The Role of Rhizobial Biodiversity in Legume Crop Productivity in the West Asian Highlands. III.Rhizobium meliloti

1995 ◽  
Vol 31 (4) ◽  
pp. 493-499 ◽  
Author(s):  
L. A. Materon ◽  
J. D. H. Keatinge ◽  
D. P. Beck ◽  
N. Yurtsever ◽  
K. Karuc ◽  
...  

SUMMARYThe native rhizobia capable of symbiosis with potential pasture legume crops for the west Asian highlands were surveyed and estimates made of the numbers and nitrogen fixing efficiency of isolates ofRhizobium melilotiwith a range of annualMedicagospecies. Soils were collected from 105 sites at elevations between 500 and 2200 m. Numbers of bacteria were generally adequate to permit efficient nodulation but the nitrogen fixing efficiency of three of the four host species with the indigenous rhizobia was often low. In contrast, nitrogen fixation inM. aculeatawas generally highly efficient. No overall geographic pattern in either numbers or efficiency of nitrogen fixation was evident. Substantial further research is required before annual medic crops can be successfully introduced into highland crop/livestock systems in Turkey and elsewhere in the west Asian highlands.Biodiversidad en elRhizobium meliloti

1995 ◽  
Vol 31 (4) ◽  
pp. 501-507 ◽  
Author(s):  
J. D. H. Keatinge ◽  
D. P. Beck ◽  
L. A. Materon ◽  
N. Yurtsever ◽  
K. Karuc ◽  
...  

SUMMARYThe native rhizobia capable of symbiosis with chickpea crops in the Turkish highlands were surveyed and estimates made of the numbers of bacteria and the nitrogen fixing efficiency of isolates of R. ciceri in symbiosis with an improved Turkish cultivar and a local landracc. Soils were collected from locations at elevations between 500 and 2200 m.Native rhizobia specific to the local landrace were more abundant than those specific to the improved cultivar but nitrogen fixation efficiencies of all isolates were consistently poor. Agronomic research priorities must include the identification of strains of rhizobia symbiotically efficient and ecologically persistent in highland soils. Comprehensive trials with these strains as artificial inoculants on chickpeas are required throughout the region.Biodiversidad en el Rhizobium ciceri


1995 ◽  
Vol 31 (4) ◽  
pp. 485-491 ◽  
Author(s):  
L. A. Materon ◽  
J. D. H. Keatinge ◽  
D. P. Beck ◽  
N. Yurtsever ◽  
K. Karuc ◽  
...  

SUMMARYThe native rhizobia capable of symbiosis with annually-sown food and forage legume crops in the Turkish highlands were surveyed and estimates made of the numbers and nitrogen fixing efficiency of native Rhizobium leguminosarum with Turkish cultivars of lentil (Lens culinaris Medik.) and vetch (Vicia sativa L.). Native rhizobia were present in medium to high numbers in most samples but the nitrogen fixation efficiency of at least half of the isolates was poor. Vetch was somewhat less specific in its rhizobial compatibility than lentil, suggesting a potential for artificial inoculation to improve the productivity and sustainability of cropping in both species especially in areas of central and eastern Anatolia where legumes are not traditionally grown.Biodiversidad en el Rhizobium leguminosarum


1995 ◽  
Vol 31 (4) ◽  
pp. 473-483 ◽  
Author(s):  
J. D. H. Keatinge ◽  
L. A. Materon ◽  
D. P. Beck ◽  
N. Yurtsever ◽  
K. Karuc ◽  
...  

SUMMARYThe numbers of bacteria and the nitrogen fixing efficiency of isolates ofRhizobium leguminosarum, R. ciceriandR. melilotiwith appropriate legume crop species were determined from soils collected from a wide range of locations in Turkey with elevations between 500 and 2200 m. For vetch and lentil nodulated byR. leguminosarum, many native rhizobia are present in most locations but they often have limited nitrogen fixation capacity. However, for chickpea nodulated byR. ciceri, relatively small numbers of bacteria and the almost universal ineffectiveness of fixation capacity point to a need for artificial seed inoculation of chickpea crops as a future agronomic priority. The wide range of bacterial numbers, considerable geographic inconsistency and generally low effectiveness of the indigenous rhizobia associated with the annualMedicagospp. suggest that inoculation would initially be a sensible precaution for all sowings.Biodiversidad del rhizobium en Asia occidental


2007 ◽  
Vol 20 (10) ◽  
pp. 1241-1249 ◽  
Author(s):  
Manuel J. Granados-Baeza ◽  
Nicolás Gómez-Hernández ◽  
Yolanda Mora ◽  
María J. Delgado ◽  
David Romero ◽  
...  

Symbiotic nitrogen-fixing bacteria express a terminal oxidase with a high oxygen affinity, the cbb3-type oxidase encoded by the fixNOQP operon. Previously, we have shown that, in Rhizobium etli CFN42, the repeated fixNOQP operons (fixNOQPd and fixNOQPf) have a differential role in nitrogen fixation. Only the fixNOQPd operon is required for the establishment of an effective symbiosis; microaerobic induction of this operon is under the control of at least three transcriptional regulators, FixKf, FnrNd, and FnrNchr, belonging to the Crp/Fnr family. In this work, we describe two novel Crp/Fnr-type transcriptional regulators (StoRd and StoRf, symbiotic terminal oxidase regulators) that play differential roles in the control of key genes for nitrogen fixation. Mutations either in stoRd or stoRf enhance the microaerobic expression of both fixNOQP reiterations, increasing also the synthesis of the cbb3-type oxidase in nodules. Despite their structural similarity, a differential role of these genes was also revealed, since a mutation in stoRd but not in stoRf enhanced both the expression of fixKf and the nitrogen-fixing capacity of R. etli CFN42.


2019 ◽  
Author(s):  
◽  
Nhung Thi Huyen Hoang

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] Nitrogen is a macronutrient that is critical for plant growth and development because it provides the building blocks of nucleic acids, proteins, chlorophyll, and energy- transfer compounds, such as ATP. Although 78% of the atmosphere is diatomic nitrogen, this form is inert and unavailable to plants due to the strong nitrogen-nitrogen triple bond. Plants can only absorb nitrogen in the forms of NH4+ or NO3-. Most of the inorganic nitrogen available to crop plants is provided through fertilizers synthesized based on the Haber-Bosch process. This process converts atmospheric nitrogen (N2) into ammonia (NH3) by a reaction with hydrogen (H2) using a metal catalyst (iron) under high temperatures (~500 [degrees]C) and high pressures (150-300 bar). Ammonia production by this method consumes a lot of energy, which is derived from burning fossil fuels. Synthetic ammonia production by the Haber-Bosch process causes losses of biodiversity through eutrophication, soil acidification and global increase in N2O atmospheric concentration, which is the third most significant greenhouse gas. An alternative approach to provide a sustainable nitrogen source to plants without causing such damage to the environment is through biological nitrogen fixation between legume species and Rhizobium bacteria. The symbiotic interaction between legume plants and rhizobia results in the formation of root nodules, specialized organs within which rhizobia convert atmospheric nitrogen into ammonia for plant consumption. In return, the legume host plants provide rhizobia with photosynthate as a carbon source for their growth. The legume - Rhizobium symbiosis is a sophisticated process that requires numerous regulators including the 20-24 nucleotide-long microRNAs which negatively regulate the expression of their target messenger RNAs. In my study, we provide two examples that demonstrate the significant role of microRNAs in the symbiotic interplay between soybean, an important legume crop, and rhizobia. In the first example, our results suggest that gma-miR319i functions as a positive regulator of nodule number during the soybean - Bradyrhizobium symbiosis by targeting the TCP33 transcription factor. Overexpression and CRISPR/cas9-mediated gene mutation of gma-miR319i increased and reduced nodule number after rhizobial inoculation, respectively. gma-miR319i and TCP33 showed an inverse expression pattern in different stages of nodule development. TCP33 modulated nodule development in a gma-miR319i dependent manner. The expression of gma-miR319i and TCP33 was differentially regulated in one soybean mutant line that exhibits a hypernodulation phenotype. In the second example, we further investigated the mechanism by which two identical microRNAs, gma-miR171o and gma-miR171q, function in modulating the spatial and temporal aspects of soybean nodulation. Although sharing the identical mature sequence, gma-miR171o and gma-miR171q genes are divergent and show unique, tissue-specific expression patterns. The expression levels of the two miRNAs are negatively correlated with that of their target genes. Ectopic expression of these miRNAs in transgenic hairy roots resulted in a significant reduction in nodule formation. Both gma-miR171o and gma-miR171q target members of the GRAS transcription factor superfamily, namely GmSCL-6 and GmNSP2. Besides those two above-mentioned examples, we were able to generate and characterize an enhancer trap insertional mutant of the NODULATION SIGNALING PATHWAY 2 (NSP2) gene which is the target gene of Gma-miR171 and also an important regulator of nodulation. Overall, our study shows the importance of microRNAs in the regulation of nitrogen-fixing symbiosis. Our results contribute to efforts to fully understand the molecular mechanisms controlling the legume - Rhizobium interaction. Our ultimate hope is that the information gained through my studies can lead to an increased utilization of biological nitrogen fixation for sustainable agriculture and environment protection.


1998 ◽  
Vol 11 (9) ◽  
pp. 878-886 ◽  
Author(s):  
Bert Boesten ◽  
Jacques Batut ◽  
Pierre Boistard

The Sinorhizobium meliloti C4-dicarboxylate transport gene (dctA) is essential for symbiotic nitrogen fixation. Under free-living conditions, the expression of dctA is fully dependent on the cognate regulatory genes dctBD. However, during symbiosis with the Medicago sativa host plant, the dctA gene is efficiently expressed even in the absence of the dctBD genes. The spatial expression of the dctA gene has been monitored in situ in mature nitrogen-fixing nodules formed by wild-type and dctD mutant strains. In nodules induced by a wild-type strain, expression was observed in both the infection zone and the nitrogen-fixing zone of the nodule. DctD-independent expression of dctA was observed with a previously described dctA∷lacZ fusion (pCU700) and was found to be confined to the fixation zone (zone III) of mature nodules. Therefore, the operation of the alternative system of symbiotic dctA activation (ASA) is concomitant with the onset of nitrogen fixation, which could be consistent with an increased need for transport of (C)4(-dicarboxylic acids by the nitrogen-fixing) bacteroids. Sequences in the 5′ part of the dctA coding region were found to be essential for the activation of the dctA∷lacZ gene fusions by the ASA. Deletion of these sequences resulted in gene fusions that were found to be strictly dependent on dctBD for expression, under all conditions tested including symbiosis. Such gene fusions allowed us to establish that the DctBD-dependent dctA expression was occurring throughout the whole nodule.


2018 ◽  
Vol 45 (2) ◽  
pp. 47 ◽  
Author(s):  
Anna V. Tsyganova ◽  
Anna B. Kitaeva ◽  
Viktor E. Tsyganov

The nitrogen-fixing nodule is a unique ecological niche for rhizobia, where microaerobic conditions support functioning of the main enzyme of nitrogen fixation, nitrogenase, which is highly sensitive to oxygen. To accommodate bacteria in a symbiotic nodule, the specialised infected cells increase in size owing to endoreduplication and are able to shelter thousands of bacteria. Bacteria are isolated from the cytoplasm of the plant cell by a membrane-bound organelle-like structure termed the symbiosome. It is enclosed by a symbiosome membrane, mainly of plant origin but with some inclusion of bacterial proteins. Within the symbiosome, bacterial cells differentiate into bacteroids a form that is specialised for nitrogen fixation. In this review, we briefly summarise recent advances in studies of differentiation both of symbiosomes and of the infected cells that accommodate them. We will consider the role of CCS52A, DNA topoisomerase VI, tubulin cytoskeleton rearrangements in differentiation of infected cells, the fate of the vacuole, and the distribution of symbiosomes in the infected cells. We will also consider differentiation of symbiosomes, paying attention to the role of NCR peptides, vesicular transport to symbiosomes, and mutant analysis of symbiosome development in model and crop legumes. Finally, we conclude that mechanisms involved in redistribution organelles, including the symbiosomes, clearly merit much more attention.


2021 ◽  
Author(s):  
Amanda K. Garcia ◽  
Bryan Kolaczkowski ◽  
Betul Kacar

The evolution of biological nitrogen fixation, uniquely catalyzed by nitrogenase enzymes, has been one of the most consequential biogeochemical innovations over life's history. Though understanding the early evolution of nitrogen fixation has been a longstanding goal from molecular, biogeochemical, and planetary perspectives, its origins remain enigmatic. In this study, we reconstructed the evolutionary histories of nitrogenases, as well as homologous maturase proteins that participate in the assembly of the nitrogenase active-site cofactor but are not able to fix nitrogen. We combined phylogenetic and ancestral sequence inference with an analysis of predicted functionally divergent sites between nitrogenases and maturases to infer the nitrogen-fixing capabilities of their shared ancestors. Our results provide phylogenetic constraints to the emergence of nitrogen fixation and suggest that nitrogenases likely emerged from maturase-like predecessors. Though the precise functional role of such a predecessor protein remains speculative, our results highlight evolutionary contingency as a significant factor shaping the evolution of a biogeochemically essential enzyme.


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