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Food fraud threats in UK post-harvest seafood supply chains; an assessment of current vulnerabilities 英国收获后海鲜供应链中的食品欺诈威胁;对当前脆弱性的评估。
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-27 DOI: 10.1038/s41538-024-00272-z
Sophie Lawrence, Christopher Elliott, Wim Huisman, Moira Dean, Saskia van Ruth
Seafood fraud is commonly reported on food fraud databases and deceptive practices are highlighted by numerous studies, with impacts on the economy, health and marine conservation. Food fraud assessments are a widely accepted fraud mitigation and prevention activity undertaken to identify possible points of deception within a supply chain. This study aims to understand the food fraud vulnerability of post-harvest seafood supply chains in the UK and determine if there are differences according to commodity, supply chain node, business size and certification status. The SSAFE food fraud vulnerability assessment tool was used to assess 48 fraud factors relating to opportunities, motivations and controls. The analysis found seafood supply chains to have a medium vulnerability to food fraud, with the highest perceived vulnerability in technical opportunities. Certification status was a stronger determinant of vulnerability than any other factor, particularly in the level of controls, a factor that also indicated a higher perceived level of vulnerability in smaller companies and the food service industry. This paper also reviews historic food fraud trends in the sector to provide additional insights and the analysis indicates that certain areas of the supply chain, including uncertified prawn supply chains, salmon supply chains and food service companies, may be at higher risk of food fraud. This study conducts an in-depth examination of food fraud vulnerability relating to the UK and for seafood supply chains and contributes to a growing body of literature identifying areas of vulnerability and resilience to food related criminality within the global food system.
食品欺诈数据库中经常有海产品欺诈的报道,许多研究都强调了欺骗行为对经济、健康和海洋保护的影响。食品欺诈评估是一种广为接受的欺诈缓解和预防活动,旨在确定供应链中可能存在的欺骗点。本研究旨在了解英国收获后海鲜供应链的食品欺诈脆弱性,并确定不同商品、供应链节点、企业规模和认证状态是否存在差异。SSAFE 食品欺诈脆弱性评估工具用于评估与机会、动机和控制有关的 48 个欺诈因素。分析发现,海鲜供应链对食品欺诈的脆弱性处于中等水平,在技术机会方面的脆弱性最高。与其他因素相比,认证状况是决定易受攻击程度的更重要因素,特别是在控制水平方面,这一因素也表明较小的公司和食品服务行业的易受攻击程度较高。本文还回顾了该行业食品欺诈的历史趋势,以提供更多的见解。分析表明,供应链的某些领域,包括未经认证的对虾供应链、三文鱼供应链和食品服务公司,可能面临更高的食品欺诈风险。本研究深入探讨了与英国有关的食品欺诈脆弱性以及海产品供应链的脆弱性,为越来越多的文献确定全球食品系统中与食品有关的犯罪的脆弱性和复原力做出了贡献。
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引用次数: 0
Characterization of spring and durum wheat using non-destructive synchrotron phase contrast X-ray microtomography during storage 利用无损同步辐射相衬 X 射线显微层析技术分析春小麦和硬质小麦在储藏期间的特征。
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-18 DOI: 10.1038/s41538-024-00271-0
Navanth S. Indore, Chithra Karunakaran, Digvir S. Jayas, Jarvis Stobbs, Miranda Vu, Kaiyang Tu, Omar Marinos
Post-harvest losses during cereal grain storage are a big concern in both developing and developed countries, where spring and durum wheat are staple food grains. Varieties under these classes behave differently under storage, which affects their end storage life. High resolution imaging data of dry as well as spoiled seed are not available for any class of wheat; therefore, an attempt was made to generate 3D data for better understanding of seed structure and changes due to spoilage. Six wheat varieties (3 varieties for each class of wheat) were stored for 5 week at 17% moisture content (wb) before scanning. Seeds were also stored in a freezer (-18 °C) for further scanning to determine if any changes occur in the structure of seeds due to freezing. Spring varieties of wheat performed better than durum varieties and freezing did not affect seed structure. Data could also help plant breeders to develop varieties that do not easily spoil, adjust grain processing techniques, and develop post-harvest recommendations for other wheat varieties.
无论是发展中国家还是发达国家,谷物储藏期间的收获后损失都是一个重大问题,而春小麦和硬质小麦是这些国家的主食谷物。这些类别下的品种在贮藏过程中表现不同,从而影响其最终贮藏寿命。目前还没有任何一类小麦的干燥种子和变质种子的高分辨率成像数据;因此,我们尝试生成三维数据,以便更好地了解种子结构和变质引起的变化。扫描前,6 个小麦品种(每类小麦 3 个品种)的种子在 17% 的含水量 (wb) 下储存 5 周。种子还被储存在冷冻室(-18 °C)中进行进一步扫描,以确定种子结构是否会因冷冻而发生任何变化。春小麦品种的表现优于硬粒小麦品种,冷冻对种子结构没有影响。这些数据还有助于植物育种者开发不易变质的品种、调整谷物加工技术以及为其他小麦品种制定收获后建议。
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引用次数: 0
First principles modelling of the ion binding capacity of finger millet 小米离子结合能力的第一原理模型
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-14 DOI: 10.1038/s41538-024-00270-1
Wei Cong Matthew Yong, Apramita Devi, Tsair-Fuh Lin, Helen F. Chappell
Finger millet, a cereal grain widely consumed in India and Africa, has gained more attention in recent years due to its high dietary fibre (arabinoxylan) and trace mineral content, and its climate resilience. The aim of this study was to understand the interactions between potassium (K+), calcium (Ca2+) and zinc (Zn2+) ions and the arabinoxylan structure and determine its ion-binding capacity. Three variations of a proposed model of the arabinoxylan structure were constructed and first principles Density Functional Theory calculations were carried out to determine the cation-binding capacity of the arabinoxylan complexes. Zn2+-arabinoxylan complexes were highly unstable and thermodynamically unfavourable in all three models. Ca2+ and K+ ions, however, form thermodynamically stable complexes, particularly involving two glucuronic acid residues as a binding pocket. Glucuronic acid residues are found to play a key role in stabilising the cation-arabinoxylan complex, and steric effects are more important to the stability than charge density. Our results highlight the most important structural features of the millet fibre regarding ion-storage capacity, and provide valuable preliminary data for confirmatory experimental studies and for the planning of clinical trials where the bioavailability of bound ions following digestion may be tested.
手指粟是一种在印度和非洲广泛食用的谷物,近年来因其膳食纤维(阿拉伯木聚糖)和微量矿物质含量较高以及对气候的适应能力而受到越来越多的关注。本研究旨在了解钾(K+)、钙(Ca2+)和锌(Zn2+)离子与阿拉伯木聚糖结构之间的相互作用,并确定其离子结合能力。我们构建了阿拉伯木聚糖结构拟议模型的三种变体,并进行了第一原理密度泛函理论计算,以确定阿拉伯木聚糖复合物的阳离子结合能力。在所有三种模型中,Zn2+-阿拉伯木聚糖复合物都极不稳定,热力学上也不利。然而,Ca2+ 和 K+ 离子却能形成热力学上稳定的复合物,特别是以两个葡萄糖醛酸残基作为结合袋。研究发现,葡萄糖醛酸残基在稳定阳离子-阿拉伯木聚糖复合物方面起着关键作用,立体效应比电荷密度对稳定性更为重要。我们的研究结果突出了小米纤维在离子存储能力方面最重要的结构特征,并为确证实验研究和临床试验规划提供了宝贵的初步数据,在临床试验中,可以对消化后结合离子的生物利用率进行测试。
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引用次数: 0
Microbial community structure of plant-based meat alternatives 植物肉类替代品的微生物群落结构。
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-13 DOI: 10.1038/s41538-024-00269-8
Franz-Ferdinand Roch, Monika Dzieciol, Narciso M. Quijada, Lauren V. Alteio, Patrick-Julian Mester, Evelyne Selberherr
A reduction in animal-based diets has driven market demand for alternative meat products, currently raising a new generation of plant-based meat alternatives (PBMAs). It remains unclear whether these substitutes are a short-lived trend or become established in the long term. Over the last few years, the trend of increasing sales and diversifying product range has continued, but publication activities in this field are currently limited mainly to market research and food technology topics. As their popularity increases, questions emerge about the safety and nutritional risks of these novel products. Even though all the examined products must be heated before consumption, consumers lack experience with this type of product and thus further research into product safety, is desirable. To consider these issues, we examined 32 PBMAs from Austrian supermarkets. Based on 16S rRNA gene amplicon sequencing, the majority of the products were dominated by lactic acid bacteria (either Leuconostoc or Latilactobacillus), and generally had low alpha diversity. Pseudomonadota (like Pseudomonas and Shewanella) dominated the other part of the products. In addition to LABs, a high diversity of different Bacillus, but also some Enterobacteriaceae and potentially pathogenic species were isolated with the culturing approach. We assume that especially the dominance of heterofermentative LABs has high relevance for the product stability and quality with the potential to increase shelf life of the products. The number of isolated Enterobacteriaceae and potential pathogens were low, but they still demonstrated that these products are suitable for their presence.
动物性饮食的减少推动了市场对替代肉类产品的需求,目前正在催生新一代植物性肉类替代品(PBMA)。这些替代品是昙花一现,还是会长期存在,目前尚不清楚。在过去的几年里,销售额不断增长,产品种类不断丰富,但这一领域的出版活动目前主要局限于市场研究和食品技术主题。随着这些新产品越来越受欢迎,有关其安全性和营养风险的问题也随之出现。尽管所有受检产品在食用前都必须加热,但消费者对这类产品缺乏经验,因此我们希望对产品的安全性进行进一步研究。为了解决这些问题,我们研究了奥地利超市中的 32 种 PBMA。根据 16S rRNA 基因扩增片段测序,大多数产品以乳酸菌(白色念珠菌或拉氏乳杆菌)为主,α-多样性普遍较低。假单胞菌(如假单胞菌和雪旺菌)在另一部分产品中占主导地位。除了 LABs 外,通过培养方法还分离出了多种不同的芽孢杆菌,以及一些肠杆菌科细菌和潜在的致病菌。我们认为,特别是异发酵 LABs 的优势与产品的稳定性和质量有很大关系,有可能延长产品的保质期。虽然分离出的肠杆菌科细菌和潜在病原体数量较少,但它们仍然表明这些产品适合它们的存在。
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引用次数: 0
Author Correction: Precision nutrition to reset virus-induced human metabolic reprogramming and dysregulation (HMRD) in long-COVID 作者更正:精准营养重置病毒诱导的长期慢性乙型肝炎患者人体代谢重编程和失调(HMRD)
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-06 DOI: 10.1038/s41538-024-00267-w
A. Satyanarayan Naidu, Chin-Kun Wang, Pingfan Rao, Fabrizio Mancini, Roger A. Clemens, Aman Wirakartakusumah, Hui-Fang Chiu, Chi-Hua Yen, Sebastiano Porretta, Issac Mathai, Sreus A. G. Naidu
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引用次数: 0
Decellularised plant scaffolds facilitate porcine skeletal muscle tissue engineering for cultivated meat biomanufacturing 脱细胞植物支架促进猪骨骼肌组织工程,用于培养肉类生物制造
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-03 DOI: 10.1038/s41538-024-00262-1
Priyatharshini Murugan, Wee Swan Yap, Hariharan Ezhilarasu, Ratima Suntornnond, Quang Bach Le, Satnam Singh, Jasmine Si Han Seah, Pei Leng Tan, Weibiao Zhou, Lay Poh Tan, Deepak Choudhury
Cultivated meat (CM) offers a sustainable and ethical alternative to conventional animal agriculture, involving cell maturation in a controlled environment. To emulate the structural complexity of traditional meat, the development of animal-free and edible scaffolds is crucial, providing vital physical and biological support during tissue development. The aligned vascular bundles of the decellularised asparagus scaffold were selected to facilitate the attachment and alignment of murine myoblasts (C2C12) and porcine adipose-derived mesenchymal stem cells (pADMSCs). Muscle differentiation was assessed through immunofluorescence staining with muscle markers, including Myosin heavy chain (MHC), Myogenin (MYOG), and Desmin. The metabolic activity of Creatine Kinase in C2C12 differentiated cells significantly increased compared to proliferated cells. Quantitative PCR analysis revealed a significant increase in Myosin Heavy Polypeptide 1 (MYH1) and MYOG expression compared to Day 0. These results highlight the application of decellularised plant scaffold (DPS) as a promising, edible material conducive to cell attachment, proliferation, and differentiation into muscle tissue. To create a CM prototype with biological mimicry, pADMSC-derived muscle and fat cells were also co-cultured on the same scaffold. The co-culture was confirmed through immunofluorescence staining of muscle markers and LipidTOX staining, revealing distinct muscle fibres and adipocytes containing lipid droplets respectively. Texture profile analysis conducted on uncooked CM prototypes and pork loin showed no significant differences in textural values. However, the pan-fried CM prototype differed significantly in hardness and chewiness compared to pork loin. Understanding the scaffolds’ textural profile enhances our insight into the potential sensory attributes of CM products. DPS shows potential for advancing CM biomanufacturing.
栽培肉(CM)为传统畜牧业提供了一种可持续的、符合道德规范的替代品,它涉及细胞在受控环境中的成熟。为了模仿传统肉类的复杂结构,开发不含动物成分且可食用的支架至关重要,它能在组织发育过程中提供重要的物理和生物支持。脱细胞芦笋支架上排列整齐的血管束有助于小鼠成肌细胞(C2C12)和猪脂肪间充质干细胞(pADMSCs)的附着和排列。肌肉分化通过肌肉标记物(包括肌球蛋白重链(MHC)、肌原蛋白(MYOG)和Desmin)的免疫荧光染色进行评估。与增殖细胞相比,C2C12 分化细胞中肌酸激酶的代谢活性明显增加。定量 PCR 分析显示,与第 0 天相比,肌球蛋白重多肽 1(MYH1)和 MYOG 的表达明显增加。这些结果突显了脱细胞植物支架(DPS)的应用前景,它是一种可食用的材料,有利于细胞附着、增殖和分化成肌肉组织。为了创建具有生物仿真性的 CM 原型,还在同一支架上共同培养了源自 pADMSC 的肌肉和脂肪细胞。肌肉标记物的免疫荧光染色和 LipidTOX 染色证实了这种共培养,分别显示出明显的肌肉纤维和含有脂滴的脂肪细胞。对未煮熟的中药原型和猪里脊肉进行的质构分析表明,两者的质构值无明显差异。不过,与猪里脊肉相比,煎煮过的中药原型在硬度和咀嚼感方面有明显差异。了解支架的纹理特征有助于我们深入了解中药产品的潜在感官属性。DPS 显示了推进中药生物制造的潜力。
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引用次数: 0
An innovative molecular approach towards the cost-effective entomological authentication of honey 一种创新的分子方法,用于对蜂蜜进行具有成本效益的昆虫鉴定
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-05-02 DOI: 10.1038/s41538-024-00268-9
Guozhi Zhang, Yanzheng Zhang, Bin Yuan, Ruth Tiang En, Shanshan Li, Huoqing Zheng, Fuliang Hu
Honey authentication and traceability are crucial not only for economic purposes but also for ensuring safety. However, the widespread adoption of cutting-edge technologies in practical applications has been hampered by complex, time-consuming sample pre-treatment processes, the need for skilled personnel, and substantial associated expenses. This study aimed to develop a simple and cost-effective molecular technique to verify the entomological source of honey. By utilizing newly designed primers, we successfully amplified the mitochondrial 16S ribosomal RNA gene of honey bees from honey, confirming the high quality of the extracted DNA. Employing RFLP analysis with AseI endonuclease, species-specific restriction patterns were generated for honey derived from six closely related honey bees of the Apis genus. Remarkably, this method was proven equally effective in identifying heat-treated and aged honey by presenting the same RFLP profiles as raw honey. As far as we know, this is the initial research of the simultaneous differentiation of honey from closely related honey bee species using the restriction endonuclease AseI and mitochondrial 16S rRNA gene fragments. As a result, it holds tremendous potential as a standardized guideline for regulatory agencies to ascertain the insect origins of honey and achieve comprehensive traceability.
蜂蜜的鉴定和可追溯性不仅对经济目的至关重要,而且对确保安全也至关重要。然而,复杂、耗时的样品预处理过程、对熟练人员的需求以及大量的相关费用阻碍了尖端技术在实际应用中的广泛采用。本研究旨在开发一种简单且经济有效的分子技术来验证蜂蜜的昆虫学来源。通过使用新设计的引物,我们成功地从蜂蜜中扩增出蜜蜂线粒体 16S 核糖体 RNA 基因,证实了所提取 DNA 的高质量。通过使用 AseI 内切酶进行 RFLP 分析,我们得出了来自六种近缘蜜蜂的蜂蜜的物种特异性限制模式。值得注意的是,这种方法在鉴别热处理蜂蜜和陈酿蜂蜜时同样有效,其 RFLP 图谱与原蜜相同。据我们所知,这是利用限制性内切酶 AseI 和线粒体 16S rRNA 基因片段同时区分近缘蜜蜂蜂蜜的首次研究。因此,它作为监管机构确定蜂蜜昆虫来源和实现全面溯源的标准化指南,具有巨大的潜力。
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引用次数: 0
Edible mycelium as proliferation and differentiation support for anchorage-dependent animal cells in cultivated meat production 可食用菌丝体在肉类栽培生产中为依赖锚定的动物细胞提供增殖和分化支持
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-04-30 DOI: 10.1038/s41538-024-00263-0
Minami Ogawa, Alex S. Kermani, Mayrene J. Huynh, Keith Baar, J. Kent Leach, David E. Block
Cultivated meat production requires bioprocess optimization to achieve cell densities that are multiple orders of magnitude higher compared to conventional cell culture techniques. These processes must maximize resource efficiency and cost-effectiveness by attaining high cell growth productivity per unit of medium. Microcarriers, or carriers, are compatible with large-scale bioreactor use, and offer a large surface-area-to-volume ratio for the adhesion and proliferation of anchorage-dependent animal cells. An ongoing challenge persists in the efficient retrieval of cells from the carriers, with conflicting reports on the effectiveness of trypsinization and the need for additional optimization measures such as carrier sieving. To surmount this issue, edible carriers have been proposed, offering the advantage of integration into the final food product while providing opportunities for texture, flavor, and nutritional incorporation. Recently, a proof of concept (POC) utilizing inactivated mycelium biomass derived from edible filamentous fungus demonstrated its potential as a support structure for myoblasts. However, this POC relied on a model mammalian cell line combination with a single mycelium species, limiting realistic applicability to cultivated meat production. This study aims to advance the POC. We found that the species of fungi composing the carriers impacts C2C12 myoblast cell attachment—with carriers derived from Aspergillus oryzae promoting the best proliferation. C2C12 myoblasts effectively differentiated on mycelium carriers when induced in myogenic differentiation media. Mycelium carriers also supported proliferation and differentiation of bovine satellite cells. These findings demonstrate the potential of edible mycelium carrier technology to be readily adapted in product development within the cultivated meat industry.
与传统细胞培养技术相比,培养肉的生产需要优化生物工艺,以实现高出多个数量级的细胞密度。这些工艺必须通过实现每单位培养基的高细胞生长生产力,最大限度地提高资源效率和成本效益。微载体(或称载体)与大规模生物反应器的使用兼容,并为依赖锚定的动物细胞的粘附和增殖提供了较大的表面积与体积比。如何从载体中有效回收细胞一直是个难题,关于胰蛋白酶化的效果以及是否需要采取其他优化措施(如筛分载体)的报道相互矛盾。为了解决这个问题,人们提出了可食用载体,它具有与最终食品一体化的优势,同时还能提供质地、风味和营养成分。最近,一项利用从可食用丝状真菌中提取的灭活菌丝体生物质的概念验证(POC)证明了其作为肌细胞支撑结构的潜力。然而,该概念验证依赖于哺乳动物细胞系模型与单一菌丝种类的结合,限制了其在肉类培养生产中的实际应用。本研究旨在推进 POC 的发展。我们发现,构成载体的真菌种类会影响 C2C12 成肌细胞的附着--其中来自黑曲霉的载体能促进最好的增殖。在成肌分化培养基中诱导时,C2C12 成肌细胞能有效地在菌丝体载体上分化。菌丝体载体还支持牛卫星细胞的增殖和分化。这些研究结果表明,可食用菌丝体载体技术可随时用于肉类栽培业的产品开发。
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引用次数: 0
Distinguishable short-term effects of tea and water drinking on human saliva redox 喝茶和喝水对人体唾液氧化还原作用的短期区别
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-04-22 DOI: 10.1038/s41538-024-00266-x
Xiangyu Meng, Pik Han Chong, Lijing Ke, Pengwei Zhang, Li Li, Binbin Song, Zhaoshuo Yu, Pingfan Rao
Food consumption can alter the biochemistry and redox status of human saliva, and the serving temperature of food may also play a role. The study aimed to explore the immediate (3 min) and delayed (30 min) effects of hot tea (57 ± 0.5 °C) ingestion and cold tea (8 ± 0.5 °C) ingestion on the salivary flow rate and salivary redox-relevant attributes. The saliva was collected from 20 healthy adults before, 3-min after and 30-min after the tea ingestion. The hot or cold deionised water at the same temperatures were used as control. The salivary flow rate and redox markers in hot tea (HBT), cold tea (CBT), hot water (HW) and cold water (CW) group were analysed and compared. The results demonstrated that neither the black tea nor the water altered the salivary flow rate; the black tea immediately increased the salivary thiol (SH) and malondialdehyde (MDA) content while reduced salivary uric acid (UA) significantly. The tea ingestion showed a tendency to elevate the ferric reducing antioxidant power (FRAP) in saliva, although not significantly. The water ingestion decreased the MDA content immediately and increased the UA level significantly. Cold water was found to induce a greater delayed increase in total salivary total protein (TPC) than the hot water. In conclusion, the black tea ingestion affects the redox attributes of human saliva acutely and significantly, while the temperature of drink makes the secondary contribution.
进食会改变人体唾液的生物化学和氧化还原状态,食物的食用温度也可能起到一定作用。本研究旨在探讨摄入热茶(57 ± 0.5 °C)和冷茶(8 ± 0.5 °C)对唾液流速和唾液氧化还原相关属性的即时(3 分钟)和延迟(30 分钟)影响。研究收集了 20 名健康成年人在饮茶前、饮茶后 3 分钟和饮茶后 30 分钟的唾液。以相同温度的热去离子水或冷去离子水作为对照。分析并比较了热茶组(HBT)、冷茶组(CBT)、热水组(HW)和冷水组(CW)的唾液流速和氧化还原标志物。结果表明,红茶和水都不会改变唾液流速;红茶会立即增加唾液中硫醇(SH)和丙二醛(MDA)的含量,同时显著降低唾液中尿酸(UA)的含量。摄入茶叶后,唾液中的铁还原抗氧化能力(FRAP)有上升趋势,但并不明显。摄入水能立即降低 MDA 含量,并显著增加尿酸水平。与热水相比,冷水诱导唾液总蛋白(TPC)延迟增加的程度更大。总之,摄入红茶会对人体唾液的氧化还原属性产生急性和显著的影响,而饮料的温度则起次要作用。
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引用次数: 0
Monitoring Indian “Superfood” Moringa oleifera Lam. – species-specific PCR-fingerprint-based authentication for more consumer safety 监测印度 "超级食品 "Moringa oleifera Lam.- 基于物种特异性 PCR 指纹鉴定,提高消费者安全
IF 6.4 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-04-13 DOI: 10.1038/s41538-024-00264-z
Sascha Wetters, Vaidurya Sahi, Lena Brosche, Annette Häser, Peter Nick
Moringa oleifera Lam. has become one of the major new superfoods commonly available in the aisles of bio-shops and health-food sections in supermarkets of North America and Europe. While most of these products appear under the generic and scientifically inconclusive term “Moringa”, the European Union, so far, has allowed commercialisation for the use in food and feed for M. oleifera only. M. oleifera is indigenous to India and South Asia, but large-scale cultivation of this species has spread to the tropical regions on all continents, with a strong focus on Africa, leading to a high risk of admixture with species like M. stenopetala (Baker f.) Cufod. that is native to Africa. In the present study, we have characterised six species of Moringa in order to develop a simple and robust authentication method for commercial products. While the plants can be discriminated based on the pinnation of the leaves, this does not work for processed samples. As alternative, we use the plastidic markers psbA-trnH igs and ycf1b to discern different species of Moringa and develop a diagnostic duplex-PCR that clearly differentiates M. oleifera from other Moringa species. This DNA-based diagnostic assay that does not rely on sequencing was validated with commercial products of “Moringa” (including teas, powders, or capsules). Our method provides a robust assay to detect adulterations, which are economically profitable for costly superfood products such as “Moringa”.
Moringa oleifera Lam.已成为北美和欧洲超市生物商店和健康食品区常见的主要新型超级食品之一。虽然这些产品中的大多数都使用了 "Moringa "这个在科学上没有定论的通用术语,但欧盟迄今为止只允许将油橄榄用于食品和饲料的商业化。M. oleifera 原产于印度和南亚,但该物种的大规模种植已蔓延到各大洲的热带地区,主要集中在非洲,导致与原产于非洲的 M. stenopetala (Baker f.) Cufod.等物种混种的高风险。在本研究中,我们对六种辣木进行了特征描述,以便为商业产品开发一种简单、可靠的鉴定方法。虽然可以根据叶片的羽状复叶来区分植物,但这对加工过的样品并不适用。作为替代方法,我们使用质体标记 psbA-trnH igs 和 ycf1b 来分辨辣木的不同种类,并开发了一种诊断性双链聚合酶链式反应(duplex-PCR),可明确区分 M. oleifera 和其他辣木种类。这种不依赖测序的基于 DNA 的诊断方法已通过 "Moringa "的商业产品(包括茶、粉末或胶囊)进行了验证。我们的方法为检测掺假提供了一种可靠的检测方法,而掺假对于像 "Moringa "这样成本高昂的超级食品来说是有利可图的。
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NPJ Science of Food
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