Molecular basis of the evolution of methylthioalkylmalate synthase and diversity of methionine-derived glucosinolates
NIPGR Digital Knowledge Repository (NDKR)
View Archive InfoField | Value | |
Title |
Molecular basis of the evolution of methylthioalkylmalate synthase and diversity of methionine-derived glucosinolates
|
|
Creator |
Kumar, Roshan
Lee, Soon Goo Augustine, Rehna Reichelt, Micheal Vassão, Daniel G. Palavalli, Manoj H. Allen, Aron Gershenzon, Jonathan Jez, Joseph M. Bisht, Naveen C. |
|
Subject |
Glucosinolates
Methylthioalkylmalate Synthase |
|
Description |
Accepted date: April 19, 2019
Methylthioalkylmalate synthase catalyzes the committed step in the side-chain elongation of methionine-derived aliphatic glucosinolates and likely evolved from the isopropylmalate synthases of leucine biosynthesis. The globally cultivated Brassica species possess diverse aliphatic glucosinolates important for plant defense and animal nutrition; however, the molecular basis for the evolution of methylthioalkylmalate synthase and its generation of natural product diversity in Brassica is poorly understood. Here we show that Brassica genomes encode multiple methylthioalkylmalate synthase that have differences in expression profiles and 2-oxo substrate preference that account for diversity of aliphatic glucosinolates across Brassica accessions. The 2.1 Å resolution x-ray crystal structure of B. juncea methylthioalkylmalate synthase identifies key active site residues responsible for controlling specificity for different 2-oxo substrates and the determinants of side-chain length in aliphatic glucosinolates. Overall, these results provide the evolutionary and biochemical foundation for diversification of glucosinolates profiles across globally-cultivated Brassica species, which could be used with ongoing breeding strategies towards manipulation of beneficial glucosinolates compounds for animal health and plant protection. The work was supported by grants BT/PR271/AGR/36/687/2011 and BT/06/IYBA/2012 of the Department of Biotechnology, India to N.C.B.; a National Science Foundation grant to J.M.J. (NSF-MCB-1614539), and the Max Planck Society to J.G. N.C.B. acknowledges Max Planck India Fellowship and NIPGR-Short Term Ovearseas Fellowship. R.K. and R.A. acknowledge financial support from UGC (India) and NIPGR, respectively. We are grateful to Central Instrumentation and Plant Growth Facilities at NIPGR. Portions of this research were carried out at the Argonne National Laboratory Structural Biology Center of the Advanced Photon Source, a national use facility operated by the University of Chicago for the Department of Energy Office of Biological and Environmental Research under Grant DE-AC02-06CH11357. |
|
Date |
2019-04-30T07:55:29Z
2019-04-30T07:55:29Z 2019 |
|
Type |
Article
|
|
Identifier |
Plant Cell, 31(7): 1633-1647
1531-298X http://223.31.159.10:8080/jspui/handle/123456789/946 http://www.plantcell.org/content/early/2019/04/25/tpc.19.00046.long https://doi.org/10.1105/tpc.19.00046 |
|
Language |
en_US
|
|
Format |
application/pdf
|
|
Publisher |
American Society of Plant Biologists
|
|