Literature DB >> 27671942

Simultaneous Removal of Multiple DNA Segments by Polymerase Chain Reactions.

Vishnu Krishnamurthy1, Kai Zhang2.   

Abstract

Precise DNA manipulation is a key enabling technology for synthetic biology. Approaches based on restriction digestion are often limited by the presence of certain restriction enzyme recognition sites. Recent development of restriction-free cloning approaches has greatly enhanced the flexibility and speed of molecular cloning. Most restriction-free cloning methods focus on DNA assembly. Much less work has been dedicated towards DNA removal. Here we introduce a protocol that allows simultaneous removal of multiple DNA segments from a plasmid using polymerase chain reactions (PCR). Our approach will be beneficial to applications in multiple sites mutagenesis, DNA library construction, genetic and protein engineering, and synthetic biology.

Keywords:  Multiplex gene removal; Polymerase chain reaction; Restriction-free cloning; Synthetic DNA assembly and manipulation; Synthetic single-stranded bridging oligos

Mesh:

Substances:

Year:  2017        PMID: 27671942     DOI: 10.1007/978-1-4939-6343-0_15

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  A restriction-free method for gene reconstitution using two single-primer PCRs in parallel to generate compatible cohesive ends.

Authors:  Fanli Zeng; Zhimin Hao; Pan Li; Yanan Meng; Jingao Dong; Yibin Lin
Journal:  BMC Biotechnol       Date:  2017-03-17       Impact factor: 2.563

  1 in total

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