Cell wall thickening in two Ulva species in response to heavy metal marine pollution

2020 ◽  
Vol 35 ◽  
pp. 101125 ◽  
Author(s):  
Safia Zeroual ◽  
Salah Eddine El Bakkal ◽  
Mounir Mansori ◽  
Sabine Lhernould ◽  
Céline Faugeron-Girard ◽  
...  
1974 ◽  
Vol 14 (2) ◽  
pp. 439-449
Author(s):  
J. BURGESS ◽  
E. N. FLEMING

The process of cell wall regeneration around cultured protoplasts isolated from tobacco mesophyll has been examined by electron microscopy. The initially formed wall contains 2 components which stain with conventional heavy metal stains. The first consists of un-branched fibres, at first oriented at right angles to the plasmalemma surface. As wall growth proceeds the fibres lengthen and assume an orientation parallel to the plasmalemma. It seems probable that this component is cellulose. The second component of the wall is more amorphous and more densely stained. It is most frequently seen in situations where leaching of materials into the medium would be expected to be minimal. The endoplasmic reticulum and the plasmalemma are the only membrane systems which appear to contribute towards wall formation. No pattern of structure has been detected to explain the orientation or method of synthesis of the microfibrillar part of the wall.


2019 ◽  
Vol 24 (9) ◽  
pp. 853-866 ◽  
Author(s):  
Ian W. McCahill ◽  
Samuel P. Hazen
Keyword(s):  

2020 ◽  
Vol 11 ◽  
Author(s):  
Samaneh Sadat Maleki ◽  
Kourosh Mohammadi ◽  
Ali Movahedi ◽  
Fan Wu ◽  
Kong Shu Ji

1976 ◽  
Vol 54 (11) ◽  
pp. 927-934 ◽  
Author(s):  
T. G. Villa ◽  
V. Notario ◽  
T. Benítez ◽  
J. R. Villanueva

An exo-1,3-β-glucanase (EC 3.2.1.—) has been purified from the culture fluid of the yeast Candida utilis, and its biochemical properties have been studied. The amino acid analysis revealed a high content of acidic amino acids. The purified enzyme had 20% carbohydrate and a net negative charge showing higher affinity for laminarin than for p-nitrophenyl-β-D-glucopyranoside and yeast cell-wall 1,3-β-glucans. In addition, the enzyme hydrolyzed the substrates starting from the nonreducing ends, releasing glucose as the exclusive hydrolysis product. The enzyme activity was strongly inhibited by lactones and also by some heavy-metal ions.


IAWA Journal ◽  
2008 ◽  
Vol 29 (1) ◽  
pp. 69-77 ◽  
Author(s):  
Alexandre Antonio Alonso ◽  
Silvia Rodrigues Machado

The origin and structure are described of the secondary protective tissue in the stem of Erythorxylum tortuosum Mart., a fire tolerant shrubby species common in Brazilian cerrado. The highly tortuous stems are covered with thick bark which is more developed at the base of the stem. After fire in the cerrado, rhytidome fragments of the burned stem flake off, revealing newly formed cork. The first periderm appears near of the terminal buds and is iniated by periclinal divisions in subepidermal cells giving rise to radial rows of cells. The first phellogen is discernible only after the differentiation of the several radial rows of cork cells. Other phellogens have their origin in successively deeper layers of the cortex. The sucessive periderms are discontinuous around the circumference. The collapsed cells with phenolic substances and the accumulated dead cells cause the formation of discontinuous blackish lines, which delimit the sucessive periderms in the rhytidome. The rhytidome contains large quantities of sclereids developed from cell wall thickening of cortex cells. The occurrence of periderm in the young parts of the stem and of rhytidome in the older parts represents pyrophytic characteristics and may explain, in part, the fire tolerance of this species.


2020 ◽  
Vol 183 (4) ◽  
pp. 1600-1611 ◽  
Author(s):  
Daisuke Sugiura ◽  
Ichiro Terashima ◽  
John R. Evans

1978 ◽  
Vol 56 (23) ◽  
pp. 2990-2999 ◽  
Author(s):  
G. Faulkner ◽  
Warwick C. Kimmins

Tissue in Phaseolus vulgaris L. cv. Pinto bean bordering local lesions induced by tobacco mosaic virus showed cell wall deposition associated with paramural body formation in a narrow ring of viable cells extending one to three cell diameters around the lesions. Deposition, which led to secondary cell wall thickening, was greatest 3–4 days after inoculation, the time when the lesion stopped expanding. Secondary cell wall thickening, of similar appearance but less pronounced, was seen in tissue bordering local lesions which continued to expand; no significant secondary cell wall thickening was observed in leaves with a nonlocalized infection. Cells bordering mechanical lesions differed markedly in fine structure from cells bordering virus and chemical lesions. It is suggested that the deposition of extra cell wall material in the wall regions of cells bordering fully expanded local lesions is associated with virus localization.


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