A recombinase-based genetic circuit for heavy metal monitoring
buir.contributor.author | Akboğa, Doğuş | |
buir.contributor.author | Saltepe, Behide | |
buir.contributor.orcid | Saltepe, Behide|0000-0002-4338-6463 | |
buir.contributor.orcid | Akboğa, Doğuş|0000-0002-0426-6135 | |
dc.citation.epage | 10 | en_US |
dc.citation.issueNumber | 2 | en_US |
dc.citation.spage | 1 | en_US |
dc.citation.volumeNumber | 12 | en_US |
dc.contributor.author | Akboğa, Doğuş | |
dc.contributor.author | Saltepe, Behide | |
dc.date.accessioned | 2023-03-02T11:44:33Z | |
dc.date.available | 2023-03-02T11:44:33Z | |
dc.date.issued | 2022-02-16 | |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.description.abstract | Rapid progress in the genetic circuit design enabled whole-cell biosensors (WCBs) to become prominent in detecting an extensive range of analytes with promise in many fields, from medical diagnostics to environmental toxicity assessment. However, several drawbacks, such as high background signal or low precision, limit WCBs to transfer from proof-of-concept studies to real-world applications, particularly for heavy metal toxicity monitoring. For an alternative WCB module design, we utilized Bxb1 recombinase that provides tight control as a switch to increase dose-response behavior concerning leakiness. The modularity of Bxb1 recombinase recognition elements allowed us to combine an engineered semi-specific heat shock response (HSR) promoter, sensitive to stress conditions including toxic ions such as cadmium, with cadmium resistance regulatory elements; a cadmium-responsive transcription factor and its cognitive promoter. We optimized the conditions for the recombinase-based cadmium biosensor to obtain increased fold change and shorter response time. This system can be expanded for various heavy metals to make an all-in-one type of WCB, even using semi-specific parts of a sensing system. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. | en_US |
dc.description.provenance | Submitted by Cem Çağatay Akgün (cem.akgun@bilkent.edu.tr) on 2023-03-02T11:44:33Z No. of bitstreams: 1 A_Recombinase-Based_Genetic_Circuit_for_Heavy_Metal_Monitoring.pdf: 1747697 bytes, checksum: d48446613b12ed82ed78c8da40f52b7f (MD5) | en |
dc.description.provenance | Made available in DSpace on 2023-03-02T11:44:33Z (GMT). No. of bitstreams: 1 A_Recombinase-Based_Genetic_Circuit_for_Heavy_Metal_Monitoring.pdf: 1747697 bytes, checksum: d48446613b12ed82ed78c8da40f52b7f (MD5) Previous issue date: 2022-02-16 | en |
dc.identifier.doi | 10.3390/bios12020122 | en_US |
dc.identifier.issn | 20796374 | |
dc.identifier.uri | http://hdl.handle.net/11693/112020 | |
dc.language.iso | English | en_US |
dc.publisher | MDPI | en_US |
dc.relation.isversionof | https://dx.doi.org/10.3390/bios12020122 | en_US |
dc.source.title | Biosensors | en_US |
dc.subject | Bxb1 recombinase | en_US |
dc.subject | Heavy metal detection | en_US |
dc.subject | Synthetic biology | en_US |
dc.subject | Toxicity | en_US |
dc.subject | Whole-cell biosensor | en_US |
dc.title | A recombinase-based genetic circuit for heavy metal monitoring | en_US |
dc.type | Article | en_US |
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