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TITLE
DECLARATION
CERTIFICATE
DEDICATION
ACKNOWLEDGEMENT
CONTENTS
ABBREVIATIONS
1. Introduction and Review of Literature
INTRODUCTION
REVIEW OF LITERATURE
1. Importance of Natural products in anticancer therapy.
1.1 Anti-tumour compounds from plants.
PLATE-Mechanism of DNA strand breakage and religation by Topoisomerase
1.2 Plant Biotechnology for the production of alkaloids
1.3. Strategies to improve product yield from plant tissue culture
1.3.1. Screening and Selection
1.3.2. Influence of growth phases
1.3.3. Differentiation and culture type.
1.3.4 Organogenesis
1.3.5 Hairy root culture
1.3.6. Culture conditions
1.3.7 Elicitation
1.3.8. Precursor feeding
1.3.9 Biotransformation
1.3.10 Inducers.
1.3.11 Immobilization
1.3.1 2 Permeabilization
1.3.13 Biosynthesis, enzymology and regulation
1.3.14 Alkaloid storage compartment
1.3.15 Genetic modification
1.3.16 Combination of treatments
1.3.1 7 Large-scale production
2. Materials And Methods
2.1 Plant Material
2.2 Chemicals
2.3 Instruments
2.4 Explants and Surface sterilization.
2.5 Preparation of nutrient medium
2.6 Culture conditions
2.7 Establishment of suspension culture
2.8 Determination of fresh weight
2.9 Determination of dry weight.
2.10 Determination of packed cell volume
2.11 Estimation of growth rates of culture.
2.12 Effect of growth hormones on callus induction and organogenesis
2.13 Hairy root cultures.
2.14 Elicitation
2.15 Two phase culture
2.16 Permeabilization
2.17 Preparation of plant extract.
2.18.Isolation and crystallization of Camptothecin (CPT)
2.19 TLC analysis.
2.20 Melting point
2.21 UV - Visible absorption spectra.
2.22 High performance liquid chromatography (HPLC)
2.23 Electron spray mass spectrometry -
2.24 Topoisomerase I and I1 inhibition assay
2.25 Statistical analysis
3. Comparison of camptothecin production from intact plants and callus culture of Ophiorrhiza mungos
3.1 Materials and Methods
3.2 Results
Plate 2- Figure: 1 Ophiorrhiza mungos mother plant
Plate 2- Figure: 2 Ophiorrhiza mungos compact callus
Plate 2- Figure: 3 Ophiorrhiza mungos friable callus
Plate 3- Figure: 1 Ophiorrhiza mungos rhizogenesis
Plate 3- Figure: 2 Ophiorrhiza mungos rooted callus
Mass Spectra of Standard Camptothecin
Mass spectra of isolated camptothecin
HPLC Profiles of Selected Samples
DISCUSSION
4. Multiple shoot cultures - a viable alternative for camptothecin production
4.1. Materials and Methods.
4.2 Results
Plate 4- Figure: 1 Ophiorrhiza mungos shoot regeneration
Plate 4- Figure: 2 Ophiorrhiza mungos multiple shoots
Plate 4- Figure: 3 Ophiorrhiza mungos multiple shoots
Plate 4- Figure: 4 Ophiorrhiza mungos multiple shootsuspension culture
HPLC Profiles of Selected Samples
Amala Cancer Research Centre-Kerala
4.3 Discussion
5. An attempt to enhance camptothecin production by precursor feeding, elicitation Permeabilization and two- phase culture.
5.1 Materials and Methods
5.2 Results
HPLC Profiles of Selected Samples
DISCUSSION
6. Comparative evaluation of camptothecin production in callus, cell suspension culture, root culture and somatic embryos of Nothapodytes foetida
6.1 Materials and Methods.
6.2 Result
Plate 5- Figure: 1 Nothapodytes foetida mother plant
Plate 5- Figure: 2 Nothapodytes foetida- callus
Plate 5- Figure: 3 Nothapodytes foetida- cell suspension culture
Plate 6- Figure: 1 Nothapodytes foetida- root regeneration
Plate 6- Figure: 2 Nothapodytes foetida- somatic embryogenesis
Plate 6- Figure: 3 Nothapodytes foetida- mature somatic embryo
Plate 6- Figure: 4 Nothapodytes foetida- regenerated roots
Plate 6- Figure: 5 Nothapodytes foetida- seedling developed from somatic embryo
HPLC Profiles of Selected Samples
6.3 Discussion
7. Summary and Conclusion
Future prospectus
BIBILIOGRAPHY