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Auswahl der wissenschaftlichen Literatur zum Thema „Frankia symbiosis“
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Zeitschriftenartikel zum Thema "Frankia symbiosis"
Benson, David R., James M. Brooks, Ying Huang, Derek M. Bickhart und Juliana E. Mastronunzio. „The Biology of Frankia sp. Strains in the Post-Genome Era“. Molecular Plant-Microbe Interactions® 24, Nr. 11 (November 2011): 1310–16. http://dx.doi.org/10.1094/mpmi-06-11-0150.
Der volle Inhalt der QuellePopovici, Jean, Gilles Comte, �milie Bagnarol, Nicole Alloisio, Pascale Fournier, Floriant Bellvert, C�dric Bertrand und Maria P. Fernandez. „Differential Effects of Rare Specific Flavonoids on Compatible and Incompatible Strains in the Myrica gale-Frankia Actinorhizal Symbiosis“. Applied and Environmental Microbiology 76, Nr. 8 (26.02.2010): 2451–60. http://dx.doi.org/10.1128/aem.02667-09.
Der volle Inhalt der QuellePopovici, Jean, Vincent Walker, Cédric Bertrand, Floriant Bellvert, Maria P. Fernandez und Gilles Comte. „Strain specificity in the Myricaceae - Frankia symbiosis is correlated to plant root phenolics“. Functional Plant Biology 38, Nr. 9 (2011): 682. http://dx.doi.org/10.1071/fp11144.
Der volle Inhalt der QuelleBerg, R. Howard. „Frankia forms infection threads“. Canadian Journal of Botany 77, Nr. 9 (18.12.1999): 1327–33. http://dx.doi.org/10.1139/b99-073.
Der volle Inhalt der QuelleMastronunzio, J. E., Y. Huang und D. R. Benson. „Diminished Exoproteome of Frankia spp. in Culture and Symbiosis“. Applied and Environmental Microbiology 75, Nr. 21 (11.09.2009): 6721–28. http://dx.doi.org/10.1128/aem.01559-09.
Der volle Inhalt der QuelleAnne-Emmanuelle, Hay, Boubakri Hasna, Buonomo Antoine, Rey Marjolaine, Meiffren Guillaume, Cotin-Galvan Laetitia, Comte Gilles und Herrera-Belaroussi Aude. „Control of Endophytic Frankia Sporulation by Alnus Nodule Metabolites“. Molecular Plant-Microbe Interactions® 30, Nr. 3 (März 2017): 205–14. http://dx.doi.org/10.1094/mpmi-11-16-0235-r.
Der volle Inhalt der QuelleMarkham, John H., und Chris P. Chanway. „Does past contact reduce the degree of mutualism in the Alnus rubra - Frankia symbiosis?“ Canadian Journal of Botany 77, Nr. 3 (20.08.1999): 434–41. http://dx.doi.org/10.1139/b98-227.
Der volle Inhalt der QuellePujic, Petar, Nicole Alloisio, Guylaine Miotello, Jean Armengaud, Danis Abrouk, Pascale Fournier und Philippe Normand. „The Proteogenome of Symbiotic Frankia alni in Alnus glutinosa Nodules“. Microorganisms 10, Nr. 3 (18.03.2022): 651. http://dx.doi.org/10.3390/microorganisms10030651.
Der volle Inhalt der QuelleRibeiro, Ana, Inês Graça, Katharina Pawlowski und Patrícia Santos. „Actinorhizal plant defence-related genes in response to symbiotic Frankia“. Functional Plant Biology 38, Nr. 9 (2011): 639. http://dx.doi.org/10.1071/fp11012.
Der volle Inhalt der QuelleWilkinson, Helen, Alice Coppock, Bethany L. Richmond, Beatriz Lagunas und Miriam L. Gifford. „Plant–Environment Response Pathway Regulation Uncovered by Investigating Non-Typical Legume Symbiosis and Nodulation“. Plants 12, Nr. 10 (12.05.2023): 1964. http://dx.doi.org/10.3390/plants12101964.
Der volle Inhalt der QuelleDissertationen zum Thema "Frankia symbiosis"
Bajwa, Balwinder Singh. „Molecular charecterisation of Frankia and Alder- Frankia symbiosis in Eastern India“. Thesis, University of North Bengal, 2004. http://hdl.handle.net/123456789/918.
Der volle Inhalt der QuelleNguyen, Thi Thanh Van. „The actinorhizal symbiosis of the earliest divergent Frankia cluster“. Doctoral thesis, Stockholms universitet, Institutionen för ekologi, miljö och botanik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-139969.
Der volle Inhalt der QuelleAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 2: Manuscript. Paper 3: Manuscript.
Oakley, Brian B. „The ecology and biogeography of the Ceanothus-Frankia symbiosis in California /“. Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/5589.
Der volle Inhalt der QuelleBenabdoun, Faïza Meriem. „Étude moléculaire des étapes précoces de la symbiose actinorhizienne Casuarina-Frankia : analyse fonctionnelle des gènes de la plante hôte contrôlant l’infection“. Thesis, Montpellier 2, 2012. http://www.theses.fr/2012MON20103/document.
Der volle Inhalt der QuelleMolecular study of the early stages of actinorhizal symbiosis Casuarina-Frankia: functional analysis of the host plant genes controlling the infectionMore than 80% of plant species are able to develop arbuscular mycorrhizal (AM) symbiosis in association with glomeromycete fungi. In contrast, only some species of the Eurosid I clade, confined to four orders and ten Angiosperm families, are able to form nitrogen-fixing root nodule symbioses with soil bacteria. This concerns plants of the legume family (Fabaceae) and Parasponia associated with Rhizobium bacteria and actinorhizal plants associated with the actinomycete Frankia. Similarly to Legumes, the actinorhizal symbiosis results in the formation of nitrogen-fixing root nodules. However, unlike legume nodule, the actinorhizal nodule has a same origin and structure than a lateral root. Thus, the study of actinorhizal nodules is of particular interest not only for investigating its specific properties but also, for determining common characteristics shared with legume nodules.We have studied the role of CgCCaMK gene during the symbiotic process and nodule organogenesis in the actinorhizal tree Casuarina glauca. CCaMK encodes a calcium and calmodulin dependent protein kinase. In the signalisation cascade leading to both nodulation and mycorrhization in legumes, this gene is acting downstream the calcium oscillations (« calcium spiking ») that occur during the early steps of the symbiotic interaction. It has been suggested that these calcium oscillations are decoded and transduced by the CCaMK protein.We have monitored the spatio-temporal expression of a PromCgCCaMK::GUS fusion during actinorhizal nodulation and have shown that reporter gene expression was correlated with the presence of Frankia along the symbiotic process. This data highlights the role of CgCCaMK during Frankia infection. In addition, we have investigated the role of the CCaMK autoinhibitory/CaM domain in actinorhizal nodule organogenesis. To achieve this goal, we have obtained truncated versions of CgCCaMK lacking the autoinhibitory/CaM domain, and then expressed them into C. glauca. We have also used truncated forms of MtCCaMK from Medicago truncatula. The expression of these CCaMK constructs from C. glauca and M. truncatula was found to induce spontaneous nodulation in the absence of Frankia bacteria. These results suggest that deregulation of the calcium and calmodulin dependent protein kinase is able to reactivate the symbiotic signalling pathway and genes acting downstream CCaMK that are needed for nodule organogenesis.Key words: Casuarina glauca, Frankia, CCaMK, infection, autoinhibition, spontaneous nodules
Abdel-Lateif, Khalid. „Flavonoids and actinorhizal symbiosis : Impact of RNA interference-mediated silencing of chalcone synthase gene on symbiosis between Casuarina glauca and Frankia“. Thesis, Montpellier 2, 2012. http://www.theses.fr/2012MON20244/document.
Der volle Inhalt der QuelleNitrogen-fixing root nodulation, confined to four plant orders, encompasses more than 14,000 Leguminosae species, and approximately 200 actinorhizal species forming symbioses with rhizobia and Frankia bacterial species, respectively. Most actinorhizal plants are capable of high rates of nitrogen fixation comparable to the nitrogen fixing symbiosis between legumes and Rhizobium. As a consequence, these plants are able to grow in poor and disturbed soils and are important elements in plant community worldwide. The basic knowledge of the symbiotic interaction between Frankia and actinorhizal plants is still poorly understood, although it offers striking differences with the Rhizobium-legume symbiosis. In the symbiosis between legumes and Rhizobium, flavonoids are key molecules for nodulation. In actinorhizal plants, the involvement of flavonoids in symbiosis is poorly understood, but because of the similarities of the infection process between some actinorhizal plants and legumes, flavonoids were proposed to act as plant signals for the bacteria Frankia. The objective of this thesis was to investigate the involvement of flavonoids during the actinorhizal nodulation process resulting from the interaction between the tropical tree Casuarina glauca and the actinomycete Frankia.Eight C. glauca genes involved in flavonoid biosynthesis were identified from a unigene database and their expression patterns were monitored by quantitative real-time PCR during the nodulation time course. Our results showed that chalcone isomerase and isoflavone reductase transcripts accumulated preferentially early after inoculation with Frankia, suggesting thus for the first time that isoflavonoids are implicated in actinorhizal nodulation. To go deeper in the understanding of the role of these molecules in actinorhizal symbiosis, we used RNA interference strategy to silence chalcone synthase, the enzyme that catalyzes the first committed step of the flavonoid pathway. Knockdown of chalcone synthase expression led to a strong reduction of specific flavonoids levels and resulted in a severely impaired nodulation. Nodule formation could be rescued by supplementation of plants with naringenin, which is an upstream intermediate in flavonoid biosynthesis. Our results provide, for the first time, direct evidence of a strong implication of flavonoids during actinorhizal nodulation
Schwob, Guillaume. „Rôle écologique de la sporulation in-planta dans les symbioses actinorhiziennes : cas de la symbiose Alnus - Frankia“. Thesis, Lyon, 2018. http://www.theses.fr/2018LYSE1037/document.
Der volle Inhalt der QuelleMicrobial biogeography would be based on the ability of microorganisms to disperse across time and space, as a function of abiotic factors such as soil properties, climate, and of biotic interactions, in particular with the host in the case of symbionts, but also on life history traits such as the ability to sporulate. Frankia sp. is a spore-forming and nitrogen-fixing actinobacterium that has a complex biogeography given its abilities for both saprophytic life and root symbiotic interaction with actinorhizal plants such as alders (Alnus, Betulaceae). Two distinct groups of Frankia lineages have been described according to a major phenotypic divergence, based on the presence (Sp+) or the absence (Sp-) of spores in planta.. To the best of our knowledge, this endophytic sporulation is an original trait in a symbiotic context and very little is known about its incidence in Frankia biogeography. This work integrates descriptive and experimental approaches on both field and laboratory areas, in order to improve the understanding of the ecological role of Frankia in planta sporulation. First, we have extended the description of the phylobiogeography of Sp+ Frankia strains to validate the previously proposed distribution pattern focused on cold environements at high altitude or high latitude. A phylogeny has been computed using a large number of nodular strains coming from the 3 continents of the Northern Hemisphere and 10 different Alnus species. Special attention was paid to geographic areas where a higher diversity was expected, in Asia, and in its glacial refuges. Second, we studied the influence of the host-plant on the distribution of Fankia Sp+ and the incidence of Sp+ in the symbiotic interaction. Experimental crosses have been performed to disentangle host and climate effects and to test the incidence of the Sp+ trait in terms of infectivity, competitiveness and host-range. Finally, we studied the ecological consequences of the Alnus/Frankia symbiotic complex, on the microbial diversity and on the nitrogen cycle functionning, with respect to the sporulation of Frankia and to the Alnus expansion on sub-/alpine grasslands. Soils analyses were performed in association with measures of nitrification and denitrification, as well as global and functional microbial diversity analyses, in Sp+, Sp- or mixed alder stands and at different colonization stages. In each part of this work, alder ectomycorhizae were analyzed to compare the distribution pattern between the two symbionts and to highlight potential interactions with the Sp+ trait of Frankia. Our results show the dominance of Sp+ strains in nodules of alder species from cold environments over the 3 continents of the Holarctic zone, with original diversity patterns in alder area of origin and in glacial refuges. Even if these strains are genetically homogenous, host-specific clusters were observed in the phylogeny. Crosses revealed that Sp+ strains were more infective and competitive than Sp- strains. Moreover, unlike Sp- strains that harbor a wide host-range, Sp+ strains have a narrower specificity leading to association’s incompatibilities and suggesting strong host dependence. For the first time, modifications of microbial communities were revealed in response to the Alnus-Frankia symbiotic complex colonization and were linked to a stimulation of the nitrogen cycle in the sub-/alpine grasslands. The first comparative results of nitrogen fixation between Sp+ and Sp- strains in natura suggest a maximal efficiency of fixation, representing almost 100% of the alder nitrogen. However, unlike previous reports in literature, no pattern was observed between Sp+ and Sp- strains, suggesting a complex effect of seasonality, alder age as well as that of nodules. Altogether, the previous results contribute to a better understanding of the Frankia biogeography drivers and allow us to discuss the expected evolution of distribution pattern in response to the global warming
Bhattacharya, Sanghati. „Characterization and diversity of selected actinorhizal haemoglobin genes and proteins with reference to Alnus-Frankia symbiosis“. Thesis, University of North Bengal, 2017. http://ir.nbu.ac.in/hdl.handle.net/123456789/2629.
Der volle Inhalt der QuelleWilcox, Dale Adrian. „Diversity of Frankia associated with Morella species of the Cape floristic region of Southern Africa“. Thesis, University of the Western Cape, 2016. http://hdl.handle.net/11394/5346.
Der volle Inhalt der QuelleFrankia is one of two partners in the globally distributed N2-fixing actinorhizal symbiosis between this filamentous soil-dwelling actinomycete and almost 300 species of host plants from eight diverse angiosperm families. The actinorhizal symbiosis is a major contributor to nitrogen reservoirs in terrestrial ecosystems, and allows actinorhizal plants to perform the role of pioneers in newly formed and nitrogen-poor soils. Frankia are differentiated into four main host-infection groups (1: Alnus/Comptonia/Myrica-infective, 2: Rosaceae/Datisca/Coriaria-infective, 3: Elaeagnaceae/Gymnostoma-infective and 4: Casuarina-infective), and there is a large degree of phylogenetic clustering within these HIGs. Of these host lineages, species from the genus Morella, from the family Myricaceae, are notable as they have the ability to establish effective partnerships with Frankia from more than one host-infection group. Africa houses 16 of the world’s 33 currently accepted Morella species, and Morella is the continents only genus containing endemic actinorhizal species. Despite this, the diversity of Frankia in symbiosis with African Morella has never been explored. To address this lack of knowledge I investigated Frankia in root nodules of six Morella species from the Cape flora of Southern Africa, as well as in rhizosphere soils from selected hosts. Partial nif H gene fragments recovered from 202 root nodules yielded 26 unique sequences, which phylogenetic analysis assigned to Frankia Cluster I (the Alnus host infection group) and Frankia Cluster III (the Elaeagnus host infection group)1. Nineteen nif H sequences were assigned to three sub-clusters within Frankia Cluster III (CC-3, CC-4 and CC-5), and the remaining seven sequences to two sub-clusters within Cluster I (CC-1 and CC-2), one of which (CC-1) is novel to the current study. Identical sequences were recovered from nodules collected at geographically distant locations, suggesting a cosmopolitan distribution within the region for some subgroups from both clusters, but more localized distribution (or tighter host-specificity) for others. Soil pH correlated with strain presence in nodules, with Cluster I sequences being associated with hosts growing in acidic soils exclusively. Furthermore, three Morella species from the Cape flora of southern Africa are promiscuous in their natural habitats, with host infection group influenced by habitat edaphic conditions. In order to explore the correlation between soil characteristics and Frankia presence in nodules, nif H soil libraries were created from selected host rhizospheres. While Cluster III sequences from these libraries corresponded closely to sequences found in nodules from the same sites, the dominant Cape Cluster I group (CC-1) was absent from all six libraries, even when present in nodules recovered from the same soils. Whether this was due to low abundance of -but strong selection for- these strains by hosts under particular conditions, or due to the absence in soil of hyphal forms of these strains could not be determined. Cluster III strains are known to be better able to persist saprophytically than their relatives from other host-infection groups. A second group of Cluster I strains, detected at only one sampling site, was present in that site's corresponding soil library. An Alnus-infective subgroup, cluster AI, which has been detected in soils collected on five continents, was also detected in the of the Cape soil libraries but never in nodules, raising questions as to this group’s ability to persist in soil in the absence of known suitable hosts. Ten Frankia strains representing all three of the numerically dominant subgroups (CC-1, CC-3 and CC-4, found in 186 of 202 root nodules) were isolated from four Morella species. These isolates represent six of the most abundant unique nodular nif H sequences found in the field survey, and display morphological and cultural characteristics typical of Frankia. Phylogenetic analysis confirmed their identity as Frankia, and multilocus analysis revealed that the isolates belong to three genospecies. Two of these genospecies fall into existing groups within the Elaeagnus-infective Cluster III, while the remaining genospecies is a novel addition to the otherwise well-described Alnus-infective Cluster I. Whole genome sequencing of a representative from each of the Cape genospecies allowed for basic annotation and genome descriptions, which agreed in each case with what has been previously found for strains from the Elaeagnus and Alnus host-infection groups, respectively. Similarly, the organization of nitrogenase gene clusters in each of the sequenced strains mirrors that found in other strains from their respective host-infection groups, indicating that this gene cluster is highly conserved in different Frankia lineages. For the first time the diversity of Frankia nodulating endemic African Morella, and present in root-associated soils of these species, has been explored. This is also the first study to report isolation and description of Frankia strains from actinorhizal plants endemic to Africa.
Pozzi, Adrien C. „Rôles adaptatifs et contraintes de la sporulation chez les microorganismes associés aux plantes : cas de la sporulation in planta dans la symbiose actinorhizienne Frankia (Frankiaceae)–Alnus (Betulaceae)“. Thesis, Lyon 1, 2014. http://www.theses.fr/2014LYO10359/document.
Der volle Inhalt der QuelleFrankia sp. is a telluric actinobacteria able to establish a root symbiosis with actinorhizal plant such as Alnus sp. Only some Frankia strains are able to sporulate in-planta, as spores can be present in (Sp+) or absent from (Sp–) the vegetal cells of the root nodule. It is to our knowledge a unique case of endophytic sporulation. However, the description and the ecological interpretation of this original life-history trait (LHT) were scarce. Our contribution to the study of the in-planta sporulation of Alnus-infective Frankia sp. combines theoretical, descriptive and experimental approaches to precise (i) the relative effect of the bacterial strain, the host-plant species and the pedoclimatic conditions on this LHT, (ii) the effect of the of the environmental variability on the distribution, diversity and selection of the trait, and (iii) the associated costs and benefits for the two symbiotic partners. We demonstrated for the first time that the in-planta sporulation is a LHT (i) specific to some Frankia lineages, (ii) major to understand their evolutionary history and (iii) significantly correlated to particular genetic features. We also shown that the occurrence of the trait varies according to the environment We also proposed a model of the evolution of the trait taking its fitness into account. We bring all the previous considerations and results to discuss the inplanta sporulation trait within a continuum of symbiotic strategies and more generally to discuss the evolutionary ecology of plant-microbe symbioses
Queiroux, Clothilde. „Signalisation moléculaire dans la symbiose Frankia-aulne“. Thesis, Lyon 1, 2009. http://www.theses.fr/2009LYO10228.
Der volle Inhalt der QuelleNitrogen is essential for cells development. It's one of the limiting factors of plant growth. The only abundant source of this component is the atmosphere which contains 80 % of dinitrogen, but this form can only be assimilated by some prokaryotes. These microorganisms are able to fix atmospheric nitrogen under freeliving condition or in symbiosis with some plants. Thus, they provide nitrogen substrates to the plant in the form of ammonium, and in return the plant provides carbon substrates from photosynthesis. It is an association with reciprocal profits for both partners. There are two major nitrogen-fixing symbioses: rhizobial symbiosis, which involves various Proteobacteria and actinorhizal symbiosis, which involves the Actinobacterium, Frankia. Bacteria enter plant root cells and develop a new organ, the nodule where nitrogen fixation takes place. Molecular bases are well characterized for rhizobial symbiosis, whereas little is known about the actinorhizal symbiosis. This fact is in part due to absence of genetic tools for Frankia. However, early steps of the interaction show some similarities. These two bacteria are able to induce root hair deformation by secreting a deforming factor, Nod factor in most rhizobial symbioses and a noncharacterized factor in the actinorhizal symbiosis. The aim of this thesis was to determine if molecular dialogue between plant and bacteria is based on universal components. This work used two approaches. One was targeted on nodC-like gene from Frankia alni ACN14a. We tried to characterize their function. Another used trancriptomic microarrays in Frankia. This technique allowed us to compare transcripts from 2 conditions: free-living cells and symbiosis. A last approach focused on aromatic compounds in Frankia. We wanted to determine if Frankia was able to use different aromatic compounds to grow. Indeed, a lot of aromatic compounds are involved in plant-bacteria interaction such as plant defense
Bücher zum Thema "Frankia symbiosis"
Normand, P., J. O. Dawson und K. Pawlowski, Hrsg. Frankia Symbiosis. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7.
Der volle Inhalt der Quelle1957-, Normand P., Dawson J. O und Pawlowski K, Hrsg. Frankia symbiosis: Proceedings of the 12th Meeting on Frankia and Actinorhizal Plants, Carry-le-Rouet, France, June 2001. Dordrecht: Kluwer Academic Publishers, 2003.
Den vollen Inhalt der Quelle findenDawson, J. O., P. Normand und K. Pawlowski. Frankia Symbiosis. Springer, 2010.
Den vollen Inhalt der Quelle findenDawson, J. O., P. Normand und K. Pawlowski. Frankia Symbiosis. Springer London, Limited, 2013.
Den vollen Inhalt der Quelle finden(Editor), P. Normand, K. Pawlowski (Editor) und J. O. Dawson (Editor), Hrsg. Frankia Symbiosis (Developments in Plant and Soil Sciences). Springer, 2003.
Den vollen Inhalt der Quelle findenJeong, Soon-Chun. Evolution and ecology of the Ceanothus-Frankia symbiosis. 1997.
Den vollen Inhalt der Quelle findenFrankia Symbioses. Springer, 2011.
Den vollen Inhalt der Quelle findenBaker, D., A. D. Akkermans, K. Huss-Danell und J. D. Tjepkema. Frankia Symbioses. Springer, 2012.
Den vollen Inhalt der Quelle findenBaker, D., A. D. Akkermans, K. Huss-Danell, J. D. Tjepkema und Akke Jitske Van der Zijpp. Frankia Symbioses. Springer, 2011.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Frankia symbiosis"
Zimpfer, J. F., C. M. Kaelke, C. A. Smyth, D. Hahn und J. O. Dawson. „Frankia inoculation, soil biota, and host tissue amendment influence Casuarina nodulation capacity of a tropical soil“. In Frankia Symbiosis, 1–10. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_1.
Der volle Inhalt der QuelleMyers, Anna K., und Louis S. Tisa. „Effect of electroporation conditions on cell viability of Frankia EuI1c“. In Frankia Symbiosis, 83–88. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_10.
Der volle Inhalt der QuelleKwon, Hyuk Jun, Chang Jae Oh, Ho Bang Kim und Chung Sun An. „Molecular cloning and characterization of adr and ivd genes from Frankia EuIK1 strain“. In Frankia Symbiosis, 89–96. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_11.
Der volle Inhalt der QuelleCournoyer, B., und D. Blaha. „Cloning, characterisation and phylogenetic analysis of the sigA σ 70 factor gene sequence from the actinomycete Frankia“. In Frankia Symbiosis, 97–106. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_12.
Der volle Inhalt der QuelleJohn, Theodore R., James Wiggington, Joyce V. Bock, Ryan Klemt und Jerry D. Johnson. „An insertion sequence unique to Frankia strain ArI5“. In Frankia Symbiosis, 107–13. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_13.
Der volle Inhalt der QuelleIgual, José M., Angel Valverde, Raúl Rivas, Pedro F. Mateos, C. Rodríguez-Barrueco, Eustoquio Martínez-Molina, Emilio Cervantes und Encarna Velázquez. „Genomic fingerprinting of Frankia strains by PCR-based techniques. Assessment of a primer based on the sequence of 16S rRNA gene of Escherichia coli“. In Frankia Symbiosis, 115–23. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_14.
Der volle Inhalt der QuelleLavire, C., und B. Cournoyer. „Progress on the genetics of the N2-fixing actinorhizal symbiont Frankia“. In Frankia Symbiosis, 125–37. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_15.
Der volle Inhalt der QuelleValverde, Claudio, und Luis Gabriel Wall. „Ammonium assimilation in root nodules of actinorhizal Discaria trinervis. Regulation of enzyme activities and protein levels by the availability of macronutrients (N, P and C)“. In Frankia Symbiosis, 139–53. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_16.
Der volle Inhalt der QuelleValverde, Claudio, und Luis Gabriel Wall. „The regulation of nodulation, nitrogen fixation and ammonium assimilation under a carbohydrate shortage stress in the Discaria trinervis-Frankia symbiosis“. In Frankia Symbiosis, 155–65. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_17.
Der volle Inhalt der QuelleKaelke, C. M., und J. O. Dawson. „Seasonal flooding regimes influence survival, nitrogen fixation, and the partitioning of nitrogen and biomass in Alnus incana ssp. rugosa“. In Frankia Symbiosis, 167–77. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-1601-7_18.
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