Single-enzyme nanoparticles
Biofilm Removal using Nanozymes
Category: Environmental Microbiology
from Melanie Richards and Thomas Eugene Cloete in Nanotechnology in Water Treatment Applications
Recently there has been a great interest in the enzymatic degradation of biofilms. Enzymes are highly selective and disrupt the structural stability of the biofilm EPS matrix. Various studies have focused on the enzymatic degradation of polysaccharides and proteins for biofilm detachment since these are the two dominant components of the EPS. Due to the structural role of proteins and polysaccharides in the EPS matrix, a combination of various proteases and polysaccharases may be successful in biofilm removal.
The biodegradability and low toxicity of enzymes also make them attractive biofilm control agents. Regardless of all the advantages associated with enzymes, they also suffer from various drawbacks given that they are relatively expensive, show insufficient stability or activity under certain conditions, and cannot be reused. Various approaches are being used to increase the stability of enzymes, including enzyme modification, enzyme immobilization, protein engineering and medium engineering. Although these conventional methods have been used frequently to improve the stability of enzymes, various new techniques, such as self-immobilization of enzymes, the immobilization of enzymes on nano-scale structures and the production of single-enzyme nanoparticles, have been developed.
Self-immobilization of enzymes entails the cross-linking of enzyme molecules with each other and yields final preparations consisting of essentially pure proteins and high concentrations of enzyme per unit volume. The activity, stability and efficiency of immobilized enzymes can be improved by reducing the size of the enzyme-carrier. Nano-scale carrier materials allow for high enzyme loading per unit mass, catalytic recycling and a reduced loss of enzyme activity. Furthermore, enzymes can be stabilized by producing single-enzyme nanoparticles consisting of single-enzyme molecules surrounded by a porous organic-inorganic network of less than a few nanometers thick.
All these new technologies of enzyme stabilization make enzymes even more attractive alternatives to other biofilm removal and control agents.
Further reading:
Recently there has been a great interest in the enzymatic degradation of biofilms. Enzymes are highly selective and disrupt the structural stability of the biofilm EPS matrix. Various studies have focused on the enzymatic degradation of polysaccharides and proteins for biofilm detachment since these are the two dominant components of the EPS. Due to the structural role of proteins and polysaccharides in the EPS matrix, a combination of various proteases and polysaccharases may be successful in biofilm removal.
The biodegradability and low toxicity of enzymes also make them attractive biofilm control agents. Regardless of all the advantages associated with enzymes, they also suffer from various drawbacks given that they are relatively expensive, show insufficient stability or activity under certain conditions, and cannot be reused. Various approaches are being used to increase the stability of enzymes, including enzyme modification, enzyme immobilization, protein engineering and medium engineering. Although these conventional methods have been used frequently to improve the stability of enzymes, various new techniques, such as self-immobilization of enzymes, the immobilization of enzymes on nano-scale structures and the production of single-enzyme nanoparticles, have been developed.
Self-immobilization of enzymes entails the cross-linking of enzyme molecules with each other and yields final preparations consisting of essentially pure proteins and high concentrations of enzyme per unit volume. The activity, stability and efficiency of immobilized enzymes can be improved by reducing the size of the enzyme-carrier. Nano-scale carrier materials allow for high enzyme loading per unit mass, catalytic recycling and a reduced loss of enzyme activity. Furthermore, enzymes can be stabilized by producing single-enzyme nanoparticles consisting of single-enzyme molecules surrounded by a porous organic-inorganic network of less than a few nanometers thick.
All these new technologies of enzyme stabilization make enzymes even more attractive alternatives to other biofilm removal and control agents.
Further reading: