Characterization of a novel thermostable NAD+-dependent formate dehydrogenase from Methylacidiphilum kamchatkense Kam1 (MkaFDH)

dc.contributor.authorZribi, Khouloud
dc.contributor.authorCiciani, Matteo
dc.contributor.authorCarreira, Agata Sofia Assuncao
dc.contributor.authorPaganin, Martina
dc.contributor.authorPozzo, Sara
dc.contributor.authorCina, Lucio
dc.contributor.authorBinay, Baris
dc.date.accessioned2025-10-29T11:29:30Z
dc.date.issued2025
dc.departmentGebze Teknik Üniversitesi
dc.description.abstractMetal-independent NAD+-dependent formate dehydrogenases (FDHs) are enzymes responsible for catalyzing the conversion of formate (HCOO-) to carbon dioxide (CO2), a biological reaction involved in microbial carbon processing and cofactor regeneration. These enzymes show large potential for environmental bioremediation and biotechnological uses. However, FDHs applications are hampered by the enzymes' limited stability under extreme conditions, such as high temperatures or extreme pH. Therefore, we aimed to identify and characterize novel metal-independent FDHs with improved activity and thermostability compared to known FDHs. By using four different FDH protein sequences, CtFDH (from Chaetomium thermophilum), MtFDH (from Myceliophthora thermophile), OpFDH (from Ogata parapolymorpha DL-1) and PseFDH (from Pseudomonas sp.101) we retrieved 18,850 FDHs sequences from the NCBI database and matched against the species present in the database of thermophilic bacteria, ThermoBase. Our phylogenetic analysis identified four distinct FDHs in thermophilic bacteria: Methylocaldum szegediense (MszFDH), Methylacidiphilum kamchatkense (MkaFDH), Mycobacterium arosiense (MarFDH) and Mycobacterium genavense (MgeFDH). We selected and characterized the MkaFDH as it was expressed in the thermophilic bacterium with the highest optimum growth (55 degrees C) among the four bacteria. The MkaFDH was cloned, and the recombinant protein was expressed in E. coli and purified. The conditions for the optimal catalytic activity for formate oxidations were screened and identified, revealing metal-independent, NAD+-restricted activity in phosphate buffer, pH 8. Importantly, the enzyme showed remarkable thermal stability and catalytic activity, showing a melting temperature (Tm) of 60.15 degrees C, as confirmed by far-UV circular dichroism (CD). Finally, the enzyme showed good thermostability for formate oxidation up to 57.5 degrees C, and its high catalytic efficiency (kcat/Km = 0.44 s- 1mM- 1) suggested its potential industrial application. Collectively, we describe here a novel FDH with relevant thermostability that can be exploited as a prototype for industrial applications.
dc.description.sponsorshipUE program PON REACT-EU
dc.description.sponsorshipEuropean Union - NextGeneration EU from the Italian Ministry of Environment and Energy Security POR H2 AdP MMES/ENEA [CUP: B93C22000630006]
dc.description.sponsorshipEuropean Research Council (ERC) [101045015]
dc.description.sponsorshipMUR
dc.description.sponsorshipEuropean Research Council (ERC) [101045015] Funding Source: European Research Council (ERC)
dc.description.sponsorshipThis research was funded by the UE program PON REACT-EU to KZ and by the European Union - NextGeneration EU from the Italian Ministry of Environment and Energy Security POR H2 AdP MMES/ENEA with the involvement of CNR and RSE, PNRR-Mission 2, Component 2, Investment 3.5 Ricerca e sviluppo sull'idrogeno, CUP: B93C22000630006 to FS, and by the European Research Council (ERC-CoG microTOUCH-101045015) to NS. This work has been supported by the initiative Dipartimenti di Eccellenza 2023-2027 (Legge 232/2016) funded by the MUR.
dc.identifier.doi10.1016/j.crbiot.2025.100306
dc.identifier.issn2590-2628
dc.identifier.scopus2-s2.0-105008808488
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1016/j.crbiot.2025.100306
dc.identifier.urihttps://hdl.handle.net/20.500.14854/11133
dc.identifier.volume10
dc.identifier.wosWOS:001519906300001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofCurrent Research in Biotechnology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20251020
dc.subjectFormate dehydrogenase (FDH)
dc.subjectFormate oxidation
dc.subjectFDH thermostability
dc.subjectFDH melting point
dc.subjectFDH phylogenetic tree
dc.titleCharacterization of a novel thermostable NAD+-dependent formate dehydrogenase from Methylacidiphilum kamchatkense Kam1 (MkaFDH)
dc.typeArticle

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