High Level Biosynthesis of a Silk-Elastin-like Protein in E. coli

被引:19
作者
Collins, Tony [1 ]
Barroca, Mario [1 ]
Branca, Fernando [1 ]
Padrao, Jorge [1 ]
Machado, Raul [1 ]
Casal, Margarida [1 ]
机构
[1] Univ Minho, Dept Biol, Ctr Mol & Environm Biol CBMA, P-4710057 Braga, Portugal
关键词
HIGH-CELL-DENSITY; ESCHERICHIA-COLI; AEROBIC CULTIVATIONS; BLOCK-COPOLYMERS; PICHIA-PASTORIS; SPIDER SILK; DNA RELEASE; EXPRESSION; CULTURES; POLYMER;
D O I
10.1021/bm5005564
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Silk-elastin-like proteins (SELPs) have enormous potential for use as customizable biomaterials in numerous biomedical and materials applications, yet success in harnessing this potential has been limited by the lack of a commercially viable industrially relevant production process. We have developed a scalable fed-batch production approach which enables a SELP volumetric productivity of 4.3 g L-1 with E. coli BL21(DE3). This is the highest SELP productivity reported to date and is SO-fold higher than that reported by other groups. As compared to typical fed-batch processes, high preinduction growth rates and low inducer and oxygen concentrations are allowed whereas reduced postinduction feeding rates are preferred. Limiting factors were identified and productivity was found to be strongly influenced by a trade-off between the rate of production and plasmid stability. The process developed is robust, reproducible, and applicable to scale up to the industrial level and moves these biopolymers a step closer to the marketplace.
引用
收藏
页码:2701 / 2708
页数:8
相关论文
共 53 条
[1]   In-situ self-assembling protein polymer gel systems for administration, delivery, and release of drugs [J].
Cappello, J ;
Crissman, JW ;
Crissman, M ;
Ferrari, FA ;
Textor, G ;
Wallis, O ;
Whitledge, JR ;
Zhou, X ;
Burman, D ;
Aukerman, L ;
Stedronsky, ER .
JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) :105-117
[2]  
Casal M., 2014, BIOBASED PLASTICS MA
[3]   Formate accumulation due to DNA release in aerobic cultivations of Escherichia coli [J].
Castan, A ;
Enfors, SO .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 77 (03) :324-328
[4]   MICRODETERMINATION OF PHOSPHORUS [J].
CHEN, PS ;
TORIBARA, TY ;
WARNER, H .
ANALYTICAL CHEMISTRY, 1956, 28 (11) :1756-1758
[5]   Ultra-high expression of a thermally responsive recombinant fusion protein in E-coli [J].
Chow, Dominic C. ;
Dreher, Matthew R. ;
Trabbic-Carlson, Kimberly ;
Chilkoti, Ashutosh .
BIOTECHNOLOGY PROGRESS, 2006, 22 (03) :638-646
[6]   Batch production of a silk-elastin-like protein in E. coli BL21 (DE3): key parameters for optimisation [J].
Collins, Tony ;
Azevedo-Silva, Joao ;
da Costa, Andre ;
Branca, Fernando ;
Machado, Raul ;
Casal, Margarida .
MICROBIAL CELL FACTORIES, 2013, 12
[7]   Overcoming acetate in Escherichia coli recombinant protein fermentations [J].
Eiteman, Mark A. ;
Altman, Elliot .
TRENDS IN BIOTECHNOLOGY, 2006, 24 (11) :530-536
[8]  
Fahnestock S R, 2000, J Biotechnol, V74, P105, DOI 10.1016/S1389-0352(00)00008-8
[9]   Elastin-like polypeptides revolutionize recombinant protein expression and their biomedical application [J].
Floss, Doreen M. ;
Schallau, Kai ;
Rose-John, Stefan ;
Conrad, Udo ;
Scheller, Juergen .
TRENDS IN BIOTECHNOLOGY, 2010, 28 (01) :37-45
[10]   Expression and purification of ELP-intein-tagged target proteins in high cell density E-coli fermentation [J].
Fong, Baley A. ;
Wood, David W. .
MICROBIAL CELL FACTORIES, 2010, 9