Abstract

Plant secondary metabolites have applications for the food, biofuel, and pharmaceutical industries. Recent advances in pathway elucidation and host expression systems now allow metabolic engineering of plant metabolic pathways to produce “new-to-nature” derivatives with novel biological activities, thereby amplifying the range of industrial uses for plant metabolites. Here we use a transient expression system in the model plant Nicotiana benthamiana to reconstitute the two-step plant-derived biosynthetic pathway for auxin (indole acetic acid) to achieve accumulation up to 500 ng/g fresh mass (FM). By expressing these plant-derived enzymes in combination with either bacterial halogenases and alternative substrates, we can produce both natural and new-to-nature halogenated auxin derivatives up to 990 ng/g FM. Proteins from the auxin synthesis pathway, tryptophan aminotransferases (TARs) and flavin-dependent monooxygenases (YUCs), could be transiently expressed in combination with four separate bacterial halogenases to generate halogenated auxin derivatives. Brominated auxin derivatives could also be observed after infiltration of the transfected N. benthamiana with potassium bromide and the halogenases. Finally, the production of additional auxin derivatives could also be achieved by co-infiltration of TAR and YUC genes with various tryptophan analogs. Given the emerging importance of transient expression in N. benthamiana for industrial scale protein and product expression, this work provides insight into the capacity of N. benthamiana to interface bacterial genes and synthetic substrates to produce novel halogenated metabolites.

Highlights

  • Many natural products that share a common scaffold have subtle modifications to the core structure that dramatically modulate the biological function of the molecule (Pickens et al, 2011)

  • We first assembled the suite of genes required for Indole-3-Acetic Acid (IAA) biosynthesis

  • Our preliminary experiments did not reveal any substantial difference in activity between the various aminotransferases when expressed in N. benthamiana but suggested that co-expression quantification was based on a calibration curve

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Summary

Introduction

Many natural products that share a common scaffold have subtle modifications to the core structure that dramatically modulate the biological function of the molecule (Pickens et al, 2011). The chemical similarity between product families mirrors a homology in genes featuring in their biosynthetic pathways. The encoded enzymes among very similar pathways can have altered substrate and product specificities. Mixing and matching enzymes from analogous pathways from different organisms, could enhance our chances of success in creating new-to-nature products with novel biological functions. The presence of a halogen affects multiple physiochemical properties of molecules including lipophilicity, size, polarity, and capacity for hydrogen bonding (Jeschke, 2010), which in turn affects biological activity. The potent anti-cancer agent salinosporamide A (marizomib) uses a chlorine atom as a stable leaving group, a crucial feature for irreversible inhibition of the proteasome in cancerous cells (Miller et al, 2011)

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