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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/15721
Title: CHEMICAL COMPOSITION OF ESSENTIAL OIL FROM IN VITRO GROWN PEPEROMIA OBTUSIFOLIA THROUGH GC-MS
Authors: SAIQA ILYAS
SHAGUFTA NAZ
FARAH ASLAM
ZAHIDA PARVEEN
AAMIR ALI
Issue Date: 7-May-2014
Publisher: Karachi: Pakistan Botanical Society
Citation: Ilyas, S., Naz, S., Aslam, F., Parveen, Z., & Ali, A. (2014). Chemical composition of essential oil from in vitro grown Peperomia obtusifolia through GC-MS. Pak. J. Bot, 46(2), 667-672.
Abstract: Apical meristems and nodal plant parts were used for mass propagation of Peperomia obtusifolia. Different concentrations of BAP (6-benzylaminopurine), TDZ (Thidiazuron) and KIN (Kinetin) were used in MS medium. The highest shoot proliferation and multiplication formation occurred in the MS basal medium containing 1.0 mg/mL BAP. Maximum number of shoots and shoot lengths were 9.80 ±0.50 and 35.40 ± 2.92 cm respectively. Rooting response was the best in MS basal medium fortified with1.0 mg/mL BAP plus 0.5 mg/mL NAA (α-naphthalene acetic acid). For acclimatization, the rooted plantlets were transferred to the greenhouse. The volatile oil of this In vitro grown P. obtusifolia was extracted by hydro-distillation and investigated by gas chromatography/mass spectrometry (GC–MS). The chromatographic analysis of oil showed 35 constituents of which, 16 volatile compounds contributing 65.0% of the total oil constituents could be identified. The major components identified in this oil were sesquiterpenes such as caryophyllene (17.17%), apiol (16.65%), α-cardinol (2.12%) and α-caryophyllene (1.90%). The monoterpenes such as R-α-Pinene (1.00%), camphene (0.84%), borneal (0.32%) and limonene (0.25%) were also identified. The tau.-muurolol (0.68%), τElemene (0.63%), copaene (0.43%) and tau.-cadinol (0.27%) were present comparatively in minor percentages. The caryophyllene oxide (2.95%) was oxygenated sesquiterpene, 3,5-Dimethoxy-4-hydroxycinnamic acid (0.53%) and asarone (0.41%) were phenyl-propanoids.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/15721
ISSN: 2070-3368
Appears in Collections:Issue 02

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