Simplified process for ethanol production from sugarcane bagasse using hydrolysate-resistant Escherichia coli strain MM160

Bioresour Technol. 2011 Feb;102(3):2702-11. doi: 10.1016/j.biortech.2010.10.143. Epub 2010 Nov 4.

Abstract

Hexose and pentose sugars from phosphoric acid pretreated sugarcane bagasse were co-fermented to ethanol in a single vessel (SScF), eliminating process steps for solid-liquid separation and sugar cleanup. An initial liquefaction step (L) with cellulase was included to improve mixing and saccharification (L+SScF), analogous to a corn ethanol process. Fermentation was enabled by the development of a hydrolysate-resistant mutant of Escherichia coli LY180, designated MM160. Strain MM160 was more resistant than the parent to inhibitors (furfural, 5-hydroxymethylfurfural, and acetate) formed during pretreatment. Bagasse slurries containing 10% and 14% dry weight (fiber plus solubles) were tested using pretreatment temperatures of 160-190°C (1% phosphoric acid, 10 min). Enzymatic saccharification and inhibitor production both increased with pretreatment temperature. The highest titer (30 g/L ethanol) and yield (0.21 g ethanol/g bagasse dry weight) were obtained after incubation for 122 h using 14% dry weight slurries of pretreated bagasse (180°C).

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cellulase / chemistry
  • Cellulose / chemistry
  • Cellulose / metabolism*
  • Escherichia coli / classification*
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Ethanol / metabolism*
  • Mutation
  • Protein Hydrolysates / metabolism*
  • Saccharum / metabolism*
  • Saccharum / microbiology*
  • Species Specificity

Substances

  • Protein Hydrolysates
  • Ethanol
  • Cellulose
  • bagasse
  • Cellulase