Nanoparticle Fabrication on Bacterial Microcompartment Surface for the Development of Hybrid Enzyme-Inorganic Catalyst (original) (raw)

Direct Assembly of Gold Nanoparticle “Shells” on Polyurethane Microsphere “Cores” and Their Application as Enzyme Immobilization Templates

Chemistry of Materials, 2003

The assembly of aqueous gold nanoparticles on the surface of polyurethane (PU) spheres leading to [gold nanoparticle shell]-[polyurethane core] structures is demonstrated. The assembly of gold nanoparticles on the polymer microspheres occurs through interaction of the nitrogens in the polymer with the nanoparticles. Such direct assembly obviates the need to perform additional surface modification of the polymer microspheres, which is an important step in other polymer-based core-shell structure protocols. The nanogold-PU material is then conjugated with the enzyme pepsin, leading to the formation of a new class of biocatalyst. In relation to the free enzyme in solution, the new bioconjugate material exhibited a slightly higher biocatalytic activity and significantly enhanced pH and temperature stability. The use of gold nanoparticle-labeled polymer microspheres in pepsin bioconjugation enables easy separation from the reaction medium and reuse of the bioconjugate over six reaction cycles.

Recent advances in nanostructured biocatalysts

Biochemical Engineering Journal, 2009

Recent years have witnessed a renaissance in the field of chemically re-engineering of enzymes to obtain highly selective and efficient biocatalysts for catalyzing processes under various conditions. The incorporation of enzyme into nanostructured materials is particularly noteworthy from a structural perspective since there are unprecedented opportunities in such systems to establish suitable microenvironments for chosen enzymes. This review summarizes recent developments in the nanostructured biocatalyst with emphasis on those formed with polymers. Based on the synthetic procedures employed, the established methods are grouped into three major categories-"grafting onto", "grafting from", and "self-assembly". The merits of the methods in enhancing enzyme stability at adverse conditions and their potential for large-scale preparation and the use of the nanostructured biocatalysts are discussed. The molecular fundamentals underlying each method are highlighted, and the use of molecular simulation as a tool for the design and application of nanostructured biocatalysts, although at a nascent stage, is presented. Finally, the problems encountered with nanostructured biocatalysts are discussed together with the future prospects of such systems.

Synthesis and Organization of Gold-Peptide Nanoparticles for Catalytic Activities

ACS omega, 2022

A significant development in the synthesis strategies of metal-peptide composites and their applications in biomedical and bio-catalysis has been reported. However, the random aggregation of gold nanoparticles provides the opportunity to find alternative fabrication strategies of gold-peptide composite nanomaterials. In this study, we used a facile strategy to synthesize the gold nanoparticles via a green and simple approach where they show self-alignment on the assembled nanofibers of ultrashort oligopeptides as a composite material. A photochemical reduction method is used, which does not require any external chemical reagents for the reduction of gold ions, and resultantly makes the gold nanoparticles of size ca. 5 nm under mild UV light exposure. The specific arrangement of gold nanoparticles on the peptide nanofibers may indicate the electrostatic interactions of two components and the interactions with the amino group of the peptide building block. Furthermore, the gold-peptide nanoparticle composites show the ability as a catalyst to degradation of environmental pollutant p-nitrophenol to p-aminophenol, and the reaction rate constant for catalysis is calculated as 0.057 min −1 at a 50-fold dilute sample of 2 mg/mL and 0.72 mM gold concentration in the composites. This colloidal strategy would help researchers to fabricate the metalized bioorganic composites for various biomedical and bio-catalysis applications.

Protection and Isolation of Bioorthogonal Metal Catalysts by Using Monolayer‐Coated Nanozymes

ChemBioChem, 2020

We present here demonstration of the protection of biorthogonal transition metal catalysts (TMCs) in biological environments using self-assembled monolayers on gold nanoparticles (AuNPs). Encapsulation of transition metal catalysts (TMCs) into this hydrophobic environment preserves catalytic activity in presence of pH conditions and complex biological media that deactivates free catalyst. Significantly, the protection afforded by these 'nanozymes' extends to isolation of the catalyst 'active site', as demonstrated by the independence of rate over a wide pH range, in strong contrast to the behavior of the free catalyst.

Inorganic nanomaterial-based biocatalysts

BMB reports, 2011

Over the years, nanostructures have been developed to enable to support enzyme usability to obtain highly selective and efficient biocatalysts for catalyzing processes under various conditions. This review summarizes recent developments in the nanostructures for enzyme supporters, typically those formed with various inorganic materials. To improve enzyme attachment, the surface of nanomaterials is properly modified to express specific functional groups. Various materials and nanostructures can be applied to improve both enzyme activity and stability. The merits of the incorporation of enzymes in inorganic nanomaterials and unprecedented opportunities for enhanced enzyme properties are discussed. Finally, the limitations encountered with nanomaterial-based enzyme immobilization are discussed together with the future prospects of such systems.

Bio-Enzyme Hybrid with Nanomaterials: A Potential Cargo as Sustainable Biocatalyst

Sustainability

With advancements in bionanotechnology, the field of nanobiocatalysts has undergone rapid growth and revolutionized various nanomaterials as novel and fascinating nanocarriers for enzyme immobilization. Nanotubes, nanofibers, nanopores, nanoparticles, and nanocomposites have been successfully developed and used as nanocarriers. The construction of robust nanobiocatalysts by combining enzymes and nanocarriers using various enzyme immobilization techniques is gaining incredible attention because of their extraordinary catalytic performance, high stability, and ease of reusability under different physical and chemical conditions. Creating appropriate surface chemistry for nanomaterials promotes their downstream applications. This review discusses enzyme immobilization on nanocarriers and highlights the techniques, properties, preparations, and applications of nanoimmobilized enzymes.

Synthesis, Characterization and Catalytic Application of Bioinspired Gold Nanoparticles

"A simple one-pot green chemical method for the biosynthesis of gold nanoparticles (AuNPs) by reducing chloroauric acid (HAuCl4) with protein extract of Rhizopus oryzae to produce novel gold nano-bio-conjugates (AuNBC) is described. AuNBCs, having sizes ranging from 5 to 65 nm, were synthesized by altering the HAuCl4–protein extract ratio. The conjugates were characterized by spectroscopic, electron microscopic, light scattering and electrophoretic mobility measurements. It was found that the aqueous AuNBC suspensions exhibited excellent stability over a wide range of ionic strength, pH and temperature. The effect of pH and ionic strength indicated that stabilization is due to electrostatic repulsion arising from the negative charge of the conjugate proteins. The AuNBCs were stable at temperatures lower than the denaturation temperature of the fungal proteins. The catalytic activity of the as-synthesized AuNBCs was quantified by analysing the reduction of p-nitrophenol by borohydride. The conjugates exhibited interesting size and shape dependent catalytic activity, which was stronger than that observed for AuNPs prepared by conventional chemical methods. The catalytic activity was found to be sensitive to both the surface-area-to-volume ratio and the thickness of the protein coating on the NP. "