格式化
辅因子
催化作用
化学
甲醇
光催化
酶
营业额
膜
甲酸脱氢酶
酶催化
组合化学
固定化酶
有机化学
生物化学
作者
Fengjuan Gu,Yan-zi Wang,Zihui Meng,WenFang Liu,Liyuan Qiu
标识
DOI:10.1016/j.catcom.2019.105903
摘要
Enzymatic conversion of CO2 into high-added chemicals is advantageous in mild reaction conditions and high specificity, for which enzyme immobilization and cofactor regeneration are often necessary. Although many efforts have been made, unfortunately, the turnover number (TN) of cofactor does not exceed 100 (~1 usually). Here, an integrated process of formate synthesis from CO2 catalyzed by hollow fiber membrane immobilized enzyme succeeded with a simple UV/TiO2 photocatalytic coenzyme regeneration was explored. By optimizing the operating conditions and NADH concentration, TN reached 125 after 4.5 h. This process can be extended to the production of methanol and other similar systems.
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