[HTML][HTML] Harnessing heterologous and endogenous CRISPR-Cas machineries for efficient markerless genome editing in Clostridium
Application of CRISPR-Cas9 systems has revolutionized genome editing across all domains
of life. Here we report implementation of the heterologous Type II CRISPR-Cas9 system in …
of life. Here we report implementation of the heterologous Type II CRISPR-Cas9 system in …
Bacterial Genome Editing with CRISPR-Cas9: Deletion, Integration, Single Nucleotide Modification, and Desirable “Clean” Mutant Selection in Clostridium beijerinckii …
CRISPR-Cas9 has been demonstrated as a transformative genome engineering tool for
many eukaryotic organisms; however, its utilization in bacteria remains limited and …
many eukaryotic organisms; however, its utilization in bacteria remains limited and …
Exploiting heterologous and endogenous CRISPR‐Cas systems for genome editing in the probiotic Clostridium butyricum
X Zhou, X Wang, H Luo, Y Wang… - Biotechnology and …, 2021 - Wiley Online Library
Clostridium butyricum has been widely used as a probiotic for humans and food animals.
However, the mechanisms of beneficial effects of C. butyricum on the host remain poorly …
However, the mechanisms of beneficial effects of C. butyricum on the host remain poorly …
Efficient genome editing in Clostridium cellulolyticum via CRISPR-Cas9 nickase
The CRISPR-Cas9 system is a powerful and revolutionary genome-editing tool for
eukaryotic genomes, but its use in bacterial genomes is very limited. Here, we investigated …
eukaryotic genomes, but its use in bacterial genomes is very limited. Here, we investigated …
[HTML][HTML] A two-plasmid inducible CRISPR/Cas9 genome editing tool for Clostridium acetobutylicum
F Wasels, J Jean-Marie, F Collas… - Journal of …, 2017 - Elsevier
CRISPR/Cas-based genetic engineering has revolutionised molecular biology in both
eukaryotes and prokaryotes. Several tools dedicated to the genomic transformation of the …
eukaryotes and prokaryotes. Several tools dedicated to the genomic transformation of the …
Genome editing using the endogenous type I CRISPR-Cas system in Lactobacillus crispatus
C Hidalgo-Cantabrana, YJ Goh… - Proceedings of the …, 2019 - National Acad Sciences
CRISPR-Cas systems are now widely used for genome editing and transcriptional
regulation in diverse organisms. The compact and portable nature of class 2 single effector …
regulation in diverse organisms. The compact and portable nature of class 2 single effector …
[HTML][HTML] Genome editing in bacteria: CRISPR-Cas and beyond
RD Arroyo-Olarte, R Bravo Rodriguez, E Morales-Ríos - Microorganisms, 2021 - mdpi.com
Genome editing in bacteria encompasses a wide array of laborious and multi-step methods
such as suicide plasmids. The discovery and applications of clustered regularly interspaced …
such as suicide plasmids. The discovery and applications of clustered regularly interspaced …
[HTML][HTML] Endogenous CRISPR-Cas system-based genome editing and antimicrobials: review and prospects
Y Li, N Peng - Frontiers in microbiology, 2019 - frontiersin.org
CRISPR-Cas systems adapt “memories” via spacers from viruses and plasmids to develop
adaptive immunity against mobile genetic elements. Mature CRISPR RNAs guide CRISPR …
adaptive immunity against mobile genetic elements. Mature CRISPR RNAs guide CRISPR …
CRISPR/Cpf1 enables fast and simple genome editing of Saccharomyces cerevisiae
R Verwaal, N Buiting‐Wiessenhaan, S Dalhuijsen… - Yeast, 2018 - Wiley Online Library
Cpf1 represents a novel single RNA‐guided CRISPR/Cas endonuclease system suitable for
genome editing with distinct features compared with Cas9. We demonstrate the functionality …
genome editing with distinct features compared with Cas9. We demonstrate the functionality …
[HTML][HTML] CRISPR-assisted editing of bacterial genomes
The targeting of nucleases to specific DNA sequences facilitates genome editing. Recent
work demonstrated that the CRISPR-associated (Cas) nuclease Cas9 can be targeted to …
work demonstrated that the CRISPR-associated (Cas) nuclease Cas9 can be targeted to …
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