iScience (Apr 2019)

Single-Stranded DNA-Binding Protein and Exogenous RecBCD Inhibitors Enhance Phage-Derived Homologous Recombination in Pseudomonas

  • Jia Yin,
  • Wentao Zheng,
  • Yunsheng Gao,
  • Chanjuan Jiang,
  • Hongbo Shi,
  • Xiaotong Diao,
  • Shanshan Li,
  • Hanna Chen,
  • Hailong Wang,
  • Ruijuan Li,
  • Aiying Li,
  • Liqiu Xia,
  • Yulong Yin,
  • A. Francis Stewart,
  • Youming Zhang,
  • Jun Fu

Journal volume & issue
Vol. 14
pp. 1 – 14

Abstract

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Summary: The limited efficiency of the available tools for genetic manipulation of Pseudomonas limits fundamental research and utilization of this genus. We explored the properties of a lambda Red-like operon (BAS) from Pseudomonas aeruginosa phage Ab31 and a Rac bacteriophage RecET-like operon (RecTEPsy) from Pseudomonas syringae pv. syringae B728a. Compared with RecTEPsy, the BAS operon was functional at a higher temperature indicating potential to be a generic system for Pseudomonas. Owing to the lack of RecBCD inhibitor in the BAS operon, we added Redγ or Pluγ and found increased recombineering efficiencies in P. aeruginosa and Pseudomonas fluorescens but not in Pseudomonas putida and P. syringae. Overexpression of single-stranded DNA-binding protein enhanced recombineering in several contexts including RecET recombination in E. coli. The utility of these systems was demonstrated by engineering P. aeruginosa genomes to create an attenuated rhamnolipid producer. Our work enhances the potential for functional genomics in Pseudomonas. : Biological Sciences; Molecular Biology; Bioengineering; Biotechnology; Cell Biology Subject Areas: Biological Sciences, Molecular Biology, Bioengineering, Biotechnology, Cell Biology