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Robust production of gamma-amino butyric acid using recombinant Corynebacterium glutamicum expressing glutamate decarboxylase from Escherichia coli

机译:使用重组大肠杆菌表达谷氨酸脱羧酶的谷氨酸棒杆菌稳健地生产γ-氨基丁酸

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摘要

Gamma-amino butyric acid (GABA) is a component of pharmaceuticals, functional foods, and the biodegradable plastic polyamide 4. Here, we report a simple and robust system to produce GABA from glucose using the recombinant Corynebacterium glutamicum strain GAD, which expresses GadB, a glutamate decarboxylase encoded by the gadB gene of Escherichia coli W3110. As confirmed by HPLC analysis, GABA fermentation by C. glutamicum GAD cultured at 30 °C in GABA Production 1 (GP1) medium containing 50 g/L glucose without the addition of glutamate yielded 8.07 ± 1.53 g/L extracellular GABA after 96h. Addition of 0.1 mM pyridoxal 5'-phosphate (PLP) was found to enhance the production of GABA, whereas Tween 40 was unnecessary for GABA fermentation. Using the optimized GABA Production 2 (GP2) medium, which contained 50 g/L glucose and 0.1 mM PLP, fermentation was performed in a flask at 30°C with 10% (v/v) seed culture of C. glutamicum GAD. GABA was produced in the culture supernatant with a yield of 12.37 ± 0.88 g/L after 72 h with a space-time yield of 0.172 g/L/h, which is the highest yield obtained to date for GABA from fermentation with glucose as a main carbon source.
机译:γ-氨基丁酸(GABA)是药物,功能性食品和可生物降解的塑料聚酰胺4的组成部分。在这里,我们报告了一种简单而强大的系统,该系统可以使用表达GadB的重组谷氨酸棒杆菌GAD从葡萄糖生产GABA,大肠杆菌W3110的gadB基因编码的谷氨酸脱羧酶。如通过HPLC分析所证实的,在96小时后,在含有50g / L葡萄糖的GABA生产1(GP1)培养基中在30℃下培养的谷氨酸棒杆菌GAD对GABA的发酵产生了8.07±1.53g / L的细胞外GABA。发现添加0.1 mM吡ido醛5'-磷酸酯(PLP)可以增强GABA的产生,而吐温40对于GABA发酵而言是不必要的。使用含有50 g / L葡萄糖和0.1 mM PLP的优化GABA生产2(GP2)培养基,在30°C的烧瓶中用10%(v / v)谷氨酸棒杆菌GAD种子培养物进行发酵。 GABA在培养上清液中产生,72小时后产量为12.37±0.88 g / L,时空产量为0.172 g / L / h,这是迄今为止以葡萄糖作为糖基化酶发酵获得的GABA的最高产量。主要碳源。

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