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Questions and Answers
Explain how the manipulation of plant growth regulators (PGRs) impacts the morphogenic pathways in micropropagation, specifically in the context of shifting from callus induction to shoot regeneration. What specific PGR concentrations and ratios are generally employed to achieve this transition?
Explain how the manipulation of plant growth regulators (PGRs) impacts the morphogenic pathways in micropropagation, specifically in the context of shifting from callus induction to shoot regeneration. What specific PGR concentrations and ratios are generally employed to achieve this transition?
During micropropagation, the shift from callus induction to shoot regeneration relies on modulating PGR concentrations. High auxin-to-cytokinin ratios favor callus formation, while reducing auxin and increasing cytokinin promotes shoot development. For callus to shoot transition, a researcher would typically reduce auxin concentrations (e.g. IAA or NAA) to below 1 mg/L and increase cytokinin concentrations (e.g. BAP or kinetin) to >1 mg/L.
Discuss the potential challenges and strategies for mitigating somaclonal variation in long-term micropropagation of ornamental plants. How do different micropropagation techniques (e.g., axillary bud proliferation vs. adventitious shoot regeneration) influence the rate and type of somaclonal variation?
Discuss the potential challenges and strategies for mitigating somaclonal variation in long-term micropropagation of ornamental plants. How do different micropropagation techniques (e.g., axillary bud proliferation vs. adventitious shoot regeneration) influence the rate and type of somaclonal variation?
Somaclonal variation poses challenges in long-term micropropagation, potentially altering key ornamental traits. Using axillary bud proliferation minimizes variation compared to adventitious shoot regeneration from callus, which has a higher mutation rate. Strategies include using stable explants (shoot tips), optimizing culture conditions and minimizing subculture cycles. Regular screening using molecular markers also helps to detect and eliminate variants.
Compare and contrast the advantages and limitations of using somatic embryogenesis versus axillary bud proliferation for mass propagation of field crops, particularly focusing on considerations related to genetic fidelity and scalability.
Compare and contrast the advantages and limitations of using somatic embryogenesis versus axillary bud proliferation for mass propagation of field crops, particularly focusing on considerations related to genetic fidelity and scalability.
Somatic embryogenesis allows high-volume propagation and genetic transformation. However, it risks somaclonal variation. Axillary bud proliferation ensures genetic fidelity but is less scalable. Somatic embryogenesis is chosen when large-scale propagation is crucial and some genetic variation is acceptable or desirable (e.g. mutation breeding). Axillary bud proliferation is better when genetic uniformity is paramount.
Evaluate the economic feasibility and scalability of implementing bioreactor systems for micropropagation of medicinal plants, considering the initial investment costs, operational expenses, and potential gains in secondary metabolite production.
Evaluate the economic feasibility and scalability of implementing bioreactor systems for micropropagation of medicinal plants, considering the initial investment costs, operational expenses, and potential gains in secondary metabolite production.
Discuss the ethical considerations associated with using micropropagation for conservation of rare and endangered plant species, specifically addressing the potential impacts on natural ecosystems and the importance of maintaining genetic diversity.
Discuss the ethical considerations associated with using micropropagation for conservation of rare and endangered plant species, specifically addressing the potential impacts on natural ecosystems and the importance of maintaining genetic diversity.
Compare the efficacy of different sterilization methods (e.g., autoclaving, chemical disinfectants, filter sterilization) in preventing microbial contamination during micropropagation. What are the advantages and disadvantages of each method, particularly concerning their impact on explant viability and subsequent plant regeneration?
Compare the efficacy of different sterilization methods (e.g., autoclaving, chemical disinfectants, filter sterilization) in preventing microbial contamination during micropropagation. What are the advantages and disadvantages of each method, particularly concerning their impact on explant viability and subsequent plant regeneration?
Analyze the role of elicitors (e.g., methyl jasmonate, salicylic acid) in enhancing the production of secondary metabolites in plant cell suspension cultures. Discuss the potential mechanisms of action of these elicitors and their impact on the expression of key genes involved in secondary metabolite biosynthesis.
Analyze the role of elicitors (e.g., methyl jasmonate, salicylic acid) in enhancing the production of secondary metabolites in plant cell suspension cultures. Discuss the potential mechanisms of action of these elicitors and their impact on the expression of key genes involved in secondary metabolite biosynthesis.
Evaluate the importance of acclimatization in micropropagation. What are the key environmental factors that need to be carefully controlled during the acclimatization phase to ensure successful transfer of plantlets from in vitro to ex vitro conditions?
Evaluate the importance of acclimatization in micropropagation. What are the key environmental factors that need to be carefully controlled during the acclimatization phase to ensure successful transfer of plantlets from in vitro to ex vitro conditions?
Discuss the challenges and strategies for maintaining genetic stability during long-term in vitro storage (cryopreservation) of plant germplasm. What molecular techniques can be used to assess the genetic integrity of plant material after cryopreservation?
Discuss the challenges and strategies for maintaining genetic stability during long-term in vitro storage (cryopreservation) of plant germplasm. What molecular techniques can be used to assess the genetic integrity of plant material after cryopreservation?
Describe the role of mycorrhizal fungi in enhancing the survival and growth of micropropagated plantlets during the acclimatization phase. What are the potential mechanisms by which mycorrhizae improve plantlet establishment in ex vitro conditions?
Describe the role of mycorrhizal fungi in enhancing the survival and growth of micropropagated plantlets during the acclimatization phase. What are the potential mechanisms by which mycorrhizae improve plantlet establishment in ex vitro conditions?
Flashcards
Micropropagation
Micropropagation
In vitro regeneration of plants from small tissue pieces (explants).
Axillary bud proliferation
Axillary bud proliferation
Shoot production enhanced from axillary buds.
Adventitious shoot regeneration
Adventitious shoot regeneration
Induction of shoots from callus or explant surfaces.
Somatic embryogenesis
Somatic embryogenesis
Embryo production from somatic cells.
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Suspension culture
Suspension culture
Cultures using cells or cell aggregates in liquid media for mass propagation.
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Disease elimination
Disease elimination
Produces pathogen-free planting material in field crops.
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Uniformity
Uniformity
Ensures genetic consistency in field crops, leading to uniform growth and yield.
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Virus-free plants
Virus-free plants
Shoot tip culture in ornamental plants results in...
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Nodal culture
Nodal culture
Efficient multiplication using nodes in ornamental plants.
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Enhanced secondary metabolite production
Enhanced secondary metabolite production
Hairy root culture in medicinal plants leads to...
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- Plant tissue culture is used in micropropagation for field, ornamental, and medicinal plants.
- Micropropagation allows for rapid clonal propagation, disease elimination, and genetic improvement across plant species.
Micropropagation Techniques
- Micropropagation involves in vitro regeneration of plants from small tissue pieces known as explants.
- The steps are: explant selection, sterilization, culture initiation, multiplication, rooting, and acclimatization.
- Explants can be shoot tips, buds, leaves, or single cells.
- Sterilization prevents microbial contamination for successful culture establishment.
- Culture media contains nutrients, vitamins, and plant growth regulators (PGRs).
- Auxins like IAA and NAA and cytokinins like BAP and kinetin are common PGRs used for shoot and root development.
- Multiplication involves repeated subculturing to increase the number of shoots or embryos.
- Rooting can occur in vitro or ex vitro, depending on the plant species and protocol.
- Acclimatization adapts plantlets to ex vitro conditions.
- Micropropagation methods:
- Axillary bud proliferation enhances shoot production from axillary buds.
- Adventitious shoot regeneration induces shoots from callus or explant surfaces.
- Somatic embryogenesis produces embryos from somatic cells.
- Suspension culture uses cells or cell aggregates in liquid media for mass propagation.
- Bioreactors are large-scale culture vessels used for efficient micropropagation.
Field Plant Applications
- Micropropagation benefits field crops by:
- Rapid propagation of elite genotypes, quickly multiplying high-yielding or disease-resistant varieties.
- Disease elimination, producing pathogen-free planting material.
- Providing Uniformity, ensuring genetic consistency for growth and yield.
- Examples of field crops propagated via tissue culture:
- Banana: Cavendish bananas are mass-produced via micropropagation.
- Potato: virus-free seed potatoes.
- Sugarcane: disease-free and high-yielding varieties.
- Rice: genetic improvement and hybrid seed production.
- Cassava: rapid multiplication of improved lines.
- Advantages for field crops:
- Faster breeding cycles which accelerates introduction of new varieties.
- Year-round propagation is independent of seasonal constraints.
- Conservation of germplasm to preserve rare or endangered varieties.
- Challenges in field plant micropropagation:
- High cost for some crops.
- somaclonal variation my cause Genetic instability.
- Acclimatization issues where plantlets may struggle to adapt.
Ornamental Plant Culture
- Micropropagation has changed ornamental plant production by:
- Rapid multiplication which quickly increases availability of desirable cultivars.
- Production of disease-free plants which Ensures healthy stock.
- Year-round availability to meets market demands regardless of season.
- Preservation of rare species which conserves unique or threatened plants.
- Popular ornamental plants propagated via tissue culture:
- Orchids: mass propagation of unique hybrids.
- Roses: production of disease-resistant and novel varieties.
- Gerbera: uniform and high-quality plants.
- Carnations: disease-free and long-lasting flowers.
- Lilies: rapid scaling up of production.
- Techniques in ornamental plant micropropagation:
- Shoot tip culture for virus-free plants.
- Nodal culture for efficient multiplication.
- Callus culture for inducing somaclonal variation and new traits.
- Advantages for the ornamental plant industry:
- Introduction of new cultivars that accelerates market entry.
- Consistent quality which meets consumer expectations.
- Lower production costs through efficient propagation.
- Challenges include:
- Somaclonal variation affecting flower color, shape, or plant habit.
- Maintaining genetic integrity with careful selection and monitoring.
- Cost-effectiveness: balancing production costs with market value.
Medicinal Plant Culture
- Micropropagation is vital in medicinal plant conservation and production:
- Multiplication of rare species prevents over-collection from wild populations.
- Production of uniform plants ensures consistent secondary metabolite content.
- Using Disease-free stock enhances plant health and metabolite yield.
- Important medicinal plants propagated via tissue culture:
- Ginseng: production of high-quality roots with consistent ginsenoside levels.
- Digitalis: uniform production of cardiac glycosides.
- Artemisia: increased artemisinin production for malaria treatment.
- Coleus: production of forskolin for pharmaceutical applications.
- Stevia: mass propagation of high-stevioside lines for sweeteners.
- Techniques in medicinal plant micropropagation:
- Hairy root culture enhances secondary metabolite production.
- Cell suspension culture enables large-scale production of bioactive compounds.
- Elicitation can increase metabolite synthesis.
- Advantages for the medicinal plant industry:
- Sustainable supply reduces pressure on wild populations.
- Consistent product quality ensures reliable medicinal properties.
- Enhanced metabolite production to increases yields of desired compounds.
- Challenges in medicinal plant micropropagation:
- Complex secondary metabolite pathways require optimization for in vitro production.
- Maintaining Genetic stability ensures consistent metabolite profiles.
- There are Regulatory issues regarding compliance with pharmaceutical standards.
- Micropropagation enhances conservation efforts for endangered medicinal plants.
- In vitro production of secondary metabolites reduces reliance on field cultivation.
- Optimization of culture conditions increases the yield of valuable compounds.
- Tissue culture contributes to drug discovery and development by providing a consistent source of plant-based compounds.
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