Characterization and immobilization of arylsulfatase on modified magnetic nanoparticles for desulfation of agar

[Display omitted] •A low cost, simple manipulation and nontoxic approach were designed for the preparation of Carboxyl-functioned Magnetic Nanoparticles (CMNPs).•CMNPs were prepared and well characterized by Fourier transform infrared spedtroscopy and scanning electron microscope.•Arylsulfatase was...

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Veröffentlicht in:International journal of biological macromolecules 2017-01, Vol.94 (Pt A), p.576-584
Hauptverfasser: Xiao, Qiong, Yin, Qin, Ni, Hui, Cai, Huinong, Wu, Changzheng, Xiao, Anfeng
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container_end_page 584
container_issue Pt A
container_start_page 576
container_title International journal of biological macromolecules
container_volume 94
creator Xiao, Qiong
Yin, Qin
Ni, Hui
Cai, Huinong
Wu, Changzheng
Xiao, Anfeng
description [Display omitted] •A low cost, simple manipulation and nontoxic approach were designed for the preparation of Carboxyl-functioned Magnetic Nanoparticles (CMNPs).•CMNPs were prepared and well characterized by Fourier transform infrared spedtroscopy and scanning electron microscope.•Arylsulfatase was successfully immobilized onto CMNPs and the catalysts exhibited good catalytic activity for the desulfation of agar.•The immobilized arylsulfatase can keep its catalytic activity after being reused seven times. Carboxyl functioned magnetic nanoparticles (CMNPs) were prepared by a simple co-precipitation method and characterized by Fourier transform infrared spedtroscopy and scanning electron microscope. The prepared CMNPs were used for covalent immobilization of the arylsulfatase which could be applied in desulfation of agar. The optimal immobilizaion conditions were obtained as follows: glutaraldehyde concentration 1.0% (v/v), cross-linking time 3h, immobilization time 3h, immobilization temperature 5°C and enzyme dose 0.62U. Increase in properties of the arylsulfatase such as optimum temperature and pH was observed after immobilization. Immobilization led to increased tolerance of enzyme to some metal ions, inhibitors and detergents. The Km and kcat of the immobilized enzyme for hydrolysis of p-NPS at pH 7.5 and at 50°C were determined to be 0.89mmol/L and 256.91s−1, respectively. The relative desulfuration rates of immobilized arylsulfatase maintained 61.7% of its initial desulfuration rates after seven cycles. After the reaction of agar with immobilized arylsulfatase for 90min at 50°C, 46% of the sulfate in the agar was removed. These results showed that the immobilization of arylsulfatase onto CMNPs is an efficient and simple way for preparation of stable arylsulfatase and have a great potential for application in enzymatic desulfation of agar.
doi_str_mv 10.1016/j.ijbiomac.2016.10.029
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Carboxyl functioned magnetic nanoparticles (CMNPs) were prepared by a simple co-precipitation method and characterized by Fourier transform infrared spedtroscopy and scanning electron microscope. The prepared CMNPs were used for covalent immobilization of the arylsulfatase which could be applied in desulfation of agar. The optimal immobilizaion conditions were obtained as follows: glutaraldehyde concentration 1.0% (v/v), cross-linking time 3h, immobilization time 3h, immobilization temperature 5°C and enzyme dose 0.62U. Increase in properties of the arylsulfatase such as optimum temperature and pH was observed after immobilization. Immobilization led to increased tolerance of enzyme to some metal ions, inhibitors and detergents. The Km and kcat of the immobilized enzyme for hydrolysis of p-NPS at pH 7.5 and at 50°C were determined to be 0.89mmol/L and 256.91s−1, respectively. The relative desulfuration rates of immobilized arylsulfatase maintained 61.7% of its initial desulfuration rates after seven cycles. After the reaction of agar with immobilized arylsulfatase for 90min at 50°C, 46% of the sulfate in the agar was removed. 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Carboxyl functioned magnetic nanoparticles (CMNPs) were prepared by a simple co-precipitation method and characterized by Fourier transform infrared spedtroscopy and scanning electron microscope. The prepared CMNPs were used for covalent immobilization of the arylsulfatase which could be applied in desulfation of agar. The optimal immobilizaion conditions were obtained as follows: glutaraldehyde concentration 1.0% (v/v), cross-linking time 3h, immobilization time 3h, immobilization temperature 5°C and enzyme dose 0.62U. Increase in properties of the arylsulfatase such as optimum temperature and pH was observed after immobilization. Immobilization led to increased tolerance of enzyme to some metal ions, inhibitors and detergents. The Km and kcat of the immobilized enzyme for hydrolysis of p-NPS at pH 7.5 and at 50°C were determined to be 0.89mmol/L and 256.91s−1, respectively. The relative desulfuration rates of immobilized arylsulfatase maintained 61.7% of its initial desulfuration rates after seven cycles. After the reaction of agar with immobilized arylsulfatase for 90min at 50°C, 46% of the sulfate in the agar was removed. These results showed that the immobilization of arylsulfatase onto CMNPs is an efficient and simple way for preparation of stable arylsulfatase and have a great potential for application in enzymatic desulfation of agar.</description><subject>Agar - chemistry</subject><subject>Agar desulfation</subject><subject>Arylsulfatase</subject><subject>Arylsulfatases - chemistry</subject><subject>Bacterial Proteins - chemistry</subject><subject>Carboxyl function</subject><subject>Chemical Precipitation</subject><subject>Cross-Linking Reagents - chemistry</subject><subject>Enzyme Stability</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Equipment Reuse</subject><subject>Ferrosoferric Oxide - chemistry</subject><subject>Glutaral - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hydrolysis</subject><subject>Immobilization</subject><subject>Kinetics</subject><subject>Magnetic nanoparticle</subject><subject>Magnetite Nanoparticles - chemistry</subject><subject>Magnetite Nanoparticles - ultrastructure</subject><subject>Nitrobenzenes - chemistry</subject><subject>Recombinant Proteins - chemistry</subject><subject>Sulfates - chemistry</subject><subject>Temperature</subject><subject>Time Factors</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPwzAQhC0EgvL4CyhHLil27NjODVTxkipxgbO1cdbgKomLnSLBr8dVKVdOXo9mdrQfIZeMzhll8no196vWhwHsvMr_LM5p1RyQGdOqKSml_JDMKBOs1IzTE3Ka0iqrsmb6mJxUSgnJaz0jYfEOEeyE0X_D5MNYwNgVfhhC6_u9FFwB8atPm97BBAmLrA2h885jVwzwNuLkbTHCGNYQ89hjKlyIRYe7yH7HG8RzcuSgT3jx-56R1_u7l8VjuXx-eFrcLkvLpZ7KptWNVooJQbHireLcUaGsBSd4YxtLXS2dlIIrRV1Tgd1CcMrVwLuKS87PyNVu7zqGjw2myQw-Wex7GDFskmGa10IopnW2yp3VxpBSRGfW0Q_5YMOo2cI2K7OHbbY9Wz3DzsHL345NO2D3F9vTzYabnQHzpZ8eo0nW42ix8xHtZLrg_-v4Ad5UlXM</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Xiao, Qiong</creator><creator>Yin, Qin</creator><creator>Ni, Hui</creator><creator>Cai, Huinong</creator><creator>Wu, Changzheng</creator><creator>Xiao, Anfeng</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201701</creationdate><title>Characterization and immobilization of arylsulfatase on modified magnetic nanoparticles for desulfation of agar</title><author>Xiao, Qiong ; Yin, Qin ; Ni, Hui ; Cai, Huinong ; Wu, Changzheng ; Xiao, Anfeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-9b898771440e23b733f047ccaf439c9c0f56f6643770f92ac2016f7f5a3d23633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Agar - chemistry</topic><topic>Agar desulfation</topic><topic>Arylsulfatase</topic><topic>Arylsulfatases - chemistry</topic><topic>Bacterial Proteins - chemistry</topic><topic>Carboxyl function</topic><topic>Chemical Precipitation</topic><topic>Cross-Linking Reagents - chemistry</topic><topic>Enzyme Stability</topic><topic>Enzymes, Immobilized - chemistry</topic><topic>Equipment Reuse</topic><topic>Ferrosoferric Oxide - chemistry</topic><topic>Glutaral - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hydrolysis</topic><topic>Immobilization</topic><topic>Kinetics</topic><topic>Magnetic nanoparticle</topic><topic>Magnetite Nanoparticles - chemistry</topic><topic>Magnetite Nanoparticles - ultrastructure</topic><topic>Nitrobenzenes - chemistry</topic><topic>Recombinant Proteins - chemistry</topic><topic>Sulfates - chemistry</topic><topic>Temperature</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiao, Qiong</creatorcontrib><creatorcontrib>Yin, Qin</creatorcontrib><creatorcontrib>Ni, Hui</creatorcontrib><creatorcontrib>Cai, Huinong</creatorcontrib><creatorcontrib>Wu, Changzheng</creatorcontrib><creatorcontrib>Xiao, Anfeng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiao, Qiong</au><au>Yin, Qin</au><au>Ni, Hui</au><au>Cai, Huinong</au><au>Wu, Changzheng</au><au>Xiao, Anfeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization and immobilization of arylsulfatase on modified magnetic nanoparticles for desulfation of agar</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2017-01</date><risdate>2017</risdate><volume>94</volume><issue>Pt A</issue><spage>576</spage><epage>584</epage><pages>576-584</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>[Display omitted] •A low cost, simple manipulation and nontoxic approach were designed for the preparation of Carboxyl-functioned Magnetic Nanoparticles (CMNPs).•CMNPs were prepared and well characterized by Fourier transform infrared spedtroscopy and scanning electron microscope.•Arylsulfatase was successfully immobilized onto CMNPs and the catalysts exhibited good catalytic activity for the desulfation of agar.•The immobilized arylsulfatase can keep its catalytic activity after being reused seven times. Carboxyl functioned magnetic nanoparticles (CMNPs) were prepared by a simple co-precipitation method and characterized by Fourier transform infrared spedtroscopy and scanning electron microscope. The prepared CMNPs were used for covalent immobilization of the arylsulfatase which could be applied in desulfation of agar. The optimal immobilizaion conditions were obtained as follows: glutaraldehyde concentration 1.0% (v/v), cross-linking time 3h, immobilization time 3h, immobilization temperature 5°C and enzyme dose 0.62U. Increase in properties of the arylsulfatase such as optimum temperature and pH was observed after immobilization. Immobilization led to increased tolerance of enzyme to some metal ions, inhibitors and detergents. The Km and kcat of the immobilized enzyme for hydrolysis of p-NPS at pH 7.5 and at 50°C were determined to be 0.89mmol/L and 256.91s−1, respectively. The relative desulfuration rates of immobilized arylsulfatase maintained 61.7% of its initial desulfuration rates after seven cycles. After the reaction of agar with immobilized arylsulfatase for 90min at 50°C, 46% of the sulfate in the agar was removed. These results showed that the immobilization of arylsulfatase onto CMNPs is an efficient and simple way for preparation of stable arylsulfatase and have a great potential for application in enzymatic desulfation of agar.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27746358</pmid><doi>10.1016/j.ijbiomac.2016.10.029</doi><tpages>9</tpages></addata></record>
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ispartof International journal of biological macromolecules, 2017-01, Vol.94 (Pt A), p.576-584
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subjects Agar - chemistry
Agar desulfation
Arylsulfatase
Arylsulfatases - chemistry
Bacterial Proteins - chemistry
Carboxyl function
Chemical Precipitation
Cross-Linking Reagents - chemistry
Enzyme Stability
Enzymes, Immobilized - chemistry
Equipment Reuse
Ferrosoferric Oxide - chemistry
Glutaral - chemistry
Hydrogen-Ion Concentration
Hydrolysis
Immobilization
Kinetics
Magnetic nanoparticle
Magnetite Nanoparticles - chemistry
Magnetite Nanoparticles - ultrastructure
Nitrobenzenes - chemistry
Recombinant Proteins - chemistry
Sulfates - chemistry
Temperature
Time Factors
title Characterization and immobilization of arylsulfatase on modified magnetic nanoparticles for desulfation of agar
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