Determination of β-carotene content and vitamin A activity of vegetables by high-performance liquid chromatography and spectrophotometry

A fast and sensitive high-performance liquid chromatographic (HPLC) method for the determination of the provitamin A, β-carotene, in vegetables is described. After alkaline saponification and organic extraction β-carotene is separated from other carotenoids on a reversed-phase HPLC column and determined by measurement of its absorbance at 445 nm. The total amount of carotenoids is determined by measurement of the absorbance at 445 nm of the extract prior to HPLC.Results are presented of the analysis of β-carotene and total carotenoids in some vegetables bought at a local market in Dar es Salaam. The percentage β-carotene, of the total carotenoid content, showed a great variation. The vitamin A activity of the vegetables was calculated from the analytical results.     

Changes in β-carotene bioaccessibility and concentration during processing of carrot puree

The effect of some process and product factors (addition of olive oil, high pressure homogenisation, subsequent thermal or high pressure pasteurisation) on β-carotene bioaccessibility and isomerisation of carrot puree was investigated. High pressure homogenisation could improve β-carotene bioaccessibility by disrupting cells, but only at a pressure higher than 50 MPa. Softening of the cell walls during a subsequent thermal pasteurisation resulted in a further increase in β-carotene bioaccessibility. Unfortunately, the high temperature also induced formation of some undesirable cis-isomers. As cell walls are probably strengthened by high pressure, high pressure pasteurisation could not positively affect the amount of bioaccessible β-carotene. Moreover, the high pressure process induced β-carotene oxidation. A positive effect of olive oil on β-carotene bioaccessibility could only be noticed in combination with a thermal pasteurisation process when β-carotene was solubilised in the oil droplets. Under high pressure however, oil can be crystallised which hinders the solubilisation of β-carotene.     

Effects of processing and packaging on vitamin C and β-carotene content of ready-to-use (RTU) vegetables

High pressure liquid chromatographic methods were used for measurement of the concentration of vitamin C and β-carotene in broccoli and green pepper. The effects of processing, packaging and storage on the levels of these nutrients in both unprocessed and processed ready-to-use (RTU) vegetables were determined. Systems investigated included: (a) unpacked and pillow packaged broccoli, and (b) unpacked, pillow, partial vacuum, and total vacuum packaged green pepper. There was a statistically significant decrease in vitamin C over a 10 day storage period of unpacked and packaged vegetables including all four packaging systems (P<0.001, overall average decrease of 11%). The overall loss of β-carotene during the 10 day storage period was not statistically significant (P=0.14). Although there was a significant loss in vitamin C during storage, in most cases there was no difference in loss of vitamin C or β-carotene between the processed and unprocessed vegetables, and the packaging systems.     

Influence of particle size on lipid digestion and β-carotene bioaccessibility in emulsions and nanoemulsions

The interest in incorporating carotenoids, such as β-carotene, into foods and beverages is growing due to their potential health benefits. However, the poor water-solubility and low bioavailability of carotenoids is currently a challenge to their incorporation into many foods. The aim of this work was to study the influence of particle size on lipid digestion and β-carotene bioaccessibility using corn oil-in-water emulsions with different initial droplet diameters: large (d₄₃ ≈ 23 μm); medium (d₄₃ ≈ 0.4 μm); and small (d₄₃ ≈ 0.2 μm). There was a progressive increase in the mean particle size of all the emulsions as they passed through a simulated gastrointestinal tract (GIT) consisting of mouth, stomach, and small intestine phases, which was attributed to droplet coalescence, flocculation, and digestion. The electrical charge on all the lipid particles became highly negative after passage through the GIT due to accumulation of anionic bile salts, phospholipids, and free fatty acids at their surfaces. The rate and extent of lipid digestion increased with decreasing mean droplet diameter (small ≈ medium ? large), which was attributed to the increase in lipid surface area exposed to pancreatic lipase with decreasing droplet size. There was also an appreciable increase in β-carotene bioaccessibility with decreasing droplet diameter (small > medium > large). These results provide useful information for designing emulsion-based delivery systems for carotenoids for food and pharmaceutical uses.     

Technical note: Rapid field test for the quantification of vitamin E, β-carotene,and vitamin A in whole blood and plasma of dairy cattle

Fast and easy tests for quantifying fat-soluble vitamins such as vitamin E and vitamin A, as well as β-carotene, in whole blood without a need to preprocess blood samples could facilitate assessment of the vitamin status of dairy cattle. The objective of this study was to validate a field-portable fluorometer/spectrophotometer assay for the rapid quantification of these vitamins in whole blood and plasma of dairy cows and calves. We measured the concentrations of vitamin E and β-carotene in whole blood and plasma from 28 dairy cows and 11 calves using the iCheck test (BioAnalyt GmbH, Teltow, Germany) and compared the results with the current analytical standard (HPLC) in 2 independent laboratories, one at the University of Potsdam (Germany) and at one at DSM Nutritional Products Ltd. (Kaiseraugst, Switzerland). For vitamin A, the HPLC measurements were done only in the laboratory in Germany. The whole-blood concentrations of vitamin E as determined by iCheck (blood-hematocrit-corrected) ranged from 1.82 to 4.99 mg/L in dairy cows and 0.34 to 3.40 mg/L in calves. These findings were moderately correlated (R² = 0.66) with the values assessed by HPLC in dairy cattle (cows + calves). When calves were excluded, the correlation was higher (R² = 0.961). The β-carotene and vitamin A values obtained by the reference method HPLC were highly correlated with the iCheck methods in whole blood (R² = 0.99 and 0.88, respectively). In plasma, we observed strong correlations between the concentrations assessed by iCheck and those of HPLC for vitamin E (R² = 0.97), β-carotene (R² = 0.98), and vitamin A (R² = 0.92) in dairy cattle (cows + calves). For vitamin E, β-carotene, and vitamin A, we compared the relationship between the differences obtained by the iCheck assay and the HPLC measurements, as well as the magnitude of measurements, using Bland–Altman plots to test for systematic bias. For all 3 vitamins, the differences values were not outside the 95% acceptability limits; we found no systematic error between the 2 methods for all 3 analytes.     

A survey of β-glucan and arabinoxylan content in wheat

BACKGROUND: Dietary fibre lowers the risk of coronary heart disease and colorectal cancer. This survey quantifies mixed link β‐glucan (MBG) and arabinoxylan (AX) in wheat and investigates relationships between the grain carbohydrates. MBG and AX contents were measured in 500 and 200 wheat accessions respectively, including diploid, tetraploid and hexaploid genotypes comprising primitive, synthetic and elite lines. RESULTS: Overall, MBG contents ranged between 1.8 and 18.0 g kg^?1 grain dry weight. In wheat–barley addition lines and triticale hexaploids the levels were 9.0–11.3 and 3.5–9.6 g kg^?1 respectively. The amounts in synthetic wheats were nearer their tetraploid parents than their diploid parents. AX and total non‐starch polysaccharide (NSP) contents ranged from 23.7 to 107.5 g kg^?1 and from 31.7 to 136.7 g kg^?1 respectively. Linear regressions showed that the relationships of starch and grain weight with NSP glucose were stronger than those with AX. CONCLUSION: The results indicated insufficient genetic diversity in the germplasm surveyed to initiate a breeding programme to increase the amount of MBG in wheat grain to 20 g kg^?1, a level considered high enough to confer a 10–15% reduction in blood cholesterol. Copyright © 2011 Society of Chemical Industry     

Degradation of β-casomorphin-7 through in vitro gastrointestinal and jejunal brush border membrane digestion

This work aimed to study the opioid peptide β-casomorphin-7 (BCM7) degradation or stability during digestion using human gastrointestinal (GI) juices and porcine jejunal brush border membrane (BBM) peptidases. Synthetic BCM7 was subjected to in vitro digestion by GI fluids obtained from human volunteers for 180 min, and to downstream degradation with porcine BBM vesicles. The BCM7 was sampled at 4 time points over 24 h after BBM addition. The digests were profiled by HPLC-electrospray ionization mass spectrometry (ESI/MS) to monitor BCM7 during GI digestion, and intact BCM7 through BBM digestion was quantified by reverse-phase (RP)-HPLC. We found that BCM7 was partly digested with human GI enzymes, as 3 proteolytic fragments in addition to f(60–66) YPFPGPI were detected: f(62–66) FPGPI, f(60–65) YPFPGP and f(61–66) PFPGPI. The RP-HPLC analysis revealed that 42% of the initial peptide was degraded after only 2 h of BBM digestion, and as much as 79% was degraded after 4-h digestion with supplementation of BBM. In conclusion, this study showed that most of BCM7 was degraded during GI and BBM digestion, although a small amount (5%) was still detected after 24-h digestion. It remains to be studied whether the small amount of intact BCM7 detected after in vitro digestion is transported via active transceptors in the human intestinal epithelial cells and enters blood circulation.     

Relation between in vitro lipid digestion and β-carotene bioaccessibility in β-carotene-enriched emulsions with different concentrations of l-α-phosphatidylcholine

In view of consumer health, it is desirable to promote the bioaccessibility of lipid-soluble compounds like carotenoids, while limiting the lipid intake. The objective of this work was to examine the relation between in vitro lipid digestion and β-carotene bioaccessibility of carrot-based model food emulsions containing water, 5% olive oil enriched with β-carotene (from carrots) and different concentrations (1–2–3–4%) of l-α-phosphatidylcholine (PHC), as an emulsifier. The lipid digestion (hydrolysis of triacylglycerols (TAGS) and incorporation of free fatty acids (FFAs) and monoacylglycerols (MAGs) in the micelles) and the β-carotene bioaccessibility (incorporation of β-carotene in the micelles) were studied after an in vitro digestion procedure wherein the stomach phase was mimicked for 2.0 h (37 °C) and the small intestinal phase was mimicked for 1.0 h, 1.5 h and 2.0 h (37 °C) (both end-over-end rotations). As a consequence, not only the influence of the emulsifier concentration, but also the influence of the duration in the small intestinal phase was investigated in this study. The oil droplet size distributions of the emulsions at different stages of digestion were shown to be dependent on the phosphatidylcholine concentration, but independent on the duration in the small intestinal phase (1.0 h–2.0 h). Furthermore, all TAGs were already hydrolysed into FFAs and MAGs after 1.0 h small intestinal phase and the incorporation of FFAs and MAGs into micelles seemed to reach a maximum for all emulsions (approximately 26.5%), independent on the phoshpatidylcholine concentration and thus on the particle size distributions. Finally, the β-carotene bioaccessibility increased with increasing phosphatidylcholine concentration, ranging from 33.2% to 79.8% for a 1% and 4% PHC emulsion respectively. No significant differences in β-carotene bioaccessibility were however noticed for the different durations in the small intestinal phase tested. In conclusion, a higher phosphatidylcholine concentration in emulsions leads to higher β-carotene bioaccessibility while the incorporation of lipids into micelles did not increase.     

Effect of Sicilian pasture feeding management on content of α-tocopherol and β-carotene in cow milk

This study was performed to evaluate α-tocopherol and β-carotene contents of pasture milk under ordinary Sicilian farming conditions. Fourteen dairy farms were allocated into 2 balanced groups on the basis of cultivated (CULT) or spontaneous (SPO) pasture type feeding. Bulk milk per farm was collected 4 times from February through April at 3-wk intervals. Pasture botanical and diet composition, diet nutritional quality, milk yield and composition were estimated each time. Pasture intake levels were calculated based on feed analyses, hay and concentrate amounts fed, and milk yield and chemical composition. According to pasture intake, the farms were split into low pasture intake (LPI; <29.5% of dry matter) and high pasture intake (HPI; >29.5% of dry matter) groups. Milk samples per farm were analyzed for α-tocopherol and β-carotene contents by HPLC. The SPO group had higher levels of α-tocopherol and β-carotene in milk (0.7 and 0.3 mg/L, respectively) and milk fat (19.0 and 7.5 mg/kg fat, respectively) compared with the CULT group in milk (0.5 and 0.2 mg/L, respectively) and milk fat (14.6 and 4.9 mg/kg, respectively). High pasture intake compared with LPI increased α-tocopherol in milk fat (18.0 and 16.0 mg/kg of fat, respectively). However, only in the SPO (not in CULT), HPI compared with LPI increased milk α-tocopherol (0.8 vs. 0.6 mg/L, respectively), milk β-carotene (0.3 vs. 0.2 mg/L, respectively), and milk fat β-carotene (8.4 vs. 6.6 mg/kg, respectively). Results may be related to the different botanical composition of the respective pasture types and pasture intake. Spontaneous pasture compared with CULT contained a higher mass proportion of Asteraceae, Fabaceae, Cruciferae, Euphorbiaceae, and Malvaceae plants. Milk and milk fat α-tocopherol levels were higher on test-days (TD)-1, TD-2, and TD-4 compared with TD-3. For HPI farms, milk fat β-carotene content was higher on the first 2 TD compared with the last 2 TD. These differences could be related to plant biological stage. On Sicilian dairy farms, the highest milk α-tocopherol and β-carotene contents may be obtained feeding high levels of SPO pasture in the spring.     

Influence of antioxidant spices on the retention of β-carotene in vegetables during domestic cooking processes

Considerable amounts of β-carotene were lost during the two domestic methods of cooking commonly used, namely, pressure cooking and open pan boiling, the loss ranging from 27 to 71% during pressure cooking and 16–67% during boiling for the four vegetables examined in this study. Pressure cooking of green leafy vegetables resulted in a greater retention of this provitamin. In the presence of red gram dhal, which is a common ingredient in the diet, there was an underestimation of β-carotene due to poor extractability. Inclusion of acidulants—tamarind and citric acid-along with these vegetables brought about some changes in the level of retention of β-carotene. The antioxidant spice turmeric generally improved the retention of β-carotene in all four vegetables studied. Onion also had a similar effect. The combinations of acidulants and antioxidant spices also improved the retention of β-carotene during cooking. This effect seemed to be additive in the case of processing of amaranth by boiling.     

Performance of selected emulsifiers and their combinations in the preparation of β-carotene nanodispersions

In this work, the characteristics of β-carotene nanodispersions prepared with sodium caseinate (SC), Tween 20, decaglycerol monolaurate (ML750) and sucrose fatty acid ester (L1695) using solvent displacement technique were compared. The mean particle size of the nanodispersions ranged from 30 nm to 206 nm, depending on the emulsifier used. SC-stabilized nanodispersions had the largest particles size, while those prepared with Tween 20 had the smallest. The mean particle size and size distribution of the nanodispersions generally remained unchanged after 8 weeks of storage time at 4 °C, but the β-carotene content in all nanodispersions decreased over time. The β-carotene in SC-stabilized nanodispersions was the most stable against oxidation among all samples, most likely due to the small specific surface area of the particles, physical barrier of SC protecting the encapsulated β-carotene against free radicals and the antioxidative activity of caseins. The combined effect of SC and ML750 or L1695 on the mean particle size and β-carotene retention was also investigated. Nanodispersions prepared with SC-ML750 or SC-L1695 showed larger mean particle sizes compared to those prepared with ML750 or L1695 alone. However, the stability of β-carotene in these systems was improved owing to the antioxidative activity of SC. This work demonstrated the importance of emulsifier in determining the characteristics and stability of β-carotene nanodispersions.     

Identification of bioactive peptides and quantification of β-casomorphin-7 from bovine β-casein A1, A2 and I after ex vivo gastrointestinal digestion

This study investigated whether different genetic variants of β-casein (β-CN) give rise to different bioactive peptides during digestion. β-CN was purified from bovine milk of genetic variants A1, A2 and I, and digested with human gastrointestinal juices in a static ex vivo model. Mass spectrometry analyses revealed that the peptide ⁶⁰YPFPGPIPN⁶⁸ was exclusively identified from variants containing proline at position 67. Most strikingly, the opioid peptide β-casomorphin-7, ⁶⁰YPFPGPI⁶⁶, was identified from both variants A1 and A2 after simulated digestion, though with concentration being somewhat higher after digestion of the variant A1, compared with variants A2 and I. The peptides ¹³⁴HLPLP¹³⁸ and ¹³³LHLPLP¹³⁸ were both identified after initial 5 min of duodenal digestion. In conclusion, genetic variation of β-CN may affect proteolysis during digestion; however, the release of β-casomorphin-7 (BCM7) does not seem to be linked solely to variant A1, as earlier suggested by relevant published literature on in vitro digestion.     

Effect of vitamin E supplementation on α-tocopherol and β-carotene concentrations in tissues from pasture- and grain-fed cattle

The effects of dietary vitamin E supplementation of grain-fed cattle on lipid oxidation and meat colour have been extensively investigated, but little attention has been given to pasture-fed cattle where meat is likely to contain naturally high amounts of α-tocopherol and carotenoids. In the work described, we evaluated the effects of pasture-feeding alone and with vitamin E supplementation on tissue levels of anti-oxidants and compared the findings with those obtained for grain-fed cattle with and without supplementation. Sorghum was the major component of the grained-based ration. α-Tocopherol concentrations in plasma, muscle and fat tissues of pasture-fed cattle were not affected by vitamin E supplementation (2500 IU/head/day for 132 days prior to slaughter) while those of grain-fed cattle increased significantly. The α-tocopherol concentrations in the supplemented grain-fed cattle were similar in muscle and liver to pasture-fed animals but were lower in their fat (P<0.05). The major carotenoid present in all tissues studied from pasture-fed was β-carotene and its contents in plasma, liver, fat and muscles were decreased (P<0.05) by supplementation with vitamin E. Carotenoids were essentially absent in grain-fed cattle except for small amounts in liver. The implication of this study for the meat industry is that cattle grazed on good pasture can achieve concentrations of α-tocopherol in muscles and other tissues at least as high as those obtained by supra-nutritional supplementation of grain-fed cattle with vitamin E. However, α-tocopherol supplementation of pasture-fed cattle reduced tissue concentrations of β-carotene, which would reduce carcase fat yellowness and make pasture-fed cattle more acceptable to some Asian markets.     

Water dispersibility of the β-carotene source and its effect on the physical,thermal, and in vitro release properties of an inclusion complex

There is a need to understand the effect of in vitro digestion on the release of β-carotene (BC) from inclusion complexes (IC) prepared with water-dispersible (WDBC) or hexane-soluble (HSBC) sources. IC were prepared by co-precipitating WDBC or HSBC with β-cyclodextrin and characterised using imaging, spectral (FTIR) and thermal techniques. Two solvent systems (absolute ethanol, AE and 4:3 ethanol–hexane, EH) were employed to compare extractability of BC during simulated co-digestion with rice as food matrix. WDBC-IC had greater yield (89% vs. 44%) but lower encapsulation efficiency (30% vs. 89%) than HSBC-IC. Imaging, FTIR and thermal data confirm inclusion complex formation. In vitro WDBC release extracted with AE decreased uniformly and was unaffected by rice, whereas HSBC extracted with EH exhibited gradual release towards intestinal digestion but decreased with rice. Fabricated microcapsules with suitable forms of BC may be applied for food fortification purposes.     

Genetic variants of bovine β- and κ-casein result in different immunoglobulin E-binding epitopes after in vitro gastrointestinal digestion

Immunoglobulin E-mediated allergy to cow milk is a common allergy in industrialized countries, mainly affecting young children and infants. β-Casein (CN) and κ-CN belong to the major allergens in cow milk. Within these milk proteins, genetic polymorphisms occur, which are characterized by substitutions or deletions of AA, resulting in different variants for each protein. Until now, these variants have not been considered when discussing the allergenic potential of bovine milk. In this study, the focus was placed on the arising peptide pattern after in vitro gastrointestinal digestion of several β- and κ-CN variants to determine resistant fragments containing IgE-binding epitopes and to identify potential differences between these variants. β-Casein A¹, A², and B, as well as κ-CN A, B, and E, were separated and isolated from milk of cows homozygous for these variants and digested with an in vitro gastrointestinal digestion model. The resulting peptides were identified using mass spectrometry and compared with previously determined epitopes. Seven β-CN and 4 κ-CN peptides, common in all β- or κ-CN variants, remained of sufficient size to harbor IgE-binding epitopes. In addition, some peptides and, consequently, epitopes differ from each other due to the AA substitution occurring in the individual variants. The distinct peptides AA 108 to 129 of β-CN A¹ and A², AA 103 to 123 of β-CN B, as well as AA 59 to 72, AA 59 to 80, and AA 58 to 80 of all 3 β-CN variants correspond to the IgE-binding epitopes AA 107 to 120 and AA 55 to 70, respectively. In κ-CN, the 2 variant-specific peptides AA 136 to 149 (κ-CN A, E) and AA 134 to 150 (κ-CN B) are congruent with the IgE-binding epitope AA 137 to 148. The present study shows that genetic polymorphisms affected the arising peptide pattern of the caseins and thus modifications in the IgE-binding epitopes occurred. As a consequence, the casein variants could show differences in their allergenicity. Studies investigating the allergenic potential of these different peptides are currently in progress.     

A chemical study of β-carotene oxidation by ozone in an organic model system and the identification of the resulting products

Carotenoids are present in many foods. Due to their polyenic chains, they undergo oxidation reactions which may give several compounds. Ozone, a powerful antimicrobial agent, is applied in the food industry due to its high reactivity and penetrability. This work presents a chemical study of the degradation of β-carotene in solutions, under the influence of ozone. The experiments were carried out at ozone concentrations ranging from 0.8 to 2.5 ppm and the β-carotene solutions were sampled and analysed from zero to seven hours of reaction. The oxidation products were collected in C18 cartridges coated with dinitrophenylhydrazine and the hydrazones formed were analysed by LC-MS. The oxidation reaction was found to follow a zero order kinetic model and the β-carotene decay ranged between 17.2% and 99.8%. Fourteen oxidation products were tentatively identified, amongst them eight which had not been cited yet in the literature as oxidation products of β-carotene.     

A simple UV-Vis spectrophotometric method for determination of β-carotene content in raw carrot, sweet potato and supplemented chicken meat nuggets

A simple, rapid and low cost analytical method for the determination of β-carotene content in four different food categories is developed and validated. This method is based on solvent extraction followed by UV-Vis spectrometric detection. Target compound was extracted with four different solvents, in which acetone appears to be an excellent extractant as recovery of the analyte at 1 μg/g concentration in spiked samples was in the range of 67.8-98.8%, with relative standard deviation (RSD) ranging between 4.8 and 6.6%. Intra- and inter-day assay precisions of the method at 0.1, 1.0 and 5.0 μg/g concentrations ranged in between 3.4 and 8.9%. The linearities for β- carotene in the pure acetone, raw carrot, sweet potato, and fortified raw and cooked chicken meat nuggets were 0.994, 0.995, 0.990, 0.984 and 0.984, respectively. For robustness, the analytical method was applied to 24 samples of four different food categories namely carrot, sweet potato and carrot and sweet potato supplemented chicken meat nuggets.     

Stability of α-tocopherol, γ-tocopherol and β-carotene during ripening of pasta-filata cheese made from raw and pasteurised milk with different vitamin contents

Ripening stability of α-tocopherol, γ-tocopherol and β-carotene in cheese was evaluated in relation to different milk vitamin content and to the use of either pasteurised or raw milk. Milk from two farms with different management systems was used to obtain different vitamin content. Milk was divided into two parts, of which only one was pasteurised. Four blocks of cheese were made from each batch and ripened for 0, 15, 30, or 60 days at 14–16 °C. There was a notable variation in cheese vitamin levels, with the differences in milk vitamin content due to farm management having the highest impact. Pasteurisation had no effect on cheese vitamin content. Cheese γ-tocopherol and β-carotene content decreased after 30 and 60 days, respectively, whereas α-tocopherol content remained stable. γ-Tocopherol appeared to be the most efficient antioxidant in cheese, followed by β-carotene. Vitamin stability was not influenced by milk vitamin content or pasteurisation.     

Purification of β-carotene 15,15′-monooxygenase from pig intestine and its enzymatic hydrolysis of pigment in soybean oil

β-Carotene 15,15′-monooxygenase was isolated and purified from the intestinal mucosa of pigs, and then, it was applied to hydrolyse the pigment in soybean oil, and thus, vitamin A fortified soybean oil was obtained. The pig intestinal mucosal protein solution was purified to a specific activity of 2.487 × 10⁻⁴ U mg⁻¹, maximum reaction velocity (V_max) of 8.42 × 10⁻⁹ mol/h and Michaelis constant (K_m) of 2.03 × 10⁻⁵ m . The protein solution had a molecular mass of 156 kDa by gel filtration. The sodium deoxycholate concentrations, optimum pH, Tween 40 amount and enzyme amount for vitamin A production in soybean oil were determined to be 6.0 mm , 8.0, 3.0% (w/v) and 0.2 U/mL enzyme, respectively. Under these conditions, β-carotene 15,15′-monooxygenase produced 14.65 mg/L vitamin A after 20 h, with a conversion yield of β-carotene of 33.29% (w/w). Therefore, the nutrients in soybean oil were improved.     

Relationship between the kinetics of β-carotene degradation and formation of norisoprenoids in the storage of dried sweet potato chips

The effects of storage temperature (10; 20; 30; 40 °C), water activity (0.13; 0.30; 0.51; 0.76) and oxygen level (0%; 2.5%; 10%; 21%) on the degradation of carotenoids and formation of volatile compounds during storage of dried sweet potato chips were evaluated. A kinetic model was developed for degradation of trans-β-carotene and it showed that breakdown followed first order kinetics with an activation energy of 64.2 kJ mol⁻¹. The difference between experimental data under laboratory or field conditions fitted and data predicted by the model was less than 10% for trans-β-carotene, or for total carotenoids. The formation of the volatile compounds, β-ionone; 5,6-epoxy-β-ionone; dihydroactinidiolide; β-cyclocitral, was measured by SPME-GC-MS and was clearly related to the degradation of trans-β-carotene. It is also suggested that carotenoid degradation in dried sweet potato was by autoxidation because of the trend in β-carotene degradation rate in relation to water activity or oxygen level.