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High expression and biosilica encapsulation of alkaline-active carbonic anhydrase for CO2 sequestration system development

•High pH stable HCA(SP-) was successfully produced in soluble form.•HCA(SP-) can retain ∼90% activity even after 2h-incubation at pH 10.•HCA(SP-)@silica can retain over 80% CO2 hydration activity after 10-time reuse at pH 10. Carbonic anhydrase (CA) is a biocatalyst for CO2 sequestration because of...

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Bibliographic Details
Published in:Chemosphere (Oxford) 2016-01, Vol.143, p.128-134
Main Authors: Min, Ki-Ha, Son, Ryeo Gang, Ki, Mi-Ran, Choi, Yoo Seong, Pack, Seung Pil
Format: Article
Language:English
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Summary:•High pH stable HCA(SP-) was successfully produced in soluble form.•HCA(SP-) can retain ∼90% activity even after 2h-incubation at pH 10.•HCA(SP-)@silica can retain over 80% CO2 hydration activity after 10-time reuse at pH 10. Carbonic anhydrase (CA) is a biocatalyst for CO2 sequestration because of its distinctive ability to accelerate CO2 hydration. High production and efficient immobilization of alkaline-active CAs are required, because one potential application of CA is its use in the alkaline solvent-based CO2 absorption/desorption process. Here, we designed and applied an α-type CA from Hahella chejuensis (HCA), which was reported as highly active in alkaline conditions, but was mostly expressed as insoluble forms. We found that the signal peptide-removed form of HCA [HCA(SP-)] was successfully expressed in the soluble form [∼70mg of purified HCA(SP-) per L of culture]. HCA(SP-) also displayed high pH stability in alkaline conditions, with maximal activity at pH 10; at this pH, ∼90% activity was maintained for 2h. Then, we prepared HCA(SP-)-encapsulated silica particles [HCA(SP-)@silica] via a spermine-mediated bio-inspired silicification method. HCA(SP-)@silica exhibited high-loading and highly stable CA activity. In addition, HCA(SP-)@silica retained more than 90% of the CA activity even after 10 cycles of use in mild conditions, and ∼80% in pH 10 conditions. These results will be useful for the development of practical CO2 sequestration processes employing CA.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2015.07.020