Slow fluorescence quenching of type A chloroplasts. Resolution into two components.

The divalent-cation-specific ionophore A23187 is used to define two components of the slow fluorescence quenching of type a spinach chloroplasts: ionophore-reversible and ionophore-resistant quenching. Ionophore-reversible quenching predominates at relatively low light intensities and approaches saturation as light levels are increased. It is sensitive to uncouplers and to 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) and is dark reversible. At high light intensities the bulk (greater than 80%) of slow fluorescence quenching is ionophore-resistant. Ionophore-resistant quenching is stimulated by carbonyl cyanide m-chlorophenyl hydrazone (CCCP) at pH 7.6 and by both CCCP and methylamine at pH 9.0. It is insensitive to DCMU and is not reversed in subsequent darkness. Taken together, the two components account for all quenching observed in Type A chloroplasts. Ionophore-reversible quenching is identified with the Mg2+-mediated fluorescence quenching described by Krause (Biochim. Biophys. Acta (1974) 333, 301-313) and by Barber and Telfer (in Membrane Transport in Plants (Dainty, J., AND Zimmermann, U., eds.), pp. 281-288, Springer-Verlag, Berlin, 1974). Ionophore-resistant quenching, a first-order process requiring high light, resembles the quenching reported by Jennings et al. (Biochim. Biophys. Acta (1976) 423, 264-274). The resolution of the fluorescence quenching phenomenon into two distinct components reconciles the apparently contradictory observations of these earlier investigations.     

Slow fluorescence quenching of Type A chloroplasts. Resolution into two components

The divalent-cation-specific ionophore A23187 is used to define two components of the slow fluorescence quenching of type a spinach chloroplasts: ionophore-reversible and ionophore-resistant quenching. Ionophore-reversible quenching predominates at relatively low light intensities and approaches saturation as light levels are increased. It is sensitive to uncouplers and to 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) and is dark reversible. At high light intensities the bulk (> 80%) of slow fluorescence quenching is ionophore-resistant. Ionophore-resistant quenching is stimulated by carbonyl cyanide m-chlorophenyl hydrazone (CCCP) at pH 7.6 and by both CCCP and methylamine at pH 9.0. It is insensitive to DCMU and is not reversed in subsequent darkness. Taken together, the two components account for all quenching observed in Type A chloroplasts.Ionophore-reversible quenching is identified with the Mg²⁺-mediated fluorescence quenching described by Krause (Biochim. Biophys. Acta (1974) 333, 301–313) and by Barber and Telfer (in Membrane Transport in Plants (Dainty, J., and Zimmermann, U., eds.), pp. 281–288, Springer-Verlag, Berlin, 1974). Ionophore-resistant quenching, a first-order process requiring high light, resembles the quenching reported by Jennings et al. (Biochim. Biophys. Acta (1976) 423, 264–274).The resolution of the fluorescence quenching phenomenon into two distinct components reconciles the apparently contradictory observations of these earlier investigations.     

Cyclic AMP and the plasma membrane potential in Neurospora crassa.

Diverse treatments, which have been shown by Slayman, C. L. (1977) in Water Relations in Membrane Transport in Plants and Animals (Jungreis, A., Hodges, T. K., Kleinzeller, A., and Schultz, S. G., eds) pp. 69-86, Academic Press, New York, to depolarize the plasma membrane of Neurospora, increase levels of adenosine 3':5'-monophosphate (cyclic AMP) in the organism. The treatments include those producing large transport fluxes of metabolizable or nonmetabolizable compounds, rapid temperature drops, and addition of agents which uncouple oxidative phosphorylation. Severe mechanical stress, which may also act to depolarize the plasma membrane, leads to increases in cyclic AMP. The maximal depolarization appears to precede the maximal cyclic AMP levels. It is proposed that the membrane depolarization produces the increased cyclic AMP levels by stimulating the plasma membrane-bound adenylate cyclase and that cyclic AMP may be important to the maintenance of membrane integrity.     

May the proton motive force be with you: A plant transporter review

As our ecosystems experience challenges associated with climate change, an improved understanding of the fundamental biochemical processes governing plant physiology is needed. Strikingly, current structural information on plant membrane transporters is severely limited compared to other kingdoms of life, with only 18 unique structures in total. To advance future breakthroughs and insight in plant cell molecular biology, structural knowledge of membrane transporters is indispensable.This review summarizes the current status of structural knowledge in the plant membrane transporter field. Plants utilize the proton motive force (PMF) to drive secondary active transport. We discuss the PMF, how it relates to secondary active transport and provide a classification of PMF driven secondary active transport, discussing recently published structures of symporters, antiporters, and uniporters from plants.     

Assimilate Transport and Partitioning in Plants: Approaches,Methods, and Facets of Research

This review, dedicated to the 100th anniversary of A.L. Kursanov's date of birth, considers the development of phloem transport studies since his book, Assimilate Transport in the Plant, was published in 1976. This book and several other fundamental publications on phloem structure and functions basically shaped this physiological issue; as a result, several international meetings by scientists working in the area were induced, and the proceedings of these meetings were published at regular intervals. Six conferences have been held to date, and six corresponding collections of papers have been published and are reviewed here along with other experimental communications and reviews. This review considers the following topics: (1) the phloem structure and the ultrastructure of specialized phloem cells, (2) the physiological functions of phloem and their regulation, (3) photosynthesis and phloem loading with assimilates, (4) phloem unloading and the related processes of plant growth and development, (5) the mechanisms of sugar and amino acid transport, (6) the levels of transport, (7) transport compartments; (8) xylem–phloem and symplast–apoplast communication; (9) phloem transport vs. the integral plant physiology, (10) transport of xenobiotics, and (11) the trophic transport networks in symbionts.     

Progress, spread and natural transmission of Bahia bark scaling of citrus in Brazil

Progress, spread and natural transmission of Bahia bark scaling of citrus were evaluated in a trial where 240 screenhouse‐nursed nucellar grapefruit plants –‘Clason’, ‘Little River Seedless’, ‘Red Blush’, ‘Reed’ and ‘Howell Seedless’ cvs – were planted alongside and 5 m apart from a 10‐year‐old symptomatic ‘Marsh Seedless’ grapefruit orchard. Plants were distributed in 16 rows of 15 trees, with three plants of each cultivar per row. Eight trial plants were kept in screen cages. Incidence of symptomatic plants was assessed at 3‐months intervals, for 5 years, and for further 2 years at irregular intervals. Cumulative maps of disease incidence were produced for each assessment date and used in all analyses. Temporal progress was analysed by nonlinear fitting of three disease progress models. Spread was characterised in three levels of spatial hierarchy by the following analyses: ordinary runs, binomial dispersion index, binary power law fitting, isopath mapping and nonlinear fitting of disease gradient models. The first symptomatic plant was detected 2 years after planting. In the last disease assessment, 5 years after the first, 98% of the unprotected plants were symptomatic. None of the screen‐caged trees showed any symptoms. Bahia bark scaling progress was polyetic and best described by the logistic model. Ordinary runs analysis showed little if any evidence of transmission between adjacent trees. Diseased plants showed a very aggregated pattern inside quadrats (D > 5 and b > 1.53). Isopath mapping showed that main spread was only because of the primary inoculum source. Secondary foci were also observed, but they were never dissociated from main initial disease focus. Disease gradient followed wind direction, starting near the original inoculum source and was best described by exponential model. These results support a hypothesis of Bahia bark scaling transmission by air‐borne vectors with limited dispersion ability.     

Focus Issue on Roots: Plant Nutrition: Root Transporters on the Move

Nutrient and water uptake from the soil is essential for plant growth and development. In the root, absorption and radial transport of nutrients and water toward the vascular tissues is achieved by a battery of specialized transporters and channels. Modulating the amount and the localization of these membrane transport proteins appears as a way to drive their activity and is essential to maintain nutrient homeostasis in plants. This control first involves the delivery of newly synthesized proteins to the plasma membrane by establishing check points along the secretory pathway, especially during the export from the endoplasmic reticulum. Plasma membrane-localized transport proteins are internalized through endocytosis followed by recycling to the cell surface or targeting to the vacuole for degradation, hence constituting another layer of control. These intricate mechanisms are often regulated by nutrient availability, stresses, and endogenous cues, allowing plants to rapidly adjust to their environment and adapt their development.Plants take up nutrients and water from the soil and transport them to the leaves to support photosynthesis and plant growth. However, most soils around the world do not provide optimal conditions for plant colonization. Consequently, plants have evolved sophisticated mechanisms to adjust to deficiency or excess of nutrients and water supply. Membrane transport proteins, including channels and transporters, play crucial roles in the uptake of nutrients and water from the soil and in their radial transport to the root vasculature. Newly synthesized membrane transport proteins have to be properly targeted to a defined compartment, usually the plasma membrane, to efficiently ensure their function. The trafficking of membrane transport proteins along the secretory pathway is tightly controlled and involves the recognition of exit signals by gatekeeper protein complexes. After reaching the plasma membrane, membrane transport proteins can be endocytosed and subsequently recycled to the cell surface or targeted to the vacuole for degradation. Because the subcellular localization of proteins directly influences their activity, modulating the localization of membrane transport proteins constitutes a powerful way to control nutrient and water uptake in plants. This review discusses the fundamental mechanisms at stake in membrane protein secretion and endocytosis, with a specific focus on membrane transport proteins, and how endogenous and exogenous cues affect their dynamics to integrate uptake of nutrients and water to plant growth conditions.     

The role of Anthocoris species (Hemiptera: Anthocoridae) in the integrated control of the damson-hop aphid (Phorodon humuli)

Field studies in 1974, 1975 and 1976 investigated integrated control of the damson-hop aphid Phorodon humuli on hops. After the aphicidal effects of an early-season soil drench of mephosfolan had declined, natural enemies controlled the aphids for the remainder of the season. Anthocorid bugs, particularly Anthocoris nemoralis, were the most abundant predators. In each year a rapid decline in aphid numbers occurred in mid- to late-July, coinciding with the peak numbers of fourth and fifth instar larvae and adults, the most voracious anthocorid stages. Aphids in the cones remained under control for the rest of the season in 1974 and 1975, and increased in 1976 but damaging numbers did not develop. When predators were excluded by caging mephosfolan-treated bines, high aphid densities developed on the leaves, and the cones were heavily infested. Plants not treated with an insecticide were almost completely defoliated by late-July. Heavily infested ‘missed bines’, due to uneven uptake of mephosfolan, attracted large numbers of anthocorids, which later dispersed into the surrounding plants.     

RAB GTPases and SNAREs at the trans-Golgi network in plants

Membrane traffic is a fundamental cellular system to exchange proteins and membrane lipids among single membrane-bound organelles or between an organelle and the plasma membrane in order to keep integrity of the endomembrane system. RAB GTPases and SNARE proteins, the key regulators of membrane traffic, are conserved broadly among eukaryotic species. However, genome-wide analyses showed that organization of RABs and SNAREs that regulate the post-Golgi transport pathways is greatly diversified in plants compared to other model eukaryotes. Furthermore, some organelles acquired unique properties in plant lineages. Like in other eukaryotic systems, the trans-Golgi network of plants coordinates secretion and vacuolar transport; however, uniquely in plants, it also acts as a platform for endocytic transport and recycling. In this review, we focus on RAB GTPases and SNAREs that function at the TGN, and summarize how these regulators perform to control different transport pathways at the plant TGN. We also highlight the current knowledge of RABs and SNAREs’ role in regulation of plant development and plant responses to environmental stimuli.

     

Assimilatverteilung in Sommergerstensorten mit unterschiedlicher Resistenz gegenüber dem Echten Mehltau (Erysiphe graminis f. sp. hordei)

Distribution of assimilates in cultivars of spring barley with different resistance against powdery mildew (Erysiphe graminis f. sp. hordei) Transport and distribution of radioactive labelled assimilates in spring barley cultivars with different degrees of resistance to powdery mildew were studied after ¹⁴CO₂-treatment of single leaves. Plants of the cultivars ‘Amsel’ (susceptible), ‘Asse’ (adult plant resistant), and ‘Rupee’ (resistant) were analyzed at the vegetative growth stage (5. leaf unfolded) and the generative growth stage (anthesis). At the vegetative growth stage the assimilate export from the mildew inoculated 5. leaf of ‘Amsel’ and ‘Rupee’ is decreased; in ‘Asse’, there is no considerable change of assimilate distribution due to infection. At the generative growth stage the assimilate export from the infected flag leaf of ‘Amsel’ is reduced when the fungus, is sporulating. In the cultivar ‘Asse’ the assimilates are bound at the infection site until the seventh day after inoculation, then the transport of assimilates to the ear is increased. In ‘Rupee’ mildew inoculation causes an enhanced assimilate transport to the ear. The changes in assimilate distribution due to mildew inoculation are discussed with respect to the different types of host-parasite-interactions and the source-sink-activities in the different cultivars.     

Trans-root potential, xylem pressure, and root cortical membrane potential of 'low-salt' maize plants as influenced by nitrate and ammonium

Upon addition of nitrate and ammonium, respectively, to the bath of intact ‘low salt’ maize plants, the cortical membrane potential and the trans-root potential changed in a similar and synchronous way as revealed by applying conventional microelectrode techniques and the xylem pressure-potential probe ( Wegner & Zimmermann 1998). Upon addition of nitrate, a hyperpolarization response was observed which was frequently preceded by a short depolarization phase. In contrast, addition of ammonium resulted in an overall depolarization response both of the cortical membrane potential and the trans-root potential. The nitrate-induced hyperpolarization response and the depolarization following the addition of ammonium were concentration-dependent. The data suggest that a tight electrical coupling exists between the cellular and tissue level in the root of the intact plant and that the resistance of the cellular (symplastic) space is much less than the resistance of the apoplast.     

植物Na+/H+逆向转运蛋白研究进展

盐胁迫主要由Na 引起,过高的Na 浓度引起的离子毒害,渗透胁迫和K ／Na 比率的不平衡使植物新陈代谢异常,这是对大多数器官造成伤害的原因。植物抵御盐胁迫的主要方式是将细胞内过多的Na 从质膜向细胞外排放和将Na 在液泡中区隔化,这一过程是由Na ／H 逆向转运蛋白完成的。本文概述了植物中Na ／H 逆向转运蛋白的发现、特征、分子生物学方面的研究,以及Na ／H 逆向转运蛋白在植物耐盐性中的重要作用。     

Influence of anaesthetics on the movement of the mobile charges in the algal cell membrane of Valonia utricularis

Voltage relaxation studies in the presence of anaesthetics were performed on cells of the giant marine alga Valonia utricularis using intracellular microelectrodes. From the decay of the initial membrane voltage which can be described by two relaxation processes the conclusion can be drawn that protein-linked, mobile charges are present which are probably involved in turgor-pressure-dependent potassium transport (Büchner, K.-H., Rosenheck, K. and Zimmermann, U. (1985) J. Membrane Biol. 88, 131-137). The anaesthetics halothane and chloroform were found to affect reversibly, procaine and tetracaine irreversibly the translocation rate k of the mobile charges at concentrations which were equal to (for halothane and chloroform) or significantly below (for procaine and tetracaine) clinical and nerve blocking levels. The concentration of the mobile charges Nt as well as the specific membrane resistance Rm and the specific membrane capacitance Cm remained unchanged in these concentration ranges. The data suggest a specific interaction of anaesthetics with specialized target sites of a transport protein to which the mobile charges are coupled.     

Rapid,combinatorial analysis of membrane compartments in intact plants with a multicolor marker set

Plant membrane compartments and trafficking pathways are highly complex, and are often distinct from those of animals and fungi. Progress has been made in defining trafficking in plants using transient expression systems. However, many processes require a precise understanding of plant membrane trafficking in a developmental context, and in diverse, specialized cell types. These include defense responses to pathogens, regulation of transporter accumulation in plant nutrition or polar auxin transport in development. In all of these cases a central role is played by the endosomal membrane system, which, however, is the most divergent and ill‐defined aspect of plant cell compartmentation. We have designed a new vector series, and have generated a large number of stably transformed plants expressing membrane protein fusions to spectrally distinct, fluorescent tags. We selected lines with distinct subcellular localization patterns, and stable, non‐toxic expression. We demonstrate the power of this multicolor ‘Wave’ marker set for rapid, combinatorial analysis of plant cell membrane compartments, both in live‐imaging and immunoelectron microscopy. Among other findings, our systematic co‐localization analysis revealed that a class of plant Rab1‐homologs has a much more extended localization than was previously assumed, and also localizes to trans‐Golgi/endosomal compartments. Constructs that can be transformed into any genetic background or species, as well as seeds from transgenic Arabidopsis plants, will be freely available, and will promote rapid progress in diverse areas of plant cell biology.     

Spatial root distribution of plants growing in vertical media for use in living walls

Background and Aims

For plants growing in living walls, the growth potential is correlated to the roots ability to utilize resources in all parts of the growing medium and thereby to the spatial root distribution. The aim of the study was to test how spatial root distribution was affected by growing medium, planting position and competition from other plants.

Methods

Five species (Campanula poscharskyana cv. ‘Stella’, Fragaria vesca cv. ‘Småland’, Geranium sanguineum cv. ‘Max Frei’, Sesleria heufleriana and Veronica officinalis cv. ‘Allgrün’) were grown in three growing media (coir and two of rockwool) in transparent boxes under greenhouse conditions. Root frequency was registered and the activity of individual root systems was studied via ¹⁵N uptake and plant dry weight was measured.

Results

Plants in coir had stronger root growth in all parts of the medium than plants in rockwool. Upwards root growth was limited for plants in the middle or lower parts of the medium and ¹⁵N measurements confirmed that only plants in the bottom of the box had active roots in the bottom of the medium. The species differed in root architecture and spatial root distribution.

Conclusions

The choice of growing medium, plant species and planting position is important for a living wall as it affects the spatial root growth of the plants.     

植物体内糖分子的长距离运输及其分子机制

植物器官(如叶、叶鞘、绿色的茎等)可以通过光合作用将CO₂合成为碳水化合物, 并经过长距离运输到达库组织(如新生组织、花粉、果实等)中进行贮存或利用。蔗糖是高等植物长距离运输碳水化合物的主要形式。蔗糖分子从源到库的运输包括源组织韧皮部的装载、维管束的运输和库组织韧皮部的卸载3个步骤。遗传学和分子生物学研究证明, 蔗糖转运蛋白、转化酶和单糖转运蛋白在糖分子的装载和卸载过程中发挥重要作用。该文综述了目前对光合产物运输过程及其调控分子机制的最新研究进展。     

Consequences of insufficient equations in models of the Münch hypothesis of phloem transport

Abstract The suggestion of concentration dependent unloading as a necessary assumption for a closed-form mathematical expression of the Münch hypothesis of phloem transport (Goeschl et at., 1976) has been recently questioned (Ferrier & Christy, 1977). Also questioned was whether previous models, known to have one less equation than dependent variables, have produced erroneous or misleading results. A review of Münch's original concepts and recent comments by several researchers indicate that an equation describing the exit of solutes from sieve tubes is essential for consistency with the Münch hypothesis. Evidence is presented to show that previous mathematical predictions and interpretations regarding ‘runaway velocities’ have resulted in part from mathematical inconsistencies and characteristics of the numerical solution procedures. Likewise, a proposal that different steady-state velocities and concentrations of transport at a given loading rate might be determined by ‘previous history’ of the system can be explained on the basis of implied relationships hidden in models with insufficient equations. Finally it is concluded that concentration dependent unloading in models of the Münch hypothesis will not detract, but rather will contribute to their usefulness in experimental testing and other research regarding phloem transport.     

Production and dormancy of wild oat (Avena fatua) seed from plants grown under soil waterstress

In 1974 wild oat plants grown from very dormant seed types fA, fB, fC originating from a single field, and in 1976 plants of type fB derived from another location were waterstressed from the time when the spikelets were just beginning to emerge until the seed was fully ripe. The seed production and dormancy of the seed were determined. Waterstress reduced the number of viable seeds per plant by 42% in 1974 and 49% in 1976. The number of viable seed produced on the tillers of the plants were reduced to a greater extent by waterstress than the number produced on their main stems. Some of the differences between the number of viable seeds produced by the three wild oat types were significant. In 1974, 78% of seed from stressed plants was dormant as compared with 90% of that from unstressed plants. Under a given soil moisture, the dormancy of the three types differed little, although seed dormancy was less in tiller seed than in main stem seed. In 1976 seed from stressed plants was 80% dormant, immediately after collection, whereas that from unstressed plants was totally dormant. Storage for 6 months at 25°C decreased these percentages to 17% and 90% and at 5°C to 72% and 98% respectively. Buried in soil immediately after collection, 66% of viable seed from stressed plants gave seedlings in the first autumn after burial as compared with 4% of seed from unstressed plants. Most of the seed from waterstressed plants gave rise to seedlings in the first autumn, and seed from non-stressed plants in the second spring. The α-amylase content was four times greater in seeds from stressed compared with non-stressed plants.     

Approaches towards understanding methionine biosynthesis in higher plants

Summary. Plants are able to synthesise all amino acids essential for human and animal nutrition. Because the concentrations of some of these dietary constituents, especially methionine, lysine, and threonine, are often low in edible plant sources, research is being performed to understand the physiological, biochemical, and molecular mechanisms that contribute to their transport, synthesis and accumulation in plants. This knowledge can be used to develop strategies allowing a manipulation of crop plants, eventually improving their nutritional quality. This article is intended to serve two purposes. The first is to provide a brief review on the physiology of methionine synthesis in higher plants. The second is to highlight some recent findings linked to the metabolism of methionine in plants due to its regulatory influence on the aspartate pathway and its implication in plant growth. This information can be used to develop strategies to improve methionine content of plants and to provide crops with a higher nutritional value. Received January 28, 2000 Accepted March 3, 2000