2 edition of Phloem unloading and post-phloem transport in developing wheat grains found in the catalog.
Phloem unloading and post-phloem transport in developing wheat grains
Written in English
|Statement||by Ning Wang.|
|The Physical Object|
|Pagination||x, 127 leaves, bound :|
|Number of Pages||127|
The post-phloem unloading pathway and the mechanism of sugar accumulation remain unclear in litchi fruit. A combination of electron microscopy, transport of phloem-mobile symplasmic tracer (carboxyfluorescein, CF) and biochemical and molecular assays was used to explore the post-phloem transport pathway and the mechanism of aril sugar. Full text of "Plasmodesmata: structure, function, role in cell communication" See other formats.
In have demonstrated the importance of FRD3- particular, the mutation in AtYSL1, which is mediated citrate efflux in Fe unloading in leaf expressed in the chalazal endosperm of the seed, (from xylem to adjacent cells) and in anther provokes a reduced accumulation of Fe and NA (from tapetum to pollen grains) (10). in mature seeds (20). Sediment Transport and Scour Phenomena GeoPlanet: Earth and Planetary Sciences p. 70 illus., 20 illus. in color. SCG Sedimentology RBGB SCJ Physical Geography RGB The state-of-the-art in fluvial hydrodynamics can be examined only through a careful exploration of the theoretical development and applied engineering technology.
(). The cellular pathway of postphloem sugar transport in developing tomato fruit. Planta , - Discovery of a switch between a symplamic to an apoplasmic pathway of sugar transport in developing tomato fruit. Citation: 70; JIF: *Patrick JW. (). Phloem unloading: Sieve element unloading and post-sieve element transport. Upload No category; Control of Primary Metabolism in Plants.
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RACER # 3146326
Phloem unloading and post-phloem transport in developing wheat (Triticum aestivum L.) grains were investigated by perfusing the endosperm cavities of attached grains. Relative unloading ratio (RUR) and the rate of sucrose release into the endosperm cavity (SRR) were calculated, respectively, from 14C import and from sucrose washout from the by: A variety of fluorescent tracers and proteins were injected via severed aphid stylets into the sieve tubes of wheat (Triticum aestivum L.) grains to evaluate the dimensions of plasmodesmal channels involved in sieve element/companion cell (SE/CC)unloading and post-phloem transport.
In the post-phloem pathway, where diffusion is the predominant mode of. Robert Turgeon, Brian G. Ayre, in Vascular Transport in Plants, Phloem loading can only be understood by detailed examination of the routes of sugar movement from mesophyll cells to sieve elements.
Mapping these routes and determining the mode of transport at different interfaces are challenging, as the pathways are complex, the distances short, and the. Sieve Tube Unloading and Post-Phloem Transport of Fluorescent Tracers and Proteins Injected into Sieve Tubes via Severed Aphid Stylets May Plant physiology (1) Wang N, Fisher DB (a) Monitoring phloem unloading and post-phloem transport by microperfusion of attached wheat grains.
Plant Physiol 7–16 PubMed Google Scholar Wang N Fischer DB (b) The use of fluorescent tracers to characterize the post- phloem transport in maternal tissue of developing wheat by: Wang N, Fisher DB.
The use of fluorescent tracers to characterize the post-phloem transport pathway in maternal tissues of developing wheat grains. Plant Physiol. ;– PubMed Google ScholarCited by: Macromolecular trafficking within the sieve element–companion cell complex, phloem unloading, and post-phloem transport were studied using the jellyfish green fluorescent protein (GFP).
The GFP gene was expressed in Arabidopsis and tobacco under the control of the AtSUC2 promoter. In wild-type Arabidopsis plants, this promoter regulates expression of the Cited by: Phloem unloading and post-phloem transport in developing wheat (Triticum aestivum L.) grains were investigated by perfusing the endosperm cavities of attached grains.
Furthermore, the GFP was unloaded in sink tissues, such as root tips, anthers, and developing leaves, and was transported subsequently through non-phloem tissues. These are watershed findings in that they indicate that plasmodesmata along the post-phloem pathway in sink tissues may accommodate the transport of relatively large by: Along the pathway between source and sink, concentrations and composition of the phloem sap may change considerably for various reasons including leakage, unloading to and reloading from transient storage compartments along the axial pathway (Fig.transport phloem) and xylem–phloem transfer (Atkins, ).Cited by: Phloem‐inspired artificial microfluidics systems such as that of Jensen et al.
() provide an extremely powerful approach to the empirical testing of mathematical and other hypotheses of phloem transport. To date, the plant transport community has not yet connected to the engineers in the lab‐on‐a‐chip field, but we expect that in Cited by: Tomato fruits and grape berries behave similarly with respect to sucrose unloading and post-phloem transport.
In young tomato fruits, when starch content is built up in plastids of the columella and inner pericarp region of the fruit (Robinson et al., ; Schaffer and Petreikov, ), unloading is mainly by: Tomato fruits and grape berries behave similarly with respect to sucrose unloading and post-phloem transport.
In young tomato fruits, when starch content is built up in plastids of the columella and inner pericarp region of the fruit (Robinson et al., ; Schaffer and Petreikov, ), unloading is mainly by: Recent developments have altered our view of molecular mechanisms that determine sink strength, defined here as the capacity of non-photosynthetic structures to compete for import of photoassimilates.
We review new findings from diverse systems, including stems, seeds, flowers, and fruits. An important advance has been the identification of new transporters and facilitators Cited by: Transport path. Sugarcane and sweet sorghum may differ in their strategies for accumulating high levels of sucrose in their stems.
In maturing sugarcane stems, sucrose transport follows a predominantly symplastic pathway when moving from the phloem into the storage parenchyma cells (Figure Figure1A 1A; Lingle, ; Moore and Cosgrove, ; Rae et al., ; Patrick. Organising Committee for International Phloem Transport Conference () Referee for 9 x scientific journals, 4 x granting agencies.
International and national working groups and committees such as: Crop Productivity - Research Imperatives Revisited (). Kettering Foundation. International Phloem Transport Conference Committee ( to. This banner text can have markup. web; books; video; audio; software; images; Toggle navigation.
Plant Mol Biol – Keown AC, Taiz L, Jones RL () The nuclear content of developing barley aleurone cells. Am J Bot – Kladnik A, Chamusco K, Dermastia M, Chourey P () Evidence of programmed cell death in post-phloem transport cell of the maternal pedicel tissue in developing caryopsis of maize.
3 Long Distance Transport of SA and Related Compounds Phloem Transport Phloem Loading Strategies The phloem is a central actor in plant growth and development, allocating organic nutrients, ions, water, hormones and other signals from the leaves to the sink organs.
developing yearling heifers to breed and calve at two years of age. Agricultural Research and Education Center, Ona W. Brown, Associate Professor, Project Leader Carbohydrate Digestion by Neonatal Foals.
Progress in neonatal care of premature and stressed foals has made nutritional support of these animals critical. Susheng Gan - Senescence Processes in Plants (Annual Plant Reviews Volume 26) () код для вставки.Karl J.
Oparka - Plasmodesmata (Annual Plant Reviews Volume 18) ( Wiley-Blackwell) код для вставки.POTATO BIOLOGY AND BIOTECHNOLOGY ADVANCES AND PERSPECTIVES Edited by and Long-Distance Transport Pathway from the mesophyll to the phloem Phloem loading Long-distance transport in the phloem Carbon Unloading into Sink Organs Symplastic and apoplastic routes of unloading Phloem unloading in the tuber.