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Production of a fusion protein of sweet potato sporamin from recombinant E.coli XL1 Blue by fed-batch fermentations

机译:分批补料发酵从重组大肠杆菌XL1 Blue生产番薯孢菌素融合蛋白

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摘要

Glucose-stat and pH-stat control strategies were employed in order to culture a recombinant E.coli XL1 Blue to produce a fusion protein of sweet potato sporamin (SPA) and glutathione S-transferase (GST) from the recombinant E.coli XL1 Blue.Cell densities up to 25 g 1~(-1) and 28.9 mg fusion protein (GST-SPA)g~(-1) cell dry weight (CDW) was achieved from a fed-batch fermentation controlled by glucose-stat strategy.A pH-stat control fermentation using glycerol as a carbon source gave E.coil up to 27 g 1~(-1) and 31.5 mg GST-SPA g~(-1) CDW.Additionally,a pH-stat control strategy using glucose as a carbon source gave E.coli up to 15 g 1~(-1) and about 22.7 mg g~(-1) CDW of GST-SPA.
机译:为了培养重组大肠杆菌XL1 Blue,采用了葡萄糖调节和pH调节策略,以从重组大肠杆菌XL1 Blue生产甘薯孢菌素(SPA)和谷胱甘肽S-转移酶(GST)的融合蛋白。通过葡萄糖固定策略控制的分批补料发酵获得了高达25 g 1〜(-1)和28.9 mg融合蛋白(GST-SPA)g〜(-1)细胞干重(CDW)的细胞密度。以甘油为碳源的pH值控制发酵可产生27 g 1〜(-1)和31.5 mg GST-SPA g〜(-1)CDW的大肠杆菌。此外,使用葡萄糖的pH值控制策略作为碳源,E.coli的GST-SPA可达15 g 1〜(-1)和22.7 mg g〜(-1)CDW。

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