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A sugar chain–dependent two-component chemical defense in Hedera helix reveals substrate-driven β-glucosidase evolution in Apiales
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Plants have evolved diverse chemical strategies to defend against herbivores and pathogens, yet the mechanisms underlying their origin and diversification remain unclear. Here, we identify a sugar chain–dependent triterpenoid saponin defense system in
Hedera helix
that exemplifies adaptive innovation in plant chemical defenses. Three glycosyltransferases sequentially assemble a glucose–glucose–rhamnose chain at the C-28 position of α-hederin to form the detoxified precursor hederacoside C. Upon tissue disruption, the β-glucosidase HhGH1 hydrolyzes the entire sugar chain, regenerating α-hederin, a potent hemolytic saponin. Reconstitution of this system in
Nicotiana benthamiana
conferred strong herbivore resistance, demonstrating its ecological functionality and portability. Intriguingly, comparative genomics and biochemical analysis revealed that β-glucosidases across Apiales diversified in response to triterpenoid glycosylation, illustrating how substrate-driven enzyme evolution and metabolic innovation together generate new adaptive defense strategies in plants.
National Academy of Sciences
Title: A sugar chain–dependent two-component chemical defense in
Hedera helix
reveals substrate-driven β-glucosidase evolution in Apiales
Description:
Plants have evolved diverse chemical strategies to defend against herbivores and pathogens, yet the mechanisms underlying their origin and diversification remain unclear.
Here, we identify a sugar chain–dependent triterpenoid saponin defense system in
Hedera helix
that exemplifies adaptive innovation in plant chemical defenses.
Three glycosyltransferases sequentially assemble a glucose–glucose–rhamnose chain at the C-28 position of α-hederin to form the detoxified precursor hederacoside C.
Upon tissue disruption, the β-glucosidase HhGH1 hydrolyzes the entire sugar chain, regenerating α-hederin, a potent hemolytic saponin.
Reconstitution of this system in
Nicotiana benthamiana
conferred strong herbivore resistance, demonstrating its ecological functionality and portability.
Intriguingly, comparative genomics and biochemical analysis revealed that β-glucosidases across Apiales diversified in response to triterpenoid glycosylation, illustrating how substrate-driven enzyme evolution and metabolic innovation together generate new adaptive defense strategies in plants.
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