期刊
CHEMISTRY & BIOLOGY
卷 19, 期 8, 页码 929-931出版社
CELL PRESS
DOI: 10.1016/j.chembiol.2012.08.004
关键词
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High-throughput screening (HTS) of enzymatic activity is important for directed evolution-based enzyme engineering. However, substrate and product diffusion can severely compromise these HTS assays. In this issue of Chemistry & Biology, Kintses and coworkers describe a microfluidic platform for the directed evolution of enzymes in droplets that allows for the screening of 10(7) mutants per round of evolution.
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