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Biosynthesis of nucleotide sugars by a promiscuous UDP-sugar pyrophosphorylase from Arabidopsis thaliana (AtUSP)
Nucleotide sugars are activated forms of monosaccharides and key intermediates of carbohydrate metabolism in all organisms. The availability of structurally diverse nucleotide sugars is particularly important for the characterization of glycosyltransferases. Given that limited methods are available...
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Published in: | Bioorganic & medicinal chemistry letters 2013-07, Vol.23 (13), p.3764-3768 |
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creator | Liu, Jun Zou, Yang Guan, Wanyi Zhai, Yafei Xue, Mengyang Jin, Lan Zhao, Xueer Dong, Junkai Wang, Wenjun Shen, Jie Wang, Peng George Chen, Min |
description | Nucleotide sugars are activated forms of monosaccharides and key intermediates of carbohydrate metabolism in all organisms. The availability of structurally diverse nucleotide sugars is particularly important for the characterization of glycosyltransferases. Given that limited methods are available for preparation of nucleotide sugars, especially their useful non-natural derivatives, we introduced herein an efficient one-step three-enzyme catalytic system for the synthesis of nucleotide sugars from monosaccharides. In this study, a promiscuous UDP-sugar pyrophosphorylase (USP) from Arabidopsis thaliana (AtUSP) was used with a galactokinase from Streptococcus pneumoniae TIGR4 (SpGalK) and an inorganic pyrophosphatase (PPase) to effectively synthesize four UDP-sugars. AtUSP has better tolerance for C4-derivatives of Gal-1-P compared to UDP-glucose pyrophosphorylase from S. pneumoniae TIGR4 (SpGalU). Besides, the nucleotide substrate specificity and kinetic parameters of AtUSP were systematically studied. AtUSP exhibited considerable activity toward UTP, dUTP and dTTP, the yield of which was 87%, 85% and 84%, respectively. These results provide abundant information for better understanding of the relationship between substrate specificity and structural features of AtUSP. |
doi_str_mv | 10.1016/j.bmcl.2013.04.090 |
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The availability of structurally diverse nucleotide sugars is particularly important for the characterization of glycosyltransferases. Given that limited methods are available for preparation of nucleotide sugars, especially their useful non-natural derivatives, we introduced herein an efficient one-step three-enzyme catalytic system for the synthesis of nucleotide sugars from monosaccharides. In this study, a promiscuous UDP-sugar pyrophosphorylase (USP) from Arabidopsis thaliana (AtUSP) was used with a galactokinase from Streptococcus pneumoniae TIGR4 (SpGalK) and an inorganic pyrophosphatase (PPase) to effectively synthesize four UDP-sugars. AtUSP has better tolerance for C4-derivatives of Gal-1-P compared to UDP-glucose pyrophosphorylase from S. pneumoniae TIGR4 (SpGalU). Besides, the nucleotide substrate specificity and kinetic parameters of AtUSP were systematically studied. AtUSP exhibited considerable activity toward UTP, dUTP and dTTP, the yield of which was 87%, 85% and 84%, respectively. These results provide abundant information for better understanding of the relationship between substrate specificity and structural features of AtUSP.</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/j.bmcl.2013.04.090</identifier><identifier>PMID: 23707255</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Arabidopsis - enzymology ; Arabidopsis - metabolism ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Carbohydrate Conformation ; Galactokinase ; Galactokinase - metabolism ; Nucleotide sugars ; Nucleotidyltransferases - metabolism ; One-pot ; Pyrophosphatases - metabolism ; Streptococcus pneumoniae ; Streptococcus pneumoniae - enzymology ; UDP-sugar pyrophosphorylase ; Uridine Diphosphate Sugars - biosynthesis ; Uridine Diphosphate Sugars - chemistry</subject><ispartof>Bioorganic & medicinal chemistry letters, 2013-07, Vol.23 (13), p.3764-3768</ispartof><rights>2013 Elsevier Ltd</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-d1051cd394c3c97a25a06b87cf6943f02b72b136b5b7ccaaa93d6fa587dfe3083</citedby><cites>FETCH-LOGICAL-c389t-d1051cd394c3c97a25a06b87cf6943f02b72b136b5b7ccaaa93d6fa587dfe3083</cites></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/23707255$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Jun</creatorcontrib><creatorcontrib>Zou, Yang</creatorcontrib><creatorcontrib>Guan, Wanyi</creatorcontrib><creatorcontrib>Zhai, Yafei</creatorcontrib><creatorcontrib>Xue, Mengyang</creatorcontrib><creatorcontrib>Jin, Lan</creatorcontrib><creatorcontrib>Zhao, Xueer</creatorcontrib><creatorcontrib>Dong, Junkai</creatorcontrib><creatorcontrib>Wang, Wenjun</creatorcontrib><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Wang, Peng George</creatorcontrib><creatorcontrib>Chen, Min</creatorcontrib><title>Biosynthesis of nucleotide sugars by a promiscuous UDP-sugar pyrophosphorylase from Arabidopsis thaliana (AtUSP)</title><title>Bioorganic & medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>Nucleotide sugars are activated forms of monosaccharides and key intermediates of carbohydrate metabolism in all organisms. The availability of structurally diverse nucleotide sugars is particularly important for the characterization of glycosyltransferases. Given that limited methods are available for preparation of nucleotide sugars, especially their useful non-natural derivatives, we introduced herein an efficient one-step three-enzyme catalytic system for the synthesis of nucleotide sugars from monosaccharides. In this study, a promiscuous UDP-sugar pyrophosphorylase (USP) from Arabidopsis thaliana (AtUSP) was used with a galactokinase from Streptococcus pneumoniae TIGR4 (SpGalK) and an inorganic pyrophosphatase (PPase) to effectively synthesize four UDP-sugars. AtUSP has better tolerance for C4-derivatives of Gal-1-P compared to UDP-glucose pyrophosphorylase from S. pneumoniae TIGR4 (SpGalU). Besides, the nucleotide substrate specificity and kinetic parameters of AtUSP were systematically studied. AtUSP exhibited considerable activity toward UTP, dUTP and dTTP, the yield of which was 87%, 85% and 84%, respectively. These results provide abundant information for better understanding of the relationship between substrate specificity and structural features of AtUSP.</description><subject>Arabidopsis - enzymology</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Carbohydrate Conformation</subject><subject>Galactokinase</subject><subject>Galactokinase - metabolism</subject><subject>Nucleotide sugars</subject><subject>Nucleotidyltransferases - metabolism</subject><subject>One-pot</subject><subject>Pyrophosphatases - metabolism</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - enzymology</subject><subject>UDP-sugar pyrophosphorylase</subject><subject>Uridine Diphosphate Sugars - biosynthesis</subject><subject>Uridine Diphosphate Sugars - chemistry</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkU1v1DAQhi0EotvCH-CAfCyHhHHs2LHEZWnLh1SplcpK3CzHdlivsnGwE6T8-zps4QiHkQ_zzKsZPwi9IVASIPz9oWyPpi8rILQEVoKEZ2hDGGcFZVA_RxuQHIpGsu9n6DylAwBhwNhLdFZRAaKq6w0aP_qQlmHau-QTDh0eZtO7MHnrcJp_6Jhwu2CNxxiOPpk5zAnvru-L3z08LjGM-5ByxaXXyeEuc3gbdettGNfIaa97rweNL7fT7uH-3Sv0otN9cq-f3gu0-3Tz7epLcXv3-evV9rYwtJFTYQnUxFgqmaFGCl3VGnjbCNNxyWgHVSuqllDe1q0wRmstqeWdrhthO0ehoRfo8pSbN_85uzSpdX_X93pw-QhFagAhgBP6f5RyXgvBqcxodUJNDClF16kx-qOOiyKgVinqoFYpapWigKksJQ-9fcqf26Ozf0f-WMjAhxPg8of88i6qZLwbjLM-OjMpG_y_8h8BckKe_A</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Liu, Jun</creator><creator>Zou, Yang</creator><creator>Guan, Wanyi</creator><creator>Zhai, Yafei</creator><creator>Xue, Mengyang</creator><creator>Jin, Lan</creator><creator>Zhao, Xueer</creator><creator>Dong, Junkai</creator><creator>Wang, Wenjun</creator><creator>Shen, Jie</creator><creator>Wang, Peng George</creator><creator>Chen, Min</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><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20130701</creationdate><title>Biosynthesis of nucleotide sugars by a promiscuous UDP-sugar pyrophosphorylase from Arabidopsis thaliana (AtUSP)</title><author>Liu, Jun ; Zou, Yang ; Guan, Wanyi ; Zhai, Yafei ; Xue, Mengyang ; Jin, Lan ; Zhao, Xueer ; Dong, Junkai ; Wang, Wenjun ; Shen, Jie ; Wang, Peng George ; Chen, Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-d1051cd394c3c97a25a06b87cf6943f02b72b136b5b7ccaaa93d6fa587dfe3083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Arabidopsis - enzymology</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Carbohydrate Conformation</topic><topic>Galactokinase</topic><topic>Galactokinase - metabolism</topic><topic>Nucleotide sugars</topic><topic>Nucleotidyltransferases - metabolism</topic><topic>One-pot</topic><topic>Pyrophosphatases - metabolism</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - enzymology</topic><topic>UDP-sugar pyrophosphorylase</topic><topic>Uridine Diphosphate Sugars - biosynthesis</topic><topic>Uridine Diphosphate Sugars - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jun</creatorcontrib><creatorcontrib>Zou, Yang</creatorcontrib><creatorcontrib>Guan, Wanyi</creatorcontrib><creatorcontrib>Zhai, Yafei</creatorcontrib><creatorcontrib>Xue, Mengyang</creatorcontrib><creatorcontrib>Jin, Lan</creatorcontrib><creatorcontrib>Zhao, Xueer</creatorcontrib><creatorcontrib>Dong, Junkai</creatorcontrib><creatorcontrib>Wang, Wenjun</creatorcontrib><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Wang, Peng George</creatorcontrib><creatorcontrib>Chen, Min</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><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Bioorganic & medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jun</au><au>Zou, Yang</au><au>Guan, Wanyi</au><au>Zhai, Yafei</au><au>Xue, Mengyang</au><au>Jin, Lan</au><au>Zhao, Xueer</au><au>Dong, Junkai</au><au>Wang, Wenjun</au><au>Shen, Jie</au><au>Wang, Peng George</au><au>Chen, Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biosynthesis of nucleotide sugars by a promiscuous UDP-sugar pyrophosphorylase from Arabidopsis thaliana (AtUSP)</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>23</volume><issue>13</issue><spage>3764</spage><epage>3768</epage><pages>3764-3768</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>Nucleotide sugars are activated forms of monosaccharides and key intermediates of carbohydrate metabolism in all organisms. The availability of structurally diverse nucleotide sugars is particularly important for the characterization of glycosyltransferases. Given that limited methods are available for preparation of nucleotide sugars, especially their useful non-natural derivatives, we introduced herein an efficient one-step three-enzyme catalytic system for the synthesis of nucleotide sugars from monosaccharides. In this study, a promiscuous UDP-sugar pyrophosphorylase (USP) from Arabidopsis thaliana (AtUSP) was used with a galactokinase from Streptococcus pneumoniae TIGR4 (SpGalK) and an inorganic pyrophosphatase (PPase) to effectively synthesize four UDP-sugars. AtUSP has better tolerance for C4-derivatives of Gal-1-P compared to UDP-glucose pyrophosphorylase from S. pneumoniae TIGR4 (SpGalU). Besides, the nucleotide substrate specificity and kinetic parameters of AtUSP were systematically studied. AtUSP exhibited considerable activity toward UTP, dUTP and dTTP, the yield of which was 87%, 85% and 84%, respectively. These results provide abundant information for better understanding of the relationship between substrate specificity and structural features of AtUSP.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>23707255</pmid><doi>10.1016/j.bmcl.2013.04.090</doi><tpages>5</tpages></addata></record> |
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subjects | Arabidopsis - enzymology Arabidopsis - metabolism Arabidopsis Proteins - metabolism Arabidopsis thaliana Carbohydrate Conformation Galactokinase Galactokinase - metabolism Nucleotide sugars Nucleotidyltransferases - metabolism One-pot Pyrophosphatases - metabolism Streptococcus pneumoniae Streptococcus pneumoniae - enzymology UDP-sugar pyrophosphorylase Uridine Diphosphate Sugars - biosynthesis Uridine Diphosphate Sugars - chemistry |
title | Biosynthesis of nucleotide sugars by a promiscuous UDP-sugar pyrophosphorylase from Arabidopsis thaliana (AtUSP) |
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