Immobilization of carbonic anhydrase for facilitated CO2 capture and separation

doi:10.1016/j.cjche.2020.06.002

Abstract

Abstract: Carbonic anhydrase (CA) as a typical metalloenzyme in biological system can accelerate the hydration/dehydration of carbon dioxide (CO₂, the major components of greenhouse gases), which performer with high selectivity, environmental friendliness and superior efficiency. However, the free form of CA is quite expensive (~RMB 3000/100 mg), unstable, and non-reusable as the free form of CA is not easy for recovery from the reaction environment, which severely limits its large-scale industrial applications. The immobilization may solve these problems at the same time. In this context, many efforts have been devoted to improving the chemical and thermal stabilities of CA through immobilization strategy. Very recently, a wide range of available inorganic, organic and hybrid compounds have been explored as carrier materials for CA immobilization, which could not only improve the tolerance of CA in hazardous environments, but also improve the efficiency and recovery to reduce the cost of large-scale application of CA. Several excellent reviews about immobilization methods and application potential of CA have been published. By contrast, in our review, we stressed on the way to better retain the biocatalytic activity of immobilized CA system based on different carrier materials and to solve the problems facing in practical operations well. The concluding remarks are presented with a perspective on constructing efficient CO₂ conversion systems through rational combining CA and advanced carrier materials.

Key words: Carbon dioxide, Carbonic anhydrase, Enzyme immobilization, Capture and separation, Carrier materials

摘要： Carbonic anhydrase (CA) as a typical metalloenzyme in biological system can accelerate the hydration/dehydration of carbon dioxide (CO₂, the major components of greenhouse gases), which performer with high selectivity, environmental friendliness and superior efficiency. However, the free form of CA is quite expensive (~RMB 3000/100 mg), unstable, and non-reusable as the free form of CA is not easy for recovery from the reaction environment, which severely limits its large-scale industrial applications. The immobilization may solve these problems at the same time. In this context, many efforts have been devoted to improving the chemical and thermal stabilities of CA through immobilization strategy. Very recently, a wide range of available inorganic, organic and hybrid compounds have been explored as carrier materials for CA immobilization, which could not only improve the tolerance of CA in hazardous environments, but also improve the efficiency and recovery to reduce the cost of large-scale application of CA. Several excellent reviews about immobilization methods and application potential of CA have been published. By contrast, in our review, we stressed on the way to better retain the biocatalytic activity of immobilized CA system based on different carrier materials and to solve the problems facing in practical operations well. The concluding remarks are presented with a perspective on constructing efficient CO₂ conversion systems through rational combining CA and advanced carrier materials.

关键词: Carbon dioxide, Carbonic anhydrase, Enzyme immobilization, Capture and separation, Carrier materials

Zhenhua Wu, Yan Nan, Yang Zhao, Xueying Wang, Shouying Huang, Jiafu Shi. Immobilization of carbonic anhydrase for facilitated CO₂ capture and separation[J]. Chinese Journal of Chemical Engineering, 2020, 28(11): 2817-2831.

Zhenhua Wu, Yan Nan, Yang Zhao, Xueying Wang, Shouying Huang, Jiafu Shi. Immobilization of carbonic anhydrase for facilitated CO₂ capture and separation[J]. 中国化学工程学报, 2020, 28(11): 2817-2831.

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Immobilization of carbonic anhydrase for facilitated CO₂ capture and separation

Immobilization of carbonic anhydrase for facilitated CO₂ capture and separation

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[1]	Chaojie Li, Xianxin Fang, Meiling Sun, Jihai Duan, Weiwen Wang. Study on two-phase cloud dispersion from liquefied CO₂ release [J]. Chinese Journal of Chemical Engineering, 2023, 60(8): 37-45.
[2]	Xun Tao, Fan Zhou, Xinlei Yu, Songling Guo, Yunfei Gao, Lu Ding, Guangsuo Yu, Zhenghua Dai, Fuchen Wang. Effect of carbon dioxide on oxy-fuel combustion of hydrogen sulfide: An experimental and kinetic modeling [J]. Chinese Journal of Chemical Engineering, 2023, 59(7): 105-117.
[3]	Xiaohong Zhou, Wenfeng Zhou, Wei Zhuang, Chenjie Zhu, Hanjie Ying, Hongman Zhang. Enhanced production of cytidine 5'-monophosphate using biocatalysis of di-enzymes immobilized on amino-functionalized sepharose [J]. Chinese Journal of Chemical Engineering, 2023, 58(6): 40-52.
[4]	Tatyana P. Adamova, Sergey S. Skiba, Andrey Yu. Manakov, Sergey Y. Misyura. Growth rate of CO₂ hydrate film on water–oil and water–gaseous CO₂ interface [J]. Chinese Journal of Chemical Engineering, 2023, 56(4): 266-272.
[5]	Bowen Jiang, Jia Liu, Guoqiang Yang, Zhibing Zhang. Efficient conversion of CO₂ into cyclic carbonates under atmospheric by halogen and metal-free poly(ionic liquid)s [J]. Chinese Journal of Chemical Engineering, 2023, 55(3): 202-211.
[6]	Mingdong Sun, Dongxin Pan, Tingting Ye, Jing Gu, Yu Zhou, Jun Wang. Ionic porous polyamide derived N-doped carbon towards highly selective electroreduction of CO₂ [J]. Chinese Journal of Chemical Engineering, 2023, 55(3): 212-221.
[7]	Mengge Shang, Jing Zhang, Jinqiang Sun, Shimo Yu, Feng Hua, Xiaoxu Xuan, Xun Sun, Serguei Filatov, Xibin Yi. Amine-functionalized mesoporous UiO-66 aerogel for CO₂ adsorption [J]. Chinese Journal of Chemical Engineering, 2023, 54(2): 36-43.
[8]	Xianglin Liu, Minjie Xu, Chenxi Cao, Zixu Yang, Jing Xu. Effects of zinc on χ-Fe₅C₂ for carbon dioxide hydrogenation to olefins: Insights from experimental and density function theory calculations [J]. Chinese Journal of Chemical Engineering, 2023, 54(2): 206-214.
[9]	Zhongyao Zhang, Ming Gao, Xiaopeng Chen, Xiaojie Wei, Jiezhen Liang, Chenghong Wu, Linlin Wang. The Joule–Thomson effect of (CO₂ + H₂) binary system relevant to gas switching reforming with carbon capture and storage (CCS) [J]. Chinese Journal of Chemical Engineering, 2023, 54(2): 215-231.
[10]	Vladimir S. Derevschikov, Janna V. Veselovskaya, Anton S. Shalygin, Dmitry A. Yatsenko, Andrey Z. Sheshkovas, Oleg N. Martyanov. Operating limits and features of direct air capture on K₂CO₃/ZrO₂ composite sorbent [J]. Chinese Journal of Chemical Engineering, 2022, 46(6): 11-20.
[11]	Jipeng Dong, Fei Wang, Guanghui Chen, Shougui Wang, Cailin Ji, Fei Gao. Fabrication of nickel oxide functionalized zeolite USY composite as a promising adsorbent for CO₂ capture [J]. Chinese Journal of Chemical Engineering, 2022, 46(6): 207-213.
[12]	Youwei Yang, Jingyu Zhang, Yueqi Gao, Busha Assaba Fayisa, Antai Li, Shouying Huang, Jing Lv, Yue Wang, Xinbin Ma. Highly dispersed nickel boosts catalysis by Cu/SiO₂ in the hydrogenation of CO₂-derived ethylene carbonate to methanol and ethylene glycol [J]. Chinese Journal of Chemical Engineering, 2022, 43(3): 77-85.
[13]	Zhen Lu, Jie He, Bogeng Guo, Yulai Zhao, Jingyu Cai, Longqiang Xiao, Linxi Hou. Efficient homogenous catalysis of CO₂ to generate cyclic carbonates by heterogenous and recyclable polypyrazoles [J]. Chinese Journal of Chemical Engineering, 2022, 43(3): 110-115.
[14]	Xin Li, Song Hong, Leiduan Hao, Zhenyu Sun. Cadmium-based metal-organic frameworks for high-performance electrochemical CO₂ reduction to CO over wide potential range [J]. Chinese Journal of Chemical Engineering, 2022, 43(3): 143-151.
[15]	Yichao Wu, Zhiwei Xie, Xiaofeng Gao, Xian Zhou, Yangzhi Xu, Shurui Fan, Siyu Yao, Xiaonian Li, Lili Lin. The highly selective catalytic hydrogenation of CO₂ to CO over transition metal nitrides [J]. Chinese Journal of Chemical Engineering, 2022, 43(3): 248-254.