Wang Jianjun, Zhu Junge, Min Cong, Wu Sheng
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, PR China.
BMC Biotechnol. 2014 May 13;14:40. doi: 10.1186/1472-6750-14-40.
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.
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.
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.
γ-内酰胺酶用于拆分γ-内酰胺,γ-内酰胺在阿巴卡韦和帕拉米韦的合成中被使用。在某些情况下,酶法因其高效率和高产量而成为最常用的方法。纤维素的纤维素结合结构域(CBD)常被用作酶固定化的生物特异性亲和基质。纤维素价格低廉,具有优异的化学和物理性质。同时,纤维素与CBD之间的结合紧密,很少发生解吸。
我们制备了来自嗜热栖热菌P2的γ-内酰胺酶基因gla的两种融合构建体。这两种构建体在γ-内酰胺酶的氨基或羧基末端融合了Cbd(来自嗜热栖热放线菌的纤维素结合结构域)。这两种构建体在大肠杆菌Rosetta(DE3)中作为两种融合蛋白异源表达。它们都能很好地固定在微晶纤维素(微晶纤维素基质)上。表观动力学参数表明,羧基末端融合蛋白(Gla-接头-Cbd)是一种更好的催化剂。微晶纤维素固定化的Gla-接头-Cbd的V(max)和k(cat)值分别为381 U mg⁻¹和4.7×10⁵ s⁻¹。游离的Gla-接头-Cbd的值分别为151 U mg⁻¹和1.8×10⁵ s⁻¹。这些数据表明,固定化后酶的催化效率得到了提高。固定化的Gla-接头-Cbd的最适温度下降了10度,从80°C降至70°C,但在60°C孵育48小时时很稳定。它在催化20批次反应中保持稳定。优化后,转化中固定化酶的浓度设定为200 mg/mL。我们发现当底物浓度超过60 mM时,固定化酶会受到抑制。最后进行了10 mL体积的转化,其中0.6 M底物被水解,拆分在9小时内完成,对映体过量值为99.5%。
纤维素是地球上最丰富的可再生材料。Cbd结构域与纤维素之间的吸附是一个生物绿色过程。纤维素固定化的融合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-内酰胺的一种有前途的催化剂。