Determinate development of nodule roots in actinomycete-induced root nodules of Myrica gale

1978 ◽  
Vol 56 (11) ◽  
pp. 1357-1364 ◽  
Author(s):  
John G. Torrey ◽  
Dale Callaham
Keyword(s):  
Root Development ◽  
Root Nodules ◽  
Cortical Cell ◽  
Gas Diffusion ◽  
Nodule Development ◽  
Nodule Formation ◽  
Low Oxygen ◽  
Cortical Cells ◽  
Continuous Growth ◽  
Myrica Gale

Young seedlings of Myrica gale L. grown in water culture were inoculated with a nodule suspension containing the effective actinomycete which induced root nodule formation. Nodule development was followed from initiation to nodule lobe formation and nodule root development using living materials and fixed nodules sectioned for light microscopy. After root hair infection and prenodule formation, three stages were observed: nodule lobe formation, a transition or arrested state, and nodule root development. The primary nodule lobe meristem originates endogenously and its formation involves pericycle, endodermis, and cortical cell derivatives. The lobe develops slowly to about 2 mm in length while the cortical cells are invaded by the actinomycete endophyte. After a period of arrest of variable duration, from a few days to several weeks, the nodule lobe meristem begins altered development, forming the elongate nodule root which undergoes slow but continuous growth to about 3- to 4-cm final length. New nodule lobe primordia are initiated endogenously at the base of existing nodules lobes, ultimately forming a cluster of nodule roots. Each nodule root, which elongates at about 0.1–1.0 mm per day, has a terminal apical meristem with reduced root cap formation and produces a modified root structure possessing an elaborate cortical intercellular space system and a reduced central cylinder. Nodule root growth is distinctive in that it shows strong negative geotropism. The endophyte is restricted to cortical cells of the nodule lobe and is totally absent from tissues of the nodule root. A probable role for nodule roots is to facilitate gas diffusion to the nitrogen-fixing endophyte site in the nodule lobe when nodules occur under conditions of low oxygen tension.

Host–endophyte interactions in effective and ineffective nodules induced by the endophyte of Myrica gale

1983 ◽  
Vol 61 (11) ◽  
pp. 2898-2909 ◽  
Author(s):  
Kathryn A. VandenBosch ◽  
John G. Torrey
Keyword(s):  
Nitrogenase Activity ◽  
Root Nodules ◽  
Seedling Development ◽  
Nodule Development ◽  
Nodule Formation ◽  
Cortical Tissue ◽  
Intercellular Spaces ◽  
Cortical Cells ◽  
Myrica Gale ◽  
Infected Cells

Suspensions of crushed root nodules of Myrica gale containing the actinomycete Frankia induced nodule formation on roots of seedlings of M. gale and Comptonia peregrina grown in nutrient water culture. Nodules formed on M. gale were normal in structure and exhibited nitrogenase activity (measured as acetylene reduction) and provided the necessary nitrogen for seedling development. These effective nodules showed typical external and internal structure with the endophyte developing both vesicles and sporangia within cortical cells of the host tissue. Small nodules formed on C. peregrina representing the primary nodule stage. They lacked nitrogenase activity and were termed ineffective. Vesicles failed to develop within these ineffective nodules. However, sporangia were formed in infected cells and within intercellular spaces of the nodule cortical tissue. In addition, prominent amyloplasts occurred in infected cells of the ineffective nodules, a feature lacking in effective nodules. Exogenously supplied combined nitrogen increased seedling growth but did not improve nodule development or endophyte morphogenesis in the ineffective nodules.

A shared gene drives lateral root development and root nodule symbiosis pathways in Lotus

Science ◽  
2019 ◽  
Vol 366 (6468) ◽  
pp. 1021-1023 ◽  
Author(s):  
Takashi Soyano ◽  
Yoshikazu Shimoda ◽  
Masayoshi Kawaguchi ◽  
Makoto Hayashi
Keyword(s):  
Root Development ◽  
Lateral Root ◽  
Root Nodule ◽  
Root Nodules ◽  
Lotus Japonicus ◽  
Cortical Cell ◽  
Cortical Cells ◽  
Lateral Root Development ◽  
Lateral Organ ◽  
Nodule Symbiosis

Legumes develop root nodules in symbiosis with nitrogen-fixing rhizobial bacteria. Rhizobia evoke cell division of differentiated cortical cells into root nodule primordia for accommodating bacterial symbionts. In this study, we show that NODULE INCEPTION (NIN), a transcription factor in Lotus japonicus that is essential for initiating cortical cell divisions during nodulation, regulates the gene ASYMMETRIC LEAVES 2-LIKE18/LATERAL ORGAN BOUNDARIES DOMAIN16a (ASL18/LBD16a). Orthologs of ASL18/LBD16a in nonlegume plants are required for lateral root development. Coexpression of ASL18a and the CCAAT box–binding protein Nuclear Factor-Y (NF-Y) subunits, which are also directly targeted by NIN, partially suppressed the nodulation-defective phenotype of L. japonicusdaphne mutants, in which cortical expression of NIN was attenuated. Our results demonstrate that ASL18a and NF-Y together regulate nodule organogenesis. Thus, a lateral root developmental pathway is incorporated downstream of NIN to drive nodule symbiosis.

scholarly journals Auxin: at the root of nodule development?

2008 ◽  
Vol 35 (8) ◽  
pp. 651 ◽  
Author(s):  
Ulrike Mathesius
Keyword(s):  
Lateral Root ◽  
De Novo ◽  
Root Nodules ◽  
Lateral Roots ◽  
Nodule Development ◽  
Nodule Formation ◽  
Cortical Cells ◽  
Lateral Root Development ◽  
Organ Differentiation ◽  
Development And Differentiation

Root nodules are formed as a result of an orchestrated exchange of chemical signals between symbiotic nitrogen fixing bacteria and certain plants. In plants that form nodules in symbiosis with actinorhizal bacteria, nodules are derived from lateral roots. In most legumes, nodules are formed de novo from pericycle and cortical cells that are re-stimulated for division and differentiation by rhizobia. The ability of plants to nodulate has only evolved recently and it has, therefore, been suggested that nodule development is likely to have co-opted existing mechanisms for development and differentiation from lateral root formation. Auxin is an important regulator of cell division and differentiation, and changes in auxin accumulation and transport are essential for lateral root development. There is growing evidence that rhizobia alter the root auxin balance as a prerequisite for nodule formation, and that nodule numbers are regulated by shoot-to-root auxin transport. Whereas auxin requirements appear to be similar for lateral root and nodule primordium activation and organ differentiation, the major difference between the two developmental programs lies in the specification of founder cells. It is suggested that differing ratios of auxin and cytokinin are likely to specify the precursors of the different root organs.

Prenodule formation and primary nodule development in roots of Comptonia (Myricaceae)

1977 ◽  
Vol 55 (17) ◽  
pp. 2306-2318 ◽  
Author(s):  
Dale Callaham ◽  
John G. Torrey
Keyword(s):  
Root Hair ◽  
Lateral Root ◽  
Lateral Roots ◽  
Cortical Cell ◽  
Host Cells ◽  
Nodule Development ◽  
Nodule Formation ◽  
Cortical Cells ◽  
Lateral Root Primordium ◽  
Root Primordium

Seedlings of the sweet fern, Comptonia peregrina (L.) Coult., grown aeroponically, were inoculated with a nodule suspension to allow infection by the actinomycete-like organism which causes nodule formation. Roots with early stages of infection and nodule initiation were fixed, embedded in resin, sectioned, and examined. Infection is infrequent in Comptonia with only a few nodules per seedling root system. Infection via root hair invasion causes the retention of the curled and deformed root hair in an intensely cytoplasmic state with ramification of multiple filamentous strands of the endophyte. A limited cortical proliferation occurs in response to the infection forming the prenodule; endophyte filaments grow radially inward from the base of the infected epidermal root hair and invade a portion of the prenodular cells resulting in their hypertrophy. Distal and proximal to the prenodule site, a number of primary nodule primordia are initiated, varying from a few up to a dozen or more. These primordia appear to develop more or less simultaneously under the stimulus of the invading endophyte; they are like lateral roots in their site of origin, occurring largely opposite the protoxylem poles and involving pericyclic and endodermal cell proliferation. They differ in that the cortical cells external to each primordium are stimulated to undergo divisions and these cortical cell derivatives are incorporated into the developing primordium. The endophyte enters the cortical tissues of the lateral root on which the prenodule has formed and then invades proximal and distal to the infection site, progressing into the cortical tissues of each of the developing nodule primordia. A cork-like layer develops on the original lateral root in areas not occupied by primordia by initiation of subepidermal cell divisions and wall thickening. Normal lateral root primordium formation occurs in the pericycle opposite the protoxylem poles and involves cellular derivatives of the pericycle and endodermis but no cortical cells, which instead are crushed and displaced by the lateral root primordium as it develops. Nodule formation clearly involves complex chemical interactions, which remain for further study, between the host cells and the invading endophyte.

Effective and ineffective root nodules in Myrica faya

1976 ◽  
Vol 194 (1116) ◽  
pp. 285-293 ◽  
Keyword(s):  
Root Nodules ◽  
Light And Electron Microscopy ◽  
Nodule Formation ◽  
Culture Solution ◽  
Myrica Gale ◽  
Main Site ◽  
Myrica Faya ◽  
Modern Methods ◽  
Infected Cells ◽  
Nodule Endophytes

In cross-inoculation trials, inocula containing the nodule endophytes of Myrica gale, M. cerifera, M. cordifolia and M. pilulifera respectively were applied to the roots of young plants of M. faya Ait. growing in nitrogen-free culture solution. All four inocula induced nodule formation, and except where the M. gale inoculum had been used the nodules were of effective type and enabled the plants bearing them to grow nearly as well as other M. faya plants associated with the normal endophyte. The nodules induced by the M. gale endophyte were very numerous, but remained small and fixed no significant amount of nitrogen, and were thus ineffective. Light and electron microscopy showed that in the effective nodules induced by the normal endophyte or by that of M. cordifolia , the endophyte was confined to a layer 1-2 cells deep near the middle of the nodule cortex, and that in respect of the width of the hyphae and their production of club-shaped internally subdivided vesicles, the endophytes resembled closely those in the nodules of the few other species of Myrica that have been studied by modern methods of microscopy. In ineffective nodules the disposition of the infected cells was unchanged, but within the cells only a sparse development of the endophyte was observed, and no vesicles were found. The finding that nodules lacking vesicles showed little or no fixation is consistent with other evidence that the vesicles normally produced by non-legume nodule endophytes are the main site of nitrogen fixation.

Effects of a Nod-factor-overproducing strain of Sinorhizobium meliloti on the expression of the ENOD40 gene in Melilotus alba

2002 ◽  
Vol 80 (9) ◽  
pp. 907-915 ◽  
Author(s):  
Walter F Giordano ◽  
Michelle R Lum ◽  
Ann M Hirsch
Keyword(s):  
Lateral Root ◽  
Sinorhizobium Meliloti ◽  
Cortical Cell ◽  
Host Cells ◽  
Nodule Development ◽  
Nodule Formation ◽  
Additional Increase ◽  
Nod Factor ◽  
Melilotus Alba ◽  
Different Strains

We have initiated studies on the molecular biology and genetics of white sweetclover (Melilotus alba Desr.) and its responses to inoculation with the nitrogen-fixing symbiont Sinorhizobium meliloti. Early nodulin genes such as ENOD40 serve as markers for the transition from root to nodule development even before visible stages of nodule formation are evident. Using Northern blot analysis, we found that the ENOD40 gene was expressed within 6 h after inoculation with two different strains of S. meliloti, one of which overproduces symbiotic Nod factors. Inoculation with this strain resulted in an additional increase in ENOD40 gene expression over a typical wild-type S. meliloti strain. Moreover, the increase in mRNA brought about by the Nod-factor-overproducing strain 24 h after inoculation was correlated with lateral root formation by using whole-mount in situ hybridization to localize ENOD40 transcripts in lateral root meristems and by counting lateral root initiation sites. Cortical cell divisions were not detected. We also found that nodulation occurred more rapidly on white sweetclover in response to the Nod-factor-overproducing strain, but ultimately there was no difference in nodulation efficiency in terms of nodule number or the number of roots nodulated by the two strains. Also, the two strains could effectively co-colonize the host when inoculated together, although a few host cells were occupied by both strains.Key words: ENOD40, Nod factor, Melilotus, Sinorhizobium, symbiosis.

Effect of rhizobia and soil nitrate on the establishment and functioning of the soybean symbiosis in the field

1984 ◽  
Vol 35 (2) ◽  
pp. 149 ◽  
Author(s):  
DF Herridge ◽  
RJ Roughley ◽  
J Brockwell
Keyword(s):  
Soil Depth ◽  
Root Nodules ◽  
Xylem Sap ◽  
Progressive Increase ◽  
Rhizobium Japonicum ◽  
Nodule Development ◽  
Initial Increase ◽  
Nodule Formation ◽  
Mineral N ◽  
Nodule Initiation

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.

XV.—The Effect of Certain Factors on the Formation of Root Nodules on Pea Plants in Aseptic Culture

1949 ◽  
Vol 63 (3) ◽  
pp. 219-229 ◽  
Author(s):  
Moira P. McGonagle
Keyword(s):  
Nicotinic Acid ◽  
Root Nodules ◽  
Nodule Development ◽  
Nodule Formation ◽  
Root Cultures ◽  
Growth Substances ◽  
Aseptic Culture ◽  
Whole Plant ◽  
Rooting Medium ◽  
Whole Plants

The experiments described in the present paper were undertaken as the outcome of an investigation into the possibility of securing nodule formation on leguminous roots cultured separately from the shoots. During that investigation it soon became clear that experiments on whole plants were necessary, in order to test the effect, on the nodulation of the normal whole plant, of certain conditions under which nodulation of root cultures was being attempted. It is thought that these observations on whole plants, though ancillary to the main investigation (which is still in progress), are of sufficient interest to be published separately. The observations are concerned with the effect of the following conditions or treatments on nodule development in a particular variety of pea:—(a) Depriving the plant of light;(b) the presence of sucrose in the rooting medium;(c) the presence of nitrate in the rooting medium; and(d) the presence of certain accessory growth substances, viz. aneurin and nicotinic acid, in the rooting medium.

scholarly journals Rhizobial Synthesized Cytokinins Contribute to But Are Not Essential for the Symbiotic Interaction Between Photosynthetic Bradyrhizobia and Aeschynomene Legumes

2013 ◽  
Vol 26 (10) ◽  
pp. 1232-1238 ◽  
Author(s):  
Kateřina Podlešáková ◽  
Joel Fardoux ◽  
Delphine Patrel ◽  
Katia Bonaldi ◽  
Ondřej Novák ◽  
...  
Keyword(s):  
Root Nodules ◽  
Rna Degradation ◽  
Nodule Development ◽  
Nodule Formation ◽  
Symbiotic Interaction ◽  
Extracellular Medium ◽  
Exogenous Addition ◽  
Bradyrhizobium Sp ◽  
Derivatives Of

Cytokinins (CK) play an important role in the formation of nitrogen-fixing root nodules. It has been known for years that rhizobia secrete CK in the extracellular medium but whether they play a role in nodule formation is not known. We have examined this question using the photosynthetic Bradyrhizobium sp. strain ORS285 which is able to nodulate Aeschynomene afraspera and A. indica using a Nod-dependent or Nod-independent symbiotic process, respectively. CK profiling showed that the most abundant CK secreted by Bradyrhizobium sp. strain ORS285 are the 2MeS (2-methylthiol) derivatives of trans-zeatin and isopentenyladenine. In their pure form, these CK can activate legume CK receptors in vitro, and their exogenous addition induced nodule-like structures on host plants. Deletion of the miaA gene showed that transfer RNA degradation is the source of CK production in Bradyrhizobium sp. strain ORS285. In nodulation studies performed with A. indica and A. afraspera, the miaA mutant had a 1-day delay in nodulation and nitrogen fixation. Moreover, A. indica plants formed considerably smaller but more abundant nodules when inoculated with the miaA mutant. These data show that CK produced by Bradyrhizobium sp. strain ORS285 are not the key signal triggering nodule formation during the Nod-independent symbiosis but they contribute positively to nodule development in Aeschynomene plants.

scholarly journals Minimal gene set from Sinorhizobium (Ensifer) meliloti pSymA required for efficient symbiosis with Medicago

2020 ◽  
Vol 118 (2) ◽  
pp. e2018015118
Author(s):  
Barney A. Geddes ◽  
Jason V. S. Kearsley ◽  
Jiarui Huang ◽  
Maryam Zamani ◽  
Zahed Muhammed ◽  
...  
Keyword(s):  
Root Nodules ◽  
Nodule Development ◽  
Nodule Formation ◽  
Protein Coding ◽  
Bacterial Gene ◽  
Gene Set ◽  
Background Strain ◽  
Genetic Components ◽  
Sustainable Agricultural Systems ◽  
Bacterial Genes

Reduction of N2 gas to ammonia in legume root nodules is a key component of sustainable agricultural systems. Root nodules are the result of a symbiosis between leguminous plants and bacteria called rhizobia. Both symbiotic partners play active roles in establishing successful symbiosis and nitrogen fixation: while root nodule development is mostly controlled by the plant, the rhizobia induce nodule formation, invade, and perform N2 fixation once inside the plant cells. Many bacterial genes involved in the rhizobia–legume symbiosis are known, and there is much interest in engineering the symbiosis to include major nonlegume crops such as corn, wheat, and rice. We sought to identify and combine a minimal bacterial gene complement necessary and sufficient for symbiosis. We analyzed a model rhizobium, Sinorhizobium (Ensifer) meliloti, using a background strain in which the 1.35-Mb symbiotic megaplasmid pSymA was removed. Three regions representing 162 kb of pSymA were sufficient to recover a complete N2-fixing symbiosis with alfalfa, and a targeted assembly of this gene complement achieved high levels of symbiotic N2 fixation. The resulting gene set contained just 58 of 1,290 pSymA protein-coding genes. To generate a platform for future synthetic manipulation, the minimal symbiotic genes were reorganized into three discrete nod, nif, and fix modules. These constructs will facilitate directed studies toward expanding the symbiosis to other plant partners. They also enable forward-type approaches to identifying genetic components that may not be essential for symbiosis, but which modulate the rhizobium’s competitiveness for nodulation and the effectiveness of particular rhizobia–plant symbioses.

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