Competition for nodulation of Pisum sativum cv. Afghanistan requires live rhibozia and a plant component

1982 ◽  
Vol 28 (2) ◽  
pp. 162-168 ◽  
Author(s):  
W. J. Broughton ◽  
Ursula Samrey ◽  
B. Ben Bohlool

Nodulation of Pisum sativum cv. Afghanistan by Rhizobium leguminosarum strain Tom can be blocked by R. leguminosarum strain PF2 (isolated from P. sativum cv. Rondo) which does not form nodules of Afghanistan peas. We tested PF2 for its ability to produce bacteriocins and other compounds inhibitory to the growth of Tom. Neither strain was antagonistic toward the other. Similarly, there was no evidence for the production of inhibitors as the rhizobia grew in the plant rhizosphere. Apart from an already noted (Broughton et al. 1980. Can. J. Microbiol. 26: 562–565) ability of PF2 to accumulate on the root surfaces two to three times faster than Tom, we could not find a reason to explain the complete blocking of nodulation. In other experiments using PF2 (and Tom) killed by exposure to massive doses of gamma irradiation, dead cells still bound to the roots but they were incapable of blocking nodulation by living Tom. Finally, when both rhizobia were used to inoculate P. sativum cv. Rondo (they both form nodules on this plant), roughly one third of the nodules contained Tom, one third contained PF2, and one third contained both strains (i.e.,there was no evidence for competition). We conclude, therefore, that competition in this system is dependent upon live bacteria and requires cooperation from the plant.


1984 ◽  
Vol 62 (8) ◽  
pp. 1682-1686 ◽  
Author(s):  
Eulogio J. Bedmar ◽  
Donald A. Phillips

Data from 14 Pisum sativum L. cultivars establish that three pea genotypes, which were previously reported to affect net H2 evolution from root nodules in air and uptake hydrogenase activity of Rhizobium leguminosarum 128C53, are not unique. Two pea lines, 'JI1205' and 'Green Arrow,' produced very active uptake hydrogenase activity in strain 128C53, and essentially no H2 was evolved in air from root nodules capable of reducing 20 μmol C2H2 ∙ plan−1 ∙ h−1. Five other cultivars produced significantly lower uptake hydrogenase activities in the same bacterial strain and had much higher rates of net H2 evolution with similar C2H2-reduction capabilities. Parallel experiments with the same cultivars nodulated by R. leguminosarum 300, an organism with no convincing uptake hydrogenase activity in any pea line, showed that 'JI1205' and 'Green Arrow' had a significantly lower relative efficiency (RE) of N2 fixation (1 − (H2 evolved in air/C2H2 reduced)) than the other five cultivars. Developmental differences among the pea lines prevented any conclusion about the advantages or disadvantages of uptake hydrogenase activity for plant growth, but in general, cultivars with high uptake hydrogenase activity and low net H2 evolution grew more slowly than those evolving large amounts of H2.



1980 ◽  
Vol 26 (4) ◽  
pp. 562-565 ◽  
Author(s):  
W. J. Broughton ◽  
A. W. S. M. van Egeraat ◽  
T. A. Lie

Nodulation of Pisum sativum cv. Afghanistan by Rhizobium leguminosarum strain Tom can be blocked by the nonnodulating R. leguminosarum strain PF2. This system was used to study the dynamics of rhizobial binding to seedling root surfaces. Appreciable numbers of 35S-labeled rhizobia bound to the root surface within 2 h after inoculation. PF2 colonized the root surfaces earlier and in greater numbers that did Tom. Radioactive extracellular polysaccharides and lipopolysaccharides from either organism failed to bind to the seedling roots in measurable quantities.



2019 ◽  
Vol 70 (1) ◽  
pp. 59-67
Author(s):  
Anna Lenart-Boroń ◽  
Tadeusz Zając ◽  
Piotr Mateusz Boroń ◽  
Agnieszka Klimek-Kopyra

SummaryThe bacterial nodulation (nod) genes are essential in the formation process of root nodules. This study was aimed to verify the occurrence of nodule-associated bacteria in two pea varieties (“Tarchalska” and “Klif ”) inoculated withRhizobiuminoculants – Nitragine™ and a noncommercial one produced by the Polish Institute of Soil Science and Plant Cultivation (IUNG). The number of colonies isolated on yeast extract mannitol (YEM) agar from the nodules of “Klif ” inoculated with IUNG inoculants was significantly higher than the number of colonies isolated from other variants. Species identification was based on sequencing of 16S rDNA, which revealed that despite careful sterilization of nodules, sequences of other bacterial species were detected. Among them, one sequence belonged toRhizobium leguminosarum(isolated from IUNG inoculant). To assess the presence of nodulation-capableRhizobium, amplification of thenodCgene was performed, which revealed that of 29 samples, 19 were positive. The remaining isolates, including reference strain and bacteria isolated from Nitragine™, lacked this gene. The results show that pea nodules harbor a very diverse community of bacteria. The lack ofnodCgene in some strains isolated from plants inoculated with Nitragine™ and with IUNG inoculant proves that even ifR. leguminosarumare abundant, they may not be efficient in nodulation.



Plants ◽  
2021 ◽  
Vol 10 (10) ◽  
pp. 2120
Author(s):  
Jessica Frigerio ◽  
Giulia Agostinetto ◽  
Valerio Mezzasalma ◽  
Fabrizio De De Mattia ◽  
Massimo Labra ◽  
...  

Medicinal plants have been widely used in traditional medicine due to their therapeutic properties. Although they are mostly used as herbal infusion and tincture, employment as ingredients of food supplements is increasing. However, fraud and adulteration are widespread issues. In our study, we aimed at evaluating DNA metabarcoding as a tool to identify product composition. In order to accomplish this, we analyzed fifteen commercial products with DNA metabarcoding, using two barcode regions: psbA-trnH and ITS2. Results showed that on average, 70% (44–100) of the declared ingredients have been identified. The ITS2 marker appears to identify more species (n = 60) than psbA-trnH (n = 35), with an ingredients’ identification rate of 52% versus 45%, respectively. Some species are identified only by one marker rather than the other. Additionally, in order to evaluate the quantitative ability of high-throughput sequencing (HTS) to compare the plant component to the corresponding assigned sequences, in the laboratory, we created six mock mixtures of plants starting both from biomass and gDNA. Our analysis also supports the application of DNA metabarcoding for a relative quantitative analysis. These results move towards the application of HTS analysis for studying the composition of herbal teas for medicinal plants’ traceability and quality control.



1988 ◽  
Vol 89 (2) ◽  
pp. 243-252
Author(s):  
L.M. Stoilov ◽  
J.S. Zlatanova ◽  
A.P. Vassileva ◽  
M.G. Ivanchenko ◽  
C.P. Krachmarov ◽  
...  

Plant nuclei have been studied with respect to the three-dimensional structure of DNA. Nucleoids derived from nuclei by non-ionic detergent and high salt treatment were analysed by sedimentation in a series of sucrose gradients containing increasing amounts of the intercalating agent ethidium bromide. In addition the nucleoid sedimentation behaviour was investigated following gamma irradiation. The results show that plant DNA is supercoiled, as is the DNA from the other eukaryotes studied, and contains approximately the same concentration of superhelical turns but probably relatively fewer DNA superhelical loops. The plant nuclear populations in all cases studied give rise to two distinct nucleoid bands. These have been characterized by electron microscopy and by their DNA and protein content. The possible origin of the two bands is discussed.



1995 ◽  
Vol 172 (2) ◽  
pp. 189-198 ◽  
Author(s):  
A. N. Fesenko ◽  
N. A. Provorov ◽  
Irina F. Orlova ◽  
V. P. Orlov ◽  
B. V. Simarov


2017 ◽  
Vol 30 (4) ◽  
pp. 312-324 ◽  
Author(s):  
George C. diCenzo ◽  
Maryam Zamani ◽  
Hannah N. Ludwig ◽  
Turlough M. Finan

The bacterium Sinorhizobium meliloti Rm2011 forms N2-fixing root nodules on alfalfa and other leguminous plants. The pSymB chromid contains a 110-kb region (the ETR region) showing high synteny to a chromosomally located region in Sinorhizobium fredii NGR234 and related rhizobia. We recently introduced the ETR region from S. fredii NGR234 into the S. meliloti chromosome. Here, we report that, unexpectedly, the S. fredii NGR234 ETR region did not complement deletion of the S. meliloti ETR region in symbiosis with Medicago sativa. This phenotype was due to the bacA gene of NGR234 not being functionally interchangeable with the S. meliloti bacA gene during M. sativa symbiosis. Further analysis revealed that, whereas bacA genes from S. fredii or Rhizobium leguminosarum bv. viciae 3841 failed to complement the Fix− phenotype of a S. meliloti bacA mutant with M. sativa, they allowed for further developmental progression prior to a loss of viability. In contrast, with Melilotus alba, bacA from S. fredii and R. leguminosarum supported N2 fixation by a S. meliloti bacA mutant. Additionally, the S. meliloti bacA gene can support N2 fixation of a R. leguminosarum bacA mutant during symbiosis with Pisum sativum. A phylogeny of BacA proteins illustrated that S. meliloti BacA has rapidly diverged from most rhizobia and has converged toward the sequence of pathogenic genera Brucella and Escherichia. These data suggest that the S. meliloti BacA has evolved toward a specific interaction with Medicago and highlights the limitations of using a single model system for the study of complex biological topics.



2001 ◽  
Vol 47 (12) ◽  
pp. 1068-1074 ◽  
Author(s):  
Chantal J. Beauchamp ◽  
Joseph W. Kloepper ◽  
Joseph J. Shaw ◽  
François-P. Chalifour


2011 ◽  
Vol 50 (No. 4) ◽  
pp. 182-187 ◽  
Author(s):  
Š. Klíčová ◽  
J. Šebánek ◽  
T. Vlašic

Flax seedlings were decapitated above the cotyledons. After one cotyledon was removed the growth of the bud of the remaining cotyledon was stronger in 90% of the plants. However, the application of the cytokinin benzyladenine (BA) to the bud of the removed cotyledon caused a growth correlative reversal and, by contrast, in 65% of the plants the bud of the removed cotyledon grew out. On the other hand, in sunflower seedlings, which have epigeal cotyledons similar to flax, after the removal of one cotyledon the growth of the axillary of the removed cotyledon was more intensive in 59% of the plants. Not even an application of BA to the remaining cotyledon of sunflower resulted in more intensive growth of the axillary of this cotyledon. When both cotyledons were left on the seedling, BA applied to one of the cotyledons of decapitated flax plants resulted in a highly significant stimulation of growth of the axillary of this cotyledon; in sunflower; however, the effect of the BA was insignificant. After decapitation of the stem of pea seedlings where both cotyledons remained, both axillaries grew out, but after a certain period of time one of them (the dominant one) achieved a growth correlative dominance over the other (inhibited). The present study is focused on whether an application of plant hormones onto the inhibited shoot is able to cause a growth correlative reversal, i.e. to change the inhibited shoot into a dominant one. The application of 0.12% BA can cause such a reversal virtually in all plants if the original difference in the length between the inhibited and dominating axillaries is 12–24 mm. A 0.12–0.5% concentration of gibberellin causes a reversal in 13–75% of the plants, but only if the difference between the dominant and inhibited shoot is 1–12 mm. A 0.03–0.25% concentration of IAA causes a reversal in 34–57% of the plants, if the difference in the length of the axillaries is 1–4 mm.



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