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Targeting hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase for lignin modification in Brachypodium distachyon
Hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase (HCT) is a central enzyme of the so-called "esters" pathway to monolignols. As originally envisioned, HCT functions twice in this pathway, to form coumaroyl shikimate and then, in the "reverse" direction, to convert caf...
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Published in: | Biotechnology for biofuels 2021-02, Vol.14 (1), p.50-50, Article 50 |
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description | Hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase (HCT) is a central enzyme of the so-called "esters" pathway to monolignols. As originally envisioned, HCT functions twice in this pathway, to form coumaroyl shikimate and then, in the "reverse" direction, to convert caffeoyl shikimate to caffeoyl CoA. The discovery of a caffeoyl shikimate esterase (CSE) that forms caffeic acid directly from caffeoyl shikimate calls into question the need for the reverse HCT reaction in lignin biosynthesis. Loss of function of HCT gives severe growth phenotypes in several dicot plants, but less so in some monocots, questioning whether this enzyme, and therefore the shikimate shunt, plays the same role in both monocots and dicots. The model grass Brachypodium distachyon has two HCT genes, but lacks a classical CSE gene. This study was therefore conducted to evaluate the utility of HCT as a target for lignin modification in a species with an "incomplete" shikimate shunt.
The kinetic properties of recombinant B. distachyon HCTs were compared with those from Arabidopsis thaliana, Medicago truncatula, and Panicum virgatum (switchgrass) for both the forward and reverse reactions. Along with two M. truncatula HCTs, B. distachyon HCT2 had the least kinetically unfavorable reverse HCT reaction, and this enzyme is induced when HCT1 is down-regulated. Down regulation of B. distachyon HCT1, or co-down-regulation of HCT1 and HCT2, by RNA interference led to reduced lignin levels, with only modest changes in lignin composition and molecular weight.
Down-regulation of HCT1, or co-down-regulation of both HCT genes, in B. distachyon results in less extensive changes in lignin content/composition and cell wall structure than observed following HCT down-regulation in dicots, with little negative impact on biomass yield. Nevertheless, HCT down-regulation leads to significant improvements in biomass saccharification efficiency, making this gene a preferred target for biotechnological improvement of grasses for bioprocessing. |
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The kinetic properties of recombinant B. distachyon HCTs were compared with those from Arabidopsis thaliana, Medicago truncatula, and Panicum virgatum (switchgrass) for both the forward and reverse reactions. Along with two M. truncatula HCTs, B. distachyon HCT2 had the least kinetically unfavorable reverse HCT reaction, and this enzyme is induced when HCT1 is down-regulated. Down regulation of B. distachyon HCT1, or co-down-regulation of HCT1 and HCT2, by RNA interference led to reduced lignin levels, with only modest changes in lignin composition and molecular weight.
Down-regulation of HCT1, or co-down-regulation of both HCT genes, in B. distachyon results in less extensive changes in lignin content/composition and cell wall structure than observed following HCT down-regulation in dicots, with little negative impact on biomass yield. Nevertheless, HCT down-regulation leads to significant improvements in biomass saccharification efficiency, making this gene a preferred target for biotechnological improvement of grasses for bioprocessing.</description><identifier>ISSN: 1754-6834</identifier><identifier>EISSN: 1754-6834</identifier><identifier>DOI: 10.1186/s13068-021-01905-1</identifier><identifier>PMID: 33640016</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>09 BIOMASS FUELS ; Alfalfa ; BASIC BIOLOGICAL SCIENCES ; Biomass ; Bioprocessing ; Biosynthesis ; Brachypodium distachyon ; Caffeic acid ; Cell walls ; Cloning ; Coenzymes ; Composition ; Enzymes ; Esterase ; Esters ; Gene expression ; Gene regulation ; Genes ; Grasses ; Lignin ; Lignin modifcation ; Lignin modification ; Magnoliopsida ; Methods ; Molecular weight ; Monocot ; NMR analysis ; Panicum virgatum ; Phenotypes ; Phenylpropanoid biosynthesis ; Phylogenetics ; Physiological aspects ; Proteins ; Questions ; RNA interference ; RNA-mediated interference ; Saccharifcation efciency ; Saccharification ; Saccharification efficiency ; Transferases</subject><ispartof>Biotechnology for biofuels, 2021-02, Vol.14 (1), p.50-50, Article 50</ispartof><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c596t-e62d19fbd0408b57b737239a79ee769a30c5052f8a150bf0d27886daddd21bde3</citedby><cites>FETCH-LOGICAL-c596t-e62d19fbd0408b57b737239a79ee769a30c5052f8a150bf0d27886daddd21bde3</cites><orcidid>0000-0001-8393-9408 ; 0000000183939408</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913460/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2502905190?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33640016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1768106$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Serrani-Yarce, Juan Carlos</creatorcontrib><creatorcontrib>Escamilla-Trevino, Luis</creatorcontrib><creatorcontrib>Barros, Jaime</creatorcontrib><creatorcontrib>Gallego-Giraldo, Lina</creatorcontrib><creatorcontrib>Pu, Yunqiao</creatorcontrib><creatorcontrib>Ragauskas, Art</creatorcontrib><creatorcontrib>Dixon, Richard A</creatorcontrib><creatorcontrib>Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>Targeting hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase for lignin modification in Brachypodium distachyon</title><title>Biotechnology for biofuels</title><addtitle>Biotechnol Biofuels</addtitle><description>Hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase (HCT) is a central enzyme of the so-called "esters" pathway to monolignols. As originally envisioned, HCT functions twice in this pathway, to form coumaroyl shikimate and then, in the "reverse" direction, to convert caffeoyl shikimate to caffeoyl CoA. The discovery of a caffeoyl shikimate esterase (CSE) that forms caffeic acid directly from caffeoyl shikimate calls into question the need for the reverse HCT reaction in lignin biosynthesis. Loss of function of HCT gives severe growth phenotypes in several dicot plants, but less so in some monocots, questioning whether this enzyme, and therefore the shikimate shunt, plays the same role in both monocots and dicots. The model grass Brachypodium distachyon has two HCT genes, but lacks a classical CSE gene. This study was therefore conducted to evaluate the utility of HCT as a target for lignin modification in a species with an "incomplete" shikimate shunt.
The kinetic properties of recombinant B. distachyon HCTs were compared with those from Arabidopsis thaliana, Medicago truncatula, and Panicum virgatum (switchgrass) for both the forward and reverse reactions. Along with two M. truncatula HCTs, B. distachyon HCT2 had the least kinetically unfavorable reverse HCT reaction, and this enzyme is induced when HCT1 is down-regulated. Down regulation of B. distachyon HCT1, or co-down-regulation of HCT1 and HCT2, by RNA interference led to reduced lignin levels, with only modest changes in lignin composition and molecular weight.
Down-regulation of HCT1, or co-down-regulation of both HCT genes, in B. distachyon results in less extensive changes in lignin content/composition and cell wall structure than observed following HCT down-regulation in dicots, with little negative impact on biomass yield. Nevertheless, HCT down-regulation leads to significant improvements in biomass saccharification efficiency, making this gene a preferred target for biotechnological improvement of grasses for bioprocessing.</description><subject>09 BIOMASS FUELS</subject><subject>Alfalfa</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Biomass</subject><subject>Bioprocessing</subject><subject>Biosynthesis</subject><subject>Brachypodium distachyon</subject><subject>Caffeic acid</subject><subject>Cell walls</subject><subject>Cloning</subject><subject>Coenzymes</subject><subject>Composition</subject><subject>Enzymes</subject><subject>Esterase</subject><subject>Esters</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>Genes</subject><subject>Grasses</subject><subject>Lignin</subject><subject>Lignin modifcation</subject><subject>Lignin modification</subject><subject>Magnoliopsida</subject><subject>Methods</subject><subject>Molecular 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hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase for lignin modification in Brachypodium distachyon</title><author>Serrani-Yarce, Juan Carlos ; Escamilla-Trevino, Luis ; Barros, Jaime ; Gallego-Giraldo, Lina ; Pu, Yunqiao ; Ragauskas, Art ; Dixon, Richard A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c596t-e62d19fbd0408b57b737239a79ee769a30c5052f8a150bf0d27886daddd21bde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>09 BIOMASS FUELS</topic><topic>Alfalfa</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biomass</topic><topic>Bioprocessing</topic><topic>Biosynthesis</topic><topic>Brachypodium distachyon</topic><topic>Caffeic acid</topic><topic>Cell walls</topic><topic>Cloning</topic><topic>Coenzymes</topic><topic>Composition</topic><topic>Enzymes</topic><topic>Esterase</topic><topic>Esters</topic><topic>Gene expression</topic><topic>Gene 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Yunqiao</creatorcontrib><creatorcontrib>Ragauskas, Art</creatorcontrib><creatorcontrib>Dixon, Richard A</creatorcontrib><creatorcontrib>Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Environment Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital 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Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biotechnology for biofuels</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Serrani-Yarce, Juan Carlos</au><au>Escamilla-Trevino, Luis</au><au>Barros, Jaime</au><au>Gallego-Giraldo, Lina</au><au>Pu, Yunqiao</au><au>Ragauskas, Art</au><au>Dixon, Richard A</au><aucorp>Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeting hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase for lignin modification in Brachypodium distachyon</atitle><jtitle>Biotechnology for biofuels</jtitle><addtitle>Biotechnol Biofuels</addtitle><date>2021-02-27</date><risdate>2021</risdate><volume>14</volume><issue>1</issue><spage>50</spage><epage>50</epage><pages>50-50</pages><artnum>50</artnum><issn>1754-6834</issn><eissn>1754-6834</eissn><abstract>Hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase (HCT) is a central enzyme of the so-called "esters" pathway to monolignols. As originally envisioned, HCT functions twice in this pathway, to form coumaroyl shikimate and then, in the "reverse" direction, to convert caffeoyl shikimate to caffeoyl CoA. The discovery of a caffeoyl shikimate esterase (CSE) that forms caffeic acid directly from caffeoyl shikimate calls into question the need for the reverse HCT reaction in lignin biosynthesis. Loss of function of HCT gives severe growth phenotypes in several dicot plants, but less so in some monocots, questioning whether this enzyme, and therefore the shikimate shunt, plays the same role in both monocots and dicots. The model grass Brachypodium distachyon has two HCT genes, but lacks a classical CSE gene. This study was therefore conducted to evaluate the utility of HCT as a target for lignin modification in a species with an "incomplete" shikimate shunt.
The kinetic properties of recombinant B. distachyon HCTs were compared with those from Arabidopsis thaliana, Medicago truncatula, and Panicum virgatum (switchgrass) for both the forward and reverse reactions. Along with two M. truncatula HCTs, B. distachyon HCT2 had the least kinetically unfavorable reverse HCT reaction, and this enzyme is induced when HCT1 is down-regulated. Down regulation of B. distachyon HCT1, or co-down-regulation of HCT1 and HCT2, by RNA interference led to reduced lignin levels, with only modest changes in lignin composition and molecular weight.
Down-regulation of HCT1, or co-down-regulation of both HCT genes, in B. distachyon results in less extensive changes in lignin content/composition and cell wall structure than observed following HCT down-regulation in dicots, with little negative impact on biomass yield. Nevertheless, HCT down-regulation leads to significant improvements in biomass saccharification efficiency, making this gene a preferred target for biotechnological improvement of grasses for bioprocessing.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>33640016</pmid><doi>10.1186/s13068-021-01905-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8393-9408</orcidid><orcidid>https://orcid.org/0000000183939408</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 09 BIOMASS FUELS Alfalfa BASIC BIOLOGICAL SCIENCES Biomass Bioprocessing Biosynthesis Brachypodium distachyon Caffeic acid Cell walls Cloning Coenzymes Composition Enzymes Esterase Esters Gene expression Gene regulation Genes Grasses Lignin Lignin modifcation Lignin modification Magnoliopsida Methods Molecular weight Monocot NMR analysis Panicum virgatum Phenotypes Phenylpropanoid biosynthesis Phylogenetics Physiological aspects Proteins Questions RNA interference RNA-mediated interference Saccharifcation efciency Saccharification Saccharification efficiency Transferases |
title | Targeting hydroxycinnamoyl CoA: shikimate hydroxycinnamoyl transferase for lignin modification in Brachypodium distachyon |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T01%3A57%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Targeting%20hydroxycinnamoyl%20CoA:%20shikimate%20hydroxycinnamoyl%20transferase%20for%20lignin%20modification%20in%20Brachypodium%20distachyon&rft.jtitle=Biotechnology%20for%20biofuels&rft.au=Serrani-Yarce,%20Juan%20Carlos&rft.aucorp=Oak%20Ridge%20National%20Laboratory%20(ORNL),%20Oak%20Ridge,%20TN%20(United%20States)&rft.date=2021-02-27&rft.volume=14&rft.issue=1&rft.spage=50&rft.epage=50&rft.pages=50-50&rft.artnum=50&rft.issn=1754-6834&rft.eissn=1754-6834&rft_id=info:doi/10.1186/s13068-021-01905-1&rft_dat=%3Cgale_doaj_%3EA653674354%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c596t-e62d19fbd0408b57b737239a79ee769a30c5052f8a150bf0d27886daddd21bde3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2502905190&rft_id=info:pmid/33640016&rft_galeid=A653674354&rfr_iscdi=true |