Broad-host-range Rhizobium species strain NGR234 secretes a family of carbamoylated, and fucosylated, nodulation signals that are O-acetylated or sulphated.
about
The nodulation of alfalfa by the acid-tolerant Rhizobium sp. strain LPU83 does not require sulfated forms of lipochitooligosaccharide nodulation signalsRhizobium sp. strain NGR234 possesses a remarkable number of secretion systemsRhizobial Nodulation Factors Stimulate Mycorrhizal Colonization of Nodulating and Nonnodulating SoybeansStructures of NodZ α1,6-fucosyltransferase in complex with GDP and GDP-fucoseNew insights into Nod factor biosynthesis: Analyses of chitooligomers and lipo-chitooligomers of Rhizobium sp. IRBG74 mutantsMolecular basis of symbiotic promiscuity.Unusual methyl-branched alpha,beta-unsaturated acyl chain substitutions in the Nod Factors of an arctic rhizobium, Mesorhizobium sp. strain N33 (Oxytropis arctobia).NolL of Rhizobium sp. strain NGR234 is required for O-acetyltransferase activity.Keys to symbiotic harmony.Structural characterization of a flavonoid-inducible Pseudomonas aeruginosa A-band-like O antigen of Rhizobium sp. strain NGR234, required for the formation of nitrogen-fixing nodulesThe Rhizobium-plant symbiosisNod factor structures, responses, and perception during initiation of nodule development.Dictyostelium discoideum fatty-acyl amidase II has deacylase activity on Rhizobium nodulation factors.The atrazine catabolism genes atzABC are widespread and highly conserved.Nodulation gene regulation in Bradyrhizobium japonicum: a unique integration of global regulatory circuits.Promiscuity of hosting nitrogen fixation in rice: an overview from the legume perspective.Exo-oligosaccharides of Rhizobium sp. strain NGR234 are required for symbiosis with various legumesPerception of Rhizobium nodulation factors by tomato cells and inactivation by root chitinasesThe NodC protein of Azorhizobium caulinodans is an N-acetylglucosaminyltransferaseLigand specificity of a high-affinity binding site for lipo-chitooligosaccharidic Nod factors in Medicago cell suspension cultures.Biosynthesis of lipooligosaccharide nodulation factors: Rhizobium NodA protein is involved in N-acylation of the chitooligosaccharide backbone.Structural elucidation of the lipopolysaccharide core region of the O-chain-deficient mutant strain A28 from Pseudomonas aeruginosa serotype 06 (International Antigenic Typing Scheme).Bradyrhizobium (Arachis) sp. strain NC92 contains two nodD genes involved in the repression of nodA and a nolA gene required for the efficient nodulation of host plants.Rhizobium sp. strain NGR234 NodZ protein is a fucosyltransferaseBiosynthesis of Rhizobium meliloti lipooligosaccharide Nod factors: NodA is required for an N-acyltransferase activity.nodZ, a unique host-specific nodulation gene, is involved in the fucosylation of the lipooligosaccharide nodulation signal of Bradyrhizobium japonicum.Flavone-enhanced accumulation and symbiosis-related biological activity of a diglycosyl diacylglycerol membrane glycolipid from Rhizobium leguminosarum biovar trifolii.Bacterial-induced calcium oscillations are common to nitrogen-fixing associations of nodulating legumes and nonlegumesWild type Rhizobium etli, a bean symbiont, produces acetyl-fucosylated, N-methylated, and carbamoylated nodulation factors.Delayed maturation of nodules reduces symbiotic effectiveness of the Lotus japonicus-Rhizobium sp. NGR234 interaction.Lipo-chitooligosaccharidic nodulation factors and their perception by plant receptors.Rhizobium meliloti NodP and NodQ form a multifunctional sulfate-activating complex requiring GTP for activity.The Rhizobium meliloti regulatory nodD3 and syrM genes control the synthesis of a particular class of nodulation factors N-acylated by (omega-1)-hydroxylated fatty acids.Functional analysis of chimeric lysin motif domain receptors mediating Nod factor-induced defense signaling in Arabidopsis thaliana and chitin-induced nodulation signaling in Lotus japonicus.Bacterial Molecular Signals in the Sinorhizobium fredii-Soybean Symbiosis.Bradyrhizobium sp. Strains that nodulate the leguminous tree Acacia albida produce fucosylated and partially sulfated nod factorsDynamics of genome architecture in Rhizobium sp. strain NGR234.Biosynthesis of a structurally novel lipid A in Rhizobium leguminosarum: identification and characterization of six metabolic steps leading from UDP-GlcNAc to 3-deoxy-D-manno-2-octulosonic acid2-lipid IVA.Activation of the cell cycle machinery and the isoflavonoid biosynthesis pathway by active Rhizobium meliloti Nod signal molecules in Medicago microcallus suspensions.Natural genomic design in Sinorhizobium meliloti: novel genomic architectures
P2860
Q24600421-2EFA6CE2-4EFB-434B-8431-90CE95BE9074Q24644572-39252483-67AE-4C75-AF0A-408E140816C1Q24671541-D1648A6A-D180-467A-891B-F176073E744DQ27676916-B6606773-CD9B-4E70-B92B-3666C49B0E56Q28821042-635B6A4B-6CC3-4D23-ACE5-A584B2372B65Q33855261-1F1D5E7D-BAB9-42F5-A648-4A54FFF77520Q33948040-792DD67E-2C5E-4DF1-90ED-65A19FED6E94Q33991184-B1988212-2669-48E8-8AE2-27A0D4EEF380Q33994648-FFDE527E-7D8A-4D64-B93F-C35D14545E29Q34048347-D428D0A2-FE06-498B-B709-159041844152Q34721828-EF7C774C-C545-4E0C-BFAD-CAE98E23C194Q34727743-4DAABBDD-E255-42CB-9EA6-7CD657CDD6C3Q34745272-5C54D3CE-924C-4C23-AF01-BB92C71EE94EQ34746750-585A6605-624F-4582-B491-EC2C373F634EQ34878543-690F1165-BDEA-4DA2-88BE-34C6CB54479AQ34983169-668D33E8-AF23-403A-B500-26F50FFEF2E2Q35075259-E6491685-3EC3-4A16-940B-33B0EC75049BQ35098965-DD3BD4E9-CD6B-4483-AC87-9A08DFC939E7Q35128816-2EABE810-0D9C-469B-9569-D600A450EAD7Q35137267-C968BA30-7499-49B2-B815-5502BEFED02FQ35156655-7924781C-C798-4211-BE61-31D79948D24BQ35599042-B5368BDA-8FB7-4D24-9148-B0310D4ECC2FQ35607055-90FB673B-210D-4496-9681-2D37E3379051Q35627944-1695D741-F7A4-45C4-AA9A-F4EA2F96CC12Q35707964-27608F21-1A78-4C0E-BDB2-065A212D1FAAQ36104994-FF91C5F0-0507-4495-8511-DFB7C7657CB2Q36109123-114B078C-FAC8-436F-99E4-F911AD25968FQ36531119-954CE85C-A702-4206-88E9-372CE081B210Q36719716-8309BCE4-0AA0-4E10-97C8-A0BCFCAB1C1EQ37118093-6A9A2320-C4B1-4363-8CFF-2972E6E34949Q38297290-4A0F5098-6AF4-4059-B299-3E0313B1DBCBQ38302842-F264087E-DF01-49E5-B12B-E8E55CCD90B8Q38308419-196FC0FD-642E-4149-BD56-D7BD9B032C2FQ38309083-2B2ECE8F-D8F3-4161-BD8B-D7A87FB77EB4Q38841605-5F8839D1-3E34-4BF7-8475-A499C1BE54ACQ39488453-834D7990-879E-45AA-9589-4ACB226EB001Q39677997-BEDC725D-985D-4D40-AACD-BE227CE1926DQ39896240-583A826B-9E2B-44C5-8FEB-A84571CBAE46Q40791085-1EBD5257-A922-4156-B3F0-37AFEB783DDCQ40830359-9DB2AEA4-BFA7-4731-8400-0D527E779DD4
P2860
Broad-host-range Rhizobium species strain NGR234 secretes a family of carbamoylated, and fucosylated, nodulation signals that are O-acetylated or sulphated.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh
1992年學術文章
@zh-hant
name
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@en
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@nl
type
label
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@en
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@nl
prefLabel
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@en
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@nl
P2093
P2860
P1476
Broad-host-range Rhizobium spe ...... are O-acetylated or sulphated.
@en
P2093
Broughton WJ
Pueppke SG
P2860
P304
P356
10.1111/J.1365-2958.1992.TB01793.X
P407
P577
1992-12-01T00:00:00Z