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.
Original language | English |
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Article number | 581675 |
Number of pages | 9 |
Journal | Frontiers in Plant Science |
Volume | 11 |
DOIs | |
Publication status | Published - 20 Nov 2020 |
Keywords
- Indole-acetic acid
- Halogenase
- Combinatorial biosynthesis
- Auxin
- Unnatural natural product
- New to nature products