• Mycobiology
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• v.28 no.1
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• pp.33-38
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• 2000

Mycelium of Hericium erinaceum isolate KU-1 was cultured in liquid medium (HL medium) and solid medium (Ko medium) at pH 4.0 in $28^{\circ}C$. 1.0% glucose or fructose was the most favorable carbon source, and 0.2% amonium acetate or $NaNO_3$ was an exellent nitrogen source for mycelial growth as well as production of antimicrobial substances. The mixture of saw dust 70% with rice bran 30% (SR medium) was the substrate for formation of sporophores. The active substrates in extracts from mycelium, culture filtrate and fruiting body were separated by TLC. The solvent for TLC was EtOAc: Chloroform: MeOH (10 : 5 : 10). Phenol-like substances appeared at Rf $0.5{\sim}0.9$, and fatty acid-like substances appeared at Rf $0.1{\sim}0.2$. The purified materials from the extracts showed antimicrobial effects to Escherichia coli, Bacillus subtilis, Staphylococcus aureus, Aspergillus niger, Candida albicans and Microsporum gypseum. The S. aureus was the most inhibited. Minimal inhibitory concentration (MIC) of purified white powder and the Hercenone derivatives against S. aureus were $5.65\;{\mu}g/ml$ and $1.85\;{\mu}g/ml$, respectively.

• Korean Journal of Veterinary Research
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• v.40 no.1
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• pp.94-100
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• 2000

This study was carried out to determine the causative agent and the epidemiological features of canine dermatitis in Tae-gu, Korea from 1997 to 1998. Specimens of collected from skin lesions were examined mycologically, parasitologically and bacteriologically. In all, 70 dogs of differing ages, gender and living environment were sampled. In mycological examination during this period, pathogenic fungi were cultured from 29(41.3%) of 70 canine specimens. Dermatophytes were cultured from 15(21.4%) and Malassezia pachydermatis were 14(20.0%) of the specimens. The frequent dermatophytes isolated were Microsporum canis (12.9%). Trichophyton mentagrophytes (4.3%), T rubrum (2.9%), T raubitschekii and M gypseum (each 1.4%). There was a high proportion of positive cultures from dogs less than 1 year and over than 3 years of age, and in some long haired breeds, but there was no significant difference between the sexes, and the living environments. Although dermatophytes were more frequently isolated in spring and winter, no significant difference was detected in the seasonal distribution of the canine dermatophytosis. Out of 70 dogs, dermatitis ectoparasites(27.1%; Demodex canis 18.6% and Sarcoptes scabie 8.6%) and bacterial pyoderma(40.4%) were diagnosed. Demodex canis and Sarcoptes scabie were common canine ectoparasites, with a higher incidence in short haired breeds and in summer and winter. Bacterial pyoderma was a higher incidence in long haired breeds, and in summer. In the pathogenic agents isolated from 57 dogs(81.4%), single infection rate was 66.7%(38 dogs) and mixed infection rate was, 35.1%(19 dogs). In the majority of mixed infection cases, Gram positive cocci and Malassezia pachydermatis (in 5 cases, 8.8%), as well as ectoparasites(in 6 cases, 10.5%) were demonstrated simultaneously.

• Journal of the Korean Wood Science and Technology
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• v.38 no.3
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• pp.242-250
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• 2010

The aim of this study was to investigate the terpenoids of Total Volatile Organic Compounds (VOCs) released during drying of Cryptomeria japonica using the thermal extractor (TE). Considering the drying process of C. japonica, temperatures of TE were set at $27^{\circ}C$, $60^{\circ}C$, $80^{\circ}C$, $100^{\circ}C$, and $120^{\circ}C$, respectively. As the result, the emission factors of VOCs and terpenoids were increased as temperature increased. The amount of terpenoids included in VOCs emission factors were 87.5%, 81.6%, 83.6%, 90.1%, and 97.3% depending on above temperatures, respectively. Especially at$100^{\circ}C$ and $120^{\circ}C$, the amount of terpenoids were measured more than 90%. ${\delta}$-cadinene was the highest yield at each temperature and 32 types of terpenoids were collected. Emitted terpenoids were classified into the sesquiterpene group which consists of 15 carbon sources. These 32 sesquiterpenes were used for determining the useful bioactivity such as antifungal activity by the agar dilution. As the result, they showed the antifungal activity against Trichophyton rubrum, Trichophyton mentagrophytes, Microsporum gypseum. The 5,000 ppm concentration of terpenoids showed a strong activity with 100% against the 3 fungi. At the 1,000 ppm concentration of terpenoids, the antifungal activities against three fungi were 95.2%, 98.7%, and 97.3%, and their activities were a little inhibited at 100 ppm concentration.

• Biomedical Science Letters
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• v.20 no.3
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• pp.139-146
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• 2014

Accurate and rapid diagnosis of dermatophytosis, a disease whose prevalence has been steadily increased, is important for successful treatment. Current laboratory methods for diagnosing dermatophytosis rely on KOH mount and fungal culture method. However, these methods have low sensitivity and are time-consuming (2~4 weeks to diagnosis). In our previous study, a rapid molecular diagnostic assay (PCR-reverse blot hybridization assay, REBA) was developed to identify the following 6 main species of dermatophytes: Trichophyton rubrum, T. mentagrophytes, T. tonsurans, Microsporum canis, M. gypseum, and Epidermophyton floccosum. However, the REBA required more evaluation to validate its use in clinical examinations. The aim of the present study was to evaluate and validate the ability of the PCR-REBA to successfully identify dermatophytes in clinical isolates from dermatophytosis patients. Both conventional identification methods and the PCR-REBA were used to assess the presence of species of dermatophytes in 148 clinical isolates. The results of the two approaches were compared, and discrepancies between the two approaches were resolved by fungal ITS1 sequence analysis. T. rubrum was the most prevalent dermatophyte identified by conventional identification methods (118/148, 79.7%) and the PCR-REBA (131/148, 88.4%). The overall rate of consistency between conventional identification methods and the PCR-REBA was 79.0% (117/148 samples). Fungal ITS1 sequence analysis showed that PCR-REBA results were correct for 93.5% (29/31) of the discrepant samples. The PCR-REBA is rapid, sensitive, and highly specific compared with conventional identification methods. Thus, the PCR-REBA is a potentially useful tool for identifying dermatophytes in clinical settings.