Resultados totales (Incluyendo duplicados): 45302
Encontrada(s) 4531 página(s)
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311326
Dataset. 2022

PROTEIN VALORIZATION FROM ORA-PRO-NOBIS LEAVES BY COMPRESSED FLUIDS BIOREFINERY EXTRACTIONS: APPENDIX A. SUPPLEMENTARY DATA

  • Torres, Talyta Mayara Silva
  • Mendiola, J. A.
  • Álvarez-Rivera, Gerardo
  • Mazzutti, Simone
  • Ibáñez, Elena
  • Cifuentes, Alejandro
  • Ferreira, Sandra R. S.
Supplementary material: Supplementary captions: Figure S1 – Kinetic behavior of the extraction yield (g 100g-1) of supercritical fluid extracts from Pereskia aculeate leaves. Conditions: 40 °C, 25 MPa and 5 SLPM CO2 flow rate. Figure S2 – Kinetic behavior of the extraction yield (g 100g-1) of gas-expanded liquid extraction (GXL EtOH 25%, GXL EtOH 45%, GXL EtOH 75%) and pressurized liquid extraction (PLE EtOH 100%) from Pereskia aculeate leaves. Conditions: 40 °C, 7 MPa and 4 mL min-1. Figure S3 – Global yield (%) from subcritical water extractions (SW) at 5, 10, 15, 20 and 30 min and conventional alkaline extraction (CA) at 45 min of Pereskia aculeate leaves. Conditions: 80°C and 10.5 MPa., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311326
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311326
HANDLE: http://hdl.handle.net/10261/311326
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311326
PMID: http://hdl.handle.net/10261/311326
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311326
Ver en: http://hdl.handle.net/10261/311326
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311326

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311333
Dataset. 2022

STRUCTURE-DIGESTIBILITY RELATIONSHIP FROM NOODLES BASED ON ORGANOCATALYTICALLY ESTERIFIED REGULAR AND WAXY CORN STARCH OBTAINED BY REACTIVE EXTRUSION USING SODIUM PROPIONATE: APPENDIX A. SUPPLEMENTARY DATA

  • Hernández-Hernández, Oswaldo
  • Julio-González, L. C.
  • Doyagüez, Elisa G.
  • Gutiérrez, Tomy J.
Multimedia component 1: Appendix. Panel A- ATR/FTIR spectra Panel B- Solid-state 13C CP MAS NMR spectra of the different feedstocks used., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311333
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311333
HANDLE: http://hdl.handle.net/10261/311333
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311333
PMID: http://hdl.handle.net/10261/311333
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311333
Ver en: http://hdl.handle.net/10261/311333
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311333

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311341
Dataset. 2022

GASTROINTESTINAL FATE OF PHENOLIC COMPOUNDS AND AMINO DERIVATIVES FROM THE COCOA SHELL: AN IN VITRO AND IN SILICO APPROACH: APPENDIX A. SUPPLEMENTARY DATA

  • Cañas, Silvia
  • Rebollo-Hernanz, Miguel
  • Braojos, Cheyenne
  • Benitez, Vanesa
  • Ferreras-Charro, Rebeca
  • Dueñas, Montserrat
  • Aguilera, Yolanda
  • Martín-Cabrejas, María A.
Supplementary data 1: Supplementary Table 1. Retention index, bioaccessibility, and potential bioavailability (%) of phenolic families from cocoa shell flour (CSF) and extract (CSE) after in vitro digestion. Supplementary Table 2. Physicochemical properties and intestinal absorption of the phenolic metabolites from the cocoa shell in silico colonic metabolism. Supplementary Figure 1. Association between the molecular weight of the cocoa shell phenolic metabolites and their Caco-2 (A) and human intestinal (B) absorption., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311341
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311341
HANDLE: http://hdl.handle.net/10261/311341
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311341
PMID: http://hdl.handle.net/10261/311341
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311341
Ver en: http://hdl.handle.net/10261/311341
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311341

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311345
Dataset. 2022

SUPPLEMENTARY INFORMATION FOR RAPID, SCALABLE ASSESSMENT OF SARS-COV-2 CELLULAR IMMUNITY BY WHOLE-BLOOD PCR

  • Guccione, Ernesto
  • Bertoletti, Antonio
  • Ochando, Jordi
All data generated during this study are inthis supplementary information files. RNA-seq source data are available as gene counts on the Gene Expression Omnibus at accession GSE178757., Supplementary information: -Reporting Summary -Supplementary Tables: Supplementary Tables 1–29., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311345
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311345
HANDLE: http://hdl.handle.net/10261/311345
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311345
PMID: http://hdl.handle.net/10261/311345
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311345
Ver en: http://hdl.handle.net/10261/311345
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311345

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311349
Dataset. 2023

DESERT LIZARD DIVERSITY WORLDWIDE: EFFECTS OF ENVIRONMENT, TIME, AND EVOLUTIONARY RATE [DATASET]

  • Tejero-Cicuéndez, Héctor
In this folder you can find the supplementary figures and tables of the paper., [Aim] Biodiversity is not uniformly distributed across the Earth's surface, even among physiographically comparable biomes in different biogeographic regions. For lizards, the world's large desert regions are characterized by extreme heterogeneity in species richness, spanning some of the most species-rich (arid Australia) and species-poor (central Asia) biomes overall. Regional differences in species diversity may arise as a consequence of the interplay of several factors (e.g., evolutionary time, diversification rate, environment), but their relative importance for biogeographic patterns remains poorly known. Here we use distributional and phylogenetic data to assess the evolutionary and ecological drivers of large-scale variation in desert lizard diversity., [Location] Deserts worldwide., [Major taxa studied] Lizards (non-snake squamates)., [Methods] We specifically test whether diversity patterns are best explained by differences in the ages of arid-adapted lineages (evolutionary time hypothesis), by regional variation in speciation rate, by geographic area of the arid systems, and by spatial variation related to the environment (climate, topography, and productivity)., [Results] We found no effect of recent speciation rate and geographic area on differences in desert lizard diversity. We demonstrate that the extreme species richness of the Australian deserts cannot be explained by greater evolutionary time, because species began accumulating more recently there than in more species-poor arid regions. We found limited support for relationships between regional lizard richness and environmental variables, but these effects were inconsistent across deserts, showing a differential role of the environment in shaping the lizard diversity in different arid regions., [Main conclusions] Our results provide evidence against several classic hypotheses for interregional variation in species richness, but also highlight the complexity of processes underlying vertebrate community richness in the world's great arid systems., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311349
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311349
HANDLE: http://hdl.handle.net/10261/311349
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311349
PMID: http://hdl.handle.net/10261/311349
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311349
Ver en: http://hdl.handle.net/10261/311349
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311349

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311362
Dataset. 2023

DECREASED RETRONASAL OLFACTION AND TASTE PERCEPTION IN OBESITY ARE RELATED TO SALIVA BIOCHEMICAL AND MICROBIOTA COMPOSITION: APPENDIX A. SUPPLEMENTARY MATERIAL

  • Calvo López-Dávalos, Paula
  • Requena, Teresa
  • Pozo-Bayón, Mª Ángeles
  • Muñoz-González, Carolina
Supplementary data 1. Supplementary Table 1. Salivary microbiota abundance (median, IQR) determined in the NW and OB groups, % diffrences between NW and OG groups and results of the Mann-Whitney test. Supplementary Table 2. Spearman correlation analyses of the intensity perceived in the seven assayed attributes versus salivary microbiota composition and salivary parameters., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311362
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311362
HANDLE: http://hdl.handle.net/10261/311362
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311362
PMID: http://hdl.handle.net/10261/311362
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311362
Ver en: http://hdl.handle.net/10261/311362
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311362

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311368
Dataset. 2023

SUPPLEMENTARY INFORMATION FOR EVALUATION OF THE ANTIOXIDANT AND NEUROPROTECTIVE ACTIVITY OF THE SEAWEED DURVILLAEA ANTARCTICA (COCHAYUYO) EXTRACTS USING PRESSURIZED LIQUIDS

  • Ruiz-Domínguez, M. C.
  • Mendiola, J. A.
  • Sánchez-Martínez, J. David
  • Bueno, Mónica
  • Cerezal-Mezquita, P.
  • Ibáñez, Elena
Supplementary Information: Fig. 1S. Standardized Pareto chart (left) for antioxidant activity (TEAC) and its corresponding response surfaces (right) of D. antarctica extracts by PLE as a function of temperature and solvent (% water: ethanol). The ± signs are interpreted in the Pareto graph according to the area of the significance of factor or interaction in the experimental design. Table S1. Regression coefficients for Extraction yield, DPPH, TEAC, and AchE activity in their original units and statistics for the fit obtained by multiple linear regression., Peer reviewed

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DOI: http://hdl.handle.net/10261/311368
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311368
HANDLE: http://hdl.handle.net/10261/311368
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311368
PMID: http://hdl.handle.net/10261/311368
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311368
Ver en: http://hdl.handle.net/10261/311368
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311368

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311369
Dataset. 2022

TABLE_2_KNOCK-OUT OF CMNAC-NOR AFFECTS MELON CLIMACTERIC FRUIT RIPENING.XLSX

  • Liu, Bin
  • Santo Domingo, Miguel
  • Mayobre, Carlos
  • Martín-Hernández, Ana Montserrat
  • Pujol, Marta
  • García-Mas, Jordi
1 table. -- Supplementary Table S2: VOCs detected in melon flesh samples. A: List of VOCs detected. B: Relative content of VOCs (ng/g frozen tissue)., Fruit ripening is an important process that affects fruit quality. A QTL in melon, ETHQV6.3, involved in climacteric ripening regulation, has been found to be encoded by CmNAC-NOR, a homologue of the tomato NOR gene. To further investigate CmNAC-NOR function, we obtained two CRISPR/Cas9-mediated mutants (nor-3 and nor-1) in the climacteric Védrantais background. nor-3, containing a 3-bp deletion altering the NAC domain A, resulted in ~8 days delay in ripening without affecting fruit quality. In contrast, the 1-bp deletion in nor-1 resulted in a fully disrupted NAC domain, which completely blocked climacteric ripening. The nor-1 fruits did not produce ethylene, no abscission layer was formed and there was no external color change. Additionally, volatile components were dramatically altered, seeds were not well developed and flesh firmness was also altered. There was a delay in fruit ripening with the nor-1 allele in heterozygosis of ~20 days. Our results provide new information regarding the function of CmNAC-NOR in melon fruit ripening, suggesting that it is a potential target for modulating shelf life in commercial climacteric melon varieties., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311369
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311369
HANDLE: http://hdl.handle.net/10261/311369
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311369
PMID: http://hdl.handle.net/10261/311369
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311369
Ver en: http://hdl.handle.net/10261/311369
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oai:digital.csic.es:10261/311369

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311371
Dataset. 2023

RAW DATA ON THE EFFECT OF RESOURCE AVAILABILITY AND HERBIVORY ON THE DEFENCE-GROWTH-REPRODUCTION TRADE-OFF OF A MASTING MEDITERRANEAN PINE

  • Larrinaga, Asier R.
  • Sampedro Pérez, Luis
  • Zas Arregui, Rafael
[General methods] The full collection of six csv files contains all the raw data used in the paper “Resource availability and herbivory alter defence-growth-reproduction trade-offs in a masting Mediterranean pine”, which is now in its pre-print version. In this article we report the results of two parallel experiments we carried out to independently asses the effect of nutrient availability and different defence induction treatments on the three-way trade-off. Thirty six ramets were allocated to the fertilization experiment, with 12 ramets of each of three genotypes being randomly assigned to one of three blocks and one of two treatments (fertilization and control). Within each block, ramets were spatially grouped in two treatment plots. Each treatment by genotype combination comprises six ramets, two per block. The remaining 45 ramets were included in the defence induction experiment and randomly assigned to one of three blocks and one of five induction treatments. Within each block, ramets were spatially grouped in five treatment plots. Each treatment by genotype combination had three ramets, one per block. In the fertilization experiment we had only two treatments (fertilized vs control). Fertilization was accomplished by applying Fertimon Rojo (Soaga S.L. 2-10-16 NPK + 2.8% Mg) and a liquid 100-20-70 NPK fertilizer applied to the substrate at the base of the trunk of each tree (see Sampedro et al. 2011 for details on this fertilizer solution). The foliar fertilization continued until the end of the experiment. In january 2010, 125 additional grams of Osmocote (KB®, Scotts, NPK 17-09-11 + 2% MgO) were also added to each tree. Fertilization was maintained throughout the whole monitoring period (2010-2015). Five treatments were assigned to the herbivory simulation experiment (applied during the first two years, 2010-2011): • Needle clipping (repeated cutting of needles tips, around 1-2 cm). • Methyl jasmonate application (brushing a 25 mM solution on debarked areas of the trunk; see details in Vázquez-González et al. 2021). • Low intensity mechanical wounding of the trunk involved making three 5 mm circular holes in the bark and phloem. • High intensity mechanical wounding of the trunk, throug six 5 mm circular hole in the bark and phloem Ramets were monitored from 2010 to 2015. Below, we provide specific details on the methods associated to its data-set and the variables it includes., [growth.csv] Ramet growth was monitored for six years, beginning in 2010. Growth monitoring involved measuring maximum tree height and stem diameter at one meter height and two orthogonal directions. Tree height was measured to the nearest dm using a telescopic measuring rod, while tree callipers were used to measure stem diameter to the nearest cm., [nutrients.csv] Nutrient content was only assessed for the fertilization experiment and for the needles produced in 2010. Needle samples were taken in 14 October 2010. Nitrogen concentration in needles was determined in a LECO elemental analyzer (model CHN 628) while phosphorus was analyzed by inductively coupled plasma optical emission spectroscopy (ICP-OES) using a Perkin-Elmer Optima 4300DV (Massachusetts, USA) at the central laboratory facilities of Universidade de Vigo – CACTI (www.uvigo.es/webs/cactiweb/). Nitrogen and P concentration were expressed in mg g-1 tissue on a dry weight basis., [phenols.csv] See “resin.csv” below, for details on the sampling protocol for defensive compounds estimation. Polyphenolics were extracted from a subsample of 30 mg of needles or phloem, by immersion in a metanol-water solution (1:1 volume) in an ultrasonic bath of 15 min, followed by centrifugation and extract dilution. Colorimetric measurements were taken with a Biorad 650 microplate reader (Bio-Rad Laboratories, Philadelphia, PA,USA) a 740 nm., [pissodes.csv] During the summer of 2011 both experiments suffered an outbreak of Pissodes castaneus. We assessed the abundance of the damage caused by this curculionid in each ramet on 16 September 2011, by visually inspecting the scars produced in the main stem and assigning them to a four category ordinal scale (none, rare, abundant and very abundant)., [reproduction.csv] Monitoring of ramet reproduction comprised measures of reproductive effort (number of female strobili and abundance of male strobili) from 2010 to 2013, and measures of reproductive output (number of ripe cones, total number of seeds produced and number and dry weight of healthy seeds) from 2012 to 2015. Strobili cohorts blooming in 2010 to 2013 were hence monitored to ripeness (in 2012 to 2015). All female flowering strobili were visually counted and ripe cones collected, while male strobili shoots were counted and their length visually estimated to the nearest 5 mm to get an estimate of male strobili abundance. Pine cones where air-dried for several weeks and then oven-dried for seven days to induce opening (35ºC). Empty and healthy seeds were discriminated by decanting them on cold water, where empty seeds remain floating on the surface. After separating healthy and empty seeds for each cone, they were oven-dried again at 35ºC before weighing them to the nearest 1 mg with a precision scale., [resin.csv] On 14 October 2010 we collected needle samples from both experiments, to assess defensive compound (non-volatile resin and total polyphenolics) and nutrient content (nitrogen and phosphorus concentration). Both needles produced in 2009 and 2010 were collected (and analysed) separately in each ramet. Nutrient content was only assessed for the fertilization experiment and for the needles produced in 2010. Defensive compounds were also determined in phloem samples collected from all ramets on 16 april 2011 but due to logistical reasons, resin content data for phloem samples in 2010 were lost. Needle and phloem sampling was hence repeated at the end of the experiment, in 2013, in order to estimate non-volatile resin concentration. Total non-volatile resin content in phloem and needle tissue was determined by gravimetric analysis. Needle and phloem fresh samples (aprox 2-5 g) were immediately covered with hexane within pre-weighed test tubes, and sonicated for 20 min at 20ºC. Resin extraction continued for 24 h at room temperature under the fume hood and then the content of the tube was filtered with GFF filters (Whatman GF⁄ D, Whatman Int. Ltd, Maidstone, Kent, UK) into a second pre-weighed tube. The whole extraction procedure was repeated with each sample and the liquid fraction from both extractions pooled before letting them dry under the fume hood. Completely dried tubes were weighed with a precision scale to the nearest 0.0001 g. The solid fraction was oven-dried at 65ºC until constant weight. Total non-volatile resin content was estimated as mg of dried extracted resin per g of dry sample. Needle and phloem samples were analysed to estimate phenol content by the Folin-Ciocalteu method (Scalbert 1992), a colorimetric protocol using the Folin-Ciocalteu reagent and tannic acid as standard. Fresh samples were immediately oven-dried at 45ºC and manually ground in a mortar with liquid nitrogen., This data were collected with the support of the Spanish Goverment (grant numbers AGL2012-40151-C03-01, AGL2015-68274-C3-2-R)., growth.csv, nutrients.csv, phenols.csv, pissode.csv, reproduction.csv, resin.csv, Peer reviewed

DOI: http://hdl.handle.net/10261/311371
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311371
HANDLE: http://hdl.handle.net/10261/311371
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311371
PMID: http://hdl.handle.net/10261/311371
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311371
Ver en: http://hdl.handle.net/10261/311371
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oai:digital.csic.es:10261/311371

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311372
Dataset. 2022

TABLE_1_KNOCK-OUT OF CMNAC-NOR AFFECTS MELON CLIMACTERIC FRUIT RIPENING.XLSX

  • Liu, Bin
  • Santo Domingo, Miguel
  • Mayobre, Carlos
  • Martín-Hernández, Ana Montserrat
  • Pujol, Marta
  • García-Mas, Jordi
1 table. -- Supplementary Table 1: List of primers and their uses., Peer reviewed

Proyecto: //
DOI: http://hdl.handle.net/10261/311372
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311372
HANDLE: http://hdl.handle.net/10261/311372
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311372
PMID: http://hdl.handle.net/10261/311372
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/311372
Ver en: http://hdl.handle.net/10261/311372
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