The diploid cotton species can constitute a valuable gene pool for the more agronomically desirable cultivated tetraploid
cultivars and offer better opportunities to study gene structure and function through gene knockouts. In order to exploit
these advantages, a regeneration system is required to achieve these transformation-based goals. Carbohydrate source and
concentration were evaluated to improve somatic embryo (SE) production and desiccation treatments to improve the
conversion efficiency of SEs to plants in a diploid Gossypium arboreum accession, A2-9 (PI-529712). Improved SE
numbers and their subsequent conversion into plantlets was achieved with a Murashige and Skoog (MS)/sucrose-based
medium M2 [0.04M sucrose, 0.3mM a-naphthaleneacetic acid (NAA)]. On this medium, 219 embryos per g initiated, and
close to 11% of these embryos germinated into plantlets. Neither a 5-d desiccation treatment of embryogenic callus
previously cultured in liquid medium nor filter paper insertion improved the numbers of SEs induced or their conversion to
plantlets. A 3-d desiccation period resulted in improved plant regeneration. When immature G. arboreum SEs induced on
M1 (0.2M glucose, 2.6mM NAA, and 0.2mM kinetin) medium underwent a 3-d desiccation treatment, 49% of these
immature SEs were converted to plantlets after a 4-wk period on M2 medium. These improved results will help to pave the
way for future genetic transformation and associated gene structure and function studies utilizing G. arboreum. These
results, in particular the 3-d desiccation treatment, can also be incorporated into regeneration protocols to improve the
regeneration efficiency of other Gossypium species.
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