Boosted large-scale production and purification of a thermostable archaeal phosphotriesterase-like lactonase for organophosphate decontamination

被引:4
|
作者
Restaino, Odile Francesca [1 ]
Borzacchiello, Maria Giovanna [1 ]
Scognamiglio, Ilaria [1 ]
Porzio, Elena [2 ]
Manco, Giuseppe [2 ]
Fedele, Luigi [1 ]
Donatiello, Cinzia [1 ]
De Rosa, Mario [1 ]
Schiraldi, Chiara [1 ]
机构
[1] Univ Naples 2, Sect Biotechnol & Mol Biol, Dept Expt Med, Naples, Italy
[2] Natl Res Council Italy, Inst Prot Biochem, Naples, Italy
关键词
High cell density cultivation; Organophosphates; Sulfolobus solfataricus; Thermostable phosphotriesterase-like lactonase; Ultrafiltration; CELL-DENSITY CULTIVATION; ESCHERICHIA-COLI; NERVE AGENTS; PROTEINS; EXPRESSION; CULTURE; ENZYME; BIOREACTOR; BACTERIA; INDUCER;
D O I
10.1007/s10295-016-1892-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
Thermostable phosphotriesterase-like lactonases (PLLs) from extremophile archaea, like SsoPox from Sulfolobus solfataricus, are attractive biotechnological tools with industrial applications as organophosphate decontaminants, but their manufacturing still remains an unresolved issue because of the high costs and the low production yields. In this paper, for the first time, an efficient biotechnological process for the production and purification of a recombinant, engineered PLL, SsoPox W263F, expressed in E. coli, has been set up by studying new induction strategies, by designing high cell density cultivations and a new membrane-based downstream process. In fed batches, the enzyme production was boosted of 69-fold up to 4660.0 U L-1 using galactose as inducer in the replacement of IPTG; the process was scalable from 2.5 up to 150 L. By coupling a single thermo-precipitation step and an ultrafiltration process, a total enzyme recovery of 77% with a purity grade of almost 80% was reached.
引用
收藏
页码:363 / 375
页数:13
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