin against 10 strains of Bacteroids thetaiotaomicron, or three strains of Bacteroides ovatus, and the more active than ciprofloxacin against one strain of Bacteroides thetaiotaomicron and three strains of Bacteroids ovatus. The MICs of KF was 63 and $250{\;}{\mu\textrm{g}}/ml$ against Aspergillus niger and Candida albicans, respectively. Antibacterial activities of KF in combination with 19 antibiotics against 14 strains and with four antifungal agents against one fungal strain were determined by paper strip diffusion method. While most of combination showed additivity, KF showed synergism with bacitracin, exfadroxil, cephradin, and meropenem for 29~57% of the strains tested. However, ofloxacin, enoxacin, sparfloxacin showed antagonism with KF for 43~71% of the strains. KF alone and in combination with bacitracin, gentamycin, neomycin, itraconazole, fluconazole, terfinafine and ketoconazole against five bacterial strains or one fungus strain synergistic effect was demonstrated against 33% of strains examined with FIC index value below 0.5 by checkerboard study. Synergistic effect of KF with gentamicin against Staphylococcus epidermidis 329 (QRS) was found by time-kill study.

• Journal of the Korean Wood Science and Technology
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• 제47권1호
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• pp.21-32
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• 2019

In order to investigate the decay process of wood treated with preservative, waterproofing agent and their compound systems, a full-cell process was applied to impregnate the sapwood of poplar (Populus cathay) at paraffin wax emulsion concentrations of 0.5% and 2.0%, Copper Azole (CA) concentrations of 0.3% and 0.5%, and their four compound systems, respectively. Leaching tests and laboratory decay resistance against the white-rot fungus Corious versicolor (L.) Murrill for treated wood were carried out according to the America Standard E11-06 and China Standard GB/T 13942.1-2009. At certain time intervals during the decay test, samples were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction technique (XRD) to investigate the time-dependent changes of chemical components and crystalline structure, thus clarifying the decay mechanisms. The results suggested that white-rot fungi degrade hemicellulose and lignin in the wood cell wall first, followed by a simultaneous degradation of polysaccharides and lignin. Besides, CA could not only slower the decomposition of both hemicellulose and lignin, but also reduce the degradation amount of hemicellulose. However, paraffin wax emulsion at high concentration had a negative effect on the impregnation of CA for the compound system treated wood.

• 한국식물병리학회:학술대회논문집
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• 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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• pp.90.1-90
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• 2003

Colonization of Pseudomonas chlororaphis O6, a nonpathogenic rhizobacterium, on the roots induced systemic resistance in cucumber plants against tai-get leaf spot, a foliar disease caused by Corynespora cassiicola. A cDNA library was constructed using mRNA extracted from the cucumber leaves 12 h after inoculation with C. cassiicola, which roots had been previously treated with O6. To identify the genes involved in the O6-mediated induced systemic resistance (ISR), we employed a subtractive hybridization method using mRNAs extracted from C cassiicola-inoculated cucumber leaves with and without previous O6 treatment on the plant roots. Differential screening of the cDNA library led to the isolation of 5 distinct genesencoding a GTP-binding protein, a putative senescence-associated protein, a galactinol synthase, a hypersensitive-induced reaction protein, and a putative aquaporin. Expressions of these genes are not induced by O6 colonization alone. Before challenge inoculation, no increase in the gene transcriptions could be detected in previously O6-treated and untreated plants but, upon subsequent inoculation with the pathogenic fungus, transcription levels in O6-treated plants rose significantly faster and stronger than in untreated plants. Therefore, the O6-mediated ISR may be associated with an enhanced capacity for the rapid and effective activation of cellular defense responses which becomes apparent only after challenge inoculation on the distal, untreated plant parts, as suggested by Conrath et al. (2002). This work was supported by a grant R11-2001-092-02006-0 from the Korea Science and Engineering Foundation through the Agricultural Plant Stress Research Center at Chonnam National University.

• 식물병연구
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• 제22권2호
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• pp.72-80
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• 2016

D. bryoniae에 의해 발생되는 덩굴마름병은 세계적으로 수박 재배에 주요한 병으로 알려져 있으며, 본 실험은 D. bryoniae에 대한 수박의 효율적인 저항성 검정법을 확립하기 위해 수행하였다. 함안 지역에서 전형적인 덩굴마름병 병징을 보이는 수박으로부터 GBS3 균주를 분리하였고 ITS 영역의 염기서열 분석을 통해 GBS3 균주는 D. bryoniae로 동정되었다. 다양한 조건에서의 포자 형성량과 형성된 포자의 5가지 생육 시기의 수박 유묘에 대해 병원력 차이를 조사하고, 이로부터 저항성 검정을 위한 간편한 접종원 대량 생산 방법을 확립하였다. 시판 중인 수박 22개 품종의 GSB3 균주에 대한 저항성 정도를 확인하고, 그 결과로부터 저항성 정도가 다른 수박 4개 품종을 선발하였다. 그리고 접종원 농도, 습실 처리 기간, 접종 후 재배온도 등의 발병 조건에 따른 이들 품종의 덩굴마름병 발생을 조사하였다. 이들 결과로부터 덩굴마름병에 대한 효율적인 수박 저항성 검정 방법으로 본엽 2엽이 충분히 전개된 수박 유묘에 $5.0{\times}10^5spores/ml$ 농도의 D. bryoniae 포자현탁액을 분무접종하고, $25^{\circ}C$ 습실에서 48시간 동안 배양 후에 항온항습실($25^{\circ}C$, 상대습도 80%)로 이동하여 하루 12시간씩 광을 처리하면서 재배하고, 접종 3-4일 후에 접종한 잎의 병반면적률을 조사하는 것을 제안하고자 한다.