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1.
Sci Total Environ ; 901: 165950, 2023 Nov 25.
Artigo em Inglês | MEDLINE | ID: mdl-37536592

RESUMO

Plastic pollution is one of the most environmental problems in the last two centuries, because of their excessive usage and their rapidly increasing production, which overcome the ability of natural degradation. Moreover, this problem become an escalating environmental issue caused by inadequate disposal, ineffective or nonexistent waste collection methods, and a lack of appropriate measures to deal with the problem, such as incineration and landfilling. Consequently, plastic wastes have become so ubiquitous and have accumulated in the environment impacting ecosystems and wildlife. The above, enhances the urgent need to explore alternative approaches that can effectively reduce waste without causing harsh environmental consequences. For example, white-rot fungi are a promising alternative to deal with the problem. These fungi produce ligninolytic enzymes able to break down the molecular structures of plastics, making them more bioavailable and allowing their degradation process, thereby mitigating waste accumulation. Over the years, several research studies have focused on the utilization of white-rot fungi to degrade plastics. This review presents a summary of plastic degradation biochemistry by white-rot fungi and the function of their ligninolytic enzymes. It also includes a collection of different research studies involving white-rot fungi to degrade plastic, their enzymes, the techniques used and the obtained results. Also, this highlights the significance of pre-treatments and the study of plastic blends with natural fibers or metallic ions, which have shown higher levels of degradation. Finally, it raises the limitations of the biotechnological processes and the prospects for future studies.

2.
Rev. colomb. biotecnol ; 17(2): 44-54, jul.-dic. 2015. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-769071

RESUMO

Los hongos de la podredumbre blanca de la madera, como Ganoderma sp., han sido utilizados alrededor del mundo por sus propiedades medicinales, ya que poseen compuestos bioactivos como los triterpenos y los polisacáridos. Esta investigación se centra en la producción de polisacáridos a escala de laboratorio y de biorreactor, a partir de Ganoderma sp., aislado en la región andina, utilizando como sustrato un residuo ligninocelulósico de la industria agrícola suplementado con glucosa y lactosa. Se encontró que las condiciones más adecuadas y viables para la producción de biomasa y polisacáridos de Ganoderma sp., son: medio Bio 3%, 10 días de incubación, lactosa 10%, pH= 4,0, T= 30°C, 300 rpm y 1 vvm. Los ensayos espectrofotométricos (fenol ácido sulfúrico y escaneo en UV entre 200 y 400 nm), enzimáticos y de infrarrojo permitieron identificar y cuantificar glucanos y algunas proteínas en los extractos, sugiriendo que los hongos endógenos de la región Andina poseen características propias de metabolitos importantes a nivel medicinal. Adicionalmente se demostró el efecto antiproliferativo en células J774, especialmente del extracto GIPSi (IC50= 86%) similar al efecto generado por estándares comerciales.


The white rot wood fungi like Ganoderma has been used worldwide because it has triterpenoids and polysaccharides with medicinal properties. This research focuses on determining the polysaccharide production conditions and laboratory and bioreactor scale, from the aforementioned fungi, isolated in the Andean region. It was used agricultural lignin-residue supplemented with glucose and lactose. We found that the most appropriate and feasible production conditions for biomass and Ganoderma polysaccharides are: Bio medium 3%, t = 10 days, 10% lactose, pH= 4,0, T= 30°C, 300 rpm and 1 vvm. The spectrophotometric, enzymatic and IR tests; allowed us to identify the presence of polysaccharides and proteins in some extracts, suggesting that the endogenous mushrooms in the Andean region also have characteristics similar to those of metabolites that are important in medicine. Additionally, the antiproliferative effect was observed in J774 sarcoma cells, particularly GIPSi extract (IC50= 86%) similar to the effect generated by commercial standards.

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