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Cited by 678

The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.

DNA assembler, an in vivo genetic method for rapid construction of biochemical pathways

Open access
Shao, Zengyi, Zhao, Hua, Zhao, Huimin·2009·Nucleic Acids Research

Abstract

The assembly of large recombinant DNA encoding a whole biochemical pathway or genome represents a significant challenge. Here, we report a new method, DNA assembler, which allows the assembly of an entire biochemical pathway in a single step via in vivo homologous recombination in Saccharomyces cerevisiae. We show that DNA assembler can rapidly assemble a functional D-xylose utilization pathway (approximately 9 kb DNA consisting of three genes), a functional zeaxanthin biosynthesis pathway (approximately 11 kb DNA consisting of five genes) and a functional combined D-xylose utilization and zeaxanthin biosynthesis pathway (approximately 19 kb consisting of eight genes) with high efficiencies (70-100%) either on a plasmid or on a yeast chromosome. As this new method only requires simple DNA preparation and one-step yeast transformation, it represents a powerful tool in the construction of biochemical pathways for synthetic biology, metabolic engineering and functional genomics studies.

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Crossref · 10.1093/nar/gkn991

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Metadata

Authors
Shao, Z., Zhao, H., & Zhao, H.
Venue
Nucleic Acids Research
Published
2008-12-12
Volume
37
Issue
2
Pages
e16-e16
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W1967210731
Cited by
678
References
31
FWCI
5.96
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: DNA assembler, an in vivo genetic method for rapid construction of biochemical pathways. https://app.cochat.ai/papers/10.1093/nar/gkn991
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Shao, Z., Zhao, H., & Zhao, H. (2009). DNA assembler, an in vivo genetic method for rapid construction of biochemical pathways. Nucleic Acids Research. https://doi.org/10.1093/nar/gkn991

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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