Genetic manipulation tools for Dietzia spp.

被引:14
|
作者
Szvetnik, A. [1 ]
Bihari, Z. [1 ]
Szabo, Z. [1 ]
Kelemen, O. [1 ]
Kiss, I. [1 ]
机构
[1] Bay Zoltan Fdn Appl Res, Inst Biotechnol, H-6726 Szeged, Hungary
关键词
Dietzia; electroporation; pNV18; pNV18Sm; transformation; SP-NOV; CORYNEBACTERIUM-GLUTAMICUM; IMPROVED ELECTROPORATION; BACTERIAL COMMUNITIES; CLONING; IDENTIFICATION; DIVERSITY; SEDIMENTS; GLYCINE; PATIENT;
D O I
10.1111/j.1365-2672.2010.04818.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To develop an applicable vector system and a transformation method for the manipulation of Dietzia spp. Methods and Results: The pNV18 Nocardia-E. coli shuttle vector was tested and found to be a replicating plasmid in Dietzia sp. E1. With the use of pNV18, an electroporation method was optimized for the transformation of Dietzia sp. E1, and a transformation efficiency suitable for genetic manipulations was achieved (2 center dot 18 x 104 transformants mu g-1 DNA). The method was also applied for the transformation of Dietzia cinnamea, D. maris, D. natronolimnaea and D. psychralcaliphila. Conclusions: The first applicable vectors and a simple electroporation protocol enabling the manipulation of several Dietzia spp. are presented. Significance and Impact of the Study: Dietzia spp. have clinical, industrial and great environmental importance; however, the analysis of the Dietzia genus is currently hampered by the lack of manipulation techniques. The presented basic tools allow the genetic analysis of several Dietzia species, including the human disease-associated Dietzia maris.
引用
收藏
页码:1845 / 1852
页数:8
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