Klebsiella oxytoca strains were constructed to produce optical pure d-lactate by pH-controlled batch fermentation in mineral salts medium. The alcohol dehydrogenase gene, adhE, and the phospho-transacetylase/acetate kinase A genes, pta-ackA, were deleted from the wild type. KMS002 (ΔadhE) and KMS004 (ΔadhE Δpta-ackA) exhibited d-lactate production as a primary pathway for the regeneration of NAD⁺. Both strains produced 11–13g/L of d-lactate in medium containing 2% (w/v) glucose with yields of 0.64–0.71g/g glucose used. In sugarcane molasses, KMS002 and KMS004 produced 22–24g/L of d-lactate with yields of 0.80–0.87g/g total sugars utilized. Both strains also utilized maltodextrin derived from cassava starch and produced d-lactate at a concentration of 33–34g/L with yields of 0.91–0.92g/g maltodextrin utilized. These d-lactate yields are higher than those reported for engineered E. coli strains.