A constitutive expression system for high-throughput screening

被引:33
|
作者
Aerts, Dirk [1 ]
Verhaeghe, Tom [1 ]
De Mey, Marjan [1 ]
Desmet, Tom [1 ]
Soetaert, Wim [1 ]
机构
[1] Univ Ghent, Dept Biochem & Microbial Technol, Ctr Expertise Ind Biotechnol & Biocatalysis, B-9000 Ghent, Belgium
来源
ENGINEERING IN LIFE SCIENCES | 2011年 / 11卷 / 01期
关键词
Constitutive expression; Directed evolution; High-throughput screening; Promoter; Sucrose phosphorylase; RECOMBINANT SUCROSE PHOSPHORYLASE; ESCHERICHIA-COLI; LEUCONOSTOC-MESENTEROIDES; DIRECTED EVOLUTION; SOLUBLE EXPRESSION; BATCH CULTURE; GENE; PROMOTER; STRATEGIES; PROTEINS;
D O I
10.1002/elsc.201000065
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
To reduce the amount of consumables and number of pipetting steps in high-throughput screening, a constitutive expression system was developed that comprises four different promoters of varying strength. The system was validated by the expression of different sucrose phosphorylase enzymes from Leuconostoc mesenteroides, Lactobacillus acidophilus and Bifidobacterium adolescentis in 96-deep-and low-well plates at three temperatures. Drastically improved soluble expression in mini-cultures was observed for the enzymes from L. mesenteroides strains by reducing the promoter strength from strong to intermediate and by expressing the proteins at lower temperatures. In contrast, the enzymes from B. adolescentis and L. acidophilus were expressed most efficiently with a strong promoter. The constitutive expression of sucrose phosphorylases in low-well plates resulted in a level of activity that is equal or even better than what was achieved by inducible expression. Therefore, our plasmid set with varying constitutive promoters will be an indispensable tool to optimize enzyme expression for high-throughput screening.
引用
收藏
页码:10 / 19
页数:10
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