Charge engineering of cellulases improves ionic liquid tolerance and reduces lignin inhibition. Issue 8 (11th March 2014)
- Record Type:
- Journal Article
- Title:
- Charge engineering of cellulases improves ionic liquid tolerance and reduces lignin inhibition. Issue 8 (11th March 2014)
- Main Title:
- Charge engineering of cellulases improves ionic liquid tolerance and reduces lignin inhibition
- Authors:
- Nordwald, Erik M.
Brunecky, Roman
Himmel, Michael E.
Beckham, Gregg T.
Kaar, Joel L. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit25216-sec-0001" sec-type="section"> <p>We report a novel approach to concurrently improve the tolerance to ionic liquids (ILs) as well as reduce lignin inhibition of <italic>Trichoderma reesei</italic> cellulase via engineering enzyme charge. Succinylation of the cellulase enzymes led to a nearly twofold enhancement in cellulose conversion in 15% (v/v) 1‐butyl‐3‐methylimidazolium chloride ([BMIM][Cl]). The improvement in activity upon succinylation correlated with the apparent preferential exclusion of the [Cl] anion in fluorescence quenching assays. Additionally, modeling analysis of progress curves of Avicel hydrolysis in buffer indicated that succinylation had a negligible impact on the apparent <italic>K</italic><sub>M</sub> of cellulase. As evidence of reducing lignin inhibition of <italic>T. reesei</italic> cellulase, succinylation resulted in a greater than twofold increase in Avicel conversion after 170 h in buffer with 1 wt% lignin. The impact of succinylation on lignin inhibition of cellulase further led to the reduction in apparent <italic>K</italic><sub>M</sub> of the enzyme cocktail for Avicel by 2.7‐fold. These results provide evidence that naturally evolved cellulases with highly negative surface charge densities may similarly repel lignin, resulting in improved cellulase activity. Ultimately, these results underscore the potential of rational charge engineering as a means of<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="bit25216-sec-0001" sec-type="section"> <p>We report a novel approach to concurrently improve the tolerance to ionic liquids (ILs) as well as reduce lignin inhibition of <italic>Trichoderma reesei</italic> cellulase via engineering enzyme charge. Succinylation of the cellulase enzymes led to a nearly twofold enhancement in cellulose conversion in 15% (v/v) 1‐butyl‐3‐methylimidazolium chloride ([BMIM][Cl]). The improvement in activity upon succinylation correlated with the apparent preferential exclusion of the [Cl] anion in fluorescence quenching assays. Additionally, modeling analysis of progress curves of Avicel hydrolysis in buffer indicated that succinylation had a negligible impact on the apparent <italic>K</italic><sub>M</sub> of cellulase. As evidence of reducing lignin inhibition of <italic>T. reesei</italic> cellulase, succinylation resulted in a greater than twofold increase in Avicel conversion after 170 h in buffer with 1 wt% lignin. The impact of succinylation on lignin inhibition of cellulase further led to the reduction in apparent <italic>K</italic><sub>M</sub> of the enzyme cocktail for Avicel by 2.7‐fold. These results provide evidence that naturally evolved cellulases with highly negative surface charge densities may similarly repel lignin, resulting in improved cellulase activity. Ultimately, these results underscore the potential of rational charge engineering as a means of enhancing cellulase function and thus conversion of whole biomass in ILs. Biotechnol. Bioeng. 2014;111: 1541–1549. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Biotechnology and bioengineering. Volume 111:Issue 8(2014:Aug.)
- Journal:
- Biotechnology and bioengineering
- Issue:
- Volume 111:Issue 8(2014:Aug.)
- Issue Display:
- Volume 111, Issue 8 (2014)
- Year:
- 2014
- Volume:
- 111
- Issue:
- 8
- Issue Sort Value:
- 2014-0111-0008-0000
- Page Start:
- 1541
- Page End:
- 1549
- Publication Date:
- 2014-03-11
- Subjects:
- Biotechnology -- Periodicals
Bioengineering -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/doi/10.1002/bip.v101.5/issuetoc ↗
http://www.interscience.wiley.com ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/bit.25216 ↗
- Languages:
- English
- ISSNs:
- 0006-3592
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3473.xml