Ancestral carbonic anhydrase with significantly enhanced stability and activity for CO2 capture and utilization

被引:1
|
作者
Yang, Chun [1 ]
Mao, Lei [1 ]
Chen, Yaxin [1 ]
Zhou, Yanhong [1 ]
Zhang, Ruifang [1 ]
Yi, Zhiwei [2 ]
Zhang, Dechao [3 ]
Zhang, Guangya [1 ]
机构
[1] Huaqiao Univ, Dept Bioengn & Biotechnol, Xiamen 361021, Fujian, Peoples R China
[2] Minist Nat Resources, Inst Oceanog 3, Technol Innovat Ctr Exploitat Marine Biol Resource, Xiamen 361005, Fujian, Peoples R China
[3] Guangzhou Lintop Informat Technol Co Ltd, Guangzhou 510000, Guangdong, Peoples R China
关键词
Enzyme engineering; Ancestral sequence reconstruction; Thermoactive enzyme; Enzymatic CO2 conversion; DIOXIDE;
D O I
10.1016/j.biortech.2025.132054
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Carbonic anhydrases (CAs) has garnered increasing attention in carbon capture, utilization and storage (CCUS) due to their ecological friendliness. However, most of them suffer susceptibility to deactivation in harsh conditions. Herein, a reliable dataset was adopted for creating ancestral CAs through an optimized ancestral sequence reconstruction (ASR) method. After prescreening, the ancestor AncCA19 was obtained and successfully expressed. The hydration activity of AncCA19 was as high as 58,859 WAU/mg, with the optimum temperature and pH obtained by esterase assay at 100 degrees C and 9, respectively. AncCA19 had the longest half-life (1.7 h) at 95 degrees C compared with existing CAs. After 2 weeks' incubation in artificial seawater at 30 degrees C or 25.0 % N-methyldiethanolamine (MDEA) at 60 degrees C, the activities remained above 47,370 WAU/mg and 6,596 WAU/mg, respectively. Thus, AncCA19, as a novel benchmark of CAs, exhibits exceptional stability in a variety CCUS applications, establishing a versatile candidate for effective CO2 capture.
引用
收藏
页数:10
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