Nature Communications (Feb 2023)
Genomics and biochemical analyses reveal a metabolon key to β-L-ODAP biosynthesis in Lathyrus sativus
- Anne Edwards,
- Isaac Njaci,
- Abhimanyu Sarkar,
- Zhouqian Jiang,
- Gemy George Kaithakottil,
- Christopher Moore,
- Jitender Cheema,
- Clare E. M. Stevenson,
- Martin Rejzek,
- Petr Novák,
- Marielle Vigouroux,
- Martin Vickers,
- Roland H. M. Wouters,
- Pirita Paajanen,
- Burkhard Steuernagel,
- Jonathan D. Moore,
- Janet Higgins,
- David Swarbreck,
- Stefan Martens,
- Colin Y. Kim,
- Jing-Ke Weng,
- Sagadevan Mundree,
- Benjamin Kilian,
- Shiv Kumar,
- Matt Loose,
- Levi Yant,
- Jiří Macas,
- Trevor L. Wang,
- Cathie Martin,
- Peter M. F. Emmrich
Affiliations
- Anne Edwards
- John Innes Centre, Norwich Research Park
- Isaac Njaci
- John Innes Centre, Norwich Research Park
- Abhimanyu Sarkar
- John Innes Centre, Norwich Research Park
- Zhouqian Jiang
- John Innes Centre, Norwich Research Park
- Gemy George Kaithakottil
- Earlham Institute, Norwich Research Park, Colney Lane
- Christopher Moore
- School of Life Sciences, University of Nottingham, University Park
- Jitender Cheema
- John Innes Centre, Norwich Research Park
- Clare E. M. Stevenson
- John Innes Centre, Norwich Research Park
- Martin Rejzek
- John Innes Centre, Norwich Research Park
- Petr Novák
- Institute of Plant Molecular Biology, Biology Centre CAS
- Marielle Vigouroux
- John Innes Centre, Norwich Research Park
- Martin Vickers
- John Innes Centre, Norwich Research Park
- Roland H. M. Wouters
- John Innes Centre, Norwich Research Park
- Pirita Paajanen
- John Innes Centre, Norwich Research Park
- Burkhard Steuernagel
- John Innes Centre, Norwich Research Park
- Jonathan D. Moore
- John Innes Centre, Norwich Research Park
- Janet Higgins
- Earlham Institute, Norwich Research Park, Colney Lane
- David Swarbreck
- Earlham Institute, Norwich Research Park, Colney Lane
- Stefan Martens
- Research and Innovation Centre, Fondazione Edmund Mach
- Colin Y. Kim
- Whitehead Institute for Biomedical Research
- Jing-Ke Weng
- Whitehead Institute for Biomedical Research
- Sagadevan Mundree
- Queensland University of Technology
- Benjamin Kilian
- Global Crop Diversity Trust
- Shiv Kumar
- International Center for Agricultural Research in the Dry Areas, Avenue Hafiane Cherkaoui
- Matt Loose
- School of Life Sciences, University of Nottingham, University Park
- Levi Yant
- School of Life Sciences, University of Nottingham, University Park
- Jiří Macas
- Institute of Plant Molecular Biology, Biology Centre CAS
- Trevor L. Wang
- John Innes Centre, Norwich Research Park
- Cathie Martin
- John Innes Centre, Norwich Research Park
- Peter M. F. Emmrich
- John Innes Centre, Norwich Research Park
- DOI
- https://doi.org/10.1038/s41467-023-36503-2
- Journal volume & issue
-
Vol. 14,
no. 1
pp. 1 – 16
Abstract
Abstract Grass pea (Lathyrus sativus L.) is a rich source of protein cultivated as an insurance crop in Ethiopia, Eritrea, India, Bangladesh, and Nepal. Its resilience to both drought and flooding makes it a promising crop for ensuring food security in a changing climate. The lack of genetic resources and the crop’s association with the disease neurolathyrism have limited the cultivation of grass pea. Here, we present an annotated, long read-based assembly of the 6.5 Gbp L. sativus genome. Using this genome sequence, we have elucidated the biosynthetic pathway leading to the formation of the neurotoxin, β-L-oxalyl-2,3-diaminopropionic acid (β-L-ODAP). The final reaction of the pathway depends on an interaction between L. sativus acyl-activating enzyme 3 (LsAAE3) and a BAHD-acyltransferase (LsBOS) that form a metabolon activated by CoA to produce β-L-ODAP. This provides valuable insight into the best approaches for developing varieties which produce substantially less toxin.