Robust one-pot multi-enzyme polysaccharide remodeling strategy for the synthesis of uniform chondroitin fragments and derivatives
The non-sulfated chondroitin backbone (CH) is the synthetic precursor of chondroitin sulfate, a linear polysaccharide with dramatic biological functions. Owing to the intrinsic characteristics of the polysaccharide biosynthetic pathway, it is still a challenge to obtain structural-defined glycans vi...
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Veröffentlicht in: | Carbohydrate research 2021-11, Vol.509, p.108442, Article 108442 |
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creator | Yang, Lin Xu, Xuan Li, Shuang Li, Yi Ling, Peixue Fang, Junqiang |
description | The non-sulfated chondroitin backbone (CH) is the synthetic precursor of chondroitin sulfate, a linear polysaccharide with dramatic biological functions. Owing to the intrinsic characteristics of the polysaccharide biosynthetic pathway, it is still a challenge to obtain structural-defined glycans via microbial fermentation or enzymatic synthesis, which hindering the illustration of CH polysaccharide functions. Herein, we report a robust one-pot multi-enzyme polysaccharide remodeling strategy to synthesize uniform CH fragments and their derivatives. CH tetrasaccharide, which was obtained from the digestion of heterogeneous CH fragments, was used as the starting material to trigger the assembly of uniform CH fragments in a one-pot multi-enzyme system. This strategy, which combined heteropolymer digestion, sugar nucleotide in situ generation, and sugar chain synchronized polymerization, provides a robust toolbox for structural-defined polysaccharides synthesis.
[Display omitted]
•Non-sulfated chondroitin tetrasaccharide was obtained by a glycan-remodeling toolbox.•Uniform CH chondroitin fragments and their derivatives were generated.•CH fragments with azido could be applied as scaffolds for sustained drug release.•Exogenous CH fragments would be used in targeted drug delivery systems. |
doi_str_mv | 10.1016/j.carres.2021.108442 |
format | Article |
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[Display omitted]
•Non-sulfated chondroitin tetrasaccharide was obtained by a glycan-remodeling toolbox.•Uniform CH chondroitin fragments and their derivatives were generated.•CH fragments with azido could be applied as scaffolds for sustained drug release.•Exogenous CH fragments would be used in targeted drug delivery systems.</description><identifier>ISSN: 0008-6215</identifier><identifier>ISSN: 1873-426X</identifier><identifier>EISSN: 1873-426X</identifier><identifier>DOI: 10.1016/j.carres.2021.108442</identifier><identifier>PMID: 34547517</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Chondroitin - chemistry ; Chondroitin Sulfates - biosynthesis ; Chondroitin Sulfates - chemical synthesis ; Chondroitin Sulfates - chemistry ; One-pot multi-enzyme ; Polysaccharide remodeling ; Polysaccharides - biosynthesis ; Polysaccharides - chemical synthesis ; Polysaccharides - chemistry ; Uniform chondroitin fragments</subject><ispartof>Carbohydrate research, 2021-11, Vol.509, p.108442, Article 108442</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright © 2021 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-158adbaa2e03d66e4e011d916bbb072598f3f7c52031478b8a383eb50f2d30a03</citedby><cites>FETCH-LOGICAL-c362t-158adbaa2e03d66e4e011d916bbb072598f3f7c52031478b8a383eb50f2d30a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0008621521002111$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34547517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Xu, Xuan</creatorcontrib><creatorcontrib>Li, Shuang</creatorcontrib><creatorcontrib>Li, Yi</creatorcontrib><creatorcontrib>Ling, Peixue</creatorcontrib><creatorcontrib>Fang, Junqiang</creatorcontrib><title>Robust one-pot multi-enzyme polysaccharide remodeling strategy for the synthesis of uniform chondroitin fragments and derivatives</title><title>Carbohydrate research</title><addtitle>Carbohydr Res</addtitle><description>The non-sulfated chondroitin backbone (CH) is the synthetic precursor of chondroitin sulfate, a linear polysaccharide with dramatic biological functions. Owing to the intrinsic characteristics of the polysaccharide biosynthetic pathway, it is still a challenge to obtain structural-defined glycans via microbial fermentation or enzymatic synthesis, which hindering the illustration of CH polysaccharide functions. Herein, we report a robust one-pot multi-enzyme polysaccharide remodeling strategy to synthesize uniform CH fragments and their derivatives. CH tetrasaccharide, which was obtained from the digestion of heterogeneous CH fragments, was used as the starting material to trigger the assembly of uniform CH fragments in a one-pot multi-enzyme system. This strategy, which combined heteropolymer digestion, sugar nucleotide in situ generation, and sugar chain synchronized polymerization, provides a robust toolbox for structural-defined polysaccharides synthesis.
[Display omitted]
•Non-sulfated chondroitin tetrasaccharide was obtained by a glycan-remodeling toolbox.•Uniform CH chondroitin fragments and their derivatives were generated.•CH fragments with azido could be applied as scaffolds for sustained drug release.•Exogenous CH fragments would be used in targeted drug delivery systems.</description><subject>Chondroitin - chemistry</subject><subject>Chondroitin Sulfates - biosynthesis</subject><subject>Chondroitin Sulfates - chemical synthesis</subject><subject>Chondroitin Sulfates - chemistry</subject><subject>One-pot multi-enzyme</subject><subject>Polysaccharide remodeling</subject><subject>Polysaccharides - biosynthesis</subject><subject>Polysaccharides - chemical synthesis</subject><subject>Polysaccharides - chemistry</subject><subject>Uniform chondroitin fragments</subject><issn>0008-6215</issn><issn>1873-426X</issn><issn>1873-426X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM2LFDEQxYMo7rj6H4jk6KXHfHTS2Ysgi1-wIIiCt5BOqmcydCdjKj3Q3vzP7aVXj56KerxXj_oR8pKzPWdcvzntvSsFcC-Y4Ktk2lY8IjtuOtm0Qv94THaMMdNowdUVeYZ4WlemO_2UXMlWtZ3i3Y78_pr7GSvNCZpzrnSaxxobSL-WCeg5jws674-uxAC0wJQDjDEdKNbiKhwWOuRC6xEoLmkdGJHmgc4prvpE_TGnUHKsMdGhuMMEqSJ1KdAAJV5cjRfA5-TJ4EaEFw_zmnz_8P7b7afm7svHz7fv7hovtagNV8aF3jkBTAatoQXGebjhuu971gl1YwY5dF4JJnnbmd44aST0ig0iSOaYvCavt7vnkn_OgNVOET2Mo0uQZ7RCdUp2Uhu1WtvN6ktGLDDYc4mTK4vlzN7Dtye7wbf38O0Gf429emiY-wnCv9Bf2qvh7WaA9c9LhGLRR0geQizgqw05_r_hD7ZbmtY</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Yang, Lin</creator><creator>Xu, Xuan</creator><creator>Li, Shuang</creator><creator>Li, Yi</creator><creator>Ling, Peixue</creator><creator>Fang, Junqiang</creator><general>Elsevier Ltd</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>202111</creationdate><title>Robust one-pot multi-enzyme polysaccharide remodeling strategy for the synthesis of uniform chondroitin fragments and derivatives</title><author>Yang, Lin ; Xu, Xuan ; Li, Shuang ; Li, Yi ; Ling, Peixue ; Fang, Junqiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-158adbaa2e03d66e4e011d916bbb072598f3f7c52031478b8a383eb50f2d30a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chondroitin - chemistry</topic><topic>Chondroitin Sulfates - biosynthesis</topic><topic>Chondroitin Sulfates - chemical synthesis</topic><topic>Chondroitin Sulfates - chemistry</topic><topic>One-pot multi-enzyme</topic><topic>Polysaccharide remodeling</topic><topic>Polysaccharides - biosynthesis</topic><topic>Polysaccharides - chemical synthesis</topic><topic>Polysaccharides - chemistry</topic><topic>Uniform chondroitin fragments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Lin</creatorcontrib><creatorcontrib>Xu, Xuan</creatorcontrib><creatorcontrib>Li, Shuang</creatorcontrib><creatorcontrib>Li, Yi</creatorcontrib><creatorcontrib>Ling, Peixue</creatorcontrib><creatorcontrib>Fang, Junqiang</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>Carbohydrate research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Lin</au><au>Xu, Xuan</au><au>Li, Shuang</au><au>Li, Yi</au><au>Ling, Peixue</au><au>Fang, Junqiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Robust one-pot multi-enzyme polysaccharide remodeling strategy for the synthesis of uniform chondroitin fragments and derivatives</atitle><jtitle>Carbohydrate research</jtitle><addtitle>Carbohydr Res</addtitle><date>2021-11</date><risdate>2021</risdate><volume>509</volume><spage>108442</spage><pages>108442-</pages><artnum>108442</artnum><issn>0008-6215</issn><issn>1873-426X</issn><eissn>1873-426X</eissn><abstract>The non-sulfated chondroitin backbone (CH) is the synthetic precursor of chondroitin sulfate, a linear polysaccharide with dramatic biological functions. Owing to the intrinsic characteristics of the polysaccharide biosynthetic pathway, it is still a challenge to obtain structural-defined glycans via microbial fermentation or enzymatic synthesis, which hindering the illustration of CH polysaccharide functions. Herein, we report a robust one-pot multi-enzyme polysaccharide remodeling strategy to synthesize uniform CH fragments and their derivatives. CH tetrasaccharide, which was obtained from the digestion of heterogeneous CH fragments, was used as the starting material to trigger the assembly of uniform CH fragments in a one-pot multi-enzyme system. This strategy, which combined heteropolymer digestion, sugar nucleotide in situ generation, and sugar chain synchronized polymerization, provides a robust toolbox for structural-defined polysaccharides synthesis.
[Display omitted]
•Non-sulfated chondroitin tetrasaccharide was obtained by a glycan-remodeling toolbox.•Uniform CH chondroitin fragments and their derivatives were generated.•CH fragments with azido could be applied as scaffolds for sustained drug release.•Exogenous CH fragments would be used in targeted drug delivery systems.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>34547517</pmid><doi>10.1016/j.carres.2021.108442</doi></addata></record> |
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subjects | Chondroitin - chemistry Chondroitin Sulfates - biosynthesis Chondroitin Sulfates - chemical synthesis Chondroitin Sulfates - chemistry One-pot multi-enzyme Polysaccharide remodeling Polysaccharides - biosynthesis Polysaccharides - chemical synthesis Polysaccharides - chemistry Uniform chondroitin fragments |
title | Robust one-pot multi-enzyme polysaccharide remodeling strategy for the synthesis of uniform chondroitin fragments and derivatives |
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