Somatic Embryogenesis: Embryos vary widely and can generally be classified into two main categories: zygotic and non-zygotic embryos. Zygotic embryos develop from the zygote, which is a fertilized egg. In contrast, non-zygotic embryos can be divided into several subtypes:
Somatic embryogenesis, the process of developing somatic embryos, is a powerful biotechnological tool with significant potential in fields such as clonal propagation and genetic transformation. This process was first demonstrated by Stewart in 1958 using carrots in a suspension culture.
Somatic embryogenesis is a process where somatic cells develop into somatic embryos. This method offers several key benefits over zygotic embryogenesis. It allows for easy monitoring of the embryogenesis process, provides control over the environment and development stages of the somatic embryos, and enables the production of a large number of embryos. Detailed NEET biology notes on somatic embryogenesis are provided in the article below.
Structural Organisation in Animals
Somatic embryogenesis is an important process in plant biotechnology where embryos are formed from somatic cells, which are regular cells not usually involved in embryo formation. These embryos develop through stages similar to those of zygotic embryos, which are formed from fertilization, and can eventually grow into whole plants. There are two main types of somatic embryogenesis: direct and indirect.
In direct somatic embryogenesis, embryos form directly from the explant (a piece of tissue taken from the plant) without first forming a callus. This method is less common but is preferred because it is faster and more efficient. Types of explants that are more likely to undergo direct somatic embryogenesis include immature zygotic embryos, pollen grains, and the outer cells of leaves.
Sexual Reproduction in Flowering Plants
Indirect somatic embryogenesis is the more common pathway. In this process, embryos develop from a callus, which is a mass of undifferentiated cells that forms from the explant. The callus is induced by culturing the explant on a medium with specific plant growth regulators (PGRs). These PGRs usually include a high concentration of auxin, such as 2,4-D, to promote cell division and growth. Once the callus has formed, the
PGRs are modified to encourage embryo development. This typically involves lowering the auxin concentration and adding cytokinins, which stimulate the development of shoots and roots. The somatic embryos then mature, gaining the ability to germinate and grow into whole plants.
Somatic embryogenesis process involves three main steps: induction of embryogenesis, embryo development, and embryo maturation.
The principle behind somatic embryogenesis is based on the totipotency of plant cells, highlighting two key aspects of plant embryogenesis:
Because somatic embryogenesis does not require fertilization, it allows for faster and large-scale plant propagation. Additionally, it facilitates genetic transformation of plants and serves as a valuable method for the cryo-storage of embryos and germplasm.
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Embryo | Funaria | Selaginella | Malvaceae |
Polyembryony | Apomixis | Pinus | Pollen Grains |
Chara | Volvox | Endosperm | Equisetum |
Somatic embryogenesis is a process that allows plants to produce embryos from somatic cells (any cell other than reproductive cells). This technique has numerous applications in agriculture, horticulture, and conservation biology. The following are stages of somatic embryogenesis:
1. Initiation: This stage begins with the selection of explant material, which is then sterilized and cultured on a medium with high levels of auxins, particularly 2,4-Dichlorophenoxyacetic acid (2,4-D), to promote the formation of embryogenic callus.Each step is essential and requires precise control of environmental conditions and growth regulators to ensure successful plant regeneration.
Somatic embryogenesis is a multifaceted process influenced by various factors. The following are the key factors affecting somatic embryogenesis:
1. Explant: This refers to the type of tissue used to start embryogenesis. In most plant species, immature zygotic embryos serve as the ideal explants. The developmental stage and genetic composition of the explant tissue also impact the process. For instance, juvenile explants typically produce more somatic embryos compared to older explants.By optimizing these factors, scientists can enhance the efficiency of somatic embryogenesis for a wider range of plant species. This technique has numerous applications in plant propagation, conservation, and genetic engineering.
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Plasma Membrane Structure | Pre-Fertilisation | Economic Importance of Algae |
Slime moulds | hypotonic solution | Post fertilisation |
Somatic embryogenesis, where plant cells transform into embryos and develop into entire plants, is a highly useful tool for researchers and agriculturists. Below are its main uses:
These are just a few of the many applications of somatic embryogenesis. As research progresses, this technique is expected to become even more significant in plant science and agriculture.
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Rhizopus | Fibrous root | Marchantia | Actinomycetes |
Nostoc | Spirogyra | Ribosomes | Liverworts |
Somatic embryogenesis and organogenesis are two techniques used in plant tissue culture:
Somatic Embryogenesis: This process imitates the natural formation of seeds, where non-reproductive cells (somatic cells) develop into embryos without fertilization. These embryos can then mature into complete plants.
Organogenesis: In this method, plant tissues are stimulated to produce new organs such as roots or shoots directly from either the original tissue or from a callus (a cluster of undifferentiated cells). There are two main pathways for organogenesis in plants:
The process is controlled by plant hormones like auxins and cytokinins, which determine the type of organ that will form. For instance, a higher concentration of auxin relative to cytokinin typically promotes root formation, while a higher concentration of cytokinin relative to auxin favors shoot formation.
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