In vitro flow cytometry-based screening platform for cellulase engineering

被引:44
|
作者
Koerfer, Georgette [1 ]
Pitzler, Christian [1 ]
Vojcic, Ljubica [1 ]
Martinez, Ronny [1 ]
Schwaneberg, Ulrich [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Worringerweg 3, D-52074 Aachen, Germany
[2] DWI RWTH Aachen eV, Forckenbeckstr 50, D-52056 Aachen, Germany
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
CELL-FREE SYNTHESIS; DIRECTED EVOLUTION; MEMBRANE-PROTEINS; DIVERSITY; SYSTEM;
D O I
10.1038/srep26128
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ultrahigh throughput screening (uHTS) plays an essential role in directed evolution for tailoring biocatalysts for industrial applications. Flow cytometry-based uHTS provides an efficient coverage of the generated protein sequence space by analysis of up to 10(7) events per hour. Cell-free enzyme production overcomes the challenge of diversity loss during the transformation of mutant libraries into expression hosts, enables directed evolution of toxic enzymes, and holds the promise to efficiently design enzymes of human or animal origin. The developed uHTS cell-free compartmentalization platform (InVitroFlow) is the first report in which a flow cytometry-based screened system has been combined with compartmentalized cell-free expression for directed cellulase enzyme evolution. InVitroFlow was validated by screening of a random cellulase mutant library employing a novel screening system (based on the substrate fluorescein-di-beta-D-cellobioside), and yielded significantly improved cellulase variants (e.g. CelA2-H288F-M1 (N273D/H288F/N468S) with 13.3-fold increased specific activity (220.60 U/mg) compared to CelA2 wildtype: 16.57 U/mg).
引用
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页数:12
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