- Title
- The structural components of the Azotobacter vinelandii iron-only nitrogenase, AnfDKG, form a protein complex within the plant mitochondrial matrix
- Creator
- Johnston, E.; Okada, S.; Wood, C. C.; Gregg, C. M.; Warden, A. C.; Rolland, V.; Gillespie, V.; Byrne, K.; Colgrave, M. L.; Eamens, A. L.; Allen, R. S.
- Relation
- Plant Molecular Biology Vol. 112, Issue 4-5, p. 279-291
- Publisher Link
- http://dx.doi.org/10.1007/s11103-023-01363-3
- Publisher
- Springer
- Resource Type
- journal article
- Date
- 2023
- Description
- A long-held goal of synthetic biology has been the transfer of a bacterial nitrogen-fixation pathway into plants to reduce the use of chemical fertiliser on crops such as rice, wheat and maize. There are three classes of bacterial nitrogenase, named after their metal requirements, containing either a MoFe-, VFe- or FeFe-cofactor, that converts N2 gas to ammonia. Relative to the Mo-nitrogenase the Fe-nitrogenase is not as efficient for catalysis but has less complex genetic and metallocluster requirements, features that may be preferable for engineering into crops. Here we report the successful targeting of bacterial Fe-nitrogenase proteins, AnfD, AnfK, AnfG and AnfH, to plant mitochondria. When expressed as a single protein AnfD was mostly insoluble in plant mitochondria, but coexpression of AnfD with AnfK improved its solubility. Using affinity-based purification of mitochondrially expressed AnfK or AnfG we were able to demonstrate a strong interaction of AnfD with AnfK and a weaker interaction of AnfG with AnfDK. This work establishes that the structural components of the Fe-nitrogenase can be engineered into plant mitochondria and form a complex, which will be a requirement for function. This report outlines the first use of Fe-nitrogenase proteins within a plant as a preliminary step towards engineering an alternative nitrogenase into crops.
- Subject
- nitrogenase; protein interactions; synthetic biology; plant biotechnology; mitochondrial engineering
- Identifier
- http://hdl.handle.net/1959.13/1484230
- Identifier
- uon:51287
- Identifier
- ISSN:0167-4412
- Rights
- x
- Language
- eng
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