Results 111 to 120 of about 91,794 (245)
A Model for the Development of the Rhizobial and Arbuscular Mycorrhizal Symbioses in Legumes and Its Use to Understand the Roles of Ethylene in the Establishment of these two Symbioses [PDF]
, 2002 We propose a model depicting the development of nodulation and arbuscular mycorrhizae. Both processes are dissected into many steps, using Pisum sativum L. nodulation mutants as a guideline. For nodulation, we distinguish two main developmental programs, Albrecht C., Albrecht C., Ardourel M., Azcon-Aguilar C., Balaji B., Balestrini R., Barker D.G., Barker S.J., Barker S.J., Barnes D.K., Bauer P., Besmer Y.L., Blancaflor E.B., Blilou I., Bonfante P., Bonfante P., Boogerd F.C., Borisov A.Y., Borisov A.Y., Borisov A.Y., Brewin N.J., Buée M., Caetano-Anolles G., Cao X.F., Cardenas L., Carroll B.J., Catoira R., Catoira R., Cavagnaro T.R., Chang C., Charon C., Ciardi J., Cohn J., Cook D., Cruz A.F., Davidson A.L., Davidson A.L., de Faria S.M., Dehio C., Drennan D.S.H., Duc G., Duc G., Dugassa G.D., Duodu S., Ehrhardt D.W., Ekdahl I., El Ghachtouli N., Engvild K.C., F C Guinel, Fang Y., Fearn J.C., Felle H.H., Felle H.H., Fernández-López M., Fuchs Y., Fukuda H., Gallaud I., Garriock M.L., Geil R.D., Geil R.D., Geitmann A., Genre A., Genre A., Geurts R., Gianinazzi-Pearson V., Giovannetti M., Giovannetti M., Glick B.R., Gollotte A., Goodlass G., Gremaud M.F., Guinel F.C., Guinel F.C., Guinel F.C., Hall M.A., Hamilton A.J., Harrison M.J., Heidstra R., Hirayama T., Hirsch A.M., Hirsch A.M., Hirsch A.M., Hirsch A.M., Hirsch A.M., Hua J., Hunter W.J., Ishii T., John P., Johnson P.R., Joshi P.A., Kneen B.E., Kneen B.E., Kneen B.E., Kobayashi I., Kolchinsky A., Kombrink E., Le Gal M.F., Lee K.H., Lee K.H., Lee K.H., Lhuissier F.G.P., Ligero F., Ligero F., Lorteau M.-A., Luschnig C., Lynch J., Markwei C.M., Markwei C.M., Marsh J.F., Martínez-Abarca F., Mateos P.F., Mathesius U., Mathesius U., Matsubara Y., Matthysse A.G., Mattoo A.K., McArthur D.A.J., Morandi D., Mort A.J., Morzhina E.V., Mylona P., Nadian H., Nagahashi G., Niebel A., Nukui N., Oldroyd G.E.D., Osborne D.J., Park S.J., Parniske M., Paruvangada V.G., Pawlowski K., Peters N.K., Peterson R.L., Postma J.G., Provorov N.A., R D Geil, Rae A.L., Reddy A.S.N., Resendes C.M., Roberts I.N., Sagan M., Sagan M., Salzer P., Santos R., Santos R., Schauser L., Schmidt J.S., Schneider A., Schultze M., Sen D., Senoo K., Smalle J., Smith F.A., Solano R., Sprent J.I., Sprent J.I., Steen D.A., Stougaard J., Stougaard J., Subba-Rao N.S., Suganuma N., Sugimoto K., Szczyglowski K., Theologis A., Timmers A.C.J., Timmers A.C.J., Todaka I., Tsyganov V.E., Tsyganov V.E., Tsyganov V.E., van Rhijn P., van Spronsen P.C., van Spronsen P.C., van Spronsen P.C., van Workum W.A.T., Vasse J., Vasse J., Vega-Hernandez M.C., Vernoud V., Vierheilig H., Vogel J.P., Voroshilova V.A., Wais R.J., Walker S.A., Wegel E., Wisniewski J.-P., Yang W.-C., Yang W.-C., Yasuta T., Young J.P.W., Yuhashi K.-I., Zaat S.A.J., Zhou L. +192 morecore +2 more sourcesWild Cicer species exhibit superior leaf photosynthetic phosphorus‐ and water‐use efficiencies compared with cultivated chickpea under low‐phosphorus conditions
New Phytologist, Volume 247, Issue 1, Page 144-159, July 2025.Summary Domesticated chickpea cultivars exhibit limited genetic diversity. This study evaluated the effects of chickpea domestication on phosphorus (P)‐use efficiency (PUE) under low‐P conditions, using a diverse Cicer collection, including wild species.
Two wild Cicer species – 54 C. reticulatum accessions and 15 C. echinospermum accessions, and seven Jiayin Pang, Simiao Li, Ulrike Mathesius, Jens Berger, Weina Zhang, Komal D. Sawant, Rajeev K. Varshney, Kadambot H. M. Siddique, Hans Lambers +8 morewiley +1 more sourceDecoding Long‐Distance Communication Under Mineral Stress: Advances in Vascular Signalling and Molecular Tools for Plant Resilience
Plant, Cell &Environment, Volume 48, Issue 7, Page 4781-4802, July 2025.ABSTRACT
Mineral nutrients are essential for plant growth, development and crop yield. Under mineral deficient conditions, plants rely on a sophisticated network of signalling pathways to coordinate their molecular, physiological, and morphological responses.Chao Xia, Juliana Miranda, David Mendoza‐Cozatl, Byung‐Kook Ham, Jianxin Ma, Cankui Zhang +5 morewiley +1 more sourceCyclic β-glucans at the bacteria–host cells interphase: One sugar ring to rule them all [PDF]
, 2018 Cyclic β‐1,2‐D‐glucans (CβG) are natural bionanopolymers present in the periplasmic space of many Proteobacteria. These molecules are sugar rings made of 17 to 25 D‐glucose units linked exclusively by β‐1,2‐glycosidic bonds.Arce Gorvel, Vilma, Ciocchini, Andres Eduardo, Comerci, Diego José, Gorvel, Jean-Pierre, Guidolin, Leticia Soledad +4 morecore +1 more sourceStructural and productive responses of signalgrass and its association with leaf area index and light interception under silvopastoral or monoculture systems
Agrosystems, Geosciences &Environment, Volume 8, Issue 2, June 2025.Abstract
Silvopastoral systems (SPSs) have emerged as one of the most prominent alternatives for grassland recovery. We evaluated the structural and productive responses of signalgrass [Urochloa decumbens (Stapf.) R. D. Webster] and its association with leaf area index (LAI) and light interception (LI) measured with different equipment across different Diego de Lima Coêlho, Alexandre Carneiro Leão de Mello, José Carlos Batista Dubeux Jr., Márcio Vieira da Cunha, Mércia Virginia Ferreira dos Santos, Erinaldo Viana de Freitas, André Pereira Freire Ferraz, Amanda Maria Gallindo dos Santos, Janerson José Coelho, Igor Lima Bretas +9 morewiley +1 more sourceNodule Initiation Elicited by Noninfective Mutants of \u3cem\u3eRhizobium phaseoli\u3c/em\u3e [PDF]
, 1985 Rhizobium phaseoli CE106, CE110, and CE115, originally derived by transposon mutagenesis (Noel et al., J. Bacteriol. 158:149-155, 1984), induced the formation of uninfected root nodule-like swellings on bean (Phaseolus vulgaris).Kaneko, Yasuko, Newcomb, Eldon H., Noel, K. Dale, Vandenbosch, Kathryn A. +3 morecore +1 more sourceDiversity of Sinorhizobium meliloti from the Central Asian Alfalfa Gene Center [PDF]
, 2002 Sinorhizobium meliloti was isolated from nodules and soil from western Tajikistan, a center of diversity of the host plants (Medicago, Melilotus, and Trigonella species).Andronov, E.E., Dammann-Kalinowski, T., Keller, M., Roumiantseva, M.L., Sharypova, L.A., Simarov, B.V., Young, J.P.W. +6 morecore +1 more sourceModulation of rhizosphere microbiota by Bacillus subtilis R31 enhances long‐term suppression of banana Fusarium wilt
iMetaOmics, Volume 2, Issue 2, June 2025.This study indicated that biocontrol bacterium B. subtilis R31 is likely to prevent and control banana Fusarium wilt through regulating the structure and function of banana rhizosphere microorganism flora (especially increasing the microbial abundance of Actinomyces), and help potential biocontrol bacteria grow into the plant roots.Ming‐Wei Shao, Hao‐Jun Chen, Ai‐Qin Huang, Li Zheng, Chun‐ji Li, Di Qin, Yun‐Hao Sun, Zheng Lin, Gang Fu, Yan‐Hong Chen, Yong‐Jian Li, Zhang‐Yong Dong, Ping Cheng, Heru Pramono, Guo‐Hui Yu, Zhi‐Min Xu, Shuang Miao, Kevin D. Hyde +17 morewiley +1 more sourceInfection of Soybean and Pea Nodules by \u3cem\u3eRhizobium\u3c/em\u3e spp. Purine Auxotrophs in the Presence of 5-aminoimidazole-4-Carboxamide Riboside [PDF]
, 1994 Purine auxotrophs of various Rhizobium species are symbiotically defective, usually unable to initiate or complete the infection process. Earlier studies demonstrated that, in the Rhizobium etli-bean symbiosis, infection by purine auxotrophs is partially Diebold, Ronald J., Newman, Jeffrey D., Noel, K. Dale, Schultz, Bruce W. +3 morecore +1 more source
