Search

Leaf spot on lemon balm is frequently observed in Korea, causing considerable damage to crops. In 2014 and 2015, the occurrence of leaf spot was observed in several production greenhouses at Suwon, Gongju, and Namwon in Korea. Symptoms on lower leaves initially developed as small, distinct, discolored lesions, which enlarged progressively turning into dark brown, angular spots surrounded by purplish-brown margins. Based on the morphological characteristics and sequence analysis of actin (ACT), translation elongation factor 1-alpha (EF-1α), internal transcribed spacer (ITS), 28S nrDNA (LSU), and RNA polymerase II second largest subunit (RPB2), the fungus associated with the lemon balm leaf spot was determined as Septoria melissae. To the best of our knowledge, this is the first report of lemon balm leaf spot caused by S. melissae in Asia as well as in Korea.

Microbial volatile compounds (MVCs) significantly influence the growth of plants and phytopathogens. However, the practical application of MVCs at the field level is limited by the fact that the concentrations at which these compounds antagonize the pathogens are often toxic for the plants. In this study, we investigated the effect of dimethyl disulfide (DMDS), one of the MVCs produced by microorganisms, on the fitness of tomato plants and its fungicidal potential against a fungal phytopathogen, Sclerotinia minor. DMDS showed strong fungicidal and plant growth promoting activities with regard to the inhibition of mycelial growth, sclerotia formation, and germination, and reduction of disease symptoms in tomato plants infected with S. minor. DMDS exposure significantly upregulated the expression of genes related to growth and defense against the pathogen in tomato. Especially, the overexpression of PR1 and PR5 suggested the involvement of the salicylic acid pathway in the induction of systemic resistance. Several morphological and ultrastructural changes were observed in the cell membrane of S. minor and the expression of ergosterol biosynthesis gene was significantly downregulated, suggesting that DMDS damaged the membrane, thereby affecting the growth and pathogenicity of the fungus. In conclusion, the tripartite interaction studies among pathogenic fungus, DMDS, and tomato revealed that DMDS played roles in antagonizing pathogen as well as improving the growth and disease resistance of tomato. Our findings provide new insights into the potential of volatile DMDS as an effective tool against sclerotial rot disease.

Microbial originated volatile organic compounds (VOCs) are reported to play significant roles in plant development and growth by interfering with the synthesis, metabolism, or signaling of phytohormones. Here, we demonstrated dimethyl disulfide (DMDS), a VOC previously known to be produced from rhizobacteria/fungi, modulated growth and root system architecture of Arabidopsis thaliana. Changes in root system architecture were correlated with auxin signalling intensities which were assessed by expression of auxin signaling reporter (i.e. DR5::GUS) and early auxin responsive genes (e.g. SAUR-AC1, GH3.1, IAA14). Ultimately, Arabidopsis mutants aborted in auxin signalling (e.g. tir1-1, arf7, arf7arf19) displayed insensitivity to DMDS in lateral root formation and suggested that DMDS can contribute to plant growth and development by modifying the root system architecture through canonical auxin signalling pathways in Arabidopsis.

Salvia farinacea Benth. (Lamiaceae) is an herbaceous perennial plant, native to Mexico and southern parts of the United States. This plant is cultivated worldwide for its ornamental value. In November 2019, hundreds of S. farinacea 'Blue Bedder" grown in a flower garden in Jeju (33°30'57"N 126°32'50"E), Korea have been found to be infected with a powdery mildew fungus. The disease severity was estimated to be 100%. Likewise in October 2020, a similar situation with this plant was also observed in a flower garden in Seoul (37°35'19"N 127°01'07"E), Korea. Leaves, stems and inflorescence of plants were covered by white, thin mycelial felt, bearing an abundance of conidiophores and conidia. Eventually, infected plants lose their ornamental value. Two voucher specimens have been deposited in the Korea University Herbarium (KUS-F31478 and F32164). Fresh materials were examined. Hyphal appressoria were nipple-shaped, but rarely found. Conidiophores (n = 30) were straight, 95 to 160 × 10 to 12 μm and produced 2 to 7 immature conidia in chains with a crenate outline. Foot-cells were cylindric and 36 to 60 μm long. Conidia (n = 30) were ellipsoid-ovoid to barrel-shaped, 32 to 38 × 18 to 24 μm, and contained conspicuous fibrosin bodies. Dark brown chasmothecia were found partly embedded in the mycelial felt on leaves, mostly hypophyllous, spherical, and 82 to 100 µm diameter, with a single ascus in each. Appendages were few, mycelioid, 1- to 4-septate, brown near the base when mature, but paler above. Asci were broadly ellipsoid to subglobose, 56 to 68 × 50 to 62 μm, sessile and 8-spored. Ascospores were colorless, oval to subglobose, and 14 to 18 × 12 to 15 µm. These characteristics were consistent with those of Podosphaera xanthii (Castagne) U. Braun & Shishkoff (Braun and Cook 2012). For further confirmation, genomic DNA was extracted from chasmothecia from KUS-F31478 and F32164. PCR amplification was performed using the primer pair ITS1F/PM6 for internal transcribed spacer (ITS) and PM3/TW14 for the large subunit (LSU) of the rDNA (Takamatsu and Kano 2001). Obtained sequences were deposited to the GenBank under the accession numbers MZ359847 and MZ359859 for ITS, MZ359858 and MZ359861 for LSU. For ITS regions 99.80-100% similarity was found with sequences MT131256 (Salvia farinacea), MT131254 (Mazus pumilus) and MT131252 (Erigeron bellioides) of P. xanthii, whereas it was 99.90% with sequences of this fungus on Echinacea purpurea (MT826247 and MT826245) for 28S rDNA gene. Pathogenicity tests were carried out by touching an infected leaf onto healthy leaves of disease-free 30 days old potted 'Blue Bedder' using replication of five plants, with five non-inoculated plants used as controls. The typical signs of powdery mildew started to develop on the inoculated leaves in 7 to 10 days, and microscopic examination revealed the morphological identity with the fungus observed from the field. All non-inoculated control plants remained symptomless. Hitherto Golovinomyces powdery mildews on Salvia spp. were reported globally (Farr and Rossman 2021). However, Podosphaera elsholtziae on Salvia sp. and P. xanthii on S. farinacea were reported from China and Taiwan (Zheng and Yu 1987, Yeh et al. 2021). To our knowledge, this is the first report of P. xanthii on S. farinacea in Korea. The occurrence of Podosphaera powdery mildew on S. farinacea could pose a serious threat to the beauty of this plant, causing premature senescence of young leaves and gray to purplish discoloration of the leaves.

Verbena bonariensis L., named as purple-top vervain or Argentinian vervain, is native to tropical South America. It is cultivated worldwide as an ornamental plant. During summer and autumn of 2020, over 50% of the leaves of V. bonariensis were found infected with powdery mildew in a flower garden in Seoul (37°35'19"N 127°01'07"E), Korea. White, superficial mycelia developed initially on the leaves and subsequently covered surfaces of leaves and stems, are resulting in leaf discoloration, early defoliation, and shoots distortion. Heavily infected plants lost ornamental value. A representative voucher specimen was deposited in the Korea University herbarium (KUS-F32168). Morphological characterization and measurements of conidiophores and conidia were carried out using fresh samples. Microscopic observation showed that aAppressoria on the superficial hypha were nipple-shaped, but rarely found or nearly absent. Conidiophores (n = 30) were cylindrical, 110 to 220 × 10 to 12 µm, and produced 2 to 5 immature conidia in chains with a sinuate outline, followed by 2 to 3 short cells. Foot-cells of conidiophores were straight, cylindrical, and 46 to 90 μm long. Conidia (n = 30) were hyaline, ellipsoid to doliiform, 28 to 40 × 18 to 24 μm with a length/width ratio of 1.3 to 2.0, and contained small be like oil-like drops, but without distinct fibrosin bodies. Primary conidia were apically rounded and sub-truncate at the base. Germ tubes were produced at perihilar position of the conidia. Chasmothecia were not observed. These morphological characteristics were typical of the conidial stage of the genus Golovinomyces (Braun and Cook 2012, Qiu et al. 2020). To identify the fungus, rDNA was extracted from the voucher sample. PCR products were amplified using the primer pair ITS1F/PM6 for internal transcribed spacer (ITS), and PM3/TW14 for the large subunit (LSU) of the rDNA (Takamatsu and Kano 2001). The resulting sequences were registered to GenBank (MW599742 for ITS, and MW599743 for LSU). Using Blast'n search of GenBank, sequences showed 100% identity for ITS and LSU with G. ambrosiae (MT355557, KX987303, MH078047 for ITS, and AB769427, AB769426 for LSU), respectively. Thus, based on morphology and molecular analysis, the isolate on V. bonariensis in Korea was identified as G. ambrosiae (Schwein.) U. Braun & R.T.A. Cook. Pathogenicity tests were carried out by touching an infected leaf onto healthy leaves of disease-free pot-grown plants using a replication of five plants, with five non-inoculated plants used as controls. After 7 days, typical powdery mildew colonies started to appear on the inoculated leaves. The fungus on inoculated leaves was morphologically identical to that originally observed in the field. All non-inoculated control leaves remained symptomless. On different global Verbena species, tThere have been many reports of Golovinomyces powdery mildews including G. cichoracearum s.lat., G. longipes, G. monardae, G. orontii s.lat., and G. verbenae (Farr and Rossman 2021). In China, G. verbenae was recorded on V.erbena phlogiflora (Liu et al. 2006). Golovinomyces powdery mildew has not been reported on Verbena spp. in Korea. Powdery mildew has been reported on V. bonariensis in California, but identity of the causal agent had not been reported. To our knowledge, this is the first report on the identity of the powdery mildew caused by G. ambrosiae on V. bonariensis in Korea. Since heavily infected plants lost ornamental value, appropriate control measures should be developed.

Benincasa hispida (Thunb.) Cogn. (syn. B. cerifera Savi, Cucurbita hispida Thunb.), called wax gourd or ash gourd, is a cucurbitaceous vine grown for medicinal purposes and commercial values of its large fruits in Southeast Asia (Al-Snafi 2013). During the summer and autumn of 2020, leaves of wax gourd were observed to be affected by powdery mildew with 100% disease incidence in an experimental plot of Jeonbuk National University (35°50'55″N, 127°07'48″E), Korea. Fungal colonies were initially circular to irregular, forming white patches on both sides of the leaves and young stems, finally covering entire leaves and causing premature senescence of the leaves and poor growth. A representative voucher specimen was deposited in the Korea University herbarium (KUS-F32171). At least 30 measurements were taken for each asexual diagnostic features. Conidiophores arising from superficial hyphae were straight, 100 to 210 μm long, and produced 3 to 7 immature conidia in chains with a crenate outline. Foot-cells were cylindrical, 46 to 74 ×10 to 12 μm, followed by 1 to 2 shorter cells. Conidia were ellipsoid-ovoid to barrel-shaped, 30 to 40 × 18 to 23 μm with a length/width ratio of 1.4 to 2.0 and contained conspicuous fibrosin bodies. Germ tubes were produced from a lateral position on conidia. Sexual stage was not observed during the growing season. The morphological characteristics of the fungus were compatible with those of Podosphaera xanthii (Castagne) U. Braun & Shishkoff (Braun and Cook 2012), a well-known cucurbitaceous powdery mildew. DNA was extracted from mycelium, and primer sets ITS1F/PM6 and PM3/TW14 were used for amplification of ITS1-5.8S-ITS2 regions and 5´-end of 28S rDNA gene, respectively (Takamatsu and Kano 2001). Sequences determined in this study were deposited to the GenBank under the accession numbers MW559231 and MW559420, respectively. The sequences for ITS regions and 28S rDNA gene showed 99.78% and 99.07% similarity respectively with those of P. xanthii (MH465242, MH465243, MT250855 for ITS, and MK357436, MT826247 for LSU). Pathogenicity was confirmed twice by pressing a diseased leaf onto young leaves of five wax gourd plants. Five non-inoculated plants were used as controls. Inoculated leaves developed symptoms after 5 days, whereas the control plants remained symptomless. The fungus present on the inoculated plants was identical morphologically to that originally observed on diseased plants. Sphaerotheca fuliginea (syn. P. xanthii) on B. hispida has been listed in Hungary, India, Japan, Singapore, and Taiwan so far (Farr and Rossman 2021). Recently, the identity of P. xanthii on B. hispida in Taiwan was confirmed with morphological examination and molecular analysis by Wu and Kirschner (2017). To our knowledge, this is the first report of powdery mildew caused by P. xanthii on B. hispida in Korea. Since wax gourd production is only recently started on a commercial scale in the southern part of Korea, powdery mildew infections pose a serious threat to the safe production of the fruits, especially in organic farming where chemical control options are limited.

In September 2013 and 2014, a significant number of kenaf plants showing symptoms of leaf spots with approximately 50% incidence were found in experimental plots in Iksan and Namwon, Korea. Leaf spots were circular to irregular, more or less vein-limited, reaching to 10 mm in diameter. The spots were initially uniformly brown to reddish brown, turning pale brown with a purplish margin and showing grayish patches on the lesion due to heavy fructification. The causative agent of the leaf spot disease was identified as Cercospora malayensis. The pathogenicity test was conducted with similar results, which fulfilled Koch's postulates. This is the first report of C. malayensis infection of kenaf in Korea.

Barley yellow dwarf virus (BYDV) belongs to Luteovirus and is limited only at phloem related tissues. An open reading frame (ORF) 4 of BYDV codes for the movement protein (MP) of BYDV gating plasmodesmata (PD) to facilitate virus movement. Like other Luteoviruses, ORF 4 of BYDV is embedded in the ORF3 but expressed from the different reading frame in leaky scanning manner. Although MP is a very important protein for systemic infection of BYDV, there was a little information. In this study, MP was characterized in terms of subcellular localization and programmed cell death (PCD). Gene of MP or its mutant (ΔMP) was expressed by Agroinfiltration method. MP was clearly localized at the nucleus and the PD, but ΔMP which was deleted distal N-terminus of MP showed no localization to PD exhibited the different target with original MP. In addition to PD localization, MP appeared associated with small granules in cytoplasm whereas ΔMP did not. MP associated with PD and small granules induced PCD, but ΔMP showed no association with PD and small granules did not exhibit PCD. Based on this study, the distal N-terminal region within MP is seemingly responsible for the localization of PD and the induction small granules and PCD induction. These results suggest that subcellular localization of BYDV MP may modulate the PCD in Nicotiana benthamiana.

Microbial volatile compounds (MVCs) significantly influence the growth of plants and phytopathogens. However, the practical application of MVCs at the field level is limited by the fact that the concentrations at which these compounds antagonize the pathogens are often toxic for the plants. In this study, we investigated the effect of dimethyl disulfide (DMDS), one of the MVCs produced by microorganisms, on the fitness of tomato plants and its fungicidal potential against a fungal phytopathogen, Sclerotinia minor. DMDS showed strong fungicidal and plant growth promoting activities with regard to the inhibition of mycelial growth, sclerotia formation, and germination, and reduction of disease symptoms in tomato plants infected with S. minor. DMDS exposure significantly upregulated the expression of genes related to growth and defense against the pathogen in tomato. Especially, the overexpression of PR1 and PR5 suggested the involvement of the salicylic acid pathway in the induction of systemic resistance. Several morphological and ultrastructural changes were observed in the cell membrane of S. minor and the expression of ergosterol biosynthesis gene was significantly downregulated, suggesting that DMDS damaged the membrane, thereby affecting the growth and pathogenicity of the fungus. In conclusion, the tripartite interaction studies among pathogenic fungus, DMDS, and tomato revealed that DMDS played roles in antagonizing pathogen as well as improving the growth and disease resistance of tomato. Our findings provide new insights into the potential of volatile DMDS as an effective tool against sclerotial rot disease.

Resveratrol has gained widespread scientific attention due to its ability to significantly extend the lifespan of yeast. However, research on the efficacy of resveratrol on lifespan extension has yielded mixed results in animal studies, making resveratrol a contentious subject. In our previous work, we reported that transgenic resveratrol rice DJ526 showed unusual health benefits beyond expectations. In this work, we established a callus culture of resveratrol rice DJ526, which contains 180 times more resveratrol than the grain, and found that resveratrol rice callus significantly extended the median lifespan of Drosophila melanogaster by up to 50% compared to the control. The resveratrol rice callus also ameliorated age-dependent symptoms, including locomotive deterioration, body weight gain, eye degeneration, and neurodegeneration of D. melanogaster with age progression. Considering that resveratrol is the most preferred antiaging compound due to its superior safety and proven mechanism against many serious adult diseases, the outstanding efficacy of resveratrol on the longevity of wild-type animals could cast a light on the development of antiaging therapeutic agents.

As carbon dioxide (CO2) concentration in the atmosphere is enormously increasing, global warming has become one of the most important issues affecting our ecosystem. Exploitation of natural energy resources and the increasing cost of raw materials drive the search for renewable energy sources. Bioethanol is known as an important renewable bioenergy source that may be used to reduce greenhouse gases (GHG) and dependency on fossil fuel. Thus bioethanol is regarded as a more environmentally friendly fuel than gasoline. Sugarcane bagasse (SCB) is a potentially renewable resource that may be used to produce bioethanol, which is one of the largest cellulosic agro-industrial by-products. Over the last decade many efforts have been made to achieve maximum prehydrolysis and sachharification efficiency to obtain higher yields of fermentable sugar and ethanol from SCB. This article presents a brief overview of bioethanol production from SCB through the biotechnological processes.

Microbe-assisted phytoremediation has been considered a promising measure for the remediation of heavy metal-polluted soil. The aim of this study was to assess the effect of diazotrophic plant growth-promoting Herbaspirillum sp. GW103 on growth and lead (Pb) and zinc (Zn) accumulation in Zea mays L. The strain GW103 exhibited plant growth-promoting traits such as indole-3-acetic acid, siderophores, and 1-aminocyclopropane-1-carboxylic deaminase. Treatment of Z. mays L. plants with GW103 significantly increased 19, 31, and 52% of plant biomass and 10, 50, and 126% of chlorophyll a contents in Pb, Zn, and Pb + Zn-amended soils, respectively. Similarly, the strain GW103 significantly increased Pb and Zn accumulation in shoots and roots of Z. mays L., which were 77 and 25% in Pb-amended soil, 42 and 73% in Zn-amended soil, and 27 and 84% in Pb + Zn-amended soil. Furthermore, addition of GW103 increased 8, 12, and 7% of total protein content, catalase, and superoxide dismutase levels, respectively, in Z. mays L. plants. The results pointed out that isolate GW103 could potentially reduce the phytotoxicity of metals and increase Pb and Zn accumulation in Z. mays L. plant.

Polymyxa graminis, a root endoparasite of several cereal species, is considered to be non-pathogenic but serves as a vector of various plant viruses belonging to the genera Bymovirus, Furovirus, and Pecluvirus. Specifically, it reduces barley productivity by transmitting the Barley Yellow Mosaic Virus (BaYMV). To date, due to its obligate biotrophic property, no artificial culturing of P. graminis was reported and its quantification was also technically challenging. Here, we developed a novel and simple method to infect P. graminis within sterile barley roots in contamination free by preparing nearly pure zoospore inoculum. Such artificial maintenance of P. graminis was verified based on the presence of various developmental stages in infected barley roots under microscope. In addition, the population of resting spores in host tissue was determined by establishing standard curve between manually counted number of spores and Ct values of 18S rDNA amplification using quantitative real-time PCR. Furthermore, it was validated that standard curve generated was also applicable to estimate the abundance of P. graminis in soil environments. In conclusion, the present study would help to generate a system to investigate the etiological causes as well as management of plant diseases caused by P. graminis and BaYMV in tissue and soil.

The aim of this study was to introduce novel Sn, Cu, Hg, and Ag nanopowders (NPs) and a composite nanopowder (NP) synthesized using Salvia miltiorrhiza Bunge (SM) root extract as a reducing and capping agent to improve the antibacterial property of dental filling materials. All of the NPs obtained were characterized using a scanning transmission electron microscope (STEM), and energy dispersive X-ray (EDX) spectrum imaging was performed to map the elemental distributions of the NP composite. Fourier transform infrared (FTIR) spectroscopy was performed to identify the role of various functional groups in all of the obtained NPs and the phyto-compound responsible for the reduction of various metal ions. The X-ray diffraction (XRD) patterns clearly illustrated the crystalline phase of the synthesized NP. The antibacterial properties of the synthesized Sn, Cu, Hg, Ag, composite NP, SM root extract, and commercial amalgam powder were evaluated. The Cu, composite NP, SM root extract and Ag NP displayed excellent antibacterial activity against dental bacteria Streptococcus mutans and Lactobacillus acidophilus. The results of this study require further evaluation for signs of metal toxicity in appropriate animal models. However, the results are encouraging for the application of metal NPs as suitable alternatives for antibiotics and disinfectants, especially in dental filling materials.

The receptor-like cytoplasmic kinases (RLCK family VII) are required for plant defense against various pathogens. Previously, OsPBL1 (ORYZA SATIVA ARABIDOPSIS PBS1-LIKE 1) was isolated from rice as a potential RSV (rice stripe virus) resistant factor, but its physiological roles in plant defense are yet to be investigated. In this study, we demonstrated that OsPBL1increased defense against P. syringae in transgenic Arabidopsis. To ascertain the role of OsPBL1 gene in plant defense, OsPBL1 tagged with HA (i.e. Hemagglutinin) was overexpressed in Arabidopsis and examined for the resistance against Pseudomonas syringae pv. tomato DC3000 (i.e. Pst DC3000). At 3 dpi of Pst DC3000, transgenic Arabidopsis lines exhibited the reduced chlorotic lesion and propagation of P. syringae, compared to wild type. Elevated pathogen resistance of transgenic lines was correlated with increased H2O2 accumulation and callose deposition on the infected leaves. It was also revealed that expression levels of salicylic acid dependent genes such as PR1, PR2, and PR5, were induced higher in transgenic lines than wild type. Taken together, our data suggested that OsPBL1 exerted the role in defense against pathogen attacks in plant via mainly facilitating salicylic acid dependent pathway.

A green, eco-friendly approach for the synthesis of silver and gold nanoparticles (AgNPs and AuNPs) using Erigeron annuus (L.) pers flower extract as both the reducing and capping agent is reported for the first time. Optimal nanoparticle production was achieved by adjusting various parameters including pH, extract concentration, metal ion concentration, and time. Initial verification of AgNP and AuNP production was done by visual observation and measuring surface plasmon spectra at 434 and 537 nm, respectively. The synthesized AgNPs and AuNPs were characterized by high resolution-transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), energy dispersive spectrophotometry (EDS), Fourier transform infrared spectroscopy (FTIR) and zeta potential. The catalytic potential of E. annuus flower extract, silver ions, synthesized AgNPs, commercial grade AgNPs, and a mixture of flower extract and AgNPs immobilized on sodium alginate hydrogel beads (Na/Al HB) was analyzed. The ability of these immobilized materials to degrade methylene blue was investigated. Commercial grade AgNPs immobilized with Na/Al HB 1.5 g/20 mL were observed to have good catalytic activity followed by a mixture of synthesized AgNPs immobilized with Na/Al HB and E. annuus flower extract immobilized with Na/Al HB at 1.5 g/20 mL. (C) 2014 King Saud University. Production and hosting by Elsevier B.V. All rights reserved.

In Korea, okra (Abelmoschus esculentus [L.] Moench) is cultivated on small family farms and experimental plots (0.5 ha). In August 2014 and 2015, okra plants of cultivar ‘Green Hope’, grown in the farms of Iksan, Korea, were observed for leaf spot symptoms. Leaf spots were circular to irregular-shaped, initially brown, and subsequently turned reddish-brown with a yellowish margin. On leaves, stromata were brown, small, and composed of a few swollen hyphal cells. The conidiophores were fasciculate, olivaceous to brown, paler toward the apex, straight to minimally curved, geniculate, 30 to 250 µm long, 3.5 to 5.0 µm wide, one- to five-septate, and with conspicuous conidial scars. Conidia (n = 50) were hyaline, acicular, subacute to obtuse at the apex, truncate to obconically truncate at the base, 2- to 20-septate, 34 to 280 × 3.4 to 6.5 µm, and with a thickened, darkened hilum at the base. The morphological characteristics were consistent with Cercospora malayensis F. Stevens & Solheim (Chupp 1953). To obtain a pure conidial suspension, conidia were collected from 50 infected leaves using sterile forceps, placed in an Eppendorf tube containing sterile water, streaked onto the surface of 2% water agar plates supplemented with 100 mg/liter of streptomycin sulfate, and transferred onto potato dextrose agar (PDA). After 7 days of incubation, fungal colonies (10 isolates) appeared off-white and flat with aerial mycelia. Voucher specimens were housed in the Korea University herbarium (KUS-F28701), and one isolate was deposited in the Korean Agricultural Culture Collection (KACC47769). Additional fungal confirmation was conducted using the internal transcribed spacer (ITS), translation elongation factor 1-α (EF), and actin (ACT) gene sequences (Groenewald et al. 2013). A BLASTn search using ITS and ACT sequences showed >99% identity with C. malayensis ITS and ACT sequences (KM489070 and KY082664), whereas EF sequences showed 97.8% identity with C. malayensis EF gene (KY082663). The ITS, EF, and ACT sequences of the isolate were deposited in GenBank (MH129519, MH129517, and MH129515). Five 4-month-old okra plants (Green Hope) were spray-inoculated with C. malayensis (KACC47769) hyphal suspensions obtained from 2-week-old colonies grown on PDA at 25°C and transferred to a greenhouse (25°C) with a 12-h photoperiod. Five control plants were inoculated with sterile water. Symptoms observed on the C. malayensis inoculated plants were 100% identical with infected field conditions. C. malayensis was reisolated from symptomatic leaf tissues, and the identity was confirmed by microscopic studies. The pathogenicity test was repeated twice. Okra leaf spots associated with C. malayensis have previously been reported from several countries but not Korea (Farr and Rossman 2019). To our knowledge, this is the first report of C. malayensis on okra in Korea. Because okra hectares may increase, the disease poses a threat to okra cultivation in Korea.

In the natural environment, plants communicate with various microorganisms (pathogenic or beneficial) and exhibit differential responses. In recent years, research on microbial volatile compounds (MVCs) has revealed them to be simple, effective and efficient groups of compounds that modulate plant growth and developmental processes. They also interfere with the signaling process. Different MVCs have been shown to promote plant growth via improved photosynthesis rates, increased plant resistance to pathogens, activated phytohormone signaling pathways, or, in some cases, inhibit plant growth, leading to death. Regardless of these exhibited roles, the molecules responsible, the underlying mechanisms, and induced specific metabolic/molecular changes are not fully understood. Here, we review current knowledge on the effects of MVCs on plants, with particular emphasis on their modulation of the salicylic acid, jasmonic acid/ethylene, and auxin signaling pathways. Additionally, opportunities for further research and potential practical applications presented.

A simple method based on alkaline extraction followed by acid precipitation can be used to form silica aquagel from corn cob ash (CCA). SEM-EDS analysis confirmed the high silicon and oxygen content of the extracted silica. XRD diffraction indicated that the obtained product was amorphous silica, while FTIR data demonstrated the presence of siloxane and silanol groups. TEM images revealed the silica to be amorphous, and have an agglomeration form with an average diameter of ∼50 nm. CCA-extracted silica (0.1 g/20 ml) was observed to have good catalytic potential with 100% removal of 12 × 10 −4 M methylene blue.

The primary step for efficient control of viral diseases is the development of simple, rapid, and sensitive virus detection. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) has been used to detect viral RNA molecules because of its simplicity and high sensitivity for a number of viruses. RT-LAMP for the detection of Potato virus X (PVX) was developed and compared with conventional reverse transcription polymerase chain reaction (RT-PCR) to demonstrate its advantages over RT-PCR. RT-LAMP reactions were conducted with or without a set of loop primers since one out of six primers showed PVX specificity. Based on real-time monitoring, RT-LAMP detected PVX around 30 min, compared to 120 min for RT-PCR. By adding a fluorescent reagent during the reaction, the extra step of visualization by gel electrophoresis was not necessary. RT-LAMP was conducted using simple inexpensive instruments and a regular incubator to evaluate whether RNA could be amplified at a constant temperature instead of using an expensive thermal cycler. This study shows the potential of RT-LAMP for the diagnosis of viral diseases and PVX epidemiology because of its simplicity and rapidness compared to RT-PCR.

This study describes an eco-friendly, rapid method for green synthesis of silver nanoparticles (Ag NPs) from an aqueous solution of silver nitrate using Pinus densiflora for. multicaulis Uyeki young cone extract in a single-pot process. Color changes, ultraviolet–visible spectra (444.5 nm), X-ray diffraction peaks (2θ = 39.68, 46.92, 68.12, and 79.10), and Fourier transform infrared spectroscopy (FT-IR) confirmed the presence of Ag NPs and phytochemicals. Transmission electron microscopy showed that the nanoparticles were mostly oval in shape, with a few triangular-shaped particles. Average particle size was 30–80 nm. Phytochemicals present in the young pine cone extract were likely responsible for the reduction of Ag+ ions. The synthesized Ag NPs (40 μg) had a 7 mm larger zone of inhibition against the skin pathogen Brevibacterium linens than commercial Ag NPs, Propionibacterium acnes (14 mm), Bacillus cereus (9 mm) and Staphylococcus epidermidis (10 mm).

This study aimed to understand the influence of heavy metals on 1-aminocyclopropane-1-carboxylate deaminase activity (ACCD) and acdS gene expression in Herbaspirillium sp. GW103. The GW103 strain ACCD activity decreased in cells grown in a medium supplemented with Pb and As, whereas cells grown in medium supplemented with Cu showed increase in enzyme activity. The GW103 strain produced 262.2 ± 6.17 μmol of α-ketobutyrate per milligram of protein per hour during ACC deamination at 25 °C after 24 h incubation. Using a PCR approach, an acdS coding-gene of 1.06 kbp was amplified in isolate GW103, showing 92% identity with Herbaspirillum seropedicae SmR1 acdS gene. Real time quantitative polymerase chain reaction results indicate that the acdS expression rate was increased (7.1-fold) in the presence of Cu, whereas it decreased (0.2- and 0.1-fold) in the presence of As and Pb.

Sclerotinia is a phytopathogenic genus of fungi that form sclerotia: black, hard, seed-like functioning bodies. Sclerotinia sclerotiorum and Sclerotinia minor are major threats to vegetable cultivation. In this study, we identified an efficient biocontrol agent against lettuce drop caused by S. minor. Initially, 43 bacterial strains isolated from Sclerotinia-infected field were screened for antifungal effects against S. minor. The selected bacterial strains (i.e. C5 and C25) conferred significant (P

Rice stripe disease is caused by the rice stripe virus (RSV) which is transmitted by the small brown plant hopper (SBPH). This disease significantly restricts rice productivity in East Asia. Major RSV resistance quantitative trait loci (QTLs) have been shown to be located on chromosome 11 in several resistant cultivars. However, the molecular identities of these QTLs are largely unknown. In this study, we identified the serine/threonine protein kinase OsPBL1 ( O RYZA S ATIVA ARABIDOPSIS PB S1-L IKE 1), a potential resistance gene to rice stripe disease, by reverse genetic screening with T-DNA insertional mutant lines. The OsPBL1 protein is highly conserved among various monocots and dicots, including Arabidopsis. Specifically, OsPBL1 exhibits 67 % amino acid sequence identity to AtPBS1 (AVRPPHB SUSCEPTIBLE1), a positive regulator of effector-triggered immunity (ETI) in Arabidopsis. Moreover, we show here that OsPBL1 transcripts are abundantly expressed in the leaves of Dongjin seedlings—an RSV-resistant—under normal growth conditions. Exogenous treatment with defense-related phytohormones such as cytokinin and salicylic acid increased the expression of OsPBL1. This gene is also modulated by the circadian rhythm. Furthermore, OsPBL1, OsPR1b, and OsPR2 transcripts were up-regulated to higher levels by SBPH treatment, which was specifically observed in RSV-resistant varieties. The OsPBL1 protein was found to localize to the nucleus and to be cleaved upon attack with either healthy or infected SBPHs. Taken together, our data indicate that OsPBL1 undergoes various transcriptional and post-translational modifications upon SBPH and/or RSV attack, similar to Arabidopsis PBS1. We propose that OsPBL1 is involved in antiviral defense signaling pathways in rice.

Oomycetes are generally known as water molds, and include diverse plant pathogenic organisms. In this review, wesummarized plant diseases mainly caused by oomycetes and highlighted ongoing trends in controlling and managingthese pathogens using eco-friendly ways.DOI: http://dx.doi.org/10.3126/njst.v15i1.12033Nepal Journal of Science and TechnologyVol. 15, No.1 (2014) 157-166

KACC10070 playing a role in reduction of ethylene in plant. The strain G19 increased the biomass of Chinese cabbage seedlings grown in the presence of 150 mM NaCl. The results indicated that the strain G19 promoted the growth of Chinese cabbage seedling under salinity stress through microbe-plant interactions.

The main objective of this study was to extract natural colorant from purple sweet potato powder (PSPP) via a water bath and ultrasound water bath using acidified ethanol (A. EtOH) as the extraction solvent. When optimizing the colorant extraction conditions of the solvents, acidified ethanol with ultrasound yielded a high extraction capacity and color intensity at pH2, temperature of 80°C, 20mL of A. EtOH, 1.5g of PSPP, time of 45min, and ultrasonic output power of 75W. Subsequently, the colorant was extracted using the optimized conditions for dyeing of textiles (leather, silk, and cotton). This natural colorant extraction technique can avoid serious environmental pollution during the extraction and is an alternative to synthetic dyes, using less solvent and simplified abstraction procedures. The extracted purple sweet potato natural colorant (PSPC) was used to dye leather, silk, and cotton fabrics in an eco-friendly approach with augmented antibacterial activity by in situ synthesis of silver nanoparticles (AgNPs) and dyeing. The optimal dyeing conditions for higher color strength (K/S) values were pH2 and 70°C for 45min. The colorimetric parameters L∗, a∗, b∗, C, and H were measured to determine the depth of the color. The Fourier transform infrared spectroscopy (FTIR) spectra of undyed control, dyed with PSPC and dyed with blend of PSPC and AgNPs treated leather, silk and cotton fabric were investigated to study the interaction among fiber type, nanoparticles, and dye. The structural morphology of leather and silk and cotton fabrics and the anchoring of AgNPs with elemental compositions were investigated by scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS). The dry and wet rubbing fastness for dye alone and dye with nanoparticles were grade 4-5 and 4, respectively. Thus, the results of the present study clearly suggest that in situ synthesis of AgNPs along with dyeing should be considered in the development of antimicrobial textile finishes.

Ethylene, a plant hormone, plays an important role inplant growth and development, and is also known as beinga stress hormone [4, 19]. It regulates a wide variety ofdevelopmental processes, including germination, root hairinitiation, root and shoot primordial formation andelongation, leaf and flower senescence and abscission, andfruit ripening [2]. The production of ethylene in plants isassociated with certain environmental and biologicalfactors such as temperature, light, gravity, nutrient, salt,and the other hormones [19]. In spite of its advantageouseffect on plants, the overproduction of ethylene in planttissues retards root growth and causes plant senescence[14]. Thus, increased ethylene level in plants correspondsnot only to induction of defense responses that help toenhance the survival of the plant under adverse conditions,but it also causes stress symptoms [7]. 1-Aminocyclopropane-1-carboxlyate (ACC), a precursorin the biosynthetic pathway of ethylene in plants [4], isconverted to ethylene by ACC oxidase. A variety ofdifferent stresses stimulate ACC synthesis, resulting in anincreased production of ethylene in plant tissue [7, 15].ACC deaminase (AcdS) is an enzyme that converts ACC to

In the present study, we synthesized silver and gold nanoparticles with a particle size of 10-20 nm, using Zingiber officinale root extract as a reducing and capping agent. Chloroauric acid (HAuCl4) and silver nitrate (AgNO3) were mixed with Z. officinale root extract for the production of silver (AgNPs) and gold nanoparticles (AuNPs). The surface plasmon absorbance spectra of AgNPs and AuNPs were observed at 436-531 nm, respectively. Optimum nanoparticle production was achieved at pH 8 and 9, 1 mM metal ion, a reaction temperature 50 °C and reaction time of 150-180 min for AgNPs and AuNPs, respectively. An energy-dispersive X-ray spectroscopy (SEM-EDS) study provides proof for the purity of AgNPs and AuNPs. Transmission electron microscopy images show the diameter of well-dispersed AgNPs (10-20 nm) and AuNPs (5-20 nm). The nanocrystalline phase of Ag and Au with FCC crystal structures have been confirmed by X-ray diffraction analysis. Fourier transform infrared spectroscopy analysis shows the respective peaks for the potential biomolecules in the ginger rhizome extract, which are responsible for the reduction in metal ions and synthesized AgNPs and AuNPs. In addition, the synthesized AgNPs showed a moderate antibacterial activity against bacterial food pathogens.

Microbiota in the niches of the rhizosphere zones can affect plant growth and responses to environmental stress conditions via mutualistic interactions with host plants. Specifically, some beneficial bacteria, collectively referred to as Plant Growth Promoting Rhizobacteria (PGPRs), increase plant biomass and innate immunity potential. Here, we report that Enterobacter sp. EJ01, a bacterium isolated from sea china pink (Dianthus japonicus thunb) in reclaimed land of Gyehwa-do in Korea, improved the vegetative growth and alleviated salt stress in tomato and Arabidopsis. EJ01 was capable of producing 1-aminocy-clopropane-1-carboxylate (ACC) deaminase and also exhibited indole-3-acetic acid (IAA) production. The isolate EJ01 conferred increases in fresh weight, dry weight, and plant height of tomato and Arabidopsis under both normal and high salinity conditions. At the molecular level, short-term treatment with EJ01 increased the expression of salt stress responsive genes such as DREB2b, RD29A, RD29B, and RAB18 in Arabidopsis. The expression of proline biosynthetic genes (i.e. P5CS1 and P5CS2) and of genes related to priming processes (i.e. MPK3 and MPK6) were also up-regulated. In addition, reactive oxygen species scavenging activities were enhanced in tomatoes treated with EJ01 in stressed conditions. GFP-tagged EJ01 displayed colonization in the rhizosphere and endosphere in the roots of Arabidopsis. In conclusion, the newly isolated Enterobacter sp. EJ01 is a likely PGPR and alleviates salt stress in host plants through multiple mechanisms, including the rapid up-regulation of conserved plant salt stress responsive signaling pathways.

This study was to investigate beneficial effects of microbial mixture on red pepper which was capable of promoting plant growth by solubilizing insoluble phosphate as well as protecting plants from pathogenic attack. Saccharomyces sp. L13 was isolated for phosphate solubilizing activity on aluminium phosphate, tricalcium phosphate, calcium hydrophosphate, and magnesium hydrophosphate. On the other hand, Bacillus sp. L32 was isolated for antagonistic activity against Phytophthora capsisi and Colletotrichum gloeosporioides, causing Phytophthora blight and Anthracnose disease in pepper, respectively. The strain L32 exhibited antagonistic activities both under dual culture assays and detached leaves assays. The each strain under the condition of mixed cultivation exhibited the same growth rates as one under pure cultivation. In greenhouse study, the mixed culture showed the both effect of plant growth promotion and reduction of disease symptom development against P. capsisi and C. gloeosporioides providing a potential as effective microbial agent for plant husbandry.

The popcorn disease caused by sclerotia forming fungi reduces the productivity of mulberry fruits in world wide. In Korea, only two species (Ciboria shiraiana and Scleromitrula shiraiana) have been reported as the major causal organisms and their morphological features are also largely unknown. Hereby, we report the first identification of another species (i.e. Ciboria carunculoides) in Korea and detailed features of their anamorphic stage. Fungi dominantly associated with sclerotia were purely isolated from infected mulberry fruits under the microscope. PCR-amplified DNA encoding 5.8S rRNA displayed 100% similarity to Ciboria carunculoides. The anamorphic features exhibited the absence of true mycelia. Instead, very short, aseptated, branched conidiophores were directly emerged from sclerotia. Phialides were usually three in number from each conidiophore, ampuliform to navicular in shape, slightly curved and tapering towards the apex. Conidia were produced from phialides and mostly found as one celled, pear shaped, not hyaline with smooth to uneven surface walled. Diversely modified features in phialides formed pseudo-mycelial structures around the host tissue. Combined all, current study is the first report of C. carunculoides isolated in Korea and the foremost detailed description of its anamorph stage.

Polyaniline/bacterial extracellular polysaccharide (Pn/EPS) nanocomposite was prepared by in situ polymerization of aniline using ammonium peroxydisulfate as oxidant. Transmission electron micrograph showed that the surface of the nanocomposite was rough, providing good possibility for adsorption of Cr(VI). Under optimized conditions, the nanocomposite removed 97.3 % (25 mg L−1) of Cr(VI) from aqueous solution. The Freundlich isotherm model and pseudo-first order rate expression better described the adsorption equilibrium of Pn/EPS nanocomposite. X-ray diffractogram peak for Cr2O3 (2θ = 24.5) in the nanocomposite confirmed the reduction of Cr(VI). Fourier transform infrared spectroscopy pattern of the nanocomposite confirmed the ionic interaction between Cr species and surface functional groups. The results of the study indicate that Pn/EPS nanocomposite could be used for the removal and detoxification of Cr(VI) from aqueous solution.

Protease production by Bacillus sp. SKK11 isolated from brackish environment was studied by solid-state fermentation with horse gram husk. Response surface methodology-based Box-Behnken design (BBD) was used to optimize the variables such as pH, maltose, and MgSO₄. The BBD design analysis showed a reasonable adjustment of the quadratic model with the experimental data. Statistics-based contour and three-dimensional (3-D) plots were generated to evaluate the changes in the response surface and to understand the relationship between the enzyme yield and the culture conditions. The maximum yield of the enzyme was observed at pH 9.0.

Silver nanoparticles have wide application in different scientific fields. The present study reports the simple and eco-friendly synthesis of silver nanoparticles using cow milk. The X-ray diffraction peaks (2θ—37.76, 46.12, 67.4, and 76.84) and scanning electron microscopy–energy dispersive spectroscopy peak, approximately at 3 keV, confirmed the presence of silver nanoparticles. Transmission electron micrograph showed that nanoparticles are mostly circular with an average size of 30–90 nm. The proteins present in cow milk could be responsible for Ag+ ions reduction. The synthesized nanoparticles (2 mM) can significantly inhibit (87.1%, 86.5%, and 83.5%) the growth of phytopathogens Colletotrichum coccodes, Monilinia sp., and Pyricularia sp.

Bioassay can be used for analysis of the biological potency of Bacillus thuringiensis (Bt) in fermentation and formulation but requires precise scheduling and several repetitions. Alternatively, this work explored if the endospore counting could be used to predict the potency of Bt technical powder. Analyses of Bt technical powers provided a strong linear relationship (r = 0.971) between the number of viable endospores and the potency of the technical powder against second instar Plutella xylostella (L.) larvae. Next, a Bt wettable powder formulation was stored at 25 and 40 °C for 12 weeks to investigate the influence of storage temperature on the prediction of insecticidal potency based on the counting. At 25 °C storage, the insecticidal potency could be predicted based on the counting, but at 40 °C the predicted insecticidal potency was much lower than the measured potency. These results suggest that the NT0423 endospore viability can be used to predict its potency in production, but the relationship may not be the same following the storage at high temperature.

Lettuce plants were grown under red, blue, or white light-emitting diode lights for four weeks after transplantation. Blue-light-treated lettuce exhibited the highest growth in view of root length, leaf area, number of leaves, chlorophyll content, and fresh and dry weight. In addition, the development of gray mold was significantly suppressed in blue-light-treated lettuce where the highest antioxidant activities were observed. The results suggest that the control efficacy of gray mold by Botrytis cinerea in lettuce is closely associated with the increase of antioxidant capacity as well as the development of compact morphology by blue-light treatment.

Prickly ash trees with shortened internodes, proliferation of shoots, phyllody and witches' brooms were observed for the first time in Korea. A phytoplasma was detected in infected trees by polymerase chain reaction amplification of 16S rDNA, 16S–23S intergenic spacer region and the fragment of rp operon sequences. The 16S rDNA sequences exhibited maximum (99.6%) similarity with Iranian lettuce phytoplasma, and the sequences of rp operon exhibited maximum (100%) similarity with golden rain phytoplasma. Based on the sequence analysis and phylogenetic studies, it was confirmed that phytoplasma infecting prickly ash trees in Korea belongs to the aster yellows group (subgroup 16SrI-B).

The effectiveness of nanoscale zero-valent iron (nZVI) to remove heavy metals from water is reduced by its low durability, poor mechanical strength, and tendency to form aggregates. A composite of zeolite and nanoscale zero-valent iron (Z–nZVI) overcomes these problems and shows good potential to remove Pb from water. FTIR spectra support nZVI loading onto the zeolite and reduced Fe 0 oxidation in the Z–nZVI composite. Scanning electron micrographs show aggregation was eliminated and transmission electron micrographs show well-dispersed nZVI in chain-like structures within the zeolite matrix. The mean surface area of the composite was 80.37 m 2 /g, much greater than zeolite (1.03 m 2 /g) or nZVI (12.25 m 2 /g) alone, as determined by BET-N 2 measurement. More than 96% of the Pb(II) was removed from 100 mL of solution containing 100 mg Pb(II)/L within 140 min of mixing with 0.1 g Z–nZVI. Tests with solution containing 1000 mg Pb(II)/L suggested that the capacity of the Z–nZVI is about 806 mg Pb(II)/g. Energy-dispersive X-ray spectroscopy showed the presence of Fe in the composite; X-ray diffraction confirmed formation and immobilization of Fe 0 and subsequent sorption and reduction of some of the Pb(II) to Pb 0 . The low quantity of Pb(II) recovered in water-soluble and Ca(NO 3 ) 2 -extractable fractions indicate low bioavailability of the Pb(II) removed by the composite. Results support the potential use of the Z–nZVI composite in permeable reactive barriers.

Polymyxa graminis, a root endoparasite of several cereal species, is considered to be non-pathogenic but serves as a vector of various plant viruses belonging to the genera Bymovirus, Furovirus, and Pecluvirus. Specifically, it reduces barley productivity by transmitting the Barley Yellow Mosaic Virus (BaYMV). To date, due to its obligate biotrophic property, no artificial culturing of P. graminis was reported and its quantification was also technically challenging. Here, we developed a novel and simple method to infect P. graminis within sterile barley roots in contamination free by preparing nearly pure zoospore inoculum. Such artificial maintenance of P. graminis was verified based on the presence of various developmental stages in infected barley roots under microscope. In addition, the population of resting spores in host tissue was determined by establishing standard curve between manually counted number of spores and Ct values of 18S rDNA amplification using quantitative real-time PCR. Furthermore, it was validated that standard curve generated was also applicable to estimate the abundance of P. graminis in soil environments. In conclusion, the present study would help to generate a system to investigate the etiological causes as well as management of plant diseases caused by P. graminis and BaYMV in tissue and soil.