Growth and toxin production of proteolytic Clostridium botulinum in aseptically steamed rice products at pH 4.6 to 6.8, packed under modified atmosphere, using a deoxidant pack

Demand for aseptically steamed rice products has been increasing rapidly in Japan over the past 10 years. In our previous study, we showed that proteolytic Clostridium botulinum produce toxins in steamed rice products packaged under a modified atmosphere of < or =0.3% oxygen. In the present study, we examined the effect of pH to control botulism risk in steamed rice products packaged under modified atmosphere (5% CO2 and 95% N2 as the balance) with the inclusion of a deoxidant pack to produce an oxygen concentration of < or =0.3%. A mixture of 10 strains of proteolytic C. botulinum (5 type A strains and 5 type B strains) was inoculated into steamed rice products at pH values between 4.6 and 6.8 prior to packaging. All samples were stored at 30 degrees C for 24 weeks. Samples at higher pH showed earlier starts of neurotoxin production. Neurotoxin was detected after 2 weeks of incubation in samples at pH 5.4 or above, whereas it took 4 weeks for the toxin to be detected in samples at pH 5.2 to 5.3 and 12 weeks in samples at pH 5.0 to 5.1. In samples at pH 4.9 or below, no toxin was detected during the experimental period. Apparent sample spoilage did not occur before C. botulinum produced neurotoxin in most of the samples. Based on these results, we conclude that aseptically steamed rice products must be packaged at pH 4.9 or below under modified atmosphere containing < or =0.3% oxygen, with the inclusion of a deoxidant pack.     

Evaluation of botulinal toxin production in packaged fresh-cut cantaloupe and honeydew melons.

The ability of Clostridium botulinum to produce toxin on cubed, packaged melons was investigated relative to microbial spoilage at various incubation temperatures and in different packaging systems. Freshly cut cubes (approximately 2.5 cm3) of cantaloupe and honeydew melons were surface inoculated with a 10 strain mixture of proteolytic and nonproteolytic spores of C. botulinum (10 to 15 cubes per package; approximately 100 total spores per package). To initially evaluate toxin production and spoilage in a passively modified atmosphere, melon cubes were loosely packaged in air in polyethylene pouches, sealed, and incubated at 7 or 15 degrees C for up to 21 days. At various sampling intervals, samples were tested for headspace oxygen and carbon dioxide levels, pH, presence of botulinal toxin, aerobic and anaerobic plate counts, and counts of yeasts and molds. During incubation, headspace oxygen levels decreased, headspace carbon dioxide levels increased, aerobic and anaerobic plate counts increased, and the pH remained constant or decreased slightly. Botulinal toxin was not detected in any cantaloupe samples or in honeydew samples incubated at 7 degrees C. Botulinal toxin was detected in some honeydew samples at 15 degrees C after 9 days of incubation, but the toxic honeydews were severely spoiled and considered organoleptically unacceptable. A similar second experiment was performed in which half of the melon cubes were treated with UV light to inactivate vegetative organisms before packaging, and these were incubated at 7, 15, or 27 degrees C. In this second experiment, toxin production occurred in the UV-treated samples at 15 degrees C with gross spoilage and at 27 degrees C with only marginal spoilage. These data indicate that inhibition of spoilage organisms with UV light could result in botulinal toxin formation in packaged melons before overt spoilage.     

Growth and toxin production by Clostridium botulinum in English-style crumpets packaged under modified atmospheres.

To determine the safety of a high moisture bakery product, packaged under modified atmospheres, challenge studies were done on English-style crumpets (water activity [a(w)] 0.990, pH 6.5) inoculated postbaking with Clostridium botulinum types A and proteolytic B spores (5 X 10(2) spores/g). Products were packaged either in air, in air with an Ageless FX200 oxygen absorbent, or in a CO2/N2 (60:40) gas mixture, stored at ambient temperature (25 degrees C), and monitored for toxicity daily. All inoculated crumpets were toxic within 4 to 6 days and were organoleptically acceptable at the time of toxigenesis. Counts of C. botulinum increased to approximately 10(5) CFU/g at the time of toxicity. To determine the effect of baking on product safety, subsequent challenge studies were done on crumpets inoculated with 5 x 10(2) spores/g (baked weight basis) prior to baking. All crumpets were toxic after only 6 days, irrespective of packaging conditions, and toxigenesis again preceded spoilage. Temperature profile studies showed that the maximum internal temperature reached during baking was 97 degrees C, and the total baking process was equivalent to 0.03 min at 121 degrees C. The actual time to toxin production in both studies (4 to 6 days) correlated well with the predicted time (3.4 days) using the U.S. Department of Agriculture Pathogen Modeling Program (version 5.1) for proteolytic strains of C. botulinum. These studies confirm that high moisture bakery products, if contaminated with C. botulinum spores either pre- or postbaking, could pose a public health hazard, if packaged in air (in a high gas barrier package where O2 was depleted and CO2 was generated during storage) or under modified atmosphere packaging conditions and stored at ambient temperature.     

菊芋全粉对米发糕贮藏品质特性的影响

目的 探究菊芋全粉添加量与米发糕品质特性之间的相关性。方法 在米发糕中添加不同比例(5%、10%、15%、20%、25%)的菊芋全粉,测定其贮藏过程(0、1、3、5、7 d)中感官品质、质构特性和体外消化特性等指标,探究菊芋全粉与米发糕品质指标之间的相关性。结果 与未添加菊芋全粉的米发糕相比,菊芋全粉的添加降低了米发糕的硬度、粘性和咀嚼性,感官评分从81.91下降到70.91,而米发糕抗性淀粉从26.02%增加至34.59%。菊芋全粉的添加能有效减缓米发糕在贮藏期间质构的劣变,贮藏第7d时,添加15%菊芋全粉的米发糕感官评分(80.83)高于对照组(66.57),且添加10%菊芋全粉的米发糕抗性淀粉高达42.23%。通过相关性分析,回复值、弹性和粘聚性是影响米发糕感官品质的主要因素,其中弹性与米发糕感官评分呈极显著负相关(P<0.01)。结论 添加菊芋全粉可有效提升米发糕的感官品质及抗消化特性,并能有效减缓米发糕在贮藏期间的质构劣变,同时也丰富了米发糕品种多样性,可为菊芋资源的开发和高值化利用、发糕制品的深度研究提供理论参考。     

Impacts of storage temperature and rice moisture content on color characteristics of rice from fields with different disease management practices

Rice downgrading due to discoloration in storage presents a significant loss to growers and processors. The objective of this study was to investigate impacts of storage temperature and rice moisture content (MC) on color characteristics of milled hybrid rice (cv. XL 745) from fields with differing production practices. Freshly-harvested rough rice from field plots treated with and without fungicide for rice disease control during production were procured and stored at four MC levels (12.5%, 16%, 19% and 21% wet basis), and at five temperatures (10 °C, 15 °C, 20 °C, 27 °C, 40 °C) for 16 weeks, with samples taken every 2 weeks. Kinetics of mold growth and rice color were determined. It was observed that at 12.5% MC, discoloration was abated across all studied temperatures and treatments until 6 weeks of storage and increased not in excess of 20% thereafter 16 weeks. As the storage MC increased to 16%, discoloration increased and became significantly notable at the highest temperature of 40 °C. By week 16, at 40 °C storage temperature, discoloration increased significantly to 87.9% and 73% for sample lots from fungicide and non-fungicide treated plots, respectively. At the highest MC (21%), increase in rice discoloration was notable as early as after 2 weeks, across all storage temperatures, and continued to increase, especially for the highest storage temperature of 40 °C, to as high as 99.1% and 96.47%, after 16 weeks, for sample lots from fungicide and non-fungicide treated plots, respectively. There was more expression of discoloration patterns on samples stored at the highest temperature of 40 °C compared to that at lower temperatures, for both categories of sample treatments and ranges of studied MCs. Although not yet widely used for rice, this study suggested that cooling technology for rice, may have potential to extend rice storability, especially by retarding discoloration in the first few weeks after harvest.     

KEEPING QUALITY OF DIFFERENT PACKAGED SALTED ATLANTIC BONITO "LAKERDA"

Quality and shelf life of salted Atlantic bonito (lakerda) packaged in brine, under vacuum and in oil conditions and stored at 4  ±  1C were studied. The sensory scores of lakerda stored in all package types at 4C were 14 weeks, respectively. The microbiological count of the vacuum-packaged lakerda was extended than that lower of other group sample. Overall results of this study showed that 9 weeks of storage of lakerda in brine was the beginning of spoilage, whereas storage of samples in oil and vacuum package delayed onset of spoilage about 2–3 weeks in terms of chemical analysis. Lakerda stored in cold storage as sensory, chemical and microbiological results for brine- and oil-packaged lakerda showed us that week 11 was the beginning of spoilage, and for vacuum-packaged lakerda, week 13 was the beginning of spoilage.

PRACTICAL APPLICATIONS

Raw fish and processed fish product is highly perishable and has a short shelf life. Packing processing is finding increasing use in the food industry because of its relative advantages versus other food processing methods in eliciting minimal changes in the flavor, microbiological and nutritional qualities of the final product. This paper illustrates the changes induced in salted fish by packaging at different types. By using oil- and vacuum-packaged treatment, shelf life of traditional-packaged (in brine) lakerda could be extended at 4C from 9 weeks to 11–13 weeks.     

多糖类食品添加剂对米饭质构特性的影响

通过扫描电镜分析,得出仙桃大米颗粒的孔隙大小为2μm 4μm;采用90Plus Particle Size Ana-lyser分析羟丙基甲基纤维素(HPMC)、麦芽糊精、瓜尔豆胶和卡拉胶在水溶液中的粒径分布大小,得出这些多糖类食品添加剂在水溶液中的粒径大小分别为897.7nm、35.9nm、125.2nm、323.5nm。在蒸制米饭的过程中添加这些多糖类食品添加剂,研究米饭样品在冷藏过程中的硬度和黏性的变化,结果表明:羟丙基甲基纤维素(HPMC)和瓜尔豆胶添加量为0%时,与添加量为0.1%,0.3%的米饭样品相比,米饭的硬度较低,而黏性则较高,添加羟丙基甲基纤维素和瓜尔豆胶加速了米饭样品的老化;麦芽糊精和卡拉胶添加量为0.1%的米饭样品与添加量为0%和0.3%的样品相比,米饭样品的硬度低于而黏性高于添加量为0%和0.3%的米饭样品,麦芽糊精和卡拉胶能够起到延缓米饭样品老化的作用。     

The storage life of chilled pork packaged under carbon dioxide

Pork cuts of longissimus dorsi muscle with overlaying fat and skin were packed under vacuum in film of low oxygen transmission rate, or under CO₂ in gas impermeable aluminium foil laminate. Cuts were stored at +3 or −1·5°C. Vacuum packaged cuts were grossly spoiled by Brochothrix thermosphacta after 2 weeks' storage at 3°C and after 5 weeks at −1·5°C. Cuts packaged under CO₂ were grossly spoiled by B. thermosphacta after 5·5 weeks' storage at 3°C. Growth of B. thermosphacta was suppressed when CO₂ packaged cuts were stored at −1·5°C. At that temperature, slow growth of enterobacteria was detected after a lag of about 18 weeks. The enterobacteria caused gross spoilage of an increasing proportion of cuts between 18 and 26 weeks. Muscle tissue with pale, soft, exudative (PSE) characteristics tended to lose colour after long storage periods, apparently because of loss of myogglobin with exudate. Until spoilage, the eating qualities of pork appeared little affected by prolonged storage.     

Cooked and brined shrimps packed in a modified atmosphere have a shelf-life of >7 months at 0 °C, but spoil in 4–6 days at 25 °C

Summary Spoilage and safety of cooked, brined and modified atmosphere packed shrimps were studied at 0, 5, 8, 15 and 25 °C. Shrimps from two sources, cold and warm waters, were brined in a sodium–chloride brine containing benzoic, citric and sorbic acids. Shelf-life was above 7 months at 0 °C but only 4–6 days at 25 °C. Apparent activation energy for the effect of temperature on shelf-life was > 100 kJ mol^-1. This pronounced effect of temperature was explained by changes in spoilage microflora at different storage temperatures. Simple and empirical mathematical models for rates of spoilage were developed for the prediction of shelf-life at different temperatures. To evaluate safety, products were challenged with Listeria monocytogenes and spores of Clostridium botulinum . Above 5 °C growth responses of L. monocytogenes followed the square root model with a T_min-value of +0.2 °C. Cl. botulinum produced toxin at the time of spoilage at 25 °C but only in shrimps with < 3% water-phase salt.     

Effects of modified atmosphere packaging on toxin production by Clostridium botulinum in raw aquacultured summer flounder fillets (Paralichthys dentatus)

Packaging fishery products under vacuum atmosphere packaging (VAC) and modified atmosphere packaging (MAP) conditions can significantly extend the shelf life of raw, refrigerated fish products. There is considerable commercial interest in marketing VAC and MAP refrigerated (never frozen) raw fish fillets. The objective of this study was to determine if Clostridium botulinum toxin development precedes microbiological spoilage in raw, refrigerated flounder fillets. Aquacultured flounder (Paralichthys dentatus) individual fish fillets either were packed with a film having an oxygen transmission rate (OTR) of 3000 cm3 m(-2) 24 h(-1) at 22.8 degrees C or were vacuum packaged or packaged under 100% CO2 with a film having an OTR of 7.8 cm3 m(-2) 24 h(-1) at 21.1 degrees C and were stored at 4 and 10 degrees C. Samples were analyzed by aerobic plate count (APC) for spoilage and qualitatively for botulinum toxin with a mouse bioassay. The results demonstrate that flounder fillets (4 degrees C) packaged with a film having an OTR of 3,000 were microbiologically spoiled (APC, > 10(7) CFU/g) on day 15, but there was no toxin formation, even after 35 days of storage. However, at 10 degrees C, toxin production occurred (day 8), but it was after microbial spoilage and absolute sensory rejection (day 5). Vacuum-packaged fillets and 100% CO2 fillets (4 degrees C) packaged with a film having an OTR of 7.8 were toxic on days 20 and 25, respectively, with microbial spoilage (APC, >10(7) CFU/g) not occurring during the tested storage period (i.e., >35 days). At 10 degrees C, in vacuum-packaged flounder, toxin formation coincided with microbiological spoilage (days 8 to 9). In the 100% CO2-packaged fillets, toxin formation occurred on day 9, with microbial spoilage occurring on day 15. This study indicates that films with an OTR of 3,000 can be used for refrigerated fish fillets and still maintain the safety of the product.     

EFFECT OF FILMS OF DIFFERENT OXYGEN TRANSMISSION RATE ON TOXIN PRODUCTION BY CLOSTRIDIUM BOTULINUM TYPE E IN VACUUM PACKAGED COLD AND HOT SMOKED TROUT FILLETS

Studies were done to determine the effect of film oxygen transmission rate (OTR) on the time to toxicity in vacuum packaged cold and hot smoked rainbow trout fillets challenged with C. botulinum type E (10² spores/g) and stored at refrigerated conditions (4C), and under mild (8C) and moderate (12C) temperature abuse conditions. While no samples were toxic at 4C, toxin was detected within 28 days at 8C for cold smoked trout fillets vacuum packaged in films with high OTR. Toxin was also detected for most vacuum packaged hot smoked trout fillets within 14–28 days at 8C, with the exception of trout fillets packaged in films with an OTR > 10,000 cc/m²/day. In most cases at 8C, spoilage, based on odor/color scores, preceded or occurred simultaneously with toxigenesis. At 12C all cold and hot smoked trout were toxic after 14–21 days and samples packaged in films with an OTR <5000 cc/m²/day became toxic before, or at the same time as, samples became spoiled. This study has shown that vacuum packaging of trout fillets in low gas barrier films, ranging in OTR from approximately 3,000 to approximately 10,000 cc/m²/day at 24C and 0% relative humidity (RH), did not prevent the growth and toxin production by C. botulinum in vacuum packaged cold and hot smoked trout fillets at 12C. Additional barriers, other than the OTR of the packaging film, need to be considered to ensure the safety of vacuum packaged trout fillets, particularly at mild to moderate temperature abuse storage conditions.     

Nonproteolytic Clostridium botulinum toxigenesis in cooked turkey stored under modified atmospheres

The ability of nonproteolytic Clostridium botulinum type B spores to grow and produce toxin in cooked, uncured turkey packaged under modified atmospheres was investigated at refrigeration and mild to moderate abuse temperatures. Cook-in-bag turkey breast was carved into small chunks, surface-inoculated with a mixture of nonproteolytic C. botulinum type B spores, packaged in O2-impermeable bags under two modified atmospheres (100% N2 and 30% CO2:70% N2), and stored at 4, 10, and 15 degrees C. Samples were analyzed for botulinal toxin and indigenous microorganisms, as well as subjected to sensory evaluation, on days 0, 7, 14, 28, 42, and 60. Given sufficient incubation time, nonproteolytic C. botulinum type B grew and produced toxin in all temperature and modified atmosphere treatment combinations. At moderate temperature abuse (15 degrees C), toxin was detected by day 7, independent of packaging atmosphere. At mild temperature abuse (10 degrees C), toxin was detected by day 14, also independent of packaging atmosphere. At refrigeration temperature (4 degrees C), toxin was detected by day 14 in product packaged under 100% N2 and by day 28 in product packaged under 30% CO2:70% N2. Reduced storage temperature significantly delayed toxin production and extended the period of sensory acceptability of cooked turkey, but even strict refrigeration did not prevent growth and toxigenesis by nonproteolytic C. botulinum. At all three storage temperatures, toxin detection preceded or coincided with development of sensory characteristics of spoilage, demonstrating the potential for consumption of toxic product when spoilage-signaling sensory cues are absent.     

Clostridium botulinum type E outgrowth and toxin production in vacuum-skin packaged shrimp

White and brown shrimp (Penaeus spp.), harvested from the Georgia coast, were inoculated with log 3-4 spores of a mixed pool of four strains of Clostridium botulinum type E (Beluga, Minnesota, G21-5, and 070). Oxygen barrier film was used to vacuum-skin package the shrimp. Packaged shrimp was stored at either 4°C or 10°C. Storage at 10°C was used to simulate temperature abuse. Anaerobes were enumerated by Most Probable Number method using TPYGT broth incubated in anaerobic jars. Clostridium botulinum toxin production was evaluated using the mouse bioassay. After six days at 10°C, botulinum toxin was detected in the packaged shrimp, but the shrimp was noticeably spoiled at this point. No botulinum toxin was detected in the packaged shrimp stored at 4°C for 21 days, although spoilage was noted after 6 days.     

Toxin production by Clostridium botulinum in pasteurized milk treated with carbon dioxide.

The addition of carbon dioxide to milk at levels of <20 mM inhibits the growth of selected spoilage organisms and extends refrigerated shelf life. Our objective was to determine if the addition of CO2 influenced the risk of botulism from milk. Carbon dioxide was added to pasteurized 2% fat milk at approximately 0, 9.1, or 18.2 mM using a commercial gas-injection system. The milk was inoculated with a 10-strain mixture of proteolytic and nonproteolytic Clostridium botulinum spore strains to yield 10(1) to 10(2) spores/ml. Milk was stored at 6.1 or 21 degrees C for 60 or 6 days, respectively, in sealed glass jars or high-density polyethylene plastic bottles. Milk stored at 21 degrees C curdled and exhibited a yogurt-like odor at 2 days and was putrid at 4 days. Botulinal toxin was detected in 9.1 mM CO2 milk at 4 days and in all treatments after 6 days of storage at 21 degrees C. All toxic samples were grossly spoiled based on sensory evaluation at the time toxin was detected. Although botulinal toxin appeared earlier in milk treated with 9.1 mM CO2 compared to both the 18.2 mM and untreated milk, gross spoilage would act as a deterrent to consumption of toxic milk. No botulinal toxin was detected in any treatment stored at 6.1 degrees C for 60 days. At 6.1 degrees C, the standard plate counts (SPCs) were generally lower in the CO2-treated samples than in controls, with 18.2 mM CO2 milk having the lowest SPC. These data indicate that the low-level addition of CO2 retards spoilage of pasteurized milk at refrigeration temperatures and does not increase the risk of botulism from treated milk stored at refrigeration or abuse temperatures.     

Packaging conditions for extended storage of chilled dark, firm, dry beef

Normal-pH (5·5-5·7) and high-pH (> 6·0) beef cuts of 500g were vacuum packaged in polyvinylidene chloride (PVDC), metalized polyester or aluminium foil laminates, or in foil laminate packs inflated with 1 litre of CO(2). During storage at + 1°C. vacuum packaged cuts developed spoilage floras of lactobacilli and enterobacteria; cuts stored under CO(2) developed floras of lactobacilli alone. Floras on all high-pH vacuum packaged cuts approached maximum numbers after 6 weeks' storage. At this time, cuts in PVDC laminate showed early symptoms of spoilage, but such symptoms did not develop in other vacuum packaged high-pH cuts until 9 or more weeks. Similarly, normal-pH cuts in PVDC film showed spoilage symptoms at 12 weeks, but such symptoms did not develop in other vacuum packaged normal-pH cuts until 15 weeks. Both normal- and high-pH cuts packaged under CO(2) were unspoiled at 15 weeks.     

Degradation of lnosinic Acid in Chicken Muscle During Aseptic Storage and Its Possible Use as an Index of Quality.

SUMMARY— Analysis of chicken breast and leg muscle stored under aseptic conditions at 0, 5, and 10°C showed that the breakdown of inosinic acid and formation of hypoxanthine depended on storage temperature and time. Over 75% loss of inosinic acid content of both breast and leg muscle occurred in 3–5 weeks at 0°, in 2–3 weeks at 5O and in about 1 week at 10°C. These storage periods correspond to the lengths of time after which quality deterioration has been detected by sensory evaluation. During the same periods of storage, the hypoxanthine content of these muscles increased gradually to a value of 200–400 fig/g of muscle.
Since the level of inosinic acid in fresh muscle is fairly constant and related to flavor, the results indicate that an objective method of quality assessment of chicken meat based on inosinic acid content is feasible. A similar test based on the hypoxanthine content is also possible, but not likely to be as satisfactory, because losses occurring as a result of "weeping" and leaching in hypoxanthine content would show an apparent quality that is higher than it should be. On the other hand, an index based on inosinic acid would reflect similar losses by lowering of quality.     

CHALLENGE STUDIES WITH CLOSTRIDIUM BOTULINUM TYPE E IN A VALUE-ADDED SURIMI PRODUCT STORED UNDER A MODIFIED ATMOSPHERE

Challenge studies were carried out on raw, cooked, and sterilized surimi nuggets, inoculated with 10⁴ spores/g of C. botulinum type E spores. All products were packaged in air and air with an Ageless SS oxygen absorbent and stored at 4, 12 and 25C. Toxin was not detected in any raw product throughout storage (28 days). The absence of toxigenesis was attributed to the low pH (4.1–4.3) due mainly to the growth of lactic acid bacteria (10⁷CFU/g). Toxin was also not detected in any cooked product after 28 days. Product pH did not decrease as previously (due to the absence of LAB), but counts of C. botulinum still decreased throughout storage.
In sterile nuggets , C. botulinum counts increased to 10⁶ cfu/g at both 12 and 25C, respectively, by 28 days. Lactic acid bacteria and Bacillus spp. were not detected throughout the 28 days storage period. Toxin was detected by days 28 and 14 at 12 and 25C, respectively, and toxigenesis preceded spoilage. The absence of toxin in cooked nuggets was attributed to the anti-botulinal role by Bacillus species, the predominant spoilage bacteria in cooked nuggets.     

冷藏卵形鲳优势腐败菌的分离鉴定及致腐能力分析

为研究卵形鲳鲹冷藏末期的优势腐败菌及其致腐能力,采用传统选择性培养结合16S rDNA序列分析法,对卵形鲳鲹4℃贮藏期间腐败菌分别进行分离纯化、菌相分析及菌属确定,并以腐败物质的产量因子Y_TVB-N/CFU为评价标准,定量分析了贮藏末期优势菌的致腐能力。结果得出,卵形鲳鲹4℃贮藏过程中共分离纯化出16株细菌,其中革兰氏阴性菌10株,革兰氏阳性菌6株,其分属6个菌属。贮藏初期（0 d）时菌相丰富,希瓦氏菌属（Shewanella sp.）、假单胞菌属（Pseudomonas sp.）、葡萄球菌属（Staphylococcus sp.）、芽孢杆菌属（Bacillus sp.）、乳酸杆菌属（Lactobacillus sp.）与肠杆菌属（Enterobacter sp.）等均有出现;中期（3 d）菌群种类有所减少,以希瓦氏菌属（Shewanella sp.）与假单胞菌属（Pseudomonas sp.）所占比例较高,后期（6 d）种类进一步减少,只有3株菌占较高,分别是2号腐败希瓦氏菌（Shewanella putrefaciens 48%）、5号奥奈达希瓦氏菌（Shewanella oneidensis 26.6%）与16号霍氏肠杆菌（Enterobacter hormaechei 19.4%）;致腐能力由高至低依次为腐败希瓦氏菌 > 奥奈达希瓦氏菌 > 霍氏肠杆菌,其中腐败希瓦式菌致腐能力显著强于另两株菌;综合贮藏末期所占比例及致腐能力结果,最终确定腐败希瓦氏菌为4℃贮藏下卵形鲳鲹的优势腐败菌。     

Extended shelf-life of unrefrigerated prerigor cooked meat

Five experiments were conducted to evaluate the microbial quality of unrefrigerated cooked prerigor beef after the application of oxygen-permeable packaging. Specific objectives were to combine the beneficial effects of aerobic packaging, meat surface acidification and prerigor rapid cooking rates on meat storage stability at ambient temperature. In the experiments, the triceps brachii muscle was dissected from one side 45 min after exanguination of the animal, and samples of 2 × 3 × 5 cm were prepared. Bags made of a strong barrier, plastic film, and a highly oxygen permeable oriented polypropylene, were used. The cooking of the packaged samples covered a number of treatments ranging from cooking in a 70°C water bath to an internal sample temperature of 65°C to cooking in 100°C water for 40 min. Reheating and multiple heat treatments were also included. The pH values of the cooked samples were determined and aerobic plate counts (log(10)/g) were determined for the cooked samples at various intervals during two weeks of storage at 22°C or at 3°C for the control samples. The results indicate that heat treatment alone did not improve shelf stability at 22°C. However, dipping the samples in 80°C solutions of 0·7% citric acid or 1·25% lactic acid for 1 min and draining for 1 min followed by packaging using oxygen permeable bags and cooking in 100°C water for 40 min consistently resulted in shelf stable products at all 22°C storage intervals. The lactic acid treatment was superior to the citric acid treatment because it completely decontaminated the samples and delayed spoilage, especially at 3°C.     

CHALLENGE STUDIES WITH PROTEOLYTIC CLOSTRIDIUM BOTULINUM IN YEAST AND CHEMICALLY LEAVENED CRUMPETS PACKAGED UNDER MODIFIED ATMOSPHERES

Challenge studies were done with proteolytic Clostridium botulinum (10³ spores/g) in yeast-and chemical-leavened crumpets (50-g) packaged in air with an ethanol vapor (2-G Ethicap®) generator or in 100% CO₂ and stored at ambient temperature (25C) for 30 days. Neurotoxin was detected in all gas- (CO₂) packaged crumpets after 5 days regardless of the method of leavening. While neurotoxin was delayed for 10 days in chemical-leavened Ethicap®-packaged crumpets, it was not detected in any similarly packaged yeast-leavened crumpets throughout storage. This inhibition of growth and neurotoxin production by C. botulinum was attributed to the production of ethanol by Saccharomyces cerevisiae in the yeast leavened crumpets, in conjunction with the ethanol vapor generated by the Ethicap® sachets (2-G), to levels to inhibitory to the growth of C. botulinum (>2.8% v/v). Subsequent challenge studies in sterile crumpets inoculated with either C. botulinum (10³ spores/g) or a co-inoculum of C. botulinum (10³ spores/g) and S. cerevisiae (10⁵ CFU/g) confirmed the significant role (p<0.001) of S. cerevisiae in enhancing the antibotulinal efficacy of ethanol vapor. These studies showed that the method of crumpet leavening could have a profound effect on the growth of and neurotoxin production by C. botulinum in crumpets packaged under modified atmospheres.