Periodicity as a Factor in the Generation of Isotropic Compressive Growth Stress Between Microfibrils in Cell Wall Formation during a Twenty-Four Hour Period

Holzforschung ◽  
2000 ◽  
Vol 54 (5) ◽  
pp. 469-473 ◽  
Author(s):  
Masato Yoshida ◽  
Yoshihiro Hosoo ◽  
Takashi Okuyama

Summary Field emission scanning electron microscopy and energy-dispersive X-ray microanalysis were used to investigate the generation of growth stress in connection with the deposition of cell wall materials along the innermost surface of radial walls during secondary wall formation of differentiating tracheids of Cryptomeria japonica. Samples were collected when the turgor pressure of the tree was low (16:00 h), and when the pressure was high (6:00 h). In samples collected at 16:00 h, cellulose microfibrils deposited on the innermost surface of radial walls were clearly evident and amorphous material was rarely found. Conversely, in samples collected at 6:00 h, cellulose microfibrils were rarely observed and the amorphous material was prevalent. Cellulose microfibrils were evident, however, after removing the amorphous material with chlorite. The concentration of potassium on the inner surface of radial walls was greater at 6:00 h than at 16:00 h. After chlorite treatment, the concentration of potassium measured in the samples collected at 6:00 h decreased to a level equivalent to that in samples collected at 16:00 h and thus potassium was found to be associated with the amorphous material on the cellulose microfibrils. The amorphous material is probably a matrix of hemicellulose and monolignol, material that is abundant on the inner surface of developing cell walls, especially during expansion (as a result of high turgor pressure) of differentiating tracheids. A matrix of hemicellulose and lignin deposited in the expanded gaps between cellulose microfibrils and daily expansion of the gaps probably produces an isotropic compressive stress (growth stress). This paper demonstrates periodicity in cell wall formation as a result of the cycles of compressive growth in the differentiating cell wall.

1969 ◽  
Vol 17 (2) ◽  
pp. 229 ◽  
Author(s):  
AB Wardrop

In Eryngium vesiculosum and E. rostratum, the leaf collenchyma is characterized by the development of a lignified secondary wall in the final stages of cell differentiation. The collenchyma wall is rich in pectic substances which are distributed uniformly. In the outer limiting region of the collenchyma wall the microfibril orientation is random and this structure is considered to be the wall formed at cell division. The collenchyma wall consists of six to eight layers in which the microfibrils are alternately transversely and longitudinally oriented. Each layer consists of a number of lamellae of microfibrils. In the secondary lignified wall the cellulose microfibrils are arranged helically, the direction of their orientation making an angle of 40-45° to the cell axis. Excised leaf segments showed greatest elongation in solutions of glucose and 3-indoleacetic acid, when the collenchyma walls were thin, and no elongation occurred in segments in which secondary wall formation had commenced. In radial sections layers of transversely oriented microfibrils could not be seen distant from the lumen although discontinuities in wall texture were apparent. Layers of transversely oriented microfibrils could be seen adjacent to the lumen. It is suggested that reorientation of layers of initially transversely oriented microfibrils takes place during elongation of the cells.


2016 ◽  
Vol 113 (40) ◽  
pp. 11360-11365 ◽  
Author(s):  
Pallinti Purushotham ◽  
Sung Hyun Cho ◽  
Sara M. Díaz-Moreno ◽  
Manish Kumar ◽  
B. Tracy Nixon ◽  
...  

Plant cell walls are a composite material of polysaccharides, proteins, and other noncarbohydrate polymers. In the majority of plant tissues, the most abundant polysaccharide is cellulose, a linear polymer of glucose molecules. As the load-bearing component of the cell wall, individual cellulose chains are frequently bundled into micro and macrofibrils and are wrapped around the cell. Cellulose is synthesized by membrane-integrated and processive glycosyltransferases that polymerize UDP-activated glucose and secrete the nascent polymer through a channel formed by their own transmembrane regions. Plants express several different cellulose synthase isoforms during primary and secondary cell wall formation; however, so far, none has been functionally reconstituted in vitro for detailed biochemical analyses. Here we report the heterologous expression, purification, and functional reconstitution of Populus tremula x tremuloides CesA8 (PttCesA8), implicated in secondary cell wall formation. The recombinant enzyme polymerizes UDP-activated glucose to cellulose, as determined by enzyme degradation, permethylation glycosyl linkage analysis, electron microscopy, and mutagenesis studies. Catalytic activity is dependent on the presence of a lipid bilayer environment and divalent manganese cations. Further, electron microscopy analyses reveal that PttCesA8 produces cellulose fibers several micrometers long that occasionally are capped by globular particles, likely representing PttCesA8 complexes. Deletion of the enzyme’s N-terminal RING-finger domain almost completely abolishes fiber formation but not cellulose biosynthetic activity. Our results demonstrate that reconstituted PttCesA8 is not only sufficient for cellulose biosynthesis in vitro but also suffices to bundle individual glucan chains into cellulose microfibrils.


1991 ◽  
Vol 82 (2) ◽  
pp. 219-224 ◽  
Author(s):  
Barbro S. M. Ingemarsson ◽  
Leif Eklund ◽  
Lennart Eliasson

2014 ◽  
Vol 48 (4) ◽  
pp. 389-397
Author(s):  
Liu Lin ◽  
Quan Xianqing ◽  
Zhao Xiaomei ◽  
Huang Lihua ◽  
Feng Shangcai ◽  
...  

2021 ◽  
Vol 22 (7) ◽  
pp. 3560
Author(s):  
Ruixue Xiao ◽  
Chong Zhang ◽  
Xiaorui Guo ◽  
Hui Li ◽  
Hai Lu

The secondary wall is the main part of wood and is composed of cellulose, xylan, lignin, and small amounts of structural proteins and enzymes. Lignin molecules can interact directly or indirectly with cellulose, xylan and other polysaccharide molecules in the cell wall, increasing the mechanical strength and hydrophobicity of plant cells and tissues and facilitating the long-distance transportation of water in plants. MYBs (v-myb avian myeloblastosis viral oncogene homolog) belong to one of the largest superfamilies of transcription factors, the members of which regulate secondary cell-wall formation by promoting/inhibiting the biosynthesis of lignin, cellulose, and xylan. Among them, MYB46 and MYB83, which comprise the second layer of the main switch of secondary cell-wall biosynthesis, coordinate upstream and downstream secondary wall synthesis-related transcription factors. In addition, MYB transcription factors other than MYB46/83, as well as noncoding RNAs, hormones, and other factors, interact with one another to regulate the biosynthesis of the secondary wall. Here, we discuss the biosynthesis of secondary wall, classification and functions of MYB transcription factors and their regulation of lignin polymerization and secondary cell-wall formation during wood formation.


2020 ◽  
Vol 50 (2) ◽  
pp. 176-186
Author(s):  
Yi MAN ◽  
RuiLi LI ◽  
YuFen BU ◽  
Na SUN ◽  
YanPing JING ◽  
...  

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