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作 者:王成梁 乔培 刘德华 孟永红 关巍[2] 杨玉文[2,4] 赵廷昌[2,4] WANG Chengliang;QIAO Pei;LIU Dehua;MENG Yonghong;GUAN Wei;YANG Yuwen;ZHAO Tingchang(College of Plant Protection,Jilin Agricultural University,Changchun 130118,Jilin,China;Institute of Plant Protection,Chinese Academy of Agricultural Sciences/State Key Laboratory for Biology of Plant Diseases and Insect Pests,Beijing 100193,China;Ledong Douzhiguo Melon and Watermelon Planting Professional Farmers Cooperative,Ledong 572541,Hainan,China;National Nanfan Research Institute(Sanya),Chinese Academy of Agricultural Sciences,Sanya 572024,Hainan,China)
机构地区:[1]吉林农业大学植物保护学院,长春130118 [2]中国农业科学院植物保护研究所/植物病虫害综合治理全国重点实验室,北京100193 [3]乐东都知果西密瓜种植农民专业合作社,海南乐东572541 [4]三亚中国农业科学院国家南繁研究院,海南三亚572024
出 处:《中国瓜菜》2024年第5期41-52,共12页China Cucurbits And Vegetables
基 金:国家重点研发计划(2023YFD1401200);海南省科技专项(ZDYF2023XDNY084);新疆维吾尔自治区重大科技专项(2023A02009);新疆生产建设兵团科技攻关项目(2022AB015);中国农业科学院科技创新工程(CAAS-ASTIP);国家西甜瓜产业技术体系(CARS-25)。
摘 要:DeoR(Deoxyribonucleoside operon repressor)家族转录因子是在原核生物中广泛存在的转录调控因子。DeoR通过调节毒力因子的表达来影响病原细菌的致病性,并且在不同的病原细菌中有不同的调控网络。为了阐明DeoR在西瓜噬酸菌中的功能和信号通路,Aac5菌株被用来构建DeoR转录因子glpR的缺失突变株及互补菌株,通过进行表型及转录水平的测定,对西瓜噬酸菌中DeoR转录因子glpR的功能进行初步探究。结果表明,缺失glpR基因后,Aac5菌株利用果糖的能力、对西瓜苗的致病能力、西瓜子叶体内生长能力以及形成生物膜的能力均显著下降,体外生长速度减慢,而抗高盐胁迫能力以及抗铜离子胁迫能力显著增强。同时,基因glpR的缺失会导致三型分泌系统基因hrpG、hrpE及hrcJ表达量显著下调,果糖利用相关基因fruA、fruB与fruK表达量显著下调,生物膜相关基因flgG表达量显著下调,与WT-fruBpGUS相比,ΔglpR-fruBpGUS的fruB的启动子活性显著减弱。以上结果表明,glpR基因在西瓜噬酸菌果糖利用、抵抗逆境胁迫以及致病过程中起重要作用。The DeoR(Deoxyribonucleoside operon repressor)family of transcription factors are transcriptional regulators that are widely present in prokaryotes.DeoR affects the pathogenicity of pathogenic bacteria by regulating the expression of virulence factors,and there are different regulatory networks in different pathogenic bacteria.In order to elucidate its function and signaling pathway in Acidovorax citrulli,Aac5 strain was used to construct the deletion mutant and complementary strain of DeoR transcription factor glpR.The function of DeoR transcription factor glpR in Acidovorax citrulli was preliminarily explored by measuring the phenotype and transcription level.The results showed that after deletion of glpR gene,the ability of Aac5 strain to utilize fructose,the pathogenicity of watermelon seedlings,the growth ability of watermelon cotyledons and the ability to form biofilm were significantly decreased,and the growth rate in vitro was slowed down.The ability to resist high salt stress and copper ion stress was significantly increased.At the same time,the deletion of the gene glpR resulted in a significant down-regulation of the type III secretion system genes hrpG,hrpE and hrcJ,a significant down-regulation of the fructose utilization-related genes fruA,fruB and fruK,and a significant down-regulation of the biofilm-related gene flgG.Compared with WT-fruBpGUS,the promoter activity of fruB inΔgl-pR-fruBpGUS was significantly reduced.The results indicated that glpR gene plays an important role in fructose utilization,resistance to stress and pathogenicity of Acidovorax citrulli.
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