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Dissolution and deacetylation of chitin in ionic liquid tetrabutylammonium hydroxide and its cascade reaction in enzyme treatment for chitin recycling
[Display omitted] •Mild ionic liquids [TBA][OH] was employed on chitin for the first time.•[TBA][OH] showed dissolution and deacetylation abilities on chitin.•Deacetylation of chitin was positively correlated with the solubility of chitin.•A combinational process of [TBA][OH] pretreatment and ReCDA...
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Published in: | Carbohydrate polymers 2020-02, Vol.230, p.115605-115605, Article 115605 |
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creator | Ma, Qinyuan Gao, Xiuzhen Bi, Xinyu Han, Qi Tu, Linna Yang, Yupeng Shen, Yanbing Wang, Min |
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•Mild ionic liquids [TBA][OH] was employed on chitin for the first time.•[TBA][OH] showed dissolution and deacetylation abilities on chitin.•Deacetylation of chitin was positively correlated with the solubility of chitin.•A combinational process of [TBA][OH] pretreatment and ReCDA were performed.•The ReCDA activity on chitin was activated with [TBA][OH] pretreatment.
Chitin is the second most abundant renewable polymer on earth, and its deacetylated derivative, chitosan, is a highly useful biopolymer. This work studied for the first time the application of ionic liquid (IL) tetrabutylammonium hydroxide ([TBA][OH]) and chitin deacetylase from Rhodococcus equi CGMCC14861 (ReCDA) for the efficient conversion of chitin into chitosan at room temperature. Results confirmed that chitin had good solubility in 18 wt% aqueous [TBA][OH] solution at 80 ℃. In addition, efficient chitin deactylation was observed with high concentrations of [TBA][OH] exceeding 12 wt% and showing potential application in chitin conversion. ReCDA activity on chitin was activated by [TBA][OH] pretreatment. Sequential and simultaneous strategies were also compared, and the results showed that the simultaneous one-pot deacetylation provided the highest acetic acid yield of 3.78 mg/g chitin powder after 24 h. This study serves as a guide for the dissolution and deacetylation of chitin to produce high value-added chitosan products. |
doi_str_mv | 10.1016/j.carbpol.2019.115605 |
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•Mild ionic liquids [TBA][OH] was employed on chitin for the first time.•[TBA][OH] showed dissolution and deacetylation abilities on chitin.•Deacetylation of chitin was positively correlated with the solubility of chitin.•A combinational process of [TBA][OH] pretreatment and ReCDA were performed.•The ReCDA activity on chitin was activated with [TBA][OH] pretreatment.
Chitin is the second most abundant renewable polymer on earth, and its deacetylated derivative, chitosan, is a highly useful biopolymer. This work studied for the first time the application of ionic liquid (IL) tetrabutylammonium hydroxide ([TBA][OH]) and chitin deacetylase from Rhodococcus equi CGMCC14861 (ReCDA) for the efficient conversion of chitin into chitosan at room temperature. Results confirmed that chitin had good solubility in 18 wt% aqueous [TBA][OH] solution at 80 ℃. In addition, efficient chitin deactylation was observed with high concentrations of [TBA][OH] exceeding 12 wt% and showing potential application in chitin conversion. ReCDA activity on chitin was activated by [TBA][OH] pretreatment. Sequential and simultaneous strategies were also compared, and the results showed that the simultaneous one-pot deacetylation provided the highest acetic acid yield of 3.78 mg/g chitin powder after 24 h. This study serves as a guide for the dissolution and deacetylation of chitin to produce high value-added chitosan products.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2019.115605</identifier><identifier>PMID: 31887900</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Cascade reaction ; Chitin ; Chitosan ; Deacetylation ; Dissolution ; Ionic liquid</subject><ispartof>Carbohydrate polymers, 2020-02, Vol.230, p.115605-115605, Article 115605</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-9ff525ab71656e20b11d1a9cde8ad1e019ad3335e566a413caafc27300e0d5c93</citedby><cites>FETCH-LOGICAL-c402t-9ff525ab71656e20b11d1a9cde8ad1e019ad3335e566a413caafc27300e0d5c93</cites><orcidid>0000-0002-8367-3758</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31887900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Qinyuan</creatorcontrib><creatorcontrib>Gao, Xiuzhen</creatorcontrib><creatorcontrib>Bi, Xinyu</creatorcontrib><creatorcontrib>Han, Qi</creatorcontrib><creatorcontrib>Tu, Linna</creatorcontrib><creatorcontrib>Yang, Yupeng</creatorcontrib><creatorcontrib>Shen, Yanbing</creatorcontrib><creatorcontrib>Wang, Min</creatorcontrib><title>Dissolution and deacetylation of chitin in ionic liquid tetrabutylammonium hydroxide and its cascade reaction in enzyme treatment for chitin recycling</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>[Display omitted]
•Mild ionic liquids [TBA][OH] was employed on chitin for the first time.•[TBA][OH] showed dissolution and deacetylation abilities on chitin.•Deacetylation of chitin was positively correlated with the solubility of chitin.•A combinational process of [TBA][OH] pretreatment and ReCDA were performed.•The ReCDA activity on chitin was activated with [TBA][OH] pretreatment.
Chitin is the second most abundant renewable polymer on earth, and its deacetylated derivative, chitosan, is a highly useful biopolymer. This work studied for the first time the application of ionic liquid (IL) tetrabutylammonium hydroxide ([TBA][OH]) and chitin deacetylase from Rhodococcus equi CGMCC14861 (ReCDA) for the efficient conversion of chitin into chitosan at room temperature. Results confirmed that chitin had good solubility in 18 wt% aqueous [TBA][OH] solution at 80 ℃. In addition, efficient chitin deactylation was observed with high concentrations of [TBA][OH] exceeding 12 wt% and showing potential application in chitin conversion. ReCDA activity on chitin was activated by [TBA][OH] pretreatment. Sequential and simultaneous strategies were also compared, and the results showed that the simultaneous one-pot deacetylation provided the highest acetic acid yield of 3.78 mg/g chitin powder after 24 h. This study serves as a guide for the dissolution and deacetylation of chitin to produce high value-added chitosan products.</description><subject>Cascade reaction</subject><subject>Chitin</subject><subject>Chitosan</subject><subject>Deacetylation</subject><subject>Dissolution</subject><subject>Ionic liquid</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u3CAUhVHUKJmmeYRWLLvxhGsMM15VVfoXKVI26RphuE4Y2TABXNV5kD5vmJ90G4SEuHz3HHEPIR-BLYGBvNosjY7dNgzLmkG7BBCSiROygPWqrYA3zTuyYNA01VrC6py8T2nDypLAzsg5h3XBGFuQf99cSmGYsgueam-pRW0wz4PeV0JPzaPLztPdDt4ZOrinyVmaMUfdTTtyHMvDNNLH2cbw11ncC7mcqNHJ6HKPRXSvV1TQP88j0lxqeUSfaR_iq0lEM5vB-YcP5LTXQ8LL43lBfv_4fn_9q7q9-3lz_fW2Mg2rc9X2vaiF7lYghcSadQAWdGssrrUFLIPRlnMuUEipG-BG697UK84YMitMyy_I54PuNoanCVNWo0sGh0F7DFNSNecg66ZmvKDigJoYUorYq210o46zAqZ2kaiNOkaidpGoQySl79PRYupGtP-7XjMowJcDgOWjfxxGlYxDb9C6Mo-sbHBvWLwAaAuj3A</recordid><startdate>20200215</startdate><enddate>20200215</enddate><creator>Ma, Qinyuan</creator><creator>Gao, Xiuzhen</creator><creator>Bi, Xinyu</creator><creator>Han, Qi</creator><creator>Tu, Linna</creator><creator>Yang, Yupeng</creator><creator>Shen, Yanbing</creator><creator>Wang, Min</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8367-3758</orcidid></search><sort><creationdate>20200215</creationdate><title>Dissolution and deacetylation of chitin in ionic liquid tetrabutylammonium hydroxide and its cascade reaction in enzyme treatment for chitin recycling</title><author>Ma, Qinyuan ; Gao, Xiuzhen ; Bi, Xinyu ; Han, Qi ; Tu, Linna ; Yang, Yupeng ; Shen, Yanbing ; Wang, Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-9ff525ab71656e20b11d1a9cde8ad1e019ad3335e566a413caafc27300e0d5c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cascade reaction</topic><topic>Chitin</topic><topic>Chitosan</topic><topic>Deacetylation</topic><topic>Dissolution</topic><topic>Ionic liquid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Qinyuan</creatorcontrib><creatorcontrib>Gao, Xiuzhen</creatorcontrib><creatorcontrib>Bi, Xinyu</creatorcontrib><creatorcontrib>Han, Qi</creatorcontrib><creatorcontrib>Tu, Linna</creatorcontrib><creatorcontrib>Yang, Yupeng</creatorcontrib><creatorcontrib>Shen, Yanbing</creatorcontrib><creatorcontrib>Wang, Min</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Qinyuan</au><au>Gao, Xiuzhen</au><au>Bi, Xinyu</au><au>Han, Qi</au><au>Tu, Linna</au><au>Yang, Yupeng</au><au>Shen, Yanbing</au><au>Wang, Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissolution and deacetylation of chitin in ionic liquid tetrabutylammonium hydroxide and its cascade reaction in enzyme treatment for chitin recycling</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2020-02-15</date><risdate>2020</risdate><volume>230</volume><spage>115605</spage><epage>115605</epage><pages>115605-115605</pages><artnum>115605</artnum><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>[Display omitted]
•Mild ionic liquids [TBA][OH] was employed on chitin for the first time.•[TBA][OH] showed dissolution and deacetylation abilities on chitin.•Deacetylation of chitin was positively correlated with the solubility of chitin.•A combinational process of [TBA][OH] pretreatment and ReCDA were performed.•The ReCDA activity on chitin was activated with [TBA][OH] pretreatment.
Chitin is the second most abundant renewable polymer on earth, and its deacetylated derivative, chitosan, is a highly useful biopolymer. This work studied for the first time the application of ionic liquid (IL) tetrabutylammonium hydroxide ([TBA][OH]) and chitin deacetylase from Rhodococcus equi CGMCC14861 (ReCDA) for the efficient conversion of chitin into chitosan at room temperature. Results confirmed that chitin had good solubility in 18 wt% aqueous [TBA][OH] solution at 80 ℃. In addition, efficient chitin deactylation was observed with high concentrations of [TBA][OH] exceeding 12 wt% and showing potential application in chitin conversion. ReCDA activity on chitin was activated by [TBA][OH] pretreatment. Sequential and simultaneous strategies were also compared, and the results showed that the simultaneous one-pot deacetylation provided the highest acetic acid yield of 3.78 mg/g chitin powder after 24 h. This study serves as a guide for the dissolution and deacetylation of chitin to produce high value-added chitosan products.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31887900</pmid><doi>10.1016/j.carbpol.2019.115605</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8367-3758</orcidid></addata></record> |
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subjects | Cascade reaction Chitin Chitosan Deacetylation Dissolution Ionic liquid |
title | Dissolution and deacetylation of chitin in ionic liquid tetrabutylammonium hydroxide and its cascade reaction in enzyme treatment for chitin recycling |
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