Induksi Embrio Globular pada Tanaman Aren (Arenga pinnata (Wurmb) Merr.)

Abstract

Sugar palm is a monocot plant belong to the Arecaceae family economically valuable and have bright prospects to be developed for food products to bio-ethanol substituting fossil fuels. This plant is usually propagated generatively yet there are a few issues being faced such as a long reproductive cycle, long seed production and dormancy, low germination capacity, and uniform seedling growth. Non-conventional plant breeding through biotechnology is the best possible alternative solution to provide good quality seedlings in order to increase sugar palm productivity. Tissue culture through somatic embryogenesis method is a technique that can be used to induce abundant and relatively uniform somatic embryos from zygotic embryos. One of the key factors when using this method which is focused in this research is the role of plant growth regulators under the auxin, cytokinin, and gibberellin groups. The objective of this study was to get the best media to produce somatic embryos from zygotic embryos of sugar palm. The obtained results are expected to be used for future sugar palm non-conventional breeding. This research was conducted at Tissue Culture Laboratory Department of Agronomy and Horticulture, Faculty of Agriculture, Bogor Agricultural University from October 2012 to April 2013. It covers the embryogenic callus induction phase, globular embryo induction phase and globular embryos maturation phase. The first phase consisted six treatments with 2,4-D, NAA, and biotin combination aiming to induce callus formation from young zygotic embryos. In the second phase, callus obtained from the first phase were subcultured to 14 different treatments with various kinetin and TIBA combination. As for the third phase, explants which were obtained from the second phase were subcultured into media with or without GA3 combination. The variables which were observed were percentage and total sterile explants, percentage and total explants which induced callus formation, average percentage of callus coverage, percentage and total explants with base apocol smaller than haustorium, percentage and total pseudo roots, percentage and total explants which induced globular embryos, percentage and total alive and mature globular embryo clumps. Sterilization using NaOCl 1.575 % and alcohol 96 % was able to provide 50-85 % sterile explants. During callus induction phase, embryogenic callus were mostly formed at treatment A5 (MS + 3 mg l-1 2,4-D + 0.2 mg l-1 NAA + 100 mg l-1 biotin) which is 73.4 % after 8 weeks. All explants were able to form globular embryos on media B3 (callus A1 to media MS + 4 mg l-1 Kinetin), B6 (callus A1 to media MS + 1 mg l-1 Kinetin + 0.1 mg l-1 TIBA), B12 (callus A2 to media MS + 0.1 mg l-1 Kinetin + 1 mg l-1 TIBA), and B14 (callus A2 to media MS + 1 mg l-1 Kinetin + 1 mg l-1 TIBA) at 2 WAT during embryo globular induction phase. During embryo globular maturation phase, media C11 (globular embryo clumps B9 to media MS + 0.1 mg l-1 GA3) was able to induce 70.8 % mature globular embryo clumps.