• Mycobiology
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• 제30권1호
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• pp.57-59
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• 2002

Anthracnose symptoms severely occurred up to 100% on leaves of May lily grown in four locations in Korea during a disease survey in 2001. The symptoms appeared as circular to irregular spots with brown to dark brown discoloration on leaves of the plant, and severely infected leaves blighted. A total of 35 isolates of Colletotrichum sp. was obtained from the spotted lesions and identified as Colletotrichum liliacearum based on the morphological and cultural characteristics. Leaf spots similar to the original anthracnose symptoms were induced on the host leaves by artificial inoculation with the isolates of the fungus. This is the first report that C. liliacearum causes anthracnose of May lily.

• The Plant Pathology Journal
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• 제36권2호
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• pp.170-178
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• 2020

The Lily mottle virus (LMoV) impedes the growth and quality of lily crops in Lanzhou, China. Recently Arabis mosaic virus (ArMV) has been detected in LMoV-infected plants in this region, causing plant stunting as well as severe foliar symptoms, and likely posing a threat to lily production. Consequently, there is a need to develop simple, sensitive, and reliable detection methods for these two viruses to prevent them from spreading. Reverse transcription (RT) loop-mediated isothermal amplification (LAMP) assays have been developed to detect LMoV and ArMV using two primer pairs that match six conserved sequences of LMoV and ArMV coat proteins, respectively. RT-LAMP assay results were visually assessed in reaction tubes using green fluorescence and gel electrophoresis. Our assays successfully detected both LMoV and ArMV in lily plants without the occurrence of viral cross-reactivity from other lily viruses. Optimal conditions for LAMP reactions were 65℃ and 60℃ for 60 min for LMoV and ArMV, respectively. Detection sensitivity for both RT-LAMP assays was a hundredfold greater than that of our comparative RT-polymerase chain reaction assays. We have also found this relatively rapid, target specific and sensitive method can also be used for samples collected in the field and may be especially useful in regions with limited or no laboratory facilities.

• The Plant Pathology Journal
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• 제20권3호
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• pp.212-219
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• 2004

Three isolates of Cucumber mosaic virus (CMV) from lily plants showing mosaic and distortion symptoms were detected by reverse-transcriptase polymerase chain reaction (RT-PCR) using primers specific to Cucumovirus genus namely, LK-CMV, LK4-CMV, and LKS-CMV. Restriction enzymes patterns of the RT-PCR products revealed that the lily isolates belonged to subgroup IA of CMV. In terms of biological properties, the lily isolates have highly similar but distinct pathogenicity as reported in other lily strains and ordinary strains of CMV. To characterize the molecular properties, cDNAs containing coat protein (CP) gene and 3' non-coding region (NCR) of RNA3 for the isolates were cloned and their nucleotide sequences were determined. The CP similarity (218 amino acids) was highly homologous (>97％) with that of subgroup I CMV strains. However, an additional 20-nulcleotide long segment was only present in 3' NCR of lily isolates, which form an additional stem-loop RNA structure. By using chimeric construct exchange cDNA containing 3'NCR of LK-CMV into the full-length cDNA clone of RNA3 of Fny-CMV, this additional segment may prove to be significant in the identification and fitness of the virus in lily plants. The pathology of zucchini squash infected by F1F2L3-CMV, a pseudorecombinant virus was showed to change drastically the severe mosaic and stunting symptom into a mild chlorotic spot on systemic leave, compared with Fny-CMV. To delimit the sequence of RNA3 affected the pathology, various RNA3 chimeras were constructed between two strains of CMV. The symptom determinants of F1F2L3-CMV were mapped to the positions amino acid 234, 239, and 250 in 3a movement protein (MP). RNA3 chimeras changed the sequences encoding three amino acids were resulted in alteration of systemic symptom.

• Journal of Plant Biology
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• 제39권3호
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• pp.197-202
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• 1996

A pollen-specific cDNA clone, LMP50, was isolated from the mature pollen cDNA library of the Easter lily. The LMP50 transcript was highly abundant in mture pollen grains but not detectable in other organs. The LMP50 cDNA clone contains 1383 nucleotides and two open reading frames. The first codes for a peptide of 15 amino acid residues. The role of this peptide is nuclear. The second encodes a protein containing 329 amino acid residues. This protein exhibited a significant homology to human tartrate-resistant acid phosphatase and porcine uteroferrin. Both of these enzymes have been suggested to play a role in iron transport. Therefore, LMP50 may act as an iron carrier protein in mature pollen grains.

• 식물병연구
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• 제27권1호
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• pp.32-37
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• 2021

2020년 전라북도 완주 소재 약용작물 전시포장에서 재배중인 범부채(Iris domestica) 140개체 가운데 3개체의 잎에서 괴사증상이 발견되었다. Reverse transcription polymerase chain reaction 검정결과 증상을 나타내는 3개체가 tomato spotted wilt virus (TSWV)에 감염된 것으로 확인되었다. 증상주로부터 분리한 TSWV 분리주 'Blackberry lily-kr1'의 전체 염기서열을 결정하였으며, 유전자 은행에 있는 다른 분리주들과 L, M, S 분절유전체 부위의 염기서열 상동성을 비교하였다. 'Blackberry lily-kr1' 분리주는 L 분절 유전체는 우리나라에서 보고한 'JJ' 분리주(MF159046) 또는 'HJ' (LC273305) 분리주와 상동성이 높았으며, M과 S 분절 유전체는 'JJ' 분리주(MF159058과 KY021439)와 가장 상동성이 높았다. MEGA X 프로그램의 maximum likelihood 방법을 이용하여 'Blackberry lily-kr1'의 다른 TSWV 분리주들과의 계통학적 연관성에 관한 분석을 한 결과 L, M, S 분절유전체 모두 고추에서 분리한 'JJ' 분리주 및 환삼덩굴(Humulus japonicas)에서 분리한 'HJ' 분리주와 높은 연관성을 보였다. 건전한 I. domestica 식물에 'Blackberry lily-kr1'을 감염시킨 Nicoatiana rustica 식물 즙액을 접종한 결과 50일 후에 잎에 괴사 또는 이중 고리형태의 괴사 증상이 형성되었다. 이는 노지에서 재배하는 범부채에서 관찰된 괴사증상이 TSWV 감염에 의한 것임을 시사하는 결과이다. 이 연구는 우리나라에서 범부채에서 TSWV 발생에 관한 최초의 보고이다.

• KSBB Journal
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• 제17권6호
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• pp.577-581
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• 2002

풍부한 식물의 화분을 이용하여 재조합단백질의 생산연구를 위하여 UreB 단백질 정보를 지닌 1.7 kb DNA를 Helicobacter pylori urease gene cluster를 지니는 pH808로보터 PCR을 통하여 증폭하고 이를 CaMV35S promoter에 연결하여 백합(Lilium longiflorum)화분내로 도입하고 기내배양을 실시하였다. 발아초기의 화분을 Agrobacterium과 함께 진공침윤시켜 ureB DNA를 형질전환시키고 kanamycin을 지니는 화분배지에서 16-24시간 배앵하여 완전한 화분관신장을 이루도록 하였다. 이들 형질전환화분의 유전자도입 및 발현을 분석하였으며 그 결과 기내배양하는 하분을 일회성의 단백질공장으로 이용할 수 있다는 가능성을 제시하였다.

• 한국환경농학회지
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• 제34권2호
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• pp.149-154
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• 2015

효모의 유용 기능을 탐색하기 위해서 참나리에 정착하는 효모 군집을 분석하였다. 본 연구에서는 잎에서 총 82 균주, 줄기에서 총 94 균주, 꽃에서는 총 97 균주를 분리하였다. 분리된 균주를 ITS 1과 4 primer를 사용하여 ITS 영역 염기서열의 계통분석을 실시한 결과, 참나리 잎에서는 Pseudozyma가 31 균주, Aureobasidium pullulans가 28 균주, Cryptococcus가 11 균주, 줄기에서는 A. pullulans가 40 균주, Cryptococcus가 23균주, Candida 11 균주, 꽃에서는 A. pullulans가 95 균주, Rhodotorula 1 균주, Metschnikowia 1 균주가 분포하였다. 특히, 참나리 잎과 줄기, 꽃 모든 시료에서 A. pullulans가 우점하였으며, 꽃에서는 97 균주 중에서 95 균주의 A. pullulans가 검출되어 한 종이 절대적으로 우점함을 알 수가 있었다. 참나리 잎에서는 82 균주 중에서 Pseudozyma가 31 균주로 가장 우점함을 보였으며, 참나리 줄기에서는 94 분리 균주 중에서 Cryptococcus가 23 균주로 두번째로 우점함을 보였다. 참나리의 부위별로 분포양상이 다름을 확인하였다. 향후 이들 효모 균주들의 바이오테크놀로지 분야에 응용을 기대해본다.

• The Plant Pathology Journal
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• 제17권6호
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• pp.381.2-381
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• 2001

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2020년도 춘계학술대회
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• pp.43-43
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• 2020

Plants regenerated from in vitro cultures are associated with chromosomal variations, which have been generally found in long-term culture. Reducing plant culture age is one of the ways to reduce genetic and epigenetic changes. The present study focused on the efficient in vitro propagation of lily cultivars and has intensified to speed up bulb propagation for cryopreservation. The multiplication process applied in this experiment uses starting material, which the newly small bulb formed from bulb-scales in two lily cultivars. The adventitious bulb from bulb-scale tissue cultured on three different media following Murashige and Skoog (MS) basal medium supplemented with 1 g/L Charcoal, MS medium containing 0.3 mg/L IAA and 0.4 mg/L BA hormone with or without Charcoal, respectively. After about seven weeks, there is little change in the number of newly propagated bulbs in small bulbs of the two media. Compared to the both mediums, the number of the propagated bulbs is increased 5 times in MS medium containing 0.3 mg/L IAA and 0.4 mg/L BA hormone without Charcoal. After about seven weeks, the results of the propagation showed that the number of the propagated bulbs is increased 5 times in MS medium containing 0.3 mg/L IAA and 0.4 mg/L BA hormone without Charcoal compared to the both mediums. The number of propagated bulbs ranged from 5 to 6 and 4 to 6 with an average of 5 in Tropicalpink and Greenstar cultivars, respectively. There is little change in the number of newly propagated bulbs in small bulbs of other media. The multiplication process applied in this study may save in vitro culture period and effort.

• 한국환경농학회지
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• 제42권4호
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• pp.396-407
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• 2023

The golden apple snail (Pomacea canaliculata) has been utilized as a natural and eco-friendly control of weeds in rice paddy fields. However, P. canaliculata can damage other crops. In this study, the effectiveness of plant extracts from various natural sources that are reportedly effective against pests in the control of P. canaliculata was investigated. The four plant extracts were effective against P. canaliculata and ranked in descending order as green tea seed (Camellia sinensis) > root of red spider lily (Lycoris radiata) > leaves of tobacco (Nicotiana tabacum) > root of sophora (Sophora flavescens). The mortality rate of P. canaliculata was increased using 200 to 2000 mg/kg of green tea seed powder. However, shrubby sophora root extract did not significantly increase the mortality rate. The LC₅₀ and LC₉₀ of green tea seed, tobacco leaves, shrubby sophora root, and red spider lily root were 900 and 2800 mg/L, 956 and 2320 mg/L, 2162 and 5325 mg/L, and 512 and 1054 mg/kg, respectively. The LC₅₀ and LC₉₀ of ground powder of C. sinensis, N. tabacum, S. flavescens and L. radiata were 248 and 646 mg/L, 403 and 733 mg/L, 409 and 905 mg/L, and 493 and 1141 mg/L, respectively. The findings indicate the remarkable control potency of green tea seeds against the golden apple snail. An organic material incorporating the four plant powders may help control green apple snail in an ecosystem-friendly manner.