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Nucleic Acids Res ; 48(16): e95, 2020 09 18.
Article in English | MEDLINE | ID: mdl-32692349

ABSTRACT

Multiplexed assays allow functional testing of large synthetic libraries of genetic elements, but are limited by the designability, length, fidelity and scale of the input DNA. Here, we improve DropSynth, a low-cost, multiplexed method that builds gene libraries by compartmentalizing and assembling microarray-derived oligonucleotides in vortexed emulsions. By optimizing enzyme choice, adding enzymatic error correction and increasing scale, we show that DropSynth can build thousands of gene-length fragments at >20% fidelity.


Subject(s)
Gene Library , Genes, Synthetic , Nucleic Acid Amplification Techniques/methods , Oligonucleotides/genetics , Emulsions/chemistry , Escherichia coli/genetics
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