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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Photosynthesis. ; Sulfur--Metabolism. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (538 pages)
    Edition: 1st ed.
    ISBN: 9781402068638
    Series Statement: Advances in Photosynthesis and Respiration Series ; v.27
    DDC: 572.46
    Language: English
    Note: Hell_FM.pdf -- Hell_CP.pdf -- Hell_Ch01.pdf -- Hell_Ch02.pdf -- Hell_Ch03.pdf -- Hell_Ch04.pdf -- Hell_Ch05.pdf -- Hell_Ch06.pdf -- Hell_Ch07.pdf -- Hell_Ch08.pdf -- Hell_Ch09.pdf -- Hell_Ch10.pdf -- Hell_Ch11.pdf -- Hell_Ch12.pdf -- Hell_Ch13.pdf -- Hell_Ch14.pdf -- Hell_Ch15.pdf -- Hell_Ch16.pdf -- Hell_Ch17.pdf -- Hell_Ch18.pdf -- Hell_Ch19.pdf -- Hell_Ch20.pdf -- Hell_Ch21.pdf -- Hell_Ch22.pdf -- Hell_Ch23.pdf -- Hell_Ch24.pdf -- Hell_Index.pdf -- Hell_BM.pdf.
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  • 2
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Plants--Effect of metals on. ; Plants--Nutrition. ; Cytology. ; Metals--metabolism. ; Plant Physiological Phenomena. ; Plant Cells. ; Cytologie. swd. ; Metall. swd. ; Nährstoff. swd. ; Pflanzenzelle. swd. ; Aufsatzsammlung.2swd. ; Electronic books.
    Description / Table of Contents: This review of the latest on function and metabolism of metal sand nutrients reaches into cellular physiology. It highlights aspects of homeostasis and sensing, signaling and regulation, and it draws parallels to other organisms, including humans.
    Type of Medium: Online Resource
    Pages: 1 online resource (311 pages)
    Edition: 1st ed.
    ISBN: 9783642106132
    Series Statement: Plant Cell Monographs ; v.17
    DDC: 571.6
    Language: English
    Note: Intro -- Role of Boron in Plant Growth and its Transport Mechanisms -- Introduction: Specialty of B -- Physiological Significance of B -- B Essentiality in Plants and Animals -- B Deficiency and Toxicity Symptoms in Plants -- RG-II-B in Cell Wall and its Requirement for Plant Growth -- Chemical Properties of B: Possible Binding Sites of B in Cell -- Identification of RG-II-B Complex in Plant Cell Walls -- Synthesis of RG-II and Physiological Roles of RG-II -- A. thaliana MUR1 for Fucose Synthesis Essential for Efficient Formation of dRG-II-B -- NpGUT1, Glucuronyltransferase 1, for Cell Adhesion and Attachment -- Changes in RG-II Properties in Response to B Nutrition -- Molecular Mechanism of B Transport in Plants -- Passive Diffusion -- Channel-mediated B Transport for Facilitation -- A. thaliana NIP5 -- 1, A Channel for Boric Acid for B Uptake Under B Limitation -- A. thaliana NIP6 -- 1, for Preferential Distribution of B into Growing Shoot Tissues -- Active B Transport System Under Limited Supply of B -- A. thaliana BOR1, the First Borate Transporter Identified in the Biological Systems -- BOR1 Degradation Via Endocytosis in Response to High B Supply -- Active B Transport System Under Toxic Level of B -- Cellular B Distribution Under Adequate and Toxic Level of B -- BOR1 Homologs Involved in High B Tolerance Through B Efflux in Plants -- Retranslocation of B -- B Transport Mechanisms in Yeast and Mammals -- Function of a BOR1 Homolog in S. cerevisiae -- Function of a BOR1 Homolog in Animals -- Conclusions and Foresights -- References -- Calcium: Not Just Another Ion -- Introduction -- Nutritional and Structural Functions of Ca2+ -- Nutritional Functions of Ca2+ -- Structural Functions of Ca2+ -- The Evolution of Ca2+ as a Signaling Molecule -- Calcium Release in Response to Signals and Stimuli. , Calcium Responses to Abiotic, Biotic Factors and Development -- Calcium Responses to Hormones -- Interconnection of Ca2+ Dynamics with other Second Messengers -- Organelles and Ca2+ -- Calcium Signaling within the Nucleus -- Calcium Regulation by the ER -- Mitochondrial Calcium Dynamics -- The Role of Chloroplasts in Cellular Calcium Homeostasis -- Channels and Transporters shaping Ca2+ Signals -- Influx of Ca2+ -- Voltage Dependent Channels -- Ligand Gated Channels -- Vacuolar and ER Ca2+ Channels -- Efflux of Calcium -- Calcium-Proton Antiporter -- Phosphorylated-type ATPases -- Signal Response Coupling of Calcium -- Differences in Salt and Mannitol Responses -- Differences in Symbiotic Calcium Responses -- Calcium Binding Proteins -- Calmodulin -- CDPKs -- CBLs and CIPKs -- Conclusions -- References -- Cell Biology of Copper -- Introduction -- Functions of Cu Proteins in Plants -- Plastocyanin -- Cytochrome c Oxidase -- Cu/Zn Superoxide Dismutase -- Ethylene Receptors -- Phytocyanins -- Laccase and Ascorbate Oxidase -- Polyphenol Oxidase -- Amine Oxidase -- Other Roles of Cu in Plants -- Cu Movement in and out of Root Cells -- Cu Uptake -- Cu Export and Intercellular Reallocation -- Root to Shoot Cu Translocation -- Excess Cu -- Intracellular Cu Delivery to Cu Protein Targets -- Chloroplast: Cu Import into the Chloroplast -- Delivery of Cu to other Compartments -- Mitochondria -- Endomembrane and Secretory Pathway -- Senescence, Reallocation, and Delivery to Reproductive Tissues -- Regulation of Copper Homeostasis -- Transcription Factors -- The Cu microRNAs -- Overview -- References -- Iron -- Introduction -- The Reduction Strategy -- The Chelation Strategy -- Regulation of the Reduction Strategy -- Regulation of the Chelation Strategy -- Fe Transport within the Plant -- Intercellular Fe Transport -- Citrate -- Nicotianamine. , Iron Transport Protein (ITP) -- Subcellular Fe Transport -- Vacuoles -- Chloroplasts -- Mitochondria -- References -- Dissecting Pathways Involved in Manganese Homeostasis and Stress in Higher Plant Cells -- Introduction -- Importance of Mn in Plants and Consequences of Mn Deficiency and Excess -- Uptake, Distribution and Detoxification -- Uptake into the Cell -- Subcellular Compartmentalisation -- The Role of CAX (Cation Exchanger) Transporters and the MTP (Metal Tolerance Protein) Family of Transporters -- The Role of Natural Resistance Associated Macrophage Protein Transporters -- Role of P-type ATPases -- ECA3 -- ECA1 and LCA1P-type ATPase -- Long-Distance Transport and Seed Loading -- Are There Transporters Yet to be Identified? -- Chaperones for Mn? -- Homeostasis and Aspects of Sensing, Signalling and Regulation -- Conclusions and Future Directions -- References -- Cell Biology of Molybdenum -- Introduction -- Molybdenum Uptake into Cells -- The Molybdenum Cofactor -- Molybdenum Cofactor Biosynthesis -- Step 1: Conversion of GTP into cPMP -- Step 2: Synthesis of Molybdopterin -- Step 3: Adenlyation of Molybdopterin -- Step 4: Molybdenum Insertion into Molybdopterin and Crosstalk to Copper Metabolism -- Allocation of the Molybdenum Cofactor -- Storage and Transfer of the Molybdenum Cofactor -- Insertion of the Molybdenum Cofactor into Molybdenum Enyzmes -- Micro-Compartmentalization and Cytoskeleton Binding -- Molybdenum Enzymes -- Xanthine Dehydrogenase -- Aldehyde Oxidase -- Sulfite Oxidase -- Nitrate Reductase -- Mitochondrial Amidoxime Reducting Component -- Posttranslational Sulfuration of Xanthine Oxidase Family-Enzymes -- Crosstalk between Molybdenum and Iron Metabolism -- Conclusion -- References -- Cellular Biology of Nitrogen Metabolism and Signaling -- Introduction -- Distribution of N Forms in Plant Cells -- N in Different Tissues. , N Cellular Distribution -- N Fluxes Within a Plant Cell -- Nitrate and Nitrite Fluxes -- Ammonium Fluxes -- Urea Transport -- Organic N Transport -- N Assimilation Pathways -- N Assimilation -- N Remobilization -- Regulation of N Uptake and Metabolism -- Regulation at the mRNA Level -- Regulation at the Protein Level -- N- Signaling: Nitric Oxide - A Special Case -- Sources for NO in Plants -- Mechanisms Through Which NO Affects Targets -- Conclusion -- References -- Phosphorus: Plant Strategies to Cope with its Scarcity -- Introduction -- Phosphorus is Needed to Sustain Life -- The Phosphorus Paradox -- Phosphorus is Necessary for Plant Welfare -- Phosphorus: Its Limited Availability -- Phosphorus in Soil -- Phosphorus Availability: Economical and Environmental Problems -- Pi Uptake and Transport by Plants -- Pi Uptake and Translocation in Whole Plant -- Pi Transporters in Plants -- The Plant Phosphate Starvation Response -- Biochemical Adaptations of Phosphate Starved Plants -- Gathering and Recycling Phosphorus from Organic Pi Pool -- Solubilizing Phosphorus from Inorganic Pi Pool -- Increasing the Pi Uptake Ratio and Translocation -- Physiological Changes -- Morphological Adaptations of Phosphate-Starved Plants -- Pi Can Modify Post-Embrionary Root Development -- RH Formation -- Root System Architecture -- Interaction with Other Organisms -- Regulation and Signaling Mechanisms of Phosphate Starvation -- Phosphate Starvation Response, a Coordinate Mechanism -- Is There a Plant Pho Regulon? -- Sensing Pi Status -- Transcriptional Factors Involved in Phosphate Starvation -- Phosphate Homeostasis -- Signaling Pathway of Phosphate Starvation Dependent of PHR1, PHO2, and MicroRNA399 -- The Role of Sugars in Phosphate Starvation -- The Role of Plant Hormones in the Regulation of Phosphate Starvation Response -- Conclusions -- References -- Potassium. , Potassium is an Essential Mineral Element -- Physiological Functions of Potassium -- Symptoms of Potassium Deficiency -- Acclimatory Responses to Potassium Starvation -- The Acquisition and Cellular Distribution of Potassium -- Potassium Acquisition by Plant Roots -- Thermodynamic Consideration of K+ Uptake and Distribution in Root Cells -- Cellular K+ Homeostasis -- Potassium Transport Within the Plant -- The Molecular Biology of K+ Transporters -- Summary -- References -- Selenium Metabolism in Plants -- Introduction -- Metabolism of Se -- From Selenate to Selenocysteine -- From Selenocysteine to Other Selenocompounds -- Genetic Engineering of Plant Se Metabolism -- Results Obtained from Various Transgenic Approaches -- Obtained Insight into Rate-controlling Steps and Se Detoxification Mechanisms -- Testing the Potential of the Transgenics for Phytoremediation, and as Fortified Foods -- New Insights into Plant Se Responses and Tolerance Mechanisms -- Results Using the Model Nonaccumulator Species Arabidopsis thaliana -- Results Using Se Hyperaccumulators and Related Nonhyperaccumulators -- Ecological Aspects of Plant Se Accumulation -- Contribution of Microbes to Se Uptake and Volatilization -- Effects of Plant Se on Ecological Partners -- Conclusions and Future Prospects -- References -- Cellular Biology of Sulfur and Its Functions in Plants -- Sulfur is an Essential Mineral Element -- Physiological Functions of Sulfur -- Symptoms of Sulfur Deficiency -- Acclimatory Responses to Sulfur Starvation -- The Acquisition and Allocation of Sulfur Compounds -- Sulfate Acquisition by Plant Roots -- Whole Plant Allocation of Sulfur Compounds -- Cellular Distribution of Sulfur-containing Compounds -- Reductive Sulfate Assimilation -- Subcellular Organization of Reactions -- Signal Mechanisms and Homeostasis of Uptake and Reductive Assimilation. , Regulation of Sulfur Amino Acids Biosynthesis.
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  • 3
    Book
    Book
    Dordrecht : Springer
    Keywords: Photosynthesis ; Sulfur Metabolism ; Photosynthese ; Schwefelstoffwechsel
    Type of Medium: Book
    Pages: XXXI, CP1- CP4, 516 S , Ill., graph. Darst
    ISBN: 9781402068621 , 140206862X
    Series Statement: Advances in photosynthesis and respiration 27
    RVK:
    Language: English
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  • 4
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The amino acid nicotianamine (NA) is essential for micronutrient metabolism in plants. Lack of NA results in a chlorotic phenotype and oxidative stress, since NA is a chelator of iron and other metal nutrients. To investigate the precise cellular function of NA in micronutrient transport and homeostasis, a protocol for the production of [14C]-labelled NA was developed. Recombinant NA synthase was used to generate [14C]-NA from [14C]-S-adenosylmethionine. After purification by solid-phase ion exchange about 66% yield was achieved. The identity of the [14C]-NA with chemically synthesized NA was demonstrated by several independent methods, including two TLC systems, two HPLC systems and immuno-detection. Moreover, biological function was shown by complementation of the Lycopersicon esculentum mutant chloronerva that is free of NA due to a defect in NA synthase. Proof-of-function for the produced [14C]-NA as a suitable tool for transport studies was provided monitoring the distribution of [14C]-NA after feeding to tomato and Ricinus communis seedlings.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2048
    Keywords: Key words: Amino acid – Glutamine synthetase – Nitrate assimilation – Nitrate reductase –Nicotiana (sulfur-deprivation) – Sulfur-deprivation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract.  Tobacco (Nicotiana tabacum L.) plants were subjected to a prolonged period of sulfur-deprivation to characterize molecular and metabolic mechanisms that permit control of primary N-metabolism under these conditions. Prior to the appearance of chlorotic lesions, sulfur-deprived tobacco leaves showed a strong decrease in the sulfate content and changes in foliar enzyme activities, mRNA accumulation and amino-acid pools. The basic amino acids glutamine, asparagine and arginine accumulated in the leaves of sulfur-deprived plants, while the foliar concentrations of aspartate, glutamate, serine or alanine remained fairly unchanged. Maximal extractable nitrate reductase (NR; EC 1.6.6.1) activity decreased strongly in response to sulfur-deprivation. The decrease in maximal extractable NR activity was accompanied by a decline in NR transcripts while the mRNAs of the plastidic glutamine synthetase (EC 6.1.3.2) or the β-subunit of the mitochondrial ATP synthase were much less affected. Nitrate first accumulated in leaves of tobacco during sulfur-deprivation but then declined. An appreciable amount of nitrate was, however, present in severely sulfur-depleted leaves. The repression of NR gene expression is, therefore, not related to the decrease in the leaf nitrate level. However, glutamine- and/or asparagine-mediated repression of NR gene transcription is a possible mechanism of control in situations when glutamine and asparagine accumulate in leaves and provides a feasible explanation for the reduction in NR activity during sulfur-deprivation. The removal of reduced nitrogen from primary metabolism by redirection and storage as arginine, asparagine or glutamine combined with the down-regulation of nitrate reduction via glutamine- and/or asparagine-mediated repression of NR gene transcription may contribute to maintaining a normal N/S balance during sulfur-deprivation and indicate that the co-ordination of N- and S-metabolism is retained under these conditions.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2048
    Keywords: Cell suspension culture ; λ-Glutamylcysteine synthetase ; Glutathione synthesis ; Nicotiana (Glutathione synthesis)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract λ-Glutamylcysteine synthetase activity (EC 6.3.2.2) was analysed in Sephacryl S-200 eluents of extracts from cell suspension cultures ofNicotiana tabacum L. cv. Samsun by determination of λ-glutamylcysteine as its monobromobimane derivative. The enzyme has a relative molecular mass (Mr) of 60000 and exhibits maximal activity at pH 8 (50% at pH 7.0 and pH9.0) and an absolute requirement for Mg2+. With 0.2mM Cd2+ or Zn2+, enzyme activity was reduced by 35% and 19%, respectively. Treatment with 5 mM dithioerythritol led to a heavy loss of activity and to dissociation into subunits (Mr 34000). Buthionine sulfoximine andl-methionine-sulfoximine, known as potent inhibitors of λ-glutamylcysteine synthetase from mammalian cells, were found to be effective inhibitors of the plant enzyme too. The apparent Km values forl-glutamate,l-cysteine, and α-aminobutyrate were, respectively, 10.4mM, 0.19 mM, and 6.36 mM. The enzyme was completely inhibited by glutathione (Ki=0.42 mM). The data indicate that the rate of glutathione synthesis in vivo may be influenced substantially by the concentration of cysteine and glutamate and may be further regulated by feedback inhibition of λ-glutamylcysteine synthetase by glutathione itself. λ-Glutamylcysteine synthetase is, like glutathione synthetase, localized in chloroplasts as well as in the cytoplasm. Chloroplasts fromPisum sativum L. isolated on a Percoll gradient contained about 72% of the λ-glutamylcysteine synthetase activity in leaf cells and 48% of the total glutathione synthetase activity. In chloroplasts ofSpinacia oleracea L. about 61% of the total λ-glutamylcysteine synthetase activity of the cells were found and 58% of the total glutathione synthetase activity. These results indicate that glutathione synthesis can take place in at least two compartments of the plant cell.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-2048
    Keywords: Key words:Arabidopsis (stm mutant) ; Gas exchange ; Gene expression ; Glutamine synthetase ; Mutant (Arabidopsis ; stm) ; Photorespiration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The regulation by photorespiration of the transcript level corresponding to plastidic glutamine synthetase (GS-2) was investigated in the leaves of Arabidopsis thaliana (L.) Heynh.. Photorespiration was suppressed by growing the plants in an atmosphere containing 300 Pa CO2. Suppression of photorespiration was demonstrated by the ability of the conditionally lethal serine hydroxymethyltransferase (SHMT)-deficient stm mutant of A. thaliana to grow normally under these conditions. In contrast to previous studies with bean or pea that were performed at very high CO2 partial pressure (2–4 kPa; Edwards and Coruzzi, 1989, Plant Cell 1: 241–248; Cock et al., 1991, Plant Mol Biol 17: 761–771), suppression of photorespiration during growth of A. thaliana in an atmosphere with 300 Pa CO2 had no effect on the leaf GS-2 transcript level. In the short term, neither suppression of photorespiration induced by the transfer of air-grown A. thaliana plants into a CO2-enriched atmosphere, nor an increase in the rate of photorespiration achieved by the transfer of high-CO2-grown A. thaliana plants into air resulted in a change in the GS-2 mRNA level. The absence of photorespiratory ammonium release in leaves of the stm mutant had no effect on the GS-2 transcript level. Overall, our data argue against a control by photorespiration of the A. thaliana leaf GS-2 mRNA pool. In contrast, regulation of the leaf SHMT mRNA level may involve a negative feedback effect of at least one metabolite derived from the glycine/serine conversion during photorespiration, as indicated by the overexpression of SHMT transcripts in the leaves of the stm mutant.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Planta 202 (1997), S. 138-148 
    ISSN: 1432-2048
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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