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2721por Kvitko, Brian H., Park, Duck Hwan, Velásquez, André C., Wei, Chia-Fong, Russell, Alistair B., Martin, Gregory B., Schneider, David J., Collmer, Alan“…The γ-proteobacterial plant pathogen Pseudomonas syringae pv. tomato DC3000 uses the type III secretion system to inject ca. 28 Avr/Hop effector proteins into plants, which enables the bacterium to grow from low inoculum levels to produce bacterial speck symptoms in tomato, Arabidopsis thaliana, and (when lacking hopQ1-1) Nicotiana benthamiana. The effectors are collectively essential but individually dispensable for the ability of the bacteria to defeat defenses, grow, and produce symptoms in plants. …”
Publicado 2009
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2722“…To identify the sources and to reduce this heterogeneity, we transformed tobacco (Nicotiana tabacum L.) BY-2 cells with a gene encoding green fluorescent protein (GFP) using Agrobacterium tumefaciens, and then introduced a simple cloning procedure to generate cell lines derived from the individual transformed cells. …”
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2723“…Sunflower (Helianthus annuus L.), wild type (wt), Rubisco-deficient (–RBC), FNR-deficient (–FNR), and Cyt b(6)f deficient (–CBF) transgenic tobacco (Nicotiana tabacum L.) were grown in a growth chamber. …”
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2724por Oh, Sung Aeong, Pal, Madhumita Das, Park, Soon Ki, Johnson, James Andrew, Twell, David“…Here, novel male gametophytic microtubule-reporter Nicotiana tabacum plants were constructed, expressing a green fluorescent protein-α-TUBULIN fusion protein (GFP-TUA6) under the control of a microspore-specific promoter. …”
Publicado 2010
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2725por Halterman, Dennis A., Chen, Yu, Sopee, Jiraphan, Berduo-Sandoval, Julio, Sánchez-Pérez, Amilcar“…In support of this finding, we observed that expression of IPI-O4 via Agrobacterium blocked recognition of IPI-O1, leading to inactivation of RB-mediated programmed cell death in Nicotiana benthamiana. CONCLUSIONS: In this study we definitively demonstrate and provide the first evidence that P. infestans can defeat an R protein through inhibition of recognition of the corresponding effector protein.…”
Publicado 2010
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2726por Matoba, Nobuyuki, Husk, Adam S., Barnett, Brian W., Pickel, Michelle M., Arntzen, Charles J., Montefiori, David C., Takahashi, Atsushi, Tanno, Kazunobu, Omura, Satoshi, Cao, Huyen, Mooney, Jason P., Hanson, Carl V., Tanaka, Haruo“…For recombinant (r)AH expression, we evaluated a tobacco mosaic virus-based system in Nicotiana benthamiana plants as a means to facilitate molecular engineering and cost-effective mass production. …”
Publicado 2010
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2727por Kim, Sang Hee, Gao, Fei, Bhattacharjee, Saikat, Adiasor, Joseph A., Nam, Ji Chul, Gassmann, Walter“…Intriguingly, when transiently expressed in Nicotiana benthamiana, SRFR1, RPS4 and SNC1 are in a common protein complex in a cytoplasmic microsomal compartment. …”
Publicado 2010
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2728por Bos, Jorunn I. B., Prince, David, Pitino, Marco, Maffei, Massimo E., Win, Joe, Hogenhout, Saskia A.“…A total of 48 effector candidates were identified, cloned, and subjected to transient overexpression in Nicotiana benthamiana to assay for elicitation of a phenotype, suppression of the Pathogen-Associated Molecular Pattern (PAMP)–mediated oxidative burst, and effects on aphid reproductive performance. …”
Publicado 2010
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2729por van Ooijen, Gerben, Lukasik, Ewa, van den Burg, Harrold A, Vossen, Jack H, Cornelissen, Ben J C, Takken, Frank L W“…Silencing of RSI2-related HSP20s in Nicotiana benthamiana compromised the hypersensitive response that is normally induced by auto-active variants of I-2 and Mi-1, a second tomato R protein. …”
Publicado 2010
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2730por Yang, Xiuling, Wang, Yu, Guo, Wei, Xie, Yan, Xie, Qi, Fan, Longjiang, Zhou, Xueping“…METHODOLOGY/PRINCIPAL FINDINGS: Solanum lycopersicum plant leaves systemically infected with Tomato yellow leaf curl China virus (TYLCCNV) alone or together with its associated betasatellite (TYLCCNB), and Nicotiana benthamiana plant leaves systemically infected with TYLCCNV alone, or together with TYLCCNB or with mutant TYLCCNB were harvested for RNA extraction; sRNA cDNA libraries were then constructed and submitted to Solexa-based deep sequencing. …”
Publicado 2011
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2731“…We have recently demonstrated that it is feasible to engineer benzylglucosinolate (BGLS) in the non-cruciferous plant Nicotiana benthamiana by transient expression of five genes from Arabidopsis thaliana. …”
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2732por Pečenková, Tamara, Hála, Michal, Kulich, Ivan, Kocourková, Daniela, Drdová, Edita, Fendrych, Matyáš, Toupalová, Hana, Žárský, Viktor“…Intracellular localization of both Exo70 proteins was studied following a GFP fusion assay and Agrobacterium-mediated transient expression of the constructs in Nicotiana benthamiana leaf epidermis. GFP-Exo70H1 localizes in the vesicle-like structures, while GFP-Exo70B2 is localized mainly in the cytoplasm. …”
Publicado 2011
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2733por Shimura, Hanako, Pantaleo, Vitantonio, Ishihara, Takeaki, Myojo, Nobutoshi, Inaba, Jun-ichi, Sueda, Kae, Burgyán, József, Masuta, Chikara“…Cucumber mosaic virus (CMV) Y satellite RNA (Y-sat) is a non-coding subviral RNA and modifies the typical symptom induced by CMV in specific hosts; Y-sat causes a bright yellow mosaic on its natural host Nicotiana tabacum. The Y-sat-induced yellow mosaic failed to develop in the infected Arabidopsis and tomato plants suggesting a very specific interaction between Y-sat and its host. …”
Publicado 2011
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2734por Castilho, Alexandra, Gattinger, Pia, Grass, Josephine, Jez, Jakub, Pabst, Martin, Altmann, Friedrich, Gorfer, Markus, Strasser, Richard, Steinkellner, Herta“…Here, we demonstrate the modulation of the plant glycosylation pathway toward the formation of human-type bisected and branched complex N-glycans. Glycoengineered Nicotiana benthamiana lacking plant-specific N-glycosylation (i.e. β1,2-xylose and core α1,3-fucose) was used to transiently express human erythropoietin (hEPO) and human transferrin (hTF) together with modified versions of human β1,4-mannosyl-β1,4-N-acetylglucosaminyltransferase (GnTIII), α1,3-mannosyl-β1,4-N-acetylglucosaminyltransferase (GnTIV) and α1,6-mannosyl-β1,6-N-acetylglucosaminyltransferase (GnTV). hEPO was expressed as a fusion to the IgG-Fc domain (EPO-Fc) and purified via protein A affinity chromatography. …”
Publicado 2011
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2735por Trenado, Helena P., Orílio, Anelise F., Márquez-Martín, Belén, Moriones, Enrique, Navas-Castillo, Jesús“…Successful infection by agroinoculation of several species of Ipomoea (including sweet potato) and Nicotiana benthamiana was confirmed by PCR, dot blot and Southern blot hybridization. …”
Publicado 2011
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2736por Dong, Suomeng, Yin, Weixiao, Kong, Guanghui, Yang, Xinyu, Qutob, Dinah, Chen, Qinghe, Kale, Shiv D., Sui, Yangyang, Zhang, Zhengguang, Dou, Daolong, Zheng, Xiaobo, Gijzen, Mark, M. Tyler, Brett, Wang, Yuanchao“…Transient expression of Avr3b in Nicotiana benthamiana increased susceptibility to P. capsici and P. parasitica, with significantly reduced accumulation of reactive oxygen species (ROS) around invasion sites. …”
Publicado 2011
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2737“…In this article, we propose a novel strategy towards the generation of seedless or less-seeded fruits by downregulation of flavonol biosynthesis in tobacco (Nicotiana tabacum cv Xanthi) through post-transcriptional gene silencing (PTGS) of FLS encoding mRNA. …”
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2738“…Transient expression assay in Nicotiana benthamiana leaves support that PIF4 directly activates YUC8 expression in vivo. …”
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2739por Savory, Elizabeth A., Zou, Cheng, Adhikari, Bishwo N., Hamilton, John P., Buell, C. Robin, Shiu, Shin-Han, Day, Brad“…We found that PscRXLR1 was up-regulated during the early stages of infection of plants, and, moreover, that heterologous expression of PscRXLR1 in Nicotiana benthamiana elicits a rapid necrosis. More interestingly, we also demonstrate that PscRXLR1 arises as a product of alternative splicing, making this the first example of an alternative splicing event in plant pathogenic oomycetes transforming a non-effector gene to a functional effector protein. …”
Publicado 2012
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2740por Macho, Alberto P., Zumaquero, Adela, Gonzalez-Plaza, Juan J., Ortiz-Martín, Inmaculada, Rufián, José S., Beuzón, Carmen R.“…In support of this notion, effectors from Pseudomonas syringae pv. tomato (Pto) DC3000 have been classified into redundant effector groups (REGs), analysing virulence of polymutants in the model plant Nicotiana benthamiana. However, using competitive index (CI) as a virulence assay, we were able to establish the individual contribution of AvrPto1(Pto) (DC3000) to Pto DC3000 virulence in tomato, its natural host, even though typically, contribution to virulence of AvrPto1 is only shown in strains also lacking AvrPtoB (also called HopAB2), a member of its REG. …”
Publicado 2012
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