El desafío de la paz: Colombia, Guatemala, Ucrania y El Salvador a la luz de los Objetivos de Desarrollo Sostenible

Recoge las ponencias expuestas por treinta y una personalidades académicas y políticas de talla internacional además de las intervenciones de las autoridades académicas de la Universidad Carlos III de Madrid y del Ministerio de Derechos Sociales y Agenda 2030, presentadas en cuatro seminarios, que comenzaron con los relativos a los procesos de paz en Colombia y Guatemala, a fines de 2021, que continuaron el 30 de marzo de 2022 con la jornada dedicada a las herramientas para buscar una solución diplomática a la guerra en Ucrania (solo un mes después de la invasión rusa) y en junio del mismo año con el relativo a los acuerdos de 1992 en El Salvador. Dichos seminarios fueron: "Los Acuerdos de Paz en Colombia, cinco años después". (Madrid, 29 y 30 de noviembre de 2021); "Los Acuerdos de Paz en Guatemala, veinticinco años después". (Madrid, 13 de diciembre de 2021); "Ucrania: Solución negociada, seguridad compartida". (Madrid, 30 de marzo de 2022); "Los Acuerdos de Paz de El Salvador, treinta años después, en el marco de la Agenda 2030". (Madrid, 22 de junio de 2022)Presentación / Juan Daniel Oliva, Carlos R. Fernández Liesa (pp.12-14). -- Prólogo / Lilith Verstrynge Revuelta, (pp. 15-16). -- Primera parte: Los acuerdos de paz en Colombia, cinco años después (p. 18). -- Apertura / Juan Romo Uroz (pp. 18-20). -- [Apertura] / Ione Belarra (pp. 20-23). -- Hacer la paz es más difícil que hacer la guerra / Juan Manuel Santos Calderón (pp. 23-27). -- No hay un acuerdo de paz que tenga un calado de reformas como el colombiano / Josefina Echavarría Álvarez (pp. 28-34). -- Juramos que nuestra única arma sería la palabra / Rodrigo Londoño Echeverri (pp. 34-38). -- Tuvisteis que hacer frente a una coyuntura política dificilísima / José Luis Rodríguez Zapatero (pp. 38-42). -- Segunda mesa: Balance, implementación y Agenda 2030 / Enrique Santiago (pp. 43-46). -- Solicito la apertura del macrocaso de la responsabilidad del Estado / Álvaro Leyva Durán (pp. 47-53). -- En Colombia existen más de cien mil desaparecidos / Luz Marina Monzón Cifuentes (pp. 54-61). -- No hay contradicción entre la búsqueda de la paz y la de la justicia / Yesid Reyes Alvarado (pp. 62-67). -- Logramos el primer acuerdo de paz con enfoque de género / Gloria Inés Ramírez (pp. 68-74). -- Segunda parte. Los Acuerdos de Paz en Guatemala, veinticinco años después (p. 75). -- Apertura / J. Daniel Oliva Martínez (pp. 75-76) , Enrique Santiago Romero (pp. 77-78). -- Guatemala es hoy un Estado capturado por mafias / José Manuel Martín Medem (pp. 78-81). -- Se firmó la paz, pero falta la construcción de una cultura de paz / Olinda Salguero (pp. 81-85). -- Guatemala se halla en el peor escenario en materia de derechos humanos desde 1986 / Velia Muralles (pp. 85-90). -- Las comisiones de la verdad registraron unas doscientas mil personas desaparecidas y ejecutadas / Erik de León (pp. 90-94). -- El problema fundamental era y es la marginación de los grupos indígenas y la pobreza extrema / Vinicio Cerezo Arévalo (pp. 94-102). -- Guatemala está peor que cuando firmamos la paz / Pablo Monsanto (pp. 103-109). -- Guatemala es un barril de pólvora con la mecha prendida / Ana Isabel Prera (pp. 109-115). -- Clausura / Ione Belarra (pp. 115-120). -- Tercera parte. Ucrania: Solución negociada, seguridad compartida (p. 121). Apertura / María Luisa González Cuéllar Serrano, Ione Belarra (pp. 122-125). -- Debemos trabajar para exponer las amenazas de esta guerra. Es necesario para sobrevivir / Noam Chomsky (pp. 125-132). -- Primera Mesa - La negociación como herramienta de resolución de conflictos / Santiago Jiménez Martín (p. 133). -- Trabajar por la paz acarrea incomprensiones y entraña riesgos / Yago Pico de Coaña (pp. 134-139). -- La Unión Europea debe volver a un papel de potencia pacífica / Gianni Labella (pp. 140-145). -- Las armas no nos salvarán / Carmen Magallón Portoles (pp. 145-149). -- Segunda mesa: Construcción de paz y seguridad compartida en Europa / Cástor Díaz Barrado (pp. 149-150). -- Un mundo sin armas nucleares es necesario y posible / Carlos Umaña (pp. 151-154). -- Pedimos una solución diplomática negociada / Mariela Kohon (pp. 155-159). -- Hay que avanzar hacia una arquitectura de seguridad europea basada en la seguridad compartida / Vicenç Fisas Armengol (pp. 159-162). -- Que la guerra en Ucrania no nos lleve a olvidar los otros conflictos armados, que también requieren nuestro apoyo / Mabel González Bustelo (pp. 163-168). -- Clausura / Carlos Fernández Liesa, Enrique Santiago (pp. 168-173). -- Cuarta parte. Los Acuerdos de Paz de El Salvador, treinta años después, en el marco de la Agenda 2030 (p. 174). -- Apertura / Montserrat Huguet Santos, Enrique Santiago (pp. 175-178). -- Hicimos la paz a través del diálogo político en medio de la guerra / Óscar Santamaría (pp. 178-182). -- Agradecemos el acompañamiento y la solidaridad de la comunidad internacional / Nidia Díaz (pp. 183-190). -- El proceso de paz no fue una confrontación ideológica / Álvaro de Soto (pp. 190-196). -- Fue el momento más importante desde la independencia nacional / Rubén Zamora (pp. 196-201). -- Segunda mesa: Los Acuerdos de Paz treinta años después: Balance, implementación y Agenda 2030 / Daniel Oliva (pp. 202-203). -- El presidente Bukele se burla de los acuerdos de paz / David Morales (pp. 203-209). -- Están en riesgo los derechos conquistados por las mujeres / Lorena Peña (pp. 209-212). -- Necesitamos una alianza en defensa de los derechos humanos / José María Tojeira (pp. 213-216). -- Tenemos que construir la unidad opositora para desplazar a esta dictadura de nuevo tipo / Maricela Ramírez (pp. 217-222). -- Clausura / Matilde Sánchez, Ione Belarra (pp. 222-224). -- Epílogo / Federico Mayor Zaragoza (pp. 225-228)

Increased riboflavin production by manipulation of inosine 5′-monophosphate dehydrogenase in Ashbya gossypii

Guanine nucleotides are the precursors of essential biomolecules including nucleic acids and vitamins such as riboflavin. The enzyme inosine-5′-monophosphate dehydrogenase (IMPDH) catalyzes the ratelimiting step in the guanine nucleotide de novo biosynthetic pathway and plays a key role in controlling the cellular nucleotide pools. Thus, IMPDH is an important metabolic bottleneck in the guanine nucleotide synthesis, susceptible of manipulation by means of metabolic engineering approaches. Herein, we report the functional and structural characterization of the IMPDH enzyme from the industrial fungus Ashbya gossypii. Our data show that the overexpression of the IMPDH gene increases the metabolic flux through the guanine pathway and ultimately enhances 40 % riboflavin production with respect to the wild type. Also, IMPDH disruption results in a 100-fold increase of inosine excretion to the culture media. Our results contribute to the developing metabolic engineering toolbox aiming at improving the production of metabolites with biotechnological interest in A. gossypii.This work was supported by grant BIO2014-56930-P from the Spanish Ministerio de Economía y Competitividad. Rubén M Buey is supported by a “Ramón y Cajal” contract from the Spanish Ministerio de Economía y Competitividad and by a Marie Curie Career Integration Grant (EB-SxIP; FP7-PEOPLE-2011-CIG-293831).Peer Reviewe

MOESM4 of Utilization of xylose by engineered strains of Ashbya gossypii for the production of microbial oils

Additional file 4. A. gossypii strains used in this study. Table of A. gossypii strains used in this study

Numerical Study of a Solar Cell to Achieve the Highest InGaN Power Conversion Efficiency for the Whole In-Content Range

A solar cell structure with a graded bandgap absorber layer based on InGaN has been proposed to overcome early predicted efficiency. Technological issues such as carrier concentration in the p- and n-type are based on the data available in the literature. The influence of carrier concentration-dependent mobility on the absorber layer has been studied, obtaining considerable improvements in efficiency and photocurrent density. Efficiency over the tandem solar cell theoretical limit has been reached. A current density of 52.95 mA/cm2, with an efficiency of over 85%, is determined for a PiN structure with an InGaN step-graded bandgap absorption layer and 65.44% of power conversion efficiency for the same structure considering piezoelectric polarization of fully-strained layers and interfaces with electron and hole surface recombination velocities of 10−3 cm/s

Ferredoxin-linked flavoenzyme defines a family of pyridine nucleotide-independent thioredoxin reductases

Ferredoxin-dependent thioredoxin reductase was identified 35 y ago in the fermentative bacterium Clostridium pasteurianum [Hammel KE, Cornwell KL, Buchanan BB (1983) Proc Natl Acad Sci USA 80:3681–3685]. The enzyme, a flavoprotein, was strictly dependent on ferredoxin as reductant and was inactive with either NADPH or NADH. This early work has not been further pursued. We have recently reinvestigated the problem and confirmed that the enzyme, here designated ferredoxin-dependent flavin thioredoxin reductase (FFTR), is a flavoprotein. The enzyme differs from ferredoxin−thioredoxin reductase (FTR), which has a signature [4Fe−4S] cluster, but shows structural similarities to NADP-dependent thioredoxin reductase (NTR). Comparative amino acid sequence analysis showed that FFTR is present in a number of clostridial species, some of which lack both FTR and an archetypal NTR. We have isolated, crystallized, and determined the structural properties of FFTR from a member of this group, Clostridium acetobutylicum, both alone and in complex with Trx. The structures showed an elongated FFTR homodimer, each monomer comprising two Rossmann domains and a noncovalently bound FAD cofactor that exposes the isoalloxazine ring to the solvent. The FFTR structures revealed an alternative domain organization compared with NTR that enables the enzyme to accommodate Fdx rather than NADPH. The results suggest that FFTR exists in a range of conformations with varying degrees of domain separation in solution and that the stacking between the two redox-active groups for the transfer of reducing equivalents results in a profound structural reorganization. A mechanism in accord with the findings is proposed.This work was supported by Spanish Ministerio de Ciencia, Innovación y Universidades Grants BFU2016-80343-P and BIO2016-75634-P. The research leading to these results received funding from the European Community’s Seventh Framework Program FP7/2007–2013 under BioStruct-X Grant Agreement 7687

A nucleotide-dependent conformational switch controls the polymerization of human IMP dehydrogenases to modulate their catalytic activity

36 p.-6 fig.+inf. supl.18 p.-8 fig.-2 tab.Inosine 5'-monophosphate dehydrogenase (IMPDH) catalyzes the rate-limiting step in the de novo GTP biosynthetic pathway and plays essential roles in cell proliferation. As a clinical target, IMPDH has been studied for decades, but it has only been within the last years that we are starting to understand the complexity of the mechanisms of its physiological regulation. Here, we report structural and functional insights into how adenine and guanine nucleotides control a conformational switch that modulates the assembly of the two human IMPDH enzymes into cytoophidia and allosterically regulates their catalytic activity. In vitro reconstituted micron-length cytoophidia-like structures show catalytic activity comparable to unassembled IMPDH but, in turn, are more resistant to GTP/GDP allosteric inhibition. Therefore, IMPDH cytoophidia formation facilitates the accumulation of high levels of guanine nucleotides when the cell requires it. Finally, we demonstrate that most of the IMPDH retinopathy-associated mutations abrogate GTP/GDP-induced allosteric inhibition and alter cytoophidia dynamics.This work was supported by the Spanish Ministerio de Ciencia, Innovación y Universidades (grants BFU2016-79237-P to R.M.B. and BIO2014-56930-P to J.L.R.).Peer reviewe

Unprecedented pathway of reducing equivalents in a diflavin-linked disulfide oxidoreductase

Flavoproteins participate in a wide variety of physiologically relevant processes that typically involve redox reactions. Within this protein superfamily, there exists a group that is able to transfer reducing equivalents from FAD to a redox-active disulfide bridge, which further reduces disulfide bridges in target proteins to regulate their structure and function. We have identified a previously undescribed type of flavin enzyme that is exclusive to oxygenic photosynthetic prokaryotes and that is based on the primary sequence that had been assigned as an NADPH-dependent thioredoxin reductase (NTR). However, our experimental data show that the protein does not transfer reducing equivalents from flavins to disulfides as in NTRs but functions in the opposite direction. High-resolution structures of the protein from Gloeobacter violaceus and Synechocystis sp. PCC6803 obtained by X-ray crystallography showed two juxtaposed FAD molecules per monomer in redox communication with an active disulfide bridge in a variant of the fold adopted by NTRs. We have tentatively named the flavoprotein "DDOR" (diflavin-linked disulfide oxidoreductase) and propose that its activity is linked to a thiol-based transfer of reducing equivalents in bacterial membranes. These findings expand the structural and mechanistic repertoire of flavoenzymes with oxidoreductase activity and pave the way to explore new protein engineering approaches aimed at designing redox-active proteins for diverse biotechnological applications.This work was supported by Spanish Ministerio de Economía, Industria y Competitividad Grants BFU2016-80343-P and BIO2016-75634-P. R.M.B. is supported by a Ramón y Cajal contract from the Spanish Ministerio de Economía, Industria y Competitividad. L.L.-M. is supported by a postdoctoral contract from Universidad de Sevilla. The research leading to these results received funding from the European Community’s Seventh Framework Program (FP7/2007–2013) under BioStruct-X Grant Agreement 7687.Peer Reviewe

Nómadas del conocimiento en contextos pedagógicos emergentes: cartografiando prácticas disruptivas en Educación Secundaria

Identificar y seleccionar proyectos que implementen pedagogías de tipo emergente y prácticas disruptivas, focalizados como estudios de casos centrados en el desarrollo de la Educación Secundaria Obligatoria y Postobligatoria. Implementar un espacio transversal de encuentro virtual («Laboratorio de pedagogías emergentes y prácticas disruptivas»