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Regulatory transcription factor (CooA)-driven carbon monoxide partial pressure sensing whole-cell biosensor

We designed and constructed a whole-cell biosensor capable of detecting the presence and quantity of carbon monoxide (CO) using the CO regulatory transcription factor. This biosensor utilizes CooA, a CO-sensing transcription regulator that activates the expression of carbon monoxide dehydrogenase (C...

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Detalles Bibliográficos
Autores principales: Kang, Byeongchan, Lee, Hyeryeong, Oh, Soyoung, Kim, Ji-Yeon, Ko, Young-Joon, Chang, In Seop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318455/
https://www.ncbi.nlm.nih.gov/pubmed/37408883
http://dx.doi.org/10.1016/j.heliyon.2023.e17391
Descripción
Sumario:We designed and constructed a whole-cell biosensor capable of detecting the presence and quantity of carbon monoxide (CO) using the CO regulatory transcription factor. This biosensor utilizes CooA, a CO-sensing transcription regulator that activates the expression of carbon monoxide dehydrogenase (CODH), to detect the presence of CO and respond by triggering the expression of a GUS reporter protein (β-glucuronidase). The GUS reporter protein is expressed from a CO-induced CooA-binding promoter (P(cooF)) by CooA and enables the effective colorimetric detection of CO. An Escherichia coli strain used to validate the biosensor showed growth and GUS activity under anaerobic conditions; this study used the inert gas (Ar) to create anaerobic conditions. The pBRCO biosensor could successfully detect the presence of CO in the headspace. Moreover, the GUS-specific activity of pBRCO according to the CO strength as partial pressure followed Michaelis-Menten kinetics (R(2) = 0.98). It was confirmed that the GUS-specific activity of pBRCO increased linearly up to 30.39 kPa (R(2) = 0.98), and thus, a quantitative analysis of CO concentration (i.e., partial pressure) was possible.