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首页> 外文期刊>Applied and Environmental Microbiology >Characterization of Erwinia chrysanthemi by pectinolytic isozyme polymorphism and restriction fragment length polymorphism analysis of PCR-amplified fragments of pel genes.
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Characterization of Erwinia chrysanthemi by pectinolytic isozyme polymorphism and restriction fragment length polymorphism analysis of PCR-amplified fragments of pel genes.

机译:通过果胶分解同工酶多态性和PCR扩增的pel基因片段的限制性片段长度多态性分析鉴定欧文氏菊。

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Conserved regions about 420 bp long of the pelADE cluster specific to Erwinia chrysanthemi were amplified by PCR and used to differentiate 78 strains of E. chrysanthemi that were obtained from different hosts and geographical areas. No PCR products were obtained from DNA samples extracted from other pectinolytic and nonpectinolytic species and genera. The pel fragments amplified from the E. chrysanthemi strains studied were compared by performing a restriction fragment length polymorphism (RFLP) analysis. On the basis of similarity coefficients derived from the RFLP analysis, the strains were separated into 16 PCR RFLP patterns grouped in six clusters, These clusters appeared to be correlated with other infraspecific levels of E. chrysanthemi classification, such as pathovar and biovar, and occasionally with geographical origin. Moreover, the clusters correlated well with the polymorphism of pectate lyase and pectin methylesterase isoenzymes. While the pectin methylesterase profiles correlated with host monocot-dicot classification, the pectate lyase polymorphism might reflect the cell wall microdomains of the plants belonging to these classes.
机译:通过PCR扩增了特异于菊花欧文氏菌的pelADE簇的约420bp长的保守区,并用于区分从不同宿主和地理区域获得的78株菊花欧文氏菌。从其他果胶分解和非果胶分解物种和属提取的DNA样品未获得PCR产物。通过进行限制性片段长度多态性(RFLP)分析,比较了从所研究的大肠杆菌菌株中扩增得到的pel片段。根据RFLP分析得出的相似性系数,将菌株分为16个簇,分为16个PCR RFLP模式。这些簇似乎与其他金黄色葡萄球菌的亚种水平相关,例如病原体和生物变体。具有地理起源。而且,这些簇与果胶酸裂合酶和果胶甲基酯酶同工酶的多态性很好地相关。虽然果胶甲基酯酶谱与宿主单子叶植物双子叶分类相关,但果胶裂合酶多态性可能反映了属于这些类别的植物的细胞壁微结构域。

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