scholarly journals Phenolic components of the primary cell wall. Feruloylated disaccharides of d-galactose and l-arabinose from spinach polysaccharide

1982 ◽  
Vol 203 (2) ◽  
pp. 493-504 ◽  
Author(s):  
S C Fry
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Spinacia Oleracea ◽  
Cell Suspension Cultures ◽  
Prolonged Treatment ◽  
Primary Cell Wall ◽  
Spinacia Oleracea L ◽  
Growing Cell ◽  
Phenolic Components ◽  
Acetic Acid Water

1. Cell walls from rapidly growing cell suspension cultures of Spinacia oleracea L. contained ferulic acid and p-coumaric acid esterified with a water-insoluble polymer. 2. Prolonged treatment with trypsin did not release may feruloyl esters from dearabinofuranosylated cell walls, and the polymer was also insoluble in phenol/acetic acid/water (2:1:1, w/v/v). 3. Treatment of the cell walls with the fungal hydrolase preparation ‘Driselase’ did liberate low-Mr feruloyl esters. The major esters were 4-O-(6-O-feruloyl-beta-D-galactopyranosyl)-D-galactose and 3?-O-feruloyl-alpha-L-arabinopyranosyl)-L-arabinose. These two esters accounted for about 60% of the cell-wall ferulate. 4. It is concluded that the feruloylation of cell-wall polymers is not a random process, but occurs at very specific sites, probably on the arabinogalactan component of pectin. 5. The possible role of such phenolic substituents in cell-wall architecture and growth is discussed.

scholarly journals Catalysts of plant cell wall loosening

F1000Research ◽  
2016 ◽  
Vol 5 ◽  
pp. 119 ◽  
Author(s):  
Daniel J. Cosgrove
Keyword(s):  
Cell Wall ◽  
Plant Cell Wall ◽  
Turgor Pressure ◽  
Wall Stress ◽  
Primary Cell Wall ◽  
Wall Structure ◽  
Xyloglucan Endotransglycosylase ◽  
Growing Cell ◽  
Tensile Forces ◽  
Wall Loosening

The growing cell wall in plants has conflicting requirements to be strong enough to withstand the high tensile forces generated by cell turgor pressure while selectively yielding to those forces to induce wall stress relaxation, leading to water uptake and polymer movements underlying cell wall expansion. In this article, I review emerging concepts of plant primary cell wall structure, the nature of wall extensibility and the action of expansins, family-9 and -12 endoglucanases, family-16 xyloglucan endotransglycosylase/hydrolase (XTH), and pectin methylesterases, and offer a critical assessment of their wall-loosening activity

scholarly journals Structure and Biomechanics during Xylem Vessel Transdifferentiation in Arabidopsis thaliana

Plants ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 1715
Author(s):  
Eleftheria Roumeli ◽  
Leah Ginsberg ◽  
Robin McDonald ◽  
Giada Spigolon ◽  
Rodinde Hendrickx ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Wall ◽  
Cell Walls ◽  
Turgor Pressure ◽  
Plant Cells ◽  
Building Blocks ◽  
Xylem Vessel ◽  
Primary Cell Wall ◽  
Individual Plant ◽  
Vessel Elements

Individual plant cells are the building blocks for all plantae and artificially constructed plant biomaterials, like biocomposites. Secondary cell walls (SCWs) are a key component for mediating mechanical strength and stiffness in both living vascular plants and biocomposite materials. In this paper, we study the structure and biomechanics of cultured plant cells during the cellular developmental stages associated with SCW formation. We use a model culture system that induces transdifferentiation of Arabidopsis thaliana cells to xylem vessel elements, upon treatment with dexamethasone (DEX). We group the transdifferentiation process into three distinct stages, based on morphological observations of the cell walls. The first stage includes cells with only a primary cell wall (PCW), the second covers cells that have formed a SCW, and the third stage includes cells with a ruptured tonoplast and partially or fully degraded PCW. We adopt a multi-scale approach to study the mechanical properties of cells in these three stages. We perform large-scale indentations with a micro-compression system in three different osmotic conditions. Atomic force microscopy (AFM) nanoscale indentations in water allow us to isolate the cell wall response. We propose a spring-based model to deconvolve the competing stiffness contributions from turgor pressure, PCW, SCW and cytoplasm in the stiffness of differentiating cells. Prior to triggering differentiation, cells in hypotonic pressure conditions are significantly stiffer than cells in isotonic or hypertonic conditions, highlighting the dominant role of turgor pressure. Plasmolyzed cells with a SCW reach similar levels of stiffness as cells with maximum turgor pressure. The stiffness of the PCW in all of these conditions is lower than the stiffness of the fully-formed SCW. Our results provide the first experimental characterization of the mechanics of SCW formation at single cell level.

Die gemeinsame Wurzel der Lyse von Escherichia coli durch Penicillin oder durch Phagen

1957 ◽  
Vol 12 (7) ◽  
pp. 421-427 ◽  
Author(s):  
W. Weidel ◽  
J. Primosigh
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Building Blocks ◽  
Diaminopimelic Acid ◽  
Wall Structure ◽  
Gram Positive ◽  
E Coli ◽  
Growing Cell ◽  
Cell Wall Disruption ◽  
Entire Cell

One of the two layers of the E. coli B cell wall is shown to possess the chemical composition typical of a gram-positive microorganism. It is this layer which lends support and strength to the entire cell wall structure, its rigidity depending up on the incorporation of building blocks made up from alanine, glutamic acid, diaminopimelic acid, muramic acid and glucosamine.Phage enzyme is an agent capable of removing these stabilizing units from the „gram-positive “ layer, thereby causing it to collapse. Penicillin appears to prevent the biosynthetic incorporation of the same stabilizing units into growing cell walls, thus producing eventually the effect of cell wall disruption in a basically similar way.The rather manifold aspects of these findings are discussed at some length.

scholarly journals The Placenta of Physcomitrium patens: Transfer Cell Wall Polymers Compared across the Three Bryophyte Groups

Diversity ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 378
Author(s):  
Jason S. Henry ◽  
Karen S. Renzaglia
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cell Wall Composition ◽  
Transfer Cells ◽  
Primary Cell ◽  
Transfer Cell ◽  
Primary Cell Wall ◽  
Slight Variation ◽  
Wall Ingrowths ◽  
Cell Wall Polymers

Following similar studies of cell wall constituents in the placenta of Phaeoceros and Marchantia, we conducted immunogold labeling TEM studies of Physcomitrium patens to determine the composition of cell wall polymers in transfer cells on both sides of the placenta. Sixteen monoclonal antibodies were used to localize cell wall epitopes in the basal walls and wall ingrowths in this moss. In general, placental transfer cell walls of P. patens contained fewer pectins and far fewer arabinogalactan proteins AGPs than those of the hornwort and liverwort. P. patens also lacked the differential labeling that is pronounced between generations in the other bryophytes. In contrast, transfer cell walls on either side of the placenta of P. patens were relatively similar in composition, with slight variation in homogalacturonan HG pectins. Compositional similarities between wall ingrowths and primary cell walls in P. patens suggest that wall ingrowths may simply be extensions of the primary cell wall. Considerable variability in occurrence, abundance, and types of polymers among the three bryophytes and between the two generations suggested that similarity in function and morphology of cell walls does not require a common cell wall composition. We propose that the specific developmental and life history traits of these plants may provide even more important clues in understanding the basis for these differences. This study significantly builds on our knowledge of cell wall composition in bryophytes in general and in transfer cells across plants.

scholarly journals Identification and characterization of plant glycerophosphodiester phosphodiesterase

2004 ◽  
Vol 379 (3) ◽  
pp. 601-607 ◽  
Author(s):  
Benoît van der REST ◽  
Norbert ROLLAND ◽  
Anne-Marie BOISSON ◽  
Myriam FERRO ◽  
Richard BLIGNY ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Wall ◽  
Cell Walls ◽  
Expression System ◽  
Gel Filtration ◽  
Cell Suspension Cultures ◽  
Cell Wall Proteins ◽  
Ammonium Sulphate Precipitation ◽  
Carrot Cell ◽  
Glycerophosphodiester Phosphodiesterase

GPX-PDE (glycerophosphodiester phosphodiesterase; EC 3.1.4.46) is a relatively poorly characterized enzyme that catalyses the hydrolysis of various glycerophosphodiesters (glycerophosphocholine, glycerophosphoethanolamine, glycerophosphoglycerol, glycerophosphoserine and bis-glycerophosphoglycerol), releasing sn-glycerol 3-phosphate and the corresponding alcohol. In a previous study, we demonstrated the existence of a novel GPX-PDE in the cell walls and vacuoles of plant cells. Since no GPX-PDE had been identified in any plant organism, the purification of GPX-PDE from carrot cell walls was attempted. After extraction of cell wall proteins from carrot cell suspension cultures with CaCl2, GPX-PDE was purified up to 2700-fold using, successively, ammonium sulphate precipitation, gel filtration and concanavalin A–Sepharose. Internal sequence analysis of a 55 kDa protein identified in the extract following 2700-fold purification revealed strong similarity to the primary sequence of GLPQ, a bacterial GPX-PDE. To confirm the identity of plant GPX-PDE, an Arabidopsis thaliana cDNA similar to that encoding the bacterial GPX-PDE was cloned and overexpressed in a bacterial expression system, and was used to raise antibodies against the putative Arabidopsis thaliana GPX-PDE. Immunochemical assays performed on carrot cell wall proteins extracted by CaCl2 treatment showed a strong correlation between GPX-PDE activity and detection of the 55 kDa protein, validating the identity of the plant GPX-PDE. Finally, various properties of the purified enzyme were investigated. GPX-PDE is a multimeric enzyme, specific for glycerophosphodiesters, exhibiting a Km of 36 µM for glycerophosphocholine and active within a wide pH range (from 4 to 10). Since these properties are similar to those of GLPQ, the bacterial GPX-PDE, the similarities between plant and bacterial enzymes are also discussed.

scholarly journals The contribution of cell wall remodeling and signaling to lateral organs formation

2020 ◽  
Vol 67 (1-2) ◽  
pp. 110-127 ◽  
Author(s):  
Zvi Duman ◽  
Avi Eliyahu ◽  
Mohamad Abu-Abied ◽  
Einat Sadot
Keyword(s):  
Cell Wall ◽  
Adventitious Root ◽  
Cell Walls ◽  
Adventitious Roots ◽  
Primary Cell ◽  
Primary Cell Wall ◽  
Root Induction ◽  
Developmental Programs ◽  
Lateral Organs ◽  
Improvement Programs

Lateral organs are formed in plants by post embryonic developmental programs. Leaves, and flowers differentiate from the shoot apical meristem and lateral roots from the primary root pericycle meristem. Adventitious roots are roots formed from non-root lateral meristematic tissues, mostly the cambium, in many cases in response to stress signals. The ability of plants to regenerate adventitious roots is fundamental for selection and breading programs which are based on vegetative propagation of elite clones. Thus, recalcitrant plants, losing their rooting capability, may form a genuine commercial barrier in agricultural and forestry improvement programs. Some cellular mechanisms underlying adventitious root formation have been revealed, but much is yet to be clarified. The plant primary cell wall is a dynamic organ that can change its form, and perceive and relay molecular signals inward and outward during certain stages of development in particular cells. Therefore, before the secondary cell wall is deposited and plants become the wood from which walls and furniture are built, and the fibers from which cloths are woven, primary cell walls actively participate in plant cell differentiation and developmental programs. While auxin is a major regulator, cell walls are important in regulating coherent formative cell division and synchronized polar elongation of cell lineages that are necessary for lateral organ induction and formation, and collaborative cell functioning. Nevertheless, little is known of how cell wall changes are molecularly sensed and translated to intracellular signals during differentiation of adventitious roots. Here we summarize recent data linking, directly or indirectly, cell wall events to auxin signaling and to lateral or adventitious root induction and formation.

scholarly journals Assessment of Primary Cell Wall Nanomechanical Properties in Internal Cells of Non-Fixed Maize Roots

Plants ◽  
2019 ◽  
Vol 8 (6) ◽  
pp. 172 ◽  
Author(s):  
Liudmila Kozlova ◽  
Anna Petrova ◽  
Boris Ananchenko ◽  
Tatyana Gorshkova
Keyword(s):  
Mechanical Properties ◽  
Cell Wall ◽  
Plant Growth ◽  
Cell Walls ◽  
Maize Root ◽  
Primary Cell ◽  
Primary Cell Wall ◽  
Tissue Cell ◽  
Nanomechanical Properties ◽  
Wall Stiffness

The mechanical properties of cell walls play a vital role in plant development. Atomic-force microscopy (AFM) is widely used for characterization of these properties. However, only surface or isolated plant cells have been used for such investigations, at least as non-embedded samples. Theories that claim a restrictive role of a particular tissue in plant growth cannot be confirmed without direct measurement of the mechanical properties of internal tissue cell walls. Here we report an approach of assessing the nanomechanical properties of primary cell walls in the inner tissues of growing plant organs. The procedure does not include fixation, resin-embedding or drying of plant material. Vibratome-derived longitudinal and transverse sections of maize root were investigated by AFM in a liquid cell to track the changes of cell wall stiffness and elasticity accompanying elongation growth. Apparent Young’s modulus values and stiffness of stele periclinal cell walls in the elongation zone of maize root were lower than in the meristem, i.e., cell walls became more elastic and less resistant to an applied force during their elongation. The trend was confirmed using either a sharp or spherical probe. The availability of such a method may promote our understanding of individual tissue roles in the plant growth processes.

scholarly journals Primary Cell Wall Modifying Proteins Regulate Wall Mechanics to Steer Plant Morphogenesis

2021 ◽  
Vol 12 ◽  
Author(s):  
Dengying Qiu ◽  
Shouling Xu ◽  
Yi Wang ◽  
Ming Zhou ◽  
Lilan Hong
Keyword(s):  
Mechanical Properties ◽  
Cell Wall ◽  
Cell Expansion ◽  
Cell Walls ◽  
Primary Cell Wall ◽  
Mechanical Forces ◽  
Cell Morphogenesis ◽  
Physical Processes ◽  
Plant Morphogenesis ◽  
Continuous Progress

Plant morphogenesis involves multiple biochemical and physical processes inside the cell wall. With the continuous progress in biomechanics field, extensive studies have elucidated that mechanical forces may be the most direct physical signals that control the morphology of cells and organs. The extensibility of the cell wall is the main restrictive parameter of cell expansion. The control of cell wall mechanical properties largely determines plant cell morphogenesis. Here, we summarize how cell wall modifying proteins modulate the mechanical properties of cell walls and consequently influence plant morphogenesis.

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