x
Filter:
Filters applied
- Enzymology
- Sandgren, MatsRemove Sandgren, Mats filter
- Hansson, HenrikRemove Hansson, Henrik filter
Publication Date
Please choose a date range between 2017 and 2019.
Author
- Karkehabadi, Saeid2
- Payne, Christina M2
- Dankmeyer, Lydia1
- Douglas, Nicholai R1
- Geronimo, Inacrist1
- Goedegebuur, Frits1
- Gualfetti, Peter1
- Gudmundsson, Mikael1
- Huynh, Vicky1
- Jana, Suvamay1
- Jones, Stephen M1
- Kaper, Thijs1
- Kelemen, Brad1
- Kelemen, Bradley R1
- Kim, Steve1
- Kruithof, Paulien1
- Lam, Anna1
- Larenas, Edmund A1
- Meier, Katlyn K1
- Mikkelsen, Nils1
- Mitchinson, Colin1
- Ntarima, Patricia1
- Piens, Kathleen1
Keyword
- molecular dynamics2
- Aspergillus1
- auxiliary activity family 9 (AA9)1
- bioenergy1
- biofuel1
- biotechnology1
- carbohydrate-binding protein1
- cellobiohydrolase1
- cellulase1
- cellulose1
- crystal structure1
- directed evolution1
- electron paramagnetic resonance (EPR)1
- enzyme kinetics1
- enzyme mechanism1
- enzyme structure1
- glycoside hydrolase1
- Hypocrea jecorina1
- inhibition mechanism1
- lytic polysaccharide monooxygenase (LPMO)1
- protein engineering1
- transglycosylation1
- Trichoderma reesei1
- X-ray crystallography1
Enzymology
3 Results
- Molecular BiophysicsOpen Access
Kinetic and molecular dynamics study of inhibition and transglycosylation in Hypocrea jecorina family 3 β-glucosidases
Journal of Biological ChemistryVol. 294Issue 9p3169–3180Published online: January 2, 2019- Inacrist Geronimo
- Patricia Ntarima
- Kathleen Piens
- Mikael Gudmundsson
- Henrik Hansson
- Mats Sandgren
- and others
Cited in Scopus: 4β-Glucosidases enhance enzymatic biomass conversion by relieving cellobiose inhibition of endoglucanases and cellobiohydrolases. However, the susceptibility of these enzymes to inhibition and transglycosylation at high glucose or cellobiose concentrations severely limits their activity and, consequently, the overall efficiency of enzyme mixtures. We determined the impact of these two processes on the hydrolytic activity of the industrially relevant family 3 β-glucosidases from Hypocrea jecorina, HjCel3A and HjCel3B, and investigated the underlying molecular mechanisms through kinetic studies, binding free energy calculations, and molecular dynamics (MD) simulations. - EnzymologyOpen Access
High-resolution structure of a lytic polysaccharide monooxygenase from Hypocrea jecorina reveals a predicted linker as an integral part of the catalytic domain
Journal of Biological ChemistryVol. 292Issue 46p19099–19109Published online: September 12, 2017- Henrik Hansson
- Saeid Karkehabadi
- Nils Mikkelsen
- Nicholai R. Douglas
- Steve Kim
- Anna Lam
- and others
Cited in Scopus: 44For decades, the enzymes of the fungus Hypocrea jecorina have served as a model system for the breakdown of cellulose. Three-dimensional structures for almost all H. jecorina cellulose-degrading enzymes are available, except for HjLPMO9A, belonging to the AA9 family of lytic polysaccharide monooxygenases (LPMOs). These enzymes enhance the hydrolytic activity of cellulases and are essential for cost-efficient conversion of lignocellulosic biomass. Here, using structural and spectroscopic analyses, we found that native HjLPMO9A contains a catalytic domain and a family-1 carbohydrate-binding module (CBM1) connected via a linker sequence. - EnzymologyOpen Access
Improving the thermal stability of cellobiohydrolase Cel7A from Hypocrea jecorina by directed evolution
Journal of Biological ChemistryVol. 292Issue 42p17418–17430Published online: August 31, 2017- Frits Goedegebuur
- Lydia Dankmeyer
- Peter Gualfetti
- Saeid Karkehabadi
- Henrik Hansson
- Suvamay Jana
- and others
Cited in Scopus: 38Secreted mixtures of Hypocrea jecorina cellulases are able to efficiently degrade cellulosic biomass to fermentable sugars at large, commercially relevant scales. H. jecorina Cel7A, cellobiohydrolase I, from glycoside hydrolase family 7, is the workhorse enzyme of the process. However, the thermal stability of Cel7A limits its use to processes where temperatures are no higher than 50 °C. Enhanced thermal stability is desirable to enable the use of higher processing temperatures and to improve the economic feasibility of industrial biomass conversion.