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The influence of pretreatment and enzyme loading on the effectiveness of batch and fed‐batch hydrolysis of corn stover
Author(s) -
Chandra Richard P.,
AuYeung Kathy,
Chanis Carolina,
Roos Alexandra A.,
Mabee Warren,
Chung Pablo A.,
Ghatora Sonia,
Saddler Jack N.
Publication year - 2010
Publication title -
biotechnology progress
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.572
H-Index - 129
eISSN - 1520-6033
pISSN - 8756-7938
DOI - 10.1002/btpr.508
Subject(s) - cellulase , corn stover , hydrolysis , cellulose , chemistry , substrate (aquarium) , enzymatic hydrolysis , xylanase , batch reactor , chromatography , nuclear chemistry , biochemistry , enzyme , catalysis , biology , ecology
To try to improve hydrolysis yields at elevated solids loadings, a comparison was made between batch and fed‐batch addition of fresh substrate at the initial and later phases of hydrolysis. Both ethanol (EPCS) and steam‐pretreated corn stover (SPCS) substrates were tested at low (5 FPU) and high (60 FPU) loadings of cellulase per gram of cellulose. The fed‐batch addition of fresh substrate resulted in a slight decrease in hydrolysis yields when compared with the corresponding batch reactions. A 72‐h hydrolysis of the SPCS substrate resulted in a hydrolysis yield of 66% compared with 51% for the EPCS substrate. When the enzyme adsorption and substrate characteristics were assessed during batch and fed‐batch hydrolysis, it appeared that the irreversible binding of cellulases to the more recalcitrant original substrate limited their access to the freshly added substrate. After 72‐h hydrolysis of the SPCS substrate at low enzyme loadings, ∼40–50% of the added cellulases were desorbed into solution, whereas only 20% of the added enzyme was released from the EPCS substrate. Both simultaneous and sequential treatments with xylanases and cellulases resulted in an up to a 20% increase in hydrolysis yields for both substrates at low enzyme loading. Simons' stain measurements indicated that xylanase treatment increased cellulose access, thus facilitating cellulose hydrolysis. © 2010 American Institute of Chemical Engineers Biotechnol. Prog., 2011