• 한국식물병리학회지
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• 제11권3호
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• pp.245-251
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• 1995

Nine hundred and ninety-two isolates of Botrytis cinerea were obtained from infected strawberries, tomatoes and cucumbers in Taejon, Gongju, Puyo, Nonsan and Kimhae in Korea. Six hundred forty-two (64.7%) isolates were benomyl resistant (BR), 245 (24.7%) were procymidone resistant (PR), and 105 (10.6%) were dichlofluanid resistant (DR). In the minimum inhibitory concentration (MIC) test, DR isolates showed mycelial growth on the PDA incorporated with 100 or 500 $\mu\textrm{g}$/ml of dichlofluanid, while dichlofluanid sensitive (DS) isolates did not grow on the PDA incorporated even with 10 $\mu\textrm{g}$/ml of dichlofluanid. Chemical concentrations for inhibition of spore germination were much lower than those for inhibition of mycelial growth. IC50 values, the effective concentrations for 50% inhibition of spore germination, for DR were 0.11~0.29 $\mu\textrm{g}$/ml, whereas they were 0.04~0.09 $\mu\textrm{g}$/ml for DS isolates. In comparison of fitness-related characteristics such as virulence, sclerotial formation, and sporulation, DR isolates were inferior to DS isolates. However, mycelial growth was little different between DR isolates and DS isolates.

• 한국식물병리학회지
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• 제11권3호
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• pp.278-281
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• 1995

An isolate of Rhizoctonia solani AG 2-2(IV) from zoysiagrass was examined on development of its teleomorph by the modified soil-on-agar culture method. The most effective growth medium for sporulation was Czapek's 1/2 agar medium added with yeast extract and peptone. The characters of teleomorph of R. solani AG 2-2 (IV) are as follows. Hymenia developed on soil surface after the development of vegetative hyphae. Basidia were barrel-shaped, short clavate or obovate and were 11.4~17.9$\times$7.1~11.4 ${\mu}{\textrm}{m}$ (mean : 15.1$\times$9.0 ${\mu}{\textrm}{m}$) in size. Sterigmata were horn-shaped and slightly bent to the inner side and 4.3~18.6 ${\mu}{\textrm}{m}$ (mean : 10.3 ${\mu}{\textrm}{m}$) in size. Two to four sterigmata developed on each basidium. Basidiospores were obovate, ellipsoid to oblong-ellipsoid, hyaline, smooth, thin walled, with an apiculus, and 3.6~10.4$\times$2.9~5.7 ${\mu}{\textrm}{m}$ (mean : 7.8$\times$4.4 ${\mu}{\textrm}{m}$) in size.

• Biotechnology and Bioprocess Engineering:BBE
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• 제10권5호
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• pp.432-443
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• 2005

Microarray technology has contributed Significantly to the understanding of bacterial genetics and transcriptional regulation. One neglected aspect of this technology has been optimization of microarray-generated signals and quality of generated information. Full genome microarrays were developed for Clostridium acetobutylicum through spotting of PCR products that were designed with minimal homology with all other genes within the genome. Using statistical analyses it is demonstrated that Signal quality is significantly improved by increasing the hybridization volume. possibly increasing the effective number of transcripts available to bind to a given spot, while changes in labeled probe amounts were found to be less sensitive to improving signal quality. In addition to Q-RT-PCR, array validation was tested by examining the transcriptional program of a mutant (M5) strain lacking the pSOL1 178-gene megaplasmid relative to the wildtype (WT) strain. Under optimal conditions, it is demonstrated that the fraction of false positive genes is 1% when considering differentially expressed genes and 7% when considering all genes with signal above background. To enhance genomic-scale understanding of organismal physiology, using data from these microarrays we estimated that $40{\sim}55%$ of the C. acetobutylicum genome is expressed at any time during batch culture, similar to estimates made for Bacillus subtilis.

• KSBB Journal
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• 제26권3호
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• pp.243-247
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• 2011

Using Bacillus subtilis spore display system, with cotG as an anchoring motif, levansucrase from Zymomonas mobilis, was displayed on the outer surface of Bacillus subtilis spore. Flow cytometry of DB104 (pSDJH-cotG-levU) spore, proved the surface localization of CotG-LevU fusion protein on the spore compared to that of DB104. Enzymatic activity of DB104 (pSDJH-cotG-levU) spore showed more than 1.5 times higher levansucrase specific activity compared to that of the host spore, which is a remarkable increase of enzymatic activity considering the existence of sacA (sucrase) and sacB (levansucrase) in the Bacillus subtilis chromosome. The spore integrity, revealed by sporulation frequency test after heat and lysozyme treatment of spore, did not changed at all in spite of the CotG-LevU fusion protein incorporation into the spore coat layer during spore formation process. These data prove again that Bacillus subtilis spore could be considered as good live immobilization vehicle for efficient bioconversion process.

• The Plant Pathology Journal
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• 제18권1호
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• pp.43-49
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• 2002

Direct effects of atmospheric ozone on conidia of the rice blast pathogen, Magnaporthe grisea, were investigated to evaluate ozone-induced effects on infection potential of the rice blast fungus. Acute ozone exposure (200 nl $1^{-1}$, 8 h $day^{-1}$3 days) during sporulation significantly affected conidial morphology, appressorium formation, and disease development on rice loaves. Ozone caused reduction in conidial size and change in conidial shape. Relative cytoplasmic volume of lipids and vacuoles were increased in ozone-exposed conidia. Inhibition of appressorium formation and simultaneous increase in endogenous levee of polyamines were found in ozone-exposed conidia. The inverse relationship between appressorium formation and level of polyamines implies that ozone-mediated increase in intracellular level of polyamines may inhibit appressorium formation in rice blast fungus. Furthermore, rice plants inoculated with ozone-fumigated conidia exhibited less severe disease development than those with unfumigated conidia. This result suggests that the anti-conidial consequence of acute ozone will eventually weaken the rice blasts potential for multiple infection cycle. This further suggests that consequently, rice blast can be transformed from an explosive disease to one that has limited epidemiological potential in the field.

• The Plant Pathology Journal
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• 제17권6호
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• pp.357-360
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• 2001

Gray mold was observed on leaves of castor bean grown in Woniu and Okcheon in Korea in October 2000. Symptoms developed in the form of spot and blight with sporulation of the causal fungi at the marginal or central parts of the leaves. A total of 25 isolates were obtained from the infected leaves of castor bean. Out of the 25 isolates, 5 isolates which originated from Woniu were identified as Botrytis cinerea, while 20 isolates from Okcheon were identified as Amphobotrys ricini based on morphological and cultural characteristics. Two isolates each of B. cinerea and A. ricini were tested for their pathogenicity to castor bean plants. Gray mold symptoms similar to those observed in the fields were induced on leaves of castor bean by artificial inoculation. This is the first report of gray mold in castor bean caused by B. cinerea and A. ricini in Korea.

• International Journal of Industrial Entomology and Biomaterials
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• 제18권2호
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• pp.125-129
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• 2009

Entomopathogenic fungi were isolated directly from a cadaver of adult Monochamus alternatus supporting fungal sporulation, using a semi-selective medium and then screened several fungal colonies. The pathogenicity of each fungus was tested using oak longicorn beetle, Moechotypa diphysis, as substitutive insect. As the result, only one of them showed high pathogenicity against M. diphysis, with up to 100% mortality within 21 days of inoculation. Selected fungus was named as MaW1 and identified by Beauveria bassiana using microscopic examination and DNA analysis. Pathogenicity was also evaluated to M. alternatus.

• 환경생물
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• 제22권4호
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• pp.487-493
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• 2004

To investigate the antifungal activity related protein in pesticidal bacteria, a bacterial strain LTD was isolated from soil collected at Gimje in Jeonbuk province, Korea, and identified as Bacillus subtilis LTD based on a API50 CHB kit and 168 rDNA sequencing. It has an antifungal activity against 9 plant pathogenic fungi in a paper disc assay. The antifungal activity- deficient mutant, B. subtilis mLTD was induced at a 5 kGy dose of $^{60}Co$ gamma radiation. Using the two-dimensional electrophoresis and the matrix assisted laser desorption ionization time-of-flight mass spectrometry, the comparison analysis of proteins between the wild and mutant were performed. A major intracellular serine proteinase IspA (MW: 32.5 kDa), a NAD (P) H dehydrogenase (MW: 20.0 kDa), and a stage II sporulation protein AA, SpoIIAA (MW: 14.3kDa) were detected only in the B. subtilis LTD. These results suggested that the functions of these proteins found only in the B. subtilis LTD could. be closely related to the antifungal activity against plant pathogenic fungi.

• 미생물학회지
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• 제28권2호
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• pp.162-168
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• 1990

토양에서 분리한 방사균 주에서 호염기성 단백질 분해효소의 생합성과 세포분화와의 관계를 규명하고자 기균사와 포자의 형성, 그리고 단백질 분해효소의 생산에 대한 배양조건의 영향을 조사하였다. 그 결과, 기질의 농도가 단백질 분해효소, 포자, 그리고 기균사의 형성의 조절에 매우 중요하며 이것은 배양액의 pH가 산성으로 변화기 문임을 알았다. 인산염완충용액을 이용하여 배양액의 pH를 6으로부터 9로 조정하여 주었을 때 단백질 분해효소의 생성은 pH가 증가함에 따라 증가하였다. 이와 같은 결과로부터 배양액의 pH가 호염기성 단백질 분해효소 생합성의 조절에 중요한 요소로 작용한다고 판단하였다. 판단하였다.

• Journal of Applied Biological Chemistry
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• 제56권3호
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• pp.165-170
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• 2013

The SCO3388 gene from Streptomyces coelicolor is homologous to tmrB, the tunicamycin resistance gene of Bacillus subtilis. The SCO3388-inactivation strain (SY-tbl-1) was generated by replacing SCO3388 with thiostrepton resistance gene. Spores of S. coelicolor derivatives were prepared on mannitol-soy flour (MS) agar on which SY-tbl-1 displayed no significant defect in growth and development. When plated on R4 agar, spores of SYtbl-1 displayed retardation in growth and sporulation, whereas its mycelium gave rise to normal growth. Thus, SCO3388 is suggested to be involved in the dormant spore germination. Expression of SCO3388 under the ermE1 promoter restored but only partially the ability to sporulate in SY-tbl-1. Neither SY-tbl-1 nor SY-tbl-1/ermE1p-SCO3388 showed a difference in tunicamycin resistance to the wild type whereas, interestingly, the introduction of ermE1p-SCO3388 dramatically enhanced spore survival to heat and detergent treatments, suggesting that SCO3388 might play a role in the maintenance of spore cell wall integrity.