The effect of methionine to cysteine substitution on the stability of formate dehydrogenase from Candida methylica

Because of its industrial importance, the FDH enzyme has been subjected to several protein engineering studies in order to stabilise it at high temperatures. In this study, methionine to cysteine substitution (M1C) and disulphide bridge formation between residues 1 (M1C) and 62 (D62C) were investigated in terms of their effect on the thermostability of cmFDH. Although the mutant cmFDHs, D62C and M1C/D62C, did not show the improvement expected in its stability, characterisation studies of individual mutants showed that the M1 residue is related to temperature stability. Catalytic efficiency (kcat/KM) of the M1C single mutant was 63% better than that of the native cmFDH and the Tm value of this mutant was measured as significantly higher than that of the native cmFDH by using fluorescence measurements and Circular Dichroism Spectra. Comparing to other studies related to Cys or Met substitution in the literature, 2 °C enhancement of Tm is a promising result for the industrially important FDH enzyme and to understand the relationship between thermostability and Met to Cys substitution.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Effects of Met to Cys substitution on thermostability of cmFDH was investigated. ► M1 residue of cmFDH is related to temperature stability and catalytic efficiency. ► Tm is approximately 51 °C and 57 °C for native cmFDH and M1C, respectively.