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Manufacturing method null of the useful material which uses the microbe and the said microbe which possess the high manifestation vector and the said high manifestation vector

机译:使用具有高表达载体和所述高表达载体的微生物和所述微生物的有用材料的制造方法无效

摘要

PURPOSE:To obtain a new vector capable of highly expressing an exogenote product using Bacillus.brevis as a host microorganism. CONSTITUTION:A highly expressing vector pHY700 expressed by a restriction enzyme map of the figure. The aforementioned highly expressing vector pHY700 is obtained by treating a well-known plasmid having a DNA fragment linking an alpha-amylase (BLA) gene of Bacillus.licheniformis to the downstream side of an MWP promoter gene of Bacillus.brevis 47 (FERM P-7224) with a restriction enzyme, linking a promoter region fragment of a main extracellular protein gene (HWP gene) of Bacillus.brevis HPD31 (FERM BP-1087) thereto, transforming the Bacillus.brevis, providing a plasmid in which the MWP promoter is converted into an HWP promoter, treating the resultant plasmid with a restriction enzyme, a ligase and a linker and removing a BLA genetic region.
机译:目的:获得一种新的载体,该载体能够使用短芽孢杆菌(Bacillus.brevis)作为宿主微生物来高度表达外源基因产物。组成:高表达载体pHY700,通过图中的限制性内切酶图表达。上述高表达载体pHY700是通过处理具有将地衣芽孢杆菌的α-淀粉酶(BLA)基因连接至短芽孢杆菌47的MWP启动子基因的下游侧的DNA片段的众所周知的质粒而获得的。 7224)用限制性酶将短芽孢杆菌HPD31(FERM BP-1087)的主要细胞外蛋白基因(HWP基因)的启动子区片段连接到其上,转化短芽孢杆菌,提供了其中MWP启动子为将其转化为HWP启动子,用限制酶,连接酶和接头处理所得质粒,并除去BLA遗传区。

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