High-Efficiency Multi-site Genomic Editing of Pseudomonas putida through Thermoinducible ssDNA Recombineering
Author:
Funder
MADONNA
BioRoboost
SYNBIO4FLAV
H2020
Comunidad de Madrid
Publisher
Elsevier BV
Subject
Multidisciplinary
Reference44 articles.
1. The Ssr protein (T1E_1405) from Pseudomonas putida DOT-T1E enables oligonucleotide-based recombineering in platform strain P. putida EM42;Aparicio;Biotechnol. J.,2016
2. Improved thermotolerance of genome-reduced Pseudomonas putida EM42 enables effective functioning of the PL/cI857 system;Aparicio;Biotechnol. J.,2019
3. A broad host range plasmid-based roadmap for ssDNA-based recombineering in gram-negative bacteria;Aparicio,2020
4. Mismatch repair hierarchy of Pseudomonas putida revealed by mutagenic ssDNA recombineering of the pyrF gene;Aparicio;Environ. Microbiol.,2019
5. Substrate and target sequence length influence RecTE(Psy) recombineering efficiency in Pseudomonas syringae;Bao;PLoS One,2012
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