Abstract

Biological nitrogen fixation emerging from the symbiosis between bacteria and crop plants holds promise to increase the sustainability of agriculture. One of the biggest hurdles for the engineering of nitrogen‐fixing organisms is an incomplete knowledge of metabolic interactions between microbe and plant. In contrast to the previously assumed supply of only succinate, we describe here the CATCH‐N cycle as a novel metabolic pathway that co‐catabolizes plant‐provided arginine and succinate to drive the energy‐demanding process of symbiotic nitrogen fixation in endosymbiotic rhizobia. Using systems biology, isotope labeling studies and transposon sequencing in conjunction with biochemical characterization, we uncovered highly redundant network components of the CATCH‐N cycle including transaminases that interlink the co‐catabolism of arginine and succinate. The CATCH‐N cycle uses N2 as an additional sink for reductant and therefore delivers up to 25% higher yields of nitrogen than classical arginine catabolism—two alanines and three ammonium ions are secreted for each input of arginine and succinate. We argue that the CATCH‐N cycle has evolved as part of a synergistic interaction to sustain bacterial metabolism in the microoxic and highly acid environment of symbiosomes. Thus, the CATCH‐N cycle entangles the metabolism of both partners to promote symbiosis. Our results provide a theoretical framework and metabolic blueprint for the rational design of plants and plant‐associated organisms with new properties to improve nitrogen fixation.

Highlights

  • Nitrogen is a fundamental element of all living organisms and the primary nutrient that impacts crop yield (Socolow, 1999)

  • While the stimulation of nitrogenase only poorly occurred in the presence of succinate as the sole nutrient, we found that the addition of arginine stimulated nitrogenase activity in B. diazoefficiens and S. meliloti by 46% Æ 4% and 116% Æ 2%, respectively, as compared to nodule extracts (Appendix Table S1)

  • We report on the CATCH-N cycle operating on the provision of the two substrates arginine and succinate by the plant as part of a specific metabolic network that drives the process of symbiotic nitrogen fixation in rhizobia

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Summary

Introduction

Nitrogen is a fundamental element of all living organisms and the primary nutrient that impacts crop yield (Socolow, 1999). The emerging field of synthetic biology provides an alternative approach to engineer designer nitrogenase gene clusters in bacteria (Temme et al, 2012; Li et al, 2016; Buren et al, 2018; Yang et al, 2018). Despite these promising results, engineered organisms based on heterologous expression of nitrogenase genes have not yet come close to the efficiency of natural rhizobia–legume symbiosis systems (Beatty & Good, 2011; Good, 2018). While the molecular mechanism of the nitrogenase reaction has been resolved with atomistic detail (Hoffman et al, 2009, 2014; Seefeldt et al, 2009; Sippel & Einsle, 2017), the precise nature of metabolic interactions between plants and bacteria to sustain the energy-intensive process of nitrogen fixation has remained an open question

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