Non-cellulosic structural polysaccharides in algal cell walls I. Xylan in siphoneous green algae

The cell walls of a number of marine algae, namely species of Bryopsis, Caulerpa, Udotea, Halimeda and Penicillus and of one freshwater alga, Dichotomosiphon , are examined using both chemical and physical techniques. It is shown that, with the possible exception of Bryopsis , cellulose is completely absent and that the walls contain instead β -l,3-linked xylan as the structural polysaccharide. Bryopsis contains, in addition, a glucan which is most abundant in the outer layers of the wall and which stains like cellulose. The xylan is microfibrillar but the microfibrils are more strongly adherent than they are in cellulose, and in some species appear in the electron microscope to be joined by short crossed rod-like bodies. The orientation of the microfibrils is found to vary, ranging from a net tendency to transverse orientation through complete randomness to almost perfect longitudinal alinement. The microfibrils are negatively birefringent, so that all walls seen in optical section, and all parallel arrays of microfibrils whether in face view or in section (except strictly transverse section) are negatively birefringent. With Bryopsis , the negative birefringence in face view is overcompensated by the positive birefringence of the incrusting glucan so that the true birefringence of the crystalline polysaccharide is observed only after the glucan is removed. The X-ray diagram of parallel arrays of microfibrils as found, for instance, in Penicillus dumetosus shows that the xylan chains are helically coiled, in harmony with the negative birefringence. It is deduced that the microfibrils consist of hexagonally packed, double-stranded helices. The diameter of the helices increases with increasing relative humidity, as water is taken into the lattice, from 13.7 Å in material dried over phosphorus pentoxide to a maximum of 1.54 Å at 65 % relative humidity when the xylan contains 30 % of its weight as water. The repeat distance along the helix axis ranges from 5.85 Å (dry) to 6.06 Å (wet), the length of a half turn of each helix containing three xylose residues. The incrusting substances in these walls often include a glucan which is said also to be 1,3-linked. The significance of the extensive differences between this xylan and cellulose are examined both as regards some of the physical properties of the respective cell walls and in relation to the taxonomic position of these plants.

The structure of the walls of the red alga Porphyra umbilicalis , a member of the Bangiaceae, has been examined by chemical and physical methods, and observations have been made on Bangia fusco-purpurea sufficient to establish that there is no essential difference in wall structure between these two algae. Mannan and xylan, which are the two major skeletal polysaccharides of these algae, are found to be spatially segregated within an individual plant. The cell walls proper contain microfibrils of β -1,3-linked xylan identical with the microfibrils found in certain siphoneous green algae and constituted therefore of parallel arrays of double-stranded helices. The incrusting substances probably include mannan and xylan. The cuticle has been shown to consist predominantly of mannan (with no or little xylan) which becomes crystalline only after treatment such as extraction with hot water. The crystalline mannan is β -1,4-linked and appears identical with the mannan which forms the walls of still another group of siphoneous green algae. No evidence has been found for any structure such as microfibrils in the cuticle; it shows at best only a granular appearance. The cell walls are clearly lamellated; they merge gradually into the intercellular material (mainly mannan) and this in turn into the dense outer sheath of the plant—the cuticle. The microfibrils of individual lamellaelie at random in all the walls with the exception of the rhizoids. The rhizoids are as a rule narrow, with thick, compact walls in which the microfibrils lie through out parallel to rhizoid length with the short cross-connexions typical of the green algae with xylan walls. The apex of the rhizoids are thin-walled and sometimes dilated. The undilated tips are characterized by a small patch of randomly arranged microfibrils at the extreme apex with a progressive tendency towards longitudinal orientation below. The implications of this structure for the growth of rhizoids is discussed.


2016 ◽  
Vol 113 (22) ◽  
pp. 6188-6193 ◽  
Author(s):  
Joanne K. Hobbs ◽  
Seunghyae M. Lee ◽  
Melissa Robb ◽  
Fraser Hof ◽  
Christopher Barr ◽  
...  

Uronates are charged sugars that form the basis of two abundant sources of biomass—pectin and alginate—found in the cell walls of terrestrial plants and marine algae, respectively. These polysaccharides represent an important source of carbon to those organisms with the machinery to degrade them. The microbial pathways of pectin and alginate metabolism are well studied and essentially parallel; in both cases, unsaturated monouronates are produced and processed into the key metabolite 2-keto-3-deoxygluconate (KDG). The enzymes required to catalyze each step have been identified within pectinolytic and alginolytic microbes; yet the function of a small ORF,kdgF, which cooccurs with the genes for these enzymes, is unknown. Here we show that KdgF catalyzes the conversion of pectin- and alginate-derived 4,5-unsaturated monouronates to linear ketonized forms, a step in uronate metabolism that was previously thought to occur spontaneously. Using enzyme assays, NMR, mutagenesis, and deletion ofkdgF,we show that KdgF proteins from both pectinolytic and alginolytic bacteria catalyze the ketonization of unsaturated monouronates and contribute to efficient production of KDG. We also report the X-ray crystal structures of two KdgF proteins and propose a mechanism for catalysis. The discovery of the function of KdgF fills a 50-y-old gap in the knowledge of uronate metabolism. Our findings have implications not only for the understanding of an important metabolic pathway, but also the role of pectinolysis in plant-pathogen virulence and the growing interest in the use of pectin and alginate as feedstocks for biofuel production.


1968 ◽  
Vol 169 (1015) ◽  
pp. 127-145 ◽  

The cell walls of a number of green seaweeds, all members of the Codiaceae and the Dasy-cladaceae and including Codium and Acetabularia , are shown to contain β -1.4-linked mannan as the sole crystalline polysaccharide in the complete absence of cellulose. The X-ray diagram of the native mannan (almost identical with that of the mannan of ivory nut and of other palm-seed endosperms) has been indexed to an orthorhombic unit cell a = 7.21 Å, b (fibre axis) = 10.27 Å, c = 8.82 Å. After treatment with alkali solutions the mannan recrystallizes in a different lattice; by analogy with cellulose we propose to name this form mannan II and the native mannan, mannan I. The lamellated walls of the central siphon of some of these algae (including Dasycladus , Batophora and Cymopolia ) may be separated into two layers. X-ray diffraction analysis and polarization microscopy show that the mannan crystallites of the outer layer tend to lie transversely to the siphon axis, with some dispersion, while those in the inner layer lie longitudinally. The inner layers therefore yield good X-ray fibre diagrams from which a provisional structure of mannan I has been derived. It has proved impossible to reveal in the electron microscope, by the techniques used, the presence of true microfibrils in these plants even when the mannan is well oriented. Electron microscope images of carbon replicas reveal at most the appearance of short rodlets some 100 Å wide. The outer and inner layers resemble respectively the primary and secondary wall layers of higher plants. Some peculiar growth habits of members of the Dasycladaceae are discussed in terms of wall architecture.


1978 ◽  
Vol 33 (5-6) ◽  
pp. 444-446 ◽  
Author(s):  
E. Steudle ◽  
A . Läuchli ◽  
A . Sievers

The identification of Ca2+ by X-ray microanalysis in statoliths could be masked by Ba2+. Using Ba2+ and Ca2+ containing standards prepared from algal cell walls and cellulose acetate films it is shown that there is no inter­ference of Ba2+ with Ca2+. Hence Ba2+ is the main cationic constituent in the statoliths of Chara rhizoids.


Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 80
Author(s):  
Robert Paszkowski ◽  
Jacek Krawczyk ◽  
Włodzimierz Bogdanowicz ◽  
Dariusz Szeliga ◽  
Jan Sieniawski

The roots of cored single-crystalline turbine blades made of a nickel-based CMSX-4 superalloy were studied. The casts were solidified by the vertical Bridgman method in an industrial ALD furnace using the spiral selector and selector continuer situated asymmetrically in the blade root transverse section. Scanning electron microscopy, the Laue diffraction and X-ray diffraction topography were used to visualize the dendrite array and the local crystal misorientation of the roots. It has been stated that heterogeneity of the dendrite array and creation of low-angle boundaries (LABs) are mostly related to the lateral dendrite branching and rapid growth of the secondary and tertiary dendrites near the surface of the continuer–root connection. These processes have an unsteady character. Additionally, the influence of the mould walls on the dendrite array heterogeneity was studied. The processes of the lateral growth of the secondary dendrites and competitive longitudinal growth of the tertiary dendrites are discussed and a method of reducing the heterogeneity of the root dendrite array is proposed.


Cells ◽  
2020 ◽  
Vol 9 (4) ◽  
pp. 1066 ◽  
Author(s):  
Gea Guerriero ◽  
Ian Stokes ◽  
Nathalie Valle ◽  
Jean-Francois Hausman ◽  
Christopher Exley

Silicon is a non-essential element for plants and is available in biota as silicic acid. Its presence has been associated with a general improvement of plant vigour and response to exogenous stresses. Plants accumulate silicon in their tissues as amorphous silica and cell walls are preferential sites. While several papers have been published on the mitigatory effects that silicon has on plants under stress, there has been less research on imaging silicon in plant tissues. Imaging offers important complementary results to molecular data, since it provides spatial information. Herein, the focus is on histochemistry coupled to optical microscopy, fluorescence and scanning electron microscopy of microwave acid extracted plant silica, techniques based on particle-induced X-ray emission, X-ray fluorescence spectrometry and mass spectrometry imaging (NanoSIMS). Sample preparation procedures will not be discussed in detail, as several reviews have already treated this subject extensively. We focus instead on the information that each technique provides by offering, for each imaging approach, examples from both silicifiers (giant horsetail and rice) and non-accumulators (Cannabis sativa L.).


2018 ◽  
Vol 24 (S2) ◽  
pp. 358-359
Author(s):  
Hayato Hiraki ◽  
Na Liu ◽  
Jian Wang ◽  
Jarvis Stobbs ◽  
Chithra Karunakaran ◽  
...  

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