High-throughput screening of filamentous fungi using nanoliter-range droplet-based microfluidics

被引:121
作者
Beneyton, Thomas [1 ]
Wijaya, I. Putu Mahendra [1 ,2 ]
Postros, Prexilia [2 ]
Najah, Majdi [2 ]
Leblond, Pascal [2 ]
Couvent, Angelique [2 ]
Mayot, Estelle [2 ]
Griffiths, Andrew D. [1 ]
Drevelle, Antoine [2 ]
机构
[1] Ecole Super Phys & Chim Ind Ville Paris ESPCI Par, CNRS UMR 8231, 10 Rue Vauquelin, F-75231 Paris 05, France
[2] Ets J Soufflet CRIS OSIRIS, BP12, F-10400 Nogent Sur Seine, France
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
PROTEIN; MANIPULATION; SURFACTANTS; ASPERGILLUS; SEPARATION; STRATEGY; PLATFORM; FUSION; CELLS;
D O I
10.1038/srep27223
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
Filamentous fungi are an extremely important source of industrial enzymes because of their capacity to secrete large quantities of proteins. Currently, functional screening of fungi is associated with low throughput and high costs, which severely limits the discovery of novel enzymatic activities and better production strains. Here, we describe a nanoliter-range droplet-based microfluidic system specially adapted for the high-throughput sceening (HTS) of large filamentous fungi libraries for secreted enzyme activities. The platform allowed (i) compartmentalization of single spores in similar to 10 nl droplets, (ii) germination and mycelium growth and (iii) high-throughput sorting of fungi based on enzymatic activity. A 10(4) clone UV-mutated library of Aspergillus niger was screened based on alpha-amylase activity in just 90 minutes. Active clones were enriched 196-fold after a single round of microfluidic HTS. The platform is a powerful tool for the development of new production strains with low cost, space and time footprint and should bring enormous benefit for improving the viability of biotechnological processes.
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页数:10
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