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Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage

Plastoglobules, which are lipoprotein structures surrounded by a single hydrophobic phospholipid membrane, are subcellular organelles in plant chromoplasts and chloroplasts. They contain neutral lipids, tocopherols, quinones, chlorophyll metabolites, carotenoids and their derivatives. Proteomic stud...

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Autores principales: Jiang, Er-Ying, Fan, Yong, Phung, Nghi-Van, Xia, Wan-Yue, Hu, Guang-Rong, Li, Fu-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160619/
https://www.ncbi.nlm.nih.gov/pubmed/37152729
http://dx.doi.org/10.3389/fmicb.2023.1143017
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author Jiang, Er-Ying
Fan, Yong
Phung, Nghi-Van
Xia, Wan-Yue
Hu, Guang-Rong
Li, Fu-Li
author_facet Jiang, Er-Ying
Fan, Yong
Phung, Nghi-Van
Xia, Wan-Yue
Hu, Guang-Rong
Li, Fu-Li
author_sort Jiang, Er-Ying
collection PubMed
description Plastoglobules, which are lipoprotein structures surrounded by a single hydrophobic phospholipid membrane, are subcellular organelles in plant chromoplasts and chloroplasts. They contain neutral lipids, tocopherols, quinones, chlorophyll metabolites, carotenoids and their derivatives. Proteomic studies indicated that plastoglobules are involved in carotenoid metabolism and storage. In this study, one of the plastid lipid-associated proteins (PAP), the major protein in plastoglobules, was selected and overexpressed in Phaeodactylum tricornutum. The diameter of the plastoglobules in mutants was decreased by a mean of 19.2% versus the wild-type, while the fucoxanthin level was increased by a mean of 51.2%. All mutants exhibited morphological differences from the wild-type, including a prominent increase in the transverse diameter. Moreover, the unsaturated fatty acid levels were increased in different mutants, including an 18.9–59.3% increase in eicosapentaenoic acid content. Transcriptomic analysis revealed that PAP expression and the morphological changes altered xanthophyll synthesis and storage, which affected the assembly of the fucoxanthin chlorophyll a/c-binding protein and expression of antenna proteins as well as reduced the non-photochemical quenching activity of diatom cells. Therefore, metabolic regulation at the suborganelle level can be achieved by modulating PAP expression. These findings provide a subcellular structural site and target for synthetic biology to modify pigment and lipid metabolism in microalgae chassis cells.
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spelling pubmed-101606192023-05-06 Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage Jiang, Er-Ying Fan, Yong Phung, Nghi-Van Xia, Wan-Yue Hu, Guang-Rong Li, Fu-Li Front Microbiol Microbiology Plastoglobules, which are lipoprotein structures surrounded by a single hydrophobic phospholipid membrane, are subcellular organelles in plant chromoplasts and chloroplasts. They contain neutral lipids, tocopherols, quinones, chlorophyll metabolites, carotenoids and their derivatives. Proteomic studies indicated that plastoglobules are involved in carotenoid metabolism and storage. In this study, one of the plastid lipid-associated proteins (PAP), the major protein in plastoglobules, was selected and overexpressed in Phaeodactylum tricornutum. The diameter of the plastoglobules in mutants was decreased by a mean of 19.2% versus the wild-type, while the fucoxanthin level was increased by a mean of 51.2%. All mutants exhibited morphological differences from the wild-type, including a prominent increase in the transverse diameter. Moreover, the unsaturated fatty acid levels were increased in different mutants, including an 18.9–59.3% increase in eicosapentaenoic acid content. Transcriptomic analysis revealed that PAP expression and the morphological changes altered xanthophyll synthesis and storage, which affected the assembly of the fucoxanthin chlorophyll a/c-binding protein and expression of antenna proteins as well as reduced the non-photochemical quenching activity of diatom cells. Therefore, metabolic regulation at the suborganelle level can be achieved by modulating PAP expression. These findings provide a subcellular structural site and target for synthetic biology to modify pigment and lipid metabolism in microalgae chassis cells. Frontiers Media S.A. 2023-04-21 /pmc/articles/PMC10160619/ /pubmed/37152729 http://dx.doi.org/10.3389/fmicb.2023.1143017 Text en Copyright © 2023 Jiang, Fan, Phung, Xia, Hu and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jiang, Er-Ying
Fan, Yong
Phung, Nghi-Van
Xia, Wan-Yue
Hu, Guang-Rong
Li, Fu-Li
Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title_full Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title_fullStr Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title_full_unstemmed Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title_short Overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
title_sort overexpression of plastid lipid-associated protein in marine diatom enhances the xanthophyll synthesis and storage
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160619/
https://www.ncbi.nlm.nih.gov/pubmed/37152729
http://dx.doi.org/10.3389/fmicb.2023.1143017
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