Composition and Calcium Binding Properties of the Water Soluble Polysaccharides in the Calcareous Alga Halimeda opuntia (L) (Chlorophyta,Udoteaceae)

The mucilages of this alga contain acid polysaccharides, some of which are Ca binding. After deproteinization and gel filtration the residue of the aqueous algal extract has the composition: 2% complexed protein, 3–4% Ca, 0.4–0.5% SiO₂, 0.03–0.04% Al, ∼ 0.005% Fe, rest: polysaccharide. The molecular weights of the major and minor polysaccharide fractions are approximately 5000 and 200000 respectively (Sephadex). Uronic acid and O-ester sulfate give a total of 0.25 μequiv. H⁺/mg polysaccharide whereas the Ca binding capacity is 2.1 μequiv./mg polysaccharide. Ca complexing of the dibasic polyacid is restricted to the low molecular species and involves the 2 acidic and unidentified nonacidic groups. The complexing strength of the polysaccharide for Ca is similar to succinate. These Ca binding polysaccharides may play a role in algal calcification.     

The extracellular polysaccharides of Rhizobium japonicum: Compositional studies

The extracellular polysaccharides of seven strains of Rhizobium japonicum were investigated by using a gas-chromatographic scheme developed for determination of the various sugars present. These polysaccharides were more heterogeneous in their composition than those of any other species of Rhizobium yet examined. Five strains (1809, 110, 123, 127, and 709) produced polysaccharides containing the same constituents, although in varying relative amounts: glucose (36–44%), galactose (7–25%), mannose (18–20%), 4-O-methylgalactose (5–13%), galacturonic acid (12–16%), and acetyl groups (4–8%). The sugars of the polysaccharide of strain 1809 were all of the d series. These are the first bacterial polysaccharides reported to contain 4-O-methylgalactose and the first Rhizobium polysaccharides in which galacturonic acid has been found. In contrast to this, the polysaccharide of strain 129 consisted of glucose (7%), galactose (51%), mannose (5%), xylose (5%), glucuronic acid (5%), and pyruvic acid (2%). The polysaccharide of strain 711 contained glucose (34%), galactose (13%), mannose (27%), and pyruvic acid (6%).     

Effects of salinity on synthesis of DNA,acidic polysaccharide,and ichthyotoxin in Gymnodinium breve

A Florida red tide organism, Gymnodinium breve Davis, an unarmored dinoflagellate, was grown in enriched sea water media at salinities 20–43% and constant illumination. Use of lowest (23%) and highest (43%) salinities resulted in death within 24 hr of inoculation, though good growth was obtained at all intermediate salinities (29–39%), in accord with field observation. Rates of synthesis of DNA, acidic polysaccharide and ichthyotoxin were determined as a function of salinity and growth constant (K₁₀). The relative rate of' synthesis of DNA or polysaccharide increased linearly with growth constant. Mean cell volumes, determined during log-phase growth, showed a positive correlation with doubling time. Hemolytic activity was detected in cell extracts only at high toxin concentrations (0.35–2.05 mg of ichthyotoxin). No significant difference was noted in hemolytic activity of extracts of cells grown in high (34%) or low (26%) salinity. The rate of toxin synthesis showed a linear decrease with the rate of DNA or polysaccharide synthesis.     

Polysaccharides of the cellular slime mold II. Change of intra- and extracellular polysaccharides during growth phase of Dictyostelium discoideum NC-4

The three intra- and extracellular polysaccharide fractions were isolated during the growth phase of Dictyostelium discoideum NC-4, and the change in content of component sugars of four fractions during the culture period was examined. Myxamoebae most extensively contain a polysaccharide fraction extracted with phenol-water (polysaccharide fraction I) in a quantity of about 15–23% per dry cell. After 15 h the uronic acid formed in the polysaccharide fraction I, and the cell, could be aggregated. The glucosamine content in the polysaccharide fraction I reached a maximum as the myxamoebae entered the exponential phase, and a large amount of galactose was produced as the cell entered the stationary phase. The phenol-water extract from the cells of the stationary phase was reacted with concanavalin-A.     

Chemical characterization of the hyphal walls of the basidiomyceteArmillaria mellea

Purified hyphal walls ofArmillaria mellea were analyzed and shown to contain glucose (59.0%), mannose (6.9%), galactose (4.2%), xylose (0.2%), ribose (traces), glucosamine (6.7%), protein (10.5%), and some lipid material (8.0%). The mucilaginous surface polysaccharide (fraction I) consisted mainly of (1–3), (1–4), and (1–6)β-glucan chains with mannose, galactose, xylose, and ribose. Fraction II was made mostly of (1–3)-linkedα-glucan. Fraction III contained mainly (1–3)-linkedβ-glucan with small amounts of mannose and galactose, and fraction IV was an alkali-insolubleβ(1–3)-glucan in close association with chitin.     

Optimization of polysaccharide and ergosterol production from Agaricus brasiliensis by fermentation process

Statistically based experimental designs were applied for the fermentation optimization of polysaccharide and ergosterol production from Agaricus brasiliensis in a stirred-fermenter. Culture temperature, agitation speed and initial pH were identified to have significant effects on polysaccharide and ergosterol production by a Plackett–Burman design. These three significant factors were subsequently optimized using steepest ascent method and Box–Behnken design. The validity of the optimum conditions was verified by separate experiments in which the polysaccharide and ergosterol yields were increased by 57% and 43%, respectively, as compared to those under unoptimized fermentation conditions.     

Production of a Novel Extracellular Polysaccharide by a Bacillus Strain Isolated from Soil

A bacterium that was isolated from soil and identified as Bacillus circulans was found to produce a highly viscous extracellular polysaccharide when it was grown aerobically in a medium containing glucose as a sole source of carbon. The product was characterized by TLC and GC analyses as a novel heteropolysaccharide consisted of rhamnose, mannose, galactose, and mannuronic acid as sugar components. A maximal yield of polysaccharide reached about 2 g/liter by jar-fermentor culture at 30°C for 48 hr with a medium containing 1% glucose, 0.05% asparagine, 0.005% yeast extract, and small amounts of inorganic salts. Some culture conditions for the production of polysaccharide were investigated with flask culture; an optimal production was attained with a medium containing 0.1–1 % glucose and 0.01–0.05% asparagine, pH 7–8, at 30°C under aerobic conditions.     

Characterization of the ‘reserve cellulose’ of the endosperm of Carum carvi as a β(1–4)-mannan

The reserve polysaccharide of the endosperm of Carum carvi consists of more than 90% mannose and was characterized as a β(1–4)-mannan. Total or partial acid hydrolysis, enzymatic breakdown or acetolysis of either palm or Carum carvi mannan yielded the same mono- and oligosaccharides, indicating a similar chemical structure of the two reserve polysaccharides. However, Carum carvi contains only traces of the alkali soluble mannan A dominant in the palm endosperm polysaccharide.     

Characterization of oversulfated chondroitin sulfate rich in 4,6‐O‐disulfated disaccharides in breast cyst fluids collected from human breast gross cysts

Glycosaminoglycans (GAGs) from breast cyst fluid (BCF) of gross cysts, subdivided into apocrine and flattened, directly collected from 27 gross‐cystic‐breast‐disease (GCBD)‐affected women were analysed. Heparan sulfate, not further investigated, and chondroitin sulfate were identified. This last polysaccharide, in a content of 25–27 µg ml^?1 BCF and having a high molecular mass (~20 000–22 000), was found rich in glucuronic acid (~96%–98%) and mainly sulfated in position 4 of the N‐acetyl‐galactosamine (~60%–64%). Moreover, the presence of ~19%–24% of uncommon 4,6‐O‐disulfated disaccharides CS‐E inside the polysaccharide chains with a high charge density of ~1.15–1.20 was determined. No substantial differences between apocrine and flattened cysts were observed. The current study describes the first effort to examine the yield and distribution of complex macromolecules like GAGs in BCF, and the understanding of their structure may help explain some functions associated with physiological and pathological conditions. Copyright © 2013 John Wiley & Sons, Ltd.     

Hemicellulose fractions and associated protein of lupin hypocotyl cell walls

The alkali extraction of polysaccharide fractions from depectinated primary cell walls of lupin hypocotyls was studied using sequential extractions at 0° and 18–22°. Aqueous 10% KOH at 0° removed hemicellulose-A (95%) heteroglycan-B (80%) and linear 1–4 linked hemicellulose-B (60%). Arabinose accounts for 88% of the monosaccharides of the linear 1–4 linked hemicellulose-B extracted between 2 and 5 h at 18–22°. Extraction of the 0° and 18–22° alkali-soluble fractions by denaturants, was also examined. 6M guanidine thiocyanate removed about 60% of the 0° 10% KOH soluble polysaccharide but little of the 18–22° soluble material. Although rapidly extracted by 10% KOH at 0° the hemicellulose-A is not extracted by this reagent. Analyses of cell walls and extracted fractions showed that there is little change in amino acid composition and little extraction of wall protein upon removal of about 60% of total wall hemicellulose with 10% KOH at 0°. It is therefore not bound to the wall through galactosylserine links. 10% KOH at 18–22° caused a marked change in composition and extracted most of the wall protein. An alkali resistant fraction high in hydroxyproline and low in serine was not extracted by 24% KOH at 18–22° in 24 hr.     

INTRACELLULAR PHOTOSYNTHATE ALLOCATION AND THE CONTROL OF ARCTIC MARINE ICE ALGAL PRODUCTION1

Ice algae are a case study in photo-autotrophic growth and metabolism under chronically low temperature and irradiance. We measured the allocation of ¹⁴C-labelled photosynthate among major classes of intracellular carbon (low molecular weight compounds, or LMW; lipid; protein; and polysaccharide) and found light-dependent changes in allocation broadly similar to photo-adaptive responses known in phytoplankton at higher temperatures; average relative allocation to protein varied inversely (10–37%) and allocation to lipids and polysaccharides directly (10–23%, and 16–21%, respectively) with the sub-inhibiting irradiance levels we employed (3.5–33.0 μE.M⁻². s⁻¹). Unlike many observations at higher temperatures, ours indicated (on average) a large and light-insensitive allocation to LMW (ca. 40%) and a greater light-sensitivity in lipid than in polysaccharide allocation. At the higher incubation irradiances, resembling in situ levels typical of areas with little (0–5 cm) snow cover, allocation to protein was often low (10–13%) compared to many observations of nutrient-sufficient or light-limited phytoplankton. Allocation to protein increased substantially (to ca. 40%) during a period of intensified tidal mixing, and assimilation numbers also attained a maximum at about the same time. Such dynamics show that the ice algae are not constrained to their often protein-poor allocation by the constantly low ambient temperature. Rather, they display marked shifts in metabolism consistent with major changes in light and inorganic nutrient supply, driven in part by the physical process of tidal mixing.     

Characterization of Soy Polysaccharide and Its In Vitro and In Vivo Evaluation for Application in Colon Drug Delivery

The objective of the present investigation was to establish potential of commercially available soy polysaccharide (Emcosoy®) for colon drug delivery. The soy polysaccharide–ethyl cellulose films were fabricated and characterized. The effect of the pectinase enzyme on the tensile strength and surface morphology of the film was evaluated. The permeation of chlorpheniramine maleate (CPM), a model hydrophilic drug from pectinase enzyme treated and untreated films was measured in pH 7.4 buffer. The soy polysaccharide–ethyl cellulose films were also incubated with Lactobacillus sp. culture for a specific duration, and effect on the CPM permeation was evaluated. The CPM capsules were coated with the soy polysaccharide–ethyl cellulose mixture, and Eudragit S100 was applied as a secondary coat. The coated CPM capsules were radiolabelled, and their in vivo transit was evaluated in human volunteers on oral administration. The pectinase enzyme had a significant influence on the tensile strength and surface morphology of the soy polysaccharide–ethyl cellulose films. The permeability of pectinase enzyme-treated and Lactobacillus sp.-treated films was significantly higher than that of untreated films. The CPM capsules were coated with the soy polysaccharide–ethyl cellulose mixture and Eudragit S100 and were successfully radiolabelled by a simple method. Gamma scintigraphic studies in human volunteers showed that the radiolabelled capsules maintained integrity for at least 9 h after oral administration. Thus, the soy polysaccharide has a potential in colon drug delivery.     

Morphospecies and genospecies of Microcystis during blooms in eutrophic Lake Taihu (China) in autumn

Microcystis colonies collected in a hypertrophic lake (Lake Taihu, China) in October and November 2012 were divided into five subsamples according to colony size (<75, 75–150, 150–300, 300–500, and >500 μm). All the subsamples collected in November were dominated with Microcystis ichthyoblabe and the percentages of M. ichthyoblabe exceeded 83%. The percentages of Microcystis aeruginosa of the subsamples in >500 μm class collected in October was 93.5%. For the sample collected in October, the percentage of M. ichthyoblabe was more than 58% in <75, 75–150, 150–300 μm classes. The 16S rDNA as well as some polysaccharide biosynthesis-related genes were analyzed to understand the phylogeny of Microcystis species. There was no variant site presented in each Microcystis subsample but a single nucleotide polymorphism (SNP) was found in 16S rDNA alignment tested using MSR1 in subsamples between the two months in the current study. Our results also showed that samples collected in two months can by divided into two parts by the phylogenetic analysis using two polysaccharide biosynthesis-related genes (espL and TagH). All the results suggested that 16S rDNA was valuable to identify seasonal succession of Microcystis genospecies and the diversity of Microcystis morphospecies would be explained by these polysaccharide biosynthesis-related genes.     

The composition and structural characteristics of polysaccharides of the brown alga Eisenia bicyclis

The present study examines the polysaccharide composition of the brown alga Eisenia bicyclis. The major polysaccharide of E. bicyclis is shown to be sodium alginate (15.8% of the dry defatted alga weight). The yields of laminaran and fucoidan were 1.4% and 1.3% of the dry defatted alga weight, respectively. The alga contains laminaran (1,3;1,6-β-D-glucan) that has a unique structure, a high content of 1,6-linked D-glucose residues (the ratio of 1,3: 1,6 linkage is 1.5: 1), and an unusually high molecular weight (19–27 kDa). The fucoidan fractions isolated from E. bicyclis are sulfated and acetylated heteropolysaccharides that differ in their sulfate content and monosaccharide composition.     

Sulfation of a polysaccharide obtained from Phellinus ribis and potential biological activities of the sulfated derivatives

The paper reports the preparation, characterization and potential biological activities of a chemically sulfated polysaccharide isolated from Phellinus ribis. Four sulfated derivatives (PRP-SI–IV) with variable degrees of substitution were obtained by the chlorosulfonic acid method, without degradation of the polysaccharide (PRP). The sulfate groups were not regularly distributed along the polysaccharide chain with a multiple substitution pattern as determined by ¹³C NMR. The sulfated derivatives except for PRP-SI showed significant inhibition effects on HepG2 cells in comparison with the native non-sulfated polysaccharide (PRP). All sulfated derivatives could block new angiogenic vessel formation in zebrafish assay, however, the effects were less than PRP.     

Radiation Protective Effect of Polysaccharide from Spirulina platensis on Plant Cells from Radiation Genetic Damage

Vicia faba seeds were treated with polysaccharide from Spirulina platensis before and after radiation. From the results of nuclear aberration frequency and types of chromosomal aberration in Vicia faba root tip ceils it is proposed that Spirulina p1antensis was a natural radioprotector. At a polysaccharide concentration of 0.1%–0.15%, radiation damage on Vicia faba could be reduced both in pretreated and posttreated groups. The effect of protection was more significant in posttreated group than in the pretreated one.     

Glycogen as Primordial Carbon Reserve and α-Glucosidase in the Genera Lynghya-Phormidium-Plectonema,Thermophilic Cyanobacteria

This work was done to characterize the structure of a photosynthetic polysaccharide and its metabolizing enzymes in cyanobacteria, which represent a link between bacteria and green plants in evolutionary terms. Filamentous cyanobacteria, occurring in an alkaline hot spring (45–50^oC, pH 8.5–9.0) in Kagoshima Prefecture, were morphologically classified in the genera Lyngbya-Phormidium-Plectonema (LPP). We found a thermostable neutral (α-glucosidase with optimum pH 6.5 in the LPP. A polysaccharide isolated from the TCA-soluble fraction of the LPP was characterized as glycogen that resembled animal glycogen in structure. We also recognized the presence of the TCA-insoluble glycogen at 32–38% of the total amount of glycogen, most of which was bound non-covalently to protein and had a similar iodine absorption spectrum to that of the TCA-soluble glycogen.     

Microwave-assisted extraction and pharmacological evaluation of polysaccharides from Posidonia oceanica

Microwave-assisted extraction was employed for the isolation of polysaccharides from Posidonia oceanica (PPO). The extracting parameters were optimized adopting response surface methodology. The highest polysaccharide yield (2.55 ± 0.09%), which is in concordance with the predicted value (2.76%), was obtained under the following conditions: extraction time 60 s, liquid–solid ratio of 50:1 (mL/g) and power of 800 W. This polysaccharide, with molecular weight of 524 KDa, characterized by gas chromatography–mass spectrometry showed that PPO was mainly composed of galactose, glucose, and arabinose with molar percentages 25.38, 24.37, and 21.64%, respectively. The pharmacological evaluation of PPO using animal models at the dose of 100 mg/kg indicated a significant anti-inflammatory activity with a percentage of inhibition of edema of 54.65% and a significant antinociceptive activity with 78.91% inhibition of writhing for peripheral analgesic activity and an increase in the hot plate reaction time for central analgesic activity.     

Isolation and characterization of a succinylated polysaccharide from the cell wall of Micrococcus agilis

A polysaccharide consisting of rhamnose, galactose, glucosamine and ester-linked succinic acid was extracted from the isolated cell walls of Micrococcus agilis by the hot water-phenol and 5% trichloroacetic acid (TCA) extraction methods. The hot water-phenol extractable polysaccharide accounted for 30% of the weight of the wall, with 23% by the TCA method. Phosphorus contents were less than 0.01% of the polysaccharide. Succinyl residues released by alkali treatment (0.1 N NaOH, 30 min, 37 degrees C) were identified by gas-liquid chromatography, and accounted for 6.3% and 5.1% of the polysaccharide purified from the hot water-phenol and TCA extracts, respectively. The polysaccharide was not bound when chromatography on Concanavalin A-Sepharose 4B (Con A/Sepharose 4B) columns was performed and it could thus be separated from any residual membrane lipomannan. The purified polysaccharide behaved as a negatively-charged polymer on electrophoresis in 1% agarose (at pH 8.6). A strong cross-reaction, unaffected by removal of the succinyl groups, was observed with type XXIII pneumococcal polysaccharide antiserum indicating the presence of L-rhamnose, linked through non-reducing, lateral end groups.     

INTRACELLULAR PHOTOSYNTHATE ALLOCATION AND THE CONTROL OF ARCTIC MARINE ICE ALGAL PRODUCTION1

Ice algae are a case study in photo-autotrophic growth and metabolism under chronically low temperature and irradiance. We measured the allocation of ¹⁴C-labelled photosynthate among major classes of intracellular carbon (low molecular weight compounds, or LMW; lipid; protein; and polysaccharide) and found light-dependent changes in allocation broadly similar to photo-adaptive responses known in phytoplankton at higher temperatures; average relative allocation to protein varied inversely (10–37%) and allocation to lipids and polysaccharides directly (10–23%, and 16–21%, respectively) with the sub-inhibiting irradiance levels we employed (3.5–33.0 μE·M⁻²·s⁻¹). Unlike many observations at higher temperatures, ours indicated (on average) a large and light-insensitive allocation to LMW (ca. 40%) and a greater light-sensitivity in lipid than in polysaccharide allocation. At the higher incubation irradiances, resembling in situ levels typical of areas with little (0–5 cm) snow cover, allocation to protein was often low (10–13%) compared to many observations of nutrient-sufficient or light-limited phytoplankton. Allocation to protein increased substantially (to ca. 40%) during a period of intensified tidal mixing, and assimilation numbers also attained a maximum at about the same time. Suck dynamics show that the ice algae are not constrained to their often protein-poor allocation by the constantly low ambient temperature. Rather, they display marked shifts in metabolism consistent with major changes in light and inorganic nutrient supply, driven in part by the physical process of tidal mixing.