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Circular Polymerase Extension Cloning of Complex Gene Libraries and Pathways

Overview of attention for article published in PLOS ONE, July 2009
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Title
Circular Polymerase Extension Cloning of Complex Gene Libraries and Pathways
Published in
PLOS ONE, July 2009
DOI 10.1371/journal.pone.0006441
Pubmed ID
Authors

Jiayuan Quan, Jingdong Tian

Abstract

High-throughput genomics and the emerging field of synthetic biology demand ever more convenient, economical, and efficient technologies to assemble and clone genes, gene libraries and synthetic pathways. Here, we describe the development of a novel and extremely simple cloning method, circular polymerase extension cloning (CPEC). This method uses a single polymerase to assemble and clone multiple inserts with any vector in a one-step reaction in vitro. No restriction digestion, ligation, or single-stranded homologous recombination is required. In this study, we elucidate the CPEC reaction mechanism and demonstrate its usage in demanding synthetic biology applications such as one-step assembly and cloning of complex combinatorial libraries and multi-component pathways.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 946 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 18 2%
United Kingdom 11 1%
Germany 6 <1%
Denmark 3 <1%
Belgium 3 <1%
Uruguay 3 <1%
Austria 2 <1%
Australia 2 <1%
Netherlands 2 <1%
Other 11 1%
Unknown 885 94%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 213 23%
Student > Master 165 17%
Researcher 163 17%
Student > Bachelor 127 13%
Student > Doctoral Student 38 4%
Other 113 12%
Unknown 127 13%
Readers by discipline Count As %
Agricultural and Biological Sciences 415 44%
Biochemistry, Genetics and Molecular Biology 243 26%
Engineering 35 4%
Chemistry 26 3%
Immunology and Microbiology 18 2%
Other 64 7%
Unknown 145 15%