scholarly journals Identification of two functional xyloglucan galactosyltransferase homologs BrMUR3 and BoMUR3 in brassicaceous vegetables

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9095
Author(s):  
Meng Wang ◽  
Zongchang Xu ◽  
Shuaiqiang Guo ◽  
Gongke Zhou ◽  
Malcolm ONeill ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Walls ◽  
Cellulose Microfibrils ◽  
Composition Analysis ◽  
Evolutionary Analysis ◽  
Cell Integrity ◽  
Additional Information ◽  
The Third ◽  
Galactose Residue ◽  
Dicotyledonous Plants

Xyloglucan (XyG) is the predominant hemicellulose in the primary cell walls of most dicotyledonous plants. Current models of these walls predict that XyG interacts with cellulose microfibrils to provide the wall with the rigidity and strength necessary to maintain cell integrity. Remodeling of this network is required to allow cell elongation and plant growth. In this study, homologs of Arabidopsis thaliana MURUS3 (MUR3), which encodes a XyG-specific galactosyltransferase, were obtained from Brassica rapa (BrMUR3) to Brassica oleracea (BoMUR3). Genetic complementation showed that BrMUR3 and BoMUR3 rescue the phenotypic defects of the mur3-3 mutant. Xyloglucan subunit composition analysis provided evidence that BrMUR3 and BoMUR3 encode a galactosyltransferase, which transfers a galactose residue onto XyG chains. The detection of XXFG and XLFG XyG subunits (restoration of fucosylated side chains) in mur3-3 mutants overexpressing BrMUR3 or BoMUR3 show that MUR3 from Brassica to Arabidopsis are comparable as they add Gal to the third xylosyl residue of the XXXG subunit. Our results provide additional information for functional dissection and evolutionary analysis of MUR3 genes derived from brassicaceous species.

Reduced pectin content of cell walls prevents stress-induced root cell elongation in Arabidopsis

2020 ◽  
Author(s):  
Xiaohui Liu ◽  
Huiying Cui ◽  
Bochao Zhang ◽  
Min Song ◽  
Shaolin Chen ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Elongation ◽  
Cell Walls ◽  
Microscopic Analysis ◽  
Root Cell ◽  
Cellulose Microfibrils ◽  
Composition Analysis ◽  
Cellulose Content ◽  
Cell Extension ◽  
Mechanistic Basis

Abstract The primary cell walls of plants provide mechanical strength while maintaining the flexibility needed for cell extension growth. Cell extension involves loosening the bonds between cellulose microfibrils, hemicelluloses and pectins. Pectins have been implicated in this process, but it remains unclear if this depends on the abundance of certain pectins, their modifications, and/or structure. Here, cell wall-related mutants of the model plant Arabidopsis were characterized by biochemical and immunohistochemical methods and Fourier-transform infrared microspectroscopy. Mutants with reduced pectin or hemicellulose content showed no root cell elongation in response to simulated drought stress, in contrast to wild-type plants or mutants with reduced cellulose content. While no association was found between the degrees of pectin methylesterification and cell elongation, cell wall composition analysis suggested an important role of the pectin rhamnogalacturonan II (RGII), which was corroborated in experiments with the RGII-modifying chemical 2β-deoxy-Kdo. The results were complemented by expression analysis of cell wall synthesis genes and microscopic analysis of cell wall porosity. It is concluded that a certain amount of pectin is necessary for stress-induced root cell elongation, and hypotheses regarding the mechanistic basis of this result are formulated.

Texture of cellulose microfibrils of root hair cell walls of Arabidopsis thaliana, Medicago truncatula, and Vicia sativa

2012 ◽  
Vol 247 (1) ◽  
pp. 60-67 ◽  
Author(s):  
M. AKKERMAN ◽  
M.A.W. FRANSSEN-VERHEIJEN ◽  
P. IMMERZEEL ◽  
L.DEN HOLLANDER ◽  
J.H.N. SCHEL ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Hair Cell ◽  
Medicago Truncatula ◽  
Root Hair ◽  
Cell Walls ◽  
Cellulose Microfibrils ◽  
Vicia Sativa ◽  
Root Hair Cell

scholarly journals Two Expansin Genes, AtEXPA4 and AtEXPB5, Are Redundantly Required for Pollen Tube Growth and AtEXPA4 Is Involved in Primary Root Elongation in Arabidopsis thaliana

Genes ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 249
Author(s):  
Weimiao Liu ◽  
Liai Xu ◽  
Hui Lin ◽  
Jiashu Cao
Keyword(s):  
Arabidopsis Thaliana ◽  
Pollen Tube ◽  
Pollen Tube Growth ◽  
Cell Walls ◽  
Root Elongation ◽  
Expression Patterns ◽  
Primary Root ◽  
Pollen Grains ◽  
Tube Growth ◽  
Cell Wall Binding

The growth of plant cells is inseparable from relaxation and expansion of cell walls. Expansins are a class of cell wall binding proteins, which play important roles in the relaxation of cell walls. Although there are many members in expansin gene family, the functions of most expansin genes in plant growth and development are still poorly understood. In this study, the functions of two expansin genes, AtEXPA4 and AtEXPB5 were characterized in Arabidopsis thaliana. AtEXPA4 and AtEXPB5 displayed consistent expression patterns in mature pollen grains and pollen tubes, but AtEXPA4 also showed a high expression level in primary roots. Two single mutants, atexpa4 and atexpb5, showed normal reproductive development, whereas atexpa4atexpb5 double mutant was defective in pollen tube growth. Moreover, AtEXPA4 overexpression enhanced primary root elongation, on the contrary, knocking out AtEXPA4 made the growth of primary root slower. Our results indicated that AtEXPA4 and AtEXPB5 were redundantly involved in pollen tube growth and AtEXPA4 was required for primary root elongation.

scholarly journals Two β-glucuronosyltransferases involved in the biosynthesis of type II arabinogalactans function in mucilage polysaccharide matrix organization in Arabidopsis thaliana

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Oyeyemi O. Ajayi ◽  
Michael A. Held ◽  
Allan M. Showalter
Keyword(s):  
Arabidopsis Thaliana ◽  
Seed Size ◽  
Seed Coat ◽  
Glucuronic Acid ◽  
Industrial Applications ◽  
Crystalline Cellulose ◽  
Sugar Residue ◽  
Composition Analysis ◽  
Cellulose Content ◽  
Type Ii

Abstract Background Arabinogalactan-proteins (AGPs) are heavily glycosylated with type II arabinogalactan (AG) polysaccharides attached to hydroxyproline residues in their protein backbone. Type II AGs are necessary for plant growth and critically important for the establishment of normal cellular functions. Despite the importance of type II AGs in plant development, our understanding of the underlying role of these glycans/sugar residues in mucilage formation and seed coat epidermal cell development is poorly understood and far from complete. One such sugar residue is the glucuronic acid residues of AGPs that are transferred onto AGP glycans by the action of β-glucuronosyltransferase genes/enzymes. Results Here, we have characterized two β-glucuronosyltransferase genes, GLCAT14A and GLCAT14C, that are involved in the transfer of β-glucuronic acid (GlcA) to type II AGs. Using a reverse genetics approach, we observed that glcat14a-1 mutants displayed subtle alterations in mucilage pectin homogalacturonan (HG) compared to wild type (WT), while glcat14a-1glcat14c-1 mutants displayed much more severe mucilage phenotypes, including loss of adherent mucilage and significant alterations in cellulose ray formation and seed coat morphology. Monosaccharide composition analysis showed significant alterations in the sugar amounts of glcat14a-1glcat14c-1 mutants relative to WT in the adherent and non-adherent seed mucilage. Also, a reduction in total mucilage content was observed in glcat14a-1glcat14c-1 mutants relative to WT. In addition, glcat14a-1glcat14c-1 mutants showed defects in pectin formation, calcium content and the degree of pectin methyl-esterification (DM) as well as reductions in crystalline cellulose content and seed size. Conclusions These results raise important questions regarding cell wall polymer interactions and organization during mucilage formation. We propose that the enzymatic activities of GLCAT14A and GLCAT14C play partially redundant roles and are required for the organization of the mucilage matrix and seed size in Arabidopsis thaliana. This work brings us a step closer towards identifying potential gene targets for engineering plant cell walls for industrial applications.

Caffeoyl Shikimate Esterase (CSE) Is an Enzyme in the Lignin Biosynthetic Pathway in Arabidopsis

Science ◽  
2013 ◽  
Vol 341 (6150) ◽  
pp. 1103-1106 ◽  
Author(s):  
Ruben Vanholme ◽  
Igor Cesarino ◽  
Katarzyna Rataj ◽  
Yuguo Xiao ◽  
Lisa Sundin ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Walls ◽  
Metabolite Profiling ◽  
Biosynthetic Pathway ◽  
Wild Type ◽  
Secondary Cell Walls ◽  
Phenolic Metabolite ◽  
In The Wild ◽  
Lignin Biosynthetic Pathway

Lignin is a major component of plant secondary cell walls. Here we describe caffeoyl shikimate esterase (CSE) as an enzyme central to the lignin biosynthetic pathway. Arabidopsis thaliana cse mutants deposit less lignin than do wild-type plants, and the remaining lignin is enriched in p-hydroxyphenyl units. Phenolic metabolite profiling identified accumulation of the lignin pathway intermediate caffeoyl shikimate in cse mutants as compared to caffeoyl shikimate levels in the wild type, suggesting caffeoyl shikimate as a substrate for CSE. Accordingly, recombinant CSE hydrolyzed caffeoyl shikimate into caffeate. Associated with the changes in lignin, the conversion of cellulose to glucose in cse mutants increased up to fourfold as compared to that in the wild type upon saccharification without pretreatment. Collectively, these data necessitate the revision of currently accepted models of the lignin biosynthetic pathway.

Review — The Orientation of Cellulose Microfibrils in the cell walls of Tracheids in Conifers

IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Outer Layer ◽  
Cell Walls ◽  
Secondary Wall ◽  
Middle Layer ◽  
Cellulose Microfibrils ◽  
Conifer Species ◽  
Predominant Orientation ◽  
Scanning Electron

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.

scholarly journals Thermal degradation of hemicellulose and cellulose in ball-milled cedar and beech wood

2021 ◽  
Vol 67 (1) ◽  
Author(s):  
Jiawei Wang ◽  
Eiji Minami ◽  
Mohd Asmadi ◽  
Haruo Kawamoto
Keyword(s):  
Thermal Degradation ◽  
Ball Milling ◽  
Cell Walls ◽  
Uronic Acid ◽  
Beech Wood ◽  
Cellulose Microfibrils ◽  
Homogeneous Distribution ◽  
Japanese Beech ◽  
Temperature Range ◽  
The Matrix

AbstractThe thermal degradation reactivities of hemicellulose and cellulose in wood cell walls are significantly different from the thermal degradation behavior of the respective isolated components. Furthermore, the degradation of Japanese cedar (Cryptomeria japonica, a softwood) is distinct from that of Japanese beech (Fagus crenata, a hardwood). Lignin and uronic acid are believed to play crucial roles in governing this behavior. In this study, the effects of ball milling for various durations of time on the degradation reactivities of cedar and beech woods were evaluated based on the recovery rates of hydrolyzable sugars from pyrolyzed wood samples. The applied ball-milling treatment cleaved the lignin β-ether bonds and reduced the crystallinity of cellulose, as determined by X-ray diffraction. Both xylan and glucomannan degraded in a similar temperature range, although the isolated components exhibited different reactivities because of the catalytic effect of uronic acid bound to the xylose chains. These observations can be explained by the more homogeneous distribution of uronic acid in the matrix of cell walls as a result of ball milling. As observed for holocelluloses, cellulose in the ball-milled woods degraded in two temperature ranges (below 320 °C and above); a significant amount of cellulose degraded in the lower temperature range, which significantly changed the shapes of the thermogravimetric curves. This report compares the results obtained for cedar and beech woods, and discusses them in terms of the thermal degradation of the matrix and cellulose microfibrils in wood cell walls and role of lignin. Such information is crucial for understanding the pyrolysis and heat treatment of wood.

Results of Archaeoparasitological and Palynological Analyzes of the Contents of the Sewage Drain of the Chorgun Tower (South-Western Crimea)

2021 ◽  
pp. 377-389
Author(s):  
Evgeniy Nedelkin ◽  
◽  
Alexander Khrustalev ◽  
Anna Babenko ◽  
Sergey Slepchenko ◽  
...  
Keyword(s):  
Intestinal Parasites ◽  
Gastrointestinal Diseases ◽  
Archaeological Research ◽  
Additional Information ◽  
The Third ◽  
15Th Century ◽  
Palynological Study ◽  
Sanitary Conditions ◽  
The Village ◽  
Constant Source

The article presents the results of an archaeoparasitological and palynological study of a sample taken from the sewage drain of the Chorgun Tower. This is a fortification on the territory of the village of Chernorechie (South-Western Crimea). According to archaeological research, the construction of the keep dates back to the third quarter of the 15th century. Four types of eggs of intestinal parasites infecting humans and synanthropic animals were identified in the sample. Regarding parasitic and infectious gastrointestinal diseases, human whipworm and roundworm eggs found in the sample are indicative of relatively unfavorable sanitary conditions of the fortification. Based on the features of the archaeoparasitological spectrum, it can be concluded that anthelminthic agents were used or food with antiparasitic effects against roundworms was consumed. The difficult sanitary and epidemiological situation was also complicated by synanthropic rodents, such as rats and domestic mice, which could be a constant source of dangerous infections in the Chorgun Keep. A palynological study of the contents of the sewage runoff made it possible to obtain additional information on the nutrition of people who used the latrine facilities in the Chorgun Keep. What is equally important is that the study demonstrates the possibilities of methods for the study of canalization as a source of bioarchaeological information.

scholarly journals Characterization of .ALPHA.-L-arabinofuranosidase related to the secondary cell walls formation in Arabidopsis thaliana

2010 ◽  
Vol 27 (3) ◽  
pp. 259-266 ◽  
Author(s):  
Hitomi Ichinose ◽  
Nobuyuki Nishikubo ◽  
Taku Demura ◽  
Satoshi Kaneko
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Walls ◽  
Secondary Cell Walls

scholarly journals A Label-free, Fast and High-specificity Technique for Plant Cell Wall Imaging and Composition Analysis

2020 ◽  
Author(s):  
Huimin Xu ◽  
Yuanyuan Zhao ◽  
Yuanzhen Suo ◽  
Yayu Guo ◽  
Yi Man ◽  
...  
Keyword(s):  
Cell Wall ◽  
Chemical Composition ◽  
Raman Scattering ◽  
Plant Cell ◽  
Cell Walls ◽  
Plant Cell Wall ◽  
Composition Analysis ◽  
Plant Cell Walls ◽  
Label Free ◽  
Wall Imaging

Abstract Background: Cell wall imaging can considerably permit direct visualization of the molecular architecture of cell walls and provide the detailed chemical information on wall polymers, which is imperative to better exploit and use the biomass polymers; however, detailed imaging and quantifying of the native composition and architecture in the cell wall remains challenging.Results: Here, we describe a label-free imaging technology, coherent Raman scattering microscopy (CRS), including coherent anti-Stokes Raman scattering (CARS) microscopy and stimulated Raman scattering (SRS) microscopy, which images the major structures and chemical composition of plant cell walls. The major steps of the procedure are demonstrated, including sample preparation, setting the mapping parameters, analysis of spectral data, and image generation. Applying this rapid approach, which will help researchers understand the highly heterogeneous structures and organization of plant cell walls.Conclusions: This method can potentially be incorporated into label-free microanalyses of plant cell wall chemical composition based on the in situ vibrations of molecules.

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