Colletotrichum gloeosporioides biomass was submitted to ethanolic extraction (78 ºC, 12 h) to remove low molecular weight compounds followed by hot aqueous extraction (100 ºC, 4 h, 4x) to obtain polysaccharides. Consecutive freezing/thawing treatments of the aqueous extract yielded a soluble fraction in cold water that was separated on five components (PI to PV) by gel exclusion chromatography on Sepharose CL-6B. The PIV was homogeneous on HPSEC/RID, with apparent MW of 2.8 x 104 g mol-1, Mw/Mn 1.17, 100% of total sugar. The PIV was composed by galactose (61%), glucose (34%) and mannose (5%). 1H and 13C NMR analysis mono- and two-dimensional, homo- (COSY) and heteronuclear (HSQC and HMBC) showed that PIV is a heteropolysacharide with a main chain constituted by β-D-galactofuranosidic units (1→5) and (1→6) linked with some of the β-D-galactofuranosidic (1→6) units substituted in O-3 by α-D-glucopiranosidic residues. Cytotoxic assays (MTT) indicated that the viability of CHO-K1 cells, when exposed to different heteropolysaccharide concentrations, did not show significant differences when compared to the viability of the negative control (CN), in the experimental times of 24 and 48 hours. These results suggest the possibility of new cytotoxic assays in other normal cell lines as well as in tumor cells.

Kojic acid (KA) is an organic acid widely used in pharmaceutical industry, mainly as a skin lightening agent. Based on the ability of KA to form complexes with ions, we found the most possible kind of complex formed with cation aluminum. KA-Al3+ complex structures were studied using potentiometric and spectrophotometric (UV) titrations, FTIR and 13C NMR. The electronic spectroscopy showed that the KA-Al3+ complexes absorb at higher wavelengths (λmax= 305 nm) than do the non-complexed KA (λmax= 269 nm), confirming complexation. The IR spectra of KA complexed and not complexed allowed us to correlate the changes in the absorption of enol and carbonyl groups in absence and presence of Al3+ in aqueous solutions. The complexation suggested by the potentiometric titration and FTIR spectroscopy are in accordance with the data obtained from NMR results. Calculations based on quantum mechanics were utilized to understand the differences found in the noncomplexed and complexed KAH electronic spectra

Agaro- and carra-oligosaccharides were produced by partial acid hydrolysis of commercial agarose and kappa-carrageenan. Di- and tetrasaccharides were purified by gel filtration chromatography and characterized by NMR (1D and 2D) spectroscopy and ESIMS. The following oligosaccharides were obtained: agarobiose, agarotetraose, kappa-carrabiose and kappa-carratetraose. Agarobiose and agarotetraose were used as standards to develop a high performance size exclusion chromatography (HPSEC) method which was utilized to study the hydrolysis rate of agarose and oligosaccharide production. Six hours of hydrolysis (0.1 M TFA, 65 ºC) produced mainly di- and tetrasaccharides. The methodology for oligosaccharide production and evaluation developed in the present work shows good potential for the production of bioactive oligosaccharides.