Optimizing culture conditions for production of intra and extracellular inulinase and invertase from Aspergillus niger ATCC 20611 by response surface methodology (RSM)

Braz J Microbiol. 2017 Jul-Sep;48(3):427-441. doi: 10.1016/j.bjm.2016.10.026. Epub 2017 Feb 10.

Abstract

The aim of this study was obtain a model that maximizes growth and production of inulinase and invertase by Aspergillus niger ATCC 20611, employing response surface methodology (RSM). The RSM with a five-variable and three-level central composite design (CCD) was employed to optimize the medium composition. Results showed that the experimental data could be appropriately fitted into a second-order polynomial model with a coefficient of determination (R2) more than 0.90 for all responses. This model adequately explained the data variation and represented the actual relationships between the parameters and responses. The pH and temperature value of the cultivation medium were the most significant variables and the effects of inoculum size and agitation speed were slightly lower. The intra-extracellular inulinase, invertase production and biomass content increased 10-32 fold in the optimized medium condition (pH 6.5, temperature 30°C, 6% (v/v), inoculum size and 150rpm agitation speed) by RSM compared with medium optimized through the one-factor-at-a-time method. The process development and intensification for simultaneous production of intra-extracellular inulinase (exo and endo inulinase) and invertase from A. niger could be used for industrial applications.

Keywords: Aspergillus niger; Intra-extracellular inulinase production; Intra-extracellular invertase production; Optimization; Response surface method (RSM).

Publication types

  • Evaluation Study

MeSH terms

  • Aspergillus niger / enzymology
  • Aspergillus niger / genetics
  • Aspergillus niger / growth & development
  • Aspergillus niger / metabolism*
  • Bioreactors / microbiology
  • Culture Media / chemistry
  • Culture Media / metabolism
  • Fermentation
  • Glycoside Hydrolases / biosynthesis*
  • Glycoside Hydrolases / genetics
  • Industrial Microbiology / methods*
  • Temperature
  • beta-Fructofuranosidase / biosynthesis*
  • beta-Fructofuranosidase / genetics

Substances

  • Culture Media
  • Glycoside Hydrolases
  • beta-Fructofuranosidase
  • inulinase