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1.
Trends Plant Sci ; 6(1): 24-30, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11164374

RESUMEN

Lipo-chitooligosaccharides produced by rhizobia are a class of signalling molecules that mediate recognition and nodule organogenesis in the legume-rhizobia symbiosis. Their synthesis is specified by the nodulation genes of rhizobia and hence they are commonly known as Nod factors. They are amphiphilic molecules and induce a variety of responses in the roots of the legume hosts. Studies using plant and rhizobial mutants and purified molecules suggest that Nod factors are recognized by more than one receptor. In this article, we review evidence about the affinity, specificity and location of these putative receptors and describe recent studies with regard to their identification.


Asunto(s)
Fabaceae/metabolismo , Lipopolisacáridos/metabolismo , Plantas Medicinales , Conformación de Carbohidratos , Lipopolisacáridos/química , Fijación del Nitrógeno
2.
Biochimie ; 81(6): 669-74, 1999 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-10433121

RESUMEN

Rhizobial lipochitooligosaccharidic Nod factors mediate the specific recognition between leguminous plants and their prokaryotic symbionts. This review summarizes recent findings on the way plants could perceive and transduce these bacterial signals. It starts by summarizing knowledge about Nod factor binding sites, before moving to the potential implications in Nod factor signal transduction of G proteins, root-hair plasma membrane depolarisation, cytoplasmic and extracellular alkalinisation and finally variations in cytoplasmic calcium concentration.


Asunto(s)
Fabaceae/microbiología , Genes Bacterianos , Lipopolisacáridos/metabolismo , Plantas Medicinales , Transducción de Señal , Sitios de Unión , Calcio/metabolismo , Membrana Celular/metabolismo , Citoplasma/metabolismo , Fabaceae/metabolismo , Proteínas de Unión al GTP/metabolismo , Fijación del Nitrógeno/genética , Raíces de Plantas
3.
Proc Natl Acad Sci U S A ; 96(8): 4704-9, 1999 Apr 13.
Artículo en Inglés | MEDLINE | ID: mdl-10200326

RESUMEN

Rhizobial lipo-chitooligosaccharides (LCOs) are signaling molecules involved in host-range recognition for the establishment of the symbiosis with leguminous plants. The major LCO of Rhizobium meliloti, the symbiont of Medicago plants contains four or five N-acetylglucosamines, O-acetylated and N-acylated with a C16:2 fatty acid on the terminal nonreducing sugar and O-sulfated on the reducing sugar. In this paper, the ligand specificity of a high-affinity binding site (Nod factor binding site 2 or NFBS2), enriched in a plasma membrane-enriched fraction of Medicago cell suspension cultures, is reported. By using chemically synthesized LCOs, the role of structural elements, important for symbiotic activities, as recognition motifs for NFBS2 was determined. The results show that the substitutions on the nonreducing sugar of the LCOs (the O-acetate group, the fatty acid, and the hydroxyl group on the C4 of the sugar) are determinants for high-affinity binding to NFBS2. In contrast, the sulfate group, which is necessary for all biological activities on Medicago, is not discriminated by NFBS2. However, the reducing sugar of the LCO seems to interact with NFBS2, because ligand binding is affected by the reduction of the free anomeric carbon and depends on the number of N-acetyl glucosamine residues. These results suggest that the recognition of the LCOs by NFBS2 is mediated by structural elements in both the lipid and oligosaccharidic moities, but not by the sulfate group.

5.
Plant J ; 7(2): 253-60, 1995 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-7704048

RESUMEN

This paper describes the characteristics of a binding site for the major, lipo-oligosaccharide Nod factor of Rhizobium meliloti in roots of the symbiotic host plant, Medicago truncatula. Chemically synthesized NodRm-IV(Ac, S, C16:2) was labelled by tritiation to a specific activity of 56 Ci mmol-1 and this ligand was shown to be biologically active in the root hair deformation assay at 10(-11) M. Binding of the ligand to a particulate fraction from roots of M. truncatula was found to be saturable and reversible with an affinity (Kd) of 86 nM and the binding characteristics were consistent with a single class of binding sites. Competition with modified Nod factors showed that the binding was independent of both the O-acetyl and the sulphyl group and did not depend on the unsaturation of the fatty acid. However, both moieties of the lipo-oligosaccharide are required for high-affinity binding since tetra-N-acetyl-chitotetraose and palmitate were found to be poor competitors of ligand binding. A binding site with analogous characteristics was also found in a similarly prepared particulate fraction of tomato roots. This binding site for Nod factors, termed NFBS1, which is present in both a leguminous and a non-leguminous plant, may have a more general role than symbiosis.


Asunto(s)
Lipopolisacáridos/metabolismo , Sitios de Unión , Secuencia de Carbohidratos , Lipopolisacáridos/síntesis química , Lipopolisacáridos/química , Medicago sativa/microbiología , Datos de Secuencia Molecular , Sinorhizobium meliloti/metabolismo , Simbiosis
6.
Biochem J ; 306 ( Pt 1): 259-64, 1995 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-7864819

RESUMEN

In this paper we describe the two-step coupled 35S-radiolabelling of the lipo-oligosaccharidic nodulation (Nod) factors of the bacterium Rhizobium meliloti to a specific radioactivity of 800 Ci/mmol. These radiolabelled Nod factors bind to a particulate fraction from roots of the bacterium's symbiotic host, Medicago truncatula, with an equilibrium dissociation constant (KD) of 117 nM, similar to that observed with a synthetic tritiated ligand. The first step of the 35S-labelling involves the synthesis of 3'-phosphoadenosine 5'-phospho[35S]sulphate ([35S]PAPS) from ATP and [35S]sulphate using yeast enzymes. The second step exploits the sulphotransferase activity of the R. meliloti NodH protein, which has been expressed in Escherichia coli, to transfer the labelled sulphate group from PAPS to non-sulphated Nod factors. This enzyme was found to be active in E. coli cultured at 18 degrees C but not 37 degrees C. NodH could also transfer the sulphate group from PAPS to a model substrate, tetra-N-acetyl chitotetraose, with apparent Km values of 56 and 70 microM respectively, and exhibited an apparent Km value for non-sulphated Nod factors of 28 microM. Coupling the two steps of the radiolabelling resulted in an efficiency of 35S incorporation from inorganic sulphate to the Nod factors of approximately 10%. These labelled factors will be a valuable tool in the search for high-affinity receptors for the lipo-oligosaccharidic nodulation factors.


Asunto(s)
Marcaje Isotópico , Lipopolisacáridos/metabolismo , Sinorhizobium meliloti/química , Radioisótopos de Azufre , Adenosina Trifosfato/metabolismo , Sitios de Unión , Unión Competitiva , Escherichia coli , Fabaceae/metabolismo , Fosfoadenosina Fosfosulfato/síntesis química , Fosfoadenosina Fosfosulfato/metabolismo , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Raíces de Plantas/metabolismo , Plantas Medicinales , Proteínas Recombinantes/metabolismo , Sulfato Adenililtransferasa/metabolismo , Sulfatos/metabolismo , Sulfotransferasas/metabolismo
8.
Eur J Biochem ; 192(1): 189-93, 1990 Aug 28.
Artículo en Inglés | MEDLINE | ID: mdl-2401291

RESUMEN

The effect of manganese on lignin peroxidase activity was studied. The enzyme was produced with a new process using an air-lift-type reactor. The experiments were performed with veratryl alcohol and a dimeric lignin model compound. It was shown that when Mn(II).lactate complex was present the amount of veratraldehyde formed and the uptake of oxygen were significantly enhanced during the aerobic oxidation of veratryl alcohol. A similar effect can be obtained with superoxide dismutase. These results strongly suggest that the superoxide anion can occur during the reaction; its scavenging by Mn(II) or superoxide dismutase generates H2O2. In contrast, no evidence for the formation of superoxide anion was found during oxidation of the lignin model, compound veratrylglycerol-beta-guaiacyl ether.


Asunto(s)
Basidiomycota/enzimología , Proteínas Fúngicas/metabolismo , Manganeso/farmacología , Peroxidasas/metabolismo , Alcoholes Bencílicos/metabolismo , Biodegradación Ambiental , Proteínas Fúngicas/aislamiento & purificación , Guaifenesina/análogos & derivados , Guaifenesina/metabolismo , Lignina/metabolismo , Oxidación-Reducción , Peroxidasas/aislamiento & purificación
9.
South Med J ; 82(1): 64-6, 1989 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-2911764

RESUMEN

We believe the focus and emphasis of this committee on informed consent is unique, and that the development of an informed consent teaching process for residents will focus on the moral and ethical issues regarding informed consent. Even more important, we believe we will emphasize the patient care aspects of informed consent and also teach residents their responsibilities for long-term patient care with regard to patients' satisfaction and understanding of their disease process.


Asunto(s)
Consentimiento Informado , Internado y Residencia , Oftalmología/educación , Enseñanza/métodos
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