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1.
Indian J Exp Biol ; 2016 Aug; 54(8): 518-524
Article in English | IMSEAR | ID: sea-178798

ABSTRACT

A successful lignocellulosic ethanol production process needs to address the technological impediments such as cost-competitiveness and sustainability of the process. Effective biomass utilization requires a repertoire of enzymes including various accessory enzymes. Developing an enzyme preparation with defined hydrolytic activities can circumvent the need for supplementing cellulases with accessory enzymes for enhanced hydrolysis. With this objective, mixture design approach was used in the present study to enhance glycoside hydrolase production of a fungal isolate, Aspergillus terreus CM20, by determining the proportion of different lignocellulosic components as enzyme inducers in the culture medium. A mixture of paddy straw and wheat straw (1.42:1.58) resulted in improved cellulolytic activities. The precipitated crude enzyme showed higher CMCase (365.03 18 IU g-1), FPase (161.48 IU g-1), avicelase (15.46 IU g-1), β-glucosidase (920.92 IU g-1) and xylanase (9627.79 IU g-1) activities. The potential of the crude enzyme for saccharification of alkali pretreated paddy straw was also tested. Under optimum conditions, saccharification released 25.0 g L-1 of fermentable sugars. This indicates the superiority of the crude enzyme produced with respect to its hydrolytic enzyme components.

2.
Article in English | IMSEAR | ID: sea-150868

ABSTRACT

Optimization is often used in pharmacy relative to formulation & processing and one may find it in literature referring to any study of formula. Optimize means to make a perfect, effective (or) functional as possible. Process optimization is the discipline of adjusting a process so as to optimize some specified set of parameters without violating some constraint. The most common goals are minimizing cost, maximizing output, and/or efficiency. This is one of major quantitative tools in industrial decision making. In the present work process parameters at developmental stages of formulation were studied extensively and after completion of the data generated during the Process Optimization of Efavirenz tablets , some critical parameters were identified and some changes are recommended in various stages of manufacturing process and finally proved that process is capable of producing a drug of required quality with proposed process.

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