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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
An embodiment of the present invention provides a genome editing vector for Eubacterium calanderi for the CRISPR/Cas9 system. The genome editing vector for Eubacterium calanderi according to an embodiment of the present invention includes a DNA sequence encoding a guide RNA (gRNA) of a target gene for cutting; DNA sequence encoding the Cas9 protein; A P rbo promoter operably linked to a DNA sequence encoding the Cas9 protein; Origin of replication derived from E. coli; Origin of replication for Eubacterium calanderi; And a marker for selecting a transformed strain. According to an embodiment of the present invention, a genome editing vector for Eubacterium calander, applicable to Eubacterium calanderi strain, which is an acetogen suitable for syngas bioconversion process, and a method for editing the genome of Eubacterium calanderi strain using the same, and This can be used to provide a transformed Eubacterium calander strain.
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机译:本发明的一个实施方案为CRISPR / CAS9系统提供了用于磁杆菌Calanderi的基因组编辑载体。根据本发明的实施方案的关于易化菌Calanderi的基因组编辑载体包括编码靶基因的引导RNA(GRNA)的DNA序列进行切割;编码Cas9蛋白的DNA序列; p rbo sub> i>启动子与编码Cas9蛋白的DNA序列可操作地连接;从大肠杆菌衍生的复制起源;盲肠Calanderi复制的起源;和用于选择转化菌株的标记。根据本发明的一个实施方案,适用于具有易用Calanderi菌株的有μuBacteriumcalander的基因组编辑载体,这是适用于合成气生物转化过程的乙酰氨基,以及使用该方法的用于编辑有μUBacteriumcalanderi菌株的基因组的方法,以及该方法可用于提供转化的异细胶囊菌株。
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