• The Plant Pathology Journal
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• v.18 no.2
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• pp.68-73
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• 2002

The influence of fungicidal spray was assessed on powdery mildew epidemics caused by Erysiphe polygoni D.C. and on yield-attributing characters of mungbean [Vigna radiata (L.) Wilczek]. Mildew attack adversely affected the yield-attributing characters of mungbean and exhibited negative significant correlation with pod length (-0.57), pods/plant (-0.74), pod weight (-0.68), 100 seeds weight (-0.69), 100 seeds swell weight (-0.59), and seed germination (-0.71). These characters had direct or indirect effects on grain yield, which was also adversely affected due to mildew attack (-0.89). Powdery mildew was significantly retarded due to the single spray of carbendazim (0.05%) at 30-day-old crop, where the apparent rate of infection (r) was minimum at 0.0095/ unit/day and with low (11.44%) powdery mildew intensity. Other fungicides like tridemorph (0.075%) and penconazole (0.05%) were equally effective against the mildew disease where the disease intensity was less than 20% and the values of r were 0.0134 and 0.039/unit/day respectively, as compared with the control at 0.267/unit/day. Fungicide spray influenced the yield-attributing characters besides controlling the disease. Such effects were more pronounced in carbendazim (0.05%)-treated plots due to its phytotonic nature where pod length (7.59cm), pods/plant (29.75), pod weight (8.16 g), 100 grain weight (3.94 g), and swell weight of 100 seed (9.49 g) were maximum resulting to the highest yield (480 kg/ha) as compared with that of control (224 kg/ha). Spray of carbendazim also improved seed germination (74.5%). Spray of other fungicides like carbendazim with copper oxychloride in 1:1 ratio, tridemorph (0.075%), and penconazole (0.05%) was equally effective against powdery mildew of mungbean. These fungicides also exhibited positive effects on yield-attributing characters of the crop and finally increased yield. These systemic fungicides were more effective in controlling powdery mildew disease of V. radiata in the rainy season compared with wettable sulphur.

• Microbiology and Biotechnology Letters
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• v.39 no.4
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• pp.387-389
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• 2011

A previous study of ours indicated that Citrus auranifoli oil possesses antifungal activity against Malassezia furfur and Malassezia pachydermatis. In this study, we evaluated the anti-M. furfur and M. pachydermatis activities of limonene, which is a major component of C. aurantifolia oil, using the disk diffusion method. We also examined cytotoxicity against human normal epithelial (Beas-2B) cells using the cytopathic effect reduction (CPE) method. The results revealed that the minimum fungicidal concentration (MFC) value of limonene is lower than the value for itraconazole. The MFC value of limonene was seen to be 7.81 ${\mu}g$/mL against M. furfur and 3.90 ${\mu}g$/mL against M. pachydermatis. MFC values of itraconazole against M. furfur and M. pachydermatis were 62.50 ${\mu}g$/mL and 31.25 ${\mu}g$/mL, respectively. In addition, it was noted that limonene was not toxic to Beas-2B cells with normal morphology at a concentration of 100 ${\mu}g$/mL. However, itraconazole exhibited weak toxicity at the same concentration. Therefore, our results indicate that limonene could potentially be effective at controlling M. furfur and M. pachydermatis infections with no cytotoxicity.

• Applied Biological Chemistry
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• v.37 no.4
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• pp.287-294
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• 1994

New 3-phenyl-1-(2-furyl)propenones, 1 and 3-phenyl-1-(2-furyl)-3-thiophenyl-propanone, 2 derivatives were synthesized, and their fungicidal activities in vitro against Botrytis cineria (BC), Valsa ceratosperma (VC), Scelerotium cepivorum (SC) and Phytophthora capsici (PC) were investigated using a generalized structure-activity relationship (SAR). The activity of 1 was superior to those of 2, and nonsubstituent, 1a and chloro group substituent, 1d of E (Syn) conformer were the most effective $(EC_{50}=10{\sim}12\;ppm)$ compound to BC. Antifungal activities were able to predict to depend essentially on the ${\beta}$ carbon and their positive charge from the results that the good correlation $(r^2=0.90)$ was observed between hydrolysis rate constant (logk) of 1 and the electronic parameter $({\sigma})$ of X-substituent on the ${\beta}-phenyl$ ring.

• Korean journal of applied entomology
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• v.7
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• pp.77-81
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• 1969

The effects of submerged method. Zentmyer's drench method. pot test and field test with materials such as Carbamisol (ammonium methyldithiocarbamic acid $30\%$), NCS (ammonium N-methyldithiocarbamate$50\%$, Similuton(ethyl phenethynylmeroury $3.3\%$), Soill(N-ethylmercuric p-toluensulfonanilide $4\%$, Captan (N-trichloromethylthio-1, 2, 3, 6-tetra-hydrophthalimide $80\%$), Difolatan(N-tetrachloroet-hylthio 4cyelohexeno-1,2-dicarboximide $80\%$, Grand(2, 3-dibromepropionitryl $20\%$, trichloronitroethylene $20\%$) and Calcium hydroxide upon occurrence of Fusarium wilt of cucumber were studied. The results are summarized as follows. 1. According to submerged method, all the compounds tested were highly inhibitory to mycelial growth of Fusarium oxysporum f. cucumerinum except calcium hydroxide. But several compounds were no inhibitory to the causal fungus except Grand and Similuton, with Zentmyer's drench method. 2. Grand was the most effective fungicide for the control of cocumber Fusarium wilt in the pot test, and followed by Similuton and calcium hydroxide. The population of Fusarium oxysporm was markedly reduced when soil was treat with Grand compared with other chemicals. 3. Fungicidal effects upon occurrence of Fusarium wilt of cucumber under the field experiment varied with the fungicides. Of the fungicides tested. Grand gave the best control, and followed by Difolatan.

• Korean journal of applied entomology
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• v.9 no.1
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• pp.1-6
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• 1970

Cadmium pentachlorophenolxanthate has been synthesized with pentachlorophenol, carbondisulfide sodium hydroxide and cadmium chloride and its fungicidal activity was tested to Pyricularia oryzae and Cochliobolus miyabeanus. The results are summarized as followes; 1) The sample V synthesized by acidifying the crude PCP-xanthate solution at pH 8, then treated with $BaCl_2\;and\;CaC_2$ showed the highest purity, and the yield was $85.1\%$. 2) The same sample of $50\%$ wettable dust formulation inhibited conidial germination of P. oryzae and C. miyabeanus completely at 10 and 20 ppm, respectively. (Fig. 1) 3) The sample of $1.5\%$ dust formulation inhibited mycelial growth of P. oryzae and C. miyabeanus with 96 and $65\%$, respectively. The results were similar to those obtained by Ceresan calcium (Fig. 2) 4) Both dust and wettable powder formulations had no phytotoxcity on rice seedlings.

• Korean Journal of Microbiology
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• v.33 no.3
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• pp.170-174
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• 1997

In order to design a novel synthetic peptide with improved fungicidal activity but low hemolytic activity, a hybrid peptide, cecropin A(l-8)-magainin 2(1-12), and its analogue peptides were synthesized by the solid phase method. Antifungal and hemolytic activities of the synthetic peptides were assessed by the growth inhibition against Trichosporon beigelii and the cell membrane lysis against human red hlood cells, respectively. Analogue 2 in which Lys at position 12 in cecropin A(1-8)-magainin 2(1-12) was substituted with Ala showed most potent antifungal activity (MIC: 2.5.$\mu$g/ml) with minimal hemolytic activity (0.5% hemolysis at the (200.$\mu$g/ml peptide). This peptide (A2), therefore, could be useful as a model for further designing potent antifungal peptides without cytotoxicity.

• Applied Biological Chemistry
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• v.35 no.5
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• pp.382-388
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• 1992

Mycelial growth inhibition activity of forty-one N-substituted phenyl 5-chloro-1,3-dimethylpyrazole-4-carboxamides against Rhizoctonia solani was analysed quantitatively by multiple regression analysis using physicochemical parameters of substituents as independent variables and $pEC_{50}$ as dependent variable. As a result, a quantitative structure-activity relationship was formulated using eight physicochemical parameters, which explains 83% of variance of the fungicidal activity. The most important parameter for the biological activity was log k', as related to the penetration and transport processes in the biological system. The activity also correlated with other hydrophobic parameters$({\pi}_2,\;{\pi}_3)$, an electronic parameter$({\Sigma}{\sigma})$, and steric parameters$(STERIMOL\;parameters\;L_3,\;L_4)$.

• Korean Journal of Pharmacognosy
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• v.5 no.3
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• pp.147-154
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• 1974

Some crude drugs in ancient literatures have been used as traditional therapeutic agent of leucorrhea mainly caused by Trichomonas vaginalis and Candida albicans. Sixty six kinds of crude drugs in ancient literatures and ten constituents were selected as sample drugs. Trichomycin standard was tested to compare with the above drugs. To determine the anti-fungal effect of these drugs on Candida albicans Yu 1200, a test organism, screening test was conducted. Antifungal activities of crude drug water extracts were observed by means of two test methods : firstly through the agar slant method and secondly the counting chamber method which was used for acknowledged drug agents upon the result of the agar slant method. And in order to improve the fungicidal effect, the organisms were stained with 0.02% methylene blue solution. The results of the above test indicated that Fritillariae Rhizoma has antifungal action in the concentration of 310mcg/ml, Coptidis Rhizoma in 620mcg/ml, Meliae Cortex, Scutellariae Radix both in 5,000mcg/ml. Baicalin, catechol among the pure isolated constituents inhibited in the range of 50mcg/ml. This score was based on 50% inhibition in comparison with amounts of control organisms. Rhei Rhizoma, Mori Radicis Cortex, Linderae Radix, and Amomi globosi Fructus showed the antifungal effect moderately in 5,000mcg/ml, and baicalein and pectolinarin in 50mcg/ml in the limit of between 35% and 50% antifungal activity. Staining with 0.02% methylene blue showed that any of the crude drug extracts was unable to stain the cells, but trichomycin in 0.86unit/ml able to stain 12% of the cells. This result means that crude drugs probably do not have fungicidal but fungistatic action.

• Horticultural Science & Technology
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• v.31 no.5
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• pp.633-639
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• 2013

Fungicide applications are required to prevent the strawberry from Botrytis fruit rot and powdery mildew that infect open strawberry flowers, however, their effects of fungicides on pollen germination of strawberry have been rarely documented, particularly those from recently developed active fungicidal ingredients. In this study we have evaluated the effects of 24 commercial fungicidal formulations and 6 organic materials on pollen germination in 3 strawberry cultivars using in vitro assays. Pollens from strawberry had higher germination rates on agar with sucrose of 18% and $25^{\circ}C$ than other tested conditions. Pollen germination rates of cvs. Seolhyang, Maehyang, and Kumhyang at 18% sucrose and $25^{\circ}C$ were 15.3, 18.4 and 30.7%, respectively. Pyraclostrobin, azoxystrobin, kresoxim-methyl, dichlofluanid, iminoctadine tris, and sulfur showed the strongest inhibitory efficacy with the germination rates of more than 93.8% compared to the no-fungicide control. Germination was not significantly affected by simeconazole and procymidone. This in vitro germination study may provide information useful for selecting fungicides in flowering stage to strawberry farmers.

• Journal of the Korean Wood Science and Technology
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• v.48 no.1
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• pp.107-116
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• 2020

Termiticidal and fungicidal activities of wood vinegar from Cinnamomum parthenoxylon (CP) stem wood have been evaluated against Coptotermes curvignathus and wood rotting fungi (Schizophyllum commune and Fomitopsis palustris). The utilized CP wood vinegar was produced in the operating temperature range 250-300℃ pyrolysis. A no-choice test was applied for evaluating termiticidal activity with 33 active termites and antifungal activity using the agar media assay. The result showed that an increase in the concentrations of CP wood vinegar significantly raised the mortality of termite. CP wood vinegar showed high termiticidal activity, organic acids (acetic acid 42.91%, 3-butenoic acid 6.89%, butanoic acid, 2-propenyl ester 2.26%), and ketones (1-hydroxy-2-propanone 5.14%, 3-methylcyclopentane-1,2-dione 2.34%) might be largely contributed to termiticidal activity in addition to other minor components. Furthermore, CP wood vinegar exhibited significant inhibition of fungal growth. These data showed that CP wood vinegar was more toxic to white-rot fungi (S. commune) than brown-rot (F. palustris). The results suggested that phenolic compounds from lignin degradation were responsible for good antifungal activity.