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CBD binding domain fused γ-lactamase from Sulfolobus solfataricus is an efficient catalyst for (-) γ-lactam production

机译:来自Sulfolobus solfataricus的CBD结合域融合γ-内酰胺酶是生产(-)γ-内酰胺的有效催化剂

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Background γ-lactamase is used for the resolution of γ-lactam which is utilized in the synthesizing of abacavir and peramivir. In some cases, enzymatic method is the most utilized method because of its high efficiency and productivity. The cellulose binding domain (CBD) of cellulose is often used as the bio-specific affinity matrix for enzyme immobilization. Cellulose is cheap and it has excellent chemical and physical properties. Meanwhile, binding between cellulose and CBD is tight and the desorption rarely happened. Results We prepared two fusion constructs of the γ-lactamase gene gla , which was from Sulfolobus solfataricus P2. These two constructs had Cbd (cellulose binding domain from Clostridium thermocellum ) fused at amino or carboxyl terminus of the γ-lactamase. These two constructs were heterogeneously expressed in E. coli rosetta (DE3) as two fusion proteins. Both of them were immobilized well on Avicel (microcrystalline cellulose matrix). The apparent kinetic parameters revealed that carboxyl terminus fused protein (Gla-linker-Cbd) was a better catalyst. The V max and k cat value of Avicel immobilized Gla-linker-Cbd were 381 U mg-1 and 4.7?×?105?s-1 respectively. And the values of the free Gla-linker-Cbd were 151 U mg-1 and 1.8?×?105?s-1 respectively. These data indicated that the catalytic efficiency of the enzyme was upgraded after immobilization. The immobilized Gla-linker-Cbd had a 10-degree temperature optimum dropping from 80°C to 70°C but it was stable when incubated at 60°C for 48?h. It remained stable in catalyzing 20-batch reactions. After optimization, the immobilized enzyme concentration in transformation was set as 200?mg/mL. We found out that there was inhibition that occurred to the immobilized enzyme when substrate concentration exceeded 60?mM. Finally a 10?mL-volume transformation was conducted, in which 0.6?M substrate was hydrolyzed and the resolution was completed within 9?h with a 99.5% ee value. Conclusions Cellulose is the most abundant and renewable material on the Earth. The absorption between Cbd domain and cellulose is a bio-green process. The cellulose immobilized fusion Gla exhibited good catalytic characters, therefore we think the cellulose immobilized Gla is a promising catalyst for the industrial preparation of (-) - γ-lactam.
机译:背景技术γ-内酰胺酶用于拆分γ-内酰胺,该酶用于合成阿巴卡韦和帕拉米韦。在某些情况下,酶促方法是最常用的方法,因为它具有很高的效率和生产率。纤维素的纤维素结合域(CBD)通常用作酶固定化的生物特异性亲和基质。纤维素价格便宜,并且具有出色的化学和物理性能。同时,纤维素和CBD之间的结合紧密,并且解吸很少发生。结果我们制备了两个Sulfolobus solfataricus P2的γ-内酰胺酶基因gla的融合构建体。这两个构建体具有在γ-内酰胺酶的氨基或羧基末端融合的Cbd(来自热纤梭菌的纤维素结合域)。这两种构建体作为两种融合蛋白在大肠埃希氏菌(DE3)中异质表达。他们两个都很好地固定在Avicel(微晶纤维素基质)上。明显的动力学参数表明,羧基末端融合蛋白(Gla-linker-Cbd)是更好的催化剂。 Avicel固定化Gla-linker-Cbd的V max 和k cat 值为381 U mg -1 和4.7?×?10 5 ?s -1 。游离Gla-linker-Cbd的值分别为151 U mg -1 和1.8?×?10 5 ?s -1 。这些数据表明,固定后该酶的催化效率得到了提高。固定化的Gla-linker-Cbd的最佳温度为10度,从80°C降至70°C,但在60°C孵育48?h时稳定。它在催化20批反应中保持稳定。优化后,固定化转化酶的浓度为200?mg / mL。我们发现,当底物浓度超过60?mM时,固定化酶会产生抑制作用。最后进行了10 µmL的体积转化,其中0.6 µM的底物被水解,分离度在9 µh内完成,ee值为99.5%。结论纤维素是地球上最丰富和可再生的材料。 Cbd结构域和纤维素之间的吸收是一种生物绿色过程。纤维素固定化的Gla表现出良好的催化特性,因此我们认为纤维素固定化的Gla是工业制备(-)-γ-内酰胺的有前途的催化剂。

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