Abstract
Previous reports of somatic embryogenesis on rose tissues involved an embryogenic callus stage with either a complicated multi-step process or low numbers of embryos being produced. We have produced somatic embryos without a callus stage from leaf explants of the cut rose cultivar `Golden Emblem' by using a two step process. Explants were obtained from microshoots of `Golden Emblem' that had been in culture for three years. All experiments were repeated twice. When explants were maintained on Murashige and Skoog (MS) with 0.4 μM NAA and 0.4 μM kinetin for 10 weeks, 10% or less of the explants produced somatic embryos. Keeping the explants on the NAA/kinetin medium for two weeks, then switching to medium with 0, 0.5, 1.0, or 10.0 μM kinetin for the remaining 8 weeks failed to increase embryo production. Decreasing the time the explants were on the NAA/kinetin medium to 8 or 12 days, and then placing explants on MS medium with 1.0 μM kinetin increased somatic embryo production to a maximum of 25%. By limiting the length of time the rose leaf explants were exposed to auxin, direct somatic embryo production was increased.
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