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1.
This study evaluated whether treating inoculated peach slices with metabisulfite or acidic solutions enhanced inactivation of Listeria monocytogenes during dehydration and storage. Inoculated (five strain mixture of L. monocytogenes, 7.9 log cfu/g) peach slices were treated, dried for 6 h at 60°C and stored aerobically at 25°C for 14 d. Predrying treatments of inoculated peach slices included: (1) no treatment (control); or 10 min immersion in: (2) sterile water, (3) 4.18% sodium metabisulfite, (4) 3.40% ascorbic acid, or (5) 0.21% citric acid solutions. Samples were plated on tryptic soy agar with 0.1% pyruvate (TSAP) and PALCAM agar for enumeration of surviving bacteria. Immersion in sterile water reduced bacterial populations on peach slices by 0.7 log cfu/g (TSAP and PALCAM). Immersion in the sodium metabisulfite solution reduced populations by 1.5–2.0 log cfu/g, while acidic pretreatments reduced populations by 0.5–0.8 log cfu/g. After 6 h of dehydration, populations on control or water immersed slices were reduced by 3.2–3.4 log cfu/g, whereas populations on slices treated with sodium metabisulfite or acidic solutions were reduced by 4.3–5.1 log cfu/g (TSAP) and 5.3–6.2 log cfu/g (PALCAM), respectively. Bacteria were detectable by direct plating at 14 d of storage, except on acid treated slices. Immersion in acidic or metabisulfite solutions, before dehydration, should enhance inactivation of L. monocytogenes contamination on peach slices during dehydration and storage. 相似文献
2.
Derrickson-Tharrington E Kendall PA Sofos JN 《International journal of food microbiology》2005,99(1):79-89
Inactivation of Escherichia coli O157:H7 was evaluated on inoculated apple slices without pretreatment or pretreated by immersing in water or acid solutions commonly used to help retain apple color during dehydration, then stored at ambient temperature or dried for 6 h. Half-ring slices (0.6 cm thick) of peeled and cored Gala apples were inoculated by immersion for 30 min in a three-strain composite inoculum of E. coli O157:H7 (7.8-8.0 CFU/g). Inoculated slices received (1) no pre-drying treatment (control); or a 10-min immersion in solutions of (2) sterile water, (3) 2.8% ascorbic acid, (4) 1.7% citric acid, (5) 50% commercial lemon juice, or (6) 50% commercial lemon juice with preservatives. Drained slices were placed in sterile plastic bags and stored at room temperature (25+/-2 degrees C) for up to 6 h or dehydrated (62.8 degrees C) for up to 6 h. Samples were plated on tryptic soy agar (TSA) and sorbitol MacConkey agar (SMAC) for direct enumeration of surviving bacteria at various time intervals. Immersion in sterile water or acidic solutions caused initial bacterial reductions of 0.9-1.3 log CFU/g on apple slices. Between 0 and 6 h of storage at room temperature, slices dipped in acidic solutions showed minor changes in bacterial populations (-0.2 to +0.6 log CFU/g) compared to a 1.1 log CFU/g increase for slices dipped in sterile water. The no treatment samples (control) showed an increase in bacterial populations of 1.3-1.5 CFU/g over the 6-h holding time. For apple slices dried at 62.8 degrees C, bacterial populations were reduced by 2.5 (SMAC) and 3.1 (TSA) log CFU/g in the control (no pre-drying treatment) samples following 6 h dehydration. The slices immersed in sterile water showed a 5.8 (SMAC) and 5.1 (TSA) reduction after 6 h of dehydration. In contrast, after 6 h of dehydration bacterial populations on the four acid-pretreated products were reduced by 6.7-7.3 log CFU/g. The results showed that acidic treatment alone was not effective in destroying E. coli O157:H7 on apple slices but did inhibit growth of the organism during holding before drying. However, pretreatment of the apple slices with common household acidulants enhanced destruction of E. coli O157:H7 during drying compared to slices dried without treatment. 相似文献
3.
The process of drying apple tissue under most conditions may be divided into two main periods viz primary and secondary falling-rate periods. For most drying conditions the secondary falling-rate period is longer and has the greater influence on the overall rate. When the drying capacity of the air is very low an initial constant-rate period may occur. The drying rate constant varies with temperature with an Arrhenius-type relationship and the available evidence suggests that temperature-induced changes in the rate may be caused by vapor pressure changes Air velocity and relative humidity have their greatest influence in the early part of the drying process Towards the end of drying, internal resistance to water movement becomes rate-controlling, and external factors have little influence. An explanation of the observed drying characteristics of apple tissue in terms of the diffusion of water vapour through a ‘skin’ of dried cells is suggested. 相似文献
4.
Mustafa Özilgen Gülbanu Güvenç Mehmet Makaraci Itila Tümer 《Zeitschrift für Lebensmitteluntersuchung und -Forschung A》1995,201(1):40-45
Drying of apple slices was studied in a conventional tray drier (initial slice thickness=0.3–1.0 cm, drier temperature=60–100 °C) and in a computer-controlled tunnel drier (initial slice thickness=0.8 cm, air tempera ture=50–100 °C, air flow rate=2.4 m/s). In most of the experiments the drying behaviour was characterized by a constant rate period, followed by a falling rate period. The constant rate drying period did not occur, and the colour of the dried slices was improved substantially with tunnel drying under computer control, when a linearly decreasing temperature profile from 100 °C to 70 °C was used. The quality improvement may be attributed partly ot the elimination of the continuous water film covering the surface in the constant rate drying period, which may serve as a medium for the reaction and transport of the chemical species.
Farbveränderungen und Gewichtsverluste von Apfelstücken während des Trocknens
Zusammenfassung Apfelscheiben (0,3–1,0 cm) wurden in einem konventionellen Hordentrockner (60 bis 100 °C) und einem rechnerkontrollierten Tunneltrockner (Scheiben 0,8 cm, Lufttemperatur 50 bis 100 °C, Luftfluß 2,4 m · s–1) getrocknet. Bei den meisten Experimenten wurde eine zweiphasige Trocknung beobachtet. Eine regelmäßige Trocknung fand dagegen bei einem gesteuerten, linearen Temperaturgradienten von 100 zu 70 °C statt. Dies verbesserte die Qualität der Produkte, offensichtlich wegen des Vermeidens einer Wasserfilm-Bildung auf den Oberflächen der Apfelstücke während des Trocknens. Ein derartiger Film kann ein Medium für Reaktionen und den Transport von Reaktanden Scin.相似文献
5.
Documented outbreaks of human illness associated with consumption of minimally processed produce have increased in recent years. This study evaluated the influence of modified treatments on inactivation of Salmonella during preparation, home-type dehydration (60 degrees C, 6h) and storage of carrot slices. Inoculated (five strains, 7.8 log cfu/g) slices were subjected to the following treatments: (i) untreated control, (ii) steam blanching (88 degrees C, 10 min), (iii) water blanching (88 degrees C, 4 min), (iv) blanching in a 0.105% citric acid solution (88 degrees C, 4 min), or (v) blanching in a 0.21% citric acid solution (88 degrees C, 4 min), dried for 6h at 60 degrees C (140 degrees F), and stored for up to 30 d. Bacterial populations were reduced by 3.8-4.1, 4.6-5.1 and 4.2-4.6 log cfu/g immediately following steam, water or citric acid blanching, respectively. After 6h of dehydration, total reductions were 1.6-1.7 (control), 4.0-5.0 (steam blanched), 4.1-4.6 (water blanched) and 4.9-5.4 (blanched in citric acid solution) log cfu/g. Populations continued to decrease throughout storage, but were still detectable by direct plating at 30 d on all samples except for those blanched in 0.21% citric acid. Results suggest that blanching carrot slices, particularly blanching in 0.21% citric acid, before drying should enhance inactivation of Salmonella during home-type dehydration and storage. 相似文献
6.
Calicioglu M Sofos JN Samelis J Kendall PA Smith GC 《International journal of food microbiology》2003,89(1):51-65
This study evaluated the influence of pre-drying marinade treatments on inactivation of acid-adapted or nonadapted Salmonella on beef jerky during preparation, drying and storage. The inoculated (five-strain composite, 6.0 log CFU/cm2) slices were subjected to the following marinades (24 h, 4 degrees C) prior to drying at 60 degrees C for 10 h and aerobic storage at 25 degrees C for 60 days: (1) no marinade, control (C), (2) traditional marinade (TM), (3) double amount of TM modified with added 1.2% sodium lactate, 9% acetic acid, and 68% soy sauce with 5% ethanol (MM), (4) dipping into 5% acetic acid and then TM (AATM), and (5) dipping into 1% Tween 20 and then into 5% acetic acid, followed by TM (TWTM). Bacterial survivors were determined on tryptic soy agar with 0.1% pyruvate and xylose-lysine-tergitol 4 (XLT4) agar. Results indicated that drying reduced bacterial populations in the order of pre-drying treatments TWTM (4.8-6.0 log CFU/cm2)> or =AATM> or =MM>TM> or =C (2.6-5.0 log CFU/cm2). Nonadapted Salmonella were significantly (P<0.05) more resistant to inactivation during drying than acid-adapted Salmonella in all treatments. Bacterial populations decreased below the detection limit (-0.4 log CFU/cm2) as early as 7 h during drying or remained detectable even after 60 days of storage, depending on acid adaptation, pre-drying treatment, and agar media. The results indicated that acid adaptation may not cause increased resistance of Salmonella to the microbial hurdles involved in jerky processing and that use of modified marinades in manufacturing jerky may improve the effectiveness of drying in inactivating Salmonella. 相似文献
7.
The objective of this study was to evaluate the influence of predrying treatments, i.e., peeling, blanching prior to inoculation, and dipping in organic acid solutions, on inactivation of Salmonella during drying (60 degrees C for 14 h) and aerobic storage (25 degrees C for 28 days) of inoculated (five-strain composite, 7.1 to 7.4 log CFU/g) Roma tomato halves. Four predrying treatments groups were established. One group received no treatment (C). In the other three groups, unpeeled-unblanched, unpeeled-blanched (steam blanched at 88 degrees C for 3 min), peeled-unblanched, and peeled-blanched tomato halves were immersed for 10 min in water (W), ascorbic acid solution (AA; 3.40%, pH 2.48), or citric acid solution (CA; 0.21%, pH 2.51). Appropriate dilutions of homogenized tomato samples were spread plated on tryptic soy agar with 0.1% pyruvate and XLT4 agar for bacterial enumeration during drying and storage. Ten minutes of immersion in W, AA, or CA reduced bacterial populations by 0.7 to 1.6 log CFU/g. After 14 h of dehydration, total log reductions in the populations of bacteria were 3.2 to 4.5 (C), 3.7 to 4.9 (W), > 5.6 to > 6.1 (AA), and 4.5 to 5.5 (CA) log CFU/g, depending on type of agar used and condition of tomato samples. During drying and storage, the order of pathogen inactivation for predrying dipping treatments was AA > CA > W > C, with AA and CA rendering bacterial populations below detectable levels ( < 1.3 log CFU/g) prior to storage and between 7 and 14 days of storage, respectively. The results also indicated that peeling and blanching of tomatoes prior to inoculation may not necessarily affect destruction of Salmonella during the drying process. Use of predrying acid dipping treatments of tomatoes, especially in AA, may improve destruction of Salmonella during the dehydration process. 相似文献
8.
Microwave vacuum drying (MVD) was investigated for apple slices enriched with quercetin derivatives by vacuum impregnation (VI). Additional freeze drying (FD) and air drying (AD) were conducted. Compared to native apples, the impregnated tissue resulted in higher moisture content, elevation of weight and significant browning, due to the incorporated VI solution. The total quercetin content and quercetin glycoside composition were not affected by MVD and FD. The vacuum conditions protect the polyphenols from oxygen dependent degradation and browning reactions. AD resulted in an average quercetin glycoside loss of 44% and undesirable changes, particularly discoloration. The degradation is caused by both non-enzymatic and enzymatic reactions. The pulsed microwave energy intake improved the drying result in structure and led to a faster drying process of 130 min. The bulk density of MVD apple chips (0.69 g/ml) ranged between 0.33 g/ml for FD and 0.75 g/ml for AD. The final moisture content was the lowest after FD (6.8 g/100 g), followed by 9.0 g/100 g after MVD and 12.7 g/100 g after AD. The shelf life was significantly influenced by storage temperature and time. After 12 month at 20 °C, the total quercetin content decreased by 21%. 相似文献
9.
Shrinkage, vitamin C degradation and aroma losses during infra-red drying of apple slices 总被引:1,自引:0,他引:1
The goal of this study was to determine the effect of drying temperature on the shrinkage, ascorbic acid (vitamin C) degradation and aroma retention of apples. Apple samples were found to shrink continuously until a water content value of 2 kg/kg d.b. The degradation of ascorbic acid followed a pseudo-first-order reaction and the degradation rate constant increased when temperature increased from 40 to 70 °C. The loss of aroma volatiles increased with temperature and drying time. 相似文献
10.
Calicioglu M Sofos JN Samelis J Kendall PA Smith GC 《Journal of food protection》2002,65(9):1394-1405
The inactivation of both acid-adapted and unadapted Escherichia coli O157:H7 during the processing of beef jerky was studied. Following inoculation with the pathogen, beef slices were subjected to different predrying marinade treatments, dried at 60 degrees C for 10 h, and stored at 25 degrees C for 60 d. The predrying treatments evaluated were as follows: (i) no treatment (C), (ii) traditional marinade (TM), (iii) double-strength TM modified with added 1.2% sodium lactate, 9% acetic acid, and 68% soy sauce with 5% ethanol (MM), (iv) dipping into 5% acetic acid for 10 min followed by application of TM (AATM), and (v) dipping into 1% Tween 20 for 15 min and then into 5% acetic acid for 10 min followed by TM (TWTM). Bacterial survivors were determined during drying and storage using tryptic soy agar with 0.1% pyruvate, modified eosin methylene blue agar, and sorbitol MacConkey agar. Results indicated that bacterial populations decreased during drying in the order of TWTM (4.9 to 6.7 log) > AATM > MM > C > or = TM (2.8 to 4.9 log) predrying treatments. Populations of acid-adapted E. coli O157:H7 decreased faster (P < 0.05) in AATM and TWTM than nonadapted cells during drying, whereas no significant difference was found in inactivation of acid-adapted and nonadapted inocula in C and TM samples. MM was more effective in inactivating the nonadapted than the adapted inoculum. Bacterial populations continued to decline during storage and dropped below the detection limit (-0.4 log10 CFU/cm2) as early as day 0 (after drying) or as late as day 60, depending on acid adaptation, predrying treatment, and agar medium. The results indicated that acid adaptation may not increase resistance to the hurdles involved in jerky processing and that use of additional antimicrobial chemicals or preservatives in jerky marination may improve the effectiveness of drying in inactivating E. coli O157:H7. 相似文献
11.
苹果片微波间歇干燥特性及模型拟合 总被引:2,自引:0,他引:2
利用微波在线检测装置将微波间歇干燥技术用于苹果片薄层干燥试验,研究了苹果片在700、600、450、250 W功率,切片厚度为3、5、7、9 mm,单次微波加热时间4、5、6、7 s下的干燥动力学特性。试验结果表明,苹果片微波间歇干燥过程属于降速干燥。微波功率、切片厚度、加热时间对干燥过程影响显著。水分有效扩散系数随着干燥功率的升高、切片厚度的增加、加热时间的延长而增加。通过模型拟合可知Weibull模型具有较高的预测精度,能很好地描述苹果片微波间歇干燥试验过程规律,利用逐步回归法,确定了Weibull模型参数α、β的表达式。模型的尺度参数α随功率增大、厚度减小、加热时间增加而减小,说明增大干燥功率、减小切片厚度、延长加热时间可以显著缩短干燥时间、提高干燥效率。功率、厚度和加热时间对形状参数β影响很小,说明干燥过程中物料状态变化较小。 相似文献
12.
Nonthermal technologies are emerging as promising alternatives to heat treatment for food processing. Ultrasound, defined as sound waves with a frequency greater than 20 kHz, has proven bactericidal effects, especially when combined with other microbial-reduction strategies such as mild heating. In this study, ultrasound treatment (sonifier probe at 20 kHz, 100% power level, 150 W acoustic power, 118 W/cm2 acoustic intensity) with or without the effect of mild heat (57 degrees C) was effective at reducing microbial levels in raw milk, Listeria monocytogenes levels inoculated in ultrahigh-temperature milk, and Escherichia coli O157:H7 in apple cider. Continuous flow ultrasound treatment combined with mild heat (57 degrees C) for 18 min resulted in a 5-log reduction of L. monocytogenes in ultrahigh-temperature milk, a 5-log reduction in total aerobic bacteria in raw milk, and a 6-log reduction in E. coli O157:H7 in pasteurized apple cider. Inactivation regressions were second-order polynomials, showing an initial period of rapid inactivation, eventually tailing off. Results indicate that ultrasound technology is a promising processing alternative for the reduction of microorganisms in liquid foods. 相似文献
13.
Microstructure analysis on pre-treated apple slices and its effect on water release during air drying 总被引:2,自引:0,他引:2
Microstructural studies have played an important role in the comprehensive understanding of some food phenomena that occur during drying processes. The aim of this work was to study the effect of four pre-treatments (immersion in boiling water, vacuum impregnation, freezing/thawing, and uni-axial compression) on apple microstructure characterized by cell cavities size parameter and how the changes induced by these pre-treatments can affect the water loss rate during air drying. The quantitative structure analysis showed that freezing/thawing and compression pre-treatments caused more damage on the apple structure, yielding larger cell cavities in comparison to vacuum impregnation and immersion in boiling water and control. Apple slices that were frozen/thawed, compressed and immersed in boiling water displayed the higher drying rates and diffusivity coefficients than the vacuum impregnated and control samples. These results allow concluding that disruption of the cell walls can be considered as a factor that affects the drying rate. 相似文献
14.
15.
Recommended drying treatments may not enhance destruction of pathogens that could be present on home-dried foods. In this study, the effects of traditional and modified treatments on Salmonella were evaluated during preparation, home-type dehydration (60 degrees C for 6 h), and storage of potato slices. Potato slices inoculated with five strains of Salmonella (8.4 log CFU/ g) were left untreated or were treated by steam blanching (88 degrees C for 10 min), water blanching (88 degrees C for 4 min), 0.105% citric acid blanching (88 degrees C for 4 min), or 0.210% citric acid blanching (88 degrees C for 4 min). Slices were then dried (6 h for 60 degrees C) and aerobically stored for up to 30 days at 25 +/- 3 degrees C. Cells were enumerated on tryptic soy agar with 0.1% pyruvate (TSAP) and on xylose lysine deoxycholate agar. Salmonella populations were reduced by 4.5 to 4.8 CFU/g and by >5.4 log CFU/g immediately following steam and water blanching, respectively. Populations were below the detection limit (0.80 log CFU/g) immediately following acid blanching, except for samples blanched in 0.105% citric acid and recovered on TSAP. After dehydration (6 h for 60 degrees C), Salmonella reductions on blanched potato slices (5.3 to 5.6 log CFU/g) were significantly greater (P < 0.05) than those on untreated samples (1.9 to 2.7 log CFU/g). Populations on all samples continued to decrease throughout 30 days of storage but still were 3.1 to 3.9 log CFU/g on untreated samples. In comparison, bacterial populations on blanched samples were undetectable by direct plating following 30 days of storage (regardless of blanching method). Blanching treatments used in this study improved the effectiveness of drying for inactivating Salmonella inoculated onto potato slices and, therefore, may enhance the safety of the product. 相似文献
16.
The effects of sodium lactate (NaL) and sodium chloride (NaCl), either alone (30 g/kg) or in combination (20+20 g/kg), on the microbiological and chemical quality of raw ground beef during vacuum-packaged storage at 2°C were investigated. The results showed that addition of NaL alone or in combination with NaCl significantly delayed the proliferation of aerobic plate counts, psychrotrophic counts, lactic acid bacteria and Enterobacteriaceae and extended the shelf life of the product up to 15 and 21 days, respectively, versus 8 days only for control. Over the storage time (21 days), NaL maintained the ground beef at almost constant pH, while the pH of control or NaCl-treated samples significantly decreased. Lipid oxidation (TBA value) was not affected by addition of NaL. At storage day 21 however, TBA values of both NaL-treated (0.309) and control (0.318) samples were significantly lower than those of samples treated with NaCl (0.463). The combination of NaCl with NaL significantly reduced the oxidative changes caused by NaCl (0.384 versus 0.463). Therefore, NaL alone or in combination with NaCl could be utilized successfully to reduce the microbial growth, maintain the chemical quality, and extend the shelf life of ground beef during refrigerated storage. 相似文献
17.
《食品与发酵工业》2019,(16):148-154
以‘红富士’苹果为试材,采用真空干燥、冰温真空干燥、冷冻真空干燥3种方法进行处理,研究其对苹果的风味、营养物质以及微观结构的影响。结果显示,冰温真空干燥的复水性介于真空干燥和冷冻真空干燥之间,说明该种方式得到的苹果片疏松程度良好。冰温真空干燥后的苹果片的可滴定酸含量最高为1.28 g/100 g,基本与新鲜苹果的酸1.305 g/100 g接近(P>0.05),可溶性固形物质量分数最高为12.57%,对Vc的保留率达80.95%,比真空干燥高43.65%,比冷冻真空干燥高40.32%;总酚含量最高,说明该种方式得到的干制品品质最好。微观结构显示,冰温真空干燥得到的苹果片形变最小,与新鲜苹果的结构最为相近,有较为规则的孔状结构,冷冻真空干燥有较小的塌陷,真空干燥组织形变较大。该研究为干燥方式在食品中的应用提供了理论基础,为冰温真空干燥技术的应用做了进一步的拓展。 相似文献
18.
为研究D-异抗坏血酸钠(D-sodium erythorbate,D-SE)处理对鲜切苹果品质的影响,将1cm3鲜切寒富苹果块分别放入0.5%、1.0%、1.5%D-SE溶液中浸泡2min后沥干,用0.11mm厚度的PE保鲜膜包装后置于4℃冷库中贮藏,每2d测定与成熟衰老相关的生理生化指标。结果表明,D-SE处理可保持苹果切块的感官品质、延缓营养物质的下降、抑制微生物的繁殖,对鲜切苹果有较好的护色效果;1.5%D-SE溶液浸泡处理能在4℃贮藏8d内保持鲜切苹果的品质,有效延迟果肉褐化进程,抑制硬度和可溶性固形物、可滴定酸及抗坏血酸含量的下降,并能延缓相对电导率和丙二醛(malondialdehyde,MDA)含量的上升,降低与酶促褐变有关的多酚氧化酶(polyphenol oxidase,PPO)活性、提高过氧化物酶(peroxidase,POD)活性。 相似文献
19.
Destruction of Escherichia coli O157:H7 was evaluated on inoculated apple slices dehydrated at two temperatures with and without application of predrying treatments. Half-ring slices (0.6 cm thick) of peeled and cored Gala apples were inoculated by immersion for 30 min in a four-strain composite inoculum of E. coli O157:H7. The inoculated slices (8.7 to 9.4 log CFU/g) either received no predrying treatment (control), were soaked for 15 min in a 3.4% ascorbic acid solution, or were steam blanched for 3 min at 88 degrees C immediately prior to drying at 57.2 or 62.8 degrees C for up to 6 h. Samples were plated on tryptic soy (TSA) and sorbitol MacConkey (SMAC) agar media for direct enumeration of surviving bacterial populations. Steam blanching changed initial inoculation levels by +0.3 to -0.7 log CFU/g, while immersion in the ascorbic acid solution reduced the inoculation levels by 1.4 to 1.6 log CFU/g. Dehydration of control samples for 6 h reduced mean bacterial populations by 2.9 log CFU/g (TSA or SMAC) at 57.2 degrees C and by 3.3 (SMAC) and 3.5 (TSA) log CFU/g at 62.8 degrees C. Mean decreases from initial inoculum levels for steam-blanched slices after 6 h of drying were 2.1 (SMAC) and 2.0 (TSA) log CFU/g at 57.2 degrees C, and 3.6 (TSA or SMAC) log CFU/g at 62.8 degrees C. In contrast, initial bacterial populations on ascorbic acid-pretreated apple slices declined by 5.0 (SMAC) and 5.1 (TSA) log CFU/g after 3 h of dehydration at 57.2 degrees C, and by 7.3 (SMAC) and 6.9 (TSA) log CFU/g after 3 h at 62.8 degrees C. Reductions on slices treated with ascorbic acid were in the range of 8.0 to 8.3 log CFU/g after 6 h of drying, irrespective of drying temperature or agar medium used. The results of immersing apple slices in a 3.4% ascorbic acid solution for 15 min prior to drying indicate that a predrying treatment enhances the destruction of E. coli O157:H7 on home-dried apple products. 相似文献