Protocols for Micropropagation of Woody Trees and Fruits

Protocols for Micropropagation of Woody Trees and Fruits

Author: S.Mohan Jain

Publisher: Springer Science & Business Media

Published: 2007-09-18

Total Pages: 548

ISBN-13: 1402063520

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Micropropagation has become a reliable and routine approach for large-scale rapid plant multiplication, which is based on plant cell, tissue and organ culture on well defined tissue culture media under aseptic conditions. A lot of research efforts are being made to develop and refine micropropagation methods and culture media for large-scale plant multiplication of several number of plant species. However, many forest and fruit tree species still remain recalcitrant to in vitro culture and require highly specific culture conditions for plant growth and development. The recent challenges on plant cell cycle regulation and the presented potential molecular mechanisms of recalcitrance are providing excellent background for understanding on totipotency and what is more development of micropropagation protocols. For large-scale in vitro plant production the important attributes are the quality, cost effectiveness, maintenance of genetic fidelity, and long-term storage. The need for appropriate in vitro plant regeneration methods for woody plants, including both forest and fruit trees, is still overwhelming in order to overcome problems facing micropropagation such as somaclonal variation, recalcitrant rooting, hyperhydricity, polyphenols, loss of material during hardening and quality of plant material. Moreover, micropropagation may be utilized, in basic research, in production of virus-free planting material, cryopreservation of endangered and elite woody species, applications in tree breeding and reforestation.


Micropropagation of Medicinal Plants: Volume 2

Micropropagation of Medicinal Plants: Volume 2

Author: T. Pullaiah

Publisher: Bentham Science Publishers

Published: 2024-03-29

Total Pages: 391

ISBN-13: 9815238310

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This volume presents information about protocols for micropropagation of more than 40 species of medicinal plants. The contents combine knowledge about the scientific principles of micropropagation with state of the art updates in tissue culture techniques presented by plant scientists. The readers will learn about techniques required to grow plants in challenging conditions that aim to reduce the impacts of injudicious harvesting, deforestation, climate change, pollution, urbanization and other factors that limit the ability to meet current demand. General topics such as biotization and pharmaceutical investigation are also included to guide readers about the significance of these plants in research and development for new medicines. The book provides protocols for micropropagation of important medicinal plants like Rauvolfia serpentina, Catharanthus roseus, Withania somnifera, Tylophora indica, Bacopa monnieri, Aloe vera, Phyllanthus amarus, Allium sativum, Moringa oleifera, Operculina turpethum, Glycyrrhiza glabra, Pterocarpus marsupium, Vetiver grass, Ruta graveolens, Tinospora cordifolia, Kaempferia, Hedychium, Decalepis hamiltonii, Saraca asoca, Wrightia tinctoria, Wrightia arborea, Artemisia absinthium, Aegle marmelos, Atropa acuminata, Atropa belladonna, Alpinia species, Hedychium species, and Cissus species. This book is a handy reference for medicinal chemists, horticulturists and pharmacists who want to learn about the growth and conservation of important medicinal herbs and plants.


Cryopreservation of Plant Germplasm I

Cryopreservation of Plant Germplasm I

Author: Y. P. S. Bajaj

Publisher: Springer Science & Business Media

Published: 2013-03-09

Total Pages: 526

ISBN-13: 3662030969

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The germ plasm of numerous plant species, especially those of forest trees, some agricultural crops, and medicinal plants, is endangered and threatened with extinction. This depletion of germplasm pools and the shrinkage of naturally occurring genetic resources have caused international concern. Conventionally, the germplasm of plants is conserved through seeds, tubers, roots, corms, rhizomes, bulbs, cuttings, etc. However, the germ plasm of a number of trees and plantation crops (such as coconut, cocao, coffee, oil palm, rubber, mango, horse chestnut, etc. ) cannot be preserved since their seed are short-lived (recalcitrant). Likewise, germplasm of vegetatively propagated crops (such as potato and cassava) cannot be stored on a long term basis and has to be grown and multiplied periodically in nurseries and fields. The plants are thus exposed to unpredictable weather conditions and diseases, with the result that instances are known where entire genetic stocks are lost. Therefore, unconventional methods are being developed for the storage and international exchange of germplasm. For this purpose in vitro cultures have been employed, but they can only enable short-to medium term preservation; moreover, cell cultures upon repeated subculture undergo genetic erosion. In view of the recent developments in the in vitro induction of genetic variability through somaclonal variation, somatic hybridization, recombinant DNA technology, etc. , new methods need to be employed for the storage of desirable cultures. In this regard freeze preservation of cells in liquid nitrogen (-196 0q, like that of semen, enables long-term storage, theoretically, for an indefinite period of time.


Influence of Benzyladenine on Shoot Forcing and Tissue Culture of Juglans Nigra L. and Quercus Rubra L.

Influence of Benzyladenine on Shoot Forcing and Tissue Culture of Juglans Nigra L. and Quercus Rubra L.

Author: Andrew Craig Holsinger

Publisher:

Published: 2008

Total Pages: 78

ISBN-13:

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Shoot production and in vitro performance of Juglans nigra L and Quercus rubra L. was studied where 0, 3, 10, 30, or 100mM benzyladenine (BA) in a 20% white exterior latex paint diluted with deionized water were applied separately to 40 cm branch segments to determine the most effective concentration of benzyladenine on bud break and shoot growth. Both shoot number and shoot length of softwood shoots decreased linearly with increasing BA concentrations applied to the branch segments of both species. When all BA treated softwood shoots were compared to the controls, the BA in the medium caused a significant increase in the number of shoots produced by explants obtained from the branch segments painted with BA. Painting with BA also increased shoot production in vitro, only if BA was also in the medium.