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植物中叶绿素水解产生的叶绿醇通过植醛进行代谢。

Phytol derived from chlorophyll hydrolysis in plants is metabolized via phytenal.

作者信息

Gutbrod Philipp, Yang Wentao, Grujicic Goran Vuk, Peisker Helga, Gutbrod Katharina, Du Lin Fang, Dörmann Peter

机构信息

Institute of Molecular Physiology and Biotechnology of Plants (IMBIO), University of Bonn, Bonn, Germany.

Institute of Molecular Physiology and Biotechnology of Plants (IMBIO), University of Bonn, Bonn, Germany; Key Laboratory of Bio-Resources and Eco-Environment of the Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, China.

出版信息

J Biol Chem. 2021 Jan-Jun;296:100530. doi: 10.1016/j.jbc.2021.100530. Epub 2021 Mar 11.

DOI:10.1016/j.jbc.2021.100530
PMID:33713704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8054155/
Abstract

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.

摘要

叶绿醇是与叶绿素以酯键结合的类异戊二烯醇,叶绿素是植物中含量最丰富的光合色素。在叶片衰老过程中,叶绿素降解会释放大量叶绿醇。然而,植物中叶绿醇的分解代谢途径尚不清楚。我们推测植物中叶绿醇的降解可能涉及其氧化为长链醛植醛。在用甲基羟胺衍生化后,使用气相色谱 - 质谱联用仪(GC-MS)对醛进行定量分析,在叶片中鉴定出了植醛,而其他长链醛(植烷醛和降植烷醛)几乎检测不到。我们发现植醛在黄化胁迫期间积累,例如盐胁迫、黑暗诱导的衰老和氮缺乏。植醛含量的增加至少部分是独立于酶活性介导的,并且与光照无关。对叶绿素降解受影响的pao1突变体中植醛积累的表征表明,植醛是一种源自叶绿素分解的真正的叶绿醇代谢产物。在其他叶绿醇代谢产物(包括vte5-2(生育酚缺陷型)和pes1 pes2(脂肪酸植醇酯缺陷型))产生受影响的突变体中,植醛的增加甚至更强烈。因此,植醛的积累受磷酸化(导致生育酚产生)或酯化(脂肪酸植醇酯产生)的竞争性替代途径控制。结果,植醛的含量维持在低水平,大概是为了最小化其由高反应性醛基引起的毒性作用,该醛基可与蛋白质的氨基形成共价键并使其失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/8c41679f62e3/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/6a32c0bada53/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/df91778d51e7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/72f67102d88a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/304c3be4d56b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/b77c4f654430/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/31fc07cfb3d7/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/853def7c0d61/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/64d6b51611bc/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/e76f372b93c5/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/8c41679f62e3/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/6a32c0bada53/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/df91778d51e7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/72f67102d88a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/304c3be4d56b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/b77c4f654430/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/31fc07cfb3d7/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/853def7c0d61/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/64d6b51611bc/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/e76f372b93c5/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea4/8054155/8c41679f62e3/gr10.jpg

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