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GENOMIC EDITING VECTOR FOR EUBACTERIUM CALLANDERI, METHOD FOR EDITING GENOME OF EUBACTERIUM CALLANDERI USING THE SAME, AND TRANSGENIC EUBACTERIUM CALLANDERI STRAINS USING THE SAME
GENOMIC EDITING VECTOR FOR EUBACTERIUM CALLANDERI, METHOD FOR EDITING GENOME OF EUBACTERIUM CALLANDERI USING THE SAME, AND TRANSGENIC EUBACTERIUM CALLANDERI STRAINS USING THE SAME
Proposed is a genomic editing vector for Eubacterium callanderi for the CRISPR/Cas9 system. The genomic editing vector for Eubacterium callanderi includes a DNA sequence encoding a guide RNA (gRNA) of a cleavage target gene; a DNA sequence encoding a Cas9 protein; a Prbo promoter that is operably linked to the DNA sequence encoding a Cas9 protein; a replication starting point derived from E. coli; a replication starting point for Eubacterium callanderi; and a marker for selecting transgenic strains. It is possible to provide a genomic editing vector for Eubacterium callanderi that can be applied to Eubacterium callanderi strains that are acetogen that is suitable for syngas biorefinery, a method for editing a genome of Eubacterium callanderi strains using the same, and transgenic Eubacterium callanderi strains using the same.
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