Abstract
The sesquiterpenoid deoxynivalenol (DON) is an important trichothecene mycotoxin produced by the cereal pathogen Fusarium graminearum. DON is synthesized in specialized subcellular structures called toxisomes. The first step in DON synthesis is catalyzed by the sesquiterpene synthase (STS), Tri5 (trichodiene synthase), resulting in the cyclization of farnesyl diphosphate (FPP) to produce the sesquiterpene trichodiene. Tri5 is one of eight putative STSs in the F. graminearum genome. To better understand the F. graminearum terpenome, the volatile and soluble fractions of fungal cultures were sampled. Stringent regulation of sesquiterpene accumulation was observed. When grown in trichothecene induction medium, the fungus produces trichothecenes as well as several volatile non-trichothecene related sesquiterpenes, whereas no volatile terpenes were detected when grown in non-inducing medium. Surprisingly, a Δtri5 deletion strain grown in inducing conditions not only ceased accumulation of trichothecenes, but also failed to produce the non-trichothecene related sesquiterpenes. To test whether Tri5 from F. graminearum may be a promiscuous STS directly producing all observed sesquiterpenes, Tri5 was cloned and expressed in E. coli and shown to produce primarily trichodiene in addition to minor, related cyclization products. Therefore, while Tri5 expression in F. graminearum is necessary for non-trichothecene sesquiterpene biosynthesis, direct catalysis by Tri5 does not explain the sesquiterpene deficient phenotype observed in the Δtri5 strain. To test whether Tri5 protein, separate from its enzymatic activity, may be required for non-trichothecene synthesis, the Tri5 locus was replaced with an enzymatically inactive, but structurally unaffected tri5N225D S229T allele. This allele restores non-trichothecene synthesis but not trichothecene synthesis. The tri5N225D S229T allele also restores toxisome structure which is lacking in the Δtri5 deletion strain. Our results indicate that the Tri5 protein, but not its enzymatic activity, is also required for the synthesis of non-trichothecene related sesquiterpenes and the formation of toxisomes. Toxisomes thus not only may be important for DON synthesis, but also for the synthesis of other sesquiterpene mycotoxins such as culmorin by F. graminearum.
Highlights
Fusarium graminearum sensu stricto [1] is a fungal pathogen of major cereal crops causing the disease Fusarium head blight (FHB) [2]
Among the most potent inducers of trichothecene biosynthesis are polyamines, including putrescine and agmatine [26], that may be the signals recognized by the fungus during the infection of plants [54]
One of the sesquiterpene peaks is trichodiene 13, the major product of the trichodiene synthase Tri5 [55]. Both α-barbatene 3 and βbisabolene 9 were produced by induced cultures, which have previously been identified as minor 1,6-cyclization products of trichodiene synthase catalyzed reactions [56,57]
Summary
Fusarium graminearum sensu stricto [1] is a fungal pathogen of major cereal crops causing the disease Fusarium head blight (FHB) [2]. As a result, understanding the physiology and pathogenesis of F. graminearum is important for combatting FHB infection, as well as for breeding resistant cereal crops. Trichothecenes encompass over 200 sesquiterpenoids, all derived from the unmodified sesquiterpene trichodiene. This shared precursor is produced by the cyclization of farnesyl pyrophosphate (FPP) by a sesquiterpene synthase (STS) called trichodiene synthase or Tri5 [6,7,8] (Fig. 1). Trichothecenes may accumulate to high levels during infection of wheat and barley by F. graminearum [9,10]
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