Results 111 to 120 of about 8,180 (237)

Glutathione and Homoglutathione Play a Critical Role in the Nodulation Process of Medicago truncatula

Molecular Plant-Microbe Interactions, 2005
Legumes form a symbiotic interaction with bacteria of the Rhizobiaceae family toproduce nitrogen-fixing root nodules under nitrogen-limiting conditions.
Pierre Frendo, Judith Harrison, Christel Norman, María Jesús Hernández Jiménez, Ghislaine Van de Sype, Alain Gilabert, Alain Puppo   +6 more
doaj   +1 more source

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 more
core   +2 more sources

Phylogenetic analysis of the family Rhizobiaceae and related bacteria by sequencing of 16S rRNA gene using PCR and DNA sequencer [PDF]

, 1993
M Yanagi
openalex   +1 more source

Pulsed-field gel electrophoresis studies of Rhizobiaceae

, 2018
The migration properties of circular, covalently closed (ccc) and linear DNAs were studied in pulsed-field gel electrophoresis as a model system for resolving large plasmids in the Rhizobiaceae. The effects of varying pulse time and agarose concentration on the electrophoretic mobility cccDNAs, ranging from 2 kilobase pairs (kb) to 16 kb, was ...
openaire   +3 more sources

The ntrPR Operon of Sinorhizobium meliloti Is Organized and Functions as a Toxin-Antitoxin Module

Molecular Plant-Microbe Interactions, 2006
The chromosomal ntrPR operon of Sinorhizobium meliloti encodes a protein pair that forms a toxin-antitoxin (TA) module, the first characterized functional TA system in Rhizobiaceae. Similarly to other bacterial TA systems, the toxin gene ntrR is preceded
Monica Bodogai, Szilamér Ferenczi, Denys Bashtovyy, Paul Miclea, Péter Papp, Ilona Dusha   +5 more
doaj   +1 more source

Apparent N Balance in Organic and Conventional Low Input Cropping Systems [PDF]

, 2007
The determination of nutrient surplus is one of the indicators of potential N losses from the agricultural system to the environment. An experiment was started in 1998 in Central Italy to evaluate the soil surface N balance of an organic and a ...
Benincasa, Paolo, Boldrini, Arianna, Guiducci, Marcello, Tei, Francesco, Tosti, Giacomo   +4 more
core  

Features of the atherosclerotic plaque microbiome in patients after carotid endarterectomy

Российский кардиологический журнал
Aim. To study the microbiome of atherosclerotic plaque biopsies in patients who underwent carotid endarterectomy (CEA).Material and methods. In this study, the microbiota profile of 76 atherosclerotic plaque samples obtained during CEA was analyzed using
E. P. Kolesova, M. A. Chernyavsky, A. G. Vanyurkin, E. V. Verkhovskaya, E. K. Zaykova, O. V. Kalinina, S. I. Sitkin, A. L. Maslyansky, V. V. Kvan, E. Yu. Vasilyeva, A. N. Yakovlev, A. Yu. Babenko, A. O. Konradi, E. V. Shlyakhto   +13 more
doaj   +1 more source

Localization of ‘Candidatus Liberibacter solanacearum' (Rhizobiales: Rhizobiaceae) in Bactericera cockerelli (Hemiptera: Triozidae) [PDF]

, 2014
W. Rodney Cooper, Venkatesan G. Sengoda, Joseph E. Munyaneza   +2 more
openalex   +1 more source

Reduction of Adenosine-5′-Phosphosulfate Instead of 3′-Phosphoadenosine-5′-Phosphosulfate in Cysteine Biosynthesis by Rhizobium meliloti and Other Members of the Family Rhizobiaceae [PDF]

, 1999
A. Pia Abola, Michael G. Willits, Richard C. Wang, Sharon R. Long   +3 more
openalex   +1 more source

Taxonomy of Rhizobiaceae revisited: proposal of a new framework for genus delimitation

, 2022
Nemanja Kuzmanović, Camilla Fagorzi, Alessio Mengoni, Florent Lassalle, George C. diCenzo   +4 more
openalex   +1 more source