Functional Characterisation of Engineered Bacterial Biosensors for Kynurenine Detection
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Abstract
The kynurenine (KYN) pathway is the major catabolic pathway for tryptophan in humans, producing several metabolites that influence health. In clinical settings, KYN levels serve as a valuable biomarker for diagnosis and prognosis of inflammatory and neurological diseases. Nevertheless, KYN detection relies on mass spectrometry analysis, which requires specialised knowledge and expertise with high operational costs. The bacterial biosensor presents as a promising tool for rapid and cost-effective targeted substance detection due to its ease of genetic modifications. Therefore, this study aimed to develop an engineered bacterial biosensor by integrating a genetic module in a plasmid designed for KYN detection harboured in an Escherichia coli chassis. The KYN biosensing component in the genetic module encodes a KYN pathway regulator (KynR) from Pseudomonas aeruginosa, driven by the PBAD arabinose-inducible promoter. Upon expression, KynR would bind to the exogenous KYN and the bacterial responding kyn promoter to express the downstream green fluorescent protein gene to emit a fluorescence signal. However, despite successful induction by arabinose and the presence of KYN, biosensors with different gene orientation and genetic components failed to produce a significant fluorescence signal. These findings suggest that the sensitivity of P. aeruginosa KynR is insufficient to detect physiological level of KYN. Further exploration of alternative biological sensing components is warranted.
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Abstract
The kynurenine (KYN) pathway is the major catabolic pathway for tryptophan in humans, producing several metabolites that influence health. In clinical settings, KYN levels serve as a valuable biomarker for diagnosis and prognosis of inflammatory and neurological diseases. Nevertheless, KYN detection relies on mass spectrometry analysis, which requires specialised knowledge and expertise with high operational costs. The bacterial biosensor presents as a promising tool for rapid and cost-effective targeted substance detection due to its ease of genetic modifications. Therefore, this study aimed to develop an engineered bacterial biosensor by integrating a genetic module in a plasmid designed for KYN detection harboured in an Escherichia coli chassis. The KYN biosensing component in the genetic module encodes a KYN pathway regulator (KynR) from Pseudomonas aeruginosa, driven by the PBAD arabinose-inducible promoter. Upon expression, KynR would bind to the exogenous KYN and the bacterial responding kyn promoter to express the downstream green fluorescent protein gene to emit a fluorescence signal. However, despite successful induction by arabinose and the presence of KYN, biosensors with different gene orientation and genetic components failed to produce a significant fluorescence signal. These findings suggest that the sensitivity of P. aeruginosa KynR is insufficient to detect physiological level of KYN. Further exploration of alternative biological sensing components is warranted.
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Funding
-
Rosetrees Trust
(Award Seedcorn2022/100007)
- Principal Award Recipient: Chien-Yi Chang
-
NIHR Newcastle Biomedical Research Centre
(Award Infrastructural support)
- Principal Award Recipient: Chien-Yi Chang
-
Newcastle University
(Award Oversea Research Scholarship)
- Principal Award Recipient: Pisit Charoenwongwatthana
-
Mahidol University
(Award PhD studentship)
- Principal Award Recipient: Pisit Charoenwongwatthana
-
Applied Microbiology International
(Award Summer Student Placement Scholarship)
- Principal Award Recipient: Wojciech Cajdler
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- last seen: 2026-05-20T01:45:00.602351+00:00
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License: CC-BY-4.0