TY - JOUR
T1 - Integrating metal organic frameworks (MOFs) and polyelectrolytes (PEs) in membrane reactors for boosting the activity of immobilized carbonic anhydrase
AU - Malankowska, Magdalena
AU - Popkov, Andrei
AU - DeMartini, Markus
AU - Jørgensen, Gustav
AU - Su, Ziran
AU - Pinelo, Manuel
PY - 2024
Y1 - 2024
N2 - Atmospheric CO2 levels are now at their highest point and the
remediation technology is being actively explored. Carbonic anhydrase
(CA) is the enzyme that can help sequester CO2 from
industrial processes. However, enzyme stability under these industrial
conditions is a big disadvantage. Herein, we propose a novel dual
reactor where we combine an Enzymatic membrane reactor (EMR) with enzyme
encapsulation in Metal-organic-framework (MOF) inside one unit − by
employing various attachment mechanisms and using polyelectrolytes in
different multilayer configurations. The polydopamine (PDA)-assisted
co-deposition approach was used for modification of pristine polysulfone
membranes. Each immobilization method was evaluated individually first,
i.e.: enzyme immobilized on a membrane, enzyme encapsulated in MOF, and
the dual reactor. In this work, immobilization of CA on a modified
membrane surface showed a 2.5-fold increase of enzyme specific activity
(558 vs 220 mU/mg), while encapsulation of CA in MOF significantly
improved its thermal stability (11 % vs 92 % of CA activity loss upon
incubation at 60 °C). Enzyme immobilized in the dual reactor
demonstrated biocatalytic activities up to 744 µU/cm2 while
retaining up to 59 % of the native membrane permeability. The results
shown in this work present the proof of concept of effective integration
of MOFs and EMRs to enhance the performance of immobilized CA. Finally,
this work shows that selected CA immobilization methods can promote
significant increases of activity, particularly at high temperatures,
and therefore immobilization cannot only be used for boosting enzyme
stability but also activity. This research can pave the way for future
exploration of different possibilities for the use of enzymes and
methods of their protection without decreasing their performance
AB - Atmospheric CO2 levels are now at their highest point and the
remediation technology is being actively explored. Carbonic anhydrase
(CA) is the enzyme that can help sequester CO2 from
industrial processes. However, enzyme stability under these industrial
conditions is a big disadvantage. Herein, we propose a novel dual
reactor where we combine an Enzymatic membrane reactor (EMR) with enzyme
encapsulation in Metal-organic-framework (MOF) inside one unit − by
employing various attachment mechanisms and using polyelectrolytes in
different multilayer configurations. The polydopamine (PDA)-assisted
co-deposition approach was used for modification of pristine polysulfone
membranes. Each immobilization method was evaluated individually first,
i.e.: enzyme immobilized on a membrane, enzyme encapsulated in MOF, and
the dual reactor. In this work, immobilization of CA on a modified
membrane surface showed a 2.5-fold increase of enzyme specific activity
(558 vs 220 mU/mg), while encapsulation of CA in MOF significantly
improved its thermal stability (11 % vs 92 % of CA activity loss upon
incubation at 60 °C). Enzyme immobilized in the dual reactor
demonstrated biocatalytic activities up to 744 µU/cm2 while
retaining up to 59 % of the native membrane permeability. The results
shown in this work present the proof of concept of effective integration
of MOFs and EMRs to enhance the performance of immobilized CA. Finally,
this work shows that selected CA immobilization methods can promote
significant increases of activity, particularly at high temperatures,
and therefore immobilization cannot only be used for boosting enzyme
stability but also activity. This research can pave the way for future
exploration of different possibilities for the use of enzymes and
methods of their protection without decreasing their performance
KW - Carbonic Anhydrase
KW - Enzymatic Membrane Reactor
KW - Enzyme immobilization
KW - Metal organic framework
U2 - 10.1016/j.cej.2024.155563
DO - 10.1016/j.cej.2024.155563
M3 - Journal article
SN - 1385-8947
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -