Cascade enzymatic reactions for efficient carbon sequestration

被引:13
|
作者
Xia, Shunxiang [1 ,2 ]
Zhao, Xueyan [1 ,2 ]
Frigo-Vaz, Benjamin [1 ,2 ]
Zheng, Wenyun [3 ]
Kim, Jungbae [4 ]
Wang, Ping [1 ,2 ]
机构
[1] Univ Minnesota, Dept Bioprod & Biosyst Engn, St Paul, MN 55108 USA
[2] Univ Minnesota, Inst Biotechnol, St Paul, MN 55108 USA
[3] E China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China
[4] Korea Univ, Dept Chem & Biol Engn, Seoul, South Korea
关键词
Carbon capture and storage; Isocitrate dehydrogenase; Aconitase; Carbon dioxide; Biocatalysis; CO2; METHANOL; DIOXIDE; CAPTURE; CYCLE; MONOETHANOLAMINE; ENZYMES; ACID;
D O I
10.1016/j.biortech.2015.01.093
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Thermochemical processes developed for carbon capture and storage (CCS) offer high carbon capture capacities, but are generally hampered by low energy efficiency. Reversible cascade enzyme reactions are examined in this work for energy-efficient carbon sequestration. By integrating the reactions of two key enzymes of RTCA cycle, isocitrate dehydrogenase and aconitase, we demonstrate that intensified carbon capture can be realized through such cascade enzymatic reactions. Experiments show that enhanced thermodynamic driving force for carbon conversion can be attained via pH control under ambient conditions, and that the cascade reactions have the potential to capture 0.5 mol carbon at pH 6 for each mole of substrate applied. Overall it manifests that the carbon capture capacity of biocatalytic reactions, in addition to be energy efficient, can also be ultimately intensified to approach those realized with chemical absorbents such as MEA. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:368 / 372
页数:5
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