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221por Kovacova, Viera, Zluvova, Jitka, Janousek, Bohuslav, Talianova, Martina, Vyskot, Boris“…The mikimopine synthase (mis) gene evolved in a different manner in the branch leading to Nicotiana tabacum and N. tomentosiformis, in the branch leading to N. glauca and in the genus Linaria. …”
Publicado 2014
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222por Djami-Tchatchou, Arnaud T., Maake, Mmapula P., Piater, Lizelle A., Dubery, Ian A.Enlace del recurso
Publicado 2015
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223por Stamler, Rio A., Holguin, Omar, Dungan, Barry, Schaub, Tanner, Sanogo, Soumaila, Goldberg, Natalie, Randall, Jennifer J.“…Inoculation of chile pepper with zoospores of non-host Phytophthora nicotianae or the chemical elicitor beta-aminobutyric acid (BABA) significantly inhibited foliar blight caused by Phytophthora capsici. …”
Publicado 2015
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224“…Exogenous applied brassinolide (BL, the most active BR) induced, while brassinazole (BRZ, a BR biosynthesis inhibitor) reduced alternative respiration and AOX1 expression in Nicotiana benthamiana. Chemical scavenging of H(2)O(2) and virus-induced gene silencing (VIGS) of NbRBOHB compromised the BR-induced alternative respiratory pathway, and this result was further confirmed by NbAOX1 promoter analysis. …”
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225“…In this study, we determined whether homologues of these LecRKs from the Solanaceous plants Nicotiana benthamiana and tomato (Solanum lycopersicum) play similar roles in defence against Phytophthora. …”
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226por Zheng, Luping, Yao, Jinai, Gao, Fangluan, Chen, Lin, Zhang, Chao, Lian, Lingli, Xie, Liyan, Wu, Zujian, Xie, Lianhui“…Fibrillarin2 is a nucleolar protein of Nicotiana benthamiana (N. benthamiana). Its cDNA was amplified by RT-PCR and inserted into expression vector pEarley101 labeled with yellow fluorescent protein (YFP). …”
Publicado 2016
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227“…In this study, we identified 16 putative Las effectors via bioinformatics, and transiently expressed them in Nicotiana benthamiana. Diverse subcellular localization with different shapes and aggregation patterns of the effector candidates were revealed by UV- microscopy after transient expression in leaf tissue. …”
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228por Zhou, Wenwu, Brockmöller, Thomas, Ling, Zhihao, Omdahl, Ashton, Baldwin, Ian T, Xu, Shuqing“…Analyzing 60 HAE-induced leaf transcriptomes from closely-related Nicotiana species revealed a key gene co-expression network (M4 module) which is co-activated with the HAE-induced JA accumulations but is elicited independently of JA, as revealed in plants silenced in JA signaling. …”
Publicado 2016
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229por Ponndorf, Daniel, Ehmke, Sven, Walliser, Benjamin, Thoss, Kerstin, Unger, Christoph, Görs, Solvig, Daş, Gürbüz, Metges, Cornelia C., Broer, Inge, Nausch, Henrik“…Different variants of the cphB coding region from Thermosynechococcus elongatus BP‐1 were transiently expressed in Nicotiana benthamiana plants. Translation and enzyme stability were optimized to produce high amounts of active CGPase. …”
Publicado 2016
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230“…The NTD is also the location for the majority of the predicted O-glycosylation sites that were variable among Nicotiana spp. The C-terminal domain (CTD) contains an Ole e 1-like domain, that was predicted to form beta-sheets that are similar in position and length among Nicotiana spp. and among stylar AGPs. …”
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231por Ligaba-Osena, Ayalew, Hankoua, Bertrand, DiMarco, Kay, Pace, Robert, Crocker, Mark, McAtee, Jesse, Nagachar, Nivedita, Tien, Ming, Richard, Tom L.“…This study investigated whether DypB, the lignin-degrading peroxidase from Rodococcus jostii, depolymerizes lignin and reduces recalcitrance in transgenic tobacco (Nicotiana benthamiana). The protein was targeted to the cytosol or the ER using ER-targeting and retention signal peptides. …”
Publicado 2017
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232“…Nectaries and nectar of the five Nicotiana species contained different amounts of sucrose, glucose, and fructose. …”
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233por Li, Zhurui, Shi, Jing, Yu, Lu, Zhao, Xiaozhen, Ran, Longlu, Hu, Deyu, Song, Baoan“…Subsequent protein sequence alignments were used to find the potential methylases and demethylases in Nicotiana tabacum (N. tabacum). Finally, reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) was used to analyse the gene expression levels of the potential methylases and demethylases in the N. tabacum leaf. …”
Publicado 2018
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234“…Through knock-down of NbTM8 by virus induced gene silencing in Nicotiana benthamiana, we show that NbTM8 represses miR172 together with another MADS-box gene, SHORT VEGETATIVE PHASE (NbSVP). …”
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235por Wang, Xuewen, Yang, Shuai, Chen, Yongdui, Zhang, Shumeng, Zhao, Qingshi, Li, Meng, Gao, Yulong, Yang, Long, Bennetzen, Jeffrey L.“…In the model plants in Nicotiana genus e.g. N. benthamiana, a comprehensive assessment of SSR content has become possible now because several Nicotiana genomes have been sequenced. …”
Publicado 2018
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236“…Transgenic plants expressing artificial microRNAs (amiRNAs) have been shown to confer specific resistance to corresponding viruses. Here, we generated Nicotiana benthamiana transgenic lines containing Oryza sativa miR528 as backbone, expressing amiRNAs targeting RNA-dependent RNA polymerase (RdRp) gene of Cymbidium mosaic virus (CymMV) and Odontoglossum ringspot virus (ORSV). …”
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237“…Among these 91 materials, we assessed the residual toxicity of 32 extracts against first instar larvae (< 5 h old) of G. molesta in the laboratory. Nicotiana tabacum L., used at the concentration of 2 mg/ml, showed the highest corrected mortality (92.0%) with a lethal time (LT(50)) value of 12.9 h. …”
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238por Grosse‐Holz, Friederike, Madeira, Luisa, Zahid, Muhammad Awais, Songer, Molly, Kourelis, Jiorgos, Fesenko, Mary, Ninck, Sabrina, Kaschani, Farnusch, Kaiser, Markus, van der Hoorn, Renier A.L.“…Agroinfiltrated Nicotiana benthamiana is a flexible and scalable platform for recombinant protein (RP) production, but its great potential is hampered by plant proteases that degrade RPs. …”
Publicado 2018
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240por Módolo, Diego G., Horn, Cynthia S., Soares, José S. M., Yunes, José A., Lima, Leila M., de Sousa, Sylvia M., Menossi, MarceloEnlace del recurso
Publicado 2018
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