期刊文献+

野油菜黄单胞菌XC3813报告质粒的构建及其表达的初步分析 被引量:1

Construction and preliminary analysis of reported plasmid of XC3813 in Xanthomonas campestris
下载PDF
导出
摘要 野油菜黄单胞菌野油菜致病变种(简称Xcc)是引起十字花科作物发生黑腐病的病原菌,在以前的研究中,证实了Xcc8004菌株基因组中一个包含三个基因XC3813-3815的新位点与致病性和胞外多糖(EPS,又称黄原胶)合成有关。将XC3813的启动子与报告基因gusA融合,构建XC3813的报告质粒pRE3813gus。通过分析报告质粒在致病相关基因rpfC、opsX和clp的突变体背景下的表达,发现rpfC和opsX的失活可使报告基因的表达分别降低42.8%和55.7%。这表明XC3813的表达可能直接或间接受rpfC和opsX基因的影响。 Xanthomonas campestris pv. campestris (Xcc) is the causal agency of the black rot disease of cruciferous plants. In previous work a novel locus, XC3813-3815, was identified to be required for full virulence and extracellular polysaccharide (EPS, also called xanthan gum) production. Here the promoter region of XC3813 was fused to the coding region of the gene gusA, resulted the reporter plasmid pRE3813gus. The gusA level of pRE3813gus, determined enzymatically and mirrors XC3813 gene expression, was tested in the wild-type background and the rpfC, opsX or clp gene mutant background. The results showed that the gusA level in rpfC and opsX mutant background was reduced 42. 8% and 55.7%, respectively, compared to that in wild-type background. This indicated that the expression of XC3813 might be regulated directly or indirectly by the gene rpfC or opsX.
出处 《广西农业生物科学》 CAS CSCD 2008年第3期212-217,共6页 Journal of Guangxi Agricultural and Biological Science
基金 国家自然科学基金重点项目(30130010) 国家自然科学基金面上项目(30470944)
关键词 野油菜黄单胞菌野油菜致病变种 XC3813 报告质粒 Xanthornonas carnpestris pv. campestris XC3813 reporter plasmid
  • 相关文献

参考文献11

  • 1SWINGS J G, CIVEROLO E L Xanthomonas [M]. London: Chapman & Hall, 1993.
  • 2LUG T, MA Z F, HU J R, et al. A novel locus involved in extracellular polysaccharide production and virulence of Xanthomonas campestris pathovar campestris [J]. Microbiol, 2007, 153 (3) : 737-746.
  • 3谭旖宁,马增凤,陆光涛,唐纪良.野油菜黄单胞菌6磷-酸葡萄糖脱氢酶基因的初步分析[J].广西农业生物科学,2007,26(3):190-195. 被引量:10
  • 4SAMBROOK J, RUSSE D W. Molecular cloning: a laboratory manual [M]. 3rd ed. New York: Cold Spring Harbor Laboratory Press, 2001.
  • 5SCHAFER A, TAUCH A, JAGER W, et al. Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum [J]. Gene, 1994, 145: 69-73.
  • 6TURNER P, BARBER C, DANNIELS M. Behaviour of the transposans Tn5 and Tn7 in Xanthomonas campestris pv. campestris [J]. Mol Gen Genet, 1984, 195: 101-107.
  • 7HENDERSON R F, BENSON J M, HAHN F F, et al. New approaches for the evaluation of pulmonary toxicity: bronehoalveolar lavage fluid analysis [J]. Fundam Appl Toxieol, 1985, 5 (3): 451-458
  • 8TANG J L, LIU Y N, BARBER C E, et al. Genetic and molecular analysis of a cluster of rpf genes involved in positive regulation of synthesis of extracellular enzymes and polysaccharide in Xanthomonas campestris pathovar campestris [J]. Mol Gen Genet, 1991, 226 (3): 409-417.
  • 9KINGSLEY M T, GABRIEL D W, MARLOW G C, et al. The opsX locus of Xanthomonas campestris affects host range and biosynthesis of lipopolysaccharide and extracellular polysaccharide [J]. J Bacteriol, 1993, 175 (18) :5839-5850.
  • 10DE CRECY-LAGARD V, GLASER P, LEJEUNE P, et al. A Xanthomonas campestris pv. campestris protein similar to eatabolite activation factor is involved in regulation of phytopathogenieity [J]. J Baeteriol, 1990, 172 (10) :5877-5883.

二级参考文献23

  • 1SWINGS J G,CIVEROLO E L.Xanthomonas[M].London:Chapman & Hall,1993.
  • 2KENNEDY J F,BRADSHAW I J.Production,properties and application of xanthan[J].Prog Ind Microbiol,1984,19:319-371.
  • 3FRAENKEL D G,BANERJEE S.Deletion mapping of zwf,the gene for a constitutive enzyme,glucose 6-phosphate dehydrogenase in Escherichia coli[J].Genetics,1972,71(4):481-489.
  • 4QIAN W,JIA Y,REN S X,et al.Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv.campestris[J].Genome Res,2005,15(6):757-767.
  • 5TURNER P,BARBER C,DANNIELS M.Behaviour of the transposans Tn5 and Tn7 in Xanthomonas campestris pv.carnpestris[J].Mol Gen Genet,1984,195:101-107.
  • 6SAMBROOK J,RUSSE D W.Molecular cloning:a Laboratory Manual[M].3rd edition.New York:Cold Spring Harbor Laboratory Press,2001.
  • 7WINDGASSEN M,URBAN A,JAEGER K E.Rapid gene inactivation in Pseudomonas aeruginosa[J].FEMS Microbiol Lett,2000,193:201-205.
  • 8SCHAFER A,TAUCH A,JAGER W,et al.Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19:selection of defined deletions in the chromosome of Corynebacterium glutamicum[J].Gene,1994,145:69-73.
  • 9DA SILVA A C,FERRO J A,REINACH F C,et al.Comparison of the genomes of two Xanthomonas pathogens with differing host specificities[J].Nature,2002,417(6887):459-463.
  • 10HARDING N E,CLEARY J M,CABANAS D K,et al.Genetic and physical analyses of a cluster of genes essential for xanthan gum biosynthesis in Xanthomonas campestris[J].J Bacteriol,1987,169:2854-2861.

共引文献11

同被引文献6

引证文献1

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部