Flow cytometry-based ultra-high-throughput screening assay for cellulase activity

被引:40
|
作者
Ostafe, Raluca [1 ,2 ]
Prodanovic, Radivoje [1 ,3 ]
Commandeur, Ulrich [1 ]
Fischer, Rainer [1 ,2 ]
机构
[1] Rhein Westfal TH Aachen, Inst Mol Biotechnol, D-52074 Aachen, Germany
[2] Fraunhofer Inst Mol Biol & Appl Ecol IME, D-52074 Aachen, Germany
[3] Univ Belgrade, Fac Chem, Belgrade 11000, Serbia
关键词
Cellulase; Fluorescence assay; Hexose oxidase; Vanadium bromoperoxidase; ViPer; FACS; Double emulsions; DIRECTED EVOLUTION; ENZYME LIBRARIES; CONVERSION;
D O I
10.1016/j.ab.2012.10.043
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a novel, ultra-high-throughput screening assay for the detection of cellulase activity based on fluorescence-activated cell sorting (FACS) and double emulsion technology. Cellulase activity is detected using a series of coupled enzymes, including hexose oxidase (HOx), which generates hydrogen peroxide from the reducing sugars released by cellulases in the presence of any natural or artificial substrate. The assay can be adapted to suit a microtiter plate format, but the highest throughput is achieved by using FACS to screen high-complexity cellulase clone libraries. Using this approach, we achieved a 12-fold enrichment of positive (cellulase-expressing) cells in cellulase reference libraries after just one sorting round. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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