Ribitol dehydrogenase (RDH) catalyzes the conversion of ribitol to d-ribulose. A novel RDH gene was cloned from Zymomonas mobilis subsp. mobilis ZM4 and overexpressed in Escherichia coli BL21(DE3). DNA sequence analysis revealed an open reading frame of 795 bp, capable of encoding a polypeptide of 266 amino acid residues with a calculated molecular mass of 28,426 Da. The gene was overexpressed in E. coli BL21(DE3) and the protein was purified as an active soluble form using glutathione S-transferase affinity chromatography. The molecular mass of the purified enzyme was estimated to be similar to 28 kDa by sodium dodecyl sulfate-polyacrylamide gel and similar to 58 KDa with gel filtration chromatography, suggesting that the enzyme is a homodimer. The enzyme had an optimal pH and temperature of 9.5 and 65A degrees C, respectively. Unlike previously characterized RDHs, Z. mobilis RDH (ZmRDH) showed an unusual dual coenzyme specificity, with a k (cat) of 4.83 s(-1) for NADH (k (cat)/K (m) = 27.3 s(-1) mM(-1)) and k (cat) of 2.79 s(-1) for NADPH (k (cat)/K (m) = 10.8 s(-1) mM(-1)). Homology modeling and docking studies of NAD(+) and NADP(+) into the active site of ZmRDH shed light on the dual coenzyme specificity of ZmRDH.