General discussion

J. R. Postgate. I enquire why there has been so little mention of stem nodulation in Sesbania spp. W hat are the modes of initial infection in these plants? C. Elmerich. The details of infection of stems of Sesbania rostrata are being studied presently. So far the signals involved in nodule initiation are unknown but the physiological steps are known. Infection of stems occurs in incipient root primordia, which are arranged in several rows vertically on each stem. It seems to involve breaks in the stem surface where these primordia emerge but do not develop into roots. Comparisons of strains of bacteria that form both stem and root nodules with those that form only root nodules suggest that the same nod genes are involved in both.

1996 ◽  
Vol 42 (2) ◽  
pp. 187-190 ◽  
Author(s):  
Kodjo Tomekpe ◽  
Marcelle Holsters ◽  
Bernard Dreyfus

Azorhizobium caulinodans ORS571 and Sinorhizobium teranga ORS51 and ORS52 are symbionts of the same host plant Sesbania rostrata. In nature, A. caulinodans nodulates more competitively the stem-located infection sites of Sesbania rostrata. Sinorhizobium strains, although frequently present in root nodules, are seldom found in stem nodules. One probable explanation for this phenomenon is the more abundant presence of Azorhizobium on the leaf and stem surfaces of the host plant. Work presented here hints at other plausible factors that determine the greater "stem specificity" of Azorhizobium. We found that under experimental conditions in which roots are not inoculated, all strains nodulated stems very well. However, ORS51 and ORS52 were much more sensitive than ORS571 to suppression of stem nodulation by previous root inoculation. The introduction of the regulatory nodD gene from A. caulinodans diminished the sensitivity to this suppression, probably by enhanced nod gene expression and subsequent Nod factor production. Our hypothesis is that the greater infectivity of ORS571 is due to a more efficient production of mitogenic Nod factors at stem-located infection sites, thereby more readily overcoming systemic suppression caused by previous root inoculations.Key words: autoregulation, nitrogen fixation, rhizobial ecology, systemic suppression of nodulation.


Genome ◽  
1989 ◽  
Vol 31 (1) ◽  
pp. 354-360 ◽  
Author(s):  
San Chiun Shen ◽  
Shui Ping Wang ◽  
Guan Qiao Yu ◽  
Jia Bi Zhu

Genes that specify nodulation (nod genes) are only active in the free-living rhizobia or in the nodule initiation state of rhizobia. As soon as the repression of nod genes occurs in the bacteroids of the nodule, nifA is induced, while ntrC is inactivated and thus the nifA-mediated nif/fix genes are turned on. Limitation of available oxygen brings about the induction of nifA, which reflects the actual status of nif/fix gene activities in symbiotic state of rhizobia. Oxygen thus appears to be a major symbiotic signal to the expression of bacteroid nif/fix genes. Mutation of nifA or shortage of nifA product in wild-type rhizobia caused by the inhibition of multicopy nifH/fixA promoters leads to an abnormal development of nodules and premature degradation of bacteroids in nodules.Key words: nitrogen fixation, nodulation, nif/fix regulation, nifA mutant.


2015 ◽  
Vol 28 (8) ◽  
pp. 847-855 ◽  
Author(s):  
Chao Wang ◽  
Haixiang Yu ◽  
Zhongming Zhang ◽  
Liangliang Yu ◽  
Xiaoshu Xu ◽  
...  

Phytosulfokine (PSK) is a tyrosine-sulfated peptide that is widely distributed in plants, participating in cell proliferation, differentiation, and innate immunity. The potential role of PSK in nodulation in legumes has not been reported. In this work, five PSK precursor genes were identified in Lotus japonicas, designated as LjPSK1 to LjPSK5. Three of them (LjPSK1, LjPSK4, and LjPSK5) were found to be expressed in nitrogen-fixing root nodules. LjPSK1 and LjPSK4 were not induced at the early stage of nodulation. Interestingly, while the expression of LjPSK4 was also found in spontaneous nodules without rhizobial colonization, LjPSK1 was not induced in these pseudo nodules. Promoter-β-glucuronidase analysis revealed that LjPSK1 was highly expressed in enlarged symbiotic cells of nodules. Exogenous addition of 1 μM synthetic PSK peptide resulted in increased nodule numbers per plant. Consistently, the number of mature nodules but not the events of rhizobial infection and nodule initiation was increased by overexpressing LjPSK1 in transgenic hairy roots, in which the expression of jasmonate-responsive genes was found to be repressed. These results suggest that PSK is a new peptide signal that regulates nodulation in legumes, probably through cross-talking with other phytohormones.


1984 ◽  
Vol 35 (2) ◽  
pp. 149 ◽  
Author(s):  
DF Herridge ◽  
RJ Roughley ◽  
J Brockwell

The symbiosis of the root-nodules of Bragg soybean [Glycine max (L.) Merrill] and the relative dependence of the plants on symbiotic and soil sources of N were evaluated in an experiment conducted on a vertisol which was high in organic- and mineral-N, free of Rhizobium japonicum, and where poor nodulation was characteristic of inoculated, new sowings. Effective inoculant containing R. japonicum strain CB 1809 was sprayed into the seed bed at three rates of application (10-fold intervals). Increasing rates of inoculant led to greater numbers of rhizobia in the rhizosphere and in the soil, and to improved nodulation. Uninoculated plants did not nodulate. High soil NO-3 (30 �g N/g, top 30 cm) did not prevent prompt, abundant colonization of rhizospheres by the bacteria from the inoculant, but nodule initiation was delayed and nodule development was retarded until 42 days after sowing. There was an acceleration in nodule formation and development between 42 and 62 days which coincided with a depletion of NO-3 from the top 60 cm of the soil profile. Nodulated and unnodulated soybeans took up NO-3 at similar times and rates to a soil depth of 90 cm; only unnodulated plants utilized soil NO-3 below 90 cm. Vacuum-extracted stem (xylem) exudate was sampled from plants throughout growth and analysed for nitrogenous solutes. The proportion of ureide-N relative to total-solutes-N in xylem sap was used as an index of symbiotic N2-fixation. The initial increase in concentrations of ureides coincided with the period of accelerated nodule formation and development between 42 and 62 days. Thereafter, there was a progressive increase in ureide concentrations in nodulated plants, and the levels were related to rate of inoculation, extent of nodulation, and to the decline in concentrations of soil NO-3. Ureide concentrations in unnodulated plants remained low throughout. The quantities of NO-3-N and �-NH2- N in xylem sap were not related to nodulation. The differences between treatments in terms of whole-plant N and grain N were less than predicted from the symbiotic parameters. This indicated that soybeans compensated for symbiotic deficiencies by more efficient exploitation of soil N and/or by more efficient redistribution of vegetative N into grain N, and that nodulation and soil NO-3 were interactive and complementary in meeting the N requirements of the crop.


1994 ◽  
Vol 49 (2) ◽  
pp. 143-151
Author(s):  
S. Rajavelu ◽  
V. C. Saralabai ◽  
M. Vivekanandan

2007 ◽  
Vol 73 (20) ◽  
pp. 6650-6659 ◽  
Author(s):  
Shino Suzuki ◽  
Toshihiro Aono ◽  
Kyung-Bum Lee ◽  
Tadahiro Suzuki ◽  
Chi-Te Liu ◽  
...  

ABSTRACT The molecular and physiological mechanisms behind the maturation and maintenance of N2-fixing nodules during development of symbiosis between rhizobia and legumes still remain unclear, although the early events of symbiosis are relatively well understood. Azorhizobium caulinodans ORS571 is a microsymbiont of the tropical legume Sesbania rostrata, forming N2-fixing nodules not only on the roots but also on the stems. In this study, 10,080 transposon-inserted mutants of A. caulinodans ORS571 were individually inoculated onto the stems of S. rostrata, and those mutants that induced ineffective stem nodules, as displayed by halted development at various stages, were selected. From repeated observations on stem nodulation, 108 Tn5 mutants were selected and categorized into seven nodulation types based on size and N2 fixation activity. Tn5 insertions of some mutants were found in the well-known nodulation, nitrogen fixation, and symbiosis-related genes, such as nod, nif, and fix, respectively, lipopolysaccharide synthesis-related genes, C4 metabolism-related genes, and so on. However, other genes have not been reported to have roles in legume-rhizobium symbiosis. The list of newly identified symbiosis-related genes will present clues to aid in understanding the maturation and maintenance mechanisms of nodules.


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