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12 ppm respectively in kernel and 0.12, 0.05, 1.15,
423 MOLLA, M.T.H.; ALAM, M.T. 0.18, 0.45%; 204, 4, 54 and 50 ppm respectively in
(Pharmaceutical Research Laboratory, Dept. of oil.
Applied Chemistry and Chemical Technology,
Rajshahi University, Rajshahi) & ISLAM, M.A.U. 424 MOSTAFA, M.; JAHAN, I.A. (BCSIR
(Dept. of Pharmacy, Rajshahi University, Rajshahi). Laboratories, Dhaka); AHMED, M. (Dept. of
Physico-Chemical and Nutritional Studies of Botany, Chittagong University, Chittagong) &
Terminalia Belerica Roxb. Seed Oil and Seed CHOUDHURY, J.U. (BCSIR Laboratories,
Kernel. J. Bio-Sci., 2007, 15, 117-126. Chittagong). Composition of Oil from the Seeds of
Cassia sophera Linn. Bang. J. Sci. Ind. Res., 2007,
Oil was extracted from Terminalia belerica Roxb. 42 (1), 75-78.
seed kernel by solvent extraction process. The
whole seed contained 12.28 % oil on dry basis. The oil obtained from the seeds of Cassia sophera
The physico-chemical properties of the oil were Linn was analyzed by GC-MS and a total of 42
determined. Moisture, ash and crude fibre contents compounds have been identified. The major
of the seed kernel were found to be 8. 43, 2.54, and constituents are palmitic acid (22.82%), linoleic
8.78% respectively. The refractive index, co- acid (8.32%), elaidic acid (19.16%), stearic acid
efficient of viscosity, specific gravity, and energy (9.86 %), 5-isopropyl -6-methyl-3-heptyne-2,5-diol
of activation of the oil were found to be 1.28, (6.44%), undecyl lauric acid (6.61%), oleic acid
403.6 millipoise at 30°C, 0.93 and 6.97 k.cal/mole (2.1%), arachidic acid (3.57%) and 3α, 7β-
respectively. The oil was found to be non-drying. dihyodxy -5 β, 6 β -epoxyc-holestane (5.9 %).
Iodine value, acid value, peroxide value,
saponification value, saponification equivalent, 425 MUNSHI, M.K.; ROY, P.K. & KABIR,
ester value, unsaponifiable matter, acetyl value, M.H. (Institute of Food and Radiation Biology,
Reichert-Meissel value, Polenske value, free fatty Atomic Energy Research Establishment, Dhaka).
acids as oleic acid and cholesterol content of the Clonal Propagation of Ginger (Zingiber officinale
oil were recorded as 107, 3.69, 3.14,189.24, Rose.) through in vitro Culture. Bang. J. Life Sci.,
296.44,185.55,1.24%, 3.78,0.719, 0.945, 0.87% 2008, 20(1), 105-109.
and 26.59 mg per 100 g oil. respectively. The oil
was qualitative and quantitative analysed for fatty Rhizome segments with axillary buds were
acid composition by TLC and GLC. The results cultured on MS medium supplemented with
showed that the fatty acids of the oil had chain different concentrations of (0.5-1.5 mg/l)
length between C 14 to C 22. The oil contained cytokinins (BA, Kin and 2iP) and also in
17.70% myristic acid, 21.6% palmitic acid, combination with a fixed concentration (1.0
45.67% oleic acid and 14.93% stearic acid. The mg/1) of the cytokinins and fow concentrations
whole kernel was analyzed for some nutrients and (0.05-0.2 mg/l) of auxin (IBA) for multiple
minerals. The kernel contained 22.57 and 8.38% shoot induction. Cent percent of explants
total lipid and protein respectively. It also produced shoots in MS with 1.0 mg/l 2iP>+ 0.2
contained 0.19mg, 0.45mg, 0.79g and 1.1mg of mg/l of IBA. Number and length of shoots were
vitamin B 1, B 2, C and A respectively per l00g of found to be higher in the same medium. Rooting
kernel. Ca, Mg. K, Na, P, Fe, Mn, Zn and Cu were of shoot was found to be best on half strength
found to be 0.3,0.02,0.2,0.2,0.01%; 23, 1, 12 and MS with 1.0 mg/l IBA.
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