Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Structural Basis for Dual Functionality of Isoflavonoid O-Methyltransferases in the Evolution of Plant Defense Responses

Journal Article · · The Plant Cell

In leguminous plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic (Medicago truncatula), and chickpea (Cicer arietinum), 4'-O-methylation of isoflavonoid natural products occurs early in the biosynthesis of defense chemicals known as phytoalexins. However, among these four species, only pea catalyzes 3-O-methylation that converts the pterocarpanoid isoflavonoid 6a-hydroxymaackiain to pisatin. In pea, pisatin is important for chemical resistance to the pathogenic fungus Nectria hematococca. While barrel medic does not biosynthesize 6a-hydroxymaackiain, when cell suspension cultures are fed 6a-hydroxymaackiain, they accumulate pisatin. In vitro, hydroxyisoflavanone 4'-O-methyltransferase (HI4'OMT) from barrel medic exhibits nearly identical steady state kinetic parameters for the 4'-O-methylation of the isoflavonoid intermediate 2,7,4'-trihydroxyisoflavanone and for the 3-O-methylation of the 6a-hydroxymaackiain isoflavonoid-derived pterocarpanoid intermediate found in pea. Protein x-ray crystal structures of HI4'OMT substrate complexes revealed identically bound conformations for the 2S,3R-stereoisomer of 2,7,4'-trihydroxyisoflavanone and the 6aR,11aR-stereoisomer of 6a-hydroxymaackiain. These results suggest how similar conformations intrinsic to seemingly distinct chemical substrates allowed leguminous plants to use homologous enzymes for two different biosynthetic reactions. The three-dimensional similarity of natural small molecules represents one explanation for how plants may rapidly recruit enzymes for new biosynthetic reactions in response to changing physiological and ecological pressures.

Research Organization:
Brookhaven National Laboratory (BNL) National Synchrotron Light Source
Sponsoring Organization:
Doe - Office Of Science
DOE Contract Number:
AC02-98CH10886
OSTI ID:
980505
Report Number(s):
BNL--93423-2010-JA
Journal Information:
The Plant Cell, Journal Name: The Plant Cell Vol. 18
Country of Publication:
United States
Language:
English

Similar Records

Structural Basis for Dual Functionality of Isoflavonoid O-Methyltransferases in the Evolution of Plant Defense Responses
Journal Article · Tue Jul 10 00:00:00 EDT 2007 · Submitted to Plant Cell · OSTI ID:909777

Three genes for metabolism of the phytoalexin maackiain in the plant pathogen Nectria haematococca: Meiotic instability and relationship to a new gene for pisatin demethylase
Journal Article · Sat Feb 29 23:00:00 EST 1992 · Applied and Environmental Microbiology; (United States) · OSTI ID:7206401

Role of oxygenases in pisatin biosynthesis and in the fungal degradation of maackiain
Journal Article · Sat Jan 31 23:00:00 EST 1987 · Plant Physiol.; (United States) · OSTI ID:6526008