RESUMO
Abstract Current trends in science education recommend the complementary use of virtual and hands-on methods of teaching. In neurobiology, for instance, there is a plethora of virtual laboratories and simulators that can be readily combined with traditional physical labs. Unfortunately, physical laboratories are almost unaffordable for many institutions due to the high cost of equipment. In this paper, we present a simple and low-cost in vivo method for demonstrating some of the basic biophysical properties of neural action potentials. The method involves the following steps: a) dissection of the ventral nerve cord of earthworm; b) electrical stimulation; c) amplification and visualization of the medial and lateral giant fibers' action potentials; and d) recording. The system showed stability, expected amplification, high signal-to-noise ratio, and an estimated total cost of US$ 5.662. We provide guidelines for assembling the system and discus its utility as a teaching alternative for low budget institutions.
Assuntos
Neurobiologia/métodos , Potenciais de Ação , Tecnologia de Baixo Custo/economia , Instituições AcadêmicasRESUMO
The biotechnology sector is continually seeking sustainable and more economical bioprocesses. Fermentation media produced with cheap components or wastes reduce production costs. Moreover, if wastes are used, they contribute to avoid environmental pollution. In this work, microbial growth media based on molasses or acidified glycerol as carbon sources and fertilizer as nitrogen source were tested for the production of a whole-cell catalyst that could be used in Cr(VI)-containing wastewater treatments. Results showed that the highest biomass production yield was obtained with a medium containing acidified glycerol 5% v/v and fertilizer 0.6% v/v. The biomass produced using this medium was immobilized in calcium alginate beads and used as catalyst in the biotransformation of Cr(VI) into Cr(III). The catalyst could be efficiently used for 5 reduction cycles of 40 mg/l Cr(VI) each. Cr(III) retention assays were performed to determine whether Cr(III) could be retained by the catalyst avoiding its solubilization in the supernatants. The retention capacity of the catalyst at 32 °C and pH 3.0 was 3 mg Cr(III)/g. Both an alternative and economical fermentation medium is here proposed for the optimization of Cr(VI)-containing wastewater treatment.
El sector industrial biotecnológico continuamente busca bioprocesos más económicos y sustentables. El uso de medios de cultivo producidos con componentes de bajo costo o con residuos reduce el presupuesto global del proceso y, particularmente si se utilizan residuos, se contribuye, además, a evitar la contaminación ambiental. En este trabajo se probaron medios de cultivo basados en melaza de caña o glicerol ácido como fuentes de carbono y energía, y fertilizante como fuente de nitrógeno, para la producción de un biocatalizador que podría ser usado para el tratamiento de aguas residuales que contienen Cr(VI). Los resultados mostraron que el mayor rendimiento de producción de biomasa se obtuvo con un medio que contenía 5% v/v de glicerol ácido y 0,6% v/v de fertilizante. Utilizando este medio se produjo la biomasa suficiente para la biotransformación de Cr(VI) a Cr(III), luego de ser inmovilizada en alginato de calcio. El proceso pudo ser aplicado eficientemente durante 5 ciclos de reducción de 40 mg/l de Cr(VI) cada uno. Además, se realizaron ensayos de retención de Cr(III) para determinar si esta especie química podría ser removida de la solución por interacción con el biocatalizador. La capacidad de retención obtenida por el biocatalizador a 32 °C y pH 3 fue de 3 mg de Cr(III)/g. De esta manera, se propone un medio de cultivo alternativo y económico para la efectivización de un tratamiento de aguas residuales que contengan Cr(VI).