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Bioproduction of single-stranded DNA from isogenic miniphage

biorxiv. 2019; 
Tyson R. Shepherd, Rebecca R. Du, Hellen Huang, View Eike-Christian Wamhoff, View Mark Bathe
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Gene Synthesis Sanger sequencing by primer walking verified the sequence of the phage DNA (External Table S1 and S2). The kit-based purification yielded 2 mg of cssDNA/L of culture, matching the yield from phenol-chloroform extraction. Endotoxins were tested using a colorimetric assay (ToxinSensor Chromogenic LAL Endotoxin Assay Kit, GenScript, NJ), showing the final product yielded endotoxin levels at 1.1 ± 0.1 E.U./ml per cssDNA concentration of 10 nM, similar to endotoxin reduction by Triton-X114 ((39); Supplementary Figure S6). Circularization of the produced cssDNA was verified by incubation with exonuclease I, showing no detectable degradation after 30 min (Figure 3d). Get A Quote

摘要

Scalable production of gene-length single-stranded DNA (ssDNA) with sequence control has applications in homology directed repair templating, gene synthesis and sequencing, scaffolded DNA origami, and archival DNA memory storage. Biological production of circular single-stranded DNA (cssDNA) using bacteriophage M13 addresses these needs at low cost. A primary goal toward this end is to minimize the essential protein coding regions of the produced, exported sequence while maintaining its infectivity and production purity, with engineered regions of sequence control. Synthetic miniphage constitutes an ideal platform for bacterial production of isogenic cssDNA, using inserts of custom sequence and size to attain t... More

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