Enhanced production of raw starch degrading enzyme using agro-industrial waste mixtures by thermotolerant Rhizopus microsporus for raw cassava chip saccharification in ethanol production

Prep Biochem Biotechnol. 2017 Sep 14;47(8):813-823. doi: 10.1080/10826068.2017.1342264. Epub 2017 Jun 21.

Abstract

In the present study, solid-state fermentation for the production of raw starch degrading enzyme was investigated by thermotolerant Rhizopus microsporus TISTR 3531 using a combination of agro-industrial wastes as substrates. The obtained crude enzyme was applied for hydrolysis of raw cassava starch and chips at low temperature and subjected to nonsterile ethanol production using raw cassava chips. The agro-industrial waste ratio was optimized using a simplex axial mixture design. The results showed that the substrate mixture consisting of rice bran:corncob:cassava bagasse at 8 g:10 g:2 g yielded the highest enzyme production of 201.6 U/g dry solid. The optimized condition for solid-state fermentation was found as 65% initial moisture content, 35°C, initial pH of 6.0, and 5 × 106 spores/mL inoculum, which gave the highest enzyme activity of 389.5 U/g dry solid. The enzyme showed high efficiency on saccharification of raw cassava starch and chips with synergistic activities of commercial α-amylase at 50°C, which promotes low-temperature bioethanol production. A high ethanol concentration of 102.2 g/L with 78% fermentation efficiency was achieved from modified simultaneous saccharification and fermentation using cofermentation of the enzymatic hydrolysate of 300 g raw cassava chips/L with cane molasses.

Keywords: Ethanol production; mixture design; raw starch degrading enzyme; solid-state fermentation; thermotolerant Rhizopus microsporus.

MeSH terms

  • Carbohydrate Metabolism
  • Ethanol / metabolism*
  • Fermentation
  • Hydrolysis
  • Industrial Waste
  • Manihot / metabolism*
  • Rhizopus / enzymology*
  • Starch / metabolism*
  • alpha-Amylases / metabolism

Substances

  • Industrial Waste
  • Ethanol
  • Starch
  • alpha-Amylases