کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2075331 | 1079328 | 2015 | 8 صفحه PDF | دانلود رایگان |
• Attractive method proposal on cactus pear biotransformation.
• Feasibility of agricultural products use in bioprocesses.
• Cold-active protease secreted by filamentous fungus isolated in Antarctica.
• Different NaCl and surfactants concentrations tolerant biocatalyst.
• Serino protease stable on all evaluated pH ranges.
Acremonium sp. L1-4B isolated from lichen in Antarctica was used to produce extracellular proteases through submerged fermentation using cactus pear extract (Opuntia ficus-indica Mill.). A 23 factorial design was applied to optimize the protease production using three independent variables, namely temperature, pH and concentration of yeast extract, was also used a Central Composite Design (CCD) under Response Surface Methodology (RSM). All variables and interactions analyzed in the factorial design were significant or marginally significant, a Central Composite Design was developed, and the Response Surface Methodology towards the highest point it was established. The experimental model was validated under 14 °C, pH 7.54, and 0.55% yeast extract, showing a protease activity of 447.65±2.6 U/mL by a prediction model of 445.48 U/mL. The enzyme showed a molecular weight of 59 kDa; it was inhibited in the presence of PMSF (serine protease); it presented optimal conditions at pH 8.0 and 50 °C; it remained stable at pH in the 3.0–9.0 range and between 10 and 40 °C; it showed a tolerance to 3000 mM NaCl as well as to surfactants, hydrogen peroxide and urea at 5%. This paper presents a proposal for an economically attractive production methodology using cactus pear as a primary source of carbon. In addition, the protease secreted by Acremonium sp. L1-4B presented a combination of biochemical characteristics that grants a promising variability of biotechnological applications.
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Journal: Biocatalysis and Agricultural Biotechnology - Volume 4, Issue 4, October 2015, Pages 737–744