Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
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Gas Fermentation-A Flexible Platform for Commercial Scale Production of Low-Carbon-Fuels and Chemicals from Waste and Renewable FeedstocksCurrent and future prospects for CRISPR-based tools in bacteriaPatterns of CRISPR/Cas9 activity in plants, animals and microbesA Narrow pH Range Supports Butanol, Hexanol, and Octanol Production from Syngas in a Continuous Co-culture of Clostridium ljungdahlii and Clostridium kluyveri with In-Line Product ExtractionDevelopment of an inducible transposon system for efficient random mutagenesis in Clostridium acetobutylicumGenome editing of Clostridium autoethanogenum using CRISPR/Cas9CRISPR/Cas9 mediated targeted mutagenesis of the fast growing cyanobacterium Synechococcus elongatus UTEX 2973.A CRISPR-Cas9 Assisted Non-Homologous End-Joining Strategy for One-step Engineering of Bacterial Genome.Sequence-specific DNA nicking endonucleases.Harnessing Type I and Type III CRISPR-Cas systems for genome editing.Toward a genetic tool development pipeline for host-associated bacteria.CRISPR-Cas9 technology: applications in genome engineering, development of sequence-specific antimicrobials, and future prospects.Development of a High-Efficiency Transformation Method and Implementation of Rational Metabolic Engineering for the Industrial Butanol Hyperproducer Clostridium saccharoperbutylacetonicum Strain N1-4.A roadmap for gene system development in Clostridium.Disruption of the Reductive 1,3-Propanediol Pathway Triggers Production of 1,2-Propanediol for Sustained Glycerol Fermentation by Clostridium pasteurianumCRISPR-based genome editing and expression control systems in Clostridium acetobutylicum and Clostridium beijerinckii.Consequences of Cas9 cleavage in the chromosome of Escherichia coli.Biomass, strain engineering, and fermentation processes for butanol production by solventogenic clostridia.Cellulosomes: bacterial nanomachines for dismantling plant polysaccharides.High throughput nanoparticle tracking analysis for monitoring outer membrane vesicle production.Harnessing heterologous and endogenous CRISPR-Cas machineries for efficient markerless genome editing in ClostridiumCas9 Nickase-Assisted RNA Repression Enables Stable and Efficient Manipulation of Essential Metabolic Genes in Clostridium cellulolyticum.Extending CRISPR-Cas9 Technology from Genome Editing to Transcriptional Engineering in the Genus Clostridium.Efficient Genome Editing of a Facultative Thermophile Using Mesophilic spCas9.Development of a CRISPR-Cas9 Tool Kit for Comprehensive Engineering of Bacillus subtilis.Efficient gene editing in Corynebacterium glutamicum using the CRISPR/Cas9 system.Challenges and Advances for Genetic Engineering of Non-model Bacteria and Uses in Consolidated Bioprocessing.Using CRISPR-Cas9-mediated genome editing to generate C. difficile mutants defective in selenoproteins synthesis.CRISPR-Cas9D10A Nickase-Assisted Genome Editing in Lactobacillus casei.Development of a CRISPR/Cas9 genome editing toolbox for Corynebacterium glutamicum.Fundamental CRISPR-Cas9 tools and current applications in microbial systems.Engineering chemical interactions in microbial communities.CRISPR/Cas9-Based Counterselection Boosts Recombineering Efficiency in Pseudomonas putida.Development of an Efficient Genome Editing Tool in Bacillus licheniformis Using CRISPR-Cas9 Nickase.Single plasmid systems for inducible dual protein expression and for CRISPR-Cas9/CRISPRi gene regulation in lactic acid bacterium Lactococcus lactis.Efficient and Scalable Precision Genome Editing in Staphylococcus aureus through Conditional Recombineering and CRISPR/Cas9-Mediated Counterselection.Genetic redundancy of senescence-associated transcription factors in Arabidopsis.Function analysis of 5'-UTR of the cellulosomal xyl-doc cluster in Clostridium papyrosolvens.Recent Developments of the Synthetic Biology Toolkit for Clostridium.Genome editing and transcriptional repression in Pseudomonas putida KT2440 via the type II CRISPR system.
P2860
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P2860
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@ast
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@en
type
label
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@ast
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@en
prefLabel
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@ast
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@en
P2093
P2860
P356
P1476
Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.
@en
P2093
Christopher L Hemme
Jizhong Zhou
Yongchao Li
Yonghua Zhu
P2860
P304
P356
10.1128/AEM.00873-15
P407
P577
2015-04-24T00:00:00Z