全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

应用高效离子交换色谱分析青枯菌的致病力分化

DOI: 10.3724/SP.J.1145.2009.00713, PP. 713-718

Keywords: 青枯菌,致病力,高效离子交换色谱,激光光散射仪

Full-Text   Cite this paper   Add to My Lib

Abstract:

应用高效离子交换色谱和激光光散射仪检测器对不同致病力的青枯菌进行分析,建立了一种快速检测青枯菌致病力分化的新方法.青枯菌纯培养物经过高效离子交换色谱分离得到3个致病力不同的特征峰,大小依次为峰3组分>峰2组分>峰1组分.对10株青枯菌进行色谱分析,并结合番茄组培苗感染试验检测其致病力,结果发现,强致病力菌株经过色谱分离只在峰3的保留时间位置出现单一特征峰,在9d内即可引起100%的番茄组培苗发病;若菌株经过色谱分离形成3个特征峰,则峰3所占的面积比越大,该菌株的致病性相对就越强.25株不同致病力青枯菌的验证试验表明了该方法的可行性,番茄组培苗发病率x与峰3面积比y之间呈现出良好的线性关系,回归方程y=0.9581x+5.4984,相关系数r=0.986.通过对青枯菌色谱行为、致病力、细胞表面黏附的epsⅰ含量三者之间相互关系的进一步研究,发现青枯菌的致病力越强,则细胞表面黏附的epsⅰ越多,峰3所占的面积比就越大.图3表6参15

References

[1]  1marquisre,mayzelk,carstensenel.cationexchangeincellwallsofgram-positivebacteria.canjmicrobiol,1976,22(7):975~982
[2]  2chenzj(陈章捷),shixz(时祥柱),linj(林娟),liust(刘树滔),yexy(叶秀云),chengr(陈躬瑞),raopf(饶平凡).separationandanalysisofanimalintestinalflorabyhighperformanceion-exchangechromatography.chinjapplenvironbiol(应用与环境生物学报),2006,12(2):278~282
[3]  4dennytp.ralstoniasolanacearum-aplantpathogenintouchwithitshost.trendsmicrobiol,2000,8(11):486~489
[4]  6linj(林娟),mac(马骋),liust(刘树滔),xiez(谢智),raopf(饶平凡).optimizationofralstoniasolanacearumpreparationmethodsbyhplcanalysis.chinabiotech(中国生物工程杂志),2006,26(5):63~68
[5]  7linj(林娟),raopf(饶平凡),mac(马骋),liust(刘树滔),xiez(谢智).studyontheseparatingconditionsofralstoniasolanacearumbyhighperformanceionexchangeliquidchromatographyanalysis.jfuzhouunivnatscied(福州大学学报自然科学版),2006,34(3):448~452
[6]  8liubo(刘波),linyz(林营志),zhuyj(葛慈斌),gecb(葛慈斌),caoy(曹宜).attenuationcharacteristicsofbacterial-wilt-diseasebiocontrolstrainanti-8098a(bacilluscereus)toralstoniasolanacearum.jagricbiotech(农业生物技术学报),2004,12(3):322~329
[7]  9linj(林娟),mac(马骋),liust(刘树滔),raopf(饶平凡).charaterizationofralstoniasolanacearumindifferentgrowthphasesbyhighperformanceionexchangeliquidchromatographyanalysis.actamicrobiolsin(微生物学报),2007,47(1):145~149
[8]  10linj(林娟),mac(马骋),liust(刘树滔),wull(吴玲玲),raopf(饶平凡).highspeedseparationandquantitationofralstoniasolanacearumofdifferentvirulencesusinghighperformanceionexchangechromatography.chinjchromatogr(色谱),2007,25(1):70~74
[9]  11orgambideg,montrozierh,servinp,rousselj,trigaletdd,trigaleta.highheterogeneityoftheexopolysaccharidesofpseudomonassolanacearumstaingmi1000andcompletestructureofthemajorpolysaccharide.jbiolchem,1991,266(13):8312~8321
[10]  15huangjz,carneybf,dennytp.acomplexnetworkregulatesexpressionofepsandothervirulencegenesofpseudomonassolanacearum.jbacteriol,1995,177(5):1259~1267
[11]  3haywardac.biologyandepidemiologyofbacterialwiltcausedbypseudomonassolanacearum.annurevphytopathol,1991,29:65~87
[12]  5genins,boucherc.ralstoniasolanacearum:secretsofamajorpathogenunveiledbyanalysisofitsgenome.molplantpathol,2002,3(3):111~118
[13]  12wilsonww,wademm,holmansc,champlinfr.statusofmethodsforassessingbacterialcellsurfacechargepropertiesbasedonzetapotentialmeasurements.jmicrobiolmethods,2001,43(3):153~164
[14]  13dicksonjs,koohmaraiem.cellsurfacechargecharacteristicsandtheirrelationshiptobacterialattachmenttomeatsurface.applenvironmicrobiol,1989,55(4):832~836
[15]  14cloughsj,leek,schellma,dennytp.atwo-componentsysteminralstonia(pseudomonas)solanacearummodulatesproductionofphca-regulatedvirulencefactorsinresponseto3-hydroxypalmiticacidmethylester.jbacteriol,1997,179(11):3639~3648

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133