Plasmid addiction systems: perspectives and applications in biotechnology

被引:99
作者
Kroll, Jens [1 ]
Klinter, Stefan [1 ]
Schneider, Cornelia [1 ]
Voss, Isabella [1 ]
Steinbuechel, Alexander [1 ]
机构
[1] Univ Munster, Inst Mol Mikrobiol & Biotechnol, D-48149 Munster, Germany
关键词
PROGRAMMED CELL-DEATH; TOXIN-ANTITOXIN SYSTEM; GENETICALLY-ENGINEERED MICROORGANISMS; SITE-SPECIFIC RECOMBINATION; RESTRICTION-MODIFICATION SYSTEMS; PAD1-ENCODED STABILITY DETERMINANT; HETEROLOGOUS-PROTEIN-PRODUCTION; OPERATOR-REPRESSOR TITRATION; MODIFICATION GENE COMPLEXES; CONDITIONAL SUICIDE SYSTEM;
D O I
10.1111/j.1751-7915.2010.00170.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
Biotechnical production processes often operate with plasmid-based expression systems in well-established prokaryotic and eukaryotic hosts such as Escherichia coli or Saccharomyces cerevisiae, respectively. Genetically engineered organisms produce important chemicals, biopolymers, biofuels and high-value proteins like insulin. In those bio-processes plasmids in recombinant hosts have an essential impact on productivity. Plasmid-free cells lead to losses in the entire product recovery and decrease the profitability of the whole process. Use of antibiotics in industrial fermentations is not an applicable option to maintain plasmid stability. Especially in pharmaceutical or GMP-based fermentation processes, deployed antibiotics must be inactivated and removed. Several plasmid addiction systems (PAS) were described in the literature. However, not every system has reached a full applicable state. This review compares most known addiction systems and is focusing on biotechnical applications.
引用
收藏
页码:634 / 657
页数:24
相关论文
共 257 条
[1]   The ratio between CcdA and CcdB modulates the transcriptional repression of the ccd poison-antidote system [J].
Afif, H ;
Allali, N ;
Couturier, M ;
Van Melderen, L .
MOLECULAR MICROBIOLOGY, 2001, 41 (01) :73-82
[2]   Identification and characterization of a novel toxin-antitoxin module from Bacillus anthracis [J].
Agarwal, Shivangi ;
Agarwal, Shivani ;
Bhatnagar, Rakesh .
FEBS LETTERS, 2007, 581 (09) :1727-1734
[3]   An Escherichia coli chromosomal ''addiction module'' regulated by 3',5'-bispyrophosphate: A model for programmed bacterial cell death [J].
Aizenman, E ;
EngelbergKulka, H ;
Glaser, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6059-6063
[4]  
Alonso JC, 1996, FEMS MICROBIOL LETT, V142, P1
[5]   New connections in the prokaryotic toxin-antitoxin network: relationship with the eukaryotic nonsense-mediated RNA decay system [J].
Anantharaman, V ;
Aravind, L .
GENOME BIOLOGY, 2003, 4 (12)
[6]  
[Anonymous], MICROB CELL FACT S1
[7]   ANTIMICROBIAL SUSCEPTIBILITY TESTING OF FRANCISELLA-TULARENSIS WITH A MODIFIED MUELLER-HINTON BROTH [J].
BAKER, CN ;
HOLLIS, DG ;
THORNSBERRY, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 22 (02) :212-215
[8]   A mutational analysis of the ColE1-encoded cell cycle regulator Rcd confirms its role in plasmid stability [J].
Balding, Claire ;
Blaby, Ian ;
Summers, David .
PLASMID, 2006, 56 (01) :68-73
[9]   Expression and immunogenicity of pertussis toxin S1 subunit-tetanus toxin fragment C fusions in Salmonella typhi vaccine strain CVD 908 [J].
Barry, EM ;
GomezDuarte, O ;
Chatfield, S ;
Rappuoli, R ;
Pizza, M ;
Losonsky, G ;
Galen, J ;
Levine, MM .
INFECTION AND IMMUNITY, 1996, 64 (10) :4172-4181
[10]   SEQUENCE OF THE RELB TRANSCRIPTION UNIT FROM ESCHERICHIA-COLI AND IDENTIFICATION OF THE RELB GENE [J].
BECH, FW ;
JORGENSEN, ST ;
DIDERICHSEN, B ;
KARLSTROM, OH .
EMBO JOURNAL, 1985, 4 (04) :1059-1066