Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis
a-d-Galactose 1-phosphate (aGal1P) is an important building block for the synthesis of nucleotide sugars that are substrates for glycosyltransferases. We have previously reported the creation of novel lactose phosphorylase enzymes that are useful for the synthesis of aGal1P from the cheap and abunda...
Saved in:
Published in: | Biotechnology letters 2009-12, Vol.31 (12), p.1873-1877 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | eng |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
recordid |
cdi_proquest_miscellaneous_36344635 |
---|---|
title |
Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis |
format |
Article |
creator |
Groeve, Manu RM Depreitere, Veerle Desmet, Tom Soetaert, Wim |
subjects |
Biotechnology Chemical synthesis Chromatography Enzymes Escherichia coli Ethyl alcohol Lactose Nucleotides Phosphorylases Precipitation Synthesis |
ispartof |
Biotechnology letters, 2009-12, Vol.31 (12), p.1873-1877 |
description |
a-d-Galactose 1-phosphate (aGal1P) is an important building block for the synthesis of nucleotide sugars that are substrates for glycosyltransferases. We have previously reported the creation of novel lactose phosphorylase enzymes that are useful for the synthesis of aGal1P from the cheap and abundant lactose. Here we describe the application of such a lactose phosphorylase in a production system using permeabilized Escherichia coli cells. After purification of the product from the reaction mixture by anion-exchange chromatography and ethanol precipitation, 9.5 grams of highly pure aGal1P were obtained from a 1l reaction volume. |
language |
eng |
source |
SpringerLink Contemporary |
identifier |
ISSN: 0141-5492 |
fulltext |
fulltext |
issn |
0141-5492 1573-6776 |
url |
http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-05-23T22%3A12%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Enzymatic%20production%20of%20%5Balpha%5D-d-galactose%201-phosphate%20by%20lactose%20phosphorolysis&rft.jtitle=Biotechnology%20letters&rft.au=Groeve,%20Manu%20RM&rft.date=2009-12-01&rft.volume=31&rft.issue=12&rft.spage=1873&rft.epage=1877&rft.pages=1873-1877&rft.issn=0141-5492&rft.eissn=1573-6776&rft_id=info:doi/10.1007/s10529-009-0087-1&rft_dat=%3Cproquest%3E1894451751%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p1225-b33eaa52fc1678ab0d9abd0ae38f1370a2aa2e3ac69fca726cf76aca9451fd293%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=211498400&rft_id=info:pmid/ |
container_title |
Biotechnology letters |
container_volume |
31 |
container_issue |
12 |
container_start_page |
1873 |
container_end_page |
1877 |
fullrecord |
<record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_36344635</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1894451751</sourcerecordid><originalsourceid>FETCH-LOGICAL-p1225-b33eaa52fc1678ab0d9abd0ae38f1370a2aa2e3ac69fca726cf76aca9451fd293</originalsourceid><addsrcrecordid>eNqFj01Lw0AQQBdRsFZ_gLfgQbys7uxn9iilVaEggp5EymSza1PSbOwmh_rrTalePOhhGHg8HjOEnAO7BsbMTQKmuKWM7SY3FA7ICJQRVBujD8mIgQSqpOXH5CSlFRtEw8yIPE2bz-0au8pl7SaWveuq2GQxZK9Yt0t8oyV9xxpdF5PPgLbLmAbc-azYZj94D-Mm1ttUpVNyFLBO_ux7j8nLbPo8uafzx7uHye2ctsC5ooUQHlHx4ECbHAtWWixKhl7kAYRhyBG5F-i0DQ4N1y4YjQ6tVBBKbsWYXO67w90fvU_dYl0l5-saGx_7tBBaSKmF-lfkwJWScle8-lMEnatcSKv0oF78Ulex3zTDv0MOpM0lY-ILcnZ7fg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><isCDI>true</isCDI><recordtype>article</recordtype><pqid>211498400</pqid></control><display><type>article</type><title>Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis</title><source>SpringerLink Contemporary</source><creator>Groeve, Manu RM ; Depreitere, Veerle ; Desmet, Tom ; Soetaert, Wim</creator><creatorcontrib>Groeve, Manu RM ; Depreitere, Veerle ; Desmet, Tom ; Soetaert, Wim</creatorcontrib><description>a-d-Galactose 1-phosphate (aGal1P) is an important building block for the synthesis of nucleotide sugars that are substrates for glycosyltransferases. We have previously reported the creation of novel lactose phosphorylase enzymes that are useful for the synthesis of aGal1P from the cheap and abundant lactose. Here we describe the application of such a lactose phosphorylase in a production system using permeabilized Escherichia coli cells. After purification of the product from the reaction mixture by anion-exchange chromatography and ethanol precipitation, 9.5 grams of highly pure aGal1P were obtained from a 1l reaction volume.</description><identifier>ISSN: 0141-5492</identifier><identifier>EISSN: 1573-6776</identifier><identifier>DOI: 10.1007/s10529-009-0087-1</identifier><language>eng</language><publisher>Dordrecht: Springer Nature B.V</publisher><subject>Biotechnology ; Chemical synthesis ; Chromatography ; Enzymes ; Escherichia coli ; Ethyl alcohol ; Lactose ; Nucleotides ; Phosphorylases ; Precipitation ; Synthesis</subject><ispartof>Biotechnology letters, 2009-12, Vol.31 (12), p.1873-1877</ispartof><rights>Springer Science+Business Media B.V. 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,787,791,27985,27986</link.rule.ids></links><search><creatorcontrib>Groeve, Manu RM</creatorcontrib><creatorcontrib>Depreitere, Veerle</creatorcontrib><creatorcontrib>Desmet, Tom</creatorcontrib><creatorcontrib>Soetaert, Wim</creatorcontrib><title>Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis</title><title>Biotechnology letters</title><description>a-d-Galactose 1-phosphate (aGal1P) is an important building block for the synthesis of nucleotide sugars that are substrates for glycosyltransferases. We have previously reported the creation of novel lactose phosphorylase enzymes that are useful for the synthesis of aGal1P from the cheap and abundant lactose. Here we describe the application of such a lactose phosphorylase in a production system using permeabilized Escherichia coli cells. After purification of the product from the reaction mixture by anion-exchange chromatography and ethanol precipitation, 9.5 grams of highly pure aGal1P were obtained from a 1l reaction volume.</description><subject>Biotechnology</subject><subject>Chemical synthesis</subject><subject>Chromatography</subject><subject>Enzymes</subject><subject>Escherichia coli</subject><subject>Ethyl alcohol</subject><subject>Lactose</subject><subject>Nucleotides</subject><subject>Phosphorylases</subject><subject>Precipitation</subject><subject>Synthesis</subject><issn>0141-5492</issn><issn>1573-6776</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFj01Lw0AQQBdRsFZ_gLfgQbys7uxn9iilVaEggp5EymSza1PSbOwmh_rrTalePOhhGHg8HjOEnAO7BsbMTQKmuKWM7SY3FA7ICJQRVBujD8mIgQSqpOXH5CSlFRtEw8yIPE2bz-0au8pl7SaWveuq2GQxZK9Yt0t8oyV9xxpdF5PPgLbLmAbc-azYZj94D-Mm1ttUpVNyFLBO_ux7j8nLbPo8uafzx7uHye2ctsC5ooUQHlHx4ECbHAtWWixKhl7kAYRhyBG5F-i0DQ4N1y4YjQ6tVBBKbsWYXO67w90fvU_dYl0l5-saGx_7tBBaSKmF-lfkwJWScle8-lMEnatcSKv0oF78Ulex3zTDv0MOpM0lY-ILcnZ7fg</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Groeve, Manu RM</creator><creator>Depreitere, Veerle</creator><creator>Desmet, Tom</creator><creator>Soetaert, Wim</creator><general>Springer Nature B.V</general><scope>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TB</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7QO</scope></search><sort><creationdate>20091201</creationdate><title>Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis</title><author>Groeve, Manu RM ; Depreitere, Veerle ; Desmet, Tom ; Soetaert, Wim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1225-b33eaa52fc1678ab0d9abd0ae38f1370a2aa2e3ac69fca726cf76aca9451fd293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biotechnology</topic><topic>Chemical synthesis</topic><topic>Chromatography</topic><topic>Enzymes</topic><topic>Escherichia coli</topic><topic>Ethyl alcohol</topic><topic>Lactose</topic><topic>Nucleotides</topic><topic>Phosphorylases</topic><topic>Precipitation</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Groeve, Manu RM</creatorcontrib><creatorcontrib>Depreitere, Veerle</creatorcontrib><creatorcontrib>Desmet, Tom</creatorcontrib><creatorcontrib>Soetaert, Wim</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Biotechnology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Groeve, Manu RM</au><au>Depreitere, Veerle</au><au>Desmet, Tom</au><au>Soetaert, Wim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic production of [alpha]-d-galactose 1-phosphate by lactose phosphorolysis</atitle><jtitle>Biotechnology letters</jtitle><date>2009-12-01</date><risdate>2009</risdate><volume>31</volume><issue>12</issue><spage>1873</spage><epage>1877</epage><pages>1873-1877</pages><issn>0141-5492</issn><eissn>1573-6776</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><notes>ObjectType-Article-2</notes><notes>ObjectType-Feature-1</notes><abstract>a-d-Galactose 1-phosphate (aGal1P) is an important building block for the synthesis of nucleotide sugars that are substrates for glycosyltransferases. We have previously reported the creation of novel lactose phosphorylase enzymes that are useful for the synthesis of aGal1P from the cheap and abundant lactose. Here we describe the application of such a lactose phosphorylase in a production system using permeabilized Escherichia coli cells. After purification of the product from the reaction mixture by anion-exchange chromatography and ethanol precipitation, 9.5 grams of highly pure aGal1P were obtained from a 1l reaction volume.</abstract><cop>Dordrecht</cop><pub>Springer Nature B.V</pub><doi>10.1007/s10529-009-0087-1</doi></addata></record> |