Initial stages of cell wall formation in the dinoflagellate Peridinium trochoideum

1975 ◽  
Vol 53 (5) ◽  
pp. 483-494 ◽  
Author(s):  
John P. Kalley ◽  
Thana Bisalputra

The formation of the cell wall in the marine dinoflagellate Peridinium trochoideum was studied using light and electron microscopy. In mature, interphase cells, densely staining inclusions termed ‘prothecal bodies’ were found distributed throughout the cytoplasm. Before ecdysis each amorphous prothecal body developed into many vesicles, each of which contained fibrous material in an electron-transparent matrix. The vast number of vesicles so formed may have increased the cell's osmotic pressure enough to initiate ecdysis. At ecdysis the thecal plates and overlying membranes were lost and a new wall was formed by deposition of intact prothecal vesicles at the protoplast surface. The newly formed wall was continuous over the protoplast and no plates existed as such

1968 ◽  
Vol 63 (3) ◽  
pp. 242-255 ◽  
Author(s):  
S. Bartnicki-Garcia ◽  
Nancy Nelson ◽  
E. Cota-Robles

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.


IAWA Journal ◽  
1992 ◽  
Vol 13 (3) ◽  
pp. 283-296 ◽  
Author(s):  
Keiji Takabe ◽  
Takaharu Miyauchi ◽  
Kazumi Fukazawa

Cell wall formation, particularly deposition of polysaccharides, of compression wood in Todo fir (Abies sacharinensis) was examined by either fluorescence and ultraviolet microscopy or by transmission electron microscopy coupled with cytochemical staining.


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 ◽  
...  

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