Phospholipid:Diacylglycerol Acyltransferase Is a Multifunctional Enzyme Involved in Membrane Lipid Turnover and Degradation While Synthesizing Triacylglycerol in the Unicellular Green Microalga Chlamydomonas reinhardtii
| dc.contributor.author | Yoon, Kangsup | |
| dc.contributor.author | Han, Danxiang | |
| dc.contributor.author | Li, Yantao | |
| dc.contributor.author | Sommerfeld, Milton | |
| dc.contributor.author | Hu, Qiang | |
| dc.date.accessioned | 2025-07-09T17:56:03Z | |
| dc.date.issued | 2012-09-01 | |
| dc.description.abstract | Many unicellular microalgae produce large amounts (∼20 to 50% of cell dry weight) of triacylglycerols (TAGs) under stress (e.g., nutrient starvation and high light), but the synthesis and physiological role of TAG are poorly understood. We present detailed genetic, biochemical, functional, and physiological analyses of phospholipid:diacylglycerol acyltransferase (PDAT) in the green microalga Chlamydomonas reinhardtii, which catalyzes TAG synthesis via two pathways: transacylation of diacylglycerol (DAG) with acyl groups from phospholipids and galactolipids and DAG:DAG transacylation. We demonstrate that PDAT also possesses acyl hydrolase activities using TAG, phospholipids, galactolipids, and cholesteryl esters as substrates. Artificial microRNA silencing of PDAT in C. reinhardtii alters the membrane lipid composition, reducing the maximum specific growth rate. The data suggest that PDAT-mediated membrane lipid turnover and TAG synthesis is essential for vigorous growth under favorable culture conditions and for membrane lipid degradation with concomitant production of TAG for survival under stress. The strong lipase activity of PDAT with broad substrate specificity suggests that this enzyme could be a potential biocatalyst for industrial lipid hydrolysis and conversion, particularly for biofuel production. | |
| dc.description.sponsorship | This work was supported by the U.S. Department of Energy (Grant DE-EE0003372) and by the Science Foundation of Arizona (Grant SRG 0438-09). | |
| dc.description.uri | https://pmc.ncbi.nlm.nih.gov/articles/PMC3480297/ | |
| dc.format.extent | 17 pages | |
| dc.genre | journal articles | |
| dc.identifier | doi:10.13016/m2myru-fdk8 | |
| dc.identifier.citation | Yoon, Kangsup, Danxiang Han, Yantao Li, Milton Sommerfeld, and Qiang Hu. "Phospholipid:Diacylglycerol Acyltransferase Is a Multifunctional Enzyme Involved in Membrane Lipid Turnover and Degradation While Synthesizing Triacylglycerol in the Unicellular Green Microalga Chlamydomonas Reinhardtii". The Plant Cell 24, no. 9 (1 September 2012): 3708–24. https://doi.org/10.1105/tpc.112.100701. | |
| dc.identifier.uri | https://doi.org/10.1105/tpc.112.100701 | |
| dc.identifier.uri | http://hdl.handle.net/11603/39365 | |
| dc.language.iso | en_US | |
| dc.publisher | Oxford University Press | |
| dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
| dc.relation.ispartof | UMBC Department of Marine Biotechnology | |
| dc.relation.ispartof | UMBC Chemistry & Biochemistry Department | |
| dc.relation.ispartof | UMBC Faculty Collection | |
| dc.rights | This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author. | |
| dc.subject | Triacylglycerol (TAG) | |
| dc.subject | Phospholipid:Diacylglycerol Acyltransferase (PDAT) | |
| dc.subject | Diacylglycerol (DAG) | |
| dc.subject | Acyl-CoA–Independent Pathway | |
| dc.subject | Galactolipids (MGDG/DGDG) | |
| dc.title | Phospholipid:Diacylglycerol Acyltransferase Is a Multifunctional Enzyme Involved in Membrane Lipid Turnover and Degradation While Synthesizing Triacylglycerol in the Unicellular Green Microalga Chlamydomonas reinhardtii | |
| dc.type | Text | |
| dcterms.creator | https://orcid.org/0000-0001-7545-1883 |
