Incorporation of β-(1,6)-linked glucooligosaccharides (pustulooligosaccharides) into plant cell wall structures

2012 ◽  
Vol 66 (9) ◽  
Author(s):  
Zuzana Zemková ◽  
Soňa Garajová ◽  
Dana Flodrová ◽  
Pavel Řehulka ◽  
Ivan Zelko ◽  
...  
Keyword(s):  
Cell Wall ◽  
Plant Cell Wall ◽  
Structural Similarity ◽  
Size Exclusion ◽  
Primary Cell Wall ◽  
Specific Cell ◽  
Specific Substrate ◽  
Xyloglucan Endotransglycosylase ◽  
Dot Blot ◽  
Wall Structures

AbstractProtein extract of germinating nasturtium (Tropaeolum majus) seeds containing xyloglucan endotransglycosylase (xyloglucan xyloglucosyl transferase, EC 2.4.1.207, abbreviated XET) exhibited the heterotransglycosylating activity with donor/acceptor substrate pair xyloglucan/sulphorhodamine labelled pustulooligosaccharides (XG/PUOS-SR) in a dot blot assay. The heterotransglycosylating activity was confirmed by the substrate-product changes during transglycosylation by HPLC size-exclusion chromatography. Another donor substrate capable of being coupled with PUOS-SR was cellulose, probably owing to its structural similarity to xyloglucan. Surprisingly, microscopic comparison of the incorporation of the labelled xyloglucan nonasaccharide XGO9-SR (specific substrate for XET) and PUOS-SR into the cell wall structures clearly showed differences in their binding to specific cell structures: the primary cell wall and the plasma membrane. These findings indicate the existence in nasturtium of XETs with different localisation, substrate specificity and, probably, function.

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

A xyloglucan-induced increase in lettuce germination and seedling elongation is not related to the degradation of the exogenous xyloglucan

Botany ◽  
2013 ◽  
Vol 91 (12) ◽  
pp. 822-829
Author(s):  
Adaucto B. Pereira-Netto ◽  
Carmen L.O. Petkowicz
Keyword(s):  
Cell Wall ◽  
High Performance ◽  
Plant Cell Wall ◽  
Building Blocks ◽  
Germination Percentage ◽  
Primary Cell ◽  
Size Exclusion ◽  
Primary Cell Wall ◽  
Hymenaea Courbaril ◽  
Cell Wall Assembly

Xyloglucans are the main hemicellulosic polysaccharides found in the primary cell walls of dicots and nongraminaceous monocots. Although xyloglucans are building blocks used in plant cell wall assembly, the function of these molecules in the structure and growth of the primary cell wall remains poorly understood. In this study, we demonstrate that treatment of lettuce seeds with a xyloglucan extracted from cotyledons of Hymenaea courbaril L. (Leguminosae (Fabaceae) – Caesalpinioideae) in the 0.1 to 10 nmol·L−1 range resulted in significantly increased germination percentage. In addition, lettuce seedlings grown in the presence of 500 nmol·L−1 xyloglucan presented a significantly larger length compared with seedlings grown in the absence of xyloglucan. Furthermore, the H. courbaril xyloglucan was not able to reverse a 2,4-dichlorophenoxy acetic acid induced inhibition of seedling elongation. High performance size exclusion chromatography (HPSEC) and high-performance liquid chromatography (HPLC) analyses indicated that the xyloglucan-induced enhancement of germination percentage and seedling elongation in lettuce does not rely on the release of monomers, i.e., glucose, xylose, and galactose from the exogenous xyloglucan.

scholarly journals AtSYP71 Is Important for Plant Cell Wall Biosynthesis and Stress Adaptation.

2021 ◽  
Author(s):  
Xiaoyue Kou ◽  
Hailong Zhang ◽  
Xiaonan Zhao ◽  
Mingjing Wang ◽  
Guochen Qin ◽  
...  
Keyword(s):  
Cell Wall ◽  
Early Development ◽  
Plant Development ◽  
Plant Cell Wall ◽  
Cell Plate ◽  
Development Stage ◽  
Cell Wall Biosynthesis ◽  
Knockout Mutant ◽  
Wall Structures ◽  
Confocal Images

Abstract Background: SYP71, the plant-specific Qc-SNARE protein, is reported to regulate vesicle trafficking. SYP71 is localized on the ER, endosome, plasma membrane and cell plate, suggesting its multiple functions. Lotus SYP71 is essential for symbiotic nitrogen fixation in nodules. AtSYP71, GmSYP71 and OsSYP71 are implicated in plant resistance to pathogenesis. To date, SYP71 regulatory role on plant development remain unclear.Results: AtSYP71-knockout mutant atsyp71-4 was lethal at early development stage. Early development of AtSYP71-knockdown mutant atsyp71-2 was delayed, and stress response was also affected. Confocal images revealed that protein secretion was blocked in atsyp71-2. Transcriptomic analysis indicated that metabolism, response to environmental stimuli pathways and apoplast components were influenced in atsyp71-2. Moreover, the contents of lignin, cellulose and flavonoids as well as cell wall structures were also altered.Conclusion: Our findings suggested that AtSYP71 is essential for plant development. AtSYP71 probably regulates plant development, metabolism and environmental adaptation by affecting cell wall homeostasis via mediating secretion of materials and regulators required for cell wall biosynthesis and dynamics.

scholarly journals Primary cell wall inspired micro containers as a step towards a synthetic plant cell

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
T. Paulraj ◽  
S. Wennmalm ◽  
D.C.F. Wieland ◽  
A. V. Riazanova ◽  
A. Dėdinaitė ◽  
...  
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Plant Cell Wall ◽  
Structural Integrity ◽  
Plant Cells ◽  
Lipid Vesicles ◽  
Primary Cell Wall ◽  
Living Plant ◽  
A Cell ◽  
Lipid Tubules

AbstractThe structural integrity of living plant cells heavily relies on the plant cell wall containing a nanofibrous cellulose skeleton. Hence, if synthetic plant cells consist of such a cell wall, they would allow for manipulation into more complex synthetic plant structures. Herein, we have overcome the fundamental difficulties associated with assembling lipid vesicles with cellulosic nanofibers (CNFs). We prepare plantosomes with an outer shell of CNF and pectin, and beneath this, a thin layer of lipids (oleic acid and phospholipids) that surrounds a water core. By exploiting the phase behavior of the lipids, regulated by pH and Mg2+ ions, we form vesicle-crowded interiors that change the outer dimension of the plantosomes, mimicking the expansion in real plant cells during, e.g., growth. The internal pressure enables growth of lipid tubules through the plantosome cell wall, which paves the way to the development of hierarchical plant structures and advanced synthetic plant cell mimics.

scholarly journals Golgi-localized GALT7 and GALT8 participate in cellulose biosynthesis

2021 ◽  
Author(s):  
Pieter Nibbering ◽  
Romain Castilleux ◽  
Gunnar Wingsle ◽  
Totte Niittylä
Keyword(s):  
Cell Wall ◽  
Golgi Apparatus ◽  
Secondary Cell Wall ◽  
Plant Cell Wall ◽  
Arabinogalactan Protein ◽  
Primary Cell Wall ◽  
Cellulose Content ◽  
Cellulose Biosynthesis ◽  
Cell Wall Assembly ◽  
Protein Levels

AbstractArabinogalactan protein (AGP) glycan biosynthesis in the Golgi apparatus contributes to plant cell wall assembly, but the mechanisms underlying this process are largely unknown. Here, we show that two putative galactosyltransferases -named GALT7 and GALT8 -from the glycosyltransferase family 31 (GT31) of Arabidopsis thaliana participate in cellulose biosynthesis. galt7galt8 mutants show primary cell wall defects manifesting as impaired growth and cell expansion in seedlings and etiolated hypocotyls, along with secondary cell wall defects, apparent as collapsed xylem vessels and reduced xylem wall thickness in the inflorescence stem. These phenotypes were associated with a ∼30% reduction in cellulose content, a ∼50% reduction in secondary cell wall CELLULOSE SYNTHASE (CESA) protein levels and reduced cellulose biosynthesis rate. CESA transcript levels were not significantly altered in galt7galt8 mutants, suggesting that the reduction in CESA levels was caused by a post-transcriptional mechanism. We provide evidence that both GALT7 and GALT8 localise to the Golgi apparatus, while quantitative proteomics experiments revealed reduced levels of the entire FLA subgroup B in the galt7galt8 mutants. This leads us to hypothesize that a defect in FLA subgroup B glycan biosynthesis reduces cellulose biosynthesis rate in galt7galt8 mutants.

Changes in Hemicellulose-associated Pectin during Softening of Peach Fruit

HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 640c-640
Author(s):  
Supreetha Hegde ◽  
Niels O. Maness
Keyword(s):  
Molecular Weight ◽  
Cell Wall ◽  
Sodium Carbonate ◽  
Middle Lamella ◽  
Apparent Molecular Weight ◽  
Primary Cell ◽  
Size Exclusion ◽  
Primary Cell Wall ◽  
Cell Wall Polysaccharide ◽  
Peach Fruit

Softening to a normal melting flesh texture in peaches involves a combined participation between polymers located in the middle lamella and primary cell wall. Pectins located in the primary cell wall polysaccharide matrix which cosolubilize when hemicellulose is extracted with KOH have received less attention than the chelator or sodium carbonate soluble pectin likely to be associated with the middle lamella. We conducted a series of extractions for cell walls prepared from softening peach fruit (47, 30, and 15 N firmness) using 0.5 m imidazole, sodium carbonate and a graded series of KOH. Hemicellulose-associated pectin was a substantial proportion of most KOH extracts (30 to 50 mole percent) and fractionated on size exclusion chromatography as a high apparent molecular weight peak which became more prominent as fruit softened and could be separated from two lower apparent molecular weight peaks by anion exchange chromatography. The nature of a hemicellulose-pectin interaction in peach was apparently by physical entrapment, versus covalent cross-linking. Softening related changes in hemicellulose-associated pectin will be addressed.

Direct visualization of cross-links in the primary plant cell wall

1990 ◽  
Vol 96 (2) ◽  
pp. 323-334 ◽  
Author(s):  
M. C. MCCANN ◽  
B. WELLS ◽  
K. ROBERTS
Keyword(s):  
Cell Wall ◽  
Plant Cell Wall ◽  
Three Dimensional ◽  
Preliminary Evidence ◽  
Cellulose Microfibrils ◽  
Primary Cell Wall ◽  
Positive Role ◽  
Extraction Step ◽  
Cross Links ◽  
Wall Construction

We have investigated the structure of the onion primary cell wall at high resolution, using shadowed replicas of rapidly frozen deep-etched specimens. We have sequentially extracted polymers from the wall and have visualized both these and the remaining structures at each extraction step. By viewing the structures in as near their native state as possible, an accurate three-dimensional picture of wall construction has been assembled, facilitated by viewing stereo pairs of micrographs. Our observations show that the physical links between cellulose microfibrils that we observe in the intact wall are generally shorter (20–40 nm) than the isolated molecules we extract (30->700nm), suggesting that lateral interactions must occur between linking polymers and cellulose in muro. These cross-links are hemicellulosic and we believe them to be xyloglucans: their removal allows increased lateral association of microfibrils. Na2CO3-extractable pectic fractions form a separate coextensive network, the removal of which does not affect basic cellulose/ hemicellulose architecture. Preliminary evidence for a lamellate model of wall construction has been obtained. In addition, we propose a positive role for hemicellulose in maintaining the ordered spacing of cellulose micronbrils, perhaps regulating wall porosity and strength. The basic wall parameters that we derive impose constraints on possible cell wall models.

Modeling the nonlinear elastic behavior of plant epidermis

Botany ◽  
2020 ◽  
Vol 98 (1) ◽  
pp. 49-64 ◽  
Author(s):  
Amir J. Bidhendi ◽  
Hongbo Li ◽  
Anja Geitmann
Keyword(s):  
Cell Wall ◽  
Test Data ◽  
Plant Cell Wall ◽  
Tissue Mechanics ◽  
Mechanical Anisotropy ◽  
Elastic Behavior ◽  
Primary Cell Wall ◽  
Uniaxial Tensile ◽  
Uniaxial Tensile Test ◽  
Highly Nonlinear

Cell growth and organ development in plants are often correlated with the tensile behavior of the primary cell wall. To understand the mechanical behavior of plant material, various mechanical testing techniques have been employed, such as tensile testing of excised tissue samples. The onion (Allium cepa L.) epidermis has emerged as a model system for plant tissue mechanics. In this study, we performed tensile tests on strips of adaxial onion epidermis. While the tissue appeared stiffer in the direction along the major growth axis compared with the transverse direction, the tensile strength of tissue was not significantly different between the two orientations, indicating a nontrivial link between the cell wall and tissue mechanical anisotropy. Importantly, we observed the stress–strain behavior of the onion epidermis under tension to be highly nonlinear. Several hyperelastic models were fitted to the test data to evaluate their capacity to describe the nonlinear deformation of onion epidermis. The Yeoh hyperelastic model could successfully simulate the uniaxial tensile test data. This study suggests that accounting for nonlinearity in the deformation of the primary tissue may be essential for the accurate interpretation of mechanical test data, and a better understanding of the mechanics of the primary plant cell wall.

The three-dimensional structure of the cell wall glycoprotein of Chlorogonium elongatum

1984 ◽  
Vol 68 (1) ◽  
pp. 271-284
Author(s):  
P.J. Shaw ◽  
G.J. Hills
Keyword(s):  
Cell Wall ◽  
Plant Cell Wall ◽  
Higher Plants ◽  
Three Dimensional ◽  
Three Dimensions ◽  
Dimensional Structure ◽  
Primary Cell Wall ◽  
Globular Domain ◽  
Higher Plant ◽  
Intersubunit Interactions

The green alga Chlorogonium elongatum, a member of the Volvocales, possesses a crystalline cell wall composed of hydroxyproline-rich glycoprotein similar to the primary cell wall glycoproteins of higher plants. Electron microscopy and computer image processing have been used to determine the crystal structure of the Chlorogonium cell wall in three dimensions to a resolution of 2.0 nm. The structure is composed of heterologous dimers. Each subunit of the dimer comprises a long, thin spacer domain and a large globular domain, which is the site of the intra- and inter-dimer interactions. There are also sites of intersubunit interactions at the opposite ends of the rod domains. We suggest that the rods are composed predominantly of glycosylated polyproline helix, as has been suggested for higher plant cell wall glycoproteins and has been shown for the cell wall glycoprotein of Chlamydomonas reinhardtii, which is closely related to Chlorogonium.

scholarly journals Carbon dots for efficient siRNA delivery and gene silencing in plants

2019 ◽  
Author(s):  
Steven. H. Schwartz ◽  
Bill Hendrix ◽  
Paul Hoffer ◽  
Rick A. Sanders ◽  
Wei Zheng
Keyword(s):  
Cell Wall ◽  
Gene Silencing ◽  
Functional Genomics ◽  
Plant Cell ◽  
Carbon Dots ◽  
Plant Cell Wall ◽  
Crop Improvement ◽  
Size Exclusion ◽  
Gene Transcript ◽  
Carbon Dot

SUMMARYThe Initiation of RNA interference (RNAi) by topically applied double stranded RNA (dsRNA) has potential applications for plant functional genomics, crop improvement and crop protection. The primary obstacle for the development of this technology is efficient delivery of RNAi effectors. The plant cell wall is a particularly challenging barrier to the delivery of macromolecules. Many of the transfection agents that are commonly used with animal cells produce nanocomplexes that are significantly larger than the size exclusion limit of the plant cell wall. Utilizing a class of very small nanoparticles called carbon dots, a method of delivering siRNA into the model plant Nicotiana benthamiana and tomato is described. Low-pressure spray application of these formulations with a spreading surfactant resulted in strong silencing of GFP transgenes in both species. The delivery efficacy of carbon dot formulations was also demonstrated by silencing endogenous genes that encode two sub-units of magnesium chelatase, an enzyme necessary for chlorophyll synthesis. The strong visible phenotypes observed with the carbon dot facilitated delivery were validated by measuring significant reductions in the target gene transcript and/or protein levels. Methods for the delivery of RNAi effectors into plants, such as the carbon dot formulations described here, could become valuable tools for gene silencing in plants with practical applications in plant functional genomics and agriculture.

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