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Preparation and characterization of affinity sorbents based on isoalloxazine‐like ligands for separation of flavoenzymes

Affinity ligands for flavoenzymes were synthesized based on the natural structure of flavo‐coenzymes. Two typical flavoenzymes, cholesterol oxidase from Brevibacterium sp. and xanthine oxidase from bovine milk, were employed as standard enzymes. Fluorescent probes were synthesized from eight isoallo...

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Published in:Journal of separation science 2011-11, Vol.34 (21), p.2940-2949
Main Authors: Xin, Yu, Yang, Hailin, Xiao, Xiaole, Zhang, Ling, Zhang, Yuran, Tong, Yanjun, Wang, Wu
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cited_by cdi_FETCH-LOGICAL-c5344-21edca51dce466021ad95409ac7a809c927818020ff8b892b61cdee674d0abb43
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container_issue 21
container_start_page 2940
container_title Journal of separation science
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creator Xin, Yu
Yang, Hailin
Xiao, Xiaole
Zhang, Ling
Zhang, Yuran
Tong, Yanjun
Wang, Wu
description Affinity ligands for flavoenzymes were synthesized based on the natural structure of flavo‐coenzymes. Two typical flavoenzymes, cholesterol oxidase from Brevibacterium sp. and xanthine oxidase from bovine milk, were employed as standard enzymes. Fluorescent probes were synthesized from eight isoalloxazine‐like chemicals and 5‐aminofluorescein. Probe–enzyme interactions were analyzed via fluorescence spectra. Chemicals with high binding abilities to flavoenzymes were coupled with Sepharose through spacers composed of epichlorohydrin, ethylenediamine, 1,3‐diaminopropane, 2‐hydroxy‐1,3‐diaminopropane, and 1,4‐diaminobutane, and subjected to adsorption analysis with flavoenzymes. The results indicated that ligands synthesized from 2,4‐dioxohexahydropyrimidine‐5‐carboxylic acid, cytosine, 7‐chloroalloxazine, and 8‐chloroalloxazine had high binding abilities to the flavoenzymes. The affinity sorbent based on these ligands revealed a high theoretical maximum adsorption (Qmax). Protein and bioactivity recoveries were tested after one step of affinity binding via chromatographic analysis on small columns. Results showed that ligands linked with sorbents through long hydrophilic spacers had higher activity recoveries.
doi_str_mv 10.1002/jssc.201100474
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Two typical flavoenzymes, cholesterol oxidase from Brevibacterium sp. and xanthine oxidase from bovine milk, were employed as standard enzymes. Fluorescent probes were synthesized from eight isoalloxazine‐like chemicals and 5‐aminofluorescein. Probe–enzyme interactions were analyzed via fluorescence spectra. Chemicals with high binding abilities to flavoenzymes were coupled with Sepharose through spacers composed of epichlorohydrin, ethylenediamine, 1,3‐diaminopropane, 2‐hydroxy‐1,3‐diaminopropane, and 1,4‐diaminobutane, and subjected to adsorption analysis with flavoenzymes. The results indicated that ligands synthesized from 2,4‐dioxohexahydropyrimidine‐5‐carboxylic acid, cytosine, 7‐chloroalloxazine, and 8‐chloroalloxazine had high binding abilities to the flavoenzymes. The affinity sorbent based on these ligands revealed a high theoretical maximum adsorption (Qmax). 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Psychology ; Isoalloxazine ring ; Ligands ; milk ; Milk - enzymology ; Other chromatographic methods ; Oxidoreductases ; Recovery ; Separation ; Sorbents ; Spacers ; Spectrometry, Fluorescence ; Surface Properties ; xanthine oxidase ; Xanthine Oxidase - chemistry ; Xanthine Oxidase - isolation &amp; purification ; Xanthine Oxidase - metabolism</subject><ispartof>Journal of separation science, 2011-11, Vol.34 (21), p.2940-2949</ispartof><rights>Copyright © 2011 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim.</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH &amp; Co. 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Sep. Science</addtitle><description>Affinity ligands for flavoenzymes were synthesized based on the natural structure of flavo‐coenzymes. Two typical flavoenzymes, cholesterol oxidase from Brevibacterium sp. and xanthine oxidase from bovine milk, were employed as standard enzymes. Fluorescent probes were synthesized from eight isoalloxazine‐like chemicals and 5‐aminofluorescein. Probe–enzyme interactions were analyzed via fluorescence spectra. Chemicals with high binding abilities to flavoenzymes were coupled with Sepharose through spacers composed of epichlorohydrin, ethylenediamine, 1,3‐diaminopropane, 2‐hydroxy‐1,3‐diaminopropane, and 1,4‐diaminobutane, and subjected to adsorption analysis with flavoenzymes. The results indicated that ligands synthesized from 2,4‐dioxohexahydropyrimidine‐5‐carboxylic acid, cytosine, 7‐chloroalloxazine, and 8‐chloroalloxazine had high binding abilities to the flavoenzymes. The affinity sorbent based on these ligands revealed a high theoretical maximum adsorption (Qmax). Protein and bioactivity recoveries were tested after one step of affinity binding via chromatographic analysis on small columns. Results showed that ligands linked with sorbents through long hydrophilic spacers had higher activity recoveries.</description><subject>Adsorption</subject><subject>Affinity</subject><subject>Affinity ligands</subject><subject>agarose</subject><subject>Analytical chemistry</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Binding</subject><subject>binding capacity</subject><subject>Biological and medical sciences</subject><subject>Brevibacterium</subject><subject>Brevibacterium - enzymology</subject><subject>Cattle</subject><subject>Chemistry</subject><subject>cholesterol</subject><subject>Cholesterol Oxidase - chemistry</subject><subject>Cholesterol Oxidase - isolation &amp; purification</subject><subject>Cholesterol Oxidase - metabolism</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>cytosine</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Exact sciences and technology</subject><subject>Flavins - chemical synthesis</subject><subject>Flavins - chemistry</subject><subject>Flavo-coenzymes</subject><subject>Flavoenzymes</subject><subject>fluorescence</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Isoalloxazine ring</subject><subject>Ligands</subject><subject>milk</subject><subject>Milk - enzymology</subject><subject>Other chromatographic methods</subject><subject>Oxidoreductases</subject><subject>Recovery</subject><subject>Separation</subject><subject>Sorbents</subject><subject>Spacers</subject><subject>Spectrometry, Fluorescence</subject><subject>Surface Properties</subject><subject>xanthine oxidase</subject><subject>Xanthine Oxidase - chemistry</subject><subject>Xanthine Oxidase - isolation &amp; purification</subject><subject>Xanthine Oxidase - metabolism</subject><issn>1615-9306</issn><issn>1615-9314</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkc1uEzEURkcIREthyxJGQgg2Cdcejz1eoghaUFWQkqrsrDseuzidjIM9aZuseASekSfB0YQUsYCV_849vvaXZU8JjAkAfTOPUY8pkLRggt3LDgkn5UgWhN3fz4EfZI9inAMQUUl4mB1QIgsOZXmYbT4Hs8SAvfNdjl2T669ppXsT3GbY9DZHa13n-nUefahN18e8xmiaPJ266LFt_S1uXGd-fv_RuiuTt-4yqWJufcjjnT6ZbIvX3nSb9cLEx9kDi200T3bjUXb-_t1scjI6_XT8YfL2dKTLgrERJabRWJJGG8Y5UIKNLBlI1AIrkFpSUZEKKFhb1ZWkNSe6MYYL1gDWNSuOsleDdxn8t5WJvVq4qE3bYmf8KioJIATlsCVf_5MkUBBaScmrhL74C537VejSOxQpWUmASigSNR4oHXyMwVi1DG6BYZ1Uapuf2uan9vmlgmc77apemGaP_w4sAS93AEaNrQ3YaRfvOCZ4SQESJwfuxrVm_Z9r1cfpdPJnE6Oh1sXe3O5rMVwpLgpRqouzY0VnsylcfDlTJ4l_PvAWvcLLkPo5nyYdA4D0uZwXvwATj88G</recordid><startdate>201111</startdate><enddate>201111</enddate><creator>Xin, Yu</creator><creator>Yang, Hailin</creator><creator>Xiao, Xiaole</creator><creator>Zhang, Ling</creator><creator>Zhang, Yuran</creator><creator>Tong, Yanjun</creator><creator>Wang, Wu</creator><general>WILEY‐VCH Verlag</general><general>WILEY-VCH Verlag</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>201111</creationdate><title>Preparation and characterization of affinity sorbents based on isoalloxazine‐like ligands for separation of flavoenzymes</title><author>Xin, Yu ; Yang, Hailin ; Xiao, Xiaole ; Zhang, Ling ; Zhang, Yuran ; Tong, Yanjun ; Wang, Wu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5344-21edca51dce466021ad95409ac7a809c927818020ff8b892b61cdee674d0abb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adsorption</topic><topic>Affinity</topic><topic>Affinity ligands</topic><topic>agarose</topic><topic>Analytical chemistry</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Binding</topic><topic>binding capacity</topic><topic>Biological and medical sciences</topic><topic>Brevibacterium</topic><topic>Brevibacterium - enzymology</topic><topic>Cattle</topic><topic>Chemistry</topic><topic>cholesterol</topic><topic>Cholesterol Oxidase - chemistry</topic><topic>Cholesterol Oxidase - isolation &amp; purification</topic><topic>Cholesterol Oxidase - metabolism</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>cytosine</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Exact sciences and technology</topic><topic>Flavins - chemical synthesis</topic><topic>Flavins - chemistry</topic><topic>Flavo-coenzymes</topic><topic>Flavoenzymes</topic><topic>fluorescence</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Isoalloxazine ring</topic><topic>Ligands</topic><topic>milk</topic><topic>Milk - enzymology</topic><topic>Other chromatographic methods</topic><topic>Oxidoreductases</topic><topic>Recovery</topic><topic>Separation</topic><topic>Sorbents</topic><topic>Spacers</topic><topic>Spectrometry, Fluorescence</topic><topic>Surface Properties</topic><topic>xanthine oxidase</topic><topic>Xanthine Oxidase - chemistry</topic><topic>Xanthine Oxidase - isolation &amp; purification</topic><topic>Xanthine Oxidase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xin, Yu</creatorcontrib><creatorcontrib>Yang, Hailin</creatorcontrib><creatorcontrib>Xiao, Xiaole</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><creatorcontrib>Zhang, Yuran</creatorcontrib><creatorcontrib>Tong, Yanjun</creatorcontrib><creatorcontrib>Wang, Wu</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xin, Yu</au><au>Yang, Hailin</au><au>Xiao, Xiaole</au><au>Zhang, Ling</au><au>Zhang, Yuran</au><au>Tong, Yanjun</au><au>Wang, Wu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and characterization of affinity sorbents based on isoalloxazine‐like ligands for separation of flavoenzymes</atitle><jtitle>Journal of separation science</jtitle><addtitle>J. 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The results indicated that ligands synthesized from 2,4‐dioxohexahydropyrimidine‐5‐carboxylic acid, cytosine, 7‐chloroalloxazine, and 8‐chloroalloxazine had high binding abilities to the flavoenzymes. The affinity sorbent based on these ligands revealed a high theoretical maximum adsorption (Qmax). Protein and bioactivity recoveries were tested after one step of affinity binding via chromatographic analysis on small columns. Results showed that ligands linked with sorbents through long hydrophilic spacers had higher activity recoveries.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag</pub><pmid>21936055</pmid><doi>10.1002/jssc.201100474</doi><tpages>10</tpages></addata></record>
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subjects Adsorption
Affinity
Affinity ligands
agarose
Analytical chemistry
Analytical, structural and metabolic biochemistry
Animals
Binding
binding capacity
Biological and medical sciences
Brevibacterium
Brevibacterium - enzymology
Cattle
Chemistry
cholesterol
Cholesterol Oxidase - chemistry
Cholesterol Oxidase - isolation & purification
Cholesterol Oxidase - metabolism
Chromatographic methods and physical methods associated with chromatography
cytosine
Enzymes and enzyme inhibitors
Exact sciences and technology
Flavins - chemical synthesis
Flavins - chemistry
Flavo-coenzymes
Flavoenzymes
fluorescence
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
Fundamental and applied biological sciences. Psychology
Isoalloxazine ring
Ligands
milk
Milk - enzymology
Other chromatographic methods
Oxidoreductases
Recovery
Separation
Sorbents
Spacers
Spectrometry, Fluorescence
Surface Properties
xanthine oxidase
Xanthine Oxidase - chemistry
Xanthine Oxidase - isolation & purification
Xanthine Oxidase - metabolism
title Preparation and characterization of affinity sorbents based on isoalloxazine‐like ligands for separation of flavoenzymes
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