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首页> 外文期刊>Biotechnology & Biotechnological Equipment >BACTERIAL GENUS XENORHABDUS (ENTEROBACTERIACEAE) PART OF THE BACTERIAL COMPLEX OF FIVE BULGARIAN POPULATIONS ENTOMOPATHOGENIC NEMATODE FROM GENUS STEINERNEMA (STE1NERNEMATWAE: RHABD1TIDA)
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BACTERIAL GENUS XENORHABDUS (ENTEROBACTERIACEAE) PART OF THE BACTERIAL COMPLEX OF FIVE BULGARIAN POPULATIONS ENTOMOPATHOGENIC NEMATODE FROM GENUS STEINERNEMA (STE1NERNEMATWAE: RHABD1TIDA)

机译:保加利亚人五种保加利亚人线虫病线虫细菌复合体的细菌XENORHABDUS(肠杆菌科)(STE1NERNEMATWAE:RHABD1TIDA)

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摘要

Twenty one bacterial strains of Xenorhabdus obtained from five nematode hosts from genus Steinernema were typed by analyzing I6S rDNA restriction patterns obtained after digestion ofPCR amplified 16S rDNAs. Three tetramer endonucleases were used. A total of 14 genotypes were identified, forming main clusters after analysis using arithmetical methods (UPMGA). To identify the strains and all genotypes, the enzymes Hae III, Alu I and Hha I were used in the analysis. From our results we could conclude that RFLP-PCR of 16S rDNA analysis is an accurate method for identifying enomopathogenic nematode bacterial symbionts.
机译:通过分析PCR扩增的16S rDNA的消化后获得的I6S rDNA限制性酶切模式,对从Steinernema属的5个线虫宿主获得的21个Xenorhabdus细菌菌株进行了分型。使用了三种四聚体核酸内切酶。使用算术方法(UPMGA)进行分析后,总共鉴定出14个基因型,形成了主要簇。为了鉴定菌株和所有基因型,在分析中使用了酶Hae III,Alu I和HhaI。从我们的结果中,我们可以得出结论,16S rDNA分析的RFLP-PCR是鉴定致病性线虫细菌共生菌的准确方法。

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