Methods and compositions for improving plant traits
Disclosed herein are methods of increasing nitrogen fixation in a non-leguminous plant. The methods can comprise exposing the plant to a plurality of bacteria. Each member of the plurality comprises one or more genetic variations introduced into one or more genes or non-coding polynucleotides of the bacteria's nitrogen fixation or assimilation genetic regulatory network, such that the bacteria are capable of fixing atmospheric nitrogen in the presence of exogenous nitrogen. The bacteria are not intergeneric microorganisms. Additionally, the bacteria, in planta, produce 1% or more of the fixed nitrogen in the plant.
1. An engineered, non-intergeneric diazotroph having increased nitrogen fixation activity as compared to an unmodified organism of the same species as said engineered, non-intergeneric diazotroph, wherein said engineered, non-intergeneric diazotroph comprises a genetic variation within one or more genes for regulating nitrogen fixation or assimilation, said genetic variation comprising genetic material that originates from at least one organism of the same species as said engineered, non-intergeneric diazotroph.
2. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph is an engineered bacterium.
3. The engineered, non-intergeneric diazotroph of claim 1 , wherein the genetic variation is within a gene in the nitrogen fixation genetic regulatory pathway.
4. The engineered, non-intergeneric diazotroph of claim 3 , wherein the genetic variation within the one or more genes for regulating nitrogen fixation or assimilation alters the activity or expression of a gene selected from the group consisting of NifA, NifL, and NifH.
5. The engineered, non-intergeneric diazotroph of claim 1 , wherein the genetic variation is within a gene in the nitrogen assimilation genetic regulatory pathway.
6. The engineered, non-intergeneric diazotroph of claim 5 , wherein the genetic variation within the one or more genes for regulating nitrogen fixation or assimilation alters the activity or expression of a gene selected from the group consisting of GlnE, AmtB, ntrB, ntrC, polynucleotide encoding glutamine synthetase, glnA, glnB, glnK, draT, polynucleotide encoding glutaminase, and glnD.
7. The engineered, non-intergeneric diazotroph of claim 1 , wherein said genetic material comprises a regulatory element.
8. The engineered, non-intergeneric diazotroph of claim 7 , wherein said regulatory element is a heterologous regulatory element.
9. The engineered, non-intergeneric diazotroph of claim 7 , wherein said regulatory element is a promoter.
10. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph has increased nitrogen fixation activity in the presence of at least 0.01 mM fixed nitrogen, as compared to an unmodified diazotroph of the same species, in the presence of the same concentration of fixed nitrogen.
11. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph has increased nitrogen fixation activity in the presence of at least 0.1 mM fixed nitrogen, as compared to an unmodified diazotroph of the same species, in the presence of the same concentration of fixed nitrogen.
12. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph has increased nitrogen fixation activity in the presence of at least 0.5 mM fixed nitrogen, as compared to an unmodified diazotroph of the same species, in the presence of the same concentration of fixed nitrogen.
13. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph has increased nitrogen fixation activity in a field, as compared to an unmodified diazotroph of the same species, in the same field.
14. The engineered, non-intergeneric diazotroph of claim 13 , wherein said field has a fixed nitrogen concentration of at least 0.01 mM.
15. The engineered, non-intergeneric diazotroph of claim 13 , wherein said field has a fixed nitrogen concentration of at least 0.1 mM.
16. The engineered, non-intergeneric diazotroph of claim 13 , wherein said field has a fixed nitrogen concentration of at least 0.5 mM.
17. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph is an epiphyte.
18. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph is an endophyte.
19. The engineered, non-intergeneric diazotroph of claim 1 , wherein said engineered, non-intergeneric diazotroph is a rhizophyte.
20. The engineered, non-intergeneric diazotroph of claim 1 , wherein the genetic material of said engineered, non-intergeneric diazotroph consists essentially of genetic material that originates from at least one organism of the same species as said engineered, non-intergeneric diazotroph.
21. A composition, comprising the engineered non-intergeneric diazotroph of claim 1 , and a plant seed.
22. The composition of claim 21 , wherein the plant seed is a non-leguminous plant seed.
23. The composition of claim 21 , wherein the plant seed is a cereal plant seed.
24. The composition of claim 21 , wherein the plant seed is a seed of a plant selected from the group consisting of: corn, wheat, and sorghum.
25. The composition of claim 21 , wherein the engineered, non-intergeneric diazotroph is coated onto the plant seed.
26. The composition of claim 25 , wherein the engineered, non-intergeneric diazotroph is within a seed coating that is coated onto the plant seed.
27. The engineered, non-intergeneric diazotroph of claim 1 , wherein the one or more genes regulating nitrogen fixation or assimilation are selected from the group consisting of nifA, nifL, nrB, ntrC, ginA, ghnB, ginK, draT, amtB, ginD, ginE, nifH, nifJ, nifD, nifK, nifY, nifE, nifN, nifU, nifS, nitV, nifW, nifZ, nifM, nitF, nifB, and nifQ.
28. The engineered, non-intergeneric diazotroph of claim 1 , wherein the genetic variation within the one or more genes for regulating nitrogen fixation or assimilation results in one or more of increased expression or activity of NifA or glutaminase, decreased expression or activity of NifL, NtrB, glutamine synthetase, GlnB, GlnK, DraT, or AmtB; decreased adenylyl-removing activity of GlnE; or decreased uridylyl-removing activity of GlnD.
29. The engineered, non-intergeneric diazotroph of claim 1 , wherein the diazotroph is a proteobacterium.