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Overexpression of Recombinant Arylsulfatase Cloned from Pseudoalteromonas carrageenovora

机译:假单胞菌角叉菜中克隆的重组芳基硫酸酯酶的过表达

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Arylsulfatase cloned from a marine bacterium, Pseudoalteromonas carrageenovora, was over-expressed in Escherichia coli. Most of the recombinant arylsulfatase was found in the cell lysate with induction up to 10 μM IPTG. However, enzyme activity was observed both in the culture supernatant and cell lysate by induction with IPTG concentration of 50-5,000 μM. Most of the recombinant enzyme was localized in the periplasmic space with 10 μM IPTG induction, while half of the enzyme was distributed in the periplasmic space with 50 μM IPTG induction. Cell growth and arylsulfatase activity did not change with the induction time, and the level of recombinant arylsulfatase expression was maintained at 4-5 U/mL after 6 to 14 hr of culture.
机译:从海洋细菌假单胞菌角叉菜中克隆出的芳基硫酸酯酶在大肠杆菌中过表达。在细胞裂解物中发现了大多数重组芳基硫酸酯酶,诱导浓度高达10μMIPTG。然而,通过用50-5,000μM的IPTG浓度诱导,在培养上清液和细胞裂解物中均观察到酶活性。大多数重组酶在IPTG诱导为10μM的情况下定位于周质空间,而在IPTG诱导为50μM的情况下,一半的酶分布在周质空间。培养6至14小时后,细胞生长和芳基硫酸酯酶活性没有随诱导时间而改变,并且重组芳基硫酸酯酶的表达水平维持在4-5U / mL。

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