Structural and physicochemical characterization of porous starch prepared by enzymatic hydrolysis,solvent-exchange,and freeze–thaw cross-linking treatments

Porous starches have been researched for applications of its characteristics, although it has been noted that different methods are used to influence the properties manifested. In this study, native starch isolated from hyacinth bean (Lablab purpureus) was used to create porous starch using three different methods, viz, solvent-exchange (SE), enzyme hydrolysis (EH), and addition of mercaptosuccinic acid known as freeze–thaw (FT). The structural characteristics (Fourier-transform infrared spectroscopy, X-Ray Diffraction) of SE and EH were very similar to those of NS. The gelatinization properties of the porous starches were higher (97.15–112.86) than those of NS (93.00–103.69). The pasting properties of SE and EH were improved, while FT did not possess any pasting abilities, this was due to its high solubility (42.92 ± 1.70) and lipophilic nature (4.63 ± 0.42). The adsorption properties of SE (4.0616.35) and EH (4.31–15.45) were similar to those of NS (3.53–15.50). The swelling power of SE (9.16 ± 0.19) and EH (9.25 ± 0.13) was similar to that of NS (9.76 ± 0.43), while the amylose contents (15.48–19.43) were lower than those of NS (20.68 ± 4.39). Only the SE (11.42 ± 3.40) from the porous starches had resistant starch present, while EH had mostly rapidly digestible (13.23 ± 0.00) and slowly digestible starch (127.16 ± 0.00). These structural and physicochemical characteristics show that these porous starches may be suitable in delivery systems, improving solubility of drugs and adsorbing dyes.     

Determination of gellan gum by capillary electrophoresis and CE–MS

Intact gellan gum (0.1% m/v) was detectable by capillary electrophoresis (CE) with UV detection. Characteristic tetrasaccharide fragments, prepared with a newly characterised gellan-degrading enzyme, provided a clearer signal that was detectable in complex food products containing other polysaccharides. Food products spiked with gellan gum could be analysed reproducibly with high accuracy and specificity by CE–ESI–MS, which is recommended as the technique of choice. Gellan gum declared as a fruit flavour drink ingredient could not be identified by CE–ESI–MS. When added to the product at the start of sample preparation, before enzyme treatment, the gum was readily detectable, demonstrating that the method was compatible with this sample type. Possible explanations for the negative results are that gellan gum was used as a trace component, with other texturing agents; that its declaration was precautionary only; or that the product contained a chemically modified form. Further work will establish whether modified gellan gums can be similarly analysed.     

Evaluation of cheese authenticity and proteolysis by HPLC and urea–polyacrylamide gel electrophoresis

Chromatographic and electrophoretic methods have been established as useful tools in characterising cheese ripening and in the detection of milk adulteration. The purpose of this work was to evaluate casein proteolysis of cheeses made from bovine, ovine or mixtures of bovine and ovine milks, as well as ovine cheese authenticity, for 30 days of ripening by HPLC and urea–polyacrylamide gel electrophoresis.Complementary information was obtained by both techniques when applied to the study of casein proteolysis during 30 days of ripening of ovine milk cheeses, ovine milk cheeses with 10% and 20% of bovine milk and bovine milk cheeses, manufactured according to the traditional Terrincho technology. For ovine cheeses, α-casein was the fraction that showed the higher degradation during cheese ripening. A similar behaviour was observed for ovine milk cheese with 10% of bovine milk. The profile for ovine milk cheese with 20% of bovine milk was more similar to that obtained for bovine cheese. Concerning bovine milk cheeses, electrophoresis was the most sensitive technique for the evaluation of proteolysis in these cheeses.Ten and 20% of bovine milk could be detected in ovine milk cheeses by urea–polyacrylamide gel electrophoresis and HPLC, respectively, even after 30 days of ripening.     

A values–beliefs–attitude model of local food consumption: An empirical study in China and Denmark

Consumers’ and policy makers’ interest in local foods is growing. Accordingly, researchers are also increasingly paying attention to the consumption of local foods. Studies have identified preference for local foods as an emergent consumer ideology called “locavorism”, but they have not yet addressed its antecedents or put it into a theoretical context. In addition, extant research provides several insights into local food buying behaviour in developed economies (e.g., USA, UK, Germany, or Italy); however, studies simultaneously conducted in developed and emerging economies are lacking. To address these research gaps, this study develops a conceptual framework with proposed relationships among values, beliefs (locavorism and fresh start mindset), and attitudes towards and intentions to purchase local foods in China and Denmark. We conducted an online survey in China and Denmark that evaluated our constructs with pre-developed multiple-item measures. Using structural equation modelling to test the integrated model, we find that values and long-term orientation are antecedents of consumer beliefs but the influences of values on consumer beliefs differ between collectivistic-dominated China and individualistic-dominated Denmark. Specifically, collectivistic values are significantly and positively related to locavorism in both countries, while individualistic values are strongly linked to locavorism only in Denmark; collectivistic values have no effects on fresh start mindset for the two samples, but individualistic values are significantly and positively related to a fresh start mindset in Denmark. In addition, consumer beliefs are significantly and positively associated with attitudes towards and intentions to buy local foods. Local food marketers can use our findings to target their communications more effectively.     

Understanding the crispy–crunchy texture of raw red pepper and its change with storage time

Red sweet peppers held in cold storage were periodically sampled at 1-week intervals over a 3-weeks period using three-point bending, puncture, cutting, and Volodkevich (coupled with acoustic emission) tests, confocal laser scanning microscopy (CLSM) and other physicochemical measurements. At each sampling, tissue specimens were soaked in mannitol solutions (0.0–0.9M) and puncture test, dimension changes and CLSM were used to identify degrees of turgidity present in osmotically manipulated pepper tissue. Pepper texture became crumbly with increased storage time due to softening and wilting processes. The Young's modulus, derived from the bending test using the single-edge notched bend geometry without notches decreased progressively during cold storage and resulted as the best mechanical parameter for measuring the loss of whole-tissue stiffness by both decreased cell wall stiffness and turgor pressure. Osmotic adjustment indicated that the pepper structure is extremely anisotropic, with the specimen's “average” relative thickness (RT) being the dimension change more affected. Incipient plasmolysis was evident in the highest mannitol concentration (0.9M), therefore, the turgor pressure of nonsoaked tissue could not be inferred. However, significant correlations were found between RT and puncture parameters such as initial slope, initial and final distances, and the number of flesh and skin force peaks, which depended on the dilation or shrinkage caused by the osmotic adjustment. During storage, soaked tissues had lower crunchy texture than nonsoaked, reflecting that cell wall stiffness plays a more significant role in determining pepper crunchiness than cell turgor pressure.     

Antioxidant potential and antimicrobial activity of chitosan–inulin conjugates obtained through the Maillard reaction

Food Science and Biotechnology - Chitosan (1%) was glycated with inulin (0.5, 1, and 2%) via the Maillard reaction at various initial pH values (5, 5.5, and 6). Higher pHs led to a greater pH drop...     

Volatile characteristics of 50 peaches and nectarines evaluated by HP–SPME with GC–MS

Using HS–SPME–GC–MS, characteristics of the volatiles of 50 peaches and nectarines representing different germplasm origins were investigated. Ten of these peaches and nectarines were studied in two successive years. Eighty-four compounds were identified. Volatile composition was relatively consistent, but the amount of total volatiles and certain individual compounds varied between years. Moreover, the composition of volatiles and their contents depended on genotypic background and germplasm origin. Total volatiles in wild peaches and a Chinese local cultivar ‘Wutao’ were much higher than in the other groups. All the peaches and nectarines could be classified into four groups by principal component analysis of the volatiles (excluding C₆ compounds): ‘Ruipan 14’ and ‘Babygold 7’ with high contents of lactones, Chinese wild peaches and ‘Wutao’ with high contents of terpenoids and esters, seven cultivars with American or European origins with high content of linalool, and others without characteristic composition of volatiles.     

Attenuation of iNOS and COX2 by blueberry polyphenols is mediated through the suppression of NF-κB activation

Treatment of BV2 microglial cells with blueberry extracts has been shown to be effective in reducing lipopolysaccharide (LPS)-induced proinflammatory mediators such as nitric oxide (NO), tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), inducible NO synthase (iNOS), and cyclooxygenase 2 (COX2). The current study explored the possibility that the down-regulation of iNOS and COX2 by blueberry extracts was mediated through NF-κB signaling pathway. A column-purified fraction of polyphenol-enriched blueberry extract (PC18) was used to treat LPS-activated BV2 cells. The results thus far showed that blueberry polyphenols significantly suppressed iNOS and COX2 promoter activities. In addition, blueberry polyphenols inhibited NF-κB nuclear translocation in LPS-activated BV2 cells. These findings suggested that the beneficial effects of blueberries may involve direct modulation of oxidative stress and/or inflammatory signaling cascades.     

Investigation of Levels and Fate of Pyridalyl in Fruit and Vegetable Samples by Fast Gas Chromatography–Mass Spectrometry

The search on pyridalyl residues, the novel insecticide, in strawberries and spring onions was evaluated. The QuEChERS technique was used for sample preparation. A fast gas chromatography–mass spectrometry (GC–MS) method was developed and validated for the analysis of pyridalyl in both matrices. Fast GC–MS was performed with a narrow-bore capillary column and a quadrupole mass detector with electron ionization and negative chemical ionization, both operating in selected ion monitoring mode. Fortification studies at 1, 5, 10, and 250 μg/kg for fruit and vegetable matrices were performed. Recoveries for all fortification levels, two ionization modes ranged from 72 to 114 %. Matrix effects were discussed. Limits of quantification were established at 1 μg/kg. Field experiments to investigate the pre-harvest interval were carried out. The proposed method was applied successfully to the determination of pyridalyl residues in samples available on Slovak market, and none of the samples contained detectable amounts of pesticides. The developed method is simple, efficient, and easy to adopt in laboratories engaged in pesticide residue analysis method.     

Simultaneous analysis of thirteen phytohormones in fruits and vegetables by SPE-HPLC–DAD

Food Science and Biotechnology - Determination of phytohormones have attracted increasing attentions in food safety field. In this study, an efficient and quantitative method was developed which...     

Identification and quantification of acetic acid bacteria in wine and vinegar by TaqMan–MGB probes

A Real-Time PCR (RT-PCR) assay was developed using TaqMan minor groove binder (MGB) probes for the specific detection and quantification of five acetic acid bacteria (AAB) species (Acetobacter pasteurianus, Acetobacter aceti, Gluconacetobacter hansenii, Gluconacetobacter europaeus and Gluconobacter oxydans) in wine and vinegar. The primers and probes, designed from the 16S rRNA gene, showed good specificity with the target AAB species. The technique was tested on AAB grown in glucose medium (GY) and inoculated samples of red wine and wine vinegar. Standard curves were constructed with the five target species in all these matrices. Quantification was linear over at least 5 log units using both serial dilution of purified DNA and cells. When this technique was tested in GY medium and inoculated matrices, at least 10²–10³ cells/ml were detected. To quantify low populations of AAB in microbiologically complex samples, a PCR enrichment including part of the 16S–23S rRNA gene ITS region was needed to increase the amount of target DNA compared to non-target DNA.     

Selenium speciation analysis of Misgurnus anguillicaudatus selenoprotein by HPLC–ICP–MS and HPLC–ESI–MS/MS

Analytical methods for selenium (Se) speciation were developed using high-performance liquid chromatography (HPLC) coupled to either inductively coupled plasma mass spectrometry (ICP?CMS) or electrospray ionization tandem mass spectrometry (ESI?CMS/MS). Separations of selenomethionine (Se-Met) and selenocysteine (Se-(Cys)₂) with favorable peak shape and resolution were obtained by both HPLC-ICP-MS and HPLC?CESI?CMS/MS. Both methods achieved low limits of detection, high sensitivity and favorable stability. With HPLC?CESI?CMS/MS, signal suppression was observed when complex matrix was co-eluted, but excellent structural characterization was still achieved. Thus, HPLC-ICP-MS is better for the detection of Se species, and HPLC?CESI?CMS/MS is essential for molecular identification and confirmation. A water-soluble selenoprotein from purified M. anguillicaudatus muscle tissue was analyzed by the two complementary systems (HPLC-ICP-MS and HPLC?CESI?CMS/MS) with high sensitivity and accuracy. The results demonstrated that Se-Met was the predominant selenoamino acid in the purified selenoprotein from M. anguillicaudatus muscle tissue, and the concentration of Se-Met in the selenoprotein was 6.280?mg/kg (dry mass). In addition, in HPLC-ICP-MS, an unknown Se-containing compound with similar polarity to Se-(Cys)₂ was discovered. Using complementary data from HPLC?CESI?CMS/MS, it was determined that this unknown Se-containing compound was not Se(Cys)_2.     

Phytoestrogenic activity of Aceriphyllum rossii and rapid identification of phytoestrogens by LC–NMR/MS and bioassay-guided isolation

Aceriphyllum rossii Engler (Saxifragaceae) has been used as a nutritious food in Korea, but only minimal studies on this plant have been undertaken. We have examined the estrogenic effect of A. rossii and have discovered its potent constituents. To identify the estrogenic activity of A. rossii, we measured the transactivation of the estrogen-responsive element (ERE) in MCF-7 cells transfected with an ERE-containing construct after treatment of the extract and fractions of A. rossii. A. rossii showed a potent estrogenic activity and gallic acid ethyl ester; quercetin and kaempferol were identified as major constituents of the active fractions by liquid chromatography–nuclear magnetic resonance spectroscopy/mass spectrometry. We confirmed quercetin and kaempferol are the major active constituents after activity-guided isolation of seven compounds: gallic acid ethyl ester (1), quercetin (2), kaempferol (3), quercetin-3-O-(6″-galloyl)-β-d-glucopyranoside (4), quercetin-3-O-β-d-glucopyranoside (5), kaempferol-3-O-(6″-galloyl)-β-d-glucopyranoside (6), and kaempferol-3-O-β-d-glucopyranoside (7). These results show A. rossii could be a possible candidate for the treatment of postmenopausal symptoms.     

De-oiled rapeseed and a protein isolate: characterization of sinapic acid derivatives by HPLC–DAD and LC–MS

De-oiled rapeseed is a rich source of proteins and phenolic compounds. The phenolic compounds, namely sinapic acid derivatives (SAD), could occur as free sinapic acid, esterified (as sinapine, the choline ester of sinapic acid) and decarboxylated (as canolol) forms. Rapeseed protein preparations containing very low phenolic compounds have been the focus of our ongoing research. A precipitated rapeseed protein isolate is investigated for SAD such as sinapine, sinapoyl glucose, canolol using HPLC–DAD and LC–MS. Profile of the phenolic compounds of de-oiled rapeseed, press cakes and the precipitated protein isolate are compared. HPLC–DAD analysis indicated SAD; particularly sinapine is the main phenolic compound of all the substrates. The protein derivation process did not remarkably alter the profile of the investigated protein isolate.     

Concentration of camu–camu juice by the coupling of reverse osmosis and osmotic evaporation processes

The objective of this work was to evaluate the technical feasibility of coupling two membrane separation processes, reverse osmosis (RO) and osmotic evaporation (OE), in order to concentrate clarified camu–camu juice, focusing on the vitamin C, phenolic compounds and antioxidant activity of the final product. The juice was firstly pre-concentrated by RO, reaching 285 g kg⁻¹ of soluble solids. During this step, the juice’s osmotic pressure showed to be the main factor controlling mass transfer. The juice was then concentrated by OE, reaching 530 g kg⁻¹ of soluble solids. Vitamin C, total phenolics and antioxidant activity levels of 94.6 g ascorbic acid kg⁻¹, 105.2 g galic acid kg⁻¹ and 762 mmol Trolox kg⁻¹, respectively, were achieved in the final product. The use of integrated membrane processes proved to be an interesting alternative to the concentration of thermosensitive juices, reaching concentration levels up to 7 times for camu–camu juice’s bioactive compounds.