Related Experiment Video
Updated: Sep 19, 2025

Author Spotlight: Discovering New Alkaloids in Plants with Advanced Mass Spectrometry Techniques
Published on: March 8, 2024
Enzymatic twists evolved stereo-divergent alkaloids in the Solanaceae family
Adam Jozwiak1, Michaela Almaria2, Jianghua Cai3
1University of California, Riverside, CA, USA. adamj@ucr.edu.
Abstract:
Steroidal alkaloids play a crucial role in plant defense and exhibit distinct stereochemistry at C25, forming either the tomato-type (25S) or eggplant-type (25R) isomers. Here, we uncover the molecular mechanisms shaping this stereochemical diversity. Phylogenetic analysis of GLYCOALKALOID METABOLISM 8 (GAME8) cytochrome P450 hydroxylases across the Solanaceae family revealed two distinct clades producing either 25S or 25R isomers. Ancestral GAME8 likely favored 25R, with gene duplications giving rise to 25S-producing enzymes in more recent Solanum species. In S. nigrum and S. dulcamara, multiple GAME8 copies generate mixed isomeric profiles. Notably, in wild S. cheesmaniae from the Galápagos, mutations in GAME8 have driven a shift from 25S back to the ancestral 25R, suggesting reverse evolution. Our findings highlight how GAME8 evolution has shaped alkaloid diversity in the genus Solanum, demonstrating a complex interplay between enzyme function, genetic variation, and evolutionary adaptation.
Related Concept Videos
Chirality in Nature
Stereoisomers
Prochirality
Stereoisomerism of Cyclic Compounds
Stereoisomerism
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation

