Alpdagtas, SaadetYucel, SevilKapkac, Handan AcelyaLiu, SiqingBinay, Baris2025-05-102025-05-1020180141-54921573-677610.1007/s10529-018-2568-62-s2.0-85047133945https://doi.org/10.1007/s10529-018-2568-6https://hdl.handle.net/20.500.14720/6198Kapkac, Handan Acelya/0000-0002-2812-1686; Alpdagtas, Saadet/0000-0002-8322-2658; Yucel, Sevil/0000-0002-9495-9321To identify a robust NADP(+) dependent formate dehydrogenase from Lactobacillus buchneri NRRL B-30929 (LbFDH) with unique biochemical properties. A new NADP(+) dependent formate dehydrogenase gene (fdh) was cloned from genomic DNA of L. buchneri NRRL B-30929. The recombinant construct was expressed in Escherichia coli BL21(DE3) with 6 x histidine at the C-terminus and the purified protein obtained as a single band of approx. 44 kDa on SDS-PAGE and 90 kDa on native-PAGE. The LbFDH was highly active at acidic conditions (pH 4.8-6.2). Its optimum temperature was 60 A degrees C and 50 A degrees C with NADP(+) and NAD(+), respectively and its T-m value was 78 A degrees C. Its activity did not decrease after incubation in a solution containing 20% of DMSO and acetonitrile for 6 h. The K-M constants were 49.8, 0.12 and 1.68 mM for formate (with NADP(+)), NADP(+) and NAD(+), respectively. An NADP(+) dependent FDH from L. buchneri NRRL B-30929 was cloned, expressed and identified with its unusual characteristics. The LbFDH can be a promising candidate for NADPH regeneration through biocatalysis requiring acidic conditions and high temperatures.eninfo:eu-repo/semantics/closedAccessAcidic Formate DehydrogenaseBiochemical And Kinetic CharacterizationHighly Nadp(+) Dependent Formate DehydrogenaseLactobacillus Buchneri Nrrl B-30929Solvent StableThermostabilityArticle407Q3Q21135114729777512WOS:000434458100013