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Bioproduction of pure, kilobase-scale single-stranded DNA
Scalable production of kilobase single-stranded DNA (ssDNA) with sequence control has applications in therapeutics, gene synthesis and sequencing, scaffolded DNA origami, and archival DNA memory storage. Biological production of circular ssDNA (cssDNA) using M13 addresses these needs at low cost. Ho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467869/ https://www.ncbi.nlm.nih.gov/pubmed/30992517 http://dx.doi.org/10.1038/s41598-019-42665-1 |
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author | Shepherd, Tyson R. Du, Rebecca R. Huang, Hellen Wamhoff, Eike-Christian Bathe, Mark |
author_facet | Shepherd, Tyson R. Du, Rebecca R. Huang, Hellen Wamhoff, Eike-Christian Bathe, Mark |
author_sort | Shepherd, Tyson R. |
collection | PubMed |
description | Scalable production of kilobase single-stranded DNA (ssDNA) with sequence control has applications in therapeutics, gene synthesis and sequencing, scaffolded DNA origami, and archival DNA memory storage. Biological production of circular ssDNA (cssDNA) using M13 addresses these needs at low cost. However, one unmet goal is to minimize the essential protein coding regions of the exported DNA while maintaining its infectivity and production purity to produce sequences less than 3,000 nt in length, relevant to therapeutic and materials science applications. Toward this end, synthetic miniphage with inserts of custom sequence and size offers scalable, low-cost synthesis of cssDNA at milligram and higher scales. Here, we optimize growth conditions using an E. coli helper strain combined with a miniphage genome carrying only an f1 origin and a β-lactamase-encoding (bla) antibiotic resistance gene, enabling isolation of pure cssDNA with a minimum sequence genomic length of 1,676 nt, without requiring additional purification from contaminating DNA. Low-cost scalability of isogenic, custom-length cssDNA is demonstrated for a sequence of 2,520 nt using a bioreactor, purified with low endotoxin levels (<5 E.U./ml). We apply these exonuclease-resistant cssDNAs to the self-assembly of wireframe DNA origami objects and to encode digital information on the miniphage genome for biological amplification. |
format | Online Article Text |
id | pubmed-6467869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64678692019-04-18 Bioproduction of pure, kilobase-scale single-stranded DNA Shepherd, Tyson R. Du, Rebecca R. Huang, Hellen Wamhoff, Eike-Christian Bathe, Mark Sci Rep Article Scalable production of kilobase single-stranded DNA (ssDNA) with sequence control has applications in therapeutics, gene synthesis and sequencing, scaffolded DNA origami, and archival DNA memory storage. Biological production of circular ssDNA (cssDNA) using M13 addresses these needs at low cost. However, one unmet goal is to minimize the essential protein coding regions of the exported DNA while maintaining its infectivity and production purity to produce sequences less than 3,000 nt in length, relevant to therapeutic and materials science applications. Toward this end, synthetic miniphage with inserts of custom sequence and size offers scalable, low-cost synthesis of cssDNA at milligram and higher scales. Here, we optimize growth conditions using an E. coli helper strain combined with a miniphage genome carrying only an f1 origin and a β-lactamase-encoding (bla) antibiotic resistance gene, enabling isolation of pure cssDNA with a minimum sequence genomic length of 1,676 nt, without requiring additional purification from contaminating DNA. Low-cost scalability of isogenic, custom-length cssDNA is demonstrated for a sequence of 2,520 nt using a bioreactor, purified with low endotoxin levels (<5 E.U./ml). We apply these exonuclease-resistant cssDNAs to the self-assembly of wireframe DNA origami objects and to encode digital information on the miniphage genome for biological amplification. Nature Publishing Group UK 2019-04-16 /pmc/articles/PMC6467869/ /pubmed/30992517 http://dx.doi.org/10.1038/s41598-019-42665-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shepherd, Tyson R. Du, Rebecca R. Huang, Hellen Wamhoff, Eike-Christian Bathe, Mark Bioproduction of pure, kilobase-scale single-stranded DNA |
title | Bioproduction of pure, kilobase-scale single-stranded DNA |
title_full | Bioproduction of pure, kilobase-scale single-stranded DNA |
title_fullStr | Bioproduction of pure, kilobase-scale single-stranded DNA |
title_full_unstemmed | Bioproduction of pure, kilobase-scale single-stranded DNA |
title_short | Bioproduction of pure, kilobase-scale single-stranded DNA |
title_sort | bioproduction of pure, kilobase-scale single-stranded dna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467869/ https://www.ncbi.nlm.nih.gov/pubmed/30992517 http://dx.doi.org/10.1038/s41598-019-42665-1 |
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