Phytol metabolism in plants. (April 2019)
- Record Type:
- Journal Article
- Title:
- Phytol metabolism in plants. (April 2019)
- Main Title:
- Phytol metabolism in plants
- Authors:
- Gutbrod, Katharina
Romer, Jill
Dörmann, Peter - Abstract:
- Abstract: Phytol, the prenyl side chain of chlorophyll, is derived from geranylgeraniol by reduction of three double bonds. Recent results demonstrated that the conversion of geranylgeraniol to phytol is linked to chlorophyll synthesis, which is catalyzed by protein complexes associated with the thylakoid membranes. One of these complexes contains light harvesting chlorophyll binding like proteins (LIL3), enzymes of chlorophyll synthesis (protoporphyrinogen oxidoreductase, POR; chlorophyll synthase, CHLG) and geranylgeranyl reductase (GGR). Phytol is not only employed for the synthesis of chlorophyll, but also for tocopherol (vitamin E), phylloquinol (vitamin K) and fatty acid phytyl ester production. Previously, it was believed that phytol is derived from reduction of geranylgeranyl-diphosphate originating from the 4-methylerythritol-5-phosphate (MEP) pathway. The identification and characterization of two kinases, VTE5 and VTE6, involved in phytol and phytyl-phosphate phosphorylation, respectively, indicated that most phytol employed for tocopherol synthesis is derived from reduction of geranylgeranylated chlorophyll to (phytol-) chlorophyll. After hydrolysis from chlorophyll, free phytol is phosphorylated by the two kinases, and phytyl-diphosphate employed for the synthesis of tocopherol and phylloquinol. The reason why some chloroplast lipids, i.e. chlorophyll, tocopherol and phylloquinol, are derived from phytol, while others, i.e. carotenoids and tocotrienols (in someAbstract: Phytol, the prenyl side chain of chlorophyll, is derived from geranylgeraniol by reduction of three double bonds. Recent results demonstrated that the conversion of geranylgeraniol to phytol is linked to chlorophyll synthesis, which is catalyzed by protein complexes associated with the thylakoid membranes. One of these complexes contains light harvesting chlorophyll binding like proteins (LIL3), enzymes of chlorophyll synthesis (protoporphyrinogen oxidoreductase, POR; chlorophyll synthase, CHLG) and geranylgeranyl reductase (GGR). Phytol is not only employed for the synthesis of chlorophyll, but also for tocopherol (vitamin E), phylloquinol (vitamin K) and fatty acid phytyl ester production. Previously, it was believed that phytol is derived from reduction of geranylgeranyl-diphosphate originating from the 4-methylerythritol-5-phosphate (MEP) pathway. The identification and characterization of two kinases, VTE5 and VTE6, involved in phytol and phytyl-phosphate phosphorylation, respectively, indicated that most phytol employed for tocopherol synthesis is derived from reduction of geranylgeranylated chlorophyll to (phytol-) chlorophyll. After hydrolysis from chlorophyll, free phytol is phosphorylated by the two kinases, and phytyl-diphosphate employed for the synthesis of tocopherol and phylloquinol. The reason why some chloroplast lipids, i.e. chlorophyll, tocopherol and phylloquinol, are derived from phytol, while others, i.e. carotenoids and tocotrienols (in some plant species) are synthesized from geranylgeraniol, remains unclear. … (more)
- Is Part Of:
- Progress in lipid research. Volume 74(2019)
- Journal:
- Progress in lipid research
- Issue:
- Volume 74(2019)
- Issue Display:
- Volume 74, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 74
- Issue:
- 2019
- Issue Sort Value:
- 2019-0074-2019-0000
- Page Start:
- 1
- Page End:
- 17
- Publication Date:
- 2019-04
- Subjects:
- Plant -- Lipid -- Chlorophyll -- Chlorophyllide -- Phytol -- Geranylgeraniol -- Tocopherol -- Tocotrienol -- Phylloquinol -- Plastoquinol -- Plastochromanol -- Isoprenoid -- Fatty acid phytyl ester -- Mevalonate -- Methylerythritol phosphate
Lipids -- Periodicals
Lipids -- Periodicals
Lipides -- Périodiques
Lipiden
572.57 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01637827 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.plipres.2019.01.002 ↗
- Languages:
- English
- ISSNs:
- 0163-7827
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6868.640000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20410.xml