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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Chem.</journal-id>
<journal-title>Frontiers in Chemistry</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Chem.</abbrev-journal-title>
<issn pub-type="epub">2296-2646</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1107619</article-id>
<article-id pub-id-type="doi">10.3389/fchem.2023.1107619</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Chemistry</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Biogenic metallic nanoparticles as enzyme mimicking agents</article-title>
<alt-title alt-title-type="left-running-head">Ngcongco et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fchem.2023.1107619">10.3389/fchem.2023.1107619</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Ngcongco</surname>
<given-names>Khanyisile</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2176402/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Krishna</surname>
<given-names>Suresh Babu Naidu</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/427245/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Pillay</surname>
<given-names>Karen</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1999393/overview"/>
</contrib> </contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>School of Life Sciences</institution>, <institution>University of KwaZulu-Natal</institution>, <addr-line>Durban</addr-line>, <country>South Africa</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Biomedical and Clinical Technology</institution>, <institution>Durban University of Technology</institution>, <addr-line>Durban</addr-line>, <country>South Africa</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/600675/overview">Sougata Ghosh</ext-link>, RK University, India</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/65356/overview">Ravindra Pratap Singh</ext-link>, Indira Gandhi National Tribal University, India</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/823120/overview">Anuja Shreeram Kulkarni</ext-link>, The Ohio State University, United States</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Karen Pillay, <email>muthusamy@ukzn.ac.za</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Nanoscience, a section of the journal Frontiers in Chemistry</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>07</day>
<month>03</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>11</volume>
<elocation-id>1107619</elocation-id>
<history>
<date date-type="received">
<day>25</day>
<month>11</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>22</day>
<month>02</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Ngcongco, Krishna and Pillay.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Ngcongco, Krishna and Pillay</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>The use of biological systems such as plants, bacteria, and fungi for the synthesis of nanomaterials has emerged to fill the gap in the development of sustainable methods that are non-toxic, pollution-free, environmentally friendly, and economical for synthesizing nanomaterials with potential in biomedicine, biotechnology, environmental science, and engineering. Current research focuses on understanding the characteristics of biogenic nanoparticles as these will form the basis for the biosynthesis of nanoparticles with multiple functions due to the physicochemical properties they possess. This review briefly describes the intrinsic enzymatic mimetic activity of biogenic metallic nanoparticles, the cytotoxic effects of nanoparticles due to their physicochemical properties and the use of capping agents, molecules acting as reducing and stability agents and which aid to alleviate toxicity. The review also summarizes recent green synthetic strategies for metallic nanoparticles.</p>
</abstract>
<kwd-group>
<kwd>biogenic metallic nanoparticles</kwd>
<kwd>nanozymes</kwd>
<kwd>capping agents</kwd>
<kwd>toxicity</kwd>
<kwd>green synthesis</kwd>
</kwd-group>
<contract-num rid="cn001">107539</contract-num>
<contract-sponsor id="cn001">National Research Foundation<named-content content-type="fundref-id">10.13039/501100001321</named-content>
</contract-sponsor>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Recent advances in nanotechnology have allowed researchers to develop devices with promising potential for use in a wide variety of applications in biomedicine, biotechnology, environmental science, and engineering (<xref ref-type="bibr" rid="B11">Bundschuh et al., 2018</xref>; <xref ref-type="bibr" rid="B23">Dan, 2020</xref>). Nanoparticles are the basic fundamental component in nanotechnology with sizes that range from 1 to 100&#xa0;nm (<xref ref-type="bibr" rid="B7">Alavi and Karimi, 2018</xref>; <xref ref-type="bibr" rid="B46">Khan et al., 2019</xref>; <xref ref-type="bibr" rid="B86">Speranza, 2021</xref>). These structures offer major advantages due to their unique physicochemical properties such as their small sizes and diverse morphologies, large surface area to volume ratio, and in the case of metallic nanoparticles, their magnetization (<xref ref-type="bibr" rid="B11">Bundschuh et al., 2018</xref>). These physicochemical properties can be exploited for a broad spectrum of applications and present possible solutions to emerging global issues such as antimicrobial resistance, environmental pollution, and energy and food production (<xref ref-type="bibr" rid="B28">Ealias and Saravanakumar, 2017</xref>).</p>
<p>There is thus a need for more sustainable methods of synthesizing nanoparticles that are non-toxic, pollution free and more environmentally friendly when compared to the conventional chemical and physical methods for nanoparticle synthesis (<xref ref-type="bibr" rid="B7">Alavi and Karimi, 2018</xref>; <xref ref-type="bibr" rid="B42">Huynh et al., 2020</xref>; <xref ref-type="bibr" rid="B9">Bahrulolum et al., 2021</xref>; <xref ref-type="bibr" rid="B99">Ying et al., 2022</xref>). Recent studies focused on the use of biological organisms including plants, bacteria, yeast, fungi, lichens or algae to synthesize nanoparticles; in a method referred to as biological synthesis (<xref ref-type="bibr" rid="B65">Patil and Chandrasekaran, 2020</xref>; <xref ref-type="bibr" rid="B63">Nguyen et al., 2021</xref>; <xref ref-type="bibr" rid="B99">Ying et al., 2022</xref>). Proteins, enzymes, phenolic compounds, amines, alkaloids and pigments are some of the molecules in plants and microorganisms that can synthesize nanoparticles due to their reduction capability (<xref ref-type="bibr" rid="B58">Nadaroglu et al., 2017</xref>). The chemical and physical methods of synthesizing nanoparticles involve the use of reducing agents and stabilizing agents for the reduction of metal ions and to prevent agglomeration of the nanoparticles, however, these agents tend to be toxic to the environment and significantly contributes to nanoparticle toxicity which is highly unfavourable especially in the biomedical field (<xref ref-type="bibr" rid="B26">de Lima et al., 2012</xref>; <xref ref-type="bibr" rid="B68">Qu et al., 2019</xref>; <xref ref-type="bibr" rid="B42">Huynh et al., 2020</xref>; <xref ref-type="bibr" rid="B61">Nayak et al., 2021</xref>). In biological synthetic methods, biological organisms can produce biomolecules that act as reducing and stabilizing agents (<xref ref-type="bibr" rid="B9">Bahrulolum et al., 2021</xref>). These agents are not harmful to the environment, and maintain the stability of the synthesized nanoparticles thereby rendering them non-toxic (<xref ref-type="bibr" rid="B58">Nadaroglu et al., 2017</xref>).</p>
<p>Earlier reviews have highlighted the nanozyme activity of various types of nanoparticles (<xref ref-type="bibr" rid="B69">Ragg et al., 2015</xref>; <xref ref-type="bibr" rid="B95">Wu et al., 2019</xref>; <xref ref-type="bibr" rid="B92">Wang et al., 2020b</xref>; <xref ref-type="bibr" rid="B37">Ge et al., 2022</xref>). Some excellent review articles have also highlighted the biogenic strategies of metallic nanoparticles and advances in their role for biomedical application (<xref ref-type="bibr" rid="B80">Singh et al., 2021a</xref>; <xref ref-type="bibr" rid="B61">Nayak et al., 2021</xref>; <xref ref-type="bibr" rid="B88">Srivastava et al., 2021</xref>; <xref ref-type="bibr" rid="B62">Nayak et al., 2022</xref>). This mini review is different in that in provides an up to date overview of various biogenic strategies for metallic nanoparticle production, the role of biogenic synthesis as capping agents and up to date use of biogenic metallic nanoparticles as nanozymes.</p>
</sec>
<sec id="s2">
<title>2 Biogenic metallic nanoparticles</title>
<p>Many different biological organisms have been found to have an ability to synthesize a variety of metallic nanoparticles, with the most recent (2018&#x2013;2022) studies presented in <xref ref-type="sec" rid="s11">Supplementary Table S1</xref> in the Supplementary Information. Although <xref ref-type="sec" rid="s11">Supplementary Table S1</xref> covers plants, bacteria, fungi and lichen as systems that can be used for metallic nanoparticle production, it should be noted that Bryophytes also have an inherent ability to produce metallic nanoparticles. To the best of our knowledge, bryophytes have not been used to produce metallic nanoparticles from 2018, and thus a review by <xref ref-type="bibr" rid="B88">Srivastava <italic>et al.</italic> (2021)</xref> gives a good overview of the bryophytes used for metallic nanoparticle production (<xref ref-type="bibr" rid="B88">Srivastava et al., 2021</xref>).</p>
<p>Plants are promising candidates for nanoparticle synthesis because they detox and reduce the accumulation of metals as they alter the chemical composition of metals making them non-toxic and thus producing nanoparticles as a by-product (<xref ref-type="bibr" rid="B58">Nadaroglu et al., 2017</xref>; <xref ref-type="bibr" rid="B103">Zhang et al., 2020</xref>). Plant extracts such as sugars, flavonoids, sapogenins, proteins, enzymes, tannins, phenolics, alkaloids, steroids, and organic acids, can be obtained from plant parts, such as leaves, stems, roots, fruit, bark, flowers, seeds and buds (<xref ref-type="bibr" rid="B56">Moodley et al., 2018</xref>; <xref ref-type="bibr" rid="B102">Yulizar et al., 2020</xref>). The extracts act as reducing agents which result in the production of nanoparticles. Recently, plant extracts from <italic>Citrus sinensis</italic>, <italic>Lawsonia inermis</italic>, <italic>Artemisia haussknechtii</italic>, <italic>Cochlospermum gossypium</italic> and <italic>Juglans regia</italic> have been reported for their use in nanoparticle synthesis (<xref ref-type="bibr" rid="B7">Alavi and Karimi, 2018</xref>; <xref ref-type="bibr" rid="B49">Kredy, 2018</xref>; <xref ref-type="bibr" rid="B87">Srivastava et al., 2019</xref>).</p>
<p>Bacteria are also target candidates in nanoparticle production because of their rapid growth, cost-effectiveness, easy culturing, and since their growth conditions and environment can be easily controlled and manipulated (<xref ref-type="bibr" rid="B58">Nadaroglu et al., 2017</xref>). The emergence of resistance mechanisms in bacteria as a means of overcoming the harmful effects of metals also contributes to their ability to biosynthesize metallic nanoparticles. These mechanisms include transitions in the redox state, the operation of efflux systems, the buildup of metals inside the cell, intracellular precipitation, and extracellular creation of complexes (<xref ref-type="fig" rid="F1">Figure 1A</xref>) (<xref ref-type="bibr" rid="B57">Moodley et al., 2021</xref>). These nanoparticles were believed to be formed through a method involving the NADH-dependent reductase enzyme, which goes through oxidation to create NAD<sup>&#x2b;</sup> and potentially, the lost free electron could turn Ag<sup>&#x2b;</sup> into AgNPs (<xref ref-type="bibr" rid="B40">Gurunathan et al., 2009</xref>; <xref ref-type="bibr" rid="B83">Sintubin et al., 2009</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Synthesis, enzyme function and toxicity of metallic nanoparticles. <bold>(A)</bold> Is a schematic representation of biosynthesis of metal nanoparticles by microorganisms, <bold>(B)</bold> depicts the enzyme mimetic activity of biogenic nanoparticles and <bold>(C)</bold> shows the mechanisms of nanoparticle toxicity. Substrates used are 3, 3&#x2032;, 5, 5&#x2032;-Tetramethylbenzidine (TMB), 3, 3&#x2032;-Diaminobenzidine (DAB), o-phenylenediamine (OPD), or 3,4-dihydroxyphenylalanine (DOPA).</p>
</caption>
<graphic xlink:href="fchem-11-1107619-g001.tif"/>
</fig>
<p>Bacteria have the ability to convert heavy metal ions into nanoparticles by reducing them (<xref ref-type="bibr" rid="B19">Capuzzo, 2021</xref>). These advantages can therefore be exploited for nanoparticle synthesis. Bacteria including <italic>Pseudomonas stutzeri</italic>, <italic>Desulfovibrio alaskensis</italic>, <italic>Morganella psychrotolerans</italic> and <italic>Lactobacillus casei</italic> were recently reported to synthesize a variety of nanoparticles (<xref ref-type="bibr" rid="B97">Xu et al., 2018</xref>; <xref ref-type="bibr" rid="B18">Capeness et al., 2019</xref>).</p>
<p>Fungi are also ideal candidates for nanoparticle synthesis as their growth is easy and cost effective for laboratories and also at the industrial scale (<xref ref-type="bibr" rid="B55">Moln&#xe1;r et al., 2018</xref>). These organisms secrete a large number of enzymes and they have a large surface area due to their mycelia which play a vital role in rapidly forming nanoparticles as these characteristics causes metal precursor salts to be quickly converted to metallic nanoparticles (<xref ref-type="bibr" rid="B47">Khandel and Shahi, 2018</xref>; <xref ref-type="bibr" rid="B51">Li et al., 2021</xref>). Fungi such as <italic>Ganoderma lucidum</italic>, <italic>Lignosus rhinocerotis</italic>, <italic>Trichoderma longibrachiatum</italic>, and <italic>Penicillium corylophilum</italic> were recently used for the synthesis of metallic nanoparticles (<xref ref-type="bibr" rid="B29">Elamawi et al., 2018</xref>; <xref ref-type="bibr" rid="B45">Katas et al., 2019</xref>; <xref ref-type="bibr" rid="B31">Fouda et al., 2020</xref>; <xref ref-type="bibr" rid="B63">Nguyen et al., 2021</xref>).</p>
</sec>
<sec id="s3">
<title>3 The intrinsic enzyme mimetic activity of biogenic metallic nanoparticles</title>
<p>Nanoparticles are known to be multifunctional and among the functions that they possess is the ability to catalyse reactions. Initially, the catalytic activity of nanoparticles was a result of the conjugation of catalysts or enzymes to the shell of the nanoparticles and therefore the nanoparticles would provide magnetic properties while the catalyst or enzyme on the surface of the nanoparticles provided the catalytic activity (<xref ref-type="bibr" rid="B36">Gao et al., 2007</xref>). This drew the interest of researchers to other possible intrinsic enzyme-like activities that nanoparticles may possess.</p>
<p>Nanoparticles exhibiting enzyme-like catalytic activities, referred to as nanozymes, act as mimic enzymes that can replace natural enzymes because natural enzymes have disadvantages in their catalytic functions due to the high cost of production, the time consuming process for production, denaturation in harsh environmental conditions and therefore must have suitable pH and temperature, and specific substrates (<xref ref-type="bibr" rid="B69">Ragg et al., 2015</xref>; <xref ref-type="bibr" rid="B3">Ahmed et al., 2019</xref>; <xref ref-type="bibr" rid="B82">Singh, 2019</xref>; <xref ref-type="bibr" rid="B70">Rastogi et al., 2021</xref>). Since nanozymes are easy to produce with low cost, have high stability, and good robustness; they are suitable candidates for applications requiring catalytic functions and were found to possess enzymatic activity identical to that of peroxidase, haloperoxidase, oxidase, catalase, hydrolase, and superoxide dismutase as summarized in <xref ref-type="fig" rid="F1">Figure 1B</xref> (<xref ref-type="bibr" rid="B69">Ragg et al., 2015</xref>; <xref ref-type="bibr" rid="B3">Ahmed et al., 2019</xref>). To date, there are more than 300 types of nanomaterials that have been found to possess the intrinsic enzyme-like activity (<xref ref-type="bibr" rid="B35">Gao and Yan, 2016</xref>).</p>
<p>Ferrihydrite nanoparticles synthesized from the bacteria <italic>Comamonas testosteroni</italic> exhibited peroxidase-like activity similar to that of horseradish peroxidase (HRP), and these nanoparticles were able to catalyze reactions of the peroxidase chromogenic agents 3, 3&#x2032;, 5, 5&#x2032;-Tetramethylbenzidine (TMB), 3, 3&#x2032;-Diaminobenzidine (DAB), and o-phenylenediamine (OPD) in the presence of H<sub>2</sub>O<sub>2</sub> (<xref ref-type="bibr" rid="B3">Ahmed et al., 2019</xref>). This peroxidase-like activity displayed by the bacteria was exploited to develop a colorimetric method for the detection of H<sub>2</sub>O<sub>2</sub> and glucose which was used for successfully detecting glucose in human serum (<xref ref-type="bibr" rid="B3">Ahmed et al., 2019</xref>). Magnetic nanoparticles referred to as magnetosomes, synthesized from <italic>Magnetospirillum gryphiswaldense</italic> (magnetotactic bacteria) also exhibit intrinsic peroxidase-like activity indicated by their ability to catalyze TMB <italic>in vitro</italic> in the presence of H<sub>2</sub>O<sub>2</sub> (<xref ref-type="bibr" rid="B39">Guo et al., 2012</xref>). The peroxidase-like activity of magnetosomes plays a role in reducing enhanced intracellular reactive oxygen species (ROS) levels generated under conditions having low oxygen and high iron concentration (<xref ref-type="bibr" rid="B39">Guo et al., 2012</xref>; <xref ref-type="bibr" rid="B52">Lin et al., 2019</xref>). ROS are very reactive chemical molecules containing oxygen, generated in cell organelles including the endoplasmic reticulum (ER), peroxisomes and the mitochondria (<xref ref-type="bibr" rid="B101">Yu et al., 2020b</xref>). This ROS elimination role is thought to be significant for the survival of magnetotactic bacteria growing under similar conditions (<xref ref-type="bibr" rid="B39">Guo et al., 2012</xref>; <xref ref-type="bibr" rid="B52">Lin et al., 2019</xref>). The peroxidase mimetic activity of magnetosomes has been used for the detection of H<sub>2</sub>O<sub>2</sub> and glucose (<xref ref-type="bibr" rid="B41">Hu et al., 2010</xref>).</p>
<p>Plant extracts contain products that comprise functional groups including phenolic acids, proteins, polyphenol, bioactive alkaloids, terpenoids and sugars, which reduce metal ions in the synthetic mechanism for nanoparticles (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). These functional groups can stabilize the synthesized nanoparticles and improve their catalytic efficiency (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). Palladium nanoparticles synthesized using gum kondagogu, a tree gum from <italic>C. gossypium</italic>, were used for developing a colorimetric assay for quantifying cholesterol from human serum based on the peroxidase-like activity exhibited by the synthesized nanoparticles (<xref ref-type="bibr" rid="B70">Rastogi et al., 2021</xref>). This study showed the potential application of the intrinsic peroxidase mimicking properties of the palladium nanoparticles for diagnostic, detection and quantification purposes (<xref ref-type="bibr" rid="B70">Rastogi et al., 2021</xref>).</p>
<p>
<italic>Prunus nepalensis</italic> fruit extract was used for synthesizing gold nanoparticles exhibiting peroxidase-like catalytic activity (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). The catalytic activity of the gold nanoparticles was confirmed by the ability to catalyze the oxidation of the substrate TMB in the presence of H<sub>2</sub>O<sub>2</sub> (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). It was found that the gold nanoparticles exhibited a higher maximum reaction velocity and affinity for TMB compared to natural horse radish peroxidase (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). The improved catalytic efficiency of the gold nanoparticles is said to have been a result of the functional groups present in the fruit extract (<xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). This peroxidase-like activity of the gold nanoparticles was exploited for a potential colorimetric immuno-sensing assay for the detection of <italic>Mycobacterium bovis</italic>, a bovine tuberculosis transmitted from cattle to humans through the &#x201c;consumption of unpasteurized milk&#x201d; (<xref ref-type="bibr" rid="B84">Smith et al., 2004</xref>; <xref ref-type="bibr" rid="B24">Das et al., 2022a</xref>). Silver nanoparticles synthesized from <italic>Cucumis sativus</italic> and <italic>Aloe vera</italic> extracts, with the <italic>A. vera</italic> extract used as a capping agent, catalyzed the reduction of methyl orange dye and <italic>para</italic>-nitro-phenol (<xref ref-type="bibr" rid="B72">Riaz et al., 2022</xref>). This indicated the potential of these nanoparticles in the degradation of nitro-phenols that are found in industrial waste.</p>
<p>Ferrihydrite nanoparticles from <italic>Trichoderma guizhouense</italic> synthesized during interaction of the fungus with hematite, whereby fungi take up minerals to form nanoparticles, also exhibited peroxidase-like activity (<xref ref-type="bibr" rid="B100">Yu et al., 2020a</xref>). Fungi interact with minerals and biomineralize them into nanoparticles, and this interaction is known as fungus-mineral interaction. The interaction is important in the transformation of rocks, minerals and metals, the degradation of rhizospheric organic matter and phosphate fixation. The generation of ROS was observed during fungal growth and therefore, the concentration of these species must be maintained at sub-toxic levels (<xref ref-type="bibr" rid="B100">Yu et al., 2020a</xref>). The peroxidase-like activity of the synthesized ferrihydrite nanoparticles reduced the generated ROS, lowering their toxic effects. It was suggested that the production of the nanoparticles caused the ROS generated during fungal growth to decrease, therefore maintaining the concentration of the ROS at sub-toxic levels.</p>
<p>The enzymatic activity of biogenic nanoparticles similar to natural enzymes presents a platform whereby they can be exploited for developing several methods for diagnostic, detection and biosensing applications. To date, there are numerous patent applications and patents that have been granted for nanozyme production and nanozyme systems which highlights the importance of these small molecules. A list of these patents and patent applications are listed in <xref ref-type="table" rid="T1">Table 1</xref>, together with a summary of various applications of biogenic nanoparticles that have recently been evaluated, highlighting the versatility of these nano molecules.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>List of Nanozyme Patent Applications and Summary of Recent Nanoparticle applications.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Invention</th>
<th align="center">Inventors</th>
<th align="center">Application number</th>
<th align="center">Year</th>
<th align="center">Country</th>
<th align="center">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">Nanozymes, methods of making nanozymes, and methods of using nanozymes</td>
<td align="center">Cao, Y.C., Liu, C., Liu, H., Wang, Z., and YangS.H.</td>
<td align="center">WO2011133504-A2</td>
<td align="center">2011</td>
<td align="center">WIPO (PCT)</td>
<td align="center">
<xref ref-type="bibr" rid="B13">Cao et al. (2011)</xref>
</td>
</tr>
<tr>
<td align="center">Synthesis method of enzyme-mimic magnetic nanocatalysts, and enzyme-mimic magnetic nanocatalysts thereby</td>
<td align="center">Jang, J., Lee, S., and Lee, J</td>
<td align="center">KR101350722B1</td>
<td align="center">2014</td>
<td align="center">South Korea</td>
<td align="center">
<xref ref-type="bibr" rid="B43">Jang et al. (2014)</xref>
</td>
</tr>
<tr>
<td align="center">Nanozymes, methods of making nanozymes, and methods of using nanozymes</td>
<td align="center">Cao, Y.C., and Liu, C</td>
<td align="center">WO2015023715A1</td>
<td align="center">2015</td>
<td align="center">WIPO (PCT)</td>
<td align="center">
<xref ref-type="bibr" rid="B16">Cao and Liu (2015)</xref>
</td>
</tr>
<tr>
<td align="center">Nanozymes, methods of making nanozymes, and methods of using nanozymes</td>
<td align="center">Cao, Y.C., and Liu, C</td>
<td align="center">US20160215279A1</td>
<td align="center">2016</td>
<td align="center">United States</td>
<td align="center">
<xref ref-type="bibr" rid="B17">Cao and Liu (2016)</xref>
</td>
</tr>
<tr>
<td align="center">Nanoparticle-attached enzyme cascades for accelerated multistep biocatalysis</td>
<td align="center">Medintz, I.L., Vranish, J.N., Ancona, M., Susumu, K., and DiazS.A.</td>
<td align="center">US20180171325A1</td>
<td align="center">2017</td>
<td align="center">United States</td>
<td align="center">
<xref ref-type="bibr" rid="B54">Medintz et al. (2017)</xref>
</td>
</tr>
<tr>
<td align="center">Stabilized polymeric nanocapsules, dispersions comprising the nanocapsules, and methods for the treatment of bacterial biofilms</td>
<td align="center">Rotello, V.M., Landis, R.F., Gupta, A., and LeeY.W.</td>
<td align="center">WO2017040024A1</td>
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<td align="center">United States</td>
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<td align="center">PD-IR nanoparticles used as peroxidase mimics</td>
<td align="center">Xia, X</td>
<td align="center">20,170,199,179</td>
<td align="center">2017</td>
<td align="center">United States</td>
<td align="center">
<xref ref-type="bibr" rid="B96">Xia (2017)</xref>
</td>
</tr>
<tr>
<td align="center">Nanozymes, methods of making nanozymes, and methods of using nanozymes</td>
<td align="center">Cao, Y.C., Liu, C., Liu, H., Wang, Z., and YangS.H.</td>
<td align="center">US 10,081,542 B2</td>
<td align="center">2018</td>
<td align="center">United States</td>
<td align="center">
<xref ref-type="bibr" rid="B14">Cao et al. (2018)</xref>
</td>
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<tr>
<td align="center">Ig E detection and allergy diagnostic method using enzyme-mimetic nanozyme-based immunoassay</td>
<td align="center">Lee, S., Lee, S., Kim, M., Shin, S., Lee, J., and Kim, M</td>
<td align="center">WO2018084340A1</td>
<td align="center">2018</td>
<td align="center">WIPO (PCT)</td>
<td align="left">
<xref ref-type="bibr" rid="B50">Lee et al. (2018)</xref>
</td>
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<tr>
<td align="center">Enzyme-encapsulated nanoparticle platform</td>
<td align="center">Ortac, I., Esener, S.C., Yayla, I.G., and Messmer, B</td>
<td align="center">US10300152B2</td>
<td align="center">2019</td>
<td align="center">United States</td>
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<xref ref-type="bibr" rid="B64">Ortac et al. (2019)</xref>
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<td align="center">RNA silencing nanozymes</td>
<td align="center">Cao, Y.C., and Jiang, T</td>
<td align="center">20210139873</td>
<td align="center">2021</td>
<td align="center">United States</td>
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<table>
<thead valign="top">
<tr>
<th align="center">Application</th>
<th align="center">
<bold>Function</bold>
</th>
<th colspan="4" align="center">
<bold>References</bold>
</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Antimicrobial Agents</td>
<td align="left">Activity against bacterial and fungal growth</td>
<td colspan="6" align="center">
<xref ref-type="bibr" rid="B27">Dong et al. (2019),</xref> <xref ref-type="bibr" rid="B5">Akpinar et al. (2021),</xref> <xref ref-type="bibr" rid="B76">Sarwer et al. (2022),</xref> <xref ref-type="bibr" rid="B85">Soliman et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">Bioremediation</td>
<td align="left">Degradation of heavy metals, pesticides, insecticides, herbicides and dyes from polluted environments</td>
<td colspan="6" align="center">
<xref ref-type="bibr" rid="B90">Tripathi et al. (2018),</xref> <xref ref-type="bibr" rid="B53">L&#xf3;pez-Miranda et al. (2019),</xref> <xref ref-type="bibr" rid="B21">Chaudhari et al. (2022),</xref> <xref ref-type="bibr" rid="B32">Gami et al. (2022),</xref> <xref ref-type="bibr" rid="B74">Salama et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">Delivery Systems</td>
<td align="left">Delivery of cancer targeting genes and therapeutic drugs</td>
<td colspan="6" align="center">
<xref ref-type="bibr" rid="B2">Abolhasani Zadeh et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">Enzyme Immobilization</td>
<td align="left">Immobilization of enzymes from reaction mixtures</td>
<td colspan="6" align="center">
<xref ref-type="bibr" rid="B30">Fotiadou et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left">MRI Contrast Agents</td>
<td align="left">Molecular imaging, diagnosis and treatment of diseases</td>
<td colspan="6" align="center">
<xref ref-type="bibr" rid="B12">Cai et al. (2019),</xref> <xref ref-type="bibr" rid="B60">Nan et al. (2021),</xref> <xref ref-type="bibr" rid="B93">Wei et al. (2021)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s4">
<title>4 Toxicity of nanoparticles and the role of capping agents</title>
<p>Nanoparticle toxicity presents a challenge, especially in areas such as biomedicine, cosmetics, agriculture and the food science, and thus there is a need for the development of nanoparticles with low cytotoxicity. The main physicochemical properties that determine toxicity of nanoparticles are size, shape, surface chemistry, surface composition, surface area to volume ratio and stability (<xref ref-type="bibr" rid="B4">Aillon et al., 2009</xref>; <xref ref-type="bibr" rid="B89">Sukhanova et al., 2018</xref>). The primary mechanisms of toxicity of metallic nanoparticles stem from them entering the cell <italic>via</italic> endocytosis, which places them within an acidic lysosome resulting in oxidation and release of metal ions. The intracellular metal ions can then exert a myriad of toxic effects as summarised in <xref ref-type="fig" rid="F1">Figure 1C</xref> (<xref ref-type="bibr" rid="B71">Repetto et al., 2010</xref>; <xref ref-type="bibr" rid="B20">Carrillo-Carrion et al., 2014</xref>).</p>
<p>Fortunately, encapsulation strategies have recently been on the radar of researchers in a bid to reduce the toxic effects of nanoparticles as it could provide stability to the nanoparticle and reduce its susceptibility to release metal ions.</p>
<p>Capping agents are molecules that play an essential role in the growth, aggregation, and physicochemical properties of nanoparticles by regulating their size, shape, geometry, and surface chemistry (<xref ref-type="bibr" rid="B44">Javed et al., 2022</xref>; <xref ref-type="bibr" rid="B79">Sidhu et al., 2022</xref>). Capping agents can firmly adsorb on the nanoparticle surface forming a single or multilayer protective coating thus providing long term nanoparticle stability (<xref ref-type="bibr" rid="B44">Javed et al., 2022</xref>). Capping agents can consist of proteins, carbohydrates, amino acids, and lipids (<xref ref-type="bibr" rid="B10">Bulgarini et al., 2021</xref>) and can prevent aggregation of nanoparticles (<xref ref-type="bibr" rid="B79">Sidhu et al., 2022</xref>).</p>
<p>Capping agents are found in biological organisms, and they can act as reducing and stability agents, an advantage that is noteworthy for biogenic nanoparticles (<xref ref-type="bibr" rid="B38">Guilger-Casagrande et al., 2021</xref>), (<xref ref-type="bibr" rid="B44">Javed et al., 2022</xref>). In addition, capping agents from biological organisms can be introduced to the chemical synthetic strategies and this has become an essential strategy in lowering the cytotoxic effects of chemically synthesized nanoparticles (<xref ref-type="bibr" rid="B79">Sidhu et al., 2022</xref>).</p>
<p>The encapsulation of nanoparticles with capping agents forms a barrier between the inner core of the nanoparticle and the surrounding environment, improving nanoparticle solubility, reactivity, interactions with biomolecules, preventing aggregation and inducing their biological functions (<xref ref-type="bibr" rid="B94">Weingart et al., 2013</xref>). A study by <xref ref-type="bibr" rid="B38">Guilger-Casagrande <italic>et al.</italic> (2021)</xref> evaluated the effects and functions of capping agents on the stability of silver nanoparticles synthesized by the fungal strain <italic>Trichoderma harzianum</italic> by comparing the stability of the nanoparticles with and without capping agents. It was found that when capping agents were removed from nanoparticles, the diameter of the nanoparticles increased and it was proposed that the reason for this may be &#x201c;subsequent aggregation of the nanoparticles&#x201d; (<xref ref-type="bibr" rid="B38">Guilger-Casagrande et al., 2021</xref>).</p>
<p>
<xref ref-type="bibr" rid="B85">Soliman <italic>et al.</italic> (2022)</xref> suggested that extracellular enzymes and proteins from <italic>Trichoderma saturnisporum</italic> acted as capping agents in the synthesis of silver and gold nanoparticles. <xref ref-type="bibr" rid="B67">Puri and Patil (2022)</xref> confirmed the presence of phytochemicals by screening <italic>Tinospora cordifolia</italic> extract used for synthesizing selenium nanoparticles. Among the phytochemicals present in the extract were phenolics and flavonoids and the hydroxyl groups of these biomolecules were proposed to act as capping agents (<xref ref-type="bibr" rid="B67">Puri and Patil, 2022</xref>). Highly stable, negatively charged, spherically shaped and nano-sized selenium nanoparticles were synthesized from the plant extracts and it was suggested that the stability of the nanoparticles was due to the phytochemicals detected in the extract (<xref ref-type="bibr" rid="B67">Puri and Patil, 2022</xref>). Silver nanoparticles synthesized using yeast extract were capped by biomolecules from the extract, and the resulting silver nanoparticles exhibited shapes, sizes and surface chemistry that exhibited good long-term stability (<xref ref-type="bibr" rid="B77">Shu et al., 2020</xref>).</p>
<p>Biogenic nanoparticles thus present a promising potential for a variety of applications with the added advantage of low toxicity due to their inherent capping potential, a feature that is lacking in physicochemical synthetic strategies that are reliant on addition of synthetic capping agents resulting in labor intensive multi-step processes (<xref ref-type="bibr" rid="B26">de Lima et al., 2012</xref>).</p>
</sec>
<sec id="s5">
<title>5 Current scenarios and challenges</title>
<p>The emergence of nanotechnology has seen nanoparticles having widespread application and being the molecule of choice, resulting in them being in high demand. Although there are numerous synthetic strategies for nanoparticle production, the physical and chemical routes pose many challenges such as the need for expensive equipment, capping agents and harmful chemicals, and production of monodisperse nanoparticles with similar morphology is not so straight forward. Green synthetic methods, using inherent biological machinery and phytochemicals as capping and stabilization agents, is therefore seen as the preferred method for nanoparticle production. However, large scale production is still seen as a challenge and researchers are daily evaluating new strategies for scaling up. One of the novel methods that could be explored for large scale production of nanoparticles is investigating the role of soil microbes in influencing plant growth and uptake of nutrients. This could have importance in nanoparticle production as soil microbes could directly affect how metals and nutrients are taken up by plants before being packaged into nanoparticles (<xref ref-type="bibr" rid="B25">Das et al., 2022b</xref>).</p>
</sec>
<sec id="s6">
<title>6 Conclusion and future prospects</title>
<p>The use of biological organisms for synthesizing nanoparticles is increasing as these organisms produce their own reducing and stabilizing agents that are involved in reducing metal ions to nanoparticles and also providing encapsulation. The biogenic nanoparticles thus have the important benefit of reduced toxicity and have immense application in a wide variety of biotechnology and biomedical fields such as drug delivery systems, scanning techniques, cosmetics, and assay systems. There is thus huge potential for exploiting biogenic nanoparticles for our advancement, however the scaling up of nanoparticle production is still an area that requires more research. An exciting area of research that could possibly result in an effective scaling up mechanism could be the role of soil microbes in plant growth as a symbiotic relationship could potentially be manipulated to allow improved metal and nutrient uptake by the plants thereby resulting in increased nanoparticle production.</p>
</sec>
</body>
<back>
<sec id="s7">
<title>Author contributions</title>
<p>KN and KP have conceptualized and prepared the manuscript. SBNK edited and critically reviewed the manuscript. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec id="s8">
<title>Funding</title>
<p>This work is based on the research supported by the National Research Foundation of South Africa (Grant number 107539). The opinions, findings and conclusions or recommendations is that of the authors and the NRF accepts no liability whatsoever in this regard.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s10">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s11">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fchem.2023.1107619/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fchem.2023.1107619/full&#x23;supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="Table1.docx" id="SM1" mimetype="application/docx" xmlns:xlink="http://www.w3.org/1999/xlink"/>
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