红莲外皮原花青素的纯化与分析

原花青素作为多酚的一大类广泛存在于天然植物中。红莲外皮原花青素粗提取物采用大孔树脂AB-8和聚酰胺柱进行两次纯化。纯化物通过红外光谱（infrared spectrum,IR）和电子喷雾离子化质谱（electrosprayionization-mass spectroscopy,ESI-MS）对成分进行分析,并通过反相液相色谱-质谱（reverse phase high-performanceliquid chromatography- mass spectroscopy,RP-HPLC-MS/MS）联用对组分进行分离鉴定。结果表明：纯化物中有9 种原花青素单体和低聚体,其中包括儿茶素和表儿茶素（m/z 289）、棓儿茶素（m/z 305）,4 种原花青定二聚体的同分异构体（m/z 577）和2 种原花青定四聚体的同分异构体（m/z 1 153）。     

基于近红外光谱技术检测红曲米中的红曲色素

采用近红外光谱技术结合化学计量学方法构建红曲米中红曲橙色素、红曲红色素、红曲黄色素的预测模型。分别采用多元线性回归(SMLR)、偏最小二乘回归(PLS)、主成分回归(PCR)构建所有色素组分的数学模型,以相关系数(R)、校正均方根误差(RMSEC)、预测均方根误差(RMSEP)、预测相对分析偏差(RPD)值来评价模型的综合性能。结果显示,MSC、SNV方法能够消除红曲米粉颗粒不均对光谱的散射影响;导数处理消除了基线漂移;对于红曲橙色素、红曲黄色素、红曲红色素三种模型均具有良好的稳定性;利用三种模型对未知红曲样品预测时,预测结果具有较高的线性,预测性能较好(RPD=2.86~5.39),可用于准确定量预测。结果表明近红外光谱技术可用于红曲色素的快速无损测定,为红曲米质量的智能化控制提供了新的途径。     

Steviol glycosides are not altered during commercial extraction and purification processes

Steviol glycosides, sweet diterpenes extracted from the shrub Stevia rebaudiana Bertoni, are approved as sweeteners in many countries throughout the world. Former heat and pH‐investigations of these glycosides have established their stability. However, due to the complex purification process, the natural authenticity has still been discussed and challenged, recently. Thus, the objective of this work was to show that the steviol glycosides are not chemically modified during the commercial extraction and purification process. Therefore, samples of three independent commercial‐scale extraction and purification batches of steviol glycosides, each batch containing a sample of the untreated stevia leaves, the first water extract and the high‐purity end product, were analysed using HPLC‐UV and HPLC‐ESI‐MS/MS. The results show that the commercial powders of extracted steviol glycosides with an estimated purity of more than or equal to 95% contain the same steviol glycosides as the dried stevia leaves and their hot water infusions, demonstrating that steviol glycosides are not affected by the purification process.     

Metabolomics reveals consistency of the shoot system in Medicago truncatula by HPLC‐UV‐ESI‐MS/MS

Flavonoids not only play crucial roles in plant development and resistance, but also provide one of the major natural sources in human nutrition. To investigate the distribution of flavonoids in the shoot system of Medicago truncatula, a high‐performance liquid chromatography coupled with electrospray ionisation tandem mass spectrometer (HPLC‐ESI‐MS/MS) method was established and then applied to determine the quantitation of flavonoids in different parts of the plant. There were twenty‐two, fifteen and eleven different kinds of flavonoids identified from the flower, leaf and stem of M. truncatula, respectively. The identified constituents were either aglycone or glycosides of the typical flavonoid backbones, such as myricetin, quercetin, luteolin, kaempferol, tricin, apigenin and laricitrin. It was found that the shoot system of M. truncatula can be differentiated by flavonoids in terms of structures and contents. Our results provide instruction to utilise the shoot system of legume crops as fodder and herb medicine in the future.     

Emerging Spectroscopic and Spectral Imaging Techniques for the Rapid Detection of Microorganisms: An Overview

Microorganism contamination and foodborne disease outbreaks are of public concern worldwide. As such, the food industry requires rapid and nondestructive methods to detect microorganisms and to control food quality. However, conventional methods such as culture and colony counting, polymerase chain reaction, and immunoassay approaches are laborious, time‐consuming and require trained personnel. Therefore, the emergence of rapid analytical methods is essential. This review introduces 6 spectroscopic and spectral imaging techniques that apply infrared spectroscopy, surface‐enhanced Raman spectroscopy, terahertz time‐domain spectroscopy, laser‐induced breakdown spectroscopy, hyperspectral imaging, and multispectral imaging for microorganism detection. Recent advances of these technologies from 2011 to 2017 are outlined. Challenges in the application of these technologies for microorganism detection in food matrices are addressed. These emerging spectroscopic and spectral imaging techniques have the potential to provide rapid and nondestructive detection of microorganisms. They should also provide complementary information to enhance the performance of conventional methods to prevent disease outbreaks and food safety problems.     

Antiglycation capacity and antioxidant activities of different pigmented Thai rice

This study investigated the antiglycation capacity and antioxidant activities of fifteen Thai rice varieties. Purple variety, Kum Rai showed the highest value of total phenolic content (245.06 ± 7.87 mg GAE/gram extract dry weight), DPPH radical scavenging activity (92.33 ± 0.49 mg Trolox/gram extract dry weight), ABTS radical scavenging activity (221.01 ± 0.25 mg Trolox/gram extract dry weight) and percentage inhibition of AGEs formation (82.03 ± 0.19%). We found that, total phenolic content and antioxidant activities (ABTS and DPPH assay) in rice varieties were highly correlated (P < 0.05) with their antiglycation capacity. These results indicated that the total phenolic content was responsible for antioxidant and antiglycation capacities of rice samples. This study is the first report on a correlation between anti‐AGEs capacity and antioxidant activities of Thai rice varieties. Our data have provided useful information for selection of rice varieties for the bioactive compounds that may improve the health of the aged and diabetic complications.     

Anti‐inflammatory properties of high pressure‐assisted extracts of Grifola frondosa in lipopolysaccharide‐activated RAW 264.7 macrophages

The aim of this study was to determine the in vitro anti‐inflammatory properties of the shake extract (SE) and the high pressure‐assisted extract (PE) of the mycelia of Grifola frondosa in a lipopolysaccharide‐stimulated RAW 264.7 macrophage model. The content of total polysaccharides and β‐glucans of PE at 600 MPa (PE‐600) was 41.2 and 6.2 mg g^?1 dry weight, respectively, which were significantly higher than SE extracts. The results showed that treatment with 500 μg mL^?1 of PE by 600 MPa (PE‐600) did not reduce RAW 264.7 cell viability but did significantly inhibit the production of LPS‐induced NO, PGE₂ and intracellular ROS. The PE‐600 inhibited the activation of NF‐kB and then reduced the production of LPS‐induced TNF‐α, IL‐6 and IL‐1β in a dose‐dependent manner. Thus, the PE could be used as an alternative extraction method for improving the extraction efficacy of G. frondosa and serve as an alternative source of anti‐inflammatory agents.     

Volatile organic compounds associated with milk spoilage by psychrotrophic bacteria

The volatile organic compounds of milk contaminated with psychrotrophic bacteria were studied by HS‐SPME and GC/MS. Pseudomonas fluorescens PS14, Pseudomonas fragi PS55, Pseudomonas mosselii PS39, Pseudomonas rhodesiae PS62 and Serratia marcescens S92 were inoculated in sterilised milk (2.5% fat) stored at either 5 °C or 10 °C. A total of 47 volatile organic compounds (VOCs) belonging to seven chemical groups were identified in the spoiled milk. Volatile organic compound patterns peculiar to the inoculate bacterial strains were highlighted. 3‐Methylbutan‐1‐ol, 2 methylpropan‐1‐ol, 3‐hydroxybutan‐2‐one, butan‐2,3‐dione, butanoic and hexanoic acids were revealed as potential chemical spoilage indexes of milk spoilage due to the activity of the five psychrotrophic strains studied.     

Κ‐CN gene polymorphism in Nili‐ravi buffalo,Achai and Sahiwal cattle of Pakistan

Kappa‐casein (κ‐CN) is the subtype of casein protein, an important constituent of bovine milk protein. The current study was undertaken to investigate the genetic polymorphism in κ‐CN gene of Nili‐ravi buffalo, Achai and Sahiwal cattle of Pakistan using polymerase chain reaction–restriction fragment length polymorphism (PCR‐RFLP) technique. The Nili‐ravi buffalo was found to be monomorphic (genotype BB only) for κ‐CN gene. Achai cattle were polymorphic for κ‐CN (having three genotypes AA, AB and BB) with a frequency of 0.70, 0.18 and 0.12, respectively, while in Sahiwal cattle, both the genotypes AA and AB were found with genotypic frequencies of 0.92 and 0.08, respectively. The presence of genotype BB in Achai cattle is surprising as it is absent in most of the cattle breeds worldwide.     

Analysis of volatile compounds in L. edodes blanched by hot water and microwave

The comprehensive flavour characterisation and volatile compounds of raw L. edodes, hot water blanching (HB) sample and microwave blanching (MB) sample were comparatively analysed by electronic nose technology and headspace solid‐phase micro‐extraction combined with gas chromatography‐mass spectrometry (HS‐SPME‐GC‐MS). Results indicated that volatile components in L. edodes markedly changed after HB and MB. Volatile compounds of raw L. edodes consisted mainly ketones, sulphide and alcohols, and 3‐octanone, as well as 1‐octen‐3‐one, were the major compounds. The content of ketones and sulphides in blanched samples markedly decreased, while the relative content of aldehydes, hydrocarbons and esters increased, which became the major volatile compounds of treatment samples. In addition, the percentage contents of esters, alcohols and sulphides in MB samples were significantly (P < 0.05) higher than that in HB samples, especially 1‐octen‐3‐ol, which contributes more to mushroom flavour. Therefore, MB is a better pretreatment method of L. edodes processing and cooking according to the results of experiment.     

Detection of Salmonella spp., Yersinia enterocolitica,Listeria monocytogenes and Campylobacter spp. by real‐time multiplex PCR using amplicon DNA melting analysis and probe‐based assay

Syto9 and probe‐based multiplex real‐time PCR assays for simultaneous detection of a group of foodborne pathogens (named SYLC group), targeting Salmonella spp. (invA gene), Yersinia enterocolitica (ystA gene), Listeria monocytogenes (hly gene) and Campylobacter spp. (rrna gene), have been developed. The Syto9 assay generates amplicon DNA melting curve with four peaks of 86.5 ± 0.5, 84 ± 0.5, 81.5 ± 0.5 and 90.5 ± 0.5 °C corresponding Salmonella spp., Y. enterocolitica, L. monocytogenes and Campylobacter spp. targets, respectively. The sensitivities of the Syto9 and TaqMan assays in artificially inoculated chicken wing rinses were in a range of 3.2 × 10² to 3.1 × 10⁴ and 9.8 × 10² to 1.9 × 10⁴ colony‐forming units per millilitre, respectively, depending on the pathogen. All tested target strains (n = 100) were correctly detected by the both assays, whereas nontarget strains (n = 100) demonstrated no cross‐reactivity representing 100% specificity. The assays are suitable for application in qualitative and quantitative detection of SYLC group pathogens in food matrices.