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نویسندگان: KARL-HERMANN KUMAR ASHWANI IMANI JAFARGHOLI NEUMANN
سری:
ISBN (شابک) : 9783030490966, 3030490963
ناشر: SPRINGER NATURE
سال نشر: 2020
تعداد صفحات: 467
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 16 مگابایت
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در صورت تبدیل فایل کتاب PLANT CELL AND TISSUE CULTURE - A TOOL IN BIOTECHNOLOGY : basics and application. به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب سلول های گیاهی و فرهنگ بافت - ابزاری در بیوتکنولوژی: اصول و کاربرد. نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Preface to First Edition Preface to Second Edition Acknowledgments In Memoriam Prof. Dr. Karl-Hermann Neumann (1936-2009) Contents About the Authors 1: Introduction References 2: Historical Developments of Cell and Tissue Culture Techniques References 3: Callus Cultures 3.1 Establishment of a Primary Culture from Explants of the Secondary Phloem of the Carrot Root 3.1.1 Sterile (Aseptic) Technique: Microbe Eradication 3.1.2 Initial Contamination 3.1.3 Latent Contamination 3.1.4 Introduced Contamination 3.1.5 Surface Sterilizing of Plant Material 3.2 Fermenter Cultures (See Also Chap. 10) 3.3 Immobilized Cell Cultures 3.4 Nutrient Media 3.5 Evaluation of Experiments 3.6 Maintenance of Strains: Cryopreservation 3.7 Some Physiological, Biochemical, and Histological Aspects References 4: Cell Suspension Cultures 4.1 Methods to Establish a Cell Suspension 4.2 Cell Population Dynamics References 5: Protoplast Cultures 5.1 Production of Protoplasts 5.2 Protoplast Fusion References 6: Haploid Techniques 6.1 Application Possibilities 6.2 Physiological and Histological Background 6.3 Methods for Practical Application 6.4 Anther and Ovary Culture 6.4.1 Anther or Microspore Culture 6.4.1.1 Materials 6.4.1.2 Procedure Plants Growing Conditions and Selection of Microspore-Containing Spikes of Bobwhite Wheat Variety 6.5 Haploid Plants References 7: Plant Propagation: Meristem Cultures, Somatic Embryogenesis Micropropagation, and Transformation of Somatic Embryos in Bior... 7.1 General Remarks and Meristem Cultures 7.2 Protocols of Some Propagation Systems 7.2.1 In Vitro Propagation of Cymbidium 7.2.2 Meristem Cultures of Raspberries 7.2.3 In Vitro Propagation of Anthurium (following Geier 1986) 7.3 Somatic Embryogenesis 7.3.1 Basics of Somatic Embryogenesis 7.3.2 Ontogenesis of Competent Cells 7.3.3 Genetic Aspects: DNA Organization 7.3.4 The Phytohormone System 7.3.5 The Protein System 7.3.6 Cell Cycle Studies 7.4 Practical Application of Somatic Embryogenesis 7.5 Artificial Seeds 7.6 Embryo Rescue 7.7 Bioreactors for Micropropagation and Genetic Transformations References 8: Some Endogenous and Exogenous Factors in Cell Culture Systems 8.1 Endogenous Factors 8.1.1 Genetic Influences 8.1.2 Physiological Status of ``Mother Tissue´´ 8.1.3 Growth Conditions of the ``Mother Plant´´ 8.2 Exogenous Factors 8.2.1 Growth Regulators 8.2.2 Nutritional Factors 8.2.2.1 Improvement of Nutrient Uptake by Transgenic Carrot Cultures 8.3 Physical Factors References 9: Primary Metabolism 9.1 Carbon Metabolism 9.1.1 Improving Photosynthesis 9.2 Nitrogen Metabolism References 10: Secondary Metabolism 10.1 Introduction 10.2 Mechanism of Production of Secondary Metabolites 10.3 Historical Background 10.4 Plant Cell Cultures and Pharmaceuticals and Other Biologically Active Compounds 10.4.1 Antitumor Compounds 10.4.1.1 Taxol 10.4.2 Anthocyanin Production 10.5 Strategies for Improvement of Metabolite Production 10.5.1 Addition of Precursors and Biotransformations 10.5.2 Immobilization of Cells (See Also Sect. 3.3) 10.5.3 Differentiation and Secondary Metabolite Production 10.5.4 Elicitation 10.5.4.1 Jasmonic Acid 10.5.4.2 Salicylic Acid 10.5.4.3 Effect of UV on Production of Secondary Metabolites in Cultured Tissues 10.6 Organ Cultures 10.6.1 Shoot Cultures 10.6.2 Root Cultures 10.6.3 Adventitious Root Culture 10.7 Genetic Engineering of Secondary Metabolites (See Also Sect. 13.6.3) 10.8 Membrane Transport and Accumulation of Secondary Metabolites 10.9 Bioreactors (See Also Sect. 3.2) 10.9.1 Technical Aspects of Bioreactor Systems 10.10 Prospects References 11: Phytohormones and Growth Regulators References 12: Cell Division, Cell Growth, and Cell Differentiation References 13: Genetic Problems and Gene Technology 13.1 Somaclonal Variations 13.1.1 Ploidy Stability 13.1.2 Some More Somaclonal Variations 13.2 DNA Fingerprinting and Characterization of Germplasm 13.3 Estimations of Genetic Diversity 13.4 Evaluation of Genetic Fidelity During Long-Term Conservation 13.5 Molecular Marker-Assisted Selection (MAS) 13.6 Modes of Plant Gene Modification 13.6.1 Classical Breeding (Wild Crossing) 13.6.2 Mutagenesis 13.6.3 Gene Technology 13.6.3.1 Genetic Modification 13.6.3.2 Transformation Techniques Indirect Gene Transfer Virus-Based Techniques Agrobacterium-Mediated Gene Transformation Direct Gene Transfer Biolistic Approaches Polyethylene Glycol (PEG) Other Transformation Methods 13.7 Agrobacterium-Mediated Transformation in Mono and Dicotyledonous Plants 13.7.1 Generation of Transgenic Wheat Plants 13.7.2 Generation of Transgenic Barley Plants 13.7.3 Stable Root Transformation System for the Functional Study of Proteins in Barley 13.7.4 Carrot Cell Culture and Transformation Procedures 13.7.5 Uses of Transgenes to Increase Host Plant Resistance to Plant Pathogens 13.7.6 Transgenic Carrot: Potential Source of Edible Vaccines 13.8 RNA Interference (RNAi) Technology 13.8.1 MicroRNA (miRNA) 13.8.2 Generation of Hypoallergenic Carrot by Means RNAi 13.9 Precise Genome Editing Tools 13.9.1 Genome Manipulation Using the DNA Repair System 13.9.2 Zinc Finger Nuclease 13.9.3 Meganucleases 13.9.4 Transcription Activator-Like Effector (TALE): A Precision Tool for DNA Editing 13.9.5 CRISPR-Cas9 System for Gene Knockout 13.9.6 Structure and Functional Mechanism of Cas9 Nuclease 13.10 CRISPR/Cas9 for Plant Genome Editing 13.11 Selectable Marker Genes 13.12 Reporter Genes 13.12.1 β-Glucuronidase (GUS) 13.12.1.1 Procedures for Assay of GUS Gene Expression Histochemical Assay 13.12.1.2 Fluorometric Assay 13.12.2 Green Fluorescent Protein (GFP) 13.12.2.1 Variants of GFP 13.13 Antibiotics Resistance Genes 13.14 Elimination of Marker Genes 13.14.1 Cre-lox Recombination-Based Systems 13.14.2 Ac/Ds System 13.14.3 Double Cassette System 13.15 Concluding Remarks References 14: Summary of Some Physiological Aspects in the Development of Plant Cell and Tissue Culture Index