CONTRIBUTION OF TOBACCO WASTE FOR AGRICULTURE

. This study aim is to explain the contribution of tobacco waste in the agricultural sector. Tobacco waste here limited to tobacco stems only. Tobacco stems are processed into bio briquettes, pellets, and liquid smoke. Biobriquettes and bio pellets can substitute the use of coal as fuel while liquid smoke can replace the use of chemical insecticides. The three products are eco-friendly and safe for the consumers. The production of these three products is a contribution manifestation of tobacco waste utilization to increase agriculture productivity, reducing fossil energy use, and minimizing tobacco stakeholders from chemical contamination both on tobacco plantation area and tobacco barns.


Introduction
World wide changes against a biotechonomy allocate new requirements for coffee commodity.The utilization of coffee plant material which adapted to the impact of climate change is one of the alternative solutions.Rising temperatures and eratic rainfall patterns pose a major risk to the future of coffee production in producing countries such as Indonesia.The planting material of coffee leaf rust tolerance is one of the alternative ways to deal with climate change.Arabica coffee which popular with its soft and unique taste contributed to 70% of world coffee production.Nevertheless, it is not tolerance with pest and disease [1] and should be planted in high land above 1200 m deep sea level.The utilization of genetically superior planting materials becomes essential for expanding biomass productivity.Leaf rust tolerant of Arabica becomes the most preferred choice due to effective results.Andungsari 1 (AS1), Andungsari 2K (AS 2K), S795 and Sigararutang are some of the commercial tolerant Arabica varieties in Indonesia.Vegetative propagation by somatic embryogenesis of those varieties supports a prospective distribution system for this purpose.Somatic embryogenesis has been successfully achieved for scale-up production in C. arabica species [2,3,4].There have been several somatic embryogenesis in C. arabica [5][6][7][8][9][10][11][12][13][14][15][16].This method has been accomplished by direct somatic embryogenesis from globular without callus formation or by indirect somatic embryogenesis through friable embryogenic callus proliferation [17].
The fundamental purpose of this research was to compare the response of germination step from the preliminary step of direct-embryogenesis from leaves explants of some Arabica varieties leaf rust tolerant.The response between plant growth regulator and varieties to induce callus, qualitative characteristic embryogenic calli and embryo germination responses were studied.

Materials and Methods
A completely randomized design of laboratory observation was carried out with coffee clones, i.e.AS2K, S795, AS1, and Sigararutang as the first factor, and 8 levels of medium treatments, i.e. 2-ip and 2,4-D for the second factor.Leaf rust tolerant varieties of Arabica coffee were subjected to chemical treatments to induce and express the embryogenic callus, based on protocol reported elsewhere [18].The eight combination of mediums are M1 (1 mg/L 2-ip and 0. Qualitative characteristics of coffee clones as responses to a different medium for direct somatic embryogenesis were observed.The embryoid will be transferred to the germination medium consisting of MS [19] medium in the absence of a plant growth regulator.Furthermore, embryo germination, open cotyledonary, root length, hypocotyl length and the number of roots were subsequently observed, the analysis of variance was performed with further Tukey post-hoc analysis to reveal the interaction effect of clone and week.

Result and Discussion
The effect of medium treatments on some qualitative characteristics of coffee embryogenic calli is inconsistently varied among clones (Table 1).The coffee clones may determine callus location with all AS2K coffee observed in vein leaf while most of S795 in the entire leaf edge.While all Sigararutang coffee observed in the entire leaf edge.Both in vein leaf and entire leaf edge were showed for AS1 coffee clon.Furthermore, the slow growth of callus for AS2K may indicate the absence of a medium effect.It is different from S795 with callus response following medium treatments varying from slow to vigorous.The best performance was Sigararutang coffee clone which was moderate and vigorous.While most of the AS 1 coffee clones exhibited slow responses.All these data may imply the importance of genetic factors and endogenous hormone posed in different coffee clones to characteristics of embryogenic calli.Type and colour of embryogenic calli were varied from brownish, yellowish and creamish between morphogenic and non morphogenic.Each treatment showed different responses of callus induction and expression of embryogenic calli due to the effect of 2-ip and 2,4-D concentration ratio from preliminary step of direct embryogenesis.This difference is due to genetic factors among varieties.The results showed that AS2K and AS1 required high concentration of cytokinins and a small concentration of auxin for callus induction (M3 medium), while embryogenic callus formation requires cytokinins with low concentration and auxin with high concentration (M2 medium).S795 requires cytokinins and auxin with high concentration for induction callus (M4 medium) but the formation of embryogenic callus requires cytokinins with low concentration and auxins with high concentration (M2 medium).The location and texture of callus were fundamentally influenced by the various combinations of medium and varieties [2].Moreover, callus growth pattern and colour were also principally influenced through the presence of various combinations of medium and varieties [2].The successful germination stage is the crucial step for the maintenance planlet before ready for the acclimatization step to avoid exaggerated plant losses in the nursery.The response of embryo germination was varied and it was largely determined by varieties.The highest percentage of embryo germination was S795 which accounts for 100% in four weeks (Figure 1).Every embryo has a different endogenous ability which is only the perfect and vigorous embryo can be survived longer in the further phase of somatic embryogenesis.An appropriate maturation embryo is a prerequisite as a beginning component to produce planlet derived from somatic embryos [20].

Conclusion
Every clone have a different response in a different medium for the characteristics of type, colour, location, and growth for direct somatic embryogenesis.The highest percentage of embryo germination is S795.Sigararutang has the longest root and hypocotyl as well as the number of root formation.AS2K coffee clone was the highest number in the response of open cotyledonary embryo.This different response between parameters was largely determined by variety.

Fig. 5 .
Fig. 5. Number of roots in different coffee clones

Table 1 .
Qualitative characteristics of coffee clones as responses to different medium for direct somatic embryogenesis (M: morphogenic; NM: non-morphogenic; SGR: Sigararutang; Vl: Vein leaf; Ele: entire leaf edges