María Esther Rodríguez
University of Cádiz
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Featured researches published by María Esther Rodríguez.
Journal of Applied Microbiology | 2010
María Esther Rodríguez; Juan José Infante; M. Molina; M. Domínguez; Laureana Rebordinos; Jesús Manuel Cantoral
Aims: To analyse the diversity of wild yeast in spontaneous fermentations of a white wine and to select the most suitable autochthonous starter yeasts. The selected yeasts would be used for inoculation of industrial fermentations in several years.
Journal of Applied Microbiology | 2017
Belén Puertas; M.J. Jiménez; Emma Cantos-Villar; Jesús Manuel Cantoral; María Esther Rodríguez
We have evaluated for the first time the impact of two commercial yeast strains (Torulaspora delbrueckii TD291 and Saccharomyces cerevisiae QA23) inoculated sequentially in musts of Chardonnay and Palomino Fino grape varieties grown under warm climate (South‐west of Spain).
International Journal of Food Microbiology | 2011
María Esther Rodríguez; Juan José Infante; Montse Molina; Laureana Rebordinos; Jesús Manuel Cantoral
The analysis of restriction fragment length polymorphism of mitochondrial DNA (mtDNA-RFLP) has been applied as a test to monitor the abundance of the starter yeast strain during industrial wine fermentations without previous isolation of yeast colonies. For white wine fermentations, we performed a rapid assay consisting in taking a sample of fermenting must, purifying the DNA from harvested cells, and obtaining the restriction patterns by digestion with the endonuclease HinfI. The same protocol, but adding an overnight cultivation step before DNA purification, was also applied to red wine fermentations. The results were compared with those obtained from the subsequent characterisation of strains, for the same samples, by analysis of the electrophoretic karyotype of isolated yeast colonies. In all cases, when the inoculated strain was dominant within the yeast population, the rapid assay anticipated the result by showing the coincidence between the restriction profiles obtained from both total cells and the inoculated strain. The results were obtained at 11 or 23 h after sampling for white- or red-wine fermentations respectively. This method allows a rapid intervention of the wine-producer if the presence of the inoculated yeasts has suffered a sudden decrease in any phase of the fermentation process.
The Open Biotechnology Journal | 2013
María Esther Rodríguez; Juan José Infante; Juan J. Mesa; Laureana Rebordinos; Jesús Manuel Cantoral
This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License.
Proteomics | 2016
Eugenia Muñoz-Bernal; Michael J. Deery; María Esther Rodríguez; Jesús Manuel Cantoral; Julie Howard; Renata Feret; Ramón Natera; Kathryn S. Lilley; Francisco Javier Fernández-Acero
Saccharomyces bayanus var. uvarum plays an important role in the fermentation of red wine from the D.O. Ribera del Duero. This is due to the special organoleptic taste that this yeast gives the wines and their ability to ferment at low temperature. To determine the molecular factors involved in the fermentation process at low temperature, a differential proteomic approach was performed by using 2D‐DIGE, comparing, qualitatively and quantitatively, the profiles obtained at 13 and 25°C. A total of 152 protein spots were identified. We detected proteins upregulated at 13°C that were shown to be related to temperature stress, the production of aromatic compounds involved in the metabolism of amino acids, and the production of fusel alcohols and their derivatives, each of which is directly related to the quality of the wines. To check the temperature effects, an aromatic analysis by GC–MS was performed. The proteomic and “aromatomic” results are discussed in relation to the oenological properties of S. bayanus var. uvarum.
Chromosoma | 2017
Silvia Portela-Bens; Manuel Alejandro Merlo; María Esther Rodríguez; Ismael Cross; Manuel Manchado; Nadezda Kosyakova; Thomas Liehr; Laureana Rebordinos
The evolution of genes related to sex and reproduction in fish shows high plasticity and, to date, the sex determination system has only been identified in a few species. Solea senegalensis has 42 chromosomes and an XX/XY chromosome system for sex determination, while related species show the ZZ/ZW system. Next-generation sequencing (NGS), multi-color fluorescence in situ hybridization (mFISH) techniques, and bioinformatics analysis have been carried out, with the objective of revealing new information about sex determination and reproduction in S. senegalensis. To that end, several bacterial artificial chromosome (BAC) clones that contain candidate genes involved in such processes (dmrt1, dmrt2, dmrt3, dmrt4, sox3, sox6, sox8, sox9, lh, cyp19a1a, amh, vasa, aqp3, and nanos3) were analyzed and compared with the same region in other related species. Synteny studies showed that the co-localization of dmrt1-dmrt2-drmt3 in the largest metacentric chromosome of S. senegalensis is coincident with that found in the Z chromosome of Cynoglossus semilaevis, which would potentially make this a sex proto-chromosome. Phylogenetic studies show the close proximity of S. senegalensis to Oryzias latipes, a species with an XX/XY system and a sex master gene. Comparative mapping provides evidence of the preferential association of these candidate genes in particular chromosome pairs. By using the NGS and mFISH techniques, it has been possible to obtain an integrated genetic map, which shows that 15 out of 21 chromosome pairs of S. senegalensis have at least one BAC clone. This result is important for distinguishing those chromosome pairs of S. senegalensis that are similar in shape and size. The mFISH analysis shows the following co-localizations in the same chromosomes: dmrt1-dmrt2-dmrt3, dmrt4-sox9-thrb, aqp3-sox8, cyp19a1a-fshb, igsf9b-sox3, and lysg-sox6.
Archive | 2012
María Esther Rodríguez; Laureana Rebordinos; Eugenia Muñoz-Bernal; Francisco Javier Fernández-Acero; Jesús Manuel Cantoral
, which were introduced in the laboratory for genetics and molecular studies in about 1935. There is, however, a second type of yeast comprising those used in industrial processes, for example, in brewing, baking and winemaking. Wine yeast and its properties have been known to humans for as long as civilizations have existed, and the earliest evidence of this yeast has been dated to Neolithic times (Mortimer, 2000). Most wine yeast strains are diploid and have a low frequency of sporulation. Another important characteristic of wine yeasts, and those used in other industries, is their highly polymorphic chromosomes: their genetic constitution is affected by the frequent and extensive mutation they undergo. These effects include (i) aneuploidy, (ii) polyploidy, (iii) amplification and deletion of chromosomal region or single gene, and (iv) the presence of hybrid chromosomes. The chromosomal polymorphism obtained by applying the technique known as pulsed field gel electrophoresis (PFGE) has been used to characterize and to classify strains that belong to the same species. In the wine industry, knowledge of the yeast species responsible for the alcoholic fermentation is important because these yeasts with their metabolism contribute significantly to the organoleptic characteristics of the finished wine (Fleet, 2008). The diverse range of yeasts associated with the vinification process can be classified in two groups. The first group is formed principally by the genera
Archives of Microbiology | 2017
Gustavo Cordero-Bueso; María Esther Rodríguez; Carlos Garrido; Jesús Manuel Cantoral
Fish & Shellfish Immunology | 2014
Ismael Cross; Manuel Alejandro Merlo; María Esther Rodríguez; Silvia Portela-Bens; Laureana Rebordinos
Archives of Microbiology | 2013
Eugenia Muñoz-Bernal; María Esther Rodríguez; Patricia Benítez; Francisco Javier Fernández-Acero; Laureana Rebordinos; Jesús Manuel Cantoral