• 식물병연구
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• 제15권2호
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• pp.101-105
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• 2009

Serratia plymuthica A21-4는 양파(Allitum fistulosum L.) 근권에서 분리된 고추 역병 생물적 방제 미생물이다. 토양 환경이 S. plymuthica A2l-4 근권정착에 미치는 영향을 알아본 결과 사질이 많이 포함되어 공극이 많은토양에 3% 중량(w/w)의 부숙된 옥수수 줄기를 첨가하고 토양 수분함양이 40% 정도, 토양온도가 $20^{\circ}C$, 토양 pH가 중성이거나 약산성 토양이 S. plymuthica A2l-4의 근권정착에 유리하였다. 그리고 토착미생물이 있는 것이 살균한 토양에서 보다 S. plymuthica A21-4의 근권정착에 유리하였다.

• 식물병연구
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• 제24권4호
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• pp.332-338
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• 2018

2011년 8월 경상북도 봉화군 재산면 농가포장 5년생 인삼포장에서 잎이 푸른색을 띈 채 급격하게 마르는 증상이 발견되었다. 잎이 시든 직후 인삼의 뿌리를 채취하였으나, 뿌리나 줄기에서 특별한 병징은 없었으며, 뿌리의 수분이 약간 빠져나간 상태였다. 이러한 증상이 발생된 지 10일이 경과된 뿌리에서는 뿌리가 물러지면서 썩는 증상이 나타났다. 이러한 병징과 건전부의 경계부위에서 세균이 분리되었으며, 이 세균에 의한 뿌리썩음병이 의심되었다. 세균을 배양한 후 건전 인삼에 접종하자, 동일한 썩음 증상이 발현되었으며, 병반으로부터 동일한 세균이 재분리되었다. 이 세균을 BioLog system에 의한 탄소원 이용여부, Vitek 2 system을 이용한 생화학적 반응, GC-MIDI Sherlock system을 이용한 지방산 조성, 16S rRNA 염기서열을 분석한 결과, 모두 Serratia plymuthica로 동정되었다. 이에 따라 인삼 뿌리에 발생하는 이 병을 Serratia plymuthica에 의한 인삼 세균뿌리썩음병으로 명명하여 보고하고자 한다.

• The Plant Pathology Journal
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• 제18권4호
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• pp.221-224
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• 2002

In vitro and in vivo activities of a biocontrol agent, Serratia plymuthica strain A2l-4, was evaluated for the control of Phytophthora blight of pepper, Strain A2l-4 inhibited mycelial growth, germination of zoosporangia and cystospores, and formation of zoospore and zoosporangia of Phytophthora capsici in vitro. In the pot experiment, incidence of Phytophthora blight of pepper in non-treated control was 100% at 14 days after inoculation, while no disease was observed in the plot treated with S. plymuthica A2l-4. In the greenhouse test, infection rate of pepper in the non-treated plots was 74.5%, while it was only 12.6％ in the plots treated with A2l-4. Results indicate that S. plymuthica A2l-4 is a potential biocontrol agent for Phytophthora blight of pepper.

• The Plant Pathology Journal
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• 제18권3호
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• pp.138-141
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• 2002

A promising biocontrol agent, A2l-4, against Phytophthora blight of pepper was selected from 351 bacterial isolates collected from rhizosphere soils and roots of onion (Allium fistulosum L.). The isolate A21-4 was identified as Serratia plymuthica based on its 16S rRNA sequence and key characteristics as compared with that of an authentic culture of S. plymuthica (ATCC No. 6109D01). The isolate readily colonized on roots of various crops including pepper when inoculated on seed and not. Strain A2l-4 showed narrow spectrum of antibiotic activity, as revealed in its strong inhibitory activity to the genera Pythium and Phytophthora, but not to Fuasrium and Rhizoctonia. In pot experiments, none of the pepper seedlings treated with A2l-4 were infected by Phytophthora capsici, while 86% of the control plants were killed by the pathogen.

• 한국미생물·생명공학회지
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• 제30권2호
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• pp.135-141
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• 2002

대파 뿌리로부터 근권미생물 146종을 분리하여 대파 흑색썩음균핵병균인 Sclerotium cepivorum에 길항하는 AL-1 균주를 최종선별하였다. 분리주 AL-1은 the procaryotes와 Bergey's mannual of systematic bacteriology의 방법과 16S rDNA의 부분염기서열을 결정하여 ribosomal database 에서 상동성 검색 등의 방법으로 Serratia plymuthica로 동정되었다. S. plymuthica AL-1은 흑색썩음균핵병균(Sclerotium cepivorum)에 대해서는 생육저지환의 크기가 15mm로 나타났으며, 고추 검은무늬병(Alternaria altrata)은 9 mm, 고추 탄저병균(Colletotrichum gleosporioids)은 13 ㎜, 도라지 줄기마름병균(Phoma sp.)은 10 ㎜, 고추 잘록병균 (Rhizoctonia solani)은 8 ㎜, 고추 흰별무의병균(Stemphylium solani)은 8 ㎜, 오이 균핵병균(Sclerotinia sclerotiorum)은 7 mm, 수박 덩굴쪼김병(Fusarium oxysporium niveum)은 7 ㎜로 길항력을 나타내었으나 참외 만고병균(Didymella bryoniae)에서는 길항력이 없었다. S. plymuthica AL-1는 1％ colloidal chitin을 첨가한 TSB 배지에서 분자량 10 kDa 이상의 분획에서는 chitinase(3.2 units/ml)가 유도 생산되었고 80℃에서 30분간 열처리할 경우 chitinase의 활성은 없어 졌으나 길항력(6.4 ㎜)은 남아있었다. 또한 분자량 10kDa 이하의 분획에서는 chitinase 활성은 없으나 길항력(5.2㎜)은 나타내었고, 80℃에서 열처리하여도 길항력(5.0mm)이 남아있어 효소 이외 다른 생리활성물질이 존재함을 확인하였다.

• The Plant Pathology Journal
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• 제23권3호
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• pp.180-186
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• 2007

The biocontrol agent, Serratia plymuthica A21-4, has been developed for controlling pepper Phytophthora blight. Serratia plymuthica A21-4 strongly inhibits the mycelial growth, zoospore formation, and cyst germination of Phytophthora capsici in vitro. The application of a cell suspension of strain A21-4 to pepper plants in pot experiments and in greenhouse successfully controlled the disease. The bacteria produced a potent antifungal substance which was a key factor in the suppression of Phytophthora capsici. The most active chemical com-pound was isolated and purified by antifungal activity-guided fractionation. The chemical structure was identified as a chlorinated macrolide $(C_{23}H_{31}O_8Cl)$ by spectroscopic (UV, IR, MS, and NMR) data, and was named macrocyclic lactone A21-4. The active compound significantly inhibited the formation of zoosporangia and zoospore and germination of cyst of P. capsici at concentrations lower than $0.0625{\mu}g/ml$. The effective concentrations of the macrocyclic lactone A21-4 for $ED_{50}$ of mycelial growth inhibition were $0.25{\mu}g/ml,\;0.25{\mu}g/ml,\;0.30{\mu}g/ml \;and\;0.75{\mu}g/ml$ against P. capsici, Pythium ultimum, Sclerotinia sclerotiorum and Botrytis cinerea, respectively.

• 생명과학회지
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• 제13권1호
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• pp.90-98
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• 2003

대파 흑색썩음균핵병균 (Sclerotium cepivorum)에 길항력을 가진 Serratia plymuthica L-1의 길항 메카니즘을 조사한기 위해 S. plymuthica L-1이 생산하는 세포외 chitinase를 정제하여 그 특성을 조사하였다. Colloidal chitin이 함유된 배지에서 생산된 S. plymuthica L-1 chitinase는 $(NH_4)_2$$_2$$SO_2$ 40~70% precipitation, affinity adsorption, DEAE-sephadex A-50 column chromatography 및 sephadex G-200 column filtration 과정을 통하여 정제하였다. 정제된 chitinase는 7.3% 회수율과 19.8의 정제도를 나타내었으며, 전기영동시 단일밴드를 얻었으며, 분자량은 55kDa로 나타났다. 정제된 chitinase의 최적 pH 및 온도는 5.5, $55^{\circ}C$이었고, 온도안정성 조사에서 정제효소는 $50^{\circ}C$까지 90%의 잔존활성을 유지하였으나 $60^{\circ}C$이상에서는 급격하게 효소활성이 실활되었다. $Ca^{2+}$, $Mn^{2+}$, $Mg^{2+}$ 등의 이온은 대략 20군 이상의 효소를 활성화시켰으나 $Cu^{2+}$이온은 약 80%의 효소활성을 억제시켰고, SDS, p-CMB, MIA 등도 효소활성을 저해하는 작용을 하였으며, colloidal chitin에 대한 Km값은 3.26 mg/$m\ell$로 나타났다. 정제효소에 의한 각종 병원균에 대한 생육 억제정도는 흑색썩음균핵병균, 고추 검은무의병균, 고추 탄저병균, 도라지 줄기마름병균, 고추 흰별무늬병균, 오이 균핵병균, 수박 덩굴쪼김병균 등에는 길항력을 나타내었으나 고추 역병균과 무 모잘록병균에서는 길항력이 아주 낮게 나타났다. 정제 chitinase에 의해 대파 흑색썩음균핵병 S.. cepivorum의 균사는 팽창과 균사 끝의 용균, 분해 및 변색현상을 관찰할 수 있었고 chitinase 기능과 Iysozyme 기능을 모두 가지고 있을 것으로 추정된다.

• The Plant Pathology Journal
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• 제22권4호
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• pp.364-368
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• 2006

Survival of biocontrol agents and their effective colonization of rhizhosphere are the essential components for successful disease suppression. The effects of hydrogel supplement on bacterial survival and disease control were evaluated in pot and in the field. Addition of 2% hydrogel material to potting soil resulted in significant enhancement of colonization of biocontrol agent Serratia plymuthica A21-4 both in soil and rhizosphere of pepper plants. Rhizosphere colonization of S. plymuthica A21-4 retrieved from 40 days old pepper seedlings indicated 100 times higher bacterial population in hydrogel treated soil than in ordinary pot soil. The pepper plants sown in hydrogelated potting soil showed higher seed germination rate and the better growth of pepper plant than those in ordinary commercial pot soil. Although the suppression of Phytophthora capsid density in the potting soil by treatment of biocontrol agent A21-4 was not significantly different between in hydrogelated soil and ordinary potting soil, the suppression of Phytophthora blight between two treatments was significantly different. A21-4 treatment in hydrogelated potting soil was completely disease-free while same treatment in ordinary potting soil revealed 36% disease incidence. Our field study under natural disease occurrence also showed significantly less disease incidence(12.3%) in the A21-4 treatment in the hydrogelated soil compared to other treatments. Yield promotion of pepper by the A21-4 treatment in the hydrogelated potting soil was also recognized. Our results indicated that hydrogel amendment with biocontrol agent in pot soil would be a good alternative to protect pepper seedlings and increase plant yield.

• The Plant Pathology Journal
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• 제21권1호
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• pp.64-67
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• 2005

The biocontrol agent Serratia plymuthica A21-4 readily colonized on the root of pepper plant and the bacterium moves to newly emerging roots continuously. The colonization of A21-4 on the pepper root was influenced by the presence ofPhytophthora capsici in the soil. When P. capsici was introduced in advance, the population density of A21-4 on the root of pepper plant was sustained more than $10^6$ cfu/g root until 3 weeks after transplanting. On the other hand, in the absence of P. capsici, the population density of A21-4 was reduced continuously and less than $10^5$ cfu/g root at 21 days after transplanting. S. plymuthica A21-4 inhibited successfully the P. capsici population in pepper root and rhizosphere soil. In the rhizosphere soil, the population density of P. capsici was not increased more than original inoculum density when A21-4 was treated, but it increased rapidly in non-treated control. Similarly, the population density of P. capsici sharply increased in the non-treated control, however the population of P. capsici in A21-4 treated plant was not increased in pepper roots. The incidence of Phytophthora blight on pepper treated with A21-4 was 12.6%, while that of non-treated pepper was 74.5% in GSNU experimental farm experiment. And in farmer's vinyl house experiment, the incidence of the disease treated with the fungicide was 27.3%, but treatment of A21-4 resulted in only 4.7% of the disease incidence, showing above 80% disease control efficacy.

• The Plant Pathology Journal
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• 제17권6호
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• pp.365.4-365
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• 2001