RESUMO
Microbial fuel cells (MFCs) are a device using microorganisms as biocatalysts for transforming chemical energy into bioelectricity. As soil is an environment with the highest number of microorganisms and diversity, we hypothesized that it should have the potential for energy generation. The soil used for the study was Mollic Gleysol collected from the surface layer (0-20 cm). Four combinations of soil MFC differing from each other in humidity (full water holding capacity [WHC] and flooding) and the carbon source (glucose and straw) were constructed. Voltage (mV) and current intensity (µA) produced by the MFCs were recorded every day or at 2-day intervals. The fastest and the most effective MFCs in voltage generation (372.2 ± 5 mV) were those constructed on the basis of glucose (MFC-G). The efficiency of straw MFCs (MFC-S) was noticeable after 2 weeks (319.3 ± 4 mV). Maximal power density (P max = 32 mW m(-2)) was achieved by the MFC-G at current density (CD) of 100 mA m(-2). Much lower values of P max (10.6-10.8 mW m(-2)) were noted in the MFC-S at CD of ca. 60-80 mA m(-2). Consequently, soil has potential for production of renewable energy.
Assuntos
Bactérias/química , Fontes de Energia Bioelétrica , Microbiologia do Solo , Solo/química , Bactérias/metabolismo , EletricidadeRESUMO
Based on the benzo[b]naphtho[1,2-d]furan and benzo[b]naphtho[1,2-d]thiophene frameworks, a series of ligands with different basic side chains (BSCs) has been synthesized and pharmacologically evaluated. Also, their binding modes have been modelled using docking techniques. It was found that the introduction of a BSC in these systems brings about a decrease of affinity for both estrogen receptors α and ß in an in vitro competitive binding assay. However, two full antagonists of the estrogen receptor ß (9c and 9f) have been discovered, with potency in the low micromolar concentration in a cell-based luciferase reporter assay, and completely devoid of activity against the α receptor at the same concentration range. Differences in the ERα/ERß binding modes have also been rationalized with the help of molecular modelling techniques. This interesting functional profile could be used to elucidate the physiological role of each ER subtype.