An easy method for quantification of anaerobic and microaerobic gene expression with fluorescent reporter proteins

Author:

Pedraz Lucas12ORCID,Torrents Eduard13ORCID

Affiliation:

1. Bacterial Infections & Antimicrobial Therapies Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science & Technology (BIST), Baldiri Reixac 15–21, 08028 Barcelona, Spain

2. Present address: Department of Microbiology & Immunology, University of British Columbia (UBC), Lower Mall Research Station, Vancouver, BC, V6T 1Z4, Canada

3. Microbiology Section, Department of Genetics, Microbiology & Statistics, University of Barcelona, 643 Diagonal Avenue, 08028, Barcelona, Spain

Abstract

Fluorescent proteins, such as green fluorescent proteins, are invaluable tools for detecting and quantifying gene expression in high-throughput reporter gene assays. However, they introduce significant inaccuracies in studies involving microaerobiosis or anaerobiosis, as oxygen is required for the maturation of these proteins' chromophores. In this study, the authors highlight the errors incurred by using fluorescent proteins under limited oxygenation by comparing standard fluorescence-based reporter gene assays to quantitative real-time PCR data in the study of a complex oxygen-regulated gene network. Furthermore, a solution to perform quantification of anaerobic and microaerobic gene expression with fluorescent reporter proteins using a microplate reader with an oxygen control system and applying pulses of full oxygenation before fluorescence measurements is provided.

Funder

Departament d'Innovació, Universitats i Empresa, Generalitat de Catalunya

‘la Caixa’ Foundation

Ministerio de Ciencia e Innovación

Publisher

Future Science Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Biotechnology

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