Structural and mechanism-based engineering of sulfotransferase CHST15 for the efficient synthesis of chondroitin sulfate E

Natural chondroitin sulfate (CS), extracted from animal cartilage, is widely used in the pharmaceuticals and foods. However, contamination with animal-derived heteropolysaccharides presents significant challenges, including potential immune responses. To address this, we developed a green and effici...

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Veröffentlicht in:Applied and environmental microbiology 2024-12, Vol.91 (1), p.e0157324
Hauptverfasser: Wang, Zhonghua, Song, Wei, Wei, Wanqing, Qi, Hejia, Meng, Weiwei, Liu, Jia, Li, Xiaomin, Gao, Cong, Liu, Liming, Hu, Guipeng, Zhou, Yiwen, Wu, Jing
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container_title Applied and environmental microbiology
container_volume 91
creator Wang, Zhonghua
Song, Wei
Wei, Wanqing
Qi, Hejia
Meng, Weiwei
Liu, Jia
Li, Xiaomin
Gao, Cong
Liu, Liming
Hu, Guipeng
Zhou, Yiwen
Wu, Jing
description Natural chondroitin sulfate (CS), extracted from animal cartilage, is widely used in the pharmaceuticals and foods. However, contamination with animal-derived heteropolysaccharides presents significant challenges, including potential immune responses. To address this, we developed a green and efficient method for synthesizing chondroitin sulfate E (CSE) via enzymatic synthesis, identifying CHST15, a sulfotransferase that catalyzes the conversion of chondroitin sulfate A (CSA) to CSE. We investigated the novel catalytic mechanism of CHST15 through quantum mechanical (QM) calculations and experimental validation, confirming its alignment with the SN2 reaction mechanism. Subsequently, we enhanced the catalytic efficiency of CHST15 using protein engineering, improving the catalytic efficiency from 18.1% in the wild type (WT) to 62.5% in the M7 mutant-a 3.5-fold increase. Finally, we constructed a six-enzyme cascade whole-cell catalyst, achieving a 72.2% conversion of 15 g/L CSA to produce CSE within 24 h. These findings offer a promising strategy for the industrial production of CSE.IMPORTANCECurrent methods for obtaining chondroitin sulfate (CS) primarily rely on tissue extraction and chemical synthesis. However, these approaches are hindered by contamination risks from animal-derived heteropolysaccharides and the technical challenges inherent in complex chemical synthesis, limiting the scalability of industrial CS production. To address this, we developed a green and efficient enzymatic biosynthesis method for chondroitin sulfate E (CSE). By identifying and engineering the sulfotransferase CHST15 from , we created a mutant ( CHST15 ) with a 3.5-fold increase in catalytic efficiency toward chondroitin sulfate A (CSA) compared to the wild-type enzyme. Additionally, we constructed a six-enzyme cascade whole-cell biocatalyst, achieving a 72.2% conversion rate from CSA to CSE. This study opens new avenues for the industrial-scale production of CSE through sustainable enzymatic processes.
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However, contamination with animal-derived heteropolysaccharides presents significant challenges, including potential immune responses. To address this, we developed a green and efficient method for synthesizing chondroitin sulfate E (CSE) via enzymatic synthesis, identifying CHST15, a sulfotransferase that catalyzes the conversion of chondroitin sulfate A (CSA) to CSE. We investigated the novel catalytic mechanism of CHST15 through quantum mechanical (QM) calculations and experimental validation, confirming its alignment with the SN2 reaction mechanism. Subsequently, we enhanced the catalytic efficiency of CHST15 using protein engineering, improving the catalytic efficiency from 18.1% in the wild type (WT) to 62.5% in the M7 mutant-a 3.5-fold increase. Finally, we constructed a six-enzyme cascade whole-cell catalyst, achieving a 72.2% conversion of 15 g/L CSA to produce CSE within 24 h. These findings offer a promising strategy for the industrial production of CSE.IMPORTANCECurrent methods for obtaining chondroitin sulfate (CS) primarily rely on tissue extraction and chemical synthesis. However, these approaches are hindered by contamination risks from animal-derived heteropolysaccharides and the technical challenges inherent in complex chemical synthesis, limiting the scalability of industrial CS production. To address this, we developed a green and efficient enzymatic biosynthesis method for chondroitin sulfate E (CSE). By identifying and engineering the sulfotransferase CHST15 from , we created a mutant ( CHST15 ) with a 3.5-fold increase in catalytic efficiency toward chondroitin sulfate A (CSA) compared to the wild-type enzyme. Additionally, we constructed a six-enzyme cascade whole-cell biocatalyst, achieving a 72.2% conversion rate from CSA to CSE. This study opens new avenues for the industrial-scale production of CSE through sustainable enzymatic processes.</description><identifier>ISSN: 0099-2240</identifier><identifier>ISSN: 1098-5336</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/aem.01573-24</identifier><identifier>PMID: 39629983</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacterial Proteins - chemistry ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biotechnology ; Catalytic converters ; Chemical synthesis ; Chondroitin sulfate ; Chondroitin Sulfates - biosynthesis ; Chondroitin Sulfates - chemistry ; Chondroitin Sulfates - metabolism ; Enzymatic synthesis ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Food contamination ; Immune response ; Industrial production ; Protein Engineering ; Protein folding ; Quantum mechanics ; Reaction mechanisms ; Sulfates ; Sulfotransferase ; Sulfotransferases - chemistry ; Sulfotransferases - genetics ; Sulfotransferases - metabolism</subject><ispartof>Applied and environmental microbiology, 2024-12, Vol.91 (1), p.e0157324</ispartof><rights>Copyright © 2024 Wang et al.</rights><rights>Copyright American Society for Microbiology Jan 2025</rights><rights>Copyright © 2024 Wang et al. 2024 Wang et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a296t-e4df26fd159a0a842273d46e0dbdc863faf1715141d154e5644c6695df2ceef73</cites><orcidid>0000-0001-6911-2041 ; 0000-0001-8505-2026 ; 0000-0001-9205-5268</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/aem.01573-24$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/aem.01573-24$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3175,27901,27902,52726,52727,52728</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39629983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Atomi, Haruyuki</contributor><creatorcontrib>Wang, Zhonghua</creatorcontrib><creatorcontrib>Song, Wei</creatorcontrib><creatorcontrib>Wei, Wanqing</creatorcontrib><creatorcontrib>Qi, Hejia</creatorcontrib><creatorcontrib>Meng, Weiwei</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Li, Xiaomin</creatorcontrib><creatorcontrib>Gao, Cong</creatorcontrib><creatorcontrib>Liu, Liming</creatorcontrib><creatorcontrib>Hu, Guipeng</creatorcontrib><creatorcontrib>Zhou, Yiwen</creatorcontrib><creatorcontrib>Wu, Jing</creatorcontrib><title>Structural and mechanism-based engineering of sulfotransferase CHST15 for the efficient synthesis of chondroitin sulfate E</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><addtitle>Appl Environ Microbiol</addtitle><description>Natural chondroitin sulfate (CS), extracted from animal cartilage, is widely used in the pharmaceuticals and foods. However, contamination with animal-derived heteropolysaccharides presents significant challenges, including potential immune responses. To address this, we developed a green and efficient method for synthesizing chondroitin sulfate E (CSE) via enzymatic synthesis, identifying CHST15, a sulfotransferase that catalyzes the conversion of chondroitin sulfate A (CSA) to CSE. We investigated the novel catalytic mechanism of CHST15 through quantum mechanical (QM) calculations and experimental validation, confirming its alignment with the SN2 reaction mechanism. Subsequently, we enhanced the catalytic efficiency of CHST15 using protein engineering, improving the catalytic efficiency from 18.1% in the wild type (WT) to 62.5% in the M7 mutant-a 3.5-fold increase. Finally, we constructed a six-enzyme cascade whole-cell catalyst, achieving a 72.2% conversion of 15 g/L CSA to produce CSE within 24 h. These findings offer a promising strategy for the industrial production of CSE.IMPORTANCECurrent methods for obtaining chondroitin sulfate (CS) primarily rely on tissue extraction and chemical synthesis. However, these approaches are hindered by contamination risks from animal-derived heteropolysaccharides and the technical challenges inherent in complex chemical synthesis, limiting the scalability of industrial CS production. To address this, we developed a green and efficient enzymatic biosynthesis method for chondroitin sulfate E (CSE). By identifying and engineering the sulfotransferase CHST15 from , we created a mutant ( CHST15 ) with a 3.5-fold increase in catalytic efficiency toward chondroitin sulfate A (CSA) compared to the wild-type enzyme. Additionally, we constructed a six-enzyme cascade whole-cell biocatalyst, achieving a 72.2% conversion rate from CSA to CSE. 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However, contamination with animal-derived heteropolysaccharides presents significant challenges, including potential immune responses. To address this, we developed a green and efficient method for synthesizing chondroitin sulfate E (CSE) via enzymatic synthesis, identifying CHST15, a sulfotransferase that catalyzes the conversion of chondroitin sulfate A (CSA) to CSE. We investigated the novel catalytic mechanism of CHST15 through quantum mechanical (QM) calculations and experimental validation, confirming its alignment with the SN2 reaction mechanism. Subsequently, we enhanced the catalytic efficiency of CHST15 using protein engineering, improving the catalytic efficiency from 18.1% in the wild type (WT) to 62.5% in the M7 mutant-a 3.5-fold increase. Finally, we constructed a six-enzyme cascade whole-cell catalyst, achieving a 72.2% conversion of 15 g/L CSA to produce CSE within 24 h. These findings offer a promising strategy for the industrial production of CSE.IMPORTANCECurrent methods for obtaining chondroitin sulfate (CS) primarily rely on tissue extraction and chemical synthesis. However, these approaches are hindered by contamination risks from animal-derived heteropolysaccharides and the technical challenges inherent in complex chemical synthesis, limiting the scalability of industrial CS production. To address this, we developed a green and efficient enzymatic biosynthesis method for chondroitin sulfate E (CSE). By identifying and engineering the sulfotransferase CHST15 from , we created a mutant ( CHST15 ) with a 3.5-fold increase in catalytic efficiency toward chondroitin sulfate A (CSA) compared to the wild-type enzyme. Additionally, we constructed a six-enzyme cascade whole-cell biocatalyst, achieving a 72.2% conversion rate from CSA to CSE. 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subjects Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Biotechnology
Catalytic converters
Chemical synthesis
Chondroitin sulfate
Chondroitin Sulfates - biosynthesis
Chondroitin Sulfates - chemistry
Chondroitin Sulfates - metabolism
Enzymatic synthesis
Escherichia coli - genetics
Escherichia coli - metabolism
Food contamination
Immune response
Industrial production
Protein Engineering
Protein folding
Quantum mechanics
Reaction mechanisms
Sulfates
Sulfotransferase
Sulfotransferases - chemistry
Sulfotransferases - genetics
Sulfotransferases - metabolism
title Structural and mechanism-based engineering of sulfotransferase CHST15 for the efficient synthesis of chondroitin sulfate E
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