Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Google Scholar citation report
Citations : 2154

Journal of Biotechnology & Biomaterials received 2154 citations as per Google Scholar report

Indexed In
  • Index Copernicus
  • Google Scholar
  • Sherpa Romeo
  • Open J Gate
  • Genamics JournalSeek
  • Academic Keys
  • ResearchBible
  • China National Knowledge Infrastructure (CNKI)
  • Access to Global Online Research in Agriculture (AGORA)
  • Electronic Journals Library
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • SWB online catalog
  • Virtual Library of Biology (vifabio)
  • Publons
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • ICMJE
Recommended Journals
Share This Page

Rapid clonal multiplication and conservation of Lavandula angustifolia â?? An aromatic and medicinal plant, using apical buds and root by in vitro techniques

7th Asia-Pacific Biotech Congress

D Leelavathi

ScientificTracks Abstracts: J Biotechnol Biomater

DOI: 10.4172/2155-952X.S1.031

Abstract
Lavandula angustifolia L. is a perennial shrub, belonging to the family Lamiaceae, cultivated for its leaves for extraction of essential oil. Oil is used in flavor, perfumery and pharmaceutical industries. In order to meet the growing demand of its oil and herbage, in vitro techniques are being used as alternative method for large scale multiplication and conservation. In the present investigation, in vitro apical bud explants were cultured on MS basal medium supplemented with BAP (8.88 μM) and NAA (2.68 μM) to induce multiple shoots. In vitro root explants were cultured on MS basal medium supplemented with BA (8.88 μM) and NAA (5.36 μM) to induce callus which was sub-cultured on same medium to obtain profuse callus. Callus was later cultured on shoot regenerating medium, MS supplemented with BAP (4.44 μM), KN (4.64 μM) and NAA (2.68 μM) to produce multiple shoots. Well developed multiple shoots developed roots on MS medium supplemented with BA (8.88 μM) and NAA (2.68 μM) and IBA (4.92 μM). The hardened, regenerated plants were acclimatized which were transferred to soil with 80% - 90% survival frequency. In vitro and in vivo leaves were subjected to phytochemical analysis for the determination of principle component. The in vitro apical buds were used for synthetic seed production using Sodium alginate and Calcium chloride as matrix and complexing agent for encapsulation. Hardened multiple shoots obtained from apical bud, root callus and synthetic seeds serve as a source of ex-situ conservation. The percentage of Linalool was found to be more in in vivo leaf when compared to in vitro propagules.
Biography
D Leelavathi is working as an Associate Professor in the Department of Botany at MES College, Bangalore. She has published 10 research papers, presented research papers in various international and national journals/conferences and is presently working on a minor research project funded by UGC. During her research she has travelled to USA and presented a paper in 4th International Conference on Medicinal plants and Herbal products held at John Hopkins University, Rockville, MD, USA, 2012.
Top