• The Plant Pathology Journal
• /
• 제22권4호
• /
• pp.381-385
• /
• 2006

Antifungal activity of Korean and Chinese lichen-forming fungi(LFF) was evaluated against plant pathogenic fungi of Botryosphaeria dothidea, Botrytis cinerea, Diaporthe actinidiae, Pestalotiopsis longiseta, Pythium sp., Rhizoctonia solani, and Sclerotium cepivorum. The LFF were isolated from Cladonia scabriuscula, Melanelia sp., Nephromopsis asahinae, Nephromopsis pallescens, Parmelia laevior, Pertusaria sp., Ramalina conduplicans, Ramalina sinensis, Ramalina sp., Umbilicaria proboscidea and Vulpicida sp. with discharged spore method. The isolates were deposited in the herbarium of Korean Lichen Research Institute(KoLRI) in Sunchon National University. The LFF of Melanelia sp., P. laevior, Pertusaria sp., R. conduplican and Ramalina sp. exhibited strong antifungal activity against all of the pathogenic fungi examined. Among them, LFF of P. laevior showed more than 90% of inhibition in fungal hyphae growth, compared with control. The results imply that LFF can be served as a promising bioresource to develop novel biofungicides. Mass cultivation of the LFF is now under progress in laboratory conditions for chemical identification of antifungal substances.

• Journal of Microbiology and Biotechnology
• /
• 제13권6호
• /
• pp.984-988
• /
• 2003

The actinomycete strain KH-6l4 possessed strong antifungal activity, especially antagonistic to the rice blast fungus, Pyricularia oryzae. Diaminopimelic acid (DAP) type and morphological and physiological characteristics, examined by scanning electron microscopy (SEM), indicated that KH-614 belonged to the genus Streptomyces. Antifungal agent produced by this strain was found to be most active, when the strain was cultured in the presence of glucose, polypeptone, and yeast extract (PY) medium for 6 days at $27^{\circ}C$. Based on the spectral report data, MS and NMR, the antifungal agent was identified as cyclo(L-leucyl-L-prolyl). According to the antimicrobial activity test measured by minimal inhibitory concentration (MIC), the cyclo(1eu-pro) exhibited the activity against Candida albicans IAM 4905, Mucor ramannianus IAM6218, Rhizoctonia solani IFO 6218, Aspergilus fumigatus ATCC 42202, Glomerella cingulata IFO 9767, Trichophton mentagrophytes ATCC 18749, and Trichophyton rubrum ATCC 44766, the order of MIC values were 50, 12.5, 5, 50, 25, 5, $5\;\mu\textrm{g}/ml$, respectively. Specifically, cyclo(1eu-pro) was one of the most effective elements against Pyricularia oryzae IFO 5994 with the MIC value of $2.5\;\mu\textrm{g}/ml$, thus indicating that cyclo(leu-pro) is a potential antifungal agent.

• Journal of Applied Biological Chemistry
• /
• 제42권1호
• /
• pp.7-11
• /
• 1999

An extracellular chitinase of the selected strong antifungal microorganism, Serratia sp. 3095, was purified by salting out, affinity adsorption, Sepadex G-100 gel fitration, Sepadex G-75 gel fitration and DEAE Sepadex A-50 chromatography. The molecular weight of the purified chitinase was estimated to be 62,000 dalton by SDS-PAGE. Optimal pH and temperature of the chitinase were pH 7.5 and 45, respectively. The enzyme retained more than 80% of the activity between pH 5.5 and pH 10.5, and below $50^{\circ}C$ but was unstable above $60^{\circ}C$, below pH 5.0. The activity of the chitinase was inhibited about 60% by $Sn^{2+}$, 40% by $Hg^{2+}$ and $Ag^+$, 70% by AHA, 40% by iodoacetate, 35% by thiourea and p-CMB, but stabilized by SDS. $K_m$ value of the purified chitinase was 3.68 mg/ml for colloidal chitin. The chitinase from Serratia sp. 3095 showed antifungal activity to Fusariurm solani.

• The Plant Pathology Journal
• /
• 제26권3호
• /
• pp.253-259
• /
• 2010

In vitro and in vivo mycofumigation effects of the volatileproducing fungus Nodulisporium sp. CF016 isolated from stem of Cinnamomum loureirii and the role of its volatile compounds were investigated against phytopathogenic fungi. The volatile compounds produced by Nodulisporium sp. CF016 inhibited and killed a wide range of plant and storage pathogens including to Pythium ultimum, Rhizoctonia solani, Fusarium oxysporum, Phytophthora capsici, Sclerotinia sclerotiorum, Colletotrichum coccodes, Magnaporthe oryzae, Alternaria panax, Botrytis cinerea and Penicillium expansum. Mycofumigation with wheat bran-rice hull cultures of Nodulisporium sp. CF016 showed in vivo antifungal activity against gray mold caused by B. cinerea and blue mold caused by P. expansum of apple. The most abundant volatile compound produced by Nodulisporium sp. CF016 was $\beta$-elemene followed by 1-methyl-1,4-cyclohexadiene, $\beta$-selinene and $\alpha$-selinene. Nodulisporium sp. CF016 could be an attractive mycofumigant in controlling postharvest diseases of various fruits including apple.

• 한국응용곤충학회지
• /
• 제13권4호
• /
• pp.205-208
• /
• 1974

전북지방의 고랭지인 무주에서 진딧물의 밀도조사를 실시한 바 다음의 결과를 얻었다. 1. 진딧물의 종류는 감자바이러스 매개진딧물 4종을 포함하여 37종이었다. 2. 진딧물의 밀도는 평야부보다 훨씬 낮다. 3. 감자바이러스 매개진딧물은 복숭아혹진딧물(Myzus persicae), 싸리수염진딧물(Aulacorthum solami), 무테두리진딧물(Lipahis erysimi), 목화진딧물(Aphis gossypii)이다. 4. 본 조사지역의 우세종은 아카시아진딧물(Aphis craccivora), 누리장진딧물(Aphis clerodendri), 무테두리진딧물(Lipaphis erysimi)이다. 5. 진딧물의 발생소장은 평야부보다 늦게 출현하고 2순쯤 빠르게 동기주로 이동한다.

• The Plant Pathology Journal
• /
• 제15권5호
• /
• pp.287-294
• /
• 1999

A technique based on the polymerase chain reaction (PCR) for the specific detection of genus Phytophthora and Phytophthora cryptogea-P. drechsleri complex group was developed using nucleotide sequence information of ribosomal DNA (rDNA) regions. The internal transcribed spacers (ITS) including 5.8S were sequenced for P. cryptogea-P. drechsleri complex group and its related species. Two pairs of oligonucleotide primers were designed. Primer pair ITS1/Phy amplified ca. 240 bp fragment in 12 out of 13 specie of Phytophthora, but not in Pythium spp., Fusarium spp.and Rhizoctonia solani. Primer pair rPhy/Pcd amplified 549 bp fragment only in P. cryptogea-P. drechsleri complex group, but not in other Phytophthora spp.and other genera. Specific PCR amplification using the primers was successful in detecting Phytophthora and P. cryptogea-P. drechsleri complex group in diseased plants.

• 한국미생물·생명공학회지
• /
• 제49권3호
• /
• pp.305-315
• /
• 2021

The cotton leafworm, Spodoptera littoralis, is a major pest in Egypt and many countries worldwide, and causes heavy economic losses. As a result, management measures to control the spread of the worm are required. S. littoralis nucleopolyhedrovirus (SpliNPV) is one of the most promising bioagents for the efficient control of insect pests. In this study, a chitinase gene (chitA) of a 1.8 kb DNA fragment was cloned and fully characterized from SpliNPV-EG1, an Egyptian isolate. A sequence of 601 amino acids was deduced when the gene was completely sequenced with a predicted molecular mass of 67 kDa for the preprotein. Transcriptional analyses using reverse transcription polymerase chain reaction (RT-PCR) revealed that chitA transcripts were detected first at 12 h post infection (hpi) and remained detectable until 168 hpi, suggesting their transcriptional regulation from a putative late promoter motif. In addition, quantitative analysis using quantitative RT-PCR showed a steady increase of 7.86-fold at 12 hpi in chitA transcription levels, which increased up to 71.4-fold at 120 hpi. An approximately 50 kDa protein fragment with chitinolytic activity was purified from ChitA-induced bacterial culture and detected by western blotting with an anti-recombinant SpliNPV chitinase antibody. Moreover, purification of the expressed ChitA recombinant protein showed in vitro growth inhibition of two different fungi species, Fusarium solani and F. oxysporum, confirming that the enzyme assembly and activity was correct. The results supported the potential role and application of the SpliNPV-ChitA protein as a synergistic agent in agricultural fungal and pest control programs.

• Parasites, Hosts and Diseases
• /
• 제60권2호
• /
• pp.143-147
• /
• 2022

Acanthamoeba keratitis (AK) is a rare ocular disease, but it is a painful and sight-threatening infectious disease. Early diagnosis and adequate treatment are necessary to prevent serious complications. While AK is frequently diagnosis via several PCR assays or Acanthamoeba-specific antibodies, a more specific and effective diagnostic method is required. This study described the production of a polyclonal peptide antibody against the periplasmic binding protein (PBP) of A. castellanii and investigated its diagnostic potential. Western blot analysis showed that the PBP antibody specifically reacted with the cell lysates of A. castellanii. However, the PBP antibody did not interact with human corneal epithelial (HCE) cells and the other 3 major causative agents of keratitis. Immunocytochemistry (ICC) results revealed the specific detection of A. castellanii trophozoites and cysts by PBP antibodies when A. castellanii were co-cultured with HCE cells. PBP antibody specificity was further confirmed by co-culture of A. castellanii trophozoites with F. solani, S. aureus, and P. aeruginosa via ICC. The PBP antibody specifically reacted with the trophozoites and cysts of A. polyphaga, A. hatchetti, A. culbertsoni, A. royreba, and A. healyi, thus demonstrated its genus-specific nature. These results showed that the PBP polyclonal peptide antibody of A. castellanii could specifically detect several species of Acanthamoeba, contributing to the development of an effective antibody-based AK diagnostics.

• 한국응용곤충학회지
• /
• 제9권1호
• /
• pp.43-48
• /
• 1970

To investigate provincial seed Potato Production farms, a Preliminary survey on the local population of the aphids was made in Sulchon alphine area, Mooju-Goon, Chollapuk-Bo where the climatic conditions were almost same as those of Taegwanryong Kangwon-Do, where Alpine Experimental station is located. This area stands from 650 to 900 metres above the sea level and divided three location of A. B, C, by altitude. A stands at 900 metres above the sea level. B at 750 metres and C at 650 metres. A and B divided three points: Al, A2, A3, and Bl, B2, B3- and divided four points-Cl, C2, C3, C4- at the distance of 300 metres apart each other. The traps were operated from July 21 to October 31, 1969. Otherwise, the traps established at Suwon (inland) and Taegwanryong where Alpine Experimental Station. A total of some 70 species including five virus vector species were identified. The Numbers of species at 10 locations, Suwon and Taegwanryong are as follows; Al-34, A2-38, A3-29, B1-25, B2-26, B3-29, C1-27, C2-14, C3-32, C4-37, species (Table 1), Suwon-49 species (including 5 virus vectors species), Taegwanryong-22 species (including 4 virus vector species). The aphids are shown in Table 1 and the Vectors are as follows: 1. Aphis gossypii Glover 2. Aulacorthum solani (Kaltenbach) 3. Lipaphis erysimi (Kaltenbach) 4. Myzus persicae(Sulzer) 5. Phorodon humuli (Schrank) Numbers of vectors versus total aphid at each locations, including inland (Suwon) and alpine area (Taegwanryong) where Alpine Experimental Station are as Fig. 1. Of a total 8,902 aphids, 6,400 $(80\%)$ were Tetraneura sp. The number of aphids devoid of the number of Tetraneura sp. are as follows; (Numbers means mean of each locations) A; 215. B; 115, C; 176 and Suwon; 2,952, Taegwanryong; 247. Densities of aphids at the locations is lower :han those at Suwon and Taegwanryong. And density of vectors at the locations, at ranged from 11 to 37, is love. than those at inland (Suwon; 197) and alpine area (Taegwanryong; 90). Thus, this area is suitable for seed potato production as Multiplication field.

• Mycobiology
• /
• 제43권3호
• /
• pp.333-338
• /
• 2015

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.