XIII.—The Polysaccharides Synthesized by Monodus subterraneus when Grown on Artificial Media under Bacteria-free Conditions.

1962 ◽  
Vol 68 (3) ◽  
pp. 171-185 ◽  
Author(s):  
Anne Beattie ◽  
Elizabeth Percival

SynopsisThis paper describes the isolation and characterization of the polysaccharides synthesized by the unicellular organism, Monodus subterraneus. Complete extraction of polysaccharide material proved difficult and the method finally adopted, after removal of colouring matter by immersion in dimethyl sulphoxide, was successive extractions with (i) cold water, (ii) hot water, (iii) aqueous ethanol, (iv) chlorite solution, and (v) dilute alkali. The major polysaccharide, isolated from (v), is a glucan. It was shown by periodate oxidation, methylation and enzymic studies to consist mainly of β-l, 4-linked glucose units. The presence of a small proportion of β-1, 3-linked glucose units, either incorporated with the β-1, 4-linked units in a single polymer of the lichenin-type or in a separate polymer of the laminarin-type, was also established. Further small quantities of this mixed glucan were also deposited from (ii) and from (iii) on keeping these extracts in the cold. Heterogeneous crude polysaccharide material was isolated from (i), (ii), (iii) and (iv) by alcohol precipitation. The sugars present in these various precipitates and their respective oxopolysaccharides were identified chromatographically, and, in the case of the major constituents, separated and characterized as crystalline derivatives. The polysaccharide extracted by cold water was found to contain glucose, mannose, galactose, xylose and 12 per cent of sulphate; that extracted by hot water comprised glucose (major), galactose (major), and possibly fucose; and that extracted by chlorite solution consisted of glucose (major), xylose (major), ribose and a trace of galactose.

Holzforschung ◽  
1999 ◽  
Vol 53 (3) ◽  
pp. 253-260 ◽  
Author(s):  
R. Sun ◽  
J.M. Fang ◽  
L. Mott ◽  
J. Bolton

Summary The polysaccharides in oil palm trunk fibre and empty fruit bunch (EFB) fibre were fractionated into cold water solubles, hot water solubles, 1% NaOH solubles, and 17.5% NaOH soluble fractions. Cellulose (approximately 42%) and hemicelluloses (approximately 33%) were the major polysaccharides in the palm trunk fibre and EFB fibre. Extractions of the lignified fibres with cold water, hot water, and 1% NaOH produced the hemicellulosic fractions, which were enriched in xylose and glucose and to a lesser extent, arabinose-, galactose-, mannose-, rhamnose-, and ribose-containing polysaccharides, together with noticeable amounts of associated lignin (4.5–31.2%). Further extraction of the delignified fibre residues with aqueous 17.5% NaOH removed the hemicellulosic fractions, which were strongly enriched in xylose-containing polysaccharides and relatively free of associated lignin (0.3–0.7%). Eight phenolic acids and aldehydes, including p-hydroxybenzoic acid, p-hydroxybenzaldehyde, vanillic acid, syringic acid, vanillin, syringaldehyde, p-coumaric acid, and ferulic acid, were detected in the mixtures of alkaline nitrobenzene oxidation of associated lignin in all the sixteen polysaccharide fractions. The results obtained showed that hemicelluloses in the cell walls of oil palm trunk and EFB fibres, are mainly bonded with lignin by syringyl units.


1974 ◽  
Vol 143 (2) ◽  
pp. 379-389 ◽  
Author(s):  
Lars-Åke Fransson ◽  
Lars Cöster ◽  
Birgitta Havsmark ◽  
Anders Malmström ◽  
Ingrid Sjöberg

Dermatan sulphate was degraded by testicular hyaluronidase and an oversulphated fraction was isolated by ion-exchange chromatography. This preparation, which contained fairly long segments derived from the non-reducing terminal portion of the molecule, was subjected to periodate oxidation under acidic conditions. The oxidized iduronic acid residues were cleaved by reduction-hydrolysis (Smith-degradation) (Fransson & Carlstedt, 1974) or by alkaline elimination. The oligosaccharides so obtained contained both GlcUA (glucuronic acid) and IdUA-SO4 (sulphated iduronic acid) residues. Copolymeric oligosaccharides obtained after alkaline elimination were cleaved by chondroitinase-AC into disaccharide and higher oligosaccharides. Since the corresponding oligosaccharides obtained by Smith-degradation were unaffected by this enzyme, it was concluded that the carbohydrate sequences were GalNAc-(IdUA-GalNAc)n-GlcUA-GalNAc. The iduronic acid-containing sequences were resistant to digestion with chondroitinase-ABC. It was demonstrated that the presence of unsulphated N-acetylgalactosamine residues in these sequences could be responsible for the observed effect. This information was obtained in an indirect way. Chemically desulphated dermatan sulphate was found to be a poor substrate for the chondroitinase-ABC enzyme. Moreover, digestion with chondroitinase-ABC of chondroitinase-AC-degraded dermatan sulphate released periodate-resistant iduronic acid-containing oligosaccharides. It is concluded that copolymeric sequences of the following structure are present in pig skin dermatan sulphate: [Formula: see text] N-acetylgalactosamine moieties surrounding IdUA-SO4 residues are unsulphated to a large extent.


Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2740 ◽  
Author(s):  
Ekaterina Baeva ◽  
Roman Bleha ◽  
Ekaterina Lavrova ◽  
Leonid Sushytskyi ◽  
Jana Čopíková ◽  
...  

Oyster mushrooms are an interesting source of biologically active glucans and other polysaccharides. This work is devoted to the isolation and structural characterization of polysaccharides from basidiocarps of the cultivated oyster mushroom, Pleurotus ostreatus. Five polysaccharidic fractions were obtained by subsequent extraction with cold water, hot water and two subsequent extractions with 1 m sodium hydroxide. Branched partially methoxylated mannogalactan and slightly branched (1→6)-β-d-glucan predominated in cold- and hot-water-soluble fractions, respectively. Alternatively, these polysaccharides were obtained by only hot water extraction and subsequent two-stage chromatographic separation. The alkali-soluble parts originating from the first alkali extraction were then fractionated by dissolution in dimethyl sulfoxide (DMSO). The polysaccharide insoluble in DMSO was identified as linear (1→3)-α-d-glucan, while branched (1→3)(1→6)-β-d-glucans were found to be soluble in DMSO. The second alkaline extract contained the mentioned branched β-d-glucan together with some proteins. Finally, the alkali insoluble part was a cell wall complex of chitin and β-d-glucans.


TAPPI Journal ◽  
2012 ◽  
Vol 11 (1) ◽  
pp. 19-26 ◽  
Author(s):  
BILJANA M. BUJANOVIC ◽  
MANGESH J. GOUNDALKAR ◽  
THOMAS E. AMIDON

In conventional pulping technologies, lignin is used mainly as a low-cost source of energy. Small quantities of industrially produced lignin are used for the production of chemicals and materials. Biorefinery technologies are emerging that have an ultimate goal of replacing fossil sources for the production of fuels and other products. To achieve this goal effectively, biorefinery technologies must take advantage of lignin as the most abundant natural aromatic polymer and use it to add higher-value products to product portfolios. Lignin has the potential to be used in making a broad range of high-quality products, including carbon fibers, thermoplastics, and oxygenated aromatic compounds. Existing processes focus primarily on the quality of cellulose and result in a severely modified and contaminated lignin of relatively low value. Lignin produced in more flexible biorefinery operations is more uniform and less contaminated than currently available industrial lignins, opening the door for broader applications of lignin and lignin products. The results of isolation and characterization of lignin dissolved during hot-water extraction and some potential applications of this lignin are discussed.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Joana M. Ferraz ◽  
Cláudio H. S. Del Menezzi ◽  
Mario R. Souza ◽  
Esmeralda Y. A. Okino ◽  
Sabrina A. Martins

The objectives of the present work were to evaluate the chemical compatibility between coir (Cocos nuciferaL.) and cement and to study treatment methods to improve this compatibility. In the inhibition test, cement hydration temperature evolution was measured in the absence and presence of untreated and treated coir fibres (cold water, hot water and NaOH), besides the addition of 4% of CaCl2. The chemical characterization of untreated and treated coir fibres was done by determining the content of extractives, lignin, and holocellulose. The inhibition test graded the untreated fibre as “extreme inhibition,” ratifying the need to provide it a treatment. Treatments done on coir fibres affected positively the compatibility between cement and fibre, reducing the inhibition. The treatments reduced the lignin coir fibres’ and extractives proportion, whose variation was significantly correlated with the reduction of the inhibitory index. These results indicate a possibility for future incorporation of these fibres into the production of mineral composites.


2008 ◽  
Vol 74 (13) ◽  
pp. 4070-4078 ◽  
Author(s):  
Anne Rønnest Stenholm ◽  
Inger Dalsgaard ◽  
Mathias Middelboe

ABSTRACT Flavobacterium psychrophilum is a serious pathogen in trout aquaculture, responsible for the diseases rainbow trout fry syndrome (RTFS) and cold water disease (CWD). Bacteriophage control of F. psychrophilum may constitute a realistic approach in the treatment of these diseases; however, a detailed understanding of the phage-host interactions is needed to evaluate the potential of F. psychrophilum bacteriophages for that purpose. Twenty-two F. psychrophilum phages from Danish rainbow trout farms were isolated and characterized. The phage genome sizes differed considerably and fell into three major size classes (8.5 to 12 kb, 48 kb, and 90 kb). The phage host ranges comprised from 5 to 23 of the 28 tested F. psychrophilum strains, and 18 of the phage isolates showed unique host ranges. Each bacterial strain had a unique pattern of susceptibility to the 22 phages, and individual strains also showed large variations (up to 107-fold differences) in susceptibility to specific phages. Phage burst size (7 to 162 phages infected cell−1) and latency period (4 to 6 h) also showed pronounced differences both between phages and, for a specific phage, between host strains. In general, the characterization documented the presence of diverse F. psychrophilum phage communities in Danish trout farms, with highly variable patterns of infectivity. The discovery and characterization of broad-host-range phages with strong lytic potential against numerous pathogenic F. psychrophilum host strains thus provided the foundation for future exploration of the potential of phages in the treatment of RTFS and CWD.


2019 ◽  
Vol 800 ◽  
pp. 289-292
Author(s):  
Andrejs Shishkin ◽  
Ieva Stafecka

The present study describes ice characterization technique by utilizing light microscopy. Two different optical setups were used and compared. For ice structure characterization, ice was formed by adding water to an ice base layer: pouring hot water (+20 °C), pouring cold water (+3 °C) and spraying of hot water (+20 °C) water. Ice substrate specimens were made (20 x 30 x 20 mm prepared in a polypropylene mould) at -20 °C for 48 h. The heat flow direction governed the orientation of the air bubbles, and set the inner structure of ice. Pouring hot water onto ice slowly solidified the top layer and created channel-like pores perpendicular to the top surface, but cold water quickly solidified the top layer and created chaotically oriented air bubbles.


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