Skip to main navigation Skip to search Skip to main content

Electrochemical and biosensing properties of an FAD-dependent glucose dehydrogenase from Trichoderma virens

  • Sudarma Dita Wijayanti
  • , Franziska Schachinger
  • , Roland Ludwig
  • , Dietmar Haltrich*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

We investigated the bioelectrochemical properties of an FAD-dependent glucose dehydrogenase from Trichoderma virens (TvGDH) and its electrochemical behaviour when immobilized on a graphite electrode. TvGDH was recently shown to have an unusual substrate spectrum and to prefer maltose over glucose as substrate, and hence could be of interest as recognition element in a maltose sensor. In this study, we determined the redox potential of TvGDH, which is –0.268 ± 0.007 V vs. SHE, and advantageously low to be used with many redox mediators or redox polymers. The enzyme was entrapped in, and wired by an osmium redox polymer (poly(1-vinylimidazole-co-allylamine)-{[Os(2,2′-bipyridine)2Cl]Cl}) with formal redox potential of +0.275 V vs. Ag|AgCl via poly(ethylene glycol) diglycidyl ether crosslinking onto a graphite electrode. When the TvGDH-based biosensor was tested with maltose it showed a sensitivity of 1.7 μA mM−1cm−2, a linear range of 0.5–15 mM, and a detection limit of 0.45 mM. Furthermore, it gave the lowest apparent Michaelis-Menten constant (KM app) of 19.2 ± 1.5 mM towards maltose when compared to other sugars. The biosensor is also able to detect other saccharides including glucose, maltotriose and galactose, these however also interfere with maltose sensing.

Original languageEnglish
Article number108480
JournalBioelectrochemistry
Volume153
DOIs
Publication statusPublished - Oct 2023

Keywords

  • Amperometry
  • FAD-dependent glucose dehydrogenase
  • GMC oxidoreductases
  • Maltose biosensor
  • Osmium polymer
  • Trichoderma virens

Fingerprint

Dive into the research topics of 'Electrochemical and biosensing properties of an FAD-dependent glucose dehydrogenase from Trichoderma virens'. Together they form a unique fingerprint.

Cite this