d-Xylonic acid is one of the top 30 most desirable chemicals to be derived from biomass sugars identified by the US Department of Energy, being applicable as a non-food substitute for d-gluconic acid and as a platform chemical. We engineered the non-conventional yeast Pichia kudriavzevii VTT C-79090T to express a d-xylose dehydrogenase coding gene from Caulobacter crescentus. With this single modification the recombinant P. kudriavzevii strain produced up to 171gL⁻¹ of d-xylonate from 171gL⁻¹d-xylose at a rate of 1.4gL⁻¹h⁻¹ and yield of 1.0g [g substrate consumed]⁻¹, which was comparable with d-xylonate production by Gluconobacter oxydans or Pseudomonas sp. The productivity of the strain was also remarkable at low pH, producing 146gL⁻¹d-xylonate at 1.2gL⁻¹h⁻¹ at pH 3.0. This is the best low pH production reported for d-xylonate. These results encourage further development towards industrial scale production.