An enzyme-loaded reactor using metal-organic framework-templated polydopamine microcapsule  被引量:5

在线阅读下载全文

作  者:Jing Wang Yongqin Lv 

机构地区:[1]Beijing Key Laboratory of Bioprocess,College of Life Science and Technology,Beijing University of Chemical Technology,Beijing 100029,China

出  处:《Chinese Journal of Chemical Engineering》2021年第1期317-325,共9页中国化学工程学报(英文版)

基  金:supported by the National Natural Science Foundation of China (31961133004, 21861132017);the National Key Research and Development Program of China (2018YFA0902200);the Fundamental Research Funds for the Central Universities (PT1917, buctrc201)。

摘  要:Ultrathin polydopamine microcapsules with hierarchical structure and porosity were prepared for the immobilization of multienzymes using metal-organic framework(MOF) as the template.The multienzyme/MOF composite was first prepared using a "one-pot" co-precipitation approach via the coordination and self-assembly of zinc ions and 2-methylimidazole in the presence of enzymes.The obtained nanoparticles were then coated with polydopamine thin layer through the self-polymerization of dopamine under alkaline condition.The polydopamine microcapsules with an ultrathin shell thickness of ~48 nm were finally generated by removing the MOF template at acidic condition.Three enzymes were encapsulated in PDA microcapsules including carbonic anhydrase(CA),formate dehydrogenase(FateDH),and glutamate dehydrogenase(GDH).FateDH that catalyzed the main reaction of CO_(2) reduction to formic acid retained 94.7% activity of equivalent free FateDH.Compared with free multienzymes,the immobilized ones embedded in PDA microcapsules exhibited 4.5-times higher of formate production and high catalytic efficiency with a co-factor-based formate yield of 342%.

关 键 词:BIOCATALYSIS ENZYME IMMOBILIZATION MICROCAPSULE Metal-organic framework Template 

分 类 号:TQ426.97[化学工程]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象