Microwave-Assisted One-Step Conversion of Wood Wastes into Levulinic Acid

This study aimed to evaluate the use of softwood and hardwood waste for the production of levulinic acid by one-stage conversion using microwave radiation combined with acid catalysis. The analysis demonstrated that the type and concentration of the acid used, the concentration of biomass in the reaction mixture and pressure value had the greatest impact on the yield of levulinic acid. The highest efficiency of carbohydrate conversion to levulinic acid, regardless of the type of raw material, was achieved using a pressure of 225 PSI and sulfuric acid as a catalyst. Maximum yield from biomass, ca. 16.5% for cherry wood chips and ca. 25% for pine chips, was obtained using sulfuric acid at a concentration of 1% v/v and 2% v/v, respectively, for the following process parameters: Exposure time 20 min, biomass concentration 3.3%, and the pressure of 225 PSI. The ratio of actual yield to theoretical yield was high: 64.7% ± 4.5% for pine chips and 43.4% ± 1.0% for cherry wood chips. High efficiency of the presented method of biomass conversion to levulinic acid indicates the possibility of its use for waste management in the wood processing industry. High concentration of levulinic acid in the post-reaction mixture allows for cost-effective extraction and purification of the compound

Evaluation of various methods of selection of B. subtilis strains capable of secreting surface-active compounds.

The aim of the study was the evaluation of a three-step method for the selection of bacterial strains capable of producing surfactin. The procedure consisted of the following steps: 1.blood agar test, 2. measurement of the surface tension (ST) of the medium using the du Nouy method before and after submerged culture, 3. qualitative and quantitative assessment of surfactin by HPLC. Forty five Bacillus subtilis natto strains producing haemolysis zones (≥3mm) were selected. Nineten of them reduced ST of the medium to ≤ 40 mN/m; in six cases, the reduction was as much as 50%. All indicated strains produced surfactin. Positive correlations (p <0.5) between the percentage reduction of ST of the medium and surfactin concentration (r = 0.44), indicate that this parameter is determinant of the ability to synthesize this compound. The blood agar test has been shown to be useful only as a pre-selection criterion for surfactin producers (18 strains selected by this method reduced ST by only ≤30%). The proposed selection strategy proved effective and made it possible to select the BS15 strain that reduced the ST of the medium to 30.56 ± 0.15 mN/m and simultaneously provided a high concentration of surfactin compared to other strains