M.L. Morales
University of Seville
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Featured researches published by M.L. Morales.
Trends in Food Science and Technology | 2002
W. Tesfaye; M.L. Morales; M.C. García-Parrilla; Ana M. Troncoso
Abstract Wine vinegar is produced in most Mediterranean countries and extensively used as a condiment, acidifying and food preserving agent. Traditional production requires maturation in wood for many years to obtain a high acetic degree and the resulting product is relatively expensive. New technologies are being designed to overcome this difficulty with the objective of producing vinegars with a similar quality and at the same time less expensive. These methods of production involve the use of submerged bacterial culture and a continuous aeration system. Recent research is focussed in improving yield and quality of the final product.
Talanta | 2010
R.M. Callejón; Ana M. Troncoso; M.L. Morales
The amino acids present in foods and beverages affect the quality of these products and they play an important role in enology. Amino acids are consumed by yeasts as a source of nitrogen during alcoholic fermentation and are precursors of aroma compounds. In this review various chromatographic methodologies for the determination of amino acids are described, and specific applications for the analysis of amino acid content are discussed. Amino acids usually need to be derivatized to make them more detectable. Several derivatizing reagents have been employed for the determination of amino acids in enological applications, and each has its advantages and disadvantages.
Journal of Chromatography A | 2010
José Manuel Amigo; Marta J. Popielarz; R.M. Callejón; M.L. Morales; Ana M. Troncoso; Mikael Agerlin Petersen; T.B. Toldam-Andersen
The most straightforward method to analyze an obtained GC-MS dataset is to integrate those peaks that can be identified by their MS profile and to perform a Principal Component Analysis (PCA). This procedure has some important drawbacks, like baseline drifts being scarcely considered or the fact that integration boundaries are not always well defined (long tails, co-eluted peaks, etc.). To improve the methodology, and therefore, the chromatographic data analysis, this work proposes the modeling of the raw dataset by using PARAFAC2 algorithm in selected areas of the GC profile and using the obtained well-resolved chromatographic profiles to develop a further PCA model. With this working method, not only the problems arising from instrumental artifacts are overcome, but also the detection of new analytes is achieved as well as better understanding of the studied dataset is obtained. As a positive consequence of using the proposed working method human time and work are saved. To exemplify this methodology the aroma profile of 36 apples being ripened were studied. The benefits of the proposed methodology (PARAFAC2+PCA) are shown in a practitioner perspective, being able to extrapolate the conclusions obtained here to other hyphenated chromatographic datasets.
Analytica Chimica Acta | 2010
R.M. Callejón; Almudena Clavijo; P. Ortigueira; Ana M. Troncoso; Patricia Paneque; M.L. Morales
Organic wines were produced at pilot scale to select the best autochthonous and commercial yeast strains to obtain wines with high organoleptic qualities. We tested the behaviour of five S. cerevisiae yeast strains and determined their volatile composition and organoleptic characteristics by sensory analysis. A total of 51 volatile compounds were quantified in the wines produced. The concentration of most of the volatile compounds was significantly influenced depending on which yeast strain was inoculated. The differences observed in the volatile composition of the wines appear to be quantitative rather than qualitative. In general, acetals were the most abundant group of volatile compounds in all the samples studied, followed by alcohols without ethanol. The highest contents of volatile compounds were found in two of the wines produced by autochthonous yeast strains. The results obtained in the sensory analysis suggest that autochthonous yeast produced wines of higher organoleptic quality because this sample gave the highest value for the general impression attribute.
Journal of Chromatography A | 2008
R.M. Callejón; A.G. González; Ana M. Troncoso; M.L. Morales
Quantification of aroma compounds in wine vinegars is challenging due to the complexity of the matrix and the low concentrations expected. A method for the determination of volatile compounds in wine vinegars employing headspace sorptive extraction-thermal desorption-gas chromatography-mass spectrometry (HSSE-TD-GC-MS) was developed. A central composite design was used to optimize the sampling condition. The proposed method was successfully validated and low detection and quantification limits was obtained. The application of the proposed methodology allows the determination of 53 compounds in different wine vinegars (red, Sherry). Five of them have been detected in wine vinegars for the first time.
Talanta | 2007
R.M. Callejón; Ana M. Troncoso; M.L. Morales
A complete methodology for the determination of chloroanisoles and chlorophenols in cork material is proposed. The determination is accomplished by means of a previous liquid-solid extraction followed by stir bar sorptive extraction (SBSE) coupled to gas chromatography-mass spectrometry (GC-MS). Two different liquid-solid extraction experiments were conducted and eight compounds considered (2,6-dichloroanisole, 2,4-dichloroanisole, 2,4,6-trichloroanisole, 2,4,6-trichlorophenol, 2,3,4,6-tetrachloroanisole, 2,3,4,6-tetrachlorophenol, pentachloroanisole and pentachlorophenol). From the results obtained we can conclude that high volume extraction extending extraction time up to 24h is the best choice if we have to release compounds from the inner surfaces of cork stoppers. Recovery percentages ranged from 51% for pentachloroanisole to 81% for 2,4-dichloroanisole. This method allows the determination of an array of compounds involved in cork taint at very low levels from 1.2ng g(-1) for 2,4,6-tricholoroanisole to 23.03ng g(-1) for 2,3,4,6-tetrachlorophenol.
Talanta | 2012
C. Ubeda; C. Balsera; Ana M. Troncoso; R.M. Callejón; M.L. Morales
A solid phase extraction method (SPE) using Isolute ENV+ cartridges was validated for the determination of ethyl carbamate (EC) in different kinds of vinegars. The method proved to be quite sensitive, precise and accurate, improving the recovery and LQD of other existing methods for the same purpose. For the optimization of the method, different pH values of the sample were tested, resulting 5.5 the most adequate. Among the 14 samples analysed, only 5 of them had contents of EC above the quantification limits, ranging between 6.73 μg/L and 56.4 μg/L. The highest value was found in red wine vinegar. Taking into account the amount of vinegar consumed in a meal and the limits established for alcoholic beverages in some countries, the levels of ethyl carbamate in the vinegars tested in this work were acceptable.
Journal of Chromatography A | 2016
R.M. Callejón; C. Ubeda; Rocío Ríos-Reina; M.L. Morales; Ana M. Troncoso
One of the most common taints in foods is a musty or earthy odour, which is commonly associated with the activity of microorganisms. Liquid foods, particularly wine and water, can be affected by this defect due to the presence of certain aromatic organic compounds at very low concentrations (ng/L) consistent with human threshold perception levels. The volatile compounds responsible for a mouldy off-aroma include approximately 20 compounds, namely, haloanisoles, geosmin, 2-methylisoborneol, several alkyl-methoxypyrazines, 1-octen-3-ol, 1-octen-3-one, trans-octenol, 3-octanone, fenchol and fenchone. Methods for determining these very low concentrations of odour compounds must be extremely sensitive and selective with efficient preconcentration treatments. A number of extraction techniques based on LLME (liquid-liquid microextraction), SPME (solid-phase microextraction) or SBSE (stir-bar sorptive extraction) can be applied and should be selected on a case-by-case basis. Moreover, recent developments in GC instrumentation coupled to different detection systems can effectively increase the selectivity and sensitivity of the analysis of target compounds.
Food Reviews International | 2009
W. Tesfaye; M.L. Morales; M.C. García-Parrilla; Ana M. Troncoso
Technical improvement of vinegar production encompasses essential modifications to obtain quality products in a relatively short period of time. There are mainly two types of acetic fermentation processes to elaborate vinegar: surface and submerged culture system. High quality products are elaborated by the surface culture system. Quality, as a degree of excellence, is a subjective concept where human sensory organs play an important role to determine the acceptability of a product by the consumer. The quality of vinegars can be evaluated by using a trained sensory panel, but more rapid and objective characterization is achieved by instrumental measurements. Physicochemical analyses are generally aimed at meeting of legislative requirements for the quality, safety and characterization of foods or condiments like vinegar. Sensory analysis is a good tool to determine the category and degree of acceptance of given vinegars. Unfortunately, sensory analysis of vinegar is very difficult to perform since the pungent sensation restricts the number of samples that can be analysed at a time. Therefore, the appropriate sensory analysis method must be clearly defined and the attributes used in discriminant analysis or descriptive tests should be precise and well recognized by the panel.
Food Chemistry | 2016
C. Ubeda; R.M. Callejón; Ana M. Troncoso; Álvaro Peña-Neira; M.L. Morales
The volatile compositions of Charmat and traditional Chilean sparkling wines were studied for the first time. For this purpose, EG-Silicone and PDMS polymeric phases were compared and, afterwards, the most adequate was selected. The best extraction method turned out to be a sequential extraction in the headspace and by immersion using two PDMS twisters. A total of 130 compounds were determined. In traditional Chilean sparkling wines, ethyl esters were significantly higher, while acetic esters and ketones were predominant in the Charmat wines. PCA and LDA confirmed the differences in the volatile profiles between the production methods (traditional vs. Charmat).