Genetic Diversity Analysis on Rep-PCR Genomic Fingerprinting and 16S rDNA Sequences of Desulfurization Bacteria

被引:1
|
作者
吕英海 [1 ]
祝加伟 [1 ]
张雨晴 [1 ]
蔡晓青 [1 ]
郭凯 [1 ]
周仕学 [1 ]
机构
[1] College of Chemical and Environmental Engineering,Shandong University of Science and Technology
关键词
16S rDNA; BOX element polymerase chain reaction(BOX-PCR); desulfurization; fingerprinting; enterobacterial repetitive intergenic consensus(ERIC)-PCR;
D O I
10.19884/j.1672-5220.2016.01.022
中图分类号
X172 [环境微生物学]; Q78 [基因工程(遗传工程)];
学科分类号
071007 ; 071012 ; 0713 ; 0836 ; 090102 ;
摘要
In order to reduce deleterious effect on environment,human health and facilities caused by original sulfides, more attention should be paid to biodesulfurization studying for fossil fuels. In this work, eight isolates were characterized by several DNA-based methods such as BOX element polymerase chain reaction( BOX-PCR), enterobacterial repetitive intergenic consensus( ERIC)-PCR and random amplification of polymorphic DNA( RAPD)-PCR. The desulfurization performance was determined by micro-coulometric method,Gibb’s assay and barium sulfate test. It was found out that ERIC-PCR displays a much higher inter-strain heterogeneity compared with using BOX. The length of the primer didnot play the most important role in bacterial classification. The combination of the analysis of repetitive-sequence-based polymerase chain reaction ngerprinting and 16 S r DNA was able to provide more effective way in the separation and identification of bacteria.According to the analysis of 16 S r DNA,the more efficient desulfurization strain should belong to Klebsiella variicola.
引用
收藏
页码:134 / 137
页数:4
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