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Featured researches published by J. Ignacio Santos.


Archive | 2009

HSQC-NMR analysis of lignin in woody (Eucalyptus globulus and Picea abies) and non-woody (Agave sisalana) ball-milled plant materials at the gel state

Jorge Rencoret; Gisela Marques; Lidia Nieto; J. Ignacio Santos

Abstract In situ analysis of lignin by 2D NMR of whole plant material was carried out by swelling finely ball-milled samples in deuterated dimethylsulfoxide (DMSO-d6 ) and sonicated so that a gel was formed in the NMR analysis tube. Solution HSQC NMR spectra of different plant materials representative for hardwood (Eucalyptus globulus), softwood (Picea abies), and non-woody plants (Agave sisalana) are presented here. The spectra show signals corresponding to those of the main plant constituents, such as lignin and polysaccharides. The lignin signals were assigned by comparing the HSQC spectra of the whole plant materials with the HSQC spectra of their respective milled-wood lignins (MWLs). In general terms, the major lignin structural features, such as the relative abundances of the main lignin substructures, the syringyl/guaiacyl ratios and the extent of γ-acetylation of the lignin side-chain observed in the HSQC spectra of the whole plant materials, matched those obtained from the HSQC spectra of the isolated MWLs. Therefore, this technique, which needs only minor amounts of lignocellulosic material and minimal sample preparation, can be useful for the rapid screening of plant lignins without the need for tedious and time-consuming lignin isolation procedures.


Holzforschung | 2009

HSQC-NMR analysis of lignin in woody (Eucalyptus globulus and Picea abies) and non-woody (Agave sisalana) ball-milled plant materials at the gel state 10th EWLP, Stockholm, Sweden, August 25–28, 2008

Jorge Rencoret; Gisela Marques; Ana Gutiérrez; Lidia Nieto; J. Ignacio Santos; Jesús Jiménez-Barbero; Ángel T. Martínez; José C. del Río

Abstract In situ analysis of lignin by 2D NMR of whole plant material was carried out by swelling finely ball-milled samples in deuterated dimethylsulfoxide (DMSO-d6 ) and sonicated so that a gel was formed in the NMR analysis tube. Solution HSQC NMR spectra of different plant materials representative for hardwood (Eucalyptus globulus), softwood (Picea abies), and non-woody plants (Agave sisalana) are presented here. The spectra show signals corresponding to those of the main plant constituents, such as lignin and polysaccharides. The lignin signals were assigned by comparing the HSQC spectra of the whole plant materials with the HSQC spectra of their respective milled-wood lignins (MWLs). In general terms, the major lignin structural features, such as the relative abundances of the main lignin substructures, the syringyl/guaiacyl ratios and the extent of γ-acetylation of the lignin side-chain observed in the HSQC spectra of the whole plant materials, matched those obtained from the HSQC spectra of the isolated MWLs. Therefore, this technique, which needs only minor amounts of lignocellulosic material and minimal sample preparation, can be useful for the rapid screening of plant lignins without the need for tedious and time-consuming lignin isolation procedures.


Bioresource Technology | 2010

Polymerization of lignosulfonates by the laccase-HBT (1-hydroxybenzotriazole) system improves dispersibility

Endry Nugroho Prasetyo; Tukayi Kudanga; Lars Østergaard; Jorge Rencoret; Ana Gutiérrez; José C. del Río; J. Ignacio Santos; Lidia Nieto; Jesús Jiménez-Barbero; Ángel T. Martínez; Jiebing Li; Göran Gellerstedt; Stéphane Lepifre; Carla Silva; Suyeon Kim; Artur Cavaco-Paulo; Bente Seljebakken Klausen; Bjart Frode Lutnaes; Gibson S. Nyanhongo; Georg M. Guebitz

The ability of laccases from Trametes villosa (TvL), Myceliophthora thermophila (MtL), Trametes hirsuta (ThL) and Bacillus subtilis (BsL) to improve the dispersion properties of calcium lignosulfonates 398 in the presence of HBT as a mediator was investigated. Size exclusion chromatography showed an extensive increase in molecular weight of the samples incubated with TvL and ThL by 107% and 572% from 28400 Da after 17h of incubation, respectively. Interestingly, FTIR spectroscopy, (13)C NMR and Py-GC/MS analysis of the treated samples suggested no substantial changes in the aromatic signal of the lignosulfonates, a good indication of the ability of TvL/ThL-HBT systems to limit their effect on functional groups without degrading the lignin backbone. Further, the enzymatic treatments led to a general increase in the dispersion properties, indeed a welcome development for its application in polymer blends.


ChemBioChem | 2009

Assessing carbohydrate-carbohydrate interactions by NMR spectroscopy: the trisaccharide epitope from the marine sponge Microciona prolifera

J. Ignacio Santos; Adriana Carvalho de Souza; F. Javier Cañada; Sonsoles Martín-Santamaría; Johannis P. Kamerling; Jesús Jiménez-Barbero

Weak recognition processes: Weak calcium‐mediated carbohydrate–carbohydrate interactions have been detected by DOSY and TRNOESY NMR methods by employing a gold glyconanoparticle as a multivalent system. In addition, 3D models of trisaccharide‐CaII‐trisaccharide complexes based on results from molecular dynamics simulations are proposed.


Glycoconjugate Journal | 2008

Versatile strategy for the synthesis of biotin-labelled glycans, their immobilization to establish a bioactive surface and interaction studies with a lectin on a biochip.

F. Javier Muñoz; Ángel Rumbero; José V. Sinisterra; J. Ignacio Santos; Sabine André; Hans-J. Gabius; Jesús Jiménez-Barbero; María J. Hernáiz

The emerging role of glycans as versatile biochemical signals in diverse aspects of cellular sociology calls for establishment of sensitive methods to monitor carbohydrate recognition by receptors such as lectins. Most of these techniques involve the immobilization of one of the binding partners on a surface, e.g. atomic force microscopy, glycan array and Surface Plasmon Resonance (SPR), hereby simulating cell surface presentation. Here, we report the synthesis of fluorescent glycoconjugates, with a functionalization strategy which avoids the frequently occurring ring opening at the reducing end for further immobilization on a surface or derivatization with biotin. In order to improve the versatility of these derivatized glycans for biological studies, a new approach for the synthesis of biotinylated and fluorescent glycans has also been realized. Finally, to illustrate their usefulness the neoglycoconjugates were immobilized on different surfaces, and the interaction analysis with a model lectin, the toxin from mistletoe, proved them to act as potent ligands, underscoring the merit of the presented synthetic approach.


Glycoconjugate Journal | 2007

NMR studies on the conformation of oligomannosides and their interaction with banana lectin.

Caroline Clavel; Ángeles Canales; Garima Gupta; J. Ignacio Santos; F. Javier Cañada; Soledad Penadés; Avadesha Surolia; Jesús Jiménez-Barbero

The conformational and dynamic behaviour of three mannose containing oligosaccharides, a tetrasaccharide with α1→2, and α1→3, and a penta and a heptasaccharide with α1→2, α1→3, and α1→6 linkages has been evaluated by molecular mechanics and dynamics simulations and NMR spectroscopical methods. It is found that they display a fair amount of conformational freedom, with one major and one minor conformation per glycosidic linkage. The evaluation of their recognition by banana lectin has also been performed by STD NMR methods and a preliminary view of their putative interaction mode has been carried out by means of docking procedures.


Bioconjugate Chemistry | 2009

Glycan Tagging to Produce Bioactive Ligands for a Surface Plasmon Resonance (SPR) Study via Immobilization on Different Surfaces

F. Javier Muñoz; Jose M. Perez; Ángel Rumbero; J. Ignacio Santos; F. Javier Cañada; Sabine André; Hans-Joachim Gabius; Jesús Jiménez-Barbero; José V. Sinisterra; María J. Hernáiz

Suitable glycan derivatives will find immediate application in the study of their interactions. Here, we present an efficient synthetic strategy to introduce a fluorescent tag functionalized with an amino group into a model disaccharide structure (lactose). This strategy led to the maintenance of bioactivity, checked by the study of the interaction of this bioconjugate with a plant lectin (mistletoe lectin 1) by NMR spectroscopy, computational docking, and surface plasmon resonance (SPR). To demonstrate the versatility of this approach, we immobilized the new glycan derivatives on different surfaces, and a comparative analysis is presented and can be successfully used for biomimetic carbohydrate-protein interaction studies on the SPR biochip.


Journal of Agricultural and Food Chemistry | 2008

Highly Acylated (Acetylated and/or p-Coumaroylated) Native Lignins from Diverse Herbaceous Plants

José C. del Río; Jorge Rencoret; Gisela Marques; Ana Gutiérrez; David Ibarra; J. Ignacio Santos; Jesús Jiménez-Barbero; Liming Zhang; Ángel T. Martínez


Holzforschung | 2008

Structural characterization of milled wood lignins from different eucalypt species

Jorge Rencoret; Gisela Marques; Ana Gutiérrez; David Ibarra; Jiebing Li; Göran Gellerstedt; J. Ignacio Santos; Jesús Jiménez-Barbero; Ángel T. Martínez; José C. del Río


Organic and Biomolecular Chemistry | 2010

Binding studies of adhesion/growth-regulatory galectins with glycoconjugates monitored by surface plasmon resonance and NMR spectroscopy

F. Javier Muñoz; J. Ignacio Santos; Ana Ardá; Sabine André; Hans-Joachim Gabius; José V. Sinisterra; Jesús Jiménez-Barbero; María J. Hernáiz

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Jorge Rencoret

Spanish National Research Council

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Ángel T. Martínez

Spanish National Research Council

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Gisela Marques

Spanish National Research Council

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Ana Gutiérrez

Spanish National Research Council

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David Ibarra

Spanish National Research Council

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F. Javier Cañada

Spanish National Research Council

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José C. del Río

Spanish National Research Council

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Lidia Nieto

Spanish National Research Council

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F. Javier Muñoz

Complutense University of Madrid

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