Loading…
Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase
Chimeric polyhydroxyalkanoate synthase PhaCAR is characterized by the capacity to incorporate unusual glycolate (GL) units and spontaneously synthesize block copolymers. The GL and 3-hydroxybutyrate (3HB) copolymer synthesized by PhaCAR is a random-homo block copolymer, poly(GL-ran-3HB)-b-poly(3HB)....
Saved in:
Published in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2022-01, Vol.86 (2), p.217-223 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03 |
---|---|
cites | cdi_FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03 |
container_end_page | 223 |
container_issue | 2 |
container_start_page | 217 |
container_title | Bioscience, biotechnology, and biochemistry |
container_volume | 86 |
creator | Tomita, Hiroya Satoh, Keigo Nomura, Christopher T Matsumoto, Ken'ichiro |
description | Chimeric polyhydroxyalkanoate synthase PhaCAR is characterized by the capacity to incorporate unusual glycolate (GL) units and spontaneously synthesize block copolymers. The GL and 3-hydroxybutyrate (3HB) copolymer synthesized by PhaCAR is a random-homo block copolymer, poly(GL-ran-3HB)-b-poly(3HB). In the present study, medium-chain-length 3-hydroxyhexanoate (3HHx) units were incorporated into this copolymer using PhaCAR for the first time. The coenzyme A (CoA) ligase from Pseudomonas oleovorans (AlkK) serves as a simple 3HHx-CoA supplying route in Escherichia coli from exogenously supplemented 3HHx. NMR analyses of the obtained polymers revealed that 3HHx units were randomly connected to 3HB units, whereas GL units were heterogeneously distributed. Therefore, the polymer is composed of 2 segments: P(3HB-co-3HHx) and P(GL-co-3HB-co-3HHx). The thermal and mechanical properties of the terpolymer indicate no contiguous P(3HB) segments in the material, consistent with the NMR results. Therefore, PhaCAR synthesized the novel block copolymer P(3HB-co-3HHx)-b-P(GL-co-3HB-co-3HHx), which is the first block polyhydroxyalkanoate copolymer comprising 2 copolymer segments. |
doi_str_mv | 10.1093/bbb/zbab198 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2599070719</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2599070719</sourcerecordid><originalsourceid>FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03</originalsourceid><addsrcrecordid>eNpdkc1uGyEUhVHUKEmTrLKvWLqqSMCMB7N0rPRHipRNsh4xzGWGlgEXZiSPn7UPUxy7UZUV6Ojwncs9CN0wesuo5Hd1Xd_talUzuTxBF4wXgpSyEB_-u5-jjyn9pJRKtmBn6DzryyUX9AL9ubchTX7oINmEg8Gb4KZZ6yYdnBqA6EA46aYmhu1Uj8MU34sdbJUPWf2MrccPSXcQre6swplgMWw3EVKyvsUJfo_gNZAI7Zjhe22fdgQp9-sAwq_zqARY-Qb30NixJ7pT1hMHvh06_BZ-eGM1Vto2ORD8buoBr7CzbQZcoVOjXILr43mJXr4-PK-_k8enbz_Wq0eiC14OpGyapS4Uk4KDmZemgHlZCDBaGEUlSMOp4twUUsjsoZQvAHTetpZmAcJQfolmB-4mhvzHNFS9TRqcUx7CmKr5QkoqqGAyW78crDqGlCKYahNtr-JUMVrt66xyndWxzuz-dASPdV7Em_dff_wvzgOkmw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2599070719</pqid></control><display><type>article</type><title>Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase</title><source>Oxford Journals Online</source><creator>Tomita, Hiroya ; Satoh, Keigo ; Nomura, Christopher T ; Matsumoto, Ken'ichiro</creator><creatorcontrib>Tomita, Hiroya ; Satoh, Keigo ; Nomura, Christopher T ; Matsumoto, Ken'ichiro</creatorcontrib><description>Chimeric polyhydroxyalkanoate synthase PhaCAR is characterized by the capacity to incorporate unusual glycolate (GL) units and spontaneously synthesize block copolymers. The GL and 3-hydroxybutyrate (3HB) copolymer synthesized by PhaCAR is a random-homo block copolymer, poly(GL-ran-3HB)-b-poly(3HB). In the present study, medium-chain-length 3-hydroxyhexanoate (3HHx) units were incorporated into this copolymer using PhaCAR for the first time. The coenzyme A (CoA) ligase from Pseudomonas oleovorans (AlkK) serves as a simple 3HHx-CoA supplying route in Escherichia coli from exogenously supplemented 3HHx. NMR analyses of the obtained polymers revealed that 3HHx units were randomly connected to 3HB units, whereas GL units were heterogeneously distributed. Therefore, the polymer is composed of 2 segments: P(3HB-co-3HHx) and P(GL-co-3HB-co-3HHx). The thermal and mechanical properties of the terpolymer indicate no contiguous P(3HB) segments in the material, consistent with the NMR results. Therefore, PhaCAR synthesized the novel block copolymer P(3HB-co-3HHx)-b-P(GL-co-3HB-co-3HHx), which is the first block polyhydroxyalkanoate copolymer comprising 2 copolymer segments.</description><identifier>ISSN: 1347-6947</identifier><identifier>EISSN: 1347-6947</identifier><identifier>DOI: 10.1093/bbb/zbab198</identifier><identifier>PMID: 34788370</identifier><language>eng</language><publisher>England</publisher><subject>3-Hydroxybutyric Acid - biosynthesis ; 3-Hydroxybutyric Acid - chemistry ; 3-Hydroxybutyric Acid - metabolism ; Acyltransferases - chemistry ; Acyltransferases - genetics ; Acyltransferases - metabolism ; Caproates - chemistry ; Caproates - metabolism ; Coenzyme A Ligases - chemistry ; Coenzyme A Ligases - genetics ; Coenzyme A Ligases - metabolism ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Magnetic Resonance Spectroscopy ; Polyhydroxybutyrates</subject><ispartof>Bioscience, biotechnology, and biochemistry, 2022-01, Vol.86 (2), p.217-223</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Japan Society for Bioscience, Biotechnology, and Agrochemistry.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03</citedby><cites>FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03</cites><orcidid>0000-0001-7967-921X</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/34788370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tomita, Hiroya</creatorcontrib><creatorcontrib>Satoh, Keigo</creatorcontrib><creatorcontrib>Nomura, Christopher T</creatorcontrib><creatorcontrib>Matsumoto, Ken'ichiro</creatorcontrib><title>Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>Chimeric polyhydroxyalkanoate synthase PhaCAR is characterized by the capacity to incorporate unusual glycolate (GL) units and spontaneously synthesize block copolymers. The GL and 3-hydroxybutyrate (3HB) copolymer synthesized by PhaCAR is a random-homo block copolymer, poly(GL-ran-3HB)-b-poly(3HB). In the present study, medium-chain-length 3-hydroxyhexanoate (3HHx) units were incorporated into this copolymer using PhaCAR for the first time. The coenzyme A (CoA) ligase from Pseudomonas oleovorans (AlkK) serves as a simple 3HHx-CoA supplying route in Escherichia coli from exogenously supplemented 3HHx. NMR analyses of the obtained polymers revealed that 3HHx units were randomly connected to 3HB units, whereas GL units were heterogeneously distributed. Therefore, the polymer is composed of 2 segments: P(3HB-co-3HHx) and P(GL-co-3HB-co-3HHx). The thermal and mechanical properties of the terpolymer indicate no contiguous P(3HB) segments in the material, consistent with the NMR results. Therefore, PhaCAR synthesized the novel block copolymer P(3HB-co-3HHx)-b-P(GL-co-3HB-co-3HHx), which is the first block polyhydroxyalkanoate copolymer comprising 2 copolymer segments.</description><subject>3-Hydroxybutyric Acid - biosynthesis</subject><subject>3-Hydroxybutyric Acid - chemistry</subject><subject>3-Hydroxybutyric Acid - metabolism</subject><subject>Acyltransferases - chemistry</subject><subject>Acyltransferases - genetics</subject><subject>Acyltransferases - metabolism</subject><subject>Caproates - chemistry</subject><subject>Caproates - metabolism</subject><subject>Coenzyme A Ligases - chemistry</subject><subject>Coenzyme A Ligases - genetics</subject><subject>Coenzyme A Ligases - metabolism</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Polyhydroxybutyrates</subject><issn>1347-6947</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkc1uGyEUhVHUKEmTrLKvWLqqSMCMB7N0rPRHipRNsh4xzGWGlgEXZiSPn7UPUxy7UZUV6Ojwncs9CN0wesuo5Hd1Xd_talUzuTxBF4wXgpSyEB_-u5-jjyn9pJRKtmBn6DzryyUX9AL9ubchTX7oINmEg8Gb4KZZ6yYdnBqA6EA46aYmhu1Uj8MU34sdbJUPWf2MrccPSXcQre6swplgMWw3EVKyvsUJfo_gNZAI7Zjhe22fdgQp9-sAwq_zqARY-Qb30NixJ7pT1hMHvh06_BZ-eGM1Vto2ORD8buoBr7CzbQZcoVOjXILr43mJXr4-PK-_k8enbz_Wq0eiC14OpGyapS4Uk4KDmZemgHlZCDBaGEUlSMOp4twUUsjsoZQvAHTetpZmAcJQfolmB-4mhvzHNFS9TRqcUx7CmKr5QkoqqGAyW78crDqGlCKYahNtr-JUMVrt66xyndWxzuz-dASPdV7Em_dff_wvzgOkmw</recordid><startdate>20220124</startdate><enddate>20220124</enddate><creator>Tomita, Hiroya</creator><creator>Satoh, Keigo</creator><creator>Nomura, Christopher T</creator><creator>Matsumoto, Ken'ichiro</creator><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><orcidid>https://orcid.org/0000-0001-7967-921X</orcidid></search><sort><creationdate>20220124</creationdate><title>Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase</title><author>Tomita, Hiroya ; Satoh, Keigo ; Nomura, Christopher T ; Matsumoto, Ken'ichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>3-Hydroxybutyric Acid - biosynthesis</topic><topic>3-Hydroxybutyric Acid - chemistry</topic><topic>3-Hydroxybutyric Acid - metabolism</topic><topic>Acyltransferases - chemistry</topic><topic>Acyltransferases - genetics</topic><topic>Acyltransferases - metabolism</topic><topic>Caproates - chemistry</topic><topic>Caproates - metabolism</topic><topic>Coenzyme A Ligases - chemistry</topic><topic>Coenzyme A Ligases - genetics</topic><topic>Coenzyme A Ligases - metabolism</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Polyhydroxybutyrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomita, Hiroya</creatorcontrib><creatorcontrib>Satoh, Keigo</creatorcontrib><creatorcontrib>Nomura, Christopher T</creatorcontrib><creatorcontrib>Matsumoto, Ken'ichiro</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>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomita, Hiroya</au><au>Satoh, Keigo</au><au>Nomura, Christopher T</au><au>Matsumoto, Ken'ichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase</atitle><jtitle>Bioscience, biotechnology, and biochemistry</jtitle><addtitle>Biosci Biotechnol Biochem</addtitle><date>2022-01-24</date><risdate>2022</risdate><volume>86</volume><issue>2</issue><spage>217</spage><epage>223</epage><pages>217-223</pages><issn>1347-6947</issn><eissn>1347-6947</eissn><abstract>Chimeric polyhydroxyalkanoate synthase PhaCAR is characterized by the capacity to incorporate unusual glycolate (GL) units and spontaneously synthesize block copolymers. The GL and 3-hydroxybutyrate (3HB) copolymer synthesized by PhaCAR is a random-homo block copolymer, poly(GL-ran-3HB)-b-poly(3HB). In the present study, medium-chain-length 3-hydroxyhexanoate (3HHx) units were incorporated into this copolymer using PhaCAR for the first time. The coenzyme A (CoA) ligase from Pseudomonas oleovorans (AlkK) serves as a simple 3HHx-CoA supplying route in Escherichia coli from exogenously supplemented 3HHx. NMR analyses of the obtained polymers revealed that 3HHx units were randomly connected to 3HB units, whereas GL units were heterogeneously distributed. Therefore, the polymer is composed of 2 segments: P(3HB-co-3HHx) and P(GL-co-3HB-co-3HHx). The thermal and mechanical properties of the terpolymer indicate no contiguous P(3HB) segments in the material, consistent with the NMR results. Therefore, PhaCAR synthesized the novel block copolymer P(3HB-co-3HHx)-b-P(GL-co-3HB-co-3HHx), which is the first block polyhydroxyalkanoate copolymer comprising 2 copolymer segments.</abstract><cop>England</cop><pmid>34788370</pmid><doi>10.1093/bbb/zbab198</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7967-921X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1347-6947 |
ispartof | Bioscience, biotechnology, and biochemistry, 2022-01, Vol.86 (2), p.217-223 |
issn | 1347-6947 1347-6947 |
language | eng |
recordid | cdi_proquest_miscellaneous_2599070719 |
source | Oxford Journals Online |
subjects | 3-Hydroxybutyric Acid - biosynthesis 3-Hydroxybutyric Acid - chemistry 3-Hydroxybutyric Acid - metabolism Acyltransferases - chemistry Acyltransferases - genetics Acyltransferases - metabolism Caproates - chemistry Caproates - metabolism Coenzyme A Ligases - chemistry Coenzyme A Ligases - genetics Coenzyme A Ligases - metabolism Escherichia coli - genetics Escherichia coli - metabolism Magnetic Resonance Spectroscopy Polyhydroxybutyrates |
title | Biosynthesis of poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate) in Escherichia coli expressing sequence-regulating polyhydroxyalkanoate synthase and medium-chain-length 3-hydroxyalkanoic acid coenzyme A ligase |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T11%3A00%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biosynthesis%20of%20poly(glycolate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate)%20in%20Escherichia%20coli%20expressing%20sequence-regulating%20polyhydroxyalkanoate%20synthase%20and%20medium-chain-length%203-hydroxyalkanoic%20acid%20coenzyme%20A%20ligase&rft.jtitle=Bioscience,%20biotechnology,%20and%20biochemistry&rft.au=Tomita,%20Hiroya&rft.date=2022-01-24&rft.volume=86&rft.issue=2&rft.spage=217&rft.epage=223&rft.pages=217-223&rft.issn=1347-6947&rft.eissn=1347-6947&rft_id=info:doi/10.1093/bbb/zbab198&rft_dat=%3Cproquest_cross%3E2599070719%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c436t-6dd8c4a1973ef26f4e2647efc7fa09e9f30a33f49791970035eec198c9f5e7f03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2599070719&rft_id=info:pmid/34788370&rfr_iscdi=true |