Title : In vitro rapid mass multiplication regeneration and enhanced secondary metabolite production of ocimum gratissimum

Type of Material: Thesis
Title: In vitro rapid mass multiplication regeneration and enhanced secondary metabolite production of ocimum gratissimum
Researcher: Chaudhary, Priyanka
Guide: Sharma, Vikas
Department: Department of Biotechnology and Microbiology
Publisher: Arni University
Place: Kangra
Year: 2018
Language: English
Subject: Biology
Biology and Biochemistry
Life Sciences
Biotechnology
Life Science
Dissertation/Thesis Note: PhD; Department of Biotechnology and Microbiology, Arni University, Kangra; 2018
Fulltext: Shodhganga

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035__|a(IN-AhILN)th_463576
040__|dIN-AhILN|aARNI_176401
041__|aeng
100__|eResearcher|aChaudhary, Priyanka
110__|aDepartment of Biotechnology and Microbiology|0U-0176|dKangra|bArni University|ein
245__|aIn vitro rapid mass multiplication regeneration and enhanced secondary metabolite production of ocimum gratissimum
260__|aKangra|c2018|bArni University
300__|dDVD
502__|d2018|bPhD|cDepartment of Biotechnology and Microbiology, Arni University, Kangra
518__|d2018|oDate of Award
518__|d2015|oDate of Registration
518__|oDate of Completion|d2018
520__|aOcimum gratissimum is an important medicinal perennial herb belonging to the family Lamiaceae and has enormous potential in cosmetic and drug industry due to occurrence of several phytoconstituents. O. gratissimum is a standout amongst the most utilized therapeutic plants as an overall wellspring of flavors and furthermore as a consolidated supply of extracts with several pharmacological activities. The demand of O.gratissimum is increasing day by day thus there is a need to conserve genetic diversity of medicinal plant resources by developing protocols for micropropagation. Therefore present study was undertaken to set up a proficient mass propagation system via nodal explants of O.gratissimum and to optimize the effect of precursor phenylalanine on the enhancement of eugenol production in vitro. Explants were surface sterilized with different sterilizing agents namely HgCl2 (0.05%- 0.5%), NaOCl (0.5%- 2.0%) and H2O2 (3.0%-10.0%) by varying their concentration and time of exposure (1-15 minutes) prior to i
650__|aBiotechnology|2UGC
650__|aLife Science|2AIU
653__|aBiology
653__|aBiology and Biochemistry
653__|aLife Sciences
700__|aSharma, Vikas|eGuide
856__|uhttp://shodhganga.inflibnet.ac.in/handle/10603/343324|yShodhganga
905__|afromsg

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