Chiral Chemopolymorphism in the Monoterpenes of Pistacia palaestina Leaves and Galls

Chirality. 2024 Aug;36(8):e23702. doi: 10.1002/chir.23702.

Abstract

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.

Keywords: Baizongia pistaciae; camphene; insect‐induced galls; limonene; polymorphism; sabinene; terpene‐4‐ol; α‐pinene; β‐pinene; δ‐3‐carene.

MeSH terms

  • Animals
  • Aphids
  • Monoterpenes* / chemistry
  • Pistacia* / chemistry
  • Plant Leaves* / chemistry
  • Plant Tumors / parasitology
  • Stereoisomerism

Substances

  • Monoterpenes