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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Trace elements. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (326 pages)
    Edition: 1st ed.
    ISBN: 9780128122433
    Language: English
    Note: Front Cover -- Plant Micronutrient Use Efficiency: Molecular and Genomic Perspectives in Crop Plants -- Copyright -- Contents -- Contributors -- Editors' Biography -- Preface -- Acknowledgments -- Chapter 1: Regulation of Micronutrient Homeostasis and Deficiency Response in Plants -- 1 Introduction -- 2 Iron -- 2.1 Acquisition from Soil -- 2.2 Regulation of Fe Homeostasis and Deficiency Response -- 3 Copper -- 3.1 Acquisition from Soil -- 3.2 Regulation of Cu Homeostasis and Deficiency Response -- 4 Zinc -- 4.1 Acquisition from Soil -- 4.2 Regulation of Zn Homeostasis and Deficiency Response -- 5 Concluding Remarks -- References -- Chapter 2: Molecular Bases of Iron Accumulation Towards the Development of Iron-Enriched Crops -- 1 Introduction -- 2 Iron Uptake From The Soil, Transport, and Storage in Roots -- 2.1 Iron Uptake in Crops -- 2.2 Strategy I, Strategy II, and a Combined Strategy -- 2.3 Root Plasma Membrane Fe Transport -- 2.4 Iron Chelation and Solubilization at the Rhizosphere -- 2.5 Vacuolar Fe Storage in Roots -- 2.6 Transcriptional Control of Fe Uptake -- 3 Long Distance Fe Transport -- 3.1 Root-to-Shoot Xylem-Dependent Fe Transport -- 3.2 Iron Movement in the Phloem -- 3.3 The Role of NA in Fe Seed Loading -- 3.4 Subcellular Fe Transport -- 3.4.1 Vacuole -- 3.4.2 Chloroplast -- 3.4.3 Mitochondria -- 4 Iron Distribution in Seeds -- 5 Different Transgenic Strategies Used to Develop Fe-Enriched Plants -- 6 Future Strategies to Develop Fe-Enriched Crops -- References -- Further Reading -- Chapter 3: Plant Responses to Iron Deficiency and Toxicity and Iron Use Efficiency in Plants -- 1 Introduction -- 2 Iron Deficiency Root Responses -- 2.1 Strategy 1: Reduction-Based Fe Uptake -- 2.2 Strategy 2: Chelation-Based Fe Uptake -- 2.3 Coexistence of Reduction and Chelation Strategies -- 3 Iron Toxicity Responses -- 4 Long-Distance Fe Transport. , 4.1 Xylem Transport -- 4.2 Phloem Transport -- 4.3 Xylem-to-Phloem Lateral Fe Transfer in Shoots -- 5 Subcellular Fe Transport and Compartmentation -- 6 Regulation of Fe Use Efficiency -- 6.1 Efficient Vs Inefficient Genotypes -- 6.2 Candidate for Fe Sensors and Signals -- 6.3 Crosstalk Between Fe and Other Elements -- 7 Conclusion and Prospects -- Acknowledgments -- References -- Chapter 4: Plant Responses to Copper: Molecular and Regulatory Mechanisms of Copper Uptake, Distribution and Accumulation i... -- 1 Copper Properties and Functions in Plants -- 2 Copper Phytoavailability and Bioavailability -- 3 Uptake, Distribution and Accumulation of Cu By Plants -- 3.1 Copper Uptake -- 3.2 Copper Transport Into Chloroplasts and Mitochondria -- 3.3 Copper Transport Through the Secretory Pathway -- 3.4 Copper Transport Into and Out of the Vacuole -- 3.5 Long-Distance Cu Transport from Roots to Shoots -- 3.6 Copper Remobilization from Senescing Organs -- 4 Molecular Responses to Cu Deficiency in Plants -- 5 The Increase of Cu Uptake and Accumulation Efficiency in Plants: Prospects for Biofortification of Crops -- References -- Further Reading -- Chapter 5: The Molecular Genetics of Zinc Uptake and Utilization Efficiency in Crop Plants -- 1 Introduction -- 2 Zinc Transport Pathway -- 2.1 The Long Distance Zn Transport in Plants -- 3 Znic Use Efficiency -- 4 Physiology of Zn Transport -- 4.1 Zrt/Irt-Like Protein -- 4.2 Heavy Metal ATPases -- 4.3 Cation Diffusion Facilitator -- 4.4 Sensing Mechanisms of Zn -- 5 Concluding Remarks -- References -- Chapter 6: Plant Response to Boron Deficiency and Boron Use Efficiency in Crop Plants -- 1 Introduction: Biological Functions of Boron -- 2 Occurrence of B in Plants -- 2.1 Uptake and Xylem Loading of B in Roots -- 2.2 Boron Distribution in Plants -- 3 Physiological and Molecular Responses to B Deficiency in Plants. , 3.1 Plant Growth -- 3.2 Plant Reproductive Development -- 3.3 Metabolism -- 3.4 Signaling Transduction -- 4 Mechanisms for Tolerance to B Deficiency and Strategies for the Improvement of B Use Efficiency -- 5 Conclusion -- References -- Chapter 7: Physiological Importance of Manganese, Cobalt and Nickel and the Improvement of Their Uptake and Utilization by ... -- 1 Introduction -- 2 Manganese -- 2.1 Importance of Mn for Plant Metabolism and Physiology -- 2.2 Uptake of Mn and Interactions With Other Nutrients -- 2.3 Manganese Transport, Distribution Among Tissues, and Utilization Efficiency by Crop Plants -- 3 Nickel -- 3.1 Importance of Ni for Plant Metabolism and Physiology -- 3.2 Uptake of Ni and Interactions With Other Nutrients -- 3.3 Nickel Transport and Distribution Among Tissues by Crop Plants -- 4 Cobalt -- 4.1 Importance of Co for Plant Metabolism and Physiology -- 4.2 Uptake of Co and Interactions With Other Nutrients -- 4.3 Cobalt Transport and Distribution Among Tissues by Crop Plants -- 5 Conclusions and Future Perspectives -- References -- Chapter 8: Roles of Molybdenum in Plants and Improvement of Its Acquisition and Use Efficiency -- 1 Introduction: Molybdenum Relevance and Its Acquisition By Plants -- 2 Molybdate Transporters -- 2.1 The MOT1 Family -- 2.2 The MOT2 Family -- 2.3 Other Plant Proteins Mediating Mo Transport -- 3 Nutrients Affecting Mo Homeostasis in Plants -- 4 Molybdenum in Symbiotic Nitrogen Fixation -- 5 Molybdenum Cofactor Biosynthesis in Eukaryotes -- 5.1 First Step: Pterin Synthesis -- 5.2 Second Step: MPT Synthesis -- 5.3 Third Step: MPT Activation -- 5.4 Fourth Step: Mo Insertion -- 6 The Sulfuration of Mo Cofactor in XOR and AO Enzymes -- 7 Storage of Mo Cofactor and Its Insertion in Molybdoenzymes -- 8 The Molybdoenzymes and Their Function -- 8.1 Xanthine Oxidoreductase/Dehydrogenase -- 8.2 Aldehyde Oxidase. , 8.3 Sulfite Oxidase -- 8.4 Nitrate Reductase -- 8.5 Amidoxime Reducing Component -- 9 Future Perspectives -- Acknowledgments -- References -- Chapter 9: Proteomics of Micronutrient Deficiency and Toxicity -- 1 Introduction -- 2 Iron -- 2.1 Iron Deficiency -- 2.1.1 Energy metabolism -- 2.1.2 Nitrogen-metabolism -- 2.1.3 Cell wall -- 2.1.4 Redox homeostasis -- 2.2 Iron Toxicity -- 3 Copper -- 3.1 Copper Deficiency -- 3.2 Copper Toxicity -- 4 Zinc -- 4.1 Zinc Deficiency -- 4.2 Zinc Toxicity -- 5 Manganese -- 5.1 Manganese Deficiency -- 5.2 Manganese Toxicity -- 6 Boron -- 6.1 Boron Deficiency -- 6.2 Boron Toxicity -- 7 Conclusions and Future Perspective -- References -- Further Reading -- Chapter 10: Oxidative Stress in Relation With Micronutrient Deficiency or Toxicity -- 1 Introduction -- 2 Generalities on Oxidative Metabolism -- 3 Iron Status and Oxidative Metabolism -- 4 Copper Status and Oxidative Metabolism -- 5 Manganese Status and Oxidative Metabolism -- 6 Zinc Status and Oxidative Metabolism -- 7 Conclusions -- References -- Chapter 11: Strategies for Increasing Micronutrient Availability in Soil for Plant Uptake -- 1 Introduction -- 2 Sources and Factors Affecting Soil Micronutrients -- 2.1 Source of Micronutrients -- 2.2 General Behavior of Micronutrients in Soils -- 2.2.1 Iron -- 2.2.2 Manganese -- 2.2.3 Zinc -- 2.2.4 Copper -- 2.2.5 Molybdenum -- 2.2.6 Boron -- 2.3 Other Factors Influencing Soil Micronutrient Availability -- 3 Distribution of Soil Available Micronutrient in the World -- 4 Agronomic Management of Micronutrients -- 5 Soil Micronutrient Availability Control in a Paddy System -- 5.1 The Effects of Fertilization and Water Management on Plant Morphology and Grain Yield -- 5.2 The Effects of Fertilization and Water Management on Micronutrient Concentration in Soil and Grain -- 6 Conclusion -- References. , Chapter 12: Micronutrients Use Efficiency of Crop-Plants Under Changing Climate -- 1 Introduction -- 2 The Importance of Micronutrients in Humans -- 3 The Role of Micronutrients in Plants -- 4 Mineral Nutrition of Crops Under Changing Climate -- 4.1 The Influence of Elevated [CO2] on Grain Minerals -- 4.1.1 Wheat -- 4.1.2 Rice -- 4.1.3 Legumes -- 4.2 The Effect of High Temperature and Drought on Crop Mineral Nutrient Concentration -- 5 Soil Nutrient Flow Under Future Climate -- 5.1 Soil Minerals Under Future Climate -- 5.2 Elevated [CO2] Influences the Mycorrhizal Associations and Root Exudates -- 5.3 Mineral Nutrition Under High Temperature and Water Stress -- 6 Mechanisms of Mineral Nutrition Under Climate Stress -- 6.1 Biomass Dilution -- 6.2 Reduction in Transpiration -- 6.3 Changes in Root Architecture -- 6.4 Change of Micronutrient Requirement -- 7 Strategies to Improve Grain Micronutrient Status Under Elevated [CO2] -- 7.1 Germplasm Screening -- 7.2 Crop Management -- 7.3 Knowledge Gaps -- 8 Conclusion -- References -- Further Reading -- Chapter 13: Micronutrient Malnutrition and Biofortification: Recent Advances and Future Perspectives -- 1 Introduction -- 2 Hunger and "Hidden Hunger" -- 3 Remedies of Micronutrient Malnutrition -- 3.1 Dietary Diversification -- 3.2 Food Supplements -- 3.3 Food Fortification -- 3.4 Biofortification -- 4 Biofortification Approaches -- 4.1 Agronomic Interventions -- 4.2 Genetic Biofortification -- 5 Reduction in Malnutrition Through Biofortification -- 5.1 Zinc Deficiency -- 5.2 Iron Deficiency -- 5.3 Vitamin A Deficiency -- 5.4 Iodine Deficiency -- 6 Climate Change and Biofortification -- 7 Conclusion and Future Research Thrusts -- Acknowledgments -- References -- Further Reading -- Chapter 14: Genomic Approaches for Micronutrients Biofortification of Rice -- 1 Introduction -- 2 Conventional Breeding Approaches. , 3 Genomics of Micronutrient Biofortification.
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Plants--Nutrition. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (420 pages)
    Edition: 1st ed.
    ISBN: 9780128112946
    Language: English
    Note: Cover -- Title page -- Copyright page -- Contents -- List of Contributors -- Editors' Biographies -- Preface -- Acknowledgments -- Chapter 1 - Molecular and genetic basis of plant macronutrient use efficiency: concepts, opportunities, and challenges -- Introduction -- Why macronutrients are important for plants? -- The role of macronutrients for a sustainable intensification of cropping systems -- Availability of nutrients in the soil -- Use of fertilizers and nutrient reserves -- Macronutrient use efficiency -- concepts and importance -- Some basic concepts -- Components of nutrient use efficiency -- Molecular and genetic basis of use efficiency of phosphate, nitrate, and potassium -- Mechanisms for nutrient uptake and transport -- Regulation of phosphate uptake -- PHR1: a master regulator -- A finely controlled network of nitrate transporters and sensors -- A complex network of potassium transporters and channels -- Modulation of the roost system architecture -- Plasticity of the root system to phosphate availability -- Root architecture responses to nitrate availability -- Root architecture responses to potassium availability -- Regulation of nutrient assimilation and remobilization -- The central role of PHO1 in phosphate homeostasis -- Nitrate assimilation and mobilization -- Potassium homeostasis -- Improvement of macronutrient use efficiency -- Concluding remarks and future perspectives -- References -- Chapter 2 - Role of nutrient-efficient plants for improving crop yields: bridging plant ecology, physiology, and molecular biology -- Introduction -- Physiology and genetics of nutrient use efficiency -- Root development in response to nutrient availability -- Root interactions with microorganisms under low nutrient availability -- Metabolism and gene regulation -- Remobilization of nutrients in the crop plant life cycle. , Finding genes for nutrient use efficiency -- Future nutrient-efficient crops -- Assessment and evaluation of nutrient use efficiency -- Ecological approaches of nutrient use efficiency -- Crop production-related approaches of nutrient use efficiency -- Nutrient balances and budgets, modeling, and life cycle assessments -- Conclusions -- References -- Chapter 3 - Macronutrient sensing and signaling in plants -- Introduction -- Plant macronutrient starvation responses -- Phosphorus -- Nitrogen -- Potassium -- Calcium -- Magnesium -- Sulfur -- Sensing of macronutrient limitations -- Phosphorus -- Nitrogen -- Potassium -- Calcium -- Sulfur -- Local and systemic signaling of macronutrient limitations -- Phosphorus -- Nitrogen -- Potassium -- Calcium -- Magnesium -- Sulfur -- Conclusion and future perspectives -- References -- Chapter 4 - The significance of nutrient interactions for crop yield and nutrient use efficiency -- Introduction -- Nutrient interactions and crop production -- Excess fertilization versus optimal fertilization -- Understanding nutrient interactions in plants to improve NUE and decrease environmental footprints -- Nutrient interactions in plants -- Synergisms and antagonisms between nutrients caused by ionic charge -- Regulatory interactions -- Metabolic interactions -- Interactive effects on root morphology -- Promising crop traits to improve overall NUE -- Nutrient uptake efficiency versus nutrient utilization efficiency -- Increased storage capacity and remobilization efficiency -- Efficient recycling and allocation to yield organ -- Root system architecture -- Effective utilization of increased atmospheric CO2 -- Conclusions -- References -- Chapter 5 - The contribution of root systems to plant nutrient acquisition -- Introduction -- Macronutrient localization and mobility. , Methods to analyze the root system architecture response to soil nutrients -- Root system architecture in response to soil nutrients -- Root system morphology and anatomy that contribute to advantageous nutrient foraging -- Genetic regulation of root system architecture changes in response to soil nutrients -- Integration of nutrient signals -- Conclusions -- Acknowledgments -- References -- Chapter 6 - Molecular genetics to discover and improve nitrogen use efficiency in crop plants -- Introduction -- NUE defined -- Strategies to improve NUE -- Increasing uptake efficiency -- Increasing uptake capacity -- Changing root morphology -- Increasing utilization efficiency -- Modifying specific leaf N -- Delayed senescence (stay green) -- Increasing remobilization efficiency -- Genetic approaches to improve NUE -- Identifying genotypic variation for NUE -- Discovering genetic loci for NUE -- Improving crop NUE using genetic information -- Transgenic approaches to improve NUE -- Targeted approach to improve NUE -- Improvement of the biotech approaches -- Future prospects -- References -- Chapter 7 - The role of root morphology and architecture in phosphorus acquisition: physiological, genetic, and molecular basis -- Introduction -- Molecular basis of RSA as a mechanism enhancing P acquisition -- The role of miRNAs in RSA and P acquisition -- Does miR399 plays a role in enhancing P uptake via modulation of RSA? -- Other miRNAs potentially involved in RSA changes in response to P -- QTL for root traits under P deficiency consistently affecting yield performance in the field -- Novel root system imaging methods and their use to investigate the role of RSA in improving P acquisition efficiency -- Conclusions -- References -- Chapter 8 - Potassium sensing, signaling, and transport: toward improved potassium use efficiency in plants -- Introduction. , Potassium transport mechanisms -- Regulatory components -- Regulatory components of K+ transport -- Regulatory components of K+ deficiency signaling -- Strategies to improve K use efficiency in plants -- Increasing K availability in plants -- Increased plant root surface to secure greater access to K in soils -- Improve the efficiency of K+ uptake and translocation in planta -- Conclusions -- References -- Chapter 9 - Understanding calcium transport and signaling, and its use efficiency in vascular plants -- Introduction -- Calcium deficiency in plants -- Calcium uptake and distribution -- Calcium uptake by roots and delivery to the xylem -- Calcium transport to the shoot -- Calcium as a signal -- Channels involved in calcium influx and signaling -- Cyclic nucleotide-gated channels -- Glutamate-like receptors -- Transporters involved in calcium efflux and signaling -- Cation/H+ exchangers -- Autoinhibited Ca2+-ATPase proteins -- Calcium sensor proteins and their involvement in plant stress responses -- Calmodulins and calmodulin-like proteins -- Calcineurin B-like proteins -- Calcium-dependent protein kinases -- Calcium use efficiency in plants -- Conclusions -- References -- Chapter 10 - The role of calcium in plant signal transduction under macronutrient deficiency stress -- Introduction -- Calcium in plants -- Membrane calcium transporters -- Calcium signatures and memory -- Calcium-binding proteins -- Role of calcium in macronutrient deficiency -- Potassium -- Transcriptional regulation -- Protein modification -- Nitrate -- Magnesium -- Conclusions and future perspectives -- References -- Chapter 11 - Magnesium homeostasis mechanisms and magnesium use efficiency in plants -- Introduction -- Morphogenesis remodeling by Mg imbalance and the mechanisms in plants -- Mg deficiency -- Mg toxicity -- Mg2+ transporters and Mg homeostasis in plant cells. , Imbalance of Mg homeostasis in plants -- Imbalance of Mg homeostasis by some stress factors -- Imbalance of Mg homeostasis by some ions -- Signaling of Mg stresses in plants -- Mg deficiency -- Mg toxicity -- Genomic perspectives of Mg stresses in plants -- Strategies for Mg use efficiency in plants -- Conclusions -- References -- Chapter 12 - Advances in understanding sulfur utilization efficiency in plants -- Introduction -- Sulfur is an essential mineral nutrient -- Sulfur in agriculture -- Why study sulfur use efficiency? -- Sulfate transport and mobilization -- High-affinity sulfate transporters responsible for uptake efficiency -- Sulfate transporters mediate efficient sulfate translocation -- Regulation and sensing -- Regulation of the sulfur starvation response -- Sulfate transporter may be a sulfur sensor -- Sulfur mobilization from stored reserves -- Glucosinolate homeostasis: management of the plant sulfur budget -- Glutathione homeostasis: management of the plant sulfur budget -- The prospects of using genetic manipulation to increase S use efficiency -- Conclusions -- References -- Chapter 13 - Water availability and nitrogen use in plants: effects, interaction, and underlying molecular mechanisms -- Introduction -- Impact of water and N interaction on crop physiology -- Effects of water availability on biological N fixation in plants -- The interplay between soil water availability and N supply -- Mechanism of water and N uptake in plants -- Molecular mechanism of the interaction between water and N uptake -- Approaches to improve NUE in water constrained environments -- Agronomic practices -- Genetic improvement of water and N-related traits -- Stay green -- Root traits -- Conclusions and future research -- Acknowledgment -- References -- Chapter 14 - NPK deficiency modulates oxidative stress in plants -- Introduction. , Reactive oxygen species and their origins.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Munksgaard International Publishers
    Physiologia plantarum 125 (2005), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: SULTR2;1 is a low-affinity sulfate transporter expressed in the vascular tissues of roots and leaves for interorgan transport of sulfate in Arabidopsis thaliana. Transgenic Arabidopsis carrying a fusion gene construct of SULTR2;1 5′-promoter region and β-glucuronidase coding sequence (GUS) demonstrated that within the reproductive tissues, SULTR2;1 is specifically expressed in the bases and veins of siliques and in the funiculus, which connects the seeds and the silique. The antisense suppression of SULTR2;1 mRNA caused decrease of sulfate contents in seeds and of thiol contents both in seeds and leaves, as compared with the wildtype (WT). The effect of antisense suppression of SULTR2;1 on seed sulfur status was determined by introducing a sulfur-indicator construct, p35S::βSRx3:GUS, which drives the expression of GUS reporter under a chimeric cauliflower mosaic virus 35S promoter containing a triplicate repeat of sulfur-responsive promoter region of soybean β-conglycinin β subunit (βSRx3). The mature seeds of F1 plants carrying both the SULTR2;1 antisense and p35S::βSRx3:GUS constructs exhibited significant accumulation of GUS activities on sulfur deficiency, as compared with those carrying only the p35S::βSRx3:GUS construct in the WT background. These results suggested that SULTR2;1 is involved in controlling translocation of sulfate into developing siliques and may modulate the sulfur status of seeds in A. thaliana.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden , USA : Munksgaard International Publishers
    Physiologia plantarum 120 (2004), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The N-terminal amino-acid sequence was determined for a major rice phloem protein with a molecular mass of 31 kDa, named RPP31. The corresponding full-length rice EST-clone was cloned based on the amino acid sequence. The predicted total amino-acid sequence of RPP31 shared high similarity with plant glutathione S-transferases (GSTs). Recombinant RPP31 produced in Escherichia coli and rice phloem sap showed GST activity. Immunocytological analysis indicated that RPP31 is localized in the phloem region of leaves. In mature leaves, the signal was restricted to sieve element–companion cell complexes, and was stronger in sieve elements than in companion cells. Although some plant GSTs are known to be induced by xenobiotics, the amount of RPP31 was not affected by treatments with an herbicide, pretilachlor, and/or its safener, fenclorim. These results suggest that RPP31 is an active GST restricted to the phloem region of normal rice leaves.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Boron deficiency hampers the productivity of 132 crops in more than 80 countries. Boron is essential in higher plants primarily for maintaining the integrity of cell walls and is also beneficial and might be essential in animals and in yeast. Understanding the molecular mechanism(s) of boron ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Physiologia plantarum 114 (2002), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 1L-myo-inositol-1-phosphate [Ins(1)P1] synthase (EC 5.5.1.4) catalyses the formation of Ins(1)P1 from glucose-6-phosphate, the first step in the biosynthesis of myo-inositol. Ins(1)P1 is a precursor of phytin (inositol hexakisphosphate), a storage form of phosphate and cations in seeds. Since sucrose and abscisic acid (ABA) are known to affect synthesis of storage compounds in seeds, we investigated the effects of ABA and sucrose on Ins(1)P1 synthase gene (RINO1) expression in cultured cells derived from the scutellum of mature rice seeds. Higher levels of RINO1 transcript accumulation were evident after treatment with either sucrose (10–100 mM) or ABA (10−8M to 10−4M). Glucose was also effective in the upregulation, whereas mannitol was not, suggesting that sucrose and glucose acted as metabolizable sugars and not as osmotica. Treatment with ABA and sucrose together resulted in much higher levels of transcript accumulation, suggesting a synergistic induction of the Ins(1)P1 synthase gene.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Nodulated (T202) and non-nodulated (T201) isolines of soybean (Glycine max [L.] Merr.) were cultivated in a rotated paddy field in Niigata, Japan. The pods, and seeds were harvested at 7-day intervals until maturity, and the subunit compositions of seed storage proteins were analyzed by SDS-PAGE. The β-subunit of β-conglycinin could scarcely be detected in the non-nodulated isoline, T201, at any period throughout seed development, although it was a major component in T202. The accumulation of α′- and α-subunits of β-conglycinin, together with the acidic and basic subunits of glycinin, appeared about one week later in seeds of T201 than in those of T202, perhaps due to a shortage of nitrogen and growth retardation. Northern hybridization could not detect the β-subunit mRNA in immature T201 seeds, while it was pronounced in T202. These results indicate that the suppression of the β-subunit in the non-nodulating isoline T201 is regulated at the level of mRNA accumulation. The α′(α)-subunit mRNAs were actively expressed in both isolines. Total nitrogen concentration was consistently lower in T201 than T202. No significant difference was observed in either the free amino acid or ureide concentrations in seeds, although the concentration of sucrose was considerably lower in T201 seeds and pods compared with T202. This result indicates the possibility that β-subunit accunmlation was regulated not only directly by total nitrogen concentration but also by carbohydrate concentrations.Nitrogen regulation of storage protein subunit levels of soybean seed were evaluated using T201 and T202. Greenhouse-grown plants were subjected to different levels and timing of nitrate treatments. The culture solution (2, 5 or 10 mM NO3–was supplied from flowering, 42 days after planting (DAP), until maturation (137 DAP), or switched from 2 to 10 mM, or from 10 to 2 mM at 61 DAP. With a continuous 2 mM NO3–treatment, seed dry weight and N concentration of the T201 plants were significantly lower than those in the T202 plants due to the lack of N2 fixation by the non nodulated T201 plants. However, when adequate NO3 was supplied, N concentration and dry weight were similar in T201 and T202 seeds. When 5 mM NO3 was supplied, the subunit proportion of the seed storage protein was similar in non-nodulating and nodulating isolines. On the other hand, when plants received a low level of NO3 (2 mM), the β-conglycinin proportion was lower in T201 than in T2O2. Furthermore, in the nodulating T202 plants treated with 10 mM NO3–the proportion of β-conglycinin increased markedly.The results indicate that non-nodulated T201 has a normal, non-defective, β-subunit gene and that limited N availability decreases accumulation of β-conglycinin, whereas high N availability increases the proportion of β-conglycinin in soybean seeds, irrespective of whether N was derived from N2 fixation or from NO3 absorption.
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 448 (2007), S. 209-212 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Silicon is an important nutrient for the optimal growth and sustainable production of rice. Rice accumulates up to 10% silicon in the shoot, and this high accumulation is required to protect the plant from multiple abiotic and biotic stresses. A gene, Lsi1, that encodes a silicon influx ...
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 9 (1991), S. 602-606 
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The soybean 7S seed storage protein, β-conglycinin, is comprised of three major subunits, α′, α, and β. Chimeric genes having β-conglycinin α′ and β subunit promoters and the β-glucuronidase gene coding sequence were constructed and electroporated into protoplasts prepared from three cultured cell lines and from tobacco mesophyll cells. The β-conglycinin promoters were active in all protoplasts examined, and their activities were 10–60% of that of the cauliflower mosaic virus 35S promoter. In electroporated protoplasts isolated from tobacco suspension cultures the time course of expression and the pattern of cell cycle dependency of the β-conglycinin promoters were similar to those of the 35S promoter. The responses to exogenously added L-methionine and abscisic acid, which are known to have differential effects on the expression of β-conglycinin promoters in cultured soybean cotyledons, were essentially the same among the promoters used. The results indicate that β-conglycinin promoters are expressed in electroporated protoplasts, but their regulation is relaxed.
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  • 10
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Tobacco plants were transformed with derivatives of a binary vector pMON505 and two kanamycin resistant lines that were nopaline positive were selected for second transformation. The plasmids used for the second transformation were derivatives of pMON850 which carries the nopaline synthase gene in addition to a gene for gentamicin resistance. Insertion of each transgene was confirmed by Southern hybridization. Surprisingly, we found that more than 50% of the doubly transformed tobacco plants were nopaline negative. Tobacco plants that were transformed only by the second vector exhibited nopaline accumulation. DNA methylation patterns at the HpaII site in the promoter region of the nopaline synthase gene did not correlate with the nopaline phenotype. In some plant lines, seedlings of the R1 generation which segregated out the second T-DNA insertion recovered the nop+ phenotype. These results indicate that nopaline accumulation was inhibited by the presence of the second T-DNA.
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