A New Escherichia coli Entry Vector Series (pIIS18) for Seamless Gene Cloning Using Type IIS Restriction Enzymes
Author(s) -
Hend Altaib,
Yuka Ozaki,
Tomoya Kozakai,
Yassien Badr,
Izumi Nomura,
Tohru Suzuki
Publication year - 2019
Publication title -
microbiology resource announcements
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.383
H-Index - 35
ISSN - 2576-098X
DOI - 10.1128/mra.00323-19
Subject(s) - cloning (programming) , restriction enzyme , escherichia coli , cleavage (geology) , molecular cloning , multiple cloning site , vector (molecular biology) , cloning vector , gene , computational biology , biology , restriction site , enzyme , genetics , microbiology and biotechnology , computer science , biochemistry , gene expression , recombinant dna , paleontology , fracture (geology) , programming language
A series of new Escherichia coli entry vectors (pIIS18-SapI, pIIS18-BsmBI, pIIS18-BsaI, pIIS18-BfuAI-1, and pIIS18-BfuAI-2) was constructed based on a modified pUC18 backbone, which carried newly designed multiple cloning sites, consisting of two facing type IIS enzyme cleavage sites and one blunt-end enzyme cleavage site. These vectors are useful for seamless gene cloning.
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