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Electrocatalytic cleavage of a lignin β-O-4 model compound and coupling with nitrogen-containing aromatics using Prussian blue analogue-derived nickel–cobalt spinel

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Journal of Energy Chemistry 2025年第1期100卷 628-636页

作者： Yi Qi Xueying Chen Bowen Liu Xuliang Lin Xueqing Qiu Yanlin Qin Guangdong Provincial Key laboratory of plant Resources Biorefinery School of Chemical Engineering and Light Industry Guangdong University of Technology Guangdong Provincial laboratory of Chemistry and Fine Chemical Engineering Jieyang Center Guangdong Basic Research Center of Excellence for Ecological Security and Green Development Guangdong University of Technology

Electrochemical conversion of lignin for the production of high-value heterocyclic aromatic compounds has great *** demonstrate the targeted synthesis and cation modulation of NiCo2O4spinel nanoboxes,synthesized via cation exchange and calcination *** catalysts exhibit excellent efficacy in the electrocatalytic conversion of lignin model compounds,specifically 2-phenoxy-1-phenylethanol,into nitrogen-containing aromatics,achieving high conversion rates and *** catalysts were synthesized via a cation exchange and calcination oxidation process,using Prussian blue nanocubes as *** porous architecture and polymetallic composition of the NiCo2O4spinel demonstrated superior performance in electrocatalytic oxidative coupling,achieving a 99.2 wt%conversion rate of the 2-phenoxy-1-phenylethanol with selectivities of 37.5 wt%for quinoline derivatives and 31.5 wt%for *** innovations include the development of a sustainable one-pot synthesis method for quinoline derivatives,the elucidation of a multistage reaction pathway involving CAO bond cleavage,hydroxyaldol condensation,and CAN bond formation,and a deeper mechanistic understanding derived from DFT *** work establishes a new strategy for lignin valorization,offering a sustainable route to produce high-value nitrogen-containing aromatics from renewable biomass under mild conditions,without the need for additional reagents.

关键词： Spinel Biomass valorization Electrocatalysis Lignin oxidation Coupling

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Progress and prospects of studies on Polymyxa graminis and its transmitted cereal viruses in China

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Progress in Natural Science:Materials International 2005年第6期15卷 481-490页

作者： CHEN Jianping*(virology and Biotechnology Institute, Zhejiang Academy of Agricultural Sciences, Key laboratory of plant virology, Ministry of Agriculture and Zhejiang Province, Hangzhou 310021, China) Key laboratory of plant virology Virology and Biotechnology Institute Zhejiang Academy of Agricultural Sciences Hangzhou 310021 China

Polymyxa graminis is a eukaryotic obligate biotrophic parasite of plant roots that belongs to a poorly studied discrete taxonomic unit informally called “plasmodiophorids”. P. graminis is nonpathogenic, but has the ability to acquire and transmit nine plant viruses which belong to genera Bymovirus and Furovirus and cause serious diseases in cereal crop species and also result in significant yield reductions in China and elsewhere. Genus Bymovirus contains barley yellow mosaic virus (BaYMV), barley mild mosaic virus (BaMMV), wheat yellow mosaic virus (WYMV), wheat spindle streak mosaic virus (WSSMV), and oat mosaic virus (OMV), and genus Furovirus contains soil-borne wheat mosaic virus (SBWMV), oat golden stripe virus (OGSV), and newly identified Chinese wheat mosaic virus (CWMV) and soil-borne cereal mosaic virus (SBCMV). All these viruses have been sequenced and their worldwide distributions have been studied. The viruses are protected by the environment within P. graminis resting spores that may remain dormant but viable for decades (probably until a suitable host plant is encountered). Spontaneous deletion mutants of SBWMV, OGSV and OMV are detected, and these deletion mutants are not transmissible by the fungus. The persistent, soil-borne nature of these diseases makes the use of virus-resistant crop varieties currently the only practical and environmentally friendly means to control them, and a large number of disease resistant germplasms have been screened.

关键词： Polymyxa graminis cereal viruses genus Bymovirus genus Furovirus.

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Leafhopper salivary carboxylesterase suppresses JA-Ile synthesis to facilitate initial arbovirus transmission in rice phloem

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plant Communications 2024年第9期5卷 116-135页

作者： Yunhua Chi Hongxiang Zhang Siyu Chen Yu Cheng Xiaofeng Zhang Dongsheng Jia Qian Chen Hongyan Chen Taiyun Wei Vector-borne Virus Research Center Fujian Province Key Laboratory of Plant VirologyInstitute of Plant VirologyFujian Agriculture and Forestry UniversityFuzhouFujian 350002China

plant jasmonoyl-L-isoleucine(JA-Ile)is a major defense signal against insect feeding,but whether or how insect salivary effectors suppress JA-Ile synthesis and thus facilitate viral transmission in the plant phloem remains *** carboxylesterases(CarEs)are the third major family of detoxification ***,we identify a new leafhopper CarE,CarE10,that is specifically expressed in salivary glands and is secreted into the rice phloem as a saliva *** CarE10 directly binds to rice jasmonate resistant 1(JAR1)and promotes its degradation by the proteasome ***,the direct association of CarE10 with JAR1 clearly impairs JAR1 enzyme activity for conversion of JA to JA-Ile in an in vitro JAIle synthesis system.A devastating rice reovirus activates and promotes the co-secretion of virions and CarE10 via virus-induced vesicles into the saliva-storing salivary cavities of the leafhopper vector and ultimately into the rice phloem to establish initial ***,a virus-mediated increase in CarE10 secretion or overexpression of CarE10 in transgenic rice plants causes reduced levels of JAR1 and thus suppresses JA-Ile synthesis,promoting host attractiveness to insect vectors and facilitating initial viral *** findings provide insight into how the insect salivary protein CarE10 suppresses host JA-Ile synthesis to promote initial virus transmission in the rice phloem.

关键词： leafhopper salivary protein CarE10 JAR1 degradation JA-Ile synthesis rice phloem initial viral transmission

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Turnip mosaic virus pathogenesis and host resistance mechanisms in Brassica

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Horticultural plant Journal 2024年第4期10卷 947-960页

作者： Guanwei Wu Xinxin Fang Tianqi Yu Jianping Chen Fei Yan State Key laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products Institute of Plant VirologyNingbo UniversityNingboZhejiang 315211China Key laboratory of Biotechnology in plant Protection of MARA and Zhejiang Province Institute of Plant VirologyNingbo UniversityNingboZhejiang 315211China

Turnip mosaic virus(TuMV)is a devastating potyvirus pathogen that infects a wide variety of both cultivated and wild Brassicaceae *** urgently need more information and understanding of TuMV pathogenesis and the host responses involved in disease development in cruciferous *** displays great versatility in viral pathogenesis,especially in its replication and intercellular ***,in the coevolutionary arms races between TuMV and its hosts,the virus has evolved to co-opt host factors to facilitate its infection and counter host defense *** review mainly focuses on recent advances in understanding the viral factors that contribute to the TuMV infection cycle and the host resistance mechanism in ***,we propose some future research directions on TuMV pathogenesis and control strategies to design durable TuMV-resistant Brassica crops.

关键词： Turnip mosaic virus Brassica Resistance genes Host factors Infection biology

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BnWRI1 coordinates fatty acid biosynthesis and photosynthesis pathways during oil accumulation in rapeseed

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Journal of Integrative plant Biology 2014年第6期56卷 582-593页

作者： Xue-Long Wu Zhi-Hong Liu Zhang-Hua Hu Rui-Zhi Huang Institute of virology and Biotechnology Zhejiang Academy of Agricultural Sciences Key Laboratory of Plant Metabolic Engineering of Zhejiang Province

Photosynthesis in“green”seeds, such as rapeseed, soybean, and Arabidopsis, plays a substantial role in the improved efficiency of oil accumulation. However, the molecular mecha-nism underpinning the coordinated expression of fatty acid （FA） biosynthesis-and photosynthesis-related genes in such develop-ing seeds remains to be elucidated. Here, we found that seed-specific overexpression of BnWRI1, a WRI1 homolog from rapeseed （Brassica napus cv. ZGY2）, results in enhanced chlorophyl content in developing seeds and increased oil content and seed mass in matured seeds. BnWRI1 was co-expressed with BnBCCP and BnCAB, two marker genes of FA biosynthesis and photosynthesis during seed development, respectively. Over-expression of BnWRI1 increased expression of both marker genes. Further, the nuclear-localized BnWRI1 protein was found to act as a transcription activator. It could bind to the GT1-element and/or GCC-box, which are widespread in the upstream regions of genes involved in FA biosynthesis and photosynthesis pathways. Accordingly, BnWRI1 could interact with promoters of BCCP2 and LHB1B2 in vivo. These results suggested that BnWRI1 may coordinate FA biosynthesis and photosynthesis pathways in developing seeds via directly stimulating expression of GT1-element and/or GCC-box containing genes.

关键词： BnWRI1 Brassica napus oil accumulation photosynthesis transcription factor

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Identification of Pns12 as the second silencing suppressor of Rice gall dwarf virus

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Science China(Life Sciences) 2011年第3期54卷 201-208页

作者： WU JianGuo WANG ChunZheng DU ZhengGuo CAI LiJun HU MeiQun WU ZuJian LI Yi XIE LianHui Institute of plant virology Fujian Agriculture and Forestry University Key Laboratory of Plant Virology of Fujian Province Fuzhou 350002 China Peking-Yale Joint Center for plant Molecular Genetics and Agrobiotechnology National Laboratory of Protein Engineering and Plant Genetic Engineering College of Life Sciences Peking University Beijing 100871 China

RNA silencing is a conserved mechanism found ubiquitously in eukaryotic *** has been used to regulate gene expression and *** addition,RNA silencing serves as an important mechanism in plants' defense against invasive nucleic acids,such as viruses,transposons,and *** a counter-defense,most plants,and some animal viruses,encode RNA silencing suppressors to interfere at one or several points of the silencing *** this study,we showed that Pns12 of RGDV (Rice gall dwarf virus) exhibits silencing suppressor activity on the reporter green fluorescent protein in transgenic Nicotiana benthamiana line ***12 of RGDV suppressed local silencing induced by sense RNA but had no effect on that induced by *** of Pns12 also enhanced Potato virus X pathogenicity in ***,these results suggested that RGDV Pns12 functions as a virus suppressor of RNA silencing,which might target an upstream step of dsRNA formation in the RNA silencing ***,we showed that Pns12 is localized mainly in the nucleus of *** leaf cells.

关键词： Rice gall dwarf virus Pns12 silencing suppressor

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Sequence Analysis of Segment 8 of Five Chinese Isolates of Rice Gall Dwarf Virus and Expression of a Main Outer Capsid Protein in Escherichia coli

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中国病毒学 2007年第4期22卷 294-300页

作者： Ming-rong DENG Xiao-lei RUAN Fu-xiu LIU Qin ZHAO Hua-ping LI laboratory of plant virology South China Agricultural University Guangzhou Guangdong 510642 China

The rice gall dwarf disease, caused by the Rice gall dwarf virus (RGDV) is a serious disease occurring in rice in many regions of Guangdong province. As a basis to control the disease we have studied the genomic diversity of a variety of isolates from different locations. Genome segment 8(S8), encoding a main outer capsid protein (Pns8) of RGDV five isolates (BL, CH, DQ, GZ, XY) from Guangdong province was cloned and sequenced. The results revealed that all the S8 segments of the five isolates consisted of 1 578 nucleotides and had a single open reading frame (ORF) extending for 1 301 nucleotides from nucleotide 21 which encoded a polypeptide of 426 amino acids with an estimated molecular weight of 47.4 kDa. The S8 full-length sequence and the ORF sequence shared 97.3%-98.8% and 97.3%-99.1% nucleotide sequence identities within the five Chinese isolates, and shared 94.8%-95.6% and 95.0%-96.0% identities with those of the Thailand isolate respectively. The deduced amino acid sequence of Pns8 in GZ isolate was identical to that in the Thailand isolate, while the amino acid sequence variability of Pns8 within five Chinese isolates ranged from 0.5% to 2.1%. These results indicate that the S8 segment of RGDV is highly conserved in different isolates from different locations. The S8 cDNA from the XY isolate was cloned into the plasmid vector pET-28b(+) and a fused expression protein with an apparent molecular mass of 51kDa was specifically detected in an analysis of Escherichia coli Rossetta(DE3)Ⅱcells. To our knowledge, this is the first report on analysis of the RGDV segment 8 sequence and genetic comparison of different RGDV isolates and their protein expression.

关键词：序列分析 8片段水稻矮化病毒大肠杆菌原核表达核衣壳蛋白

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Genome analysis of Heliothis virescens ascovirus 3h isolated from China

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Virologica Sinica 2017年第2期32卷 147-154页

作者： Guo-Hua Huang Dian-Hai Hou Manli Wang Xiao-Wen Cheng Zhihong Hu State Key laboratory of virology Microorganisms & Viruses Culture Collection CenterWuhan Institute of VirologyChinese Academy of Sciences Hunan Provincial Key laboratory for Biology and Control of plant Diseases and Insect Pests Institute of VirologyHunan Agricultural University Department of Microbiology 32 Pearson HallMiami University

No ascovirus isolated from China has been sequenced so far. Therefore, in this study, we aimed to sequence the genome of Heliothis virescens ascovirus 3h （HvAV-3h） using the 454 pyrosequencing technology. The genome was found to be 190,519-bp long with a G＋C content of 45.5%. We also found that it encodes 185 hypothetical open reading frames （ORFs） along with at least 50 amino acids, including 181 ORFs found in other ascoviruses and 4 unique ORFs. Gene-parity plots and phylogenetic analysis revealed a close relationship between HvAV-3h and three other HvAV-3a strains and a distant relationship with Spodoptera frugiperda ascovirus la （SfAV-la）, Trichoplusia ni ascovirus 6a （TnAV-6a）, and Diadromus pulchellus ascovirus 4a （DpAV-4a）. Among the 185 potential genes encoded by the genome, 44 core genes were found in all the sequenced ascoviruses. In addition, 25 genes were found to be conserved in all ascoviruses except DpAV-4a. In the HvAV-3h genome, 24 baculovirus repeat ORFs （bros） were present, and the typical homologous repeat regions （hrs） were absent. This study supplies information important for understanding the conservation and functions of ascovirus genes as well as the variety of ascoviral genomes.

关键词： Heliothis virescens ascovirus 3h (HvAV-3h) genome organization bro genes phylogenetic relationship

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Suppression of Jasmonic Acid-Mediated Defense by Viral-Inducible MicroRNA319 Facilitates Virus Infection in Rice

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Molecular plant 2016年第9期9卷 1302-1314页

作者： Chao Zhang Zuomei Ding Kangcheng Wu Liang Yang Yang Li Zhen Yang Shan Shi Xiaojuan Liu Shanshan Zhao Zhirui Yang Yu Wang Luping Zheng Juan Wei Zhenguo Du Aihong Zhang Hongqin Miao Yi Li Zujian Wu Jianguo Wu Fujian Province Key laboratory of plant virology Institute of Plant Virology Fujian Agriculture and Forestry University Fuzhou Fujian 350002 China The State Key laboratory of Protein and plant Gene Research College of Life Sciences Peking University Beijing 100871 China / plant Protection Institute Hebei Academy of Agriculture and Forestry Sciences Baoding 071000 China These authors contributed equally to this article.

MicroRNAs （miRNAs） are pivotal modulators of plant development and host-virus interactions. However, the roles and action modes of specific miRNAs involved in viral infection and host susceptibility remain largely unclear. In this study, we show that Rice ragged stunt virus （RRSV） infection caused increased accumulation of miR319 but decreased expression of miR319-regulated TCP （TEOSINTE BRANCHED/ CYCLOIDEA/PCF） genes, especially TCP21, in rice plants. Transgenic rice plants overexpressing miP,319 or downregulating TCP21 exhibited disease-like phenotypes and showed significantly higher susceptibility to RRSV in comparison with the wild-type plants. In contrast, only mild disease symptoms were observed in RRSV-infected lines overexpressing TCP21 and especially in the transgenic plants overexpressing miR319- resistant TCP21. Both RRSV infection and overexpression of miR319 caused the decreased endogenous jasmonic acid （JA） levels along with downregulated expression of JA biosynthesis and signaling-related genes in rice. However, treatment of rice plants with methyl jasmonate alleviated disease symptoms caused by RRSV and reduced virus accumulation. Taken together, our results suggest that the induction of miR319 by RRSV infection in rice suppresses JA-mediated defense to facilitate virus infection and symp- tom development.

关键词： miR319 rice ragged stunt virus RRSV TCP21 viral infection jasmonic acid

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Genome Analysis of Dasineura jujubifolia Toursvirus 2,A Novel Ascovirus

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Virologica Sinica 2020年第2期35卷 134-142页

作者： Jun Wang Minglu Yang Haibing Xiao Guo-Hua Huang Fei Deng Zhihong Hu State Key laboratory of virology and National Virus Resource Center Wuhan Institute of VirologyChinese Academy of SciencesWuhan 430071China Tarim University Alar 843300China Hunan Provincial Key laboratory for Biology and Control of plant Diseases and Insect Pests Institute of VirologyHunan Agricultural UniversityChangsha 410128China

So far,ascoviruses have only been identified from Lepidoptera host insects and their transmission vectors-endoparasitic ***,we reported the first finding of a complete novel ascovirus genome from a Diptera insect,Dasineura ***,sequence fragments with homology to ascoviruses were incidentally identified during metagenomic sequencing of the mitochondria of ***(Cecidomyiidae,Diptera)which is a major pest on Ziziphus *** a full circular viral genome was assembled from the metagenomic data,which has an A+T percentage of 74%and contains 142,600 bp with 141 open reading frames(ORFs).Among the 141 ORFs,37 were conserved in all sequenced ascoviruses(core genes)including proteins predicted to participate in DNA replication,gene transcription,protein modification,virus assembly,lipid metabolism and ***-gene families including those encode for baculovirus repeated open reading frames(BROs),myristylated membrane proteins,RING/U-box E3 ubiquitin ligases,and ATP-binding cassette(ABC)transporters were found in the virus *** analysis showed that the newly identified virus belongs to genus Toursvirus of Ascoviridae,and is therefore named as Dasineura jujubifolia toursvirus 2(DjTV-2a).The virus becomes the second reported species of the genus after Diadromus pulchellus toursvirus 1(DpTV-1a).The genome arrangement of DjTV-2a is quite different from that of DpTV-1a,suggesting these two viruses separated in an early time of *** results suggest that the ascoviruses may infect a much broader range of hosts than our previous knowledge,and shed lights on the evolution of ascoviruses and particularly on that of the toursviruses.

关键词： Dasineura jujubifolia toursvirus 2(DjTV-2a) Ascovirus Toursvirus

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