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More Than One Enzyme: Exploring Alternative FMN-Dependent L-Lactate Oxidases for Biosensor Development.
Tsvik, Lidiia; Zhang, Shulin; O'Hare, Danny; Haltrich, Dietmar; Sützl, Leander.
Afiliación
  • Tsvik L; Laboratory of Food Biotechnology, Department of Food Science and Technology, University of Natural Resources and Life Sciences, Muthgasse 11, Wien, Vienna A-1190, Austria.
  • Zhang S; Doctoral Programme 'Biomolecular Technology of Proteins (BioToP)', University of Natural Resources and Life Sciences, Muthgasse 18, Wien, Vienna A-1190, Austria.
  • O'Hare D; Department of Bioengineering, Imperial College London, London SW72AZ, U.K.
  • Haltrich D; Department of Bioengineering, Imperial College London, London SW72AZ, U.K.
  • Sützl L; Laboratory of Food Biotechnology, Department of Food Science and Technology, University of Natural Resources and Life Sciences, Muthgasse 11, Wien, Vienna A-1190, Austria.
ACS Omega ; 9(27): 29442-29452, 2024 Jul 09.
Article en En | MEDLINE | ID: mdl-39005781
ABSTRACT
The α-hydroxy acid oxidoreductase (HAOx) family contains a diverse group of enzymes that can be applied in biosensors for L-lactate detection, most prominently lactate oxidase (LOx). The limited availability and a lack of diversity of L-lactate-oxidizing enzymes have currently hindered advancements in L-lactate biosensor development. Until now, the field has mostly relied on a single, commercially available enzyme, namely Aerococcus viridans L-lactate oxidase (AvLOx). In this study, we present newly discovered alternative L-lactate oxidases that exhibit a narrow substrate specificity and varied kinetic efficiencies toward L-lactate, making them suitable for integration into existing biosensor configurations. Some of these FMN-dependent L-lactate oxidases could be obtained in substantial amounts from routine E. coli expression, potentially facilitating commercial production. Using electrochemical characterization with a mediated biosensor setup, we present 7 enzymes that perform comparable or even better than commercial AvLOx. Finally, we show that their electrochemical performance is not directly correlating with their biochemical performance, making predictions of the suitability of enzymes for biosensor applications extremely difficult. Our research emphasizes the significance of expanding the enzyme toolbox of L-lactate oxidases for the development of improved L-lactate biosensors.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2024 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2024 Tipo del documento: Article País de afiliación: Austria