• Mycobiology
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• 제42권2호
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• pp.174-180
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• 2014

We analyzed the genetic diversity of Cylindrocarpon destructans isolates obtained from Korean ginseng (i.e., Panax ginseng) roots by performing virulence tests and nuclear ribosomal gene internal transcribed spacer (ITS) and mitochondrial small subunit (mt SSU) rDNA sequence analysis. The phylogenetic relationship analysis performed using ITS DNA sequences and isolates from other hosts helped confirm that all the Korean C. destructans isolates belonged to Nectria/Neonectria radicicola complex. The results of in vivo and ex vivo virulence tests showed that the C. destructans isolates could be divided into two groups according to their distinctive difference in virulence and the genetic diversity. The highly virulent Korean isolates in pathogenicity group II (PG II), together with foreign isolates from P. ginseng and P. quinquefolius, formed a single group. The weakly virulent isolates in pathogenicity group I, together with the foreign isolates from other host plants, formed another group and exhibited a greater genetic diversity than the isolates of PG II, as confirmed by the mt SSU rDNA sequence analysis. In addition, as the weakly virulent Korean isolates were genetically very similar to the foreign isolates from other hosts, they were likely to originate from hosts other than the ginseng plants.

• 농업과학연구
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• 제10권2호
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• pp.269-276
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• 1983

전국(全國)에서 수집(收集)한 50개(固) 참깨종자(種子) sample을 blotter법(法)으로 조사(調査)하였던 바 Alternaria sesami는 29개(固) sample에서 최고(最高) 37%, Corynespora cassiicola는 38개(固) sample에서 최고(最高) 76%의 높은 비율(比率)로 검출(檢出)되었다. A. sesami와 C. cauiicola에 각각(各各) 심(甚)하게 이병(罹病)된 종자(種子)는 종자부패(種子腐敗)를 일으켜 전혀 발아(發芽)하지 못하며 일부(一部) 이병(罹病)된 종자(種子)는 발아(發芽)하더라도 곧 유묘감염(幼苗感染)이 되어 유근(柳根)이나 자엽(子葉)의 일부(一部)가 갈변(褐變)하며 고사(枯死)하였다. 종자전염성(種子傳染性) A. sesami와 C. cassiicola에 대(對)한 몇가지 종자소독제(種子消毒劑)의 효과(效果)를 조사(調査)하였던 바 A. sesami의 종자감염(種子感染)에 대(對)하여는 Busan 30의 소독효과(消毒效果)가 높았고 C. cassiicola의 종자감염(種子感染)에 대(對)하여는 Benlate T와 Homai의 소독효과(消毒效果)가 탁월(卓越)하였다.

• 한국미생물·생명공학회지
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• 제18권4호
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• pp.437-441
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• 1990

근채류 식물의 근부원인이 되는 식물병원균 Fusarium solani의 생육을 강력히 길항하는 생물반제균 Pseudomonas stutzeri YPL-1을 모균주로 하여 UV나 NTG로 돌연변이시킴으로써 길항능이 증강된 강력한 생물방제균을 유전적으로 육종하고자 하였다. 그 결과 길항기작의 원인인 외막가수분해효소 chitinase 생산능이 2.5배, 2.0배 정도로 증강된, 동시에 길항능도 모균주에 비해 1.7배, 1.5배 정도로 비례해서 증강된, 강력한 우수 길항변이주 P.stutzeri YPL-M26(UV)과 P.stutzeri YPL-M178(NTG)을 유전적으로 육종할 수 있었다. 길항종강변이주에 의한 F.solani의 생육억제기작도 모균주에서와 같이 고분자 물질인 chitinase를 주로 하는 외막가수분해효소에 의한 것으로 확인되었고, 균사신장억제율도 조사해 본 결과 조효소액 첨가 경우 24시간째에는 모균주 경우 87.1 정도인데 비해 거의 100의 생육억제율을 나타내는 강력한 생물반제균으로 유전적 육종을 할 수 있었다. 한편 변이주와 모균주의 효소에서도 그 최적반응 pH등 각종 효소학적 특성이 동일하였다.

• Weed & Turfgrass Science
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• 제2권3호
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• pp.306-311
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• 2013

Pythium aphanidermatum에 의한 잎마름병(pythium blights)이 chewing fescue "Jamestowm II" 품종에서 2011년 6월 상순에 대구대학교 시험포장에서 발생하였다. 잔디에 발병증상은 잎 끝으로부터 잎마름 증상과 뿌리 썩음증상이 나타나고, 잎색은 진한갈색,회 갈색으로 나타났다. 병원균은 병든 잎과 지제부에서 분리를 하였으며, 동정을 위하여 PDA에서 배양하였다. 균사에는 잎 같은 포자가 복잡한 구조로 부풀어져 있고, 균사로부터 구별되지 않은 실같은 포자낭이 있다. 리보소옴 DNA의 염기서열을 분석한 결과, 유전자은행 DB에 P. aphanidermatum 균주 와의 100% 상동성을 나타낸다는 것을 확인하였다. 병원성은 chewing fescue, creeping bentgrass 및 Kentucky bluegrass에서 코흐의 원칙에 따라 확인하였다. 이것은 chewing fescue 종에서 P. aphanidermatum 에 의한 잎마름병을 국내에서 처음보고 한다.

• 한국식물병리학회지
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• 제14권5호
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• pp.452-457
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• 1998

Thirty-eight isolates of Phytophthora sp. caused rots on roots and basal stems were collected from five flowering plants from 1992 to 1997 at eight cultivation areas in Korea. All the isolates were identified as P. nicotianae based on following characteristics. The fungus produced markedly papillate, not caducous and ovoid to spherical sporangia, abundant chlamydospores, and small oospores with amphigynous antheridia only when paired with either A1 or A2 mating type. All isolates grew well at 35$^{\circ}C$ and showed distinct arachnoid colony patterns on CMA and PDA. Sizes of sporangia and chlamydospores of five representative isolates from each plant averaged 43-52$\times$30-38 ${\mu}{\textrm}{m}$ and 28 ~34 ${\mu}{\textrm}{m}$. Mating type of the isolates was either A1 or A2, and oogonia and oospores were measured as 28~31 ${\mu}{\textrm}{m}$ and 21~25 ${\mu}{\textrm}{m}$. PCR-RFLP analysis of rDNA of the five isolates resulted that restriction band patterns of the small subunit and ITS regions were identical to a perilla isolate of P. nicotianae, but distinct from P. cactorum and P. capsici. Cross inoculation tests showed that the five isolates had pathogenicity to lily, christmas cactus, anthurium, baby's breath and carnation with different degrees. However, each isolate showed stronger pathogenicity to its corresponding original host than others. Among five lily cultivars Georgia and Quririna were more susceptible than Napoli and others. This is first report of Phytophthora root and stem rot of lily, Christmas cactus, anthurium, baby's breath and monochoria in Korea.

• Mycobiology
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• 제34권2호
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• pp.99-103
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• 2006

Toxicity of the fungicide Flutolanil was in vitro tested against 20 isolates of Macrophomina phaseolina and cotton seedlings of ten commercial cotton cultivars. The isolates were recovered from roots of cotton plants obtained from different cotton-growing areas in Egypt. Most of the tested isolates were sensitive to Flutolanil; however, they varied in sensitivity. Twenty-five percent of the isolates were highly sensitive where $IC_{50}$ ranged from < 1 to $5.1{\mu}g/ml$, 20% of the isolates were sensitive where $IC_{50}$ ranged from 15 to $30{\mu}g/ml$, 45% of the isolates were moderately sensitive where $IC_{50}$ ranged from 46 to $58.5{\mu}g/ml$, and 10% of the isolates were not much sensitive (tolerant) where $IC_{50}$ was > $100{\mu}g/ml$. Flutolanil was very safe on both shoots and roots of the tested cultivars ($IC_{50}\;>\;100{\mu}g/ml$). Treating cotton seeds with Flutolanil resulted in highly significant (P < 0.01) reductions in pathogenicity of 18 isolates and a significant reduction (P < 0.05) in pathogenicity of isolate $M_{29}.\;M_{1}$ was the only isolate, which was insensitive to the application of Flutolanil. In vivo toxicity to Flutolanil was not correlated with its in vitro toxicity. However, a highly significant correlation (r = 0.60, P < 0.01) was observed between pathogenicity of isolates and the in vivo toxicity of the fungicide.

• Journal of Microbiology and Biotechnology
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• 제20권12호
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• pp.1605-1613
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• 2010

Twenty-nine P. polymyxa strains isolated from rhizospheres of various crops were clustered into five genotypic groups on the basis of BOX-PCR analysis. The characteristics of several plant growth-promoting factors among the isolates revealed the distinct attributes in each allocated group. Under gnotobiotic conditions, inoculation of pepper roots with P. polymyxa isolates significantly increased the biomass in 17 of total 29 treated plants with untreated plants. Experiments on induced systemic resistance (ISR) against bacterial spot pathogen Xanthomonas axonopodis pv. vesicatoria in pepper by P. polymyxa strains were conducted and only one isolate (KNUC265) was selected. Further studies into ISR mediation by the KNUC265 strain against the soft-rot pathogen Erwinia carotovora subsp. carotovora in tobacco demonstrated that the tobacco seedlings exposed to either bacterial volatiles or diffusible metabolites exhibited a reduction in disease severity. In conclusion, ISR and plant growth promotion triggered by P. polymyxa isolates were systemically investigated on pepper for the first time. The P. polymyxa KNUC265 strain, which elicited both ISR and plant growth promotion, could be potentially used in improving the yield of pepper and possibly of other crops.

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

• Journal of Ginseng Research
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• 제4권1호
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• pp.104-120
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• 1980

The effects of temperature on transpiration, chlorophyll content, frequency and aperture of stomata, and leaf temperature of Panax ginseng were reviewed. Temperature changes of soil and air under spade roof were also reviewed. Growth responses of responses of ginseng plant at various temperature were assessed in relation to suseptibillity of ginseng plants. Reasonable management of ginseng fields was suggested based on the response of ginseng to various temperatures. Stomata frequency may be increased under high temperature during leaf$.$growing stage. Stomata aperture increased by high temperature but the increase of both frequency and aperture appears not enough for transpiration to overcome high temperature encountered during summer in most fields. Serial high temperature disorder, i.e high leaf temperature, chlorophyll loss, inhibition of photosynthesis, increased respiration and wilting might be alleviated by high humidity and abundant water supply to leaf. High air temperature which limits light transmission rate inside the shade roof, induces high soil temperature(optimum soil temperature 16∼18$^{\circ}C$) and both(especially the latter) are the principal factors to increase alternaria blight, anthracnose, early leaf fall, root rot and high missing rate of plant resulting in poor yield. High temperature disorder was lessen by abundant soil water(optimum 17∼21%) and could be decreased by lowering the content of availability of phosphorus and nitrogen in soil consequently resulting in less activity of microorganisms. Repeated plowing of fields during preparation seems to be effective for sterilization of pathogenic microoganisms by high soil temperature only on surface of soils. Low temperature damage appeared at thowing of soils and emergence stage of ginseng but reports were limited. Most limiting factor of yield appeared as physiological disorder and high pathogen activity due to high temperature during summer(about three months).

• Journal of Ginseng Research
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• 제44권2호
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• pp.332-340
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• 2020

Background: The valuable medicinal plant Panax ginseng has high pharmaceutical efficacy because it produces ginsenosides. However, its yields decline because of a root-rot disease caused by Ilyonectria mors-panacis. Because species within Ilyonectria showed variable aggressiveness by altering ginsenoside concentrations in inoculated plants, we investigated how such infections might regulate the biosynthesis of ginsenosides and their related signaling molecules. Methods: Two-year-old ginseng seedlings were treated with I. mors-panacis and I. robusta. Roots from infected and pathogen-free plants were harvested at 4 and 16 days after inoculation. We then examined levels or/and expression of genes of ginsenosides, salicylic acid (SA), jasmonic acid (JA), and reactive oxygen species (ROS). We also checked the susceptibility of those pathogens to ROS. Results: Ginsenoside biosynthesis was significantly suppressed and increased in response to infection by I. mors-panacis and I. robusta, respectively. Regulation of JA was significantly higher in I. robusta-infected roots, while levels of SA and ROS were significantly higher in I. mors-panacis-infected roots. Catalase activity was significantly higher in I. robusta-infected roots followed in order by mock roots and those infected by I. mors-panacis. Moreover, I. mors-panacis was resistant to ROS compared with I. robusta. Conclusion: Infection by the weakly aggressive I. robusta led to the upregulation of ginsenoside production and biosynthesis, probably because only a low level of ROS was induced. In contrast, the more aggressive I. mors-panacis suppressed ginsenoside biosynthesis, probably because of higher ROS levels and subsequent induction of programmed cell death pathways. Furthermore, I. mors-panacis may have increased its virulence by resisting the cytotoxicity of ROS.