首页> 外国专利> BACILLUS VELEZENSIS A-68-DERIVED CELLULASE GENE AND E.COLI A-68 STRAIN TRANSFORMED BY INTRODUCING THE SAME

BACILLUS VELEZENSIS A-68-DERIVED CELLULASE GENE AND E.COLI A-68 STRAIN TRANSFORMED BY INTRODUCING THE SAME

机译:引入相同杆菌转化芽孢杆菌的A-68纤维素酶基因和大肠杆菌A-68菌株

摘要

PURPOSE: A gene of Bacillus velezensis-derived cellulase and a recombinant E.coli A-68 recombinant strain transformed by introducing the same are provided to enhance productivity and efficiency of strains.;CONSTITUTION: A Bacillus velezensis A-68(deposit number KACC 91178P)-derived cellulase is encoded by a gene having a sequence of sequence number 1. A recombinant vector for expressing cellulase in E.coli is prepared by linking the gene of sequence number 1 to p-TGEM T-easy vector. The recombinant E.coli A-68(deposit number KACC 91335P) is prepared by transforming through introduction of the recombinant vector pTA-68. A method for producing cellulase comprises a step of culturing the recombinant E.coli A-68 in a medium containing 50g/L of rice bran and 2.5 g/L of yeast extract at pH 7.3 and 35°C.;COPYRIGHT KIPO 2012
机译:目的:提供一种芽孢杆菌来源的纤维素酶基因和通过导入该酶转化的重组大肠杆菌A-68重组菌株,以提高菌株的生产力和效率。;组成:芽孢杆菌(Bacillus velezensis)A-68(保藏号KACC 91178P)源自纤维素的纤维素酶由具有序列号1的序列的基因编码。通过将序列号1的基因与p-TGEM T-easy载体连接,制备用于在大肠杆菌中表达纤维素酶的重组载体。通过导入重组载体pTA-68进行转化来制备重组大肠杆菌A-68(保藏号KACC 91335P)。纤维素酶的生产方法包括在pH 7.3和35℃,含有50g / L米糠和2.5g / L酵母提取物的培养基中培养重组大肠杆菌A-68的步骤; COPYRIGHT KIPO 2012

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