In situ microscopy reveals reversible cell wall swelling in kelp sieve tubes: one mechanism for turgor generation and flow control?

Kelps, brown algae (Phaeophyceae) of the order Laminariales, possess sieve tubes for the symplasmic long‐distance transport of photoassimilates that are evolutionarily unrelated but structurally similar to the tubes in the phloem of vascular plants. We visualized sieve tube structure and wound responses in fully functional, intact Bull Kelp (Nereocystis luetkeana [K. Mertens] Postels & Ruprecht 1840). In injured tubes, apparent slime plugs formed but were unlikely to cause sieve tube occlusion as they assembled at the downstream side of sieve plates. Cell walls expanded massively in the radial direction, reducing the volume of the wounded sieve elements by up to 90%. Ultrastructural examination showed that a layer of the immediate cell wall characterized by circumferential cellulose fibrils was responsible for swelling and suggested that alginates, abundant gelatinous polymers of the cell wall matrix, were involved. Wall swelling was rapid, reversible and depended on intracellular pressure, as demonstrated by pressure‐injection of silicon oil. Our results revive the concept of turgor generation and buffering by swelling cell walls, which had fallen into oblivion over the last century. Because sieve tube transport is pressure‐driven and controlled physically by tube diameter, a regulatory role of wall swelling in photoassimilate distribution is implied in kelps.     

Structure of functional soybean sieve elements

Soybean (Glycine max cv. Bragg) petiolar tissue containing translocated ¹⁴C-sucrose was quick frozen, freeze-substituted in acetone or propylene oxide and embedded in Epon. This procedure allowed cytological observations on sieve elements whose functional condition could be verified by microautoradiography. Sieve elements and companion cells were essentially free of ice damage. Aside from a P-protein crystal, the central portion of the sieve tube lumen was devoid of stainable content except in the vicinity of sieve plates. Various sized clumps of stacked endoplasmic reticulum (ER) lined the wall. Superficially, the ER “membranes” seemed to consist of parallel arrays of 100 Å protein fibrils. Although that possibility could not be excluded, it seemed more likely that the fibrils were actually between ER cisternae and that the lipoprotein ER membrane could not be detected readily due to the loss of lipids during tissue preparation. The amount and distribution of proteinaceous material in the vicinity of sieve plates was variable but, when present, still consisted almost entirely of 100 Å fibrils organized into membrane-like arrays. Stacks of ER in various degrees of disorganization and a few 100 Å fibrils were found near sieve plates, with some fibrils extending through the pores. However, most (70%) of the sieve plate pores were essentially free from obstruction. The observations favor an osmotically generated pressure flow mechanism of translocation in soybean.     

Organelle movement and fibrillar elements of the cytoskeleton in the angiosperm pollen tube

Summary Continuous observation of organelles and other cytoplasmic inclusions in the older stretches of living pollen tubes of Iris pseudacorus shows that in the more attentuated parts of the protoplast they move along single, mainly longitudinally oriented fibrils, corresponding to those previously isolated from other species and shown to contain bundles of uniformly polarised actin microfilaments. The traffic associated with each fibril is unidirectional, but organelles move along them independently, sometimes with conspicuously different velocities. Larger columns of cytoplasm passing along the tube are associated with several such fibrils, as revealed in occasional discontinuities and also in columns isolated from the tube in suitable medium without fixation. The dimensions of the individual fibrils suggest that the bundles of actin microfilaments are not likely to be enclosed in a unit membrane corresponding to a tonoplast. If so, the nature of the continuous cavities traversed by numerous fibrils in the older parts of the pollen tube requires reappraisal, since these are more likely to be volumes of attentuated cytoplasm comparable with that of the central cavity of the sieve tube than vacuoles of the normal plant-cell type.     

Tubular and Fibrillar Components in the Phloem of Brassica Chinensis L. Leaves

Abstract

Electron microscopical observations of the phloem of Brassica chinensis L. leaves, healthy or infected by turnip yellow mosaic virus, have shown that the «slime», characteristic proteic component of the sieve cell protoplast, is present as tubules or fibrils, free in the cellular cytoplasm or localized in the cisternae of the endoplasmic reticulum. In this paper it was thought to follow the ontogensis and evolution of the «slime» in parallel with the differentiation of the sieve tube and at the same time to contribute to the solution of the problem concerning the origin and probable function of this proteic material.     

Ultrastructure of P-protein inHevea brasiliensis during sieve-tube development and after wounding

Summary P-protein and the changes it undergoes after wounding of sieve tubes of secondary phloem in one- to two-year old shoots ofHevea brasiliensis has been studied using electron microscopy. The P-protein in the form of tubules with a diameter of 8–9 nm and a lumen of 2–2.5 nm occurred in differentiating sieve elements and appeared as compact bodies which consisted of small aggregates of the tubules. As the sieve elements matured, these P-protein bodies dispersed with a disaggregation of the tubules before they turned into striated fibrils, 10–11 nm in diameter. In wounding experiments, as the mature sieve elements collapsed after cutting, their striated P-protein converted into tubules. These tubules were the same in ultrastructure as the tubules in differentiating sieve elements and they often were arranged in crystalline aggregates.     

Wall fibrils ingerminating sporangiospores of Gilbertella persicaria (Mucorales)

Summary In germinated sporangiospores of Gilbertella persicaria, negatively contrasted fibrils, 20–70 Å diam, are seen in thin sections of the inner vegetative wall that is continuous with the germ tube wall. The fibrils are randomly oriented in a loose network in this wall and in the germ tube wall. Germ tubes have an additional surface layer of fine, positively contrasted fibrils which appear as a nap-like coating on the hyphae. Patterns of wall fibril orientation are not revealed by transverse sections of spore and germ tube walls, whereas oblique and tangential sections are favorable for examining cell wall architecture in situ. Staining patterns show textural and compositional differences among various wall layers.     

Fine structure of P-protein filaments from Ricinus communis

Summary Exudate from the phloem of Ricinus communis L. was negatively stained, examined in the electron microscope, and the filamentous components compared with those in fixed, sectioned material. In the exudate, two main fibrillar components were observed. One component has a diameter of 20±0.35 (standard error) nm, the other of 14.1±0.34 nm. This second compoent has projections along its length measuring 5 by 14 nm and spaced at intervals of 6.5–10 nm. Fibrils have been found possessing characteristics of both fibril types, suggesting some structural relationship between the two, possibly an interconvertibility. Several other types of fibrils occurred less frequently in the exudate. The exudate also contains torus-shaped structures measuring 13.5–15 nm in diameter. Sections of mature sieve elements of Ricinus and Acer rubrum L. contain fibrils structurally similar to the 14-nm fibrils from the exudate of Ricinus. Ricinus exudate was also fixed and pelleted in the ultracentrifuge. Thin sections of the pellet afforded cross-sectional views of the 20-nm fibrils, and showed that these fibrils apparently have a solid core. Possible models for the structure of the 20-nm filaments are described.     

Accumulation,selection and covariation of amino acids in sieve tube sap of tansy (Tanacetum vulgare) and castor bean (Ricinus communis): evidence for the function of a basic amino acid transporter and the absence of a γ‐amino butyric acid transporter

Sieve tube sap was obtained from Tanacetum by aphid stylectomy and from Ricinus after apical bud decapitation. The amino acids in sieve tube sap were analyzed and compared with those from leaves. Arginine and lysine accumulated in the sieve tube sap of Tanacetum more than 10‐fold compared to the leaf extracts and they were, together with asparagine and serine, preferably selected into the sieve tube sap, whereas glycine, methionine/tryptophan and γ‐amino butyric acid were partially or completely excluded. The two basic amino acids also showed a close covariation in sieve tube sap. The acidic amino acids also grouped together, but antagonistic to the other amino acids. The accumulation ratios between sieve tube sap and leaf extracts were smaller in Ricinus than in Tanacetum. Arginine, histidine, lysine and glutamine were enriched and preferentially loaded into the phloem, together with isoleucine and valine. In contrast, glycine and methionine/tryptophan were partially and γ‐amino butyric acid almost completely excluded from sieve tube sap. The covariation analysis grouped arginine together with several neutral amino acids. The acidic amino acids were loaded under competition with neutral amino acids. It is concluded from comparison with the substrate specificities of already characterized plant amino acid transporters, that an AtCAT1‐like transporter functions in phloem loading of basic amino acids, whereas a transporter like AtGAT1 is absent in phloem. Although Tanacetum and Ricinus have different minor vein architecture, their phloem loading specificities for amino acids are relatively similar.     

Glass microelectrode measurements of sieve tube membrane potentials in internode discs and petiole strips of tomato (Solanum lycopersicum L.)

Summary In tissue slices of tomato (Solanum lycopersicum L.) sieve tube membrane potentials (E_m) were measured by use of glass microelectrodes. In internode discs, the potential differences (pd) of phloem cells near the cut surface fell into two distinct categories with average values of –66 and –109 mV. More distant from the cut surface the values decreased to averages of –71 and –140 mV. These pds were associated with phloem parenchyma cells and sieve tube/companion cell complexes, respectively. In petiole strips, pds were recorded from cells which were identified by iontophoretic injection of fluorescent dye. Averages in two different bathing media, were –140/–146mV, –149/–152mV, and –70/–68mV for sieve tubes, companion cells, and phloem parenchyma cells, respectively. The membrane potentials recorded from sieve tubes were transiently reduced upon sucrose addition. Reduction by CCCP and KCN was more permanent. Sieve tube E_ms recovered more slowly from potassium than from sucrose-induced depolarizations. Light/ dark (L/D) responses were minute (±3 mV). The limitations of the present experimentation are evaluated with special reference to the question as whether the recorded E_ms represent sieve tube membrane potentials occurring in the intact plant.Abbreviations CCCP carbonyl cyanide m-chlorophenylhydrazone - D dark(ness) - E_m membrane potential - L light - LYCH Lucifer yellow CH - pd potential difference - SE standard error     

Filament formation in vitro of a sieve tube protein from Cucurbita maxima and Cucurbita pepo

Summary Phloem proteins of the sieve tube exudate from Cucurbita maxima Duch. and Cucurbita pepo L. were investigated as to their filament forming ability in vitro. From the two main proteins (116000 dalton, 30000 dalton) only the 116000 dalton protein was found to form reversibly distinct filaments of 6–7 nm diameter upon removal of SH-protecting agents from the buffer, whereas the 30000 dalton protein was precipitated as amorphous material under these conditions. The protein filaments were similar to the filaments ocurring within the sieve tube cells in vivo.Abbreviations SDS sodium dodecyl sulfate - TCA trichloroacetic acid     

Composition and fine structure of minor veins inTetragonia leaf

Summary Mesophyll containing the minor veins from leaves ofTetragonia expansa Murr. was examined in preparation for a study of effects of beet yellows virus on the leaf tissues of this plant. The sieve elements throughout the minor veins exhibit the characteristics commonly found in this type of cell in dicotyledons. The cells are connected with one another by sieve plates and with contiguous parenchyma cells by branched plasmodesmata. Mature sieve elements are enucleate and lack ribosomes. No tonoplast was discerned in these cells. Mitochondria, plastids, and sparse endoplasmic reticulum are retained in mature cells. The plastids, which contain a massive fibrous ring of proteinaceous material, resemble the sieve element plastids ofBeta. The P-protein in the sieve elements is occasionally composed of tubules; more commonly it is represented by loose helices. The tracheary elements have scalariform secondary thickenings. In regions free of these thickenings, the primary wall largely disintegrates; only some loosely arranged fibrils remain. The mesophyll and vascular parenchyma cells contain the various organelles characteristic of living plant cells but vary in degree of vacuolation and in density of cytoplasm. Some vascular parenchyma cells have particularly dense protoplasts. They contain numerous ribosomes and their background matrix consists of a dense population of fine fibrils. Occasional vascular parenchyma cells contain the tubular spiny cell component first recognized inBeta. This work was supported in part by National Science Foundation grant GB-5506.     

Endoplasmic reticulum and crystalline fibrils in the root protophloem of Nymphoides peltata

Endoplasmic reticulum in the root protophloem of Nymphoides peltata (S.G. Gmel.) O. Kuntze changes form as sieve elements differentiate. In immature sieve elements the individual endoplasmic reticulum (ER) cisternae form large irregular aggregates in the cytoplasm. In older immature sieve elements the ER aggregates are more ordered and membranes in them are convoluted. Although convoluted ER predominates in immature sieve elements the ER of the mature sieve elements consists mainly of flattened stacks of ER cisternae. Some of these stacks of ER may be derived from the existing convoluted ER. Crystalline fibrils first appear in the cytoplasm of the sieve element when the ER starts to aggregate. The crystalline fibrils move to the parietal layer of the sieve element along with the aggregates of ER. A possible ontogenetic relationship between ER and crystalline fibrils is discussed.Abbreviation ER endoplasmic reticulum     

The fine structure of the sieve tubes of Salix caprea (L.) and its relation to the electroosmotic theory

Summary The sieve plate pores of Salix caprea in preparations fixed in glutaraldehyde are normally found to be occupied by slime fibrils showing periodic banding such as occur in a number of other species. Arguments are put forward to suggest that the occurence of fibrils in this position is natural and not an artefact of preparation. The sieve tubes further possess prominent and persistent nucleoli showing a radiating structure of tubules. The endoplasmic reticulum often occurs in parietal stacks reminiscent of other species.This evidence is discussed in relation to the electroosmotic theory of translocation.This work formed part of that submitted for the degree of Ph. D. of the University of London by U. Mishra.     

SIEVE TUBES AND CALLOSE IN ELODEA LEAVES

Detachment and incubation of Elodea leaves promoted callose synthesis in all cells, especially in epidermal pits and in sieve tubes. Phloem was detected in the midrib by fluorescent staining of callose induced to form on sieve plates. In EM views of mature sieve elements nucleus and tonoplast were lacking, mictoplasm replaced cytoplasm, mitochondria were fewer in number, and large plastids contained crystalline inclusion bodies. Slime was present as compact aggregates and as individual fibrils in mictoplasm and sieve pores. Deposition of callose is considered in relation to the blockage concept of callose function.     

Über den Feinbau verdickter (nacré) Wände und der Plastiden in den Siebröhren vonAnnona undMyristica

Zusammenfassung Die verdickten (nacré) inneren Wände der Siebröhren von Annonaceen, vonMyristica, Illicium undKadsura geben mit spezifischen Farbstoffen eine positive Cellulosereaktion. Untersuchungen über ihre Feinstruktur zeigen, daß sie sich aus bevorzugt parallel verlaufenden Fibrillen (Durchmesser 100–200 Å) zusammensetzen. Die Paralleltextur ist wahrscheinlich für den Perlmutterglanz der Wände mitverantwortlich. Die Wandverdickungen entstehen bereits in sehr jungen plasmareichen Siebröhren und engen das Siebröhrenlumen im Laufe ihrer Differenzierung bis auf weniger als die Hälfte des Ausgangswertes ein. - Die Siebröhren-Plastiden von Annonaceen undMyristica enthalten einen Proteineinschluß, z. T. zusätzlich auch Stärkekörner.

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On the fine structure of nacreous walls and of plastids in the sieve tubes ofAnnona andMyristica

Summary Wall thickenings (nacreous walls) in sieve tubes ofAnnonaceae, ofMyristica, Illicium, andKadsura give positive reactions with dyes staining cellulose walls. In electron microscopic investigations their composition of 100–200 Å wide fibrils can be depicted. The predominant parallel arrangement of the fibrils is suggested to be one of the conditions for the pearly luster of the wall thickenings. The formation of nacreous walls is initiated in young sieve tubes; finally the wall thickenings may occlude more than half of their cross-sectional area.—Sieve-tube plastids fromAnnonaceae andMyristica contain protein inclusions and often supplementary starch grains.

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Meinem Lehrer, Herrn Prof. Dr.Walter Schumacher, in Dankbarkeit zum 70. Geburtstag.     

The Relative Contributions of Sugars from Assimilating Leaves and Stem Storage Cells to the Sieve Tube Sap in Willow Cuttings

A method is described for the measurement of the relative contributions of sugars from the assimilating leaves and stem storage cells to the sieve tube sap in leafy cuttings of Salix viminalis L. In these experiments sieve tube sap was collected as honeydew from a small colony of aphids, Tuberolachnus salignus (Gmelin). Using this method it has been shown that in cuttings maintained under continuous illumination prior to experimentation, the leaves contribute about 75 per cent of the total sugars in the sieve tube sap. With cuttings which have been stored by keeping them in darkness, the level of labile carbohydrates in the stem storage cells decreases, in comparison with those growing in light, and the percentage of sugars in the sieve tube sap supplied by the leaves rises to 90 per cent.     

Phloem transport of abscisic acid in Ricinus communis L. seedlings

Sieve tube sap exuded from the cut hypocotyl of castor bean seedlings (Ricinus communis L.) was found to contain 0.2–0.5 mmol m^?3abscisic acid (ABA). The ABA concentration in the sieve tube sap always exceeded that in root pressure exudate under a wide range of water supply. Exudation of sieve tube sap from the cut hypocotyls caused water loss, and this induced ‘water shortage’ in the cotyledons which resulted in the ABA concentration in the cotyledons increasing by 3-fold and that in the sieve tube sap increasing by up to 50-fold within 7h. The wounded surface of the cut hypocotyl was not responsible for the ABA increase. Incubation of the cotyledons of endosperm-free seedlings in various ABA concentrations (up to 100 mmol m^?3) increased the ABA concentration in sieve tube sap. The concomitant increase in ABA, both in cotyledons and in sieve tube sap, had no effect on the phloem loading of sucrose, K⁺ and Mg²⁺ within the experimental period, i.e. up to 10h. It can be concluded that (i) the phloem is an important transport path for ABA, (ii) water stress at the phloem loading sites elevates phloem-mobile ABA, which may then serve as a water stress signal for sinks, for example stem and roots (not only for stomata), and (iii) the ABA concentration of cells next to or in the phloem is more important than the average ABA content in the whole cotyledon for determining the ABA concentration in sieve tube sap.     

The effect of low temperature on sucrose,ATP and potassium concentrations and fluxes in the sieve tubes of willow

Summary Experiments have been performed on the effect of localised low (0°C) temperature application on solute concentration and fluxes in the sieve elements of willow. Sieve tube exudate was obtained via the severed stylets of the aphid Tuberolachnus salignus (Gmelin). In stem segments, low temperature caused a fall in both the concentration and flux of sucrose. No recovery was observed during a 24 h cold application period. The concentrations of ATP and potassium were generally also reduced, though the effect on the fluxes of these solutes was not as marked. Both ATP and potassium appear to be translocated along the sieve tubes of stem segments as evidenced by girdling experiments. In leafy cuttings low temperature consistently reduced the concentration of sucrose in the sieve tube exudate. These data are discussed in relation to previous work on low temperature effects on the phloem transport system of willow.     

Physiological implications of the Münch-Horwitz theory of phloem transport: effects of loading rates*

Abstract Predicted effects of phloem loading rates on the five profiles of unloading rate, osmotic water flux, pressure, transport speed and concentration, in hypothetical sieve tubes with different sink properties, were calculated using the steady-state mathematical expression of the Münch hypothesis of phloem transport. The prediction that increased loading rates always increases the concentration, and generally increase the speed of translocates through the sieve tube, is emphasized since these parameters are accessible for experimental testing. This particular prediction contrasts with a previous prediction (Tyree, Christy, & Ferrier, 1974), that where concentration was held constant at the loading end, concentration along the rest of the sieve tube would decrease, while speed would increase greatly. Where the unloading mechanism was assigned saturable (enzyme-like) kinetics, increased loading rates (in the range well below the V_max of the sink) caused both transport speed and concentration to increase. However, as loading rates approached the V_max of the sinks, speed reached a maximum and then declined, and concentration increased substantially. This was particularly true at very high values of Km, e.g. > 0.1 mol cm^?3.