Direct organogenesis from leaf and internode explants of. This new plant regeneration method will open up new avenues in plant tissue culture and genetic engineering methodologies in maize. Failure in regeneration of rooted plants in high number limits the application of tissue culture technologies for safflower improvement. Torenia fournieri, the wishbone flower, is used for this laboratory exercise because the in vitro production of adventitious shoots from torenia is easy to control, seeds are easy to obtain, and. Organogenesis is the process that develops all the tissues and organs of the organism from three germ layers of the embryo. Auxins can be used alone in both petioles and roots explant to regenerate complete plants. May 25, 2016 direct organogenesis, embryogenesis, micro grafting, meristem culture and its importance for fruit crops 1. Vitamin c, known for its antioxidative properties, has also enhanced shoot growth and rooting. Since embryo is an independent structure and does not have vascular supply, it is not supposed to be the plant organ. Plant tissue culture the culture and maintenance of plant cells and organs the culture of plant seeds, organs, tissues, cells, or protoplasts on nutrient media under sterile conditions the growth and development of plant seeds, organs, tissues, cells or protoplasts on nutrient media under sterile axenic conditions the in vitro, aseptic plant culture for any purpose. Organogenesis involves inducing the vegetative tissue to form organs shoot or root which eventually develop into a complete. High frequency regeneration of plants via callusmediated. Direct organogenesis from cotyledons in cultivars of. The gesneriaceous perennial plant, lysionotus serratus, has been used in traditional chinese medicine.
Tissue culture techniques are very scanty in bambara groundnut and should be. In culture, the explant develops into callus tissue in a medium containing either a particular concentration of auxin or a definite auxincytokinin ratio. Alstroemeria is an important pot plant and cut flower in the ornamental plant. The plant hormone auxin is thought to be a central regulator of organ patterning given its concentration gradient patterns across the sam. View organogenesis in plant tissue culture ppts online, safely and virusfree. Direct organogenesis the root explants harvested from the in vitro grown seedling are considered as an excellent material for culture initiation as compared to mature plant explant and the degree of contamination is very less. Tissue culture the maintenance or growth of tissue the maintenance or growth of tissue, in vitro, in a way that may allow differentiation and preservation of their function. The plant cell, tissue or organ culture of many ornamental species and their regeneration are essential for providing the material and systems for their.
Shoot organogenesis and plant regeneration from leaf explants. Borthakurbb a plant tissue culture laboratory, botanical survey of india, eastern regional centre, meghalaya793003, india b department of botany, gauhati university, assam, india. In the micropropagation step figure 1a, after 90120 days of culture, the plantlets were cut into segments of approximately 1. Direct and indirect organogenesis and plant regeneration of an industrial plant kenaf hibiscus cannabinus l var. Direct and indirect shoot organogenesis strategies for. What is the difference between organogenesis and somatic. Direct and indirect plant regeneration from various explants of eastern cottonwood clones populus deltoides bartram ex marsh. In vitro direct and indirect organogenesis and plant regeneration of kenaf hibiscus cannabinus l var. Direct organogenesis, embryogenesis, micro grafting, meristem. Th d f dh l d l f h l d lhe production of dihaploid plants from haploid cultures sh h hortens the time taken to achieve uniform homozygous lines and varieties 3. The better quality planting material is a basic need of growers for boosting productivity. Sorghum tissue culture and regeneration protocols mostly follow either organogenesis maheswari et al. An efficient protocol to induce shoot buds regeneration in citrus clementina cultivars monreal, sra 63 and sra 64 by direct organogenesis has been developed using cotyledons as explants.
Shoot buds were obtained both from blade petiole transition zones and midribs of fully expanded leaves. In vitro plant regeneration through somatic embryogenesis and direct shoot organogenesis in cenchrus ciliaris 1. Direct organogenesis transformat a, b organogenesis somatic embryogenesis. Tissue culture produces clones, in which all product cells have the same genotype unless affected by mutation during culture. Organogenesis in vitro culture techniques plant biotechnology. The below mentioned article provides an overview on the organogenesis in plant tissue culture. This paper for the first time reports reliable and an efficient method for in vitro direct shoot organogenesis and plant regeneration from split nodal explants of maize derived from seedling.
In the use of plant tissue culture technique for propagation, organogenesis. Chavan 1,2, 1department of botany, yashavantrao chavan institute of science, satara, india. Pdf direct shoot organogenesis from in vitroderived mature leaf. Tissue culture the maintenance or growth of tissue, in vitro, in a way that may allow differentiation and preservation of their function. Pdf plant regeneration from direct and indirect organogenesis. Direct organogenesis from leaf and internode explants of in vitro raised wintergreen plant gaultheria fragrantissima r. Direct organogenesis from cold treated in vitro leaf. Rhizogenesis, caulogenesis and organogenesis abt2012026047n. Feb 04, 2014 an efficient protocol for direct shoot organogenesis has been developed for the medicinal plant aerva lanata l. This protocol may find application in citrus genetic improvement programs. This has been achieved in many plant species by altering the hormonal combination of the culture media.
Embryogenesis and organogenesis are two important processes in the development of an organism. Direct somatic embryogenesis and organogenesis pathway of. Plants have been propagated by direct organogenesis for improved. Shoot organogenesis and plant regeneration from leaf.
Ebrahimie e, habashi aa, mohammadiedehcheshmeh m, ghannadha m, ghareyazie b, yazdiamadi b 2006 direct shoot regeneration from mature embryo as a rapid and genotypeindependent pathway in tissue culture of heterogeneous diverse sets of cumin cuminum cyminum l. Box 2 organogenesis in tobacco nicotiana tabacum organogenesis from tobacco pith callus is the classical example of how varying plant growth regulator regimes can be used to manipulate the pattern of regener ation from plant tissue cultures. A laboratory exercise to demonstrate direct and indirect. With these objectives, this investigation was done on shoot regeneration via direct organogenesis from leafy petiole explants of gerbera jamesonii royal soft pink. Jun 29, 2017 if necessary nutrients, hormones and growth promoters are provided, a single plant cell can differentiate into a mature plant. Effect of vitamins on in vitro organogenesis of plant. Vitamin, organogenesis, in vitro, plant tissue culture, plant propagation. Our goal is to develop a secure and stable in vitro clonal repository of elite medicinal plant germplasm that will ensure future availability of desirable pharmacological active chemotypes. In vitro organogenesis in the callus tissue derived from a small piece of plant tissue, isolated cells, isolated protoplasts, microspores etc. The regeneration of plant or plant organs only taken place by the expression of cellular totiopotency of the callus tissues. Difference between organogenesis and somatic embryogenesis. Murashige and skoog 1962 ms medium was supplemented with 0. Direct organogenesis, embryogenesis, micro grafting, meristem culture and its importance for fruit crops 1. The production of direct buds or shoots from a tissue with no intervening callus stage is called direct organogenesis.
Somatic embryogenesis is an artificial process in which a plant or embryo is derived from a single somatic cell. As an important fiber crop, many potential applications of kenaf are being identified and developed in 21 century, especially in developed countries such as america, japan, and france and malaysia as well. Direct organogenesis in indian spinach plant cell, tissue. Direct shoot organogenesis and plant regeneration in safflower. Callus cultures were induced from leaf, stem and cotyledonary explants of momordica charantia, at different auxin and cytokinin concentrations either in single or in combination in ms medium. Organogenesis is the phase of embryonic development that starts at the end of gastrulation and continues until birth. Direct organogenesis and plant regeneration in preconditioned. Plant tissue culture, cell culture or micropropagation is the technique of producing selected plants of known desirable agriculture qualities, in large numbers of plants from small pieces of plant in relatively short period times. Direct organogenesis involves the emergence of adventitious organs directly from the meristematic region of the explants without callus phase and important to ensure clonal fidelity.
Direct and indirect method of plant regeneration from root. Organogenesis in vitro depends on the balance of auxin and cytokinins and the ability of the tissue to respond to phytohormones during culture. Section b someatic embryogenesis and organogenesis in plant. Direct organogenesis explant meristemoid primordium in many plants, subculturing of callus results in undesired variations of clones somaclonal variations. Direct organogenesis and plant regeneration in preconditioned tissue cultures of. Somatic embryogenesis and direct as well as indirect. Somatic embryos are formed from plant cells that are not normally involved in the development of embryos, i. Also, both methods involve in the induction of vegetative tissue with the use of different plant growth regulators. In plant tissue culture, organogenesis is a process of differentiation by which plant organs like roots, shoots, buds etc. The main objective in plant cultures is to regenerate a plant or plant organ from the callus culture. Pdf micropropagation of pothomorphe umbellata via direct. Efficient in vitro direct shoot organogenesis from.
The first step in organogenesis is establishing where organ primordia will form. Plant development through organogenesis is the formation. Such medium is known as callus inducing or initiation medium. Embryogenesis is the process that forms an embryo from a zygote developed from the syngamy. A simple and efficient direct shoot organogenesis method. Direct and indirect organogenesis of clivia miniata and assessment of dna methylation changes in various regenerated plantlets article pdf available in plant cell reports 317. Basic techniques of cell and tissue culture, surface sterilization, aseptic tissue transfer, concept of totipotency. Tissue culture is the culture and maintenance of plant cells or organs in sterile, nutritionally and environmentally supportive conditions in vitro. In vitro plant regeneration of sweetpotato through direct shoot. May 28, 2016 direct organogenesis, embryogenesis, micro grafting, meristem culture and its importance for fruit crops 1.
In addition, vitamin d causes cell elongation and meristematic cell division. Direct somatic embryogenesis and organogenesis pathway of plant regeneration can seldom occur. Plants have been propagated by direct organogenesis for improved multiplication rates, production of transgenic plants, and most importantly for clonal propagation. Tissue culture techniques are applied for micropropagation and production of pathogenfree plants.
In the use of plant tissue culture technique for propagation, organogenesis and somatic embryogenesis are the two alternative pathways in addition to direct shoot culture. An efficient system was developed for direct plant regeneration from in vitroderived leaf explants of embelia ribes burm. Rapid progress in plant molecular biology has great potentials to contribute to the breeding of novel ornamental plants utilizing recombinant dna technology. Thidiazuroninduced highfrequency direct shoot organogenesis of cannabis sativa l. Tissue culture as a pl ant production technique for horticultural crops akinidowu, p. Chapter 1 in vitro plant regeneration through somatic. Direct organogenesis from leaf and internode explants of in. For in vitro tissue culture experiments, statistical analysis were performed with jmp software version 9 using tukey kramer hsd test to determines significant differences among treatment at p. The below mentioned article provides a study note on organogenesis. The production of direct buds or shoots from a tissue with no intervening callus stage. Ericaceae through direct organogenesis from leaf, internode stem without axillary bud, and root explants of in vitro raised seedlings has been developed. In the direct shoot organogenesis step, root segments of 2. Direct organogenesis from cotyledons in cultivars of citrus. Plant regeneration through organogenesis can occur either directly or indirectly thorpe et al.
Tissue culture of the species began in the early 1980s. Citrus clementina, cotyledons, direct organogenesis, plant regeneration, tissue culture. No endosperm or seed coat is formed around a somatic embryo. Organogenesis is the formation of organs, either shoots or roots.
Thidiazuroninduced highfrequency direct shoot organogenesis. Plant tissue culture relies on the fact that many plant cells have the ability to regenerate a whole plant totipotency. Direct shoot organogenesis from leaf explants of embelia. In vitro plant regeneration from direct and indirect. For both genotypes, the optimum bap concentration for direct organogenesis from. Tissue culture as a plant production technique for. With plant cultures, this is the process by which the tissue or explant is first subdivide, then transferred into fresh culture medium.
It also has a great development potential as an ornamental plant with its attractive foliage and beautiful flowers. A laboratory exercise on direct and indirect organogenesis from leaf explants is presented for students of plant tissue culture or plant propagation. Micropropagation of pothomorphe umbellata via direct organogenesis from leaf explants article pdf available in plant cell tissue and organ culture 601. The main advantage of somatic embryogenesis in plants is that when the plant is infected, a mature plant can be made from a single unaffected cell using this process. Plant tissue culture is used widely in plant science. Direct and indirect plant regeneration from various explants. The in vitro procedure involved three steps that included induction of shoot initials from leaf tissue, regeneration and elongation of shoots from the shoot initials, and rooting of shoots. The gerbera market would benefit from an efficient and simple protocol for high rate regeneration for propagation and genetic engineering. Pdf direct and indirect organogenesis of clivia miniata.
The best callogenic response was observed from all. Direct adventitious organogenesis callus to organogenesis somatic embryogenesis. Plant organogenesis can be induced in tissue culture and used to regenerate plants. Organogenesis root, shoot and leaves but not embryo are the organs that are induced in plant tissue culture. Plant regeneration by somatic embryogenesis and organogenesis used for. Induction of direct organogenesis from aerial explants of. The type of organ that is formed depends on the relative concentrations of the hormones in the medium. Regeneration of begonia plantlets by direct organogenesis.
High efficiency direct shoot organogenesis from leaf segments. The biochemical engineer can grow plant cells in liquid culture on a large scalebioreactor 2. Regeneration of begonia plantlets by direct organogenesis y. Murashige and skoogs basal medium supplemented with naphthaleneacetic acid and benzyladenine each at 1 mg l. In vitro organogenesis and plant regeneration from leaves of solanum candidum lindl, s. Considering the limitations, a protocol for in vitro tissue culture of nodal segments containing axillary buds is needed to propagate elite c. Kb6 by zeti ermiena surya bt mat hussin a thesis submitted in fulfilment of the requirements for the degree of. An efficient propagation and regeneration system via direct shoot organogenesis from leaf explant was established in this study. Direct organogenesis and plant regeneration in preconditioned tissue. Nutritional requirement of cell in vitro, various types of nutrient media. Pdf an efficient system was developed for direct plant regeneration from in vitro derived leaf explants. To avoid this, direct regeneration of the explants into plantlets can be tried. Somatic embryogenesis and direct as well as indirect shoot organogenesis are the most commonly used micropropagation techniques in plant tissue culture.
Organogenesis and somatic embryogenesis are two pathways used in plant tissue culture for the vegetative propagation of plants. Tdz is a phenylureatype and potent cytokinin for plant tissue culture 31. During organogenesis, the three germ layers formed from gastrulation. Protocol for rapid regeneration of the important medicinal plant gaultheria fragrantissima wall. Typically indirect organogenesis is more important for transgenic plant production. Direct organogenesis, embryogenesis, micro grafting. The hofmeister principle states that new organs form in the location maximally distant from previous primordia. Plant regeneration via direct shoot organogenesis from.
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