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1.
Int J Biol Macromol ; 104(Pt A): 953-962, 2017 Nov.
Article En | MEDLINE | ID: mdl-28668613

Chitin is the second most abundant polysaccharide in biomass after cellulose and the term chitosan usually refers to a family of polymers obtained after chitin deacetylation. The aim of this work was the preparation and the characterization of chitin and chitosan from the gladius (pen) of the European squid (Loligo vulgaris). A high level of deproteinization (more than 80%) was recorded using Alcalase® with an enzyme/protein ratio of 10U/mg. The demineralization of the gladius was completely achieved within 8h at room temperature in HCl. 13C NMR, FTIR, and XRD diffractograms of prepared chitin and chitosan were taken and then degree of deacetylation of chitosan was calculated using 13C CP/MAS-NMR Spectroscopic. Further, in vitro antioxidant capacity of chitosan was evaluated on 1,1-diphenyl-2-picrylhydrazyl method (IC50=3.2mgmL-1) and the ß-carotene bleaching assay (IC50=3.3mgmL-1). Antimicrobial activity was also investigated and assays indicated that prepared chitosan exhibited marked inhibitory activity against all microbial strains tested. Additionally, chitosan was tested such as clarifying agent for apple juice and showed powerful clarification capability, without affecting nutritional value. Furthermore, the results suggested that prepared chitosan could be used as alternative additive in pharmaceutical preparations and food industry.


Chitin/chemistry , Chitosan/chemistry , Chitosan/pharmacology , Decapodiformes/chemistry , Fruit and Vegetable Juices , Malus/chemistry , Animals , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Antioxidants/chemistry , Antioxidants/isolation & purification , Antioxidants/pharmacology , Biphenyl Compounds/chemistry , Chitosan/isolation & purification , Picrates/chemistry , beta Carotene/chemistry
2.
Int J Biol Macromol ; 87: 163-71, 2016 Jun.
Article En | MEDLINE | ID: mdl-26920243

Chitin was recovered through enzymatic deproteinization of the Norway lobster (Nephrops norvegicus) processing by-products. The obtained chitin was characterized and converted into chitosan by N-deacetylation, the acid-soluble form of chitin. Chitosan samples were then characterized by Fourier transform infrared spectroscopy (FTIR) and 13 Cross polarization magic angle spinning nuclear magnetic resonance (CP/MAS)-NMR spectroscopy. The antimicrobial activity and anti-proliferative capacity of chitosan were evaluated. Antimicrobial activity assays indicated that prepared chitosan exhibited marked inhibitory activity against the bacterial and fungal strains tested. Further, cytotoxic effects of chitosan samples on human colon carcinoma cells HCT116 was evaluated using the MTT assay. Chitosan showed the antiproliferative capacity against the colon-cancer-cell HCT116 in a dose dependent manner with IC50 of 4.6mg/ml. Indeed, HCT116 cell proliferation was significantly inhibited (p<0.05) between 13.5 and 67.5% at 0.5-6mg/mL of chitosan after 24h of cell treatment. The chitosan showed high antitumor activity which seemed to be dependent on its characteristics such as acetylation degree.


Anti-Bacterial Agents/pharmacology , Antineoplastic Agents/pharmacology , Chitin/pharmacology , Chitosan/pharmacology , Decapoda/chemistry , Industrial Waste , Acetylation , Animals , Anti-Bacterial Agents/chemistry , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Bacteria/drug effects , Cell Proliferation/drug effects , Chitin/chemistry , Chitin/isolation & purification , Chitosan/chemistry , Chitosan/isolation & purification , HCT116 Cells , Humans
3.
Fish Physiol Biochem ; 41(6): 1587-96, 2015 Dec.
Article En | MEDLINE | ID: mdl-26242460

The objective of this study was to determine the effect of two levels of inclusion of xylan oligosaccharides (XOS) extracted from corncob on growth, feed utilization, immune status and disease resistance of Mediterranean sea bass (Dicentrarchus labrax) fingerlings. Specimens of 4.75 ± 0.69 g at initial density of 2.7 ± 0.13 kg/m(3) were fed during 12 weeks at 0 g kg(-1) diet, 5 g kg(-1) diet and 10 g kg(-1) diet, dietary XOS level of inclusion in a commercial sea bass diet. Feeding the fish at both XOS dietary inclusion levels significantly increased weight gain, protein efficiency ratio and feed conversion ratio. Feeding of supplemented diets to fish led to reducing mortalities after challenging with A. hydrophila. The haematological and immunological parameters were assayed in both pre-challenged and post-challenged groups. There was an increased trend in red blood corpuscles, white blood corpuscles, pack cell volume, haemoglobin (Hb %) and serum protein content in treated groups over the control as time elapsed with the feeding trials. The serum immunoglobulin level and lysozyme activity showed an increased trend in the fed groups. Histological features of the liver showed lower lipid vacuolization and regular-shaped morphology of hepatocytes around the sinusoidal spaces denoting a better utilization of dietary nutrients supported with the morphometric data. In conclusion, XOS added at a designated dose (5 g kg(-1) diet) in the diet improves growth and stimulates the immunity and makes D. labrax fingerlings more resistant to infection by A. hydrophila.


Animal Feed/analysis , Bass/growth & development , Dietary Supplements , Xylans/chemistry , Animal Nutritional Physiological Phenomena , Animals , Bass/immunology , Blood Proteins/analysis , Erythrocyte Count , Hemoglobins/analysis , Hepatocytes/cytology , Immunity, Innate , Immunoglobulins/blood , Leukocyte Count , Liver/growth & development , Muramidase/blood , Zea mays/chemistry
4.
Int J Biol Macromol ; 75: 283-9, 2015 Apr.
Article En | MEDLINE | ID: mdl-25647621

Sulfated polysaccharides were extracted from gray triggerfish (GTSP) and smooth hound (SHSP) skins. Their chemical and physical characteristics were determined using X-ray diffraction and Infrared spectroscopic analysis. The antibacterial activities of GTSP and SHSP against Listeria monocytogenes (ATCC 43251), Staphylococcus aureus (ATCC 25923), Enterococcus faecalis (ATCC 29212), Escherichia coli (ATCC 25922), Salmonella enterica (ATCC 43972) and Enterobacter sp were evaluated by determining clear growth inhibition zone diameters and the minimum inhibitory concentration (MIC) values and by essays in liquid media. GTSP and SHSP were fractionated by a Diethylaminoethyl-cellulose chromatography. Fraction FGII, from GTSP, and fraction FSII, from SHSP, showed the most important inhibitory effects against the tested bacterial species. The sulfated polysaccharides from fish skins did not show hemolytic activity towards bovine erythrocytes. Overall, the results suggested that those polysaccharides could offer promising sources of polysaccharides for future application as dietary ingredients in the nutraceutical industry.


Anti-Infective Agents/isolation & purification , Anti-Infective Agents/pharmacology , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Skin/chemistry , Sulfates/isolation & purification , Sulfates/pharmacology , Animals , Antifungal Agents/pharmacology , Bacteria/drug effects , Cattle , Chromatography, Ion Exchange , DEAE-Cellulose/chemistry , Fishes , Fungi/drug effects , Hemolysis/drug effects , Microbial Sensitivity Tests , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction
5.
Int J Biol Macromol ; 72: 1143-51, 2015 Jan.
Article En | MEDLINE | ID: mdl-25301697

The characteristics, biological properties, and purification of sulfated polysaccharides extracted from squid (Loligo vulgaris) skin were investigated. Their chemical and physical characteristics were determined using X-ray diffraction and infrared spectroscopic analysis. Sulfated polysaccharides from squid skin (SPSS) contained 85.06% sugar, 2.54% protein, 1.87% ash, 8.07% sulfate, and 1.72% uronic acid. The antioxidant properties of SPSS were investigated based on DPPH radical-scavenging capacity (IC50 = 19.42 mg mL(-1)), hydrogen peroxide-scavenging activity (IC50 = 0.91 mg mL(-1)), and ß-carotene bleaching inhibition (IC50 = 2.79 mg mL(-1)) assays. ACE-inhibitory activity of SPSS was also investigated (IC50 = 0.14 mg mL(-1)). Further antimicrobial activity assays indicated that SPSS exhibited marked inhibitory activity against the bacterial and fungal strains tested. Those polysaccharides did not display hemolytic activity towards bovine erythrocytes. Fractionation by DEAE-cellulose column chromatography showed three major absorbance peaks. Results of this study suggest that sulfated polysaccharides from squid skin are attractive sources of polysaccharides and promising candidates for future application as dietary ingredients.


Loligo/chemistry , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Skin/chemistry , Sulfates/isolation & purification , Sulfates/pharmacology , Angiotensin-Converting Enzyme Inhibitors/pharmacology , Animals , Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Antioxidants/pharmacology , Cattle , Chromatography, DEAE-Cellulose , Chromatography, Ion Exchange , Free Radical Scavengers/pharmacology , Hemolysis/drug effects , Hydrogen Peroxide/chemistry , Microbial Sensitivity Tests , Peptidyl-Dipeptidase A/metabolism , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction , beta Carotene/chemistry
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