Characterization of olive paste volatiles to predict the sensory quality of virgin olive oil

One of the main challenges that virgin olive oil producers face today is an accurate prediction of the sensory quality of the final product prior to the milling of the olives. The possibility that olive paste aroma can be used as a predictive measurement of virgin olive oil quality is studied in this paper. The study was centered on distinguishing the aroma of olive pastes that produced virgin olive oils without sensory defects from the aroma of olive pastes the virgin olive oils of which showed sensory defects. Olive pastes were analyzed by solid‐phase microextraction‐gas chromatography and a sensor system based on metal oxide sensors. Forty‐four volatile compounds were identified in olive pastes, all of them being also present in virgin olive oil. Six volatile compounds – acetic acid, octane, methyl benzene, (E)‐2‐hexenal, hexyl acetate and 3‐methyl‐1‐butanol – distinguished both kinds of pastes with only five misclassified samples. Five metal oxide sensors were able to classify the olive pastes with only two erroneous classifications.     

Sensory Assessment of Microencapsulated Fish Oil Powder

The aim of the study was to investigate the influence of microencapsulation by spray drying on fish oil sensory quality. Evaluated fish oil powders were coated with modified cellulose, skim milk powder and a mixture of fish gelatin and cornstarch. Samples were stored in the presence of air and under vacuum and then sensory evaluated. It was shown that fish oil powders were very susceptible to oxidation resulting in off-flavor formation. Odor profiles of samples stored in the presence of air were unstable and showed increases in undesirable odor attributes, which were significantly correlated with peroxide value, especially in the case of samples formed by spray drying. Elimination of air from the packaging improved stability of all samples during storage in both odor profile and peroxide value. The main conclusion of this study is that microencapsulation, especially by spray drying, provokes strong changes in fish oil sensory quality. Microencapsulated fish oil powder is not stable and rapidly oxidizes in the presence of air. However, its stability may be improved when stored under vacuum.     

Characterization of volatile compounds and triacylglycerol profiles of nut oils using SPME‐GC‐MS and MALDI‐TOF‐MS

Several nut oil varieties mainly used as culinary and overall healthy food ingredients were subject of the present study. Headspace solid‐phase microextraction combined with gas chromatography‐mass spectrometry was employed in order to determine the qualitative composition of volatile compounds. Furthermore, matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry was used in order to assess the profiles and relative composition of the prevalent triacylglycerols (TAG) within the oils. The headspace of the majority of oil samples was dominated by high contents of acetic acid (up to 42%) and hexanal (up to 32%). As nut oils are typically gained by cold‐pressing from previously roasted nuts, characteristic pyrazine derivatives as well as degradation products of long‐chain fatty acids were detected. TAG analysis of these oils revealed a quite homogeneous composition dominated by components of the C₅₂ and C₅₄ group composed mainly of oleic (18:1), linoleic (18:2), stearic (18:0) and palmitic (16:0) acid residues representing together between 65 and 95% of the investigated nut oils. The TAG profiles showed characteristic patterns which can be used as ‘fingerprints’ of the genuine oils. Nut oils exhibiting quite similar fatty acid composition (e.g. hazelnut, pistachio and beech oil) could be clearly discriminated based on TAG showing significant differences between the oils.     

Determination of 3‐MCPD esters in edible oil – methods of analysis and comparability of results

The discovery of fatty acid esters of 3‐chloropropane‐1,2‐diol (3‐MCPD) in edible oil products initiated food monitoring campaigns in many EU Member States. As the determination of 3‐MCPD esters was new to most laboratories, questions on the reliability of the produced analysis data were raised. In response to this, the Institute for Reference Materials and Measurements (IRMM) of the European Commission's Joint Research Centre (JRC) organised a proficiency test on the determination of 3‐chloropropane‐1,2‐diol esters (3‐MCPD esters) in edible oils. The aim of this proficiency test was to scrutinise the capabilities of official food control laboratories, private food control laboratories as well as laboratories from food industry to determine the 3‐MCPD esters content of edible oils. The study was carried out in accordance with “The International Harmonised Protocol for the Proficiency Testing of Analytical Chemistry Laboratories” and ISO Guide 43. The test materials dispatched to the participants were: refined palm oil, extra virgin olive oil spiked with 3‐chloropropane‐1,2‐dioleate and 3‐MCPD standard solution in sodium chloride. Altogether 41 laboratories from 11 EU Member States, Switzerland and Macedonia subscribed for participation in the study. The analysis task was to determine the 3‐MCPD esters content as total 3‐MCPD content of the test samples. Participants were free to choose their analysis methods. In total, 34 laboratories reported results to the organisers of the study. The performance of laboratories in the determination of 3‐MCPD esters in edible oils was expressed by z‐scores. About 56% of the participants performed satisfactorily in the determination of 3‐MCPD esters in palm oil and 85% for the spiked extra virgin olive oil test sample. The study revealed that the direct transesterification of the sample without the prior removal of glycidol esters might lead to strong positive bias.     

Accurate determination of hexanal in beef bouillons by headspace solid‐phase microextraction gas‐chromatography mass‐spectrometry

Lipid oxidation has great impact on the quality of food products through flavor and taste deterioration, reduction in nutritive value, and potential toxicity of the oxidized food components. Flavor and taste deterioration can be easily perceived and it represents one of the major causes of consumer complaints in the food industry. The deterioration of sensory properties is due to the decomposition products of hydroperoxides that easily isomerize and degrade into volatile compounds. Volatile products are responsible for flavor and taste deterioration. In this study, we present the development of the solid‐phase microextraction gas chromatography‐mass spectrometry (SPME‐GC‐MS) technique to quantify low amounts (μg/g range) of secondary oxidation products, i.e. hexanal. The optimization of SPME parameters is a difficult task because of the possibility of further formation of volatile products during analysis. Different parameters such as type of fiber, exposure time of the fiber to the sample headspace and the optimal temperature of absorption have also been investigated. The complete validation of the method was achieved by the determination of linearity, limits of detection and quantification and repeatability. We demonstrated that the SPME method is a valuable tool for the quantification of low amounts of secondary oxidation products such as hexanal. Therefore, this technique can be used to detect early formation of volatiles.     

Fatty acid profile,oxidative stability,and sensory properties of breast meat from turkeys fed diets with a different n‐6/n‐3 PUFA ratio

The objective of this study was to determine the effect of diets with a different n‐6/n‐3 PUFAs ratio (7.31, 4.43, and 0.99), resulting from the addition of different dietary oils: soybean, rapeseed, and linseed (diets S, R, and L, respectively), on the fatty acid (FA) profile, oxidative status, and sensory properties of turkey breast meat. After 15 wk of feeding, breast meat yield and chemical properties of the meat were similar in all groups. Raw breast meat of R turkeys had a significantly higher content of all‐trans‐retinol and α‐tocopherol, compared with S and L. The physicochemical properties of breast meat, including pH, color, drip loss, and cooking loss, did not differ significantly. Cooked meat samples differed significantly with respect to the concentrations of oleic acid, linoleic acid (S and R>L), and linolenic acid (S and R<L). Compared with S and R, breast meat of L turkeys was characterized by higher concentrations of total PUFAs (35.1 vs. 30.1 and 29.3%), a significantly lower n‐6/n‐3 PUFAs ratio (1.51 vs. 5.43 and 5.07%) and a higher thiobarbituric acid reactive substances content (TBARS; 31.9 vs. 26.4 and 26.7 nmol/g). After 4 months of deep‐freeze storage the n‐6/n‐3 PUFAs ratio did not deteriorate. It may be concluded that replacing soybean oil with linseed oil, but not with rapeseed oil, increased the proportion of PUFAs in the total FAs pool and improved the n‐6/n‐3 PUFAs ratio, yet it also adversely affected the sensory properties and oxidative stability of meat. Both raw and stored breast meat from L turkeys was susceptible to oxidative changes, as manifested by the significantly higher TBARS concentrations (17.07 and 81.06) compared with those of the S group (10.91 and 53.00 nmol/g, respectively). Practical applications: Studies investigating the possibility of increasing the health benefits of poultry meat have been performed mostly on broilers, while the problem remains poorly researched in turkeys. Our findings show that linseed oil, in contrast to rapeseed oil, is a good source of PUFAs, in particular n‐3 PUFAs, that can be effectively transferred from feed to carcass lipids. However, desirable changes in the fatty acid profile are accompanied by increased susceptibility to lipid oxidation and deterioration of the sensory properties of meat. Thus, the linseed oil content of turkey diets should be reduced, or diets supplemented with linseed oil should be fed for shorter periods of time to alleviate the negative effects of linseed oil on the sensory attributes and oxidative status of meat.     

The Chemical Properties and Volatile Compounds of Virgin Olive Oil from Oueslati Variety: Influence of Maturity Stages in Olives

The aim of the present work was to investigate the influence of fruit ripening on oil quality and volatile compounds in an attempt to establish an optimum harvesting time for Oueslati olives, the minor olive variety cultivated in Tunisia. Our results showed that many analytical parameters, i.e., peroxide value, UV absorbance at 232–270 nm, chlorophyll pigments, carotenoids and oleic acid contents decreased during ripening, whilst linolenic acid increased. Free acidity remained practically stable with a very slight rise at the highest maturity index. The volatile compounds emitted by the Oueslati olive oil were characterized and quantified by HS‐SPME‐GC‐EIMS. Twenty‐three volatile compounds were identified, mainly aldehydes, sesquiterpenes and esters. The results show variations in the volatile fractions and quality parameters of Oueslati extra virgin olive oil obtained at different olive‐ripening stages. Fifteen sesquiterpenes were identified for the first time in this cultivar, mainly hydrocarbon derivatives, but also oxygenated ones. On the basis of the quality parameters and volatile fractions studied, the best stage of Oueslati olive fruits for oil processing seems to be at ripeness index about 3.0. Indeed, these results suggested the possibility of using sesquiterpenes for olive authenticity and traceability and demonstrated that the volatile fractions can be used as indicators of the degree of ripening of the olives used to obtain the corresponding virgin olive oils.     

Reduction of petroleum hydrocarbons content from an engine oil refinery wastewater using a continuous stirred tank reactor monitored by spectrometry tools

BACKROUND: Hydrocarbon contamination of groundwater resources has become a major environmental and human health concern in many parts of the world. Microbial degradation of hydrocarbons, through either naturally occurring processes or engineered systems, has been successfully used to reduce concentrations of these pollutants. In order to develop an aerobic bioreactor tailored for this purpose, the present study aims to investigate petroleum contaminated wastewater remediation and toxicity reduction by acclimated microbial consortium enriched in a continuous stirred tank bioreactor (CSTR). Characterization and quantification of refinery wastewater components were performed by gas chromatography mass spectrometry (GC/MS) and Fourier transform infrared (FTIR) spectroscopy. RESULTS: The petroleum hydrocarbons were significantly degraded (97%) by the microbial consortium. After continuous aerobic treatment in the CSTR, the COD_effluent and BOD_5effluent average removals were high reaching 97% and 78%, respectively. Also, strong degradation of C10? C35 n‐alkanes was observed. The concomitant use of GC/MS and FTIR proved to be a useful complementary tool to assess the impact of treatment strategies on hydrocarbon‐contaminated wastewater. In addition, the toxicity of the contaminated wastewater decreased drastically after bioremediation. CONCLUSION: This work shows the ability of this consortium to degrade hydrocarbons and reduce toxicity, which makes them useful candidates for environmental restoration applications at other hydrocarbon‐contaminated environments. Copyright © 2011 Society of Chemical Industry