Scanlon Thomas C, Dostal Sarah M, Griswold Karl E
Thayer School of Engineering, Dartmouth College, Hanover, New Hampshire, 03755.
Biotechnol Bioeng. 2014 Feb;111(2):232-43. doi: 10.1002/bit.25019. Epub 2013 Aug 29.
We describe an ultra-high-throughput screening platform enabling discovery and/or engineering of natural product antibiotics. The methodology involves creation of hydrogel-in-oil emulsions in which recombinant microorganisms are co-emulsified with bacterial pathogens; antibiotic activity is assayed by use of a fluorescent viability dye. We have successfully utilized both bulk emulsification and microfluidic technology for the generation of hydrogel microdroplets that are size-compatible with conventional flow cytometry. Hydrogel droplets are ∼25 pL in volume, and can be synthesized and sorted at rates exceeding 3,000 drops/s. Using this technique, we have achieved screening throughputs exceeding 5 million clones/day. Proof-of-concept experiments demonstrate efficient selection of antibiotic-secreting yeast from a vast excess of negative controls. In addition, we have successfully used this technique to screen a metagenomic library for secreted antibiotics that kill the human pathogen Staphylococcus aureus. Our results establish the practical utility of the screening platform, and we anticipate that the accessible nature of our methods will enable others seeking to identify and engineer the next generation of antibacterial biomolecules.
我们描述了一种超高通量筛选平台,可用于发现和/或改造天然产物抗生素。该方法包括创建油包水凝胶乳液,其中重组微生物与细菌病原体共同乳化;使用荧光活力染料测定抗生素活性。我们已成功利用批量乳化和微流控技术生成与传统流式细胞术尺寸兼容的水凝胶微滴。水凝胶微滴体积约为25皮升,合成和分选速率超过每秒3000滴。使用该技术,我们实现了每天超过500万个克隆的筛选通量。概念验证实验证明了能从大量阴性对照中有效筛选出分泌抗生素的酵母。此外,我们已成功使用该技术筛选宏基因组文库,以寻找可杀死人类病原体金黄色葡萄球菌的分泌抗生素。我们的结果确立了该筛选平台的实际效用,并且我们预计我们方法的易操作性将使其他寻求鉴定和改造下一代抗菌生物分子的人能够使用。