دورية أكاديمية

Manufacturing DNA in E. coli yields higher-fidelity DNA than in vitro enzymatic synthesis

التفاصيل البيبلوغرافية
العنوان: Manufacturing DNA in E. coli yields higher-fidelity DNA than in vitro enzymatic synthesis
المؤلفون: Steven J. Hersch, Siddarth Chandrasekaran, Jamie Lam, Nafiseh Nafissi, Roderick A. Slavcev
المصدر: Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 2, Pp 101227- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Genetics
LCC:Cytology
مصطلحات موضوعية: DNA replication fidelity, DNA manufacturing, DNA synthesis, mutation rate, SacB, E. coli, Genetics, QH426-470, Cytology, QH573-671
الوصف: Biotechnologies such as gene therapy have brought DNA vectors to the forefront of pharmaceuticals. The quality of starting material plays a pivotal role in determining final product quality. Here, we examined the fidelity of DNA replication using enzymatic methods (in vitro) compared to plasmid DNA produced in vivo in E. coli. Next-generation sequencing approaches rely on in vitro polymerases, which have inherent limitations in sensitivity. To address this challenge, we introduce a novel assay based on loss-of-function (LOF) mutations in the conditionally toxic sacB gene. Our findings show that DNA production in E. coli results in significantly fewer LOF mutations (80- to 3,000-fold less) compared to enzymatic DNA replication methods such as polymerase chain reaction (PCR) and rolling circle amplification (RCA). These results suggest that using DNA produced by PCR or RCA may introduce a substantial number of mutation impurities, potentially affecting the quality and yield of final pharmaceutical products. Our study underscores that DNA synthesized in vitro has a significantly higher mutation rate than DNA produced traditionally in E. coli. Therefore, utilizing in vitro enzymatically produced DNA in biotechnology and biomanufacturing may entail considerable fidelity-related risks, while using DNA starting material derived from E. coli substantially mitigates this risk.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2329-0501
Relation: http://www.sciencedirect.com/science/article/pii/S2329050124000433; https://doaj.org/toc/2329-0501
DOI: 10.1016/j.omtm.2024.101227
URL الوصول: https://doaj.org/article/b6793fb4ec164648ba4953d192db0dc7
رقم الأكسشن: edsdoj.b6793fb4ec164648ba4953d192db0dc7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23290501
DOI:10.1016/j.omtm.2024.101227