ABSTRACT
Polysaccharide-functionalized silver nanoparticles (Oc-AgNPs) with a mean diameter of 15 nm were utilized as a novel and effective fluorescence-sensing platform for nucleic acid detection. Tests on the oligonucleotide sequences associated with the human immunodeficiency virus as a model system showed that the Oc-AgNPs effectively absorbed and quenched dye-labeled single-stranded DNA through strong hydrogen bonding interactions and slight electrostatic attractive interactions. The proposed system efficiently differentiated between complementary and mismatched nucleic acid sequences with high selectivity and good reproducibility at room temperature.
Subject(s)
HIV/genetics , Nanoparticles/chemistry , Oligonucleotides/analysis , Polysaccharides/chemistry , Silver/chemistry , DNA, Single-Stranded , Fluorescent Dyes , Kinetics , Reproducibility of Results , Spectrometry, Fluorescence/instrumentation , Spectrometry, Fluorescence/methods , Static ElectricityABSTRACT
Three partially purified polysaccharides were extracted from Phellinus linteus mycelia using hot water, 1% (NH4)2C2O4, and 1.25M NaOH/0.05% NaBH4, and the extracts were named PL-W, PL-A, and, PL-N respectively. PL-N mainly comprised xylose and arabinose with a high molecular weight (Mw) and the highest carbohydrate and uronic acid contents. PL-W and PL-A were mainly composed of glucose with high and low Mw fractions in various ratios. All three polysaccharides existed as compact coils in aqueous solutions and exhibited strong scavenging capacity and antioxidant activities in a concentration-dependent manner. The polysaccharides also had high uronic acid and carbohydrate contents and strong antioxidant activities. The Mws, monosaccharide compositions, and chemical structures of the polysaccharides also affected their antioxidant activities. PL-A and PL-N had better antioxidant activities and could thus be developed as potential natural antioxidant agents for applications in food additives and biomedical industries.
Subject(s)
Basidiomycota/chemistry , Free Radical Scavengers/isolation & purification , Fungal Polysaccharides/isolation & purification , Biphenyl Compounds/chemistry , Borohydrides/chemistry , Cell Line, Tumor , Cell Survival/drug effects , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Free Radicals/chemistry , Fungal Polysaccharides/chemistry , Fungal Polysaccharides/pharmacology , Hot Temperature , Humans , Molecular Weight , Picrates/chemistry , Sodium Hydroxide/chemistry , Solvents/chemistry , Water/chemistryABSTRACT
Regioselective oxidation was applied to commercial curdlan for the preparation of its water-soluble derivatives with improved antioxidant activities, using a 4-acetamido-2,2, 6,6-tetramethylpiperidine-1-oxyl radical/NaClO/NaClO2 system at pH 4.8 and 40°C. The structural features, molecular properties, and chain conformations of the oxidised curdlans were determined using Fourier transform (FT) infrared and FT Raman spectroscopy, carbon nuclear magnetic resonance, X-ray diffraction, and size-exclusion chromatography with multi-angle laser-light scattering analyses. The C6 primary hydroxyls of curdlan were successfully oxidised into carboxylate groups with less depolymerization, and no aldehyde groups were formed during oxidation. The crystalline region of curdlan was destroyed after oxidation. The oxidised curdlans formed random coils in aqueous solution, and the chain became more flexible and expanded with increasing carboxylate contents from 2.07mmol/g to 4.87mmol/g. The high polyglucuronic acid derivative (Cur-24) showed the best antioxidant activity in TEAC and FRAP assays, thus it could be explored as novel potential antioxidants for dietary and therapeutic applications.
Subject(s)
Antioxidants/chemistry , Cyclic N-Oxides/chemistry , beta-Glucans/chemistry , Carbohydrate Conformation , Multigene Family , Oxidation-Reduction , Spectroscopy, Fourier Transform Infrared , X-Ray DiffractionABSTRACT
A facile, simple, and eco-friendly method using 4-acetamido-2,2,6,6-tetramethypiperidine-1-oxyl radical-oxidized curdlan (Oc) as both reducing and stabilizing agents was developed for the fabrication of silver nanoparticles (AgNPs) from silver nitrate (AgNO3). The structure, morphology, and particle size of the as-prepared AgNPs were investigated by ultraviolet-visible spectroscopy, transmission electron microscopy, energy dispersive X-ray spectrometry, X-ray diffraction, and dynamic laser light scattering. The well-dispersed AgNPs were sphere like with a mean diameter of 15 nm. Their formation was dependent on reaction duration, reaction temperature, Oc concentration, and AgNO3 concentration. Fourier transform-infrared and Raman spectra demonstrated that the as-prepared AgNPs can readily bind covalently with the carboxylate groups of Oc through the strong monodentate interaction in the reaction medium.