Merle Geraldine, Fradette Sylvie, Madore Eric, Barralet Jake E
Faculty of Dentistry, and §Division of Orthopedics, Department of Surgery, Faculty of Medicine, McGill University , Montreal, Quebec H3A 0C7, Canada.
Langmuir. 2014 Jun 17;30(23):6915-9. doi: 10.1021/la501333s. Epub 2014 Jun 5.
Biomimetic carbonation carried out with carbonic anhydrase (CA) in CO2-absorbing solutions, such as methyldiethanolamine (MDEA), is one approach that has been developed to accelerate the capture of CO2. However, there are several practical issues, such as high cost and limited enzyme stability, that need to be overcome. In this study, the capacity of CA immobilization on a porous solid support was studied to improve the instability in the tertiary amine solvent. We have shown that a 63% porosity macroporous carbon foam support makes separation and reuse facile and allows for an efficient supply and presentation of CO2 to an aqueous solvent and the enzyme catalytic center. These enzymatic supports conserved 40% of their initial activity after 42 days at 70 °C in an amine solvent, whereas the free enzyme shows no activity after 1 h in the same conditions. In this work, we have overcome the technical barrier associated with the recovery of the biocatalyst after operation, and most of all, these electropolymerized enzymatic supports have shown a remarkable increase of thermal stability in an amine-based CO2 sequestration solvent.
在诸如甲基二乙醇胺(MDEA)等二氧化碳吸收溶液中利用碳酸酐酶(CA)进行仿生碳酸化反应,是一种已被开发用于加速二氧化碳捕集的方法。然而,存在一些实际问题,如成本高和酶稳定性有限,这些问题需要克服。在本研究中,研究了碳酸酐酶在多孔固体载体上的固定化能力,以改善其在叔胺溶剂中的不稳定性。我们已经表明,孔隙率为63%的大孔碳泡沫载体使分离和再利用变得容易,并能有效地将二氧化碳供应并呈现给水性溶剂和酶催化中心。这些酶促载体在70℃的胺溶剂中42天后仍保留其初始活性的40%,而游离酶在相同条件下1小时后就没有活性了。在这项工作中,我们克服了与操作后生物催化剂回收相关的技术障碍,最重要的是,这些电聚合酶促载体在基于胺的二氧化碳封存溶剂中显示出热稳定性的显著提高。