The Ssr protein (T1E_1405) fromPseudomonas putidaDOT-T1E enables oligonucleotide-based recombineering in platform strainP. putidaEM42
出版年份 2016 全文链接
标题
The Ssr protein (T1E_1405) fromPseudomonas putidaDOT-T1E enables oligonucleotide-based recombineering in platform strainP. putidaEM42
作者
关键词
-
出版物
Biotechnology Journal
Volume 11, Issue 10, Pages 1309-1319
出版商
Wiley
发表日期
2016-07-01
DOI
10.1002/biot.201600317
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
- (2016) Sudhir Kumar et al. MOLECULAR BIOLOGY AND EVOLUTION
- A highly precise and portable genome engineering method allows comparison of mutational effects across bacterial species
- (2016) Ákos Nyerges et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Pseudomonas putida—a versatile host for the production of natural products
- (2015) Anita Loeschcke et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Pseudomonas putidaKT2440 Strain Metabolizes Glucose through a Cycle Formed by Enzymes of the Entner-Doudoroff, Embden-Meyerhof-Parnas, and Pentose Phosphate Pathways
- (2015) Pablo I. Nikel et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Transient overexpression of DNA adenine methylase enables efficient and mobile genome engineering with reduced off-target effects
- (2015) Rebecca M. Lennen et al. NUCLEIC ACIDS RESEARCH
- A functional recT gene for recombineering of Clostridium
- (2014) Hongjun Dong et al. JOURNAL OF BIOTECHNOLOGY
- Pseudomonas 2.0: genetic upgrading of P. putida KT2440 as an enhanced host for heterologous gene expression
- (2014) Esteban Martínez-García et al. Microbial Cell Factories
- Rapid editing and evolution of bacterial genomes using libraries of synthetic DNA
- (2014) Ryan R Gallagher et al. Nature Protocols
- Biotechnological domestication of pseudomonads using synthetic biology
- (2014) Pablo I. Nikel et al. NATURE REVIEWS MICROBIOLOGY
- Conditional DNA repair mutants enable highly precise genome engineering
- (2014) Ákos Nyerges et al. NUCLEIC ACIDS RESEARCH
- SEVA 2.0: an update of the Standard European Vector Architecture for de-/re-construction of bacterial functionalities
- (2014) Esteban Martínez-García et al. NUCLEIC ACIDS RESEARCH
- CRISPR–Cas9-assisted recombineering in Lactobacillus reuteri
- (2014) Jee-Hwan Oh et al. NUCLEIC ACIDS RESEARCH
- Direct Mutagenesis of Thousands of Genomic Targets Using Microarray-Derived Oligonucleotides
- (2014) Mads T. Bonde et al. ACS Synthetic Biology
- MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
- (2013) K. Katoh et al. MOLECULAR BIOLOGY AND EVOLUTION
- RNA-guided editing of bacterial genomes using CRISPR-Cas systems
- (2013) Wenyan Jiang et al. NATURE BIOTECHNOLOGY
- Recombineering in Corynebacterium glutamicum combined with optical nanosensors: a general strategy for fast producer strain generation
- (2013) Stephan Binder et al. NUCLEIC ACIDS RESEARCH
- Metabolic potential of the organic-solvent tolerantPseudomonas putida DOT-T1E deduced from its annotated genome
- (2013) Zulema Udaondo et al. Microbial Biotechnology
- Industrial biotechnology of Pseudomonas putida and related species
- (2012) Ignacio Poblete-Castro et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- The Entner-Doudoroff pathway empowersPseudomonas putida KT2440 with a high tolerance to oxidative stress
- (2012) Max Chavarría et al. ENVIRONMENTAL MICROBIOLOGY
- High efficiency recombineering in lactic acid bacteria
- (2012) Jan-Peter van Pijkeren et al. NUCLEIC ACIDS RESEARCH
- The Standard European Vector Architecture (SEVA): a coherent platform for the analysis and deployment of complex prokaryotic phenotypes
- (2012) Rafael Silva-Rocha et al. NUCLEIC ACIDS RESEARCH
- Improving Lambda Red Genome Engineering in Escherichia coli via Rational Removal of Endogenous Nucleases
- (2012) Joshua A. Mosberg et al. PLoS One
- Substrate and Target Sequence Length Influence RecTEPsy Recombineering Efficiency in Pseudomonas syringae
- (2012) Zhongmeng Bao et al. PLoS One
- Multiplexed in Vivo His-Tagging of Enzyme Pathways for in Vitro Single-Pot Multienzyme Catalysis
- (2012) Harris H. Wang et al. ACS Synthetic Biology
- Exploring optimization parameters to increase ssDNA recombineering inLactococcus lactisandLactobacillus reuteri
- (2012) Jan-Peter van Pijkeren et al. Bioengineered
- pBAM1: an all-synthetic genetic tool for analysis and construction of complex bacterial phenotypes
- (2011) Esteban Martínez-García et al. BMC MICROBIOLOGY
- Engineering multiple genomic deletions in Gram-negative bacteria: analysis of the multi-resistant antibiotic profile of Pseudomonas putida KT2440
- (2011) Esteban Martínez-García et al. ENVIRONMENTAL MICROBIOLOGY
- Precise Manipulation of Chromosomes in Vivo Enables Genome-Wide Codon Replacement
- (2011) Farren J. Isaacs et al. SCIENCE
- Recombineering Using RecTE from Pseudomonas syringae
- (2010) B. Swingle et al. APPLIED AND ENVIRONMENTAL MICROBIOLOGY
- Scarless and sequential gene modification in Pseudomonas using PCR product flanked by short homology regions
- (2010) Rubing Liang et al. BMC MICROBIOLOGY
- Molecular characterization of Rifr mutations in Pseudomonas aeruginosa and Pseudomonas putida
- (2009) Tatjana Jatsenko et al. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
- Programming cells by multiplex genome engineering and accelerated evolution
- (2009) Harris H. Wang et al. NATURE
- Enzymatic assembly of DNA molecules up to several hundred kilobases
- (2009) Daniel G Gibson et al. NATURE METHODS
- The dif/Xer Recombination Systems in Proteobacteria
- (2009) Christophe Carnoy et al. PLoS One
- Use of the lambda Red recombinase system to rapidly generate mutants in Pseudomonas aeruginosa
- (2008) Biliana Lesic et al. BMC MOLECULAR BIOLOGY
- Identification and analysis of recombineering functions from Gram-negative and Gram-positive bacteria and their phages
- (2008) S. Datta et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started