Efficacy of extract and essential oil of Lantana indica Roxb. against food contaminating moulds and aflatoxin B1 production

The study investigates the antifungal and antiaflatoxigenic efficacy of Lantana indica against Aspergillus flavus , a key storage fungus. The leaf essential oil of L. indica was found more active than leaf extracts. The oil absolutely inhibited the growth of A. flavus at 1.5 mg mL⁻¹ while ethanolic and chloroform extracts of leaf show MIC at 7.5 and 10.0 mg mL⁻¹ concentrations respectively. The oil also showed pronounced antiaflatoxigenic efficacy and completely inhibited the aflatoxin B₁ production at 0.75 mg mL⁻¹. The ethanolic and chloroformic extracts inhibited the aflatoxin B₁ production at 5.0 and 7.5 mg mL⁻¹, respectively while other extracts exhibited poor efficacy. The L. indica essential oil exhibited broad fungitoxic spectrum against twelve different storage moulds. The present findings may recommend the L. indica essential oil and its bioactive leaf extracts as natural preservative would of immense significance in view of the environmental and toxicological implications by indiscriminate use of synthetic pesticides .     

Optimising the free radical scavenging activity of shrimp protein hydrolysate produced with alcalase using response surface methodology

Response surface methodology (RSM) was used to optimise the hydrolysis parameters of Acetes chinensis by Alcalase 2.4L in order to obtain a hydrolysate with potent radical scavenging activity. The parameters were temperature, pH and enzyme concentration/substrate concentration (E/S) ratio with degree of hydrolysis (DH) being the response. The results showed that the optimum condition was: temperature at 57 °C, pH at 8.0, E/S ratio at 2.6AU 100 g⁻¹ shrimp, hydrolysis time 3 h. The DH was 26.32%, the hydroxyl radical scavenging activity was up to 88.12% and the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity was 35.61%. The gel column filtration chromatography by a Sephadex G-25 column yielded five fractions. The molecular weight of the most potent free radical scavenging activity fraction ranged from 915 to 207 Da, its IC₅₀ for hydroxyl radical was 0.03 mg mL⁻¹, and IC₅₀ for DPPH radical was 8.86 mg mL⁻¹.     

Antioxidant and toxicity tests of roasted noni (Morinda citrifolia) leaf infusion

The antioxidant properties and toxicity profile of roasted noni ( Morinda citrifolia L . ) leaf infusion were evaluated. The 2,2-diphenylpicrylhydrazyl (DPPH) radical scavenging activity was greater than green tea infusion (81.6 ± 0.9% vs. 57.5 ± 1.8%, P  < 0.001). The mean quercetin and kaempferol contents of roasted noni leaf infusion, as prepared by the consumer, were 0.24 ± 0.01 and 0.14 ± 0.01 μg mL⁻¹, respectively. Tannic acid content was 10 ± 1 μg mL⁻¹. The infusion was non-mutagenic in the reverse mutation test in Salmonella typhimurium and did not induce primary DNA damage in E. coli PQ37. Further, no significant primary DNA damage was induced by 5,15-dimethylmorindol, which was the only detectable anthraquinone in noni leaves. The infusion was not cytotoxic in the 24 h brine shrimp toxicity test (LC₅₀ > 1 mg mL⁻¹), nor was there any evidence of acute oral toxicity from the freeze–dried infusion in Sprague–Dawley rats (LD₅₀ > 2000 mg kg⁻¹ b.w.).     

Biochemical changes in cut vs. intact lamb's lettuce (Valerianella olitoria) leaves during storage

Consumers are oriented towards fresh-cut vegetables that provide phytonutrients useful for preventing stress-related diseases. The aim of this work was to evaluate the cut operations on the quality changes of lamb's lettuce ( Valerianella olitoria L.) cv. Trofy during storage at 4 °C for 8 days. Results showed that chlorophyll and carotenoids reduction was observed after 8 days of storage. In both treatments, total carotenoids after 8 days decreased from 20 to 16 mg g⁻¹ FW. Free and total phenols increased with storage in both treatments. Total phenols were 23% higher in control (32 μmol g⁻¹ FW) compared to cut leaves (25 μmol g⁻¹ FW) after 8 days of storage. Anthocyanins increased after 8 days and reached 30 mg 100 g⁻¹ FW without significant difference between treatments. Ascorbic acid (AsA) and dehydroascorbic (DHA) acid increased in cut leaves compared to control. After 1 day AsA concentration was 3 300 nmol g⁻¹ FW in cut leaves, while in control leaves was 1 500 nmol g⁻¹ FW. Analogously AsA + DHA was higher in cut leaves, 4 100 nmol g⁻¹ FW, while in control leaves the mean was 3 000 nmol g⁻¹ FW. After 5 days of storage the values of AsA returned to initial values, while AsA + DHA were lower.     

Effects of high pressure treatment on the quality and storage of kimchi

The effects of high pressure treatment on the microflora and storage of kimchi were investigated. In a bacterial suspension, numbers of Lactobacillus plantarum were reduced by 6 logs by 500 MPa, at 25 °C for 10 min. Kimchi juice did not alter the rate of inactivation of lactic acid bacteria by high pressure treatment. There was no change in the texture of kimchi subjected to a pressure of 400 MPa, but an increase in cutting force was observed at 600 MPa. When kimchi was pressurized at 400 MPa for 10 min at 25 °C and subsequently stored at 20 °C for 4 weeks, the total number of viable cells stayed at 10³ CFU mL⁻¹. High pressure treatment above 400 MPa prevented excessive acidification that typically occurs during the extended storage of kimchi. The inflation of pouches as a result of accumulated carbon dioxide was also prevented by high pressure treatment. Although colour changes were accelerated by high pressure treatment, this study demonstrates that high pressure treatment can be used to control overripening during the distribution and storage of kimchi products.     

Sensory Acceptability and Stability of Probiotic Microorganisms and Vitamin C in Fermented Acerola (Malpighia emarginata DC.) Ice Cream

ABSTRACT:  Six fermented acerola ice creams were produced, containing different starter cultures ( Bifidobacterium longum , Bi.lactis , and traditional yogurt starter culture— Streptococcus thermophilus and Lactobacillus delbrueckii spp. bulgaricus ) and final pH (5 and 4.5). The ice creams were evaluated for probiotic culture viability, vitamin C stability, and sensory acceptance. Mix fermentations were stopped when pH 5.0 and 5.5 were attained. However, after the addition of acerola pulp the determined pH were 4.5 and 5, respectively. Mixes were frozen and stored for 15 wk at −18 °C. The viable counts for probiotic cultures remained above the recommended minimum limit of 10⁶ cfu/g during 15 wk storage even in products with pH 4.5. Vitamin C concentration remained around 140 mg/100 g of product. The attributes of aroma, taste, texture, and overall acceptance obtained scores in the range of 5.15 to 7.22. The fermented acerola ice cream was a suitable food for the delivery of vitamin C and Bifidobacterium strains with excellent viability and acceptable sensory characteristics.     

A modified colorimetric method for the estimation of β-cyclodextrin using phenolphthalein

The binding equilibrium between β-cyclodextrin and phenolphthalein has been used to develop a method for the estimation of β-cyclodextrin in solution. From logarithmic plots of amounts of β-cyclodextrin against absorbance at 554 nm, a relation log X  = (log A  − log Y )/ B was found, which gave an estimate of β-cyclodextrin in the concentration range 0.0045 mg mL⁻¹ (3.96 μm) to 4.7 mg mL⁻¹ (4.14 mm), where X =  intercept and B  = slope. This method was found to be highly reproducible and reliable.     

Oxidative stability of brined anchovies (Engraulis encrasicholus) with plant extracts

The effect of brining with plant extracts on the oxidative stability of anchovies was investigated during storage. The brining process was done in 15 g 100 mL⁻¹ of sodium chloride solution with water, and with myrtle, rosemary and nettle extracts. Brined anchovies were stored at 4 ± 1  ° C for 28 days. Brining with plant extracts slowed down the lipid oxidation of anchovies. The highest antioxidant effect was observed in brined anchovies with rosemary and myrtle extracts during storage as indicated by peroxide value (POV), thiobarbituric acid reactive substance and oxidative rancidity (OR) scores. Furthermore, OR scores in brined anchovies were well correlated with thiobarbituric acid reactive substance ( r ² = 0.66, P  < 0.01) and POV ( r ² = 0.87; P  < 0.01). The fatty acid profiles were similar among the brined anchovies with plant extracts. These results suggest that brining with rosemary, myrtle and to a lesser extent, nettle extracts prevents development of oxidation in lipids of anchovies during storage.     

The effect of storage at tropical ambient temperature on the quality and shelf life of grouper (Plectropomus maculatus)

Groupers ( Plectropomus maculatus ) were harvested from holding tanks and stored in ice until assessment rated them unacceptable. Groupers were also subjected to periods (2–12 h) of storage at tropical ambient (29–31 °C) immediately after harvest but prior to cooling in ice. The storage life of grouper stored continuously in ice was 18 days. A 2-h delay before cooling in ice approximately halves the storage life and for every further hour of malstorage the shelf-life was further reduced by approximately 1 day. The total volatile basic nitrogen (TVBN) and hypoxanthine contents were found to be good indicators of freshness in groupers, which were only acceptable with contents <31 mg N 100 per g and <2.0 μmoles g^–1, respectively and all unacceptable at >37 mg N 100 per g and 2.3 μmoles g^–1 respectively. TMA-N was found not be a reliable indicator of freshness.     

Probiotic potential and sensory properties of coconut flan supplemented with Lactobacillus paracasei and Bifidobacterium lactis

The effect of probiotic cultures on sensory performance of coconut flan during storage at 5 °C and the viability of these micro organisms for up to 28 days were investigated. Sensory analyses of the product were performed after 7, 14 and 21 days of storage. Coconut flans were produced with no addition of cultures (T1, control), or supplemented with Bifidobacterium lactis (T2), Lactobacillus paracasei (T3) and B. lactis  +  L. paracasei (T4). Populations of L. paracasei and B. lactis as single or in co-culture remained above 7 log CFU g⁻¹ during the entire storage period. Viability of L. paracasei was higher for T3. All products were well accepted and no significant differences ( P  > 0.05) were detected between the coconut flans studied. The addition of L. paracasei and B. lactis to coconut flan resulted in its having great potential as a functional food, which has high sensory acceptability.     

Radical scavenging and antimicrobial activity of horsetail (Equisetum arvense L.) extracts

A reversed-phase high performance liquid chromatography (RP-HPLC) separation on C₈ column and quantitative method were developed to analyse hydroxyl derivatives of benzoic and cinnamic acid and flavonoids in horsetail ( Equisetum arvense L.) extracts. Total phenolic content of n -butanol, ethyl acetate and water extracts, determined by the Folin-Ciocalteu method, was 96.4, 26.4 and 15.4 mg g⁻¹ of dry extracts, respectively. The antioxidative activity of horsetail extracts was tested by measuring their ability to scavenge stable 2,2-diphenyl-1-picrylhydrazyl (DPPH) and reactive hydroxyl radicals by electron spin resonance spectroscopy. The results demonstrated that the free radical scavenging activity (versus both DPPH and hydroxyl radicals) depended on the type and concentration of applied extracts; the highest DPPH (EC₅₀ = 0.65 mg mL⁻¹) and hydroxyl radical scavenging activities (EC₅₀ = 0.74 mg mL⁻¹) were obtained in the case of n -butanol extract. The radical scavenging activity of extracts significantly correlated with total phenolic content. The antimicrobial tests showed that ethyl acetate and n -butanol extracts inhibited the growth of tested bacteria.     

Comparison of high pressure treatment and thermal pasteurization effects on the quality and shelf life of guava puree

The effects of high pressures and thermal pasteurization on the survival of microorganisms, enzyme inactivation and quality changes of guava puree during storage at 4°C were investigated and compared with untreated samples. After treatment at a pressure of 600MPa and 25°C for 15 min, the microorganisms in guava puree were inactivated to less than 10 cfu mL⁻¹ and the product exhibited no change in colour, pectin, cloud and ascorbic acid content as compared with fresh samples. The inactivation of enzymes in guava puree by thermal pasteurization was greater than by high pressures. The microbial count in guava puree reduced to 200 cfu mL⁻¹ and the product showed marked changes in viscosity, turbidity and colour when heated at 88–90°C for 24s. The content of pectin, cloud and ascorbic acid as well as colour in untreated and high pressurized (400MPa) guava puree gradually decreased, whereas these changes were not observed in pasteurized (88–90°C) and high pressurized (6000MPa) puree during storage at 4°C for 60 days. The guava puree treated at 600MPa and 25°C for 15 min retained good quality similar to the freshly extracted puree after storage at 4°C for 40 days.     

Composition, sensory quality and respiration during ripening and storage of edible wild mango (Irvingia gabonensis)

The effects of tree and room ripening and of storage at chill temperatures and at 26–29°C on the sensory quality, composition and respiration of edible wild mango fruits were investigated.
Fruits harvested at the mature green stage and ripened at 26–29°C were slightly preferred to tree-ripened fruits in colour and texture. Apart from a lower moisture content, room-ripened fruits were comparable in composition with tree-ripened fruits. During storage at 26–29°C, CO₂ production increased sharply from 22 ml kg^-1 h^-1 at the end of the first day, reaching a maximum of 91 ml kg^-1 on day 5 and declining thereafter; O₂ consumption followed a similar trend. The respiratory climacteric coincided with the onset of ripening. Fruits held at 12–15°C developed symptoms of chilling injury including pitting and black spots in mature green fruits, and brownish discoloration, pitting, surface scald, excessive softening and decay in ripe fruits.     

The effects of ice storage on inosine monophosphate, inosine, hypoxanthine, and biogenic amine formation in European catfish (Silurus glanis) fillets

European catfish fillets in ice were evaluated by measuring nucleotide components and biogenic amine contents and these then compared with sensory and microbiological assessment during the 21 days of iced storage. Analyses were carried out using two different rapid HPLC methods for nucleotid degradation products and biogenic amine contents in European catfish fillets. Sensory evaluation showed that storage life of European catfish found to be 14–18 days. Initial inosine monophosphate (IMP) level was 12.6 μmol g^­1 and then decreased during the rest of storage period. Inosine (INO) level increased rapidly until 7 days of storage. Hypoxanthine (Hx) level increased almost linearly with storage time. The most accumulated biogenic amines were putrescine, cadaverine, spermidine, spermine, and serotonin in all the European catfish fillets during the storage, although the formation of biogenic amines levels was fluctuated. Histamine was only detectable at 4 and 7 days of storage as low as 1 mg 100 g^­1 fish. Total viable count in European catfish increased rapidly with storage time and reached ≤10⁹ cfu g^­1 when the fillets were not acceptable for consumption.     

Natural preservative ingredient from marine alga Ulva lactuca L.

The contents of total chlorophyll (T-Chl), carotenoids and phenolics compounds were quantified in the biomasses of Ulva lactuca grown either in normal or artificial sea water under indoor conditions. The antioxidant and antibacterial activities of U. lactuca crude organic extracts ( Ulva- COEs) were determined. Thirty-four compounds in Ulva- COEs were characterised by thin layer chromatography and high-performance liquid chromatography. The major compounds were chlorophyll a (Chl a ) (15.60–30.90%) and b (Chl b ) (12.20–14.89%) , 9-cis β-carotene (13.12–14.47%), α-carotene (11.44–11.47%) and all-trans β-carotene (6.16–29.70%, of total carotenoids).The Ulva- COEs exhibited remarkable antioxidant activity, with an IC₅₀ (concentration which causes a 50% of DPPH radical scavenging activity) values ranged from 16.5 and 18.7 μg mL⁻¹, which could be compared with the synthetic antioxidants: α-tocopherol (14.4 μg mL⁻¹), butylated hydroxyanisol (13.1 μg mL⁻¹) and butylated hydroxyltoluene (13.1 μg mL⁻¹). Also, Ulva- COEs exhibited great potential antibacterial activities against six bacterial strains, with minimal inhibitory concentration values ranged from 0.40 to 0.35 mg mL⁻¹.     

Rapid and sensitive determination of formaldehyde in some beverages and foods by flow-injection fluorimetric analysis

A simple and sensitive flow-injection (FI) method for rapid determination of formaldehyde in beverage and food products has been developed. Adopting stop-flow technique, the proposed method distinctly improved the sensitivity of FI fluorimetric method for the determination of formaldehyde based on Hantzsch reaction with cyclohexane-1,3-dione. The fluorescent intensity was proportional to formaldehyde concentrations ranging 0.1 ng mL⁻¹ to 1.000 μg mL⁻¹, and the detection limit ( S / N  = 3) was 0.04 ng mL⁻¹ of formaldehyde. The relative standard deviations ( n  = 11) for determination of 0.100 and 0.005 μg mL⁻¹ of formaldehyde were 1.3% and 2.1%, respectively. The analytical frequency was 18 samples per hour. This method was applied directly for the determination of formaldehyde in diluted beverages and extraction solutions of foods, and the results obtained correlated well with those obtained by the standard method in which a sample pretreatment of steam distillation was required.     

Microbial growth and colour of minimally processed shiitake mushroom stored at different temperatures

The effect of storage temperature on the microbiological and sensory characteristics of minimally processed shiitake was investigated. Shiitake mushrooms were washed, sanitised, packed in polystyrene trays, overwrapped with plastic film and stored at 7, 10 or 15 °C. Microbial counts, polyphenoloxidase activity, external lightness ( L* ) and acceptance tests were conducted. Mesophilic, aerobic psychrotrophic bacteria, yeasts and moulds predominated during storage. Pseudomonas was detected after 10 days' storage showing an increase of, approximately, 7 log cycles at 15 °C. Mushroom rejection occurred when the microbial population was lower than 10⁶ CFU g⁻¹, suggesting that, other factors, such as browning, affect mushroom spoilage more than microbial activity. Mushrooms treated with citric or ascorbic acids maintained high L * value during 10 days. The shelf life of minimally processed shiitake mushrooms was 10 days at 7 °C, but less than 5 days at 10 °C, and approximately 3 days at 15 °C.     

Oat-based Symbiotic Beverage Fermented by Lactobacillus plantarum, Lactobacillus paracasei ssp. casei, and Lactobacillus acidophilus

ABSTRACT: Oats and probiotics have long been recognized for their health benefits. The objectives of this study were (1) to study the ability of Lactobacillus plantarum (B-28), Lactobacillus paracasei ssp. casei (B-29) isolated from a traditional Bulgarian cereal-based fermented beverage, and Lactobacillus acidophilus from Chr. Hansen, Milwaukee, Wis., U.S.A., to remove cholesterol from the media and to adhere to the Caco-2 cell line, (2) to optimize the fermentation conditions to develop a beverage using these probiotics and oats with acceptable sensory and nutritional qualities, and (3) to assess the quality and shelf-life of this beverage and survivability of probiotics in the beverage. Lactobacillus acidophilus , B-28, and B-29 were found to remove 70.67%± 2.35%, 20.26%± 2.63%, and 16.75%± 3.83% of cholesterol from media and the percentage of adhesion was 4.69%± 0.78%, 1.92%± 0.78%, and 8.36%± 0.78%, respectively. The blend of oat flour, sugar, inulin, and whey protein concentrate was cooked in water and fermented for 12 h at 37°C by 2 ± 10⁶ colony-forming units (CFU) /mL each of B-28 and B-29 and 2 ± 10⁸ CFU/mL of L. acidophilus . The beverage had 0.87%± 0.03% of dietary fiber and had better sensory qualities compared with the commercially available similar product. The probiotics survived for 10 wk of storage at 4°C, except for L. acidophilus , which survived for about 4 wk. The population of B-28 was 1.77 ± 10⁶ to 1.29 ± 10⁷ CFU/mL and that of B-29 was 7.39 ± 10⁷ to 4.49 ± 10⁸ CFU/mL throughout the storage period. The oat-based symbiotic beverage is a functional drink providing both probiotics and prebiotics at the same time.     

Storage characteristics of sous vide cooked roast beef

The technological, microbiological, and sensory storage characteristics of low temperature sous vide cooked roast beef were investigated. the effect of two heat treatments, 59°C (P₇₀¹⁰in core 8.4) and 62°C (P₇₀¹⁰ in core 15.9) on the stability of spiced roast beef made from Musculus semitendinosus with a high initial microbial load were compared as well as storage temperatures of 2 and 10°C. Although chilling baths with circulating water were used, recommended chilling rates for sous vide products could not be attained. Yield was significantly higher at 59°C and at a storage temperature of 2°C but decreased during storage. At 62°C the meat became significantly more tender than at 59°C as measured by shear force. No differences in microbiology were observed between heating regimes. At low storage temperature products were microbiologically stable over a 35-day period. At 10°C, however, a rise in psychrotrophic aerobic counts and occasional pack swelling was observed. In a commercial scale experiment conducted with sous vide cooked (62°C) beef with low initial counts, no increase in aerobic counts was observed at 2, 5 and 10°C while swelling occurred in 28% of the packages stored at 10°C and in none at 2 and 5°C. the swelling was due to different types of gas-producing clostridia. Warmed-over flavour (as TBARS) showed no development during storage in intact packages, while slicing and serving the roast beef under commercial conditions resulted in a marked increase to < 100 μmole kg⁻¹. In spiced roast beef only minor changes in off-odour and off-flavour of the product were observed during 23 days of storage at 2°C.