Directed evolution of an ultrastable carbonic anhydrase for highly efficient carbon capture from flue gas

被引:136
|
作者
Alvizo, Oscar [1 ]
Nguyen, Luan J. [2 ]
Savile, Christopher K. [1 ]
Bresson, Jamie A. [1 ]
Lakhapatri, Satish L. [3 ]
Solis, Earl O. P. [2 ]
Fox, Richard J. [4 ]
Broering, James M. [5 ]
Benoit, Michael R. [1 ]
Zimmerman, Sabrina A. [6 ]
Novick, Scott J. [1 ]
Liang, Jack [1 ]
Lalonde, James J. [1 ]
机构
[1] Codexis Inc, Redwood City, CA 94063 USA
[2] Calysta Energy Inc, Menlo Pk, CA 94025 USA
[3] Siluria Technol Inc, San Francisco, CA 94158 USA
[4] Pioneer HiBred Int Inc, Johnston, IA 50131 USA
[5] Novozymes Inc, Franklinton, NC 27525 USA
[6] BP Biofuels, San Diego, CA 92121 USA
关键词
carbonic anhydrase; directed evolution; carbon capture; SATURATION MUTAGENESIS; ABSORPTION; STABILITY; KINETICS;
D O I
10.1073/pnas.1411461111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Carbonic anhydrase (CA) is one of nature's fastest enzymes and can dramatically improve the economics of carbon capture under demanding environments such as coal-fired power plants. The use of CA to accelerate carbon capture is limited by the enzyme's sensitivity to the harsh process conditions. Using directed evolution, the properties of a beta-class CA from Desulfovibrio vulgaris were dramatically enhanced. Iterative rounds of library design, library generation, and high-throughput screening identified highly stable CA variants that tolerate temperatures of up to 107 degrees C in the presence of 4.2 M alkaline amine solvent at pH > 10.0. This increase in thermostability and alkali tolerance translates to a 4,000,000-fold improvement over the natural enzyme. At pilot scale, the evolved catalyst enhanced the rate of CO2 absorption 25-fold compared with the noncatalyzed reaction.
引用
收藏
页码:16436 / 16441
页数:6
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