Production of functional inclusion bodies in endotoxin-free Escherichia coli

被引:46
作者
Rueda, Fabian [1 ,2 ,3 ]
Cano-Garrido, Olivia [1 ,2 ,3 ]
Mamat, Uwe [4 ]
Wilke, Kathleen [4 ]
Seras-Franzoso, Joaquin [1 ,2 ,3 ]
Garcia-Fruitos, Elena [1 ,2 ,3 ]
Villaverde, Antonio [1 ,2 ,3 ]
机构
[1] Univ Autonoma Barcelona, Inst Biotecnol & Biomed, Bellaterra 08193, Cerdanyola Del, Spain
[2] Univ Autonoma Barcelona, Dept Genet & Microbiol, Bellaterra 08193, Cerdanyola Del, Spain
[3] CIBER BBN, Bellaterra 08193, Cerdanyola Del, Spain
[4] Leibniz Ctr Med & Biosci, Res Ctr Borstel, Div Struct Biochem, D-23845 Borstel, Germany
关键词
E; coli; Recombinant protein; Inclusion bodies; Endotoxin; LPS; LPS-free; PROTEIN SOLUBILITY; REMOVAL; BIOMATERIALS; AGGREGATION; SCAFFOLDS; FACTORIES; AMYLOIDS; BACTERIA; DELIVERY;
D O I
10.1007/s00253-014-6008-9
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
Escherichia coli is the workhorse for gene cloning and production of soluble recombinant proteins in both biotechnological and biomedical industries. The bacterium is also a good producer of several classes of protein-based self-assembling materials such as inclusion bodies (IBs). Apart from being a relatively pure source of protein for in vitro refolding, IBs are under exploration as functional, protein-releasing materials in regenerative medicine and protein replacement therapies. Endotoxin removal is a critical step for downstream applications of therapeutic proteins. The same holds true for IBs as they are often highly contaminated with cell-wall components of the host cells. Here, we have investigated the production of IBs in a recently developed endotoxin-free E. coli strain. The characterization of IBs revealed this mutant as a very useful cell factory for the production of functional endotoxin-free IBs that are suitable for the use at biological interfaces without inducing endotoxic responses in human immune cells.
引用
收藏
页码:9229 / 9238
页数:10
相关论文
共 45 条
[1]  
[Anonymous], 1989, Molecular Cloning: A Laboratory
[2]   Functional Amyloids Signal Their Arrival [J].
Badtke, Matthew P. ;
Hammer, Neal D. ;
Chapman, Matthew R. .
SCIENCE SIGNALING, 2009, 2 (80)
[3]   Supramolecular organization of protein-releasing functional amyloids solved in bacterial inclusion bodies [J].
Cano-Garrido, Olivia ;
Rodriguez-Carmona, Escarlata ;
Diez-Gil, Cesar ;
Vazquez, Esther ;
Elizondo, Elisa ;
Cubarsi, Rafael ;
Seras-Franzoso, Joaquin ;
Luis Corchero, Jose ;
Rinas, Ursula ;
Ratera, Imma ;
Ventosa, Nora ;
Veciana, Jaume ;
Villaverde, Antonio ;
Garcia-Fruitos, Elena .
ACTA BIOMATERIALIA, 2013, 9 (04) :6134-6142
[4]   New challenges and opportunities for industrial biotechnology [J].
Chen, Guo-Qiang .
MICROBIAL CELL FACTORIES, 2012, 11
[5]   The nanoscale properties of bacterial inclusion bodies and their effect on mammalian cell proliferation [J].
Diez-Gil, Cesar ;
Krabbenborg, Sven ;
Garcia-Fruitos, Elena ;
Vazquez, Esther ;
Rodriguez-Carmona, Escarlata ;
Ratera, Imma ;
Ventosa, Nora ;
Seras-Franzoso, Joaquin ;
Cano-Garrido, Olivia ;
Ferrer-Miralles, Neus ;
Villaverde, Antonio ;
Veciana, Jaume .
BIOMATERIALS, 2010, 31 (22) :5805-5812
[6]   Structure and function of lipopolysaccharides [J].
Erridge, C ;
Bennett-Guerrero, E ;
Poxton, IR .
MICROBES AND INFECTION, 2002, 4 (08) :837-851
[7]  
Ferrer-Miralles N., 2013, CRIT REV BI IN PRESS
[8]   Bacterial cell factories for recombinant protein production; expanding the catalogue [J].
Ferrer-Miralles, Neus ;
Villaverde, Antonio .
MICROBIAL CELL FACTORIES, 2013, 12
[9]   Microbial factories for recombinant pharmaceuticals [J].
Ferrer-Miralles, Neus ;
Domingo-Espin, Joan ;
Corchero, Jose Luis ;
Vazquez, Esther ;
Villaverde, Antonio .
MICROBIAL CELL FACTORIES, 2009, 8
[10]   Aggregation as bacterial inclusion bodies does not imply inactivation of enzymes and fluorescent proteins -: art. no. 27 [J].
García-Fruitós, E ;
González-Montalbán, N ;
Morell, M ;
Vera, A ;
Ferraz, RM ;
Arís, A ;
Ventura, S ;
Villaverde, A .
MICROBIAL CELL FACTORIES, 2005, 4 (1)