4.6 Article

Functional Expression of a Mo-Cu-Dependent Carbon Monoxide Dehydrogenase (CODH) and Its Use as a Dissolved CO Bio-microsensor

Journal

ACS SENSORS
Volume 6, Issue 7, Pages 2772-2782

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.1c01243

Keywords

Mo-Cu carbon monoxide dehydrogenase (Mo-Cu CODH); CO oxidation; Clark-type sensor; CO bio-microsensor; CO2 microsensor

Funding

  1. National Research Foundation of Korea (NRF) - Korean Government [2020R1A2C3009210]
  2. C1 Gas Refinery Program through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2021M3D3A1A01079730]
  3. BK21 Plus
  4. Grundfos Foundation
  5. National Research Foundation of Korea [2020R1A2C3009210] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study reports the successful heterologous expression of a Mo-Cu-containing carbon monoxide dehydrogenase (Mo-Cu CODH) from Hydrogenophaga pseudoflava in Escherichia coli, with the L-subunit showing CO oxidation activity. The expressed protein was used to construct a CO biomicrosensor with a linear response to CO concentration and high sensitivity and performance. This CO biomicrosensor has potential as an analytical tool for monitoring dissolved CO concentration dynamics in natural or synthetic systems.
Herein, we report the heterologous expression in Escherichia coli of a Mo-Cu-containing carbon monoxide dehydrogenase (Mo-Cu CODH) from Hydrogenophaga pseudoflava, which resulted in an active protein catalyzing CO oxidation to CO2. By supplying the E. coli growth medium with Na2MoO4 (Mo) and CuSO4 (Cu), the Mo-Cu CODH metal cofactors precursors, the expressed L-subunit was found to have CO-oxidation activity even without the M- and S- subunits. This successful expression of CO-oxidizing-capable single L-subunit provides direct evidence of its role as the catalytic center of Mo-Cu CODH that has not been discovered and studied before. Subsequently, we used the expressed protein to construct a CO bio-microsensor based on a newly developed fast and sensitive Clark-type CO2 transducer using an aprotic solvent/ionic liquid electrolyte. The CO biomicrosensor exhibited a linear response to CO concentration in the 0-9 mu M range, with a limit of detection (LOD) of 15 nM CO. The sensor uses a mixture of Mo-Cu CODH's L-subunit/Mo, Cu cofactors/methylene blue, confined in the enzyme chamber that is placed in front of a CO2 transducer. The optimized sensor's sensitivity and performance were retained to levels of at least 80% for 1 week of continuous polarization and operation in an aqueous medium. We have also demonstrated the use of an alkaline front-trap solution to make a completely O-2/CO2 interference-free microsensor. The CO bio-microsensor developed in this study is potentially useful as an analytical tool for the detection of trace CO in dissolved form for monitoring dissolved CO concentration dynamics in natural or synthetic systems.

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