Pistacia palaestina 叶子和瘿中单萜的手性化学多态性。

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2024-08-13 DOI:10.1002/chir.23702
Einat Bar, Rachel Davidovich-Rikanati, Shashank Saini, Moshe Inbar, Efraim Lewinsohn
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引用次数: 0

摘要

Pistacia palaestina Boiss.是地中海灌木丛中的一种常见树木。这种植物的叶片会积累防御性单萜,在蚜虫Baizongia penaire诱发的虫瘿中,单萜的含量会大大增加。我们以前曾发现单萜烯含量在不同树木之间存在明显的化学多态性,但这些单萜烯的手性尚不清楚。虽然大多数植物物种都会积累特定化合物的一种对映体形式,但巴桐个体积累的主要单萜烯的手性具有化学多态性。我们在此报告了九种不同自然生长的棕榈树叶片和树瘿中柠檬烯、α-和β-蒎烯、莰烯、桧烯、δ-3-蒈烯和萜烯-4-醇含量的明显对映体差异。有趣的是,昆虫诱导的虫瘿单萜烯成分是每棵树最初表现出的特定对映体多态性的增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chiral Chemopolymorphism in the Monoterpenes of Pistacia palaestina Leaves and Galls

Chiral Chemopolymorphism in the Monoterpenes of Pistacia palaestina Leaves and Galls

Pistacia palaestina Boiss. is a common tree in the Mediterranean maquis. The leaves of this plant accumulate defensive monoterpenes, whose levels greatly increase in galls induced by the aphid Baizongia pistaciae. We previously found a significant chemopolymorphism in monoterpene content among individual trees, but the chirality of these monoterpenes was unknown. Although most plant species specifically accumulate one enantiomeric form of a given compound, P. palaestina individuals display chemopolymorphism in the chirality of the key monoterpenes accumulated. We report here a marked enantiomeric variation for the limonene, α- and β-pinene, camphene, sabinene, δ-3-carene, and terpene-4-ol content in leaves and galls of nine different naturally growing P. palaestina trees. Interestingly, insect-induced gall monoterpene composition is an augmentation of the specific enantiopolymorphism originally displayed by each individual tree.

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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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