26 research outputs found
Co-Enzymes based nanoflowers incorporated-magnetic carbon nanotubes: A new generation nanocatalyst for superior removal of cationic and anionic dyes with great repeated use
Synthetic dyes leading to substantial discharge in various industrial areas such as textile, plastics, food, and cosmetics, have growingly threatened all livings. Although enzymes have been used for dye degradation, weak stability against changes in reaction environment, lack of reusability and high cost have strictly limited their use. Herein, we have developed co-enzymes nanoflowers incorporated-magnetic carbon nanotube nanocomposite as a novel and efficient nanocatalyst for superior degradation of malachite green (MG) and acid orange 7 (AO7) as model cationic and anionic dyes with excellent cyclic use. The HRP-Lac NF@mCNT nanocomposite (NC) containing horseradish peroxidase-laccase nanoflower (HRP-Lac NF) and iron oxide nanoparticles (Fe(3)O(4)NPs) decorated magnetic carbon nanotube (mCNT) was systematically employed in dye degradation as functions of pH, reaction time, dye type and reusability. This HRP-Lac NF@mCNT nanocomposite acted as one malfunctional nanoplatform since both HRP and Lac enzymes were used for rapid and efficient dye removal, Fe3O4 NPs provided cyclic use and omitting the centrifugation step, and CNT functioned as a unique platform for NFs and Fe3O4 NPs deposition. We demonstrated that HRP-Lac NF@mCNT NC induced similar to 90 % MG and similar to 85% AO7 decolorization in 20 min at pH 7.4 while it almost completely decolorized MG and AO7 in 60 min. In addition, similar to 95% MG and similar to 85% AO7 decolorization were accomplished even after 16 cycling use of HRP-Lac NF@mCNT NC. We claim that HRP-Lac NF@mCNT NC induced dye decolorization with dual mechanisms, enzymatic degradation, and physical adsorption. (C) 2021 Elsevier B.V. All rights reserved
Preparation of magnetic horseradish peroxidase-laccase nanoflower for rapid and efficient dye degradation with dual mechanism and cyclic use
Herein, we developed magnetic co-enzymes nanocomposite called mHRP-Lac NF consisting of horseradish peroxidase (HRP), laccase (Lac) incorporated copper II ions (Cu2+) in phosphate buffered saline (PBS) solution and used as an excellent dye degradation agent against a cationic dye, malachite green (MG) and an anionic azo dye acid orange 7 (AO7) under various pH values. Benefiting from the magnetic property, mHRP-Lac NF was repeatedly used for efficient dye degradation
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Quantitative Kelvin probe force microscopy of current-carrying devices
Kelvin probe force microscopy (KPFM) should be a key tool for characterizing the device physics of nanoscale electronics because it can directly image electrostatic potentials. In practice, though, distant connective electrodes interfere with accurate KPFM potential measurements and compromise its applicability. A parameterized KPFM technique described here determines these influences empirically during imaging, so that accurate potential profiles can be deduced from arbitrary device geometries without additional modeling. The technique is demonstrated on current-carrying single-walled carbon nanotubes (SWNTs), directly resolving average resistances per unit length of 70 kΩ/μm in semimetallic SWNTs and 200 kΩ/μm in semiconducting SWNTs. © 2013 American Institute of Physics
Formation of functional nanobiocatalysts with a novel and encouraging immobilization approach and their versatile bioanalytical applications
The discovery of functional organic-inorganic hybrid nanoflowers (FNFs) consisting of proteins/enzymes as the organic components and Cu(ii) ion as the inorganic component has made an enormous impact on enzyme immobilization studies. The FNFs synthesized by an encouraging and novel approach not only showed high stabilities but also much enhanced catalytic activities as compared to free and conventionally immobilized enzymes. A recent development demonstrated that FNF formation has moved beyond the initial discovery in which enzymes and Cu2+ ions used as the organic and inorganic parts, respectively, are replaced with new organic (chitosan, amino acid and plant extracts) and inorganic (Cu2+ and Fe2+) materials. The new organic materials incorporated into FNFs act as Fenton-like agents and then show peroxidase-like activity owing to the metal ions and the porous structure of FNFs in the presence of hydrogen peroxide (H2O2). All FNFs have been widely utilized in many different scientific and industrial fields due to their greatly enhanced activities and stabilities. This review focuses primarily on the preparation, characterization, and bioanalytical applications of FNFs and explains the mechanisms of their formation and enhanced activities and stabilities
In Situ Synthesis of Horseradish Peroxidase Nanoflower@Carbon Nanotube Hybrid Nanobiocatalysts with Greatly Enhanced Catalytic Activity
Organic–inorganic hybrid nanoflowers (NFs) consisting
of
horseradish peroxidase (HRP) and copper II (Cu2+) are successfully
synthesized with the involvement of carbon nanotubes (CNTs) by in
situ and post-modification methods. Catalytic activities of in situ
synthesized HRP-NF@CNT (HRP-NF@CNT-Is) and post-modification-synthesized
HRP-NF@CNTs (HRP-NF@CNT-Pm) are systematically examined. The 30 mg
CNTs incorporated HRP-NF@CNT-Is (HRP-NF@CNT-30Is) exhibits greatly
increased catalytic activity and stability toward 3,3′,5,5′-tetramethylbenzidine
(TMB), thanks to the synergistic effect between HRP-NF and CNTs and
the peroxidase-like activity of CNTs in the presence of hydrogen peroxide
(H2O2). While HRP-NF@CNT-30Is retains almost
85% of its initial activity even after 10 cycles, HRP-NF (without
CNTs) loses half of its initial activity at the same experimental
conditions. We study how two experimental parameters, the pH values
and temperatures, influence the catalytic activity of HRP-NF@CNT-30Is,
in addition to the fact that HRP-NF@CNT-30Is is employed to detect
the presence of H2O2 and glutathione (GSH) with
colorimetric and spectrophotometric readouts. For instance, HRP-NF@CNT-30Is
is used to sensitively detect H2O2 in the range
of 20 to 300 μM with an LOD of 2.26 μM. The catalytic
activity of HRP-NF@CNT-30Is is suppressed in the presence of GSH,
and then an obvious color change from blue to nearly colorless is
observed. Using this strategy, GSH is also sensitively determined
in the range of 20–200 μM with an LOD of 11.2 μM.
We expect that HRP-NF@CNTs can be used as a promising and novel nanobiocatalyst
for various biomedical and industrial applications in the near future
Quantitative Kelvin probe force microscopy of current-carrying devices
Kelvin probe force microscopy (KPFM) should be a key tool for characterizing the device physics of nanoscale electronics because it can directly image electrostatic potentials. In practice, though, distant connective electrodes interfere with accurate KPFM potential measurements and compromise its applicability. A parameterized KPFM technique described here determines these influences empirically during imaging, so that accurate potential profiles can be deduced from arbitrary device geometries without additional modeling. The technique is demonstrated on current-carrying single-walled carbon nanotubes (SWNTs), directly resolving average resistances per unit length of 70 kΩ/μm in semimetallic SWNTs and 200 kΩ/μm in semiconducting SWNTs. © 2013 American Institute of Physics
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Processive Incorporation of Deoxynucleoside Triphosphate Analogs by Single-Molecule DNA Polymerase I (Klenow Fragment) Nanocircuits.
DNA polymerases exhibit a surprising tolerance for analogs of deoxyribonucleoside triphosphates (dNTPs), despite the enzymes' highly evolved mechanisms for the specific recognition and discrimination of native dNTPs. Here, individual DNA polymerase I Klenow fragment (KF) molecules were tethered to a single-walled carbon nanotube field-effect transistor (SWCNT-FET) to investigate accommodation of dNTP analogs with single-molecule resolution. Each base incorporation accompanied a change in current with its duration defined by τclosed. Under Vmax conditions, the average time of τclosed was similar for all analog and native dNTPs (0.2 to 0.4 ms), indicating no kinetic impact on this step due to analog structure. Accordingly, the average rates of dNTP analog incorporation were largely determined by durations with no change in current defined by τopen, which includes molecular recognition of the incoming dNTP. All α-thio-dNTPs were incorporated more slowly, at 40 to 65% of the rate for the corresponding native dNTPs. During polymerization with 6-Cl-2APTP, 2-thio-dTTP, or 2-thio-dCTP, the nanocircuit uncovered an alternative conformation represented by positive current excursions that does not occur with native dNTPs. A model consistent with these results invokes rotations by the enzyme's O-helix; this motion can test the stability of nascent base pairs using nonhydrophilic interactions and is allosterically coupled to charged residues near the site of SWCNT attachment. This model with two opposing O-helix motions differs from the previous report in which all current excursions were solely attributed to global enzyme closure and covalent-bond formation. The results suggest the enzyme applies a dynamic stability-checking mechanism for each nascent base pair
Formation of functional nanobiocatalysts with a novel and encouraging immobilization approach and their versatile bioanalytical applications
The discovery of functional organic-inorganic hybrid nanoflowers (FNFs)
consisting of proteins/enzymes as the organic components and Cu(ii) ion
as the inorganic component has made an enormous impact on enzyme
immobilization studies. The FNFs synthesized by an encouraging and novel
approach not only showed high stabilities but also much enhanced
catalytic activities as compared to free and conventionally immobilized
enzymes. A recent development demonstrated that FNF formation has moved
beyond the initial discovery in which enzymes and Cu2+ ions used as the
organic and inorganic parts, respectively, are replaced with new organic
(chitosan, amino acid and plant extracts) and inorganic (Cu2+ and Fe2+)
materials. The new organic materials incorporated into FNFs act as
Fenton-like agents and then show peroxidase-like activity owing to the
metal ions and the porous structure of FNFs in the presence of hydrogen
peroxide (H2O2). All FNFs have been widely utilized in many different
scientific and industrial fields due to their greatly enhanced
activities and stabilities. This review focuses primarily on the
preparation, characterization, and bioanalytical applications of FNFs
and explains the mechanisms of their formation and enhanced activities
and stabilities
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Electronic measurements of single-molecule catalysis by cAMP-dependent protein kinase A.
Single-molecule studies of enzymes open a window into their dynamics and kinetics. A single molecule of the catalytic domain of cAMP-dependent protein kinase A (PKA) was attached to a single-walled carbon nanotube device for long-duration monitoring. The electronic recording clearly resolves substrate binding, ATP binding, and cooperative formation of PKA's catalytically functional, ternary complex. Using recordings of a single PKA molecule extending over 10 min and tens of thousands of binding events, we determine the full transition probability matrix and conversion rates governing formation of the apo, intermediate, and closed enzyme configurations. We also observe kinetic rates varying over 2 orders of magnitude from one second to another. Anti-correlation of the on and off rates for PKA binding to the peptide substrate, but not ATP, demonstrates that regulation of enzyme activity results from altering the stability of the PKA-substrate complex, not its binding to ATP. The results depict a highly dynamic enzyme offering dramatic possibilities for regulated activity, an attribute useful for an enzyme with crucial roles in cell signaling
Electronic measurements of single-molecule catalysis by cAMP-dependent protein kinase A.
Single-molecule studies of enzymes open a window into their dynamics and kinetics. A single molecule of the catalytic domain of cAMP-dependent protein kinase A (PKA) was attached to a single-walled carbon nanotube device for long-duration monitoring. The electronic recording clearly resolves substrate binding, ATP binding, and cooperative formation of PKA's catalytically functional, ternary complex. Using recordings of a single PKA molecule extending over 10 min and tens of thousands of binding events, we determine the full transition probability matrix and conversion rates governing formation of the apo, intermediate, and closed enzyme configurations. We also observe kinetic rates varying over 2 orders of magnitude from one second to another. Anti-correlation of the on and off rates for PKA binding to the peptide substrate, but not ATP, demonstrates that regulation of enzyme activity results from altering the stability of the PKA-substrate complex, not its binding to ATP. The results depict a highly dynamic enzyme offering dramatic possibilities for regulated activity, an attribute useful for an enzyme with crucial roles in cell signaling