Biosynthesis and differential spatial distribution of the 3‐deoxyanthocyanidins apigenidin and luteolinidin at the interface of a plant‐cyanobacteria symbiosis exposed to cold

Abstract

AbstractAquatic ferns of the genus Azolla (Azolla) form highly productive symbioses with filamentous cyanobacteria fixing N2 in their leaf cavities, Nostoc azollae. Stressed symbioses characteristically turn red due to 3‐deoxyanthocyanidin (DA) accumulation, rare in angiosperms and of unknown function. To understand DA accumulation upon cold acclimation and recovery, we integrated laser‐desorption‐ionization mass‐spectrometry‐imaging (LDI‐MSI), a new Azolla filiculoides genome‐assembly and annotation, and dual RNA‐sequencing into phenotypic analyses of the symbioses. Azolla sp. Anzali recovered even when cold‐induced DA‐accumulation was inhibited by abscisic acid. Cyanobacterial filaments generally disappeared upon cold acclimation and Nostoc azollae transcript profiles were unlike those of resting stages formed in cold‐resistant sporocarps, yet filaments re‐appeared in leaf cavities of newly formed green fronds upon cold‐recovery. The high transcript accumulation upon cold acclimation of AfDFR1 encoding a flavanone 4‐reductase active in vitro suggested that the enzyme of the first step in the DA‐pathway may regulate accumulation of DAs in different tissues. However, LDI‐MSI highlighted the necessity to describe metabolite accumulation beyond class assignments as individual DA and caffeoylquinic acid metabolites accumulated differentially. For example, luteolinidin accumulated in epithelial cells, including those lining the leaf cavity, supporting a role for the former in the symbiotic interaction during cold acclimation.