Versatile plasmid-based expression systems for Gram-negative bacteria-General essentials exemplified with the bacterium Ralstonia eutropha H16

被引:21
|
作者
Gruber, Steffen [1 ]
Schwab, Helmut [1 ]
Koefinger, Petra [1 ]
机构
[1] Graz Univ Technol, Inst Mol Biotechnol, NAWI Graz, A-8010 Graz, Austria
关键词
BROAD-HOST-RANGE; RECOMBINANT PROTEIN EXPRESSION; COPY-NUMBER CONTROL; COMPLETE NUCLEOTIDE-SEQUENCE; CLONING VECTOR PBBR1MCS; ESCHERICHIA-COLI; MOLECULAR CHARACTERIZATION; ALCALIGENES-EUTROPHUS; GENETIC ORGANIZATION; EFFICIENT PRODUCTION;
D O I
10.1016/j.nbt.2015.03.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Gram-negative bacterium Escherichia coli is currently the most efficient and widely used prokaryotic host for recombinant protein and metabolite production. However, due to some limitations and to various interesting features of other Gram-negative bacteria efficient vector systems applicable to a broad range are desired. Basic building blocks for plasmid-based vectors include besides the need for a suitable selection marker in the first line a proper replication and maintenance system. In addition to these basic requirements, further elements are needed for Gram-negative bacteria beyond E. coli, such as Pseudomonas pudita, Ralstonia eutropha, Burkholderia glumae or Acinetobacter sp.. Established building blocks have to be adapted and new building blocks providing the desired functions need to be identified and exploited. This minireview addresses so far described and used genetic elements for broad host range replication, efficient plasmid maintenance, and conjugative plasmid transfer as well as expression elements and protein secretion signals. The industrially important bacterium R. eutropha H16 was chosen as a model organism to provide specific data on the effectivity and utility of building blocks based on such genetic elements.
引用
收藏
页码:552 / 558
页数:7
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