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1.
Rev. argent. microbiol ; 46(2): 144-149, jun. 2014. tab, ilus, graf
Article in English | LILACS | ID: lil-734576

ABSTRACT

Ganoderma lucidum (Curtis) P. Karst es un hongo causante de pudrición blanca, capaz de degradar la lignina de la madera y otros sustratos en los que crece. En este trabajo se evaluó la capacidad de dos cepas de esta especie de producir la enzima ligninolítica lacasa. Asimismo, se ensayó la inducción de esta enzima con diferentes compuestos fenólicos e iones metálicos, y se encontró que el ácido ferúlico y el cobre fueron los mejores inductores de la lacasa entre los agentes evaluados. También se encontró que los dos tipos de inductores (fenólicos y metálicos) producen distintos patrones electroforéticos de actividad lacasa. Las concentraciones óptimas de los inductores fueron establecidas mediante un diseño factorial. Se estimó la estabilidad térmica de la lacasa en un amplio rango de pH ácidos, y se comprobó que a pH más altos la enzima es más termoestable.


Ganoderma lucidum (Curtis) P. Karst is a white rot fungus that is able to degrade the lignin component in wood. The ability of two strains of this species to produce the ligninolytic enzyme laccase was assessed. After the evaluation of induction with heavy metals and phenolic compounds, it was found that among the tested substances, copper and ferulic acid are the best laccase inducers. It was also observed that the two types of inducers (phenolic and metallic) produce different electrophoretic patterns of laccase activity. Optimized concentrations of inducers were obtained through a factorial design and the thermal stability of optimized supernatants was studied at a wide range of acidic pH. We found that the enzyme is more thermostable at higher pH values.


Subject(s)
Laccase/biosynthesis , Reishi/drug effects , Reishi/metabolism , Coumaric Acids , Copper/pharmacology , Manganese/pharmacology , Phenols/pharmacology
2.
Braz. j. microbiol ; 45(2): 721-729, Apr.-June 2014. ilus, graf, tab
Article in English | LILACS | ID: lil-723139

ABSTRACT

DNJ, an inhibitor of α-glucosidase, is used to suppress the elevation of postprandial hyperglycemia. In this study, we focus on screening an appropriate microorganism for performing fermentation to improve DNJ content in mulberry leaf. Results showed that Ganoderma lucidum was selected from 8 species and shown to be the most effective in improvement of DNJ production from mulberry leaves through fermentation. Based on single factor and three factor influence level tests by following the Plackett-Burman design, the optimum extraction yield was analyzed by response surface methodology (RSM). The extracted DNJ was determined by reverse-phase high performance liquid chromatograph equipped with fluorescence detector (HPLC-FD). The results of RSM showed that the optimal condition for mulberry fermentation was defined as pH 6.97, potassium nitrate content 0.81% and inoculums volume 2 mL. The extraction efficiency reached to 0.548% in maximum which is 2.74 fold of those in mulberry leaf.


Subject(s)
1-Deoxynojirimycin/isolation & purification , 1-Deoxynojirimycin/metabolism , Enzyme Inhibitors/isolation & purification , Enzyme Inhibitors/metabolism , Morus/metabolism , Reishi/metabolism , Biotechnology/methods , Chromatography, High Pressure Liquid , Culture Media/chemistry , Fermentation , Hydrogen-Ion Concentration , Plant Leaves/metabolism , Reishi/growth & development , Technology, Pharmaceutical/methods
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