Journalists’ vision of the evolution of the (metaphorical) ecosystem of communication on health and biomedicine / Visión de los periodistas sobre la evolución del ecosistema (metafórico) de la comunicación sobre salud y biomedicina

This article analyses specialist journalists’ perception of transformations in public communication on health and biomedicine in Spain over the last two decades. A total of 20 semi-structured interviews were carried out. The analysis uses the metaphorical concept of “ecosystem”. According to the interviewees, the main “environmental” changes are technological (stressing the expansion and diversity of online information and the impact of social media). They perceive a multiplication and diversification among “information source-species”. Among these, the visibility of specialist sources (researchers and healthcare professionals) and civil associations (patients and consumers) has increased, but “opportunistic species”, such as promoters of fake news and pseudo-medicine, have also emerged. Health journalists rate their profession satisfactorily, while recognising that their working “environment” has deteriorated and perceiving a threat in the dependence on clickbait and social media positioning

Journalists’ vision of the evolution of the (metaphorical) ecosystem of communication on health and biomedicine / Visión de los periodistas sobre la evolución del ecosistema (metafórico) de la comunicación sobre salud y biomedicina

This article analyses specialist journalists’ perception of transformations in public communication on health and biomedicine in Spain over the last two decades. A total of 20 semi-structured interviews were carried out. The analysis uses the metaphorical concept of “ecosystem”. According to the interviewees, the main “environmental” changes are technological (stressing the expansion and diversity of online information and the impact of social media). They perceive a multiplication and diversification among “information source-species”. Among these, the visibility of specialist sources (researchers and healthcare professionals) and civil associations (patients and consumers) has increased, but “opportunistic species”, such as promoters of fake news and pseudo-medicine, have also emerged. Health journalists rate their profession satisfactorily, while recognising that their working “environment” has deteriorated and perceiving a threat in the dependence on clickbait and social media positioning

Metallo-organic ensembles of tritopic subphthalocyanine ligands

"This is the peer reviewed version of the following article: M. Ángel Revuelta-Maza, Ettore Fazio, Gema de la Torre and Tomás Torres, Metallo-organic ensembles of tritopic subphthalocyanine ligands, Journal of Porphyrins and PhthalocyaninesVol. 21, No. 12, pp. 782-789 (2017), which has been published in final form at https://doi.org/10.1142/S1088424617500882I. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use Self-Archived Versions"Organic building blocks containing amines and aldehydes can be used for the preparation of complex metallo-organic structures, such as M2L3 triple helicates or face-capped M4L4 tetrahedral cages, through the formation of both dynamic covalent and coordinative linkages during the self-Assembly process. Herein we describe how the subcomponent self-Assembly method can be succesfully applied over a triamine-functionalized subphthalocyanine (SubPc) ligand to build metallo-supramolecular helicates. Two isomeric SubPcs (C1-SubPc1 and C3-SubPc1) have been prepared from the corresponding C1-SubPcI3 and C3-SubPcI3 precursors under optimized Suzuki conditions. We selected the tritopic C3-SubPc1 derivative as ligand for the subcomponent self-Assembly experiments, which involved the reaction with 2-formylpyridine and different Fe(II) salts. The self-Assembly process was mainly studied by mass spectrometry (ESI direct injection techniques), and in all the conditions applied, we could observe the formation of helicate-Type Fe2SubPc3 structures and/or Fe2SubPc4 species, which can be considered as open precursors of Fe4SubPc4 tetrahedral cages. © 2017 World Scientific Publishing Company.Financial support from Comunidad de Madrid, Spain (S2013/MIT- 2841, FOTOCARBON), and Spanish MICINN (CTQ2014-52869-P) is acknowledged

Responsible Research and Innovation: an opportunity to develop creative skills at Higher Education

[EN] During the last decades, research and innovation have experienced a revolution that has lead to new challenge, and creativity has been identified as a main skill for professional success. In this context, not only concerns about involving society in research and innovation processes have been increasing but also to make this process responsible. Responsible Research and Innovation (RRI) has been defined as the approach for making research and innovation a collaborative, intergenerational and democratic process. The HEIRRI project aims to integrate RRI at all stages of education with the creation of different programs in Higher Eduaction. The aim of this study is assess how creativity has been developed in an RRI framework in the HEIRRI Summer School programme troughout an Inquiry-Based Learning (IBL) approach. On the basis of the results, this paper highlights that the IBL approach, but also the RRI framework foster creativity development in a research proposal design but also that have an impact on how researchers’ perceive their profession. This paper concludes that integral elements of this pedagogical approach and RRI, such as discussion, multidisciplinarity and including different voices and perspectives are main ingredients to promote creativity in research and innovation processes and have a transformative potential.http://ocs.editorial.upv.es/index.php/HEAD/HEAD18Rodríguez, G.; Saladié, N.; Revuelta, G.; Vizuete, C.; Llorente, C.; Carrió, M. (2018). Responsible Research and Innovation: an opportunity to develop creative skills at Higher Education. Editorial Universitat Politècnica de València. 1255-1262. https://doi.org/10.4995/HEAD18.2018.8187OCS1255126

Biosorption of nickel, cobalt, zinc and copper ions by Serratia marcescens strain 16 in mono and multimetallic systems

The metallurgical industry is one of the main sources of heavy metal pollution, which represents a severe threat to life. Metals can be removed from aqueous solutions by using microbial biomasses. This paper analyses the heavy metal biosorption capacity of Serratia marcescens strain 16 in single and multimetallic systems. The results obtained show that Co(II), Ni(II) and Zn(II) biosorption in monometallic systems is two to three times higher than in the presence of bi-metallic and multimetallic solutions. Fourier transform infrared spectroscopy confirmed that carbonyl, carboxyl and hydroxyl were the main functional groups, as well as the amide bands I and II involved in metal uptake, which are present in external structures of the bacterial cell. The results obtained demonstrated the viability of S. marcescens strain 16 as a biosorbent for the design of eco-friendly technologies for the treatment of waste liquor.The authors would like to acknowledge the financial support provided by the Iberoamerican PhD Program (UCA-UH), the AUIP and by the International Foundation of Science (Grant C/4078-2)

Optimization of nickel and cobalt biosorption by native Serratia marcescens strains isolated from serpentine deposits using response surface methodology

The treatment of metal-polluted wastes is a challenging issue of environmental concern. Metals can be removed using microbial biomass, and this is an interesting approach towards the design of eco-friendly technologies for liquid waste treatment. The study reported here aimed to optimize nickel and cobalt biosorption from aqueous solutions using three native metal-resistant Serratia marcescens strains. Ni(II) and Co(II) biosorption by S. marcescens strains was found to fit better to Langmuir's model, with maximum uptake capacities of 13.5 mg g(-1) for Ni(II) ions and 19.9 mg g(-1) for Co(II) ions. Different experimental conditions of initial metal concentration, pH, initial biomass, and temperature were optimized using the Plackett-Burman method, and, finally, biomass and metal concentration were studied using the response surface methodology (RSM) to improve biosorption. The optimum uptake capacities for Co(II) ions by the three biosorbents used were obtained for initial metal concentrations of 35-40 mg L-1 and an initial biomass of 6 mg. For Ni(II) ions, the optimum uptake capacity was achieved with 1 mg of initial biomass for S. marcescens C-1 and C-19, and with 7 mg for S. marcescens C-16, with initial concentrations of 20-50 mg L-1. The results obtained demonstrate the viability of native S. marcescens strains as biosorbents for Ni(II) and Co(II) removal. This study also contributes to our understanding of the potential uses of serpentine microbial populations for the design of environmental cleanup technologies

Study of the role played by NfsA, NfsB nitroreductase and NemA flavin reductase from Escherichia coli in the conversion of ethyl 2-(2′-nitrophenoxy)acetate to 4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one (D-DIBOA), a benzohydroxamic acid with interesting biological properties

Benzohydroxamic acids, such as 4-hydroxy-(2H)- 1,4-benzoxazin-3(4H)-one (D-DIBOA), exhibit interesting herbicidal, fungicidal and bactericidal properties. Recently, the chemical synthesis of D-DIBOA has been simplified to only two steps. In a previous paper, we demonstrated that the second step could be replaced by a biotransformation using Escherichia coli to reduce the nitro group of the precursor, ethyl 2-(2′-nitrophenoxy)acetate and obtain D-DIBOA. The NfsA and NfsB nitroreductases and the NemA xenobiotic reductase of E. coli have the capacity to reduce one or two nitro groups from a wide variety of nitroaromatic compounds, which are similar to the precursor. By this reason, we hypothesised that these three enzymes could be involved in this biotransformation. We have analysed the biotransformation yield (BY) of mutant strains in which one, two or three of these genes were knocked out, showing that only in the double nfsA/nfsB and in the triple nfsA/nfsB/nemA mutants, the BY was 0%. These results suggested that NfsA and NfsB are responsible for the biotransformation in the tested conditions. To confirm this, the nfsA and nfsB open reading frames were cloned into the pBAD expression vector and transformed into the nfsA and nfsB single mutants, respectively. In both cases, the biotransformation capacity of the strains was recovered (6.09±0.06% as in the wild-type strain) and incremented considerably when NfsA and NfsB were overexpressed (40.33%±9.42% and 59.68%±2.0% respectively)

Optimization of the Biocatalysis for D-DIBOA Synthesis Using a Quick and Sensitive New Spectrophotometric Quantification Method

D-DIBOA (4-hydroxy-(2H)-1,4-benzoxazin-3-(4H)-one) is an allelopathic-derived compound with interesting herbicidal, fungicidal, and insecticide properties whose production has been successfully achieved by biocatalysis using a genetically engineered Escherichia coli strain. However, improvement and scaling-up of this process are hampered by the current methodology for D-DIBOA quantification, which is based on high-performance liquid chromatographic (HPLC), a time-consuming technique that requires expensive equipment and the use of environmentally unsafe solvents. In this work, we established and validated a rapid, simple, and sensitive spectrophotometric method for the quantification of the D-DIBOA produced by whole-cell biocatalysis, with limits of detection and quantification of 0.0165 and 0.0501 mu mol center dot mL(-1) respectively. This analysis takes place in only a few seconds and can be carried out using 100 mu L of the sample in a microtiter plate reader. We performed several whole-cell biocatalysis strategies to optimize the process by monitoring D-DIBOA production every hour to keep control of both precursor and D-DIBOA concentrations in the bioreactor. These experiments allowed increasing the D-DIBOA production from the previously reported 5.01 mM up to 7.17 mM (43% increase). This methodology will facilitate processes such as the optimization of the biocatalyst, the scaling up, and the downstream purification