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461por Bollmann, Stephanie R., Press, Caroline M., Tyler, Brett M., Grünwald, Niklaus J.“…We identified AGO homologs across many representative oomycete and stramenopile species, and annotated representative homologs in P. sojae. Furthermore, we demonstrate variable transcript levels of all identified AGO homologs in comparison to previously identified Dicer-like (DCL) and RNA-dependent RNA polymerase (RDR) homologs. …”
Publicado 2018
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462por Liu, Tingli, Song, Tianqiao, Zhang, Xiong, Yuan, Hongbo, Su, Liming, Li, Wanlin, Xu, Jing, Liu, Shiheng, Chen, Linlin, Chen, Tianzi, Zhang, Meixiang, Gu, Lichuan, Zhang, Baolong, Dou, Daolong“…Here we show that Phytophthora sojae and Verticillium dahliae secrete isochorismatases (PsIsc1 and VdIsc1, respectively) that are required for full pathogenesis. …”
Publicado 2014
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463por Ortiz, Gastón Ezequiel, Noseda, Diego Gabriel, Ponce Mora, María Clara, Recupero, Matías Nicolás, Blasco, Martín, Albertó, Edgardo“…From these four strains with the highest productivity, the proteolytic extract of A. sojae ATCC 20235 was shown to be an appropriate biocatalyst for hydrolysis of casein and gelatin substrates, increasing its antioxidant activities in 35% and 125%, respectively.…”
Publicado 2016
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464“…Combining the inorganic chemical silver nitrate (AgNO(3)) with the wall glucan elicitor (WGE) from the soybean pathogen Phytophthora sojae had an additive effect on the elicitation of soybean seeds, resulting in a yield of up to 745.1 µg gt(−1) glyceollin I. …”
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465“…It has been reported that the RXLR motif of P. sojae Avr1b, which is a close homolog of AVR3a, is required for binding to phosphatidylinositol monophosphates (PIPs). …”
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466por Chambard, Marie, Ben Mlouka, Mohamed Amine, Jing, Lun, Plasson, Carole, Cosette, Pascal, Leprince, Jérôme, Follet-Gueye, Marie-Laure, Driouich, Azeddine, Nguema-Ona, Eric, Boulogne, Isabelle“…This peptide is derived from the pathogenic oomycete Phytophthora sojae. In this study, the root and the RET responses to elicitation were dissected and sequenced using transcriptional, proteomic and metabolomic approaches. …”
Publicado 2022
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467por Attah, Victoria, Milner, David S, Fang, Yufeng, Yan, Xia, Leonard, Guy, Heitman, Joseph, Talbot, Nicholas J., Richards, Thomas A“…Using a combination of phylogenomic analysis and functional assays, we investigate the diversification of a horizontally-transferred xyloglucanase gene family in the model oomycete species Phytophthora sojae. Our analyses detect 11 genes retained in P. sojae among a complex pattern of gene duplications and losses. …”
Publicado 2023
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468“…Its expression was induced by Phytophthora sojae infection, salinity and drought stresses, and treatment with methyl jasmonate (MeJA) or ethephon (ETH). …”
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469por Huang, Jie, Gu, Lianfeng, Zhang, Ying, Yan, Tingxiu, Kong, Guanghui, Kong, Liang, Guo, Baodian, Qiu, Min, Wang, Yang, Jing, Maofeng, Xing, Weiman, Ye, Wenwu, Wu, Zhe, Zhang, Zhengguang, Zheng, Xiaobo, Gijzen, Mark, Wang, Yuanchao, Dong, Suomeng“…Here we demonstrate that PsAvr3c, an avirulence effector from oomycete plant pathogen Phytophthora sojae, physically binds to and stabilizes soybean serine/lysine/arginine-rich proteins GmSKRPs. …”
Publicado 2017
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470“…Two new Diaporthe species (D.camelliae-oleiferae and D.hunanensis) were proposed and described herein, and C.oleifera was revealed to be new host records of D.hubeiensis and D.sojae. This study indicated there is a potential of more undiscovered Diaporthe species from C.oleifera in China.…”
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471por Lin, Long, Yang, Zixiang, Tao, Min, Shen, Danyu, Cui, Chuanbin, Wang, Pingping, Wang, Limin, Jing, Maofeng, Qian, Guoliang, Shao, Xiaolong“…Here, we showed that OH11 could also control a variety of plant Phytophthora diseases caused by three major oomycetes (P. sojae, P. capsici and P. infestans). We provided abundant evidence to prove that OH11 protected host plants from Phytophthora pathogen infection by inhibiting mycelial growth, digesting cysts, suppressing cyst germination, and eliciting plant immune responses. …”
Publicado 2023
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472por Gajendran, Kamal, Gonzales, Michael D., Farmer, Andrew, Archuleta, Eric, Win, Joe, Waugh, Mark E., Kamoun, Sophien“…PFGD contains transcript, genomic, gene expression and functional assay data for Phytophthora infestans, which causes late blight of potato, and Phytophthora sojae, which affects soybeans. Automated analyses are performed on all sequence data, including consensus sequences derived from clustered and assembled expressed sequence tags. …”
Publicado 2006
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473“…The DREAM5 Systems Genetics B Challenge solicited algorithms to predict soybean plant resistance to the pathogen Phytophthora sojae from training sets including phenotype, genotype, and gene expression data. …”
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474por Zhang, Li-Ming, Yao, Jia-Zhi, Li, Yang, Li, Kai, Chen, Hong-Xia, Zhang, You-Zhi, Li, Yun-Feng“…Our previous study has also shown that administration of the total flavonoids, isolated from the extract of Xiaobuxin-Tang (XBXT, mild mind-easing decoction), comprising four Chinese medicines including Haematitum, Flos Inulae, Folium Phyllostachydis Henonis, and Semen Sojae Preparatum, exerted significant antidepressant-like effect in chronically mildly stressed rats, possibly mediated by serotonergic activation. …”
Publicado 2012
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475por Guin, Krishnendu, Chen, Yao, Mishra, Radha, Muzaki, Siti Rawaidah BM, Thimmappa, Bhagya C, O'Brien, Caoimhe E, Butler, Geraldine, Sanyal, Amartya, Sanyal, Kaustuv“…Identification of putative centromeres in closely related Candida sojae, Candida viswanathii and Candida parapsilosis indicates loss of ancestral HIR-associated centromeres and establishment of evolutionary new centromeres (ENCs) in C. albicans. …”
Publicado 2020
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476“…Glyceollins, produced to induce disease resistance responses against specific species, such as an incompatible pathogen Phytophthora sojae in soybeans, have the potential to exhibit anti-inflammatory activity in RAW 264.7 cells. …”
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477por Guo, Y.S., Crous, P.W., Bai, Q., Fu, M., Yang, M.M., Wang, X.H., Du, Y.M., Hong, N., Xu, W.X., Wang, G.P.“…Phylogenetic analyses based on five loci (ITS, TEF, CAL, HIS, and TUB) coupled with morphology of 113 representative isolates revealed that 19 Diaporthe species were isolated, representing 13 known species (including D. caryae, D. cercidis, D. citrichinensis, D. eres, D. fusicola, D. ganjae, D. hongkongensis, D. padina, D. pescicola, D. sojae, D. taoicola, D. unshiuensis and D. velutina) and six new species described here as D. acuta, D. chongqingensis, D. fulvicolor, D. parvae, D. spinosa and D. zaobaisu. …”
Publicado 2020
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478“…Aspergillus is an important fungal genus used for the fermentation of Asian foods; this genus is referred to as koji mold in Japan and China. A. oryzae, A. sojae, and A. tamari are used in the production of miso and shoyu in Japan, but a comprehensive taxonomic study of Aspergillus isolated from Meju, a fermented soybean starting material for traditional soy sauce and soybean paste in Korea, has not been conducted. …”
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479“…In the presence of Sb5 exudates, colonization of rhododendron leaf discs by 12 Phytophthora species/isolates was significantly enhanced, single zoospores of P. nicotianae infected annual vinca and P. sojae race 25 successfully attacked a non-host plant, Nicotiana benthamiana as well as resistant soybean cultivars with RPS1a or RPS3a. …”
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480por Yang, Min, Duan, Shengchang, Mei, Xinyue, Huang, Huichuan, Chen, Wei, Liu, Yixiang, Guo, Cunwu, Yang, Ting, Wei, Wei, Liu, Xili, He, Xiahong, Dong, Yang, Zhu, Shusheng“…P. cactorum had a higher utilization and detoxification ability against ginsenosides–a group of defense compounds from Panax notoginseng–compared with the narrow host pathogen P. sojae. The elevated expression levels of detoxification enzymes and hydrolase activity-associated genes after exposure to ginsenosides further supported that the high detoxification and utilization ability of P. cactorum play a crucial role in the rapid adaptability of the pathogen to host plant defense compounds and fungicides.…”
Publicado 2018
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