Big bluestem (Andropogon gerardii Vitman) and little bluestem [Schizachyrium scoparium (Michaux) Nash.] are native to the North America and are important forage grasses and ornamental grasses. Both grasses are proposed as ideal biomass producers for cellulosic ethanol production. To apply genetic transformation, which is an important tool for incorporating desirable agronomic traits into plants to both species, however requires an efficient and reproducible regeneration protocol. We used mature caryopses from big and little bluestem as explants and tested the effect of various combinations of 2,4-dichlorophenoxyacetic acid (2,4-D) (1, 2,3,4 or 5 mg l(-1)) and kinetin (KT) (0, 0.1 or 0.2 mg l(-1)) on embryogenic callus induction with LS as the basal medium. The highest percentage of embryogenic calli induction occurred on medium containing 2, 4-D alone at 2 mg l(-1) for 'Bison' and on medium containing 4 mg l(-1) 2, 4-D alone for 'Bonilla' big bluestem. For little bluestem, the highest percentage of embryogenic callus induction occurred on medium containing 3 mg l(-1) 2, 4-D plus 0.1 mg l(-1) kinetin, suggesting that addition of KT is beneficial. Shoot regeneration took placeon LS basal medium without any plant growth regulator for both species, although the addition of KT increased both regeneration frequency and the number of shoots produced per callus. Rooting of shoots reaching about 2 cm long occurred readily with or without alpha-naphthateneacetic acid (NAA). Rooted plantlets were all successfully established in the soil. (C) 2009 Elsevier B.V. All rights reserved.