毕赤酵母Gpn12异戊烯基转移酶NovQ催化合成MK-3
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国家高技术研究发展计划 (863计划) (No. 2014AA021704),安徽省自然科学基金 (Nos. 1308085MA07,1608085QC46),中国科学院科技服务网络计划 (STS项目) “高值生物基化学品关键技术研发及示范 (No. KFJ-SW-STS-164)”资助。


Synthesis of vitamin K2 by isopentenyl transferase NovA in Pichia pastoris Gpn12
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National High Technology Research and Development Program of China (863 Proogram) (No. 2014AA021704), Anhui Provincial Natural Science Foundation (Nos. 1308085MA07, 1608085QC46), Research and Demonstration of Key Technology of High Value Bio-based Chemicals (STS Project) (No. KFJ-SW-STS-164).

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    摘要:

    对异戊烯基转移酶NovQ在毕赤酵母Gpn12异源表达过程中诱导剂甲醇添加量进行了探究,并以毕赤酵母Gpn12全细胞为酶源,以甲萘醌、异戊烯醇为前体,催化合成维生素K2 (MK-3)。每24 h添加2%甲醇时,NovQ表达量提高约36%。考察摇瓶中初始pH、温度、甲醇添加量、前体 (甲萘醌、异戊烯醇) 添加量、催化时间、十六烷基三甲基溴化铵 (CTAB) 添加量等7个因素对Gpn12全细胞催化合成MK-3的影响,发现催化温度、甲萘醌添加量、催化时间影响显著,对3个显著因素进行响应面优化得出催化条件为:催化温度31.56 ℃,甲萘醌添加量295.54 mg/L,催化时间15.87 h,优化后的摇瓶MK-3产量达到98.47 mg/L,与响应面预测结果一致,较优化前对照组提高了35%。在30 L发酵罐进行生物催化实验,催化时间24 h,细胞催化剂浓度220 g (干重)/L,MK-3产量达到189.67 mg/L。该方法为Gpn12规模化生产MK-3奠定了一定的基础。

    Abstract:

    The effect of methanol addition on the heterologous expression of isoprenyl transferase NovQ was studied in Pichia pastoris Gpn12, with menadione and isopentenol as precursors to catalyze vitamin K2 (MK-3) synthesis. The expression of NovQ increased by 36% when 2% methanol was added every 24 h. The influence of initial pH, temperature, methanol addition, precursors (menadione, isopentenol) addition, catalytic time and cetyltrimethyl-ammonium bromide (CTAB) addition were explored in the P. pastoris whole-cell catalytic synthesis process of MK-3 in shaking flask. Three significant factors were then studied by response surface method. The optimal catalytic conditions obtained were as follows: catalytic temperature 31.56 ℃, menadione 295.54 mg/L, catalytic time 15.87 h. Consistent with the response surface prediction results, the optimized yield of MK-3 reached 98.47 mg/L in shaking flask, 35% higher than that of the control group. On this basis, the production in a 30-L fermenter reached 189.67 mg/L when the cell catalyst of 220 g/L (dry weight) was used to catalyze the synthesis for 24 h. This method laid the foundation for the large-scale production of MK-3 by P. pastoris Gpn12.

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吴锡华,李哲敏,刘会,王鹏,王丽,方雪,孙小雯,倪文枫,杨强,郑之明,赵根海. 毕赤酵母Gpn12异戊烯基转移酶NovQ催化合成MK-3[J]. 生物工程学报, 2018, 34(1): 140-148

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  • 收稿日期:2017-04-13
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  • 在线发布日期: 2018-01-05
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