Somatic embryogenesis and shoot regeneration from intact seedlings of Phaseolus acutifolius A., P. aureus (L.) Wilczek,P. coccineus L., and P. wrightii L.

A rapid, one-step procedure has been developed for inducing direct organogenesis and somatic embryogenesis in cultures of Phaseolus coccineus L., P. acutifolius A., P. aureus L. [Vigna radiata L. Wilczek] and P. wrightii L. Development of somatic embryos and shoot buds occurred within 6–8 weeks of culture from intact seedlings raised on MS (Murashige and Skoog 1962) medium supplemented with N⁶-benzylaminopurine (BAP). Shoot buds or embryoids originated from subepidermal tissue of the regions adjacent to the shoot apex, hypocotyl and cotyledonary axils. While P. acutifolius and P. aureus were regenerated via shoot formation and P. wrightii by somatic embryogenesis, both embryogenesis and shoot regeneration were observed in P. coccineus. Relatively higher levels of BAP, 50–80 M, were found to be optimal for inducing regeneration while lower concentrations were ineffective. About 40–70 shoots and 70–250 somatic embryos were produced per responding seedling. Regenerated shoots and somatic embryos developed into whole plants on a basal medium or the one supplemented with 1 M naphthaleneacetic acid.     

Gibberellic-acid causes flowering in the short-day plants Panicum miliaceum L., P. miliare lamk., and Setaria italica (L.) P. Beauv.

Treatment with gibberellic acid (GA₃) causes formation of flowers in Panicum ciliaceum and Panicum miliare, two short-day plants, under long days (continuous light), and hastens the emergence of ears in Setaria italica, a quantitative short-day plant, under both inductive and non-inductive photoperiods. The GA₃-induced inflorescences, however, remain short and bear only few spikelets; in the two Panicum species, the spikelets also remain sterile.