Phytol is the isoprenoid alcohol bound in ester linkage to chlorophyll, the most abundant photosynthetic pigment in plants. During leaf senescence, large amounts of phytol are released by chlorophyll degradation. However, the pathway of phytol catabolism in plants is unknown. We hypothesized that phytol degradation in plants might involve its oxidation into the long-chain aldehyde phytenal. Using GC-MS for aldehyde quantification after derivatization with methylhydroxylamine, phytenal was identified in leaves, whereas other long-chain aldehydes (phytanal and pristanal) were barely detectable. We found that phytenal accumulates during chlorotic stresses, for example, salt stress, dark-induced senescence, and nitrogen deprivation. The increase in the phytenal content is mediated at least in part independently of enzyme activities, and it is independent of light. Characterization of phytenal accumulation in the pao1 mutant affected in chlorophyll degradation revealed that phytenal is an authentic phytol metabolite derived from chlorophyll breakdown. The increase in phytenal was even stronger in mutants affected in the production of other phytol metabolites including vte5-2 (tocopherol deficient) and pes1 pes2 (fatty acid phytyl ester deficient). Therefore, phytenal accumulation is controlled by competing, alternative pathways of phosphorylation (leading to tocopherol production) or esterification (fatty acid phytyl ester production). As a consequence, the content of phytenal is maintained at low levels, presumably to minimize its toxic effects caused by its highly reactive aldehyde group that can form covalent bonds with and inactivate the amino groups of proteins.
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http://dx.doi.org/10.1016/j.jbc.2021.100530 | DOI Listing |
Plant J
March 2022
Institute of Molecular Physiology and Biotechnology of Plants (IMBIO), University of Bonn, Karlrobert-Kreiten-Straße 13, 53115, Bonn, Germany.
During chlorophyll degradation, large amounts of the isoprenoid alcohol phytol are released. The pathway of phytol catabolism has been studied in humans, because chlorophyll is part of the human diet, but little is known for plants. In humans, phytanoyl-CoA derived from phytol is degraded via α-oxidation by phytanoyl-CoA hydroxylase (PAHX) and 2-hydroxy-phytanoyl-CoA lyase (HPCL).
View Article and Find Full Text PDFJ Biol Chem
August 2021
Division of Biology, Kansas State University, Manhattan, Kansas, USA. Electronic address:
Understanding the pathways involved in chlorophyll breakdown provides a molecular map to the color changes observed in plant life on a global scale each fall. Surprisingly, little is known about the fate of phytol, chlorophyll's 20-carbon branched-chain tail, during this process. A recent study from Gutbrod et al.
View Article and Find Full Text PDFJ Biol Chem
August 2021
Institute of Molecular Physiology and Biotechnology of Plants (IMBIO), University of Bonn, Bonn, Germany. Electronic address:
Phytol is the isoprenoid alcohol bound in ester linkage to chlorophyll, the most abundant photosynthetic pigment in plants. During leaf senescence, large amounts of phytol are released by chlorophyll degradation. However, the pathway of phytol catabolism in plants is unknown.
View Article and Find Full Text PDFZhong Yao Cai
November 2012
Hunan University of Chinese Medicine, Changsha 410208, China.
Objective: To study the chemical constituents from the leaf of Hydnocarpus hainanensis.
Methods: Compounds were isolated and purified by silica gel and Sephadex LH-20 column chromatography, their structures were identified by spectroscopic analysis.
Results: Nine compounds were isolated and identified as glutinol (I), fernenol (II), lupeol (III), a-armyrin (IV), 2, 9-dimethyldeca-2, 8-diene (V), phytenal (VI), phytol (VII), 3, 7, 11,15-tetramethylhexadecane-1,2-diol ( VI), 3, 5-dimethoxy-4-hydroxybenzaldehyde (IX).
Zhongguo Zhong Yao Za Zhi
November 2006
Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
Objective: To investigate the chemical constituents of red alga Corallina pilulifera.
Method: Compounds were isolated by normal phase silica gel and Sephadex LH - 20 gel column chromatography, reverse phase HPLC and recrystallization. Their structures were elucidated by spectroscopic methods including MS, 1H-NMR, 13C-NMR, HSQC, HMBC.
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