Nanozymes-based biosensors for food quality and safety

https://doi.org/10.1016/j.trac.2020.115841Get rights and content

Highlights

  • Nanozymes are used for biosensing of analytes relevant to food quality and safety.

  • Metallic, non-metallic, and organomettalic nanozymes are discussed.

  • Mechanisms of peroxidase and oxidase enzymes mimicking of nanozymes described.

  • Color-change signaling is the most popular nanozyme detection mechanism.

  • Nanozymes structure should be improved to enhance their catalytic ability and specificity.

Abstract

Nanozymes are nanomaterials, both metallic and non-metallic, that have the ability to catalyze biochemical reactions just as natural enzymes do. Since their discovery in 2007, nanozymes are exploited as nanoscale enzymatic mimics, which are now at the forefront for various biosensing applications. Compared with natural enzymes, nanozymes offer several advantages such as relatively higher stability, lower cost, easier modification, and inherently more efficient. Past research on the structure and catalytic principles of nanozymes has brought into focus various developments of nanozyme-based biosensors. Herein we introduce several typical nanozymes, primarily those belonging to the peroxidase and oxidase families. The enzyme mimicking mechanisms of these nanozymes are presented, which primarily result in colorimetric signals suitable for simple and easy biosensing. Emphasis is placed on nanozyme-based biosensors for detecting chemical contaminants, such as ions and pesticide residues, and biological contaminants, such as pathogens and biotoxins, that can compromise food quality and safety. In the future, more optimizations and improvements could be in the structure of nanozymes to enhance their catalysis ability and specificity. Overall, nanozymes possess great potential for biosensing in food and non-food applications.

Introduction

Natural enzymes are powerful biocatalysts for substrate conversion due to their specific recognition abilities and relatively high catalytic activities under mild environmental conditions in most cases. These enzymes find ubiquitous uses in myriad of laboratories and industries for performing biochemical reactions [1]. However, the use of natural enzymes is beset with such drawbacks as insufferable price, unstable structure, high sensitivity to external conditions, low reusability etc. [2,3]. Therefore, numerous researches have been focused on finding appropriate substitutes for enzymes with similar active site and catalytic properties. Some enzyme mimics include catalytic cyclodextrins, polymers, supramolecules, porphyrins, and dendrimers [[4], [5], [6], [7]].

In 2007, Yan et al. reported peroxidase enzyme-like activity of ferromagnetic nanoparticles (Fe3O4 NPs) and pointed out that with catalytic activity similar to that of protein/RNA which specifically acts as peroxidase enzyme in nature, inorganic NPs could directly trigger and accelerate oxidation of peroxidase substrates in the presence of hydrogen peroxide (H2O2) [8]. Since then, several other NPs have been identified to have biocatalytic activity either alone or as hybrids in conjunction with other biomolecular ligands [9]. Wei and Wang coined the term ‘nanozyme’ to describe NPs that possess the ability to mimic enzymatic action [10]. In addition to good recognition and biocatalytic activity, nanozymes offer prolonged life and high stability all at a cost lower than that of natural enzymes [11]. Consequently, nanozymes are increasingly employed in a number of applications such as biosensing, cancer therapy, environmental protection, and antibacterial treatment [[12], [13], [14], [15]].

Nanozyme-based biosensors (NBs) are popular in different areas, food quality safety evaluation, clinical disease diagnosis, biological metabolite measurement, and environmental pollutant monitoring (Fig. 1). To date, there has been only limited review of information on NBs, especially focusing on food quality and safety [16,17]. To fill this gap, herein we present a more comprehensive review of NBs in food analysis, along with discussion on major catalytic mechanisms of nanozymes for biosensing.

Section snippets

Predominant catalytic mechanisms of nanozyme for biosensing

Since the discovery of the first nanozyme (Fe3O4 NPs), hundreds of nanomaterials have been found to function as biocatalysts. According to the catalytic mechanisms the nanozymes mimic, two primary enzyme families have been identified (1) oxidoreductases (e.g., oxidase and peroxidase): and (2) hydrolases (e.g., nuclease and protease) [18]. In this review, we primarily focus on oxidoreductase family of nanozymes. The nanocomposites of NBs with several representative nanomaterials are shown in

Applications of nanozymes for biosensing

As an emerging class of enzyme-like nanomaterials, nanozymes rival other materials for biosensing applications. Biosensors comprising nanozyme provide highly accurate and precise sensing of various targets including Ebola virus, tumor cells, and glucose [[59], [60], [61]]. In this section our focus is on biosensing applications relevant to food quality and safety monitoring.

Summary and future perspectives

The discovery of nanozymes has established an impressive bridge connecting nanomaterials and biological enzymes. This has facilitated great strides in tailoring enzyme mimics into nanoscale and at the same time, provided an alternative way for mediating different biological events.

Up to now, most nanozyme research has focused on the oxidoreductase-type nanomaterials (e.g., oxidase, peroxidase, catalase and superoxide dismutase). Despite all of them showing high catalytic rate, peroxidase-type

References (136)

  • L. Hu et al.

    Copper nanoclusters as peroxidase mimetics and their applications to H2O2 and glucose detection

    Anal. Chim. Acta

    (2013)
  • X.X. Wang et al.

    BSA-stabilized Au clusters as peroxidase mimetics for use in xanthine detection

    Biosens. Bioelectron.

    (2011)
  • H. Liu et al.

    A sensitive hydrogen peroxide biosensor using ultra-small CuInS2 nanocrystals as peroxidase mimics

    Sensor. Actuator. B Chem.

    (2015)
  • V. Figueroa-Espi et al.

    Conjugation of manganese ferrite nanoparticles to an anti Sticholysin monoclonal antibody and conjugate applications

    Colloids Surfaces A Physicochem. Eng. Aspects

    (2011)
  • D. Bhattacharya et al.

    Development of phosphonate modified Fe(1− x) MnxFe2O4 mixed ferrite nanoparticles: novel peroxidase mimetics in enzyme linked immunosorbent assay

    Talanta

    (2011)
  • L. Huang et al.

    Facet-selective response of trigger molecule to CeO2 {1 1 0} for up-regulating oxidase-like activity

    Chem. Eng. J.

    (2017)
  • D. Duan et al.

    Nanozyme-strip for rapid local diagnosis of Ebola

    Biosens. Bioelectron.

    (2015)
  • Y. Liu et al.

    Amino acid-mediated ‘turn-off/turn-on’nanozyme activity of gold nanoclusters for sensitive and selective detection of copper ions and histidine

    Biosens. Bioelectron.

    (2017)
  • Y. Wang et al.

    Enhancing sensitivity and selectivity in a label-free colorimetric sensor for detection of iron (II) ions with luminescent molybdenum disulfide nanosheet-based peroxidase mimetics

    Biosens. Bioelectron.

    (2016)
  • Z. Mohammadpour et al.

    A new label free colorimetric chemosensor for detection of mercury ion with tunable dynamic range using carbon nanodots as enzyme mimics

    Chem. Eng. J.

    (2014)
  • G. Lakatos et al.

    Ecotoxicological studies and risk assessment on the cyanide contamination in Tisza river

    Toxicol. Lett.

    (2003)
  • E. Avşar et al.

    Formation of cyanide complexes of cobalt (II) and manganese (II)

    Polyhedron

    (1987)
  • C.W. Lien et al.

    Visual detection of cyanide ions by membrane-based nanozyme assay

    Biosens. Bioelectron.

    (2018)
  • X. Li et al.

    Highly sensitive and specific colorimetric detection of phosphate by using Zr (Ⅳ) to synergistically suppress the peroxidase-mimicking activity of hydrophilic Fe3O4 nanocubes

    Sensor. Actuator. B Chem.

    (2019)
  • K.Y. Wang et al.

    Hemin-incorporated nanoflowers as enzyme mimics for colorimetric detection of foodborne pathogenic bacteria

    Bioorg. Med. Chem. Lett.

    (2018)
  • T. Jiang et al.

    Sensitive detection of Escherichia coli O157: H7 using Pt–Au bimetal nanoparticles with peroxidase-like amplification

    Biosens. Bioelectron.

    (2016)
  • J. Han et al.

    Nanozyme-based lateral flow assay for the sensitive detection of Escherichia coli O157: H7 in milk

    J. Dairy Sci.

    (2018)
  • L. Zhang et al.

    Rapid and visual detection of Listeria monocytogenes based on nanoparticle cluster catalyzed signal amplification

    Biosens. Bioelectron.

    (2016)
  • Y. Liu et al.

    A multicolorimetric assay for rapid detection of Listeria monocytogenes based on the etching of gold nanorods

    Anal. Chim. Acta

    (2019)
  • W. Lai et al.

    Enzyme-controlled dissolution of MnO2 nanoflakes with enzyme cascade amplification for colorimetric immunoassay

    Biosens. Bioelectron.

    (2017)
  • S.X. Zhang et al.

    Polyacrylic acid-coated cerium oxide nanoparticles: an oxidase mimic applied for colorimetric assay to organophosphorus pesticides

    Biosens. Bioelectron.

    (2016)
  • J. Wei et al.

    Nanozyme-assisted technique for dual mode detection of organophosphorus pesticide

    Ecotoxicol. Environ. Saf.

    (2019)
  • N. Bagheri et al.

    Sensitive biosensing of organophosphate pesticides using enzyme mimics of magnetic ZIF-8

    Spectrochim. Acta Part A Mol. Biomol. Spectrosc.

    (2019)
  • Y.-C. Chang et al.

    A highly selective and sensitive nanosensor for the detection of glyphosate

    Talanta

    (2016)
  • C. Xiu et al.

    Melamine in milk products in China: examining the factors that led to deliberate use of the contaminant

    Food Pol.

    (2010)
  • P. Ni et al.

    Visual detection of melamine based on the peroxidase-like activity enhancement of bare gold nanoparticles

    Biosens. Bioelectron.

    (2014)
  • Y. Chang et al.

    BSA-stabilized Au clusters as peroxidase mimetic for colorimetric detection of Ag+

    Sensor. Actuator. B Chem.

    (2016)
  • S. Nisha et al.

    A review on methods, application and properties of immobilized enzyme

    Chem. Sci. Rev. Lett.

    (2012)
  • M. Misson et al.

    Nanobiocatalyst advancements and bioprocessing applications

    J. R. Soc. Interface

    (2015)
  • G. Wulff

    Enzyme-like catalysis by molecularly imprinted polymers

    Chem. Rev.

    (2002)
  • Z. Dong et al.

    Artificial enzymes based on supramolecular scaffolds

    Chem. Soc. Rev.

    (2012)
  • L. Gao et al.

    Intrinsic peroxidase-like activity of ferromagnetic nanoparticles

    Nat. Nanotechnol.

    (2007)
  • H. Wei et al.

    Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes

    Chem. Soc. Rev.

    (2013)
  • M.K. Masud et al.

    Nanoarchitectured peroxidase-mimetic nanozymes: mesoporous nanocrystalline α-or γ-iron oxide?

    J. Mater. Chem. B

    (2019)
  • H. Wang et al.

    Recent Advances in Nanozyme Research

    (2018)
  • J. Wu et al.

    Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes (II)

    Chem. Soc. Rev.

    (2019)
  • V. Singh et al.

    Graphene oxide synergistically enhances antibiotic efficacy in vancomycin-resistant staphylococcus aureus

    ACS Appl. Bio Mater.

    (2019)
  • K. Fan et al.

    In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy

    Nat. Commun.

    (2018)
  • Y. Huang et al.

    Nanozymes: classification, catalytic mechanisms, activity regulation, and applications

    Chem. Rev.

    (2019)
  • X. Wang et al.

    Nanozymes in bionanotechnology: from sensing to therapeutics and beyond

    Inorg. Chem. Front.

    (2016)
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