Journal
PLANTS-BASEL
Volume 12, Issue 5, Pages -Publisher
MDPI
DOI: 10.3390/plants12051111
Keywords
maize specialized metabolism; defense; sesquiterpenoids; Fusarium; terpene synthase
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In maize, fungal-elicited immune responses lead to the production of various sesquiterpenoids and diterpenoids as antibiotics. Through metabolic profiling, a chromosome 1 locus associated with five candidate sesquiterpenoids was identified. Enzyme co-expression studies confirmed the production of specific terpenoids by ZmTPS27 and ZmTPS8. In vitro bioassays showed that the terpenoid cubebol, produced by ZmTPS8, exhibits significant antifungal activity.
In maize (Zea mays), fungal-elicited immune responses include the accumulation of terpene synthase (TPS) and cytochrome P450 monooxygenases (CYP) enzymes resulting in complex antibiotic arrays of sesquiterpenoids and diterpenoids, including alpha/beta-selinene derivatives, zealexins, kauralexins and dolabralexins. To uncover additional antibiotic families, we conducted metabolic profiling of elicited stem tissues in mapping populations, which included B73 x M162W recombinant inbred lines and the Goodman diversity panel. Five candidate sesquiterpenoids associated with a chromosome 1 locus spanning the location of ZmTPS27 and ZmTPS8. Heterologous enzyme co-expression studies of ZmTPS27 in Nicotiana benthamiana resulted in geraniol production while ZmTPS8 yielded alpha-copaene, delta-cadinene and sesquiterpene alcohols consistent with epi-cubebol, cubebol, copan-3-ol and copaborneol matching the association mapping efforts. ZmTPS8 is an established multiproduct alpha-copaene synthase; however, ZmTPS8-derived sesquiterpene alcohols are rarely encountered in maize tissues. A genome wide association study further linked an unknown sesquiterpene acid to ZmTPS8 and combined ZmTPS8-ZmCYP71Z19 heterologous enzyme co-expression studies yielded the same product. To consider defensive roles for ZmTPS8, in vitro bioassays with cubebol demonstrated significant antifungal activity against both Fusarium graminearum and Aspergillus parasiticus. As a genetically variable biochemical trait, ZmTPS8 contributes to the cocktail of terpenoid antibiotics present following complex interactions between wounding and fungal elicitation.
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