Salvador Fabela, Camilo P Martínez-Reyes, Rene Arredondo-Hernandez, Gonzalo Castillo-Rojas, Patricia Orduña, Enrique O Graue-Hernández, Yolanda López-Vidal
{"title":"Bacterial Fluorescence-Based Biosensor for Detecting Propionate in Culture Media for Diagnostic Applications.","authors":"Salvador Fabela, Camilo P Martínez-Reyes, Rene Arredondo-Hernandez, Gonzalo Castillo-Rojas, Patricia Orduña, Enrique O Graue-Hernández, Yolanda López-Vidal","doi":"10.1177/11772719261455896","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Engineering bacteria for disease diagnosis and treatment is an emerging area of medical research that involves assessing short-lived molecules in complex, dynamic environments. Detecting metabolites <i>in situ</i> offers significant opportunities for identifying responsive cellular populations. Among suitable targets for this technology are short-chain fatty acids, such as propionate, that play crucial roles in human health and disease.</p><p><strong>Objective: </strong>To develop a bacterial fluorescence-based biosensor capable of detecting propionate levels at the millimolar scale in low-volume samples across different culture media and optimize its application protocol.</p><p><strong>Methods: </strong>Using <i>Escherichia coli</i> strain BL21(DE3) transformed with the pPro24-GFP plasmid, which contains the green fluorescent protein (<i>GFP</i>) gene under the control of a propionate-inducible promoter, we achieved reliable propionate detection with a threshold of 10 mM in a small volume (750 μL).</p><p><strong>Results: </strong>The fluorescence-based biosensor functioned in both Luria-Bertani and Dulbecco's modified Eagle media, producing fluorescence intensities of 3863 ± 957 arbitrary units. Validation using a portable Qubit<sup>®</sup> 3.0 fluorometer yielded a receiver operating characteristic curve with a Cohen's kappa of 0.716, indicating substantial agreement. Proof-of-concept experiments using flow cytometry and mock fecal samples (healthy feces + 100 mM propionate) successfully detected the elevated propionate levels.</p><p><strong>Conclusion: </strong>This cost-effective, easy-to-use protocol provides a proof-of-concept for propionate detection in biological samples, with potential future applications in clinical diagnostics, particularly for gastrointestinal disorders in which propionate serves as a biomarker, where it could be used to monitor disease progression and therapeutic interventions.</p>","PeriodicalId":47060,"journal":{"name":"Biomarker Insights","volume":"21 ","pages":"11772719261455896"},"PeriodicalIF":1.9000,"publicationDate":"2026-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13213109/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomarker Insights","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/11772719261455896","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Engineering bacteria for disease diagnosis and treatment is an emerging area of medical research that involves assessing short-lived molecules in complex, dynamic environments. Detecting metabolites in situ offers significant opportunities for identifying responsive cellular populations. Among suitable targets for this technology are short-chain fatty acids, such as propionate, that play crucial roles in human health and disease.
Objective: To develop a bacterial fluorescence-based biosensor capable of detecting propionate levels at the millimolar scale in low-volume samples across different culture media and optimize its application protocol.
Methods: Using Escherichia coli strain BL21(DE3) transformed with the pPro24-GFP plasmid, which contains the green fluorescent protein (GFP) gene under the control of a propionate-inducible promoter, we achieved reliable propionate detection with a threshold of 10 mM in a small volume (750 μL).
Results: The fluorescence-based biosensor functioned in both Luria-Bertani and Dulbecco's modified Eagle media, producing fluorescence intensities of 3863 ± 957 arbitrary units. Validation using a portable Qubit® 3.0 fluorometer yielded a receiver operating characteristic curve with a Cohen's kappa of 0.716, indicating substantial agreement. Proof-of-concept experiments using flow cytometry and mock fecal samples (healthy feces + 100 mM propionate) successfully detected the elevated propionate levels.
Conclusion: This cost-effective, easy-to-use protocol provides a proof-of-concept for propionate detection in biological samples, with potential future applications in clinical diagnostics, particularly for gastrointestinal disorders in which propionate serves as a biomarker, where it could be used to monitor disease progression and therapeutic interventions.