scholarly journals Cell wall structure and formation of maturing fibres of moso bamboo ( Phyllostachys pubescens ) increase buckling resistance

2011 ◽  
Vol 9 (70) ◽  
pp. 988-996 ◽  
Author(s):  
Xiaoqing Wang ◽  
Haiqing Ren ◽  
Bo Zhang ◽  
Benhua Fei ◽  
Ingo Burgert
Keyword(s):  
Cell Wall ◽  
Mechanical Stability ◽  
Moso Bamboo ◽  
Wall Structure ◽  
Wall Thickening ◽  
Phyllostachys Pubescens ◽  
Vascular Bundles ◽  
Buckling Resistance ◽  
Cellulose Fibrils ◽  
Transverse Rigidity

The mechanical stability of the culms of monocotyledonous bamboos is highly attributed to the proper embedding of the stiff fibre caps of the vascular bundles into the soft parenchymatous matrix. Owing to lack of a vascular cambium, bamboos show no secondary thickening growth that impedes geometrical adaptations to mechanical loads and increases the necessity of structural optimization at the material level. Here, we investigate the fine structure and mechanical properties of fibres within a maturing vascular bundle of moso bamboo, Phyllostachys pubescens , with a high spatial resolution. The fibre cell walls were found to show almost axially oriented cellulose fibrils, and the stiffness and hardness of the central part of the cell wall remained basically consistent for the fibres at different regions across the fibre cap. A stiffness gradient across the fibre cap is developed by differential cell wall thickening which affects tissue density and thereby axial tissue stiffness in the different regions of the cap. The almost axially oriented cellulose fibrils in the fibre walls maximize the longitudinal elastic modulus of the fibres and their lignification increases the transverse rigidity. This is interpreted as a structural and mechanical optimization that contributes to the high buckling resistance of the slender bamboo culms.

Molecular xylem cell wall structure of an inclined Cycas micronesica stem, a tropical gymnosperm

IAWA Journal ◽  
2010 ◽  
Vol 31 (1) ◽  
pp. 3-11 ◽  
Author(s):  
Clemens M. Altaner ◽  
Michael C. Jarvis ◽  
Jack B. Fisher ◽  
Thomas E. Marler
Keyword(s):  
Cell Wall ◽  
Compression Wood ◽  
Lignin Content ◽  
Microfibril Angle ◽  
Picea Sitchensis ◽  
Wall Structure ◽  
Crystalline Cellulose ◽  
Cellulose Structure ◽  
Molecular Features ◽  
Cellulose Fibrils

The molecular structure of tracheid walls of an inclined eccentrically grown stem of Cycas micronesica K.D. Hill did not differ between the upper and lower side. The absence the typical molecular features of compression wood tracheids, i.e. an increased galactose and lignin content as well as an increased microfibril angle, indicated that cycads do not have the ability to form even very mild forms of compression wood, which lacks anatomical features commonly observed in compression wood. Analysis of the sugar monomers in Cycas micronesica tracheids did reveal a rather unique composition of the non-cellulosic polysaccharides for a gymnosperm. The low mannose and high xylose content resembled a cell wall matrix common in angiosperms. The crystalline cellulose structure in Cycas micronesica tracheids closely resembled those of secondary cell walls in Picea sitchensis (Bong.) Carr. tracheids. However, the spacing between the sheets of cellulose chains was wider and the cellulose fibrils appeared to form larger aggregates than in Sitka spruce tracheids.

scholarly journals Biosynthetic labeling with 3-O-propargylcaffeyl alcohol reveals in vivo cell-specific patterned lignification in loquat fruits during development and postharvest storage

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Nan Zhu ◽  
Chenning Zhao ◽  
Yuqing Wei ◽  
Chongde Sun ◽  
Di Wu ◽  
...  
Keyword(s):  
Cell Wall ◽  
Lignin Content ◽  
Wall Layer ◽  
Wall Structure ◽  
Vascular Bundles ◽  
Precise Localization ◽  
In Planta ◽  
Cell Wall Modification ◽  
Fruit Flesh

AbstractLignification is a major cell wall modification that often results in the formation of sophisticated subcellular patterns during plant development or in response to environmental stresses. Precise localization of the spatiotemporal deposition of lignin is of great importance for revealing the lignification regulatory mechanism of individual cells. In loquat fruits, lignification typically increases the flesh lignin content and firmness, reducing their edibility and processing quality. However, the precise localization of the spatiotemporal active zones of lignification inside loquat fruit flesh remains poorly understood, and little is known about the contribution of patterned lignification to cell wall structure dynamics and the subsequent fruit-quality deterioration. Here, we performed an emerging bioorthogonal chemistry imaging technique to trace the in vivo patterned lignification dynamics in cells of loquat fruit flesh during development and storage. In developing fruits, lignified cells (LCs) and vascular bundles (VBs) were the zones of active lignification, and ring-like LCs deposited lignin at both the inner wall layer and the outer periphery sides. The domino effect of the generation of LCs was preliminarily visualized. In mature fruits, the newly formed lignin in the flesh of fruits during storage was specifically deposited in the corners and middle lamellae of parenchyma cells surrounding the VBs, resulting in the development of a reticular structure. Based on the findings, distinct spatiotemporal patterned lignification modes for different flesh cells in loquat fruits were proposed. These findings provide loquat lignification dynamics together with spatiotemporal data that can improve our understanding of the lignification process in planta.

In situ detection of the fracture behaviour of moso bamboo (Phyllostachys pubescens) by scanning electron microscopy

Holzforschung ◽  
2016 ◽  
Vol 70 (12) ◽  
pp. 1183-1190 ◽  
Author(s):  
Huanrong Liu ◽  
Xiaoqing Wang ◽  
Xiubiao Zhang ◽  
Zhengjun Sun ◽  
Zehui Jiang
Keyword(s):  
Fracture Toughness ◽  
Fracture Behaviour ◽  
Synergistic Effects ◽  
Microstructural Analysis ◽  
Interfacial Debonding ◽  
Moso Bamboo ◽  
Phyllostachys Pubescens ◽  
Vascular Bundles ◽  
Scanning Electron

Abstract The remarkable fracture toughness of bamboo culms is highly attributed to the proper embedding of the stiff fibre caps of the vascular bundles into the soft parenchyma matrix. In this study, the fracture behaviour of small specimens of moso bamboo (Phyllostachys pubescens) in tension and bending were investigated in situ with a scanning electron microscope (SEM) to visualise crack initiation and propagation within bamboo tissues and its interactions with the structural components (fibres and parenchyma tissues). Fracture surfaces were studied by field-emission SEM. The fracture of bamboo in either tension or bending was non-catastrophic, and cracks propagated in a tortuous manner with massive interfacial delamination. The stiff fibre bundles played an important role in restraining crack propagation, acting as bridges to inhibit cracks opening and also as “crack stoppers” inducing extensive crack-deflections. Microstructural analysis of the fractured surfaces revealed that substantial interfacial debonding, sliding and fibre pull-outs occurred at various length scales, which are believed to be effective in dissipating the crack energy. The synergistic effects of crack-deflection, crack-bridging and interfacial debonding are regarded to be mainly responsible for the remarkable fracture toughness of bamboo.

Bacterial Peptidoglycan Stapling with Functionalized D-Amino Acids

2019 ◽  
Author(s):  
Sylvia L. Rivera ◽  
Akbar Espaillat ◽  
Arjun K. Aditham ◽  
Peyton Shieh ◽  
Chris Muriel-Mundo ◽  
...  
Keyword(s):  
Cell Wall ◽  
Clinical Success ◽  
Bacterial Species ◽  
Enzymatic Reaction ◽  
Amino Acid Derivative ◽  
Wall Structure ◽  
Live Bacteria ◽  
Cross Links ◽  
Osmotic Lysis ◽  
Bacterial Peptidoglycan

Transpeptidation reinforces the structure of cell wall peptidoglycan, an extracellular heteropolymer that protects bacteria from osmotic lysis. The clinical success of transpeptidase-inhibiting β-lactam antibiotics illustrates the essentiality of these cross-linkages for cell wall integrity, but the presence of multiple, seemingly redundant transpeptidases in many bacterial species makes it challenging to determine cross-link function precisely. Here we present a technique to covalently link peptide strands by chemical rather than enzymatic reaction. We employ bio-compatible click chemistry to induce triazole formation between azido- and alkynyl-D-alanine residues that are metabolically installed in the cell walls of Gram-positive and Gram-negative bacteria. Synthetic triazole cross-links can be visualized by substituting azido-D-alanine with azidocoumarin-D-alanine, an amino acid derivative that undergoes fluorescent enhancement upon reaction with terminal alkynes. Cell wall stapling protects the model bacterium Escherichia coli from β-lactam treatment. Chemical control of cell wall structure in live bacteria can provide functional insights that are orthogonal to those obtained by genetics.<br>

Recent Developments in the Downstream Processing of Phycobiliproteins from Algae: A Review

2021 ◽  
Vol 06 ◽  
Author(s):  
Ayekpam Chandralekha Devi ◽  
G. K. Hamsavi ◽  
Simran Sahota ◽  
Rochak Mittal ◽  
Hrishikesh A. Tavanandi ◽  
...  
Keyword(s):  
Cell Wall ◽  
Large Scale ◽  
Downstream Processing ◽  
Review Article ◽  
Current Status ◽  
Wall Structure ◽  
Scale Production ◽  
Cell Wall Disruption ◽  
Recent Developments ◽  
Macro Algae

Abstract: Algae (both micro and macro) have gained huge attention in the recent past for their high commercial value products. They are the source of various biomolecules of commercial applications ranging from nutraceuticals to fuels. Phycobiliproteins are one such high value low volume compounds which are mainly obtained from micro and macro algae. In order to tap the bioresource, a significant amount of work has been carried out for large scale production of algal biomass. However, work on downstream processing aspects of phycobiliproteins (PBPs) from algae is scarce, especially in case of macroalgae. There are several difficulties in cell wall disruption of both micro and macro algae because of their cell wall structure and compositions. At the same time, there are several challenges in the purification of phycobiliproteins. The current review article focuses on the recent developments in downstream processing of phycobiliproteins (mainly phycocyanins and phycoerythrins) from micro and macroalgae. The current status, the recent advancements and potential technologies (that are under development) are summarised in this review article besides providing future directions for the present research area.

scholarly journals A Metzincin and TIMP-Like Protein Pair of a Phage Origin Sensitize Listeria monocytogenes to Phage Lysins and Other Cell Wall Targeting Agents

2021 ◽  
Vol 9 (6) ◽  
pp. 1323
Author(s):  
Etai Boichis ◽  
Nadejda Sigal ◽  
Ilya Borovok ◽  
Anat A. Herskovits
Keyword(s):  
Cell Wall ◽  
Listeria Monocytogenes ◽  
Mammalian Cells ◽  
Protein Pair ◽  
Growth Conditions ◽  
Wall Structure ◽  
Antibiotic Resistant ◽  
Extracellular Milieu ◽  
Virion Release ◽  
Genes Encoding

Infection of mammalian cells by Listeria monocytogenes (Lm) was shown to be facilitated by its phage elements. In a search for additional phage remnants that play a role in Lm’s lifecycle, we identified a conserved locus containing two XRE regulators and a pair of genes encoding a secreted metzincin protease and a lipoprotein structurally similar to a TIMP-family metzincin inhibitor. We found that the XRE regulators act as a classic CI/Cro regulatory switch that regulates the expression of the metzincin and TIMP-like genes under intracellular growth conditions. We established that when these genes are expressed, their products alter Lm morphology and increase its sensitivity to phage mediated lysis, thereby enhancing virion release. Expression of these proteins also sensitized the bacteria to cell wall targeting compounds, implying that they modulate the cell wall structure. Our data indicate that these effects are mediated by the cleavage of the TIMP-like protein by the metzincin, and its subsequent release to the extracellular milieu. While the importance of this locus to Lm pathogenicity remains unclear, the observation that this phage-associated protein pair act upon the bacterial cell wall may hold promise in the field of antibiotic potentiation to combat antibiotic resistant bacterial pathogens.

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