scholarly journals Effective Concentration of Ionic Liquids for Enhanced Saccharification of Cellulose

2018 ◽  
Vol 2 (4) ◽  
pp. 47 ◽  
Author(s):  
Kazuhiko Tanimura ◽  
Yoshiko Ooe ◽  
Keishi Suga ◽  
Hiroshi Umakoshi
Keyword(s):  
Ionic Liquids ◽  
Trichoderma Viride ◽  
Enzymatic Saccharification ◽  
Tryptophan Fluorescence ◽  
Crystalline Cellulose ◽  
Adsorption Model ◽  
Langmuir Adsorption ◽  
Intrinsic Tryptophan Fluorescence ◽  
Heat Treated ◽  
Rate Limiting

In an aqueous enzymatic saccharification using cellulase, the dissolution of crystalline cellulose is one of the rate-limiting steps. Insoluble cellulose powder was preliminarily heat-treated with ionic liquids (ILs), such as [Bmim][Cl] (1-butyl-3-methylimidazolium chloride) and [Amim][Cl] (1-allyl-3-methylimidazolium chloride), which enable the production of soluble cellulose. On the other hand, the presence of ILs leads to a denaturation of enzymes. Using cellulase from Trichoderma viride, the effects of [Bmim][Cl] and [Amim][Cl] in the enzymatic saccharification were compared. The production of glucose was optimized with 5 wt%-ILs, both for [Bmim][Cl] and for [Amim][Cl]. The significant inhibiting effects of ILs (IL concentration >10 wt%) could be due to the denaturation of cellulase, because the peak shifts of intrinsic tryptophan fluorescence were observed in the presence of 7.5 wt%-ILs. To analyze kinetic parameters, the Langmuir adsorption model and the Michaelis-Menten model were employed. The investigation suggests that [Amim][Cl] can provide soluble cellulose more efficiently, and can promote enzymatic saccharification in the IL concentration below 5 wt%.

scholarly journals Stability of cellulase in ionic liquids: correlations between enzyme activity and COSMO-RS descriptors

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Jacob Nedergaard Pedersen ◽  
Bianca Pérez ◽  
Zheng Guo
Keyword(s):  
Hydrogen Bond ◽  
Enzyme Activity ◽  
Ionic Liquids ◽  
Bond Energy ◽  
Crucial Role ◽  
Enzymatic Saccharification ◽  
Cellulase Activity ◽  
Cellulose Dissolution ◽  
Ion Size ◽  
Selection Of

AbstractIonic liquids (ILs) are effective in pretreating cellulose for enhanced enzymatic saccharification, however ILs can inactivate cellulases. To guide the selection of ILs, the activity of cellulase was correlated with COSMO-RS calculations and descriptors of ILs including hydrogen bond (H-bond) basicity/acidity, polarity and ion size. Trends were deduced using an anion-series and a cation-series of ionic liquids in aqueous solutions. The activity in the cation-series was best correlated with the size of varied cations, whereas the activity in the anion-series showed a pronounced correlation to H-bond basicity and polarity of different anions. COSMO-RS was further used to predict the solubility of cellulose in ILs, which was correlated with cellulase activity on IL-pretreated cellulose. The best correlations were found between the enzyme activity in the anion-series ILs and the logarithmic activity coefficients, the H-bond energy, H-bond basicity and polarizability, underlining that the anion plays a crucial role in cellulose dissolution.

scholarly journals The Effect of Deposition Time on the Surface Coverage of Sublimation Deposited Solid-Phase Glycine and Proline Molecules Measured by Scanning Tunneling Microscopy

Molecules ◽  
2020 ◽  
Vol 25 (13) ◽  
pp. 2962
Author(s):  
Young-Sang Youn
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Room Temperature ◽  
Deposition Time ◽  
Surface Coverage ◽  
Solid Phase ◽  
Scanning Tunneling ◽  
Adsorption Model ◽  
Tunneling Microscopy ◽  
Langmuir Adsorption ◽  
Stm Images

The effect of deposition time on the surface coverage of sublimation deposited solid-phase glycine and proline molecules onto a Ge(100) surface was studied at room temperature using scanning tunneling microscopy (STM). The STM images obtained at various coverages of glycine and proline adsorbed on the Ge(100) surface showed that (i) the adsorption rate for both molecules gradually decreased with increasing deposition time, obeying the Langmuir adsorption model, and (ii) the coverage of glycine on the Ge(100) surface is higher than that of proline under the same deposition conditions, which may be due to the differences in their molecular weight or molecular sticking probability.

scholarly journals Determination of the absolute CH4 adsorption using simplified local density theory and comparison with the modified Langmuir adsorption model

RSC Advances ◽  
2018 ◽  
Vol 8 (72) ◽  
pp. 41509-41516
Author(s):  
Yeyu Zhang ◽  
Shaonan Zhang ◽  
Zhicheng Wang ◽  
Hucheng Deng ◽  
Minghui Qi ◽  
...  
Keyword(s):  
Shale Gas ◽  
Local Density ◽  
Gas Storage ◽  
Adsorption Model ◽  
Gas Reservoirs ◽  
Methane Recovery ◽  
Langmuir Adsorption ◽  
Langmuir Adsorption Model ◽  
Ch4 Adsorption

Accurately determining the adsorbed amount of CH4 on shale is significant for understanding the mechanisms of shale gas storage and shale methane recovery from shale gas reservoirs.

scholarly journals Inactivation of sarcoplasmic-reticulum Ca2+-ATPase in low-frequency-stimulated muscle results from a modification of the active site

1992 ◽  
Vol 285 (1) ◽  
pp. 303-309 ◽  
Author(s):  
S Matsushita ◽  
D Pette
Keyword(s):  
Sarcoplasmic Reticulum ◽  
Active Site ◽  
Low Frequency ◽  
Fluorescein Isothiocyanate ◽  
Tryptophan Fluorescence ◽  
Atp Binding ◽  
Binding Characteristics ◽  
Intrinsic Tryptophan Fluorescence ◽  
Inactive Form ◽  
Induced Changes

Molecular changes underlying the partial inactivation of the sarcoplasmic-reticulum (SR) Ca(2+-) ATPase in low-frequency-stimulated fast-twitch muscle were investigated in the present study. The specific Ca(2+)-ATPase activity, as well as the ATP- and acetyl phosphate-driven Ca2+ uptakes by the SR, were reduced by approx. 30% in 4-day-stimulated muscle. Phosphoprotein formation of the enzyme in the presence of ATP or Pi was also decreased to the same extent. Measurements of ATP binding revealed a 30% decrease in binding to the enzyme. These changes were accompanied by similar decreases in the ligand-induced (ATP, ADP, Pi) intrinsic tryptophan fluorescence. A decreased binding of fluorescein isothiocyanate (FITC) corresponded to the lower ATP binding and phosphorylation of the enzyme. Moreover, Pi-induced changes in fluorescence of the FITC-labelled enzyme did not differ between SR from stimulated and contralateral muscles, indicating that Ca(2+)- ATPase molecules which did not bind FITC were responsible for the decreased Pi-dependent phosphorylation, and therefore represented the inactive form of the enzyme. No differences existed between the Ca(2+)-induced changes in the intrinsic fluorescence of SR from stimulated and contralateral muscles which fit their similar Ca(2+)-binding characteristics. Taking the proposed architecture of the Ca2(+)-ATPase into consideration, our results suggest that the inactivation relates to a circumscribed structural alteration of the enzyme in sections of the active site consisting of the nucleotide-binding and phosphorylation domains.

scholarly journals Substrate-induced conformational transition in human phenylalanine hydroxylase as studied by surface plasmon resonance analyses: the effect of terminal deletions, substrate analogues and phosphorylation

2003 ◽  
Vol 369 (3) ◽  
pp. 509-518 ◽  
Author(s):  
Anne J. STOKKA ◽  
Torgeir FLATMARK
Keyword(s):  
Surface Plasmon Resonance ◽  
Surface Plasmon ◽  
Plasmon Resonance ◽  
Phenylalanine Hydroxylase ◽  
Conformational Transition ◽  
Tryptophan Fluorescence ◽  
Catalytic Core ◽  
Intrinsic Tryptophan Fluorescence ◽  
Human Phenylalanine Hydroxylase ◽  
Activity State

The optical biosensor technique, based on the surface plasmon resonance (SPR) phenomenon, was used for real-time measurements of the slow conformational transition (isomerization) which occurs in human phenylalanine hydroxylase (hPAH) on the binding/dissociation of l-phenylalanine (l-Phe). The binding to immobilized tetrameric wt-hPAH resulted in a time-dependent increase in the refractive index (up to approx. 3min at 25°C) with an end point of approx. 75RU (resonance units)/(pmolsubunit/mm2). By contrast, the contribution of binding the substrate (165Da) to its catalytic core enzyme [ΔN(1—102)/ΔC(428—452)-hPAH] was only approx. 2RU/(pmolsubunit/mm2). The binding isotherm for tetrameric and dimeric wt-hPAH revealed a [S]0.5-value of 98±7μM (h = 1.0) and 158±11μM, respectively, i.e. for the tetramer it is slightly lower than the value (145±5μM) obtained for the co-operative binding (h = 1.6±0.4) of l-Phe as measured by the change in intrinsic tryptophan fluorescence. The responses obtained by SPR and intrinsic tryptophan fluorescence are both considered to be related to the slow reversible conformational transition which occurs in the enzyme upon l-Phe binding, i.e. by the transition from a low-activity state ('T-state') to a relaxed high-activity state ('R-state') characteristic of this hysteretic enzyme, however, the two methods reflect different elements of the transition. Studies on the N- and C-terminal truncated forms revealed that the N-terminal regulatory domain (residues 1—117) plus catalytic domain (residues 118—411) were required for the full signal amplitude of the SPR response. Both the on- and off-rates for the conformational transition were biphasic, which is interpreted in terms of a difference in the energy barrier and the rate by which the two domains (catalytic and regulatory) undergo a conformational change. The substrate analogue 3-(2-thienyl)-l-alanine revealed an SPR response comparable with that of l-Phe on binding to wild-type hPAH.

Mild pretreatment and enzymatic saccharification of cellulose with recycled ionic liquids towards one-batch process

2012 ◽  
Vol 90 (2) ◽  
pp. 805-813 ◽  
Author(s):  
Thomas Auxenfans ◽  
Sébastien Buchoux ◽  
Karim Djellab ◽  
Carine Avondo ◽  
Eric Husson ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Enzymatic Saccharification ◽  
Batch Process

scholarly journals Sodium hydroxide modified rice husk for enhanced removal of copper ions

2018 ◽  
Vol 78 (7) ◽  
pp. 1615-1623 ◽  
Author(s):  
N. Priyantha ◽  
H. K. W. Sandamali ◽  
T. P. K. Kulasooriya
Keyword(s):  
Heavy Metal ◽  
Adsorption Capacity ◽  
Rice Husk ◽  
Copper Ions ◽  
Maximum Adsorption Capacity ◽  
Adsorption Model ◽  
Natural Form ◽  
Langmuir Adsorption ◽  
Pseudo Second Order ◽  
Heavy Metal Adsorbent

Abstract Although rice husk (RH) is a readily available, natural, heavy metal adsorbent, adsorption capacity in its natural form is insufficient for certain heavy metal ions. In this context, the study is based on enhancement of the adsorption capacity of RH for Cu(II). NaOH modified rice husk (SRH) shows higher extent of removal for Cu(II) ions than that of heated rice husk (HRH) and HNO3 modified rice husk (NRH). The extent of removal of SRH is increased with the concentration of NaOH, and the optimum NaOH concentration is 0.2 mol dm−3, used to modify rice husk for further studies. The surface area of SRH is 215 m2 g−1, which is twice as much as that of HRH according to previous studies. The sorption of Cu(II) on SRH obeys the Langmuir adsorption model, leading to the maximum adsorption capacity of 1.19 × 104 mg kg−1. Kinetics studies show that the interaction of Cu(II) with SRH obeys pseudo second order kinetics. The X-ray fluorescence spectroscopy confirms the adsorption of Cu(II) on SRH, while desorption studies confirm that Cu(II) adsorbed on SRH does not leach it back to water under normal conditions.

scholarly journals Intrinsic tryptophan fluorescence spectroscopy reliably determines galectin-ligand interactions

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Paulina Sindrewicz ◽  
Xiaoxin Li ◽  
Edwin A. Yates ◽  
Jeremy E. Turnbull ◽  
Lu-Yun Lian ◽  
...  
Keyword(s):  
Fluorescence Spectroscopy ◽  
Tryptophan Fluorescence ◽  
Intrinsic Tryptophan Fluorescence ◽  
Ligand Interactions
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