Integrative bacterial artificial chromosomes for DNA integration into the Bacillus subtilis chromosome

被引:12
|
作者
Juhas, Mario [1 ]
Ajioka, James W. [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Tennis Court Rd, Cambridge CB2 1QP, England
基金
英国工程与自然科学研究理事会;
关键词
Bacterial artificial chromosome; Chromosomal integration; lambda red recombineering; mVenus; RecA homologous recombination; HORIZONTAL GENE-TRANSFER; IV SECRETION SYSTEMS; ESCHERICHIA-COLI; GENOMIC ISLANDS; FLUORESCENT PROTEIN; CELL; CLONING; VECTOR; TRANSFORMATION; CONSTRUCTION;
D O I
10.1016/j.mimet.2016.03.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bacillus subtilis is a well-characterized model bacterium frequently used for a number of biotechnology and synthetic biology applications. Novel strategies combining the advantages of B. subtilis with the DNA assembly and editing tools of Escherichia coli are crucial for B. subtilis engineering efforts. We combined Gibson Assembly and lambda red recombineering in E. coli with RecA-mediated homologous recombination in B. subtilis for bacterial artificial chromosome-mediated DNA integration into the well-characterized amyE target locus of the B. subtilis chromosome. The engineered integrative bacterial artificial chromosome iBAC(cav) can accept any DNA fragment for integration into B. subtilis chromosome and allows rapid selection of transformants by B. subtilis-specific antibiotic resistance and the yellow fluorescent protein (mVenus) expression. We used the developed iBAC(cav)-mediated system to integrate 10 kb DNA fragment from E. coli K12 MG1655 into B. subtilis chromosome. iBAC(cav)mediated chromosomal integration approach will facilitate rational design of synthetic biology applications in B. subtilis. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:1 / 7
页数:7
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