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Recruiting a new substrate for triacylglycerol synthesis in plants: the monoacylglycerol acyltransferase pathway
Monoacylglycerol acyltransferases (MGATs) are predominantly associated with lipid absorption and resynthesis in the animal intestine where they catalyse the first step in the monoacylglycerol (MAG) pathway by acylating MAG to form diacylglycerol (DAG). Typical plant triacylglycerol (TAG) biosynthesi...
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Published in: | PloS one 2012-04, Vol.7 (4), p.e35214-e35214 |
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description | Monoacylglycerol acyltransferases (MGATs) are predominantly associated with lipid absorption and resynthesis in the animal intestine where they catalyse the first step in the monoacylglycerol (MAG) pathway by acylating MAG to form diacylglycerol (DAG). Typical plant triacylglycerol (TAG) biosynthesis routes such as the Kennedy pathway do not include an MGAT step. Rather, DAG and TAG are synthesised de novo from glycerol-3-phosphate (G-3-P) by a series of three subsequent acylation reactions although a complex interplay with membrane lipids exists.
We demonstrate that heterologous expression of a mouse MGAT acyltransferase in Nicotiana benthamiana significantly increases TAG accumulation in vegetative tissues despite the low levels of endogenous MAG substrate available. In addition, DAG produced by this acyltransferase can serve as a substrate for both native and coexpressed diacylglycerol acyltransferases (DGAT). Finally, we show that the Arabidopsis thaliana GPAT4 acyltransferase can produce MAG in Saccharomyces cerevisiae using oleoyl-CoA as the acyl-donor.
This study demonstrates the concept of a new method of increasing oil content in vegetative tissues by using MAG as a substrate for TAG biosynthesis. Based on in vitro yeast assays and expression results in N. benthamiana, we propose that co-expression of a MAG synthesising enzyme such as A. thaliana GPAT4 and a MGAT or bifunctional M/DGAT can result in DAG and TAG synthesis from G-3-P via a route that is independent and complementary to the endogenous Kennedy pathway and other TAG synthesis routes. |
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We demonstrate that heterologous expression of a mouse MGAT acyltransferase in Nicotiana benthamiana significantly increases TAG accumulation in vegetative tissues despite the low levels of endogenous MAG substrate available. In addition, DAG produced by this acyltransferase can serve as a substrate for both native and coexpressed diacylglycerol acyltransferases (DGAT). Finally, we show that the Arabidopsis thaliana GPAT4 acyltransferase can produce MAG in Saccharomyces cerevisiae using oleoyl-CoA as the acyl-donor.
This study demonstrates the concept of a new method of increasing oil content in vegetative tissues by using MAG as a substrate for TAG biosynthesis. Based on in vitro yeast assays and expression results in N. benthamiana, we propose that co-expression of a MAG synthesising enzyme such as A. thaliana GPAT4 and a MGAT or bifunctional M/DGAT can result in DAG and TAG synthesis from G-3-P via a route that is independent and complementary to the endogenous Kennedy pathway and other TAG synthesis routes.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0035214</identifier><identifier>PMID: 22523576</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acylation ; Acyltransferase ; Acyltransferases - metabolism ; Agriculture ; Animals ; Arabidopsis ; Arabidopsis - metabolism ; Arabidopsis thaliana ; Baking yeast ; Bioaccumulation ; Biology ; Biosynthesis ; Carthamus tinctorius ; Diacylglycerol O-acyltransferase ; Diacylglycerol O-Acyltransferase - metabolism ; Diglycerides ; Enzymes ; Fatty acids ; Food ; Futures ; Genes ; Glycerol ; Glycerol-3-phosphate ; Glycerol-3-Phosphate O-Acyltransferase - metabolism ; Glycerophosphates - metabolism ; Hyperglycemia ; Insulin resistance ; Intestine ; Kinases ; Lipids ; Membrane lipids ; Metabolic Networks and Pathways ; Mice ; Monoglycerides - metabolism ; Nicotiana - enzymology ; Phosphatase ; Phosphates ; Plants (botany) ; Rodents ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - enzymology ; Seeds ; Tissues ; Transferases ; Trends ; Triglycerides ; Triglycerides - biosynthesis</subject><ispartof>PloS one, 2012-04, Vol.7 (4), p.e35214-e35214</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Petrie et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Petrie et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6074-e6981a387a5da0ff0b54b5b6f560cc6cfb4eb183bcfc997bd9e030f6909c18c33</citedby><cites>FETCH-LOGICAL-c6074-e6981a387a5da0ff0b54b5b6f560cc6cfb4eb183bcfc997bd9e030f6909c18c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1324573746/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1324573746?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22523576$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bonaventure, Gustavo</contributor><creatorcontrib>Petrie, James R</creatorcontrib><creatorcontrib>Vanhercke, Thomas</creatorcontrib><creatorcontrib>Shrestha, Pushkar</creatorcontrib><creatorcontrib>El Tahchy, Anna</creatorcontrib><creatorcontrib>White, Adam</creatorcontrib><creatorcontrib>Zhou, Xue-Rong</creatorcontrib><creatorcontrib>Liu, Qing</creatorcontrib><creatorcontrib>Mansour, Maged P</creatorcontrib><creatorcontrib>Nichols, Peter D</creatorcontrib><creatorcontrib>Singh, Surinder P</creatorcontrib><title>Recruiting a new substrate for triacylglycerol synthesis in plants: the monoacylglycerol acyltransferase pathway</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Monoacylglycerol acyltransferases (MGATs) are predominantly associated with lipid absorption and resynthesis in the animal intestine where they catalyse the first step in the monoacylglycerol (MAG) pathway by acylating MAG to form diacylglycerol (DAG). Typical plant triacylglycerol (TAG) biosynthesis routes such as the Kennedy pathway do not include an MGAT step. Rather, DAG and TAG are synthesised de novo from glycerol-3-phosphate (G-3-P) by a series of three subsequent acylation reactions although a complex interplay with membrane lipids exists.
We demonstrate that heterologous expression of a mouse MGAT acyltransferase in Nicotiana benthamiana significantly increases TAG accumulation in vegetative tissues despite the low levels of endogenous MAG substrate available. In addition, DAG produced by this acyltransferase can serve as a substrate for both native and coexpressed diacylglycerol acyltransferases (DGAT). Finally, we show that the Arabidopsis thaliana GPAT4 acyltransferase can produce MAG in Saccharomyces cerevisiae using oleoyl-CoA as the acyl-donor.
This study demonstrates the concept of a new method of increasing oil content in vegetative tissues by using MAG as a substrate for TAG biosynthesis. Based on in vitro yeast assays and expression results in N. benthamiana, we propose that co-expression of a MAG synthesising enzyme such as A. thaliana GPAT4 and a MGAT or bifunctional M/DGAT can result in DAG and TAG synthesis from G-3-P via a route that is independent and complementary to the endogenous Kennedy pathway and other TAG synthesis routes.</description><subject>Acylation</subject><subject>Acyltransferase</subject><subject>Acyltransferases - metabolism</subject><subject>Agriculture</subject><subject>Animals</subject><subject>Arabidopsis</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Baking yeast</subject><subject>Bioaccumulation</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Carthamus tinctorius</subject><subject>Diacylglycerol O-acyltransferase</subject><subject>Diacylglycerol O-Acyltransferase - metabolism</subject><subject>Diglycerides</subject><subject>Enzymes</subject><subject>Fatty acids</subject><subject>Food</subject><subject>Futures</subject><subject>Genes</subject><subject>Glycerol</subject><subject>Glycerol-3-phosphate</subject><subject>Glycerol-3-Phosphate O-Acyltransferase - 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Typical plant triacylglycerol (TAG) biosynthesis routes such as the Kennedy pathway do not include an MGAT step. Rather, DAG and TAG are synthesised de novo from glycerol-3-phosphate (G-3-P) by a series of three subsequent acylation reactions although a complex interplay with membrane lipids exists.
We demonstrate that heterologous expression of a mouse MGAT acyltransferase in Nicotiana benthamiana significantly increases TAG accumulation in vegetative tissues despite the low levels of endogenous MAG substrate available. In addition, DAG produced by this acyltransferase can serve as a substrate for both native and coexpressed diacylglycerol acyltransferases (DGAT). Finally, we show that the Arabidopsis thaliana GPAT4 acyltransferase can produce MAG in Saccharomyces cerevisiae using oleoyl-CoA as the acyl-donor.
This study demonstrates the concept of a new method of increasing oil content in vegetative tissues by using MAG as a substrate for TAG biosynthesis. Based on in vitro yeast assays and expression results in N. benthamiana, we propose that co-expression of a MAG synthesising enzyme such as A. thaliana GPAT4 and a MGAT or bifunctional M/DGAT can result in DAG and TAG synthesis from G-3-P via a route that is independent and complementary to the endogenous Kennedy pathway and other TAG synthesis routes.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22523576</pmid><doi>10.1371/journal.pone.0035214</doi><tpages>e35214</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acylation Acyltransferase Acyltransferases - metabolism Agriculture Animals Arabidopsis Arabidopsis - metabolism Arabidopsis thaliana Baking yeast Bioaccumulation Biology Biosynthesis Carthamus tinctorius Diacylglycerol O-acyltransferase Diacylglycerol O-Acyltransferase - metabolism Diglycerides Enzymes Fatty acids Food Futures Genes Glycerol Glycerol-3-phosphate Glycerol-3-Phosphate O-Acyltransferase - metabolism Glycerophosphates - metabolism Hyperglycemia Insulin resistance Intestine Kinases Lipids Membrane lipids Metabolic Networks and Pathways Mice Monoglycerides - metabolism Nicotiana - enzymology Phosphatase Phosphates Plants (botany) Rodents Saccharomyces cerevisiae Saccharomyces cerevisiae - enzymology Seeds Tissues Transferases Trends Triglycerides Triglycerides - biosynthesis |
title | Recruiting a new substrate for triacylglycerol synthesis in plants: the monoacylglycerol acyltransferase pathway |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T05%3A12%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Recruiting%20a%20new%20substrate%20for%20triacylglycerol%20synthesis%20in%20plants:%20the%20monoacylglycerol%20acyltransferase%20pathway&rft.jtitle=PloS%20one&rft.au=Petrie,%20James%20R&rft.date=2012-04-16&rft.volume=7&rft.issue=4&rft.spage=e35214&rft.epage=e35214&rft.pages=e35214-e35214&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0035214&rft_dat=%3Cgale_plos_%3EA477082455%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c6074-e6981a387a5da0ff0b54b5b6f560cc6cfb4eb183bcfc997bd9e030f6909c18c33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1324573746&rft_id=info:pmid/22523576&rft_galeid=A477082455&rfr_iscdi=true |