Characterization of a novel thermostable NAD+-dependent formate dehydrogenase from Methylacidiphilum kamchatkense Kam1 (MkaFDH)
| dc.contributor.author | Zribi, Khouloud | |
| dc.contributor.author | Ciciani, Matteo | |
| dc.contributor.author | Carreira, Agata Sofia Assuncao | |
| dc.contributor.author | Paganin, Martina | |
| dc.contributor.author | Pozzo, Sara | |
| dc.contributor.author | Cina, Lucio | |
| dc.contributor.author | Binay, Baris | |
| dc.date.accessioned | 2025-10-29T11:29:30Z | |
| dc.date.issued | 2025 | |
| dc.department | Gebze Teknik Üniversitesi | |
| dc.description.abstract | Metal-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.sponsorship | UE program PON REACT-EU | |
| dc.description.sponsorship | European Union - NextGeneration EU from the Italian Ministry of Environment and Energy Security POR H2 AdP MMES/ENEA [CUP: B93C22000630006] | |
| dc.description.sponsorship | European Research Council (ERC) [101045015] | |
| dc.description.sponsorship | MUR | |
| dc.description.sponsorship | European Research Council (ERC) [101045015] Funding Source: European Research Council (ERC) | |
| dc.description.sponsorship | This 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.doi | 10.1016/j.crbiot.2025.100306 | |
| dc.identifier.issn | 2590-2628 | |
| dc.identifier.scopus | 2-s2.0-105008808488 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.uri | https://doi.org/10.1016/j.crbiot.2025.100306 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14854/11133 | |
| dc.identifier.volume | 10 | |
| dc.identifier.wos | WOS:001519906300001 | |
| dc.identifier.wosquality | N/A | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.relation.ispartof | Current Research in Biotechnology | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WOS_20251020 | |
| dc.subject | Formate dehydrogenase (FDH) | |
| dc.subject | Formate oxidation | |
| dc.subject | FDH thermostability | |
| dc.subject | FDH melting point | |
| dc.subject | FDH phylogenetic tree | |
| dc.title | Characterization of a novel thermostable NAD+-dependent formate dehydrogenase from Methylacidiphilum kamchatkense Kam1 (MkaFDH) | |
| dc.type | Article |








