Effects of germination and kilning on the phenolic compounds and nutritional properties of quinoa (Chenopodium quinoa) and kiwicha (Amaranthus caudatus)

Quinoa (Chenopodium quinoa) and kiwicha (Amaranthus caudatus) are nutritious pseudocereals that originate from the Andean region. The aim of this research was to study the effect of germination and the subsequent kilning on the phenolic compounds and proximate composition in selected Peruvian varieties of quinoa (“Chullpi”) and kiwicha (“Oscar Blanco”). The germination process was carried out for 24, 48 and 72 h at 22 °C, and the kilning was performed with samples germinated for 72 h by drying the seeds at 90 °C for 5 min. Both processes increased the protein content of the samples. However, lipid content was reduced during germination. On the other hand, germination and kilning clearly increased the concentration of total phenolic compounds in both quinoa and kiwicha. Germination for 72 h either with or without kilning process resulted in a significant (p < 0.05) increase in the total content of phenolics compared to untreated materials, which was especially due to coumaric acid and a kaempferol tri-glycoside in quinoa and caffeoylquinic acid in kiwicha. Based on the results, germination and kilning may improve the nutritional quality of the Andean grains, encouraging the usage of the processed grains as ingredients in functional products for people with special gluten-free or vegetarian diets.     

快速滤过型净化法结合高效液相色谱-串联质谱同时检测人参中的5种农药残留

基于人参样品基质特点，采用快速滤过型净化法 (m-PFC) 结合高效液相色谱-串联质谱 (HPLC-MS/MS)，建立了人参中嘧菌酯、苯醚甲环唑、吡虫啉、茚虫威和噻嗪酮5种农药残留同时检测的分析方法。该方法具有较低的检出限 (0.03~0.18 μg/kg) 和定量限 (0.11~0.59 μg/kg)，其定量限较中国国家标准GB 2763—2016中规定的对人参中苯醚甲环唑和嘧菌酯的最大残留限量 (MRL) (0.5~1 mg/kg) 低3个数量级，5种农药的线性范围在1~500 μg/L之间。在2、10、50、100和300 μg/kg的添加水平下，方法的平均回收率均在76%~115%之间，相对标准偏差 (RSD) 均小于11%，回收率较好且方法稳定。与传统样品前处理方法相比，该方法具有操作简单、省时省力和灵敏度高等优点。将该方法应用于市售6份人参样品中5种农药残留的检测，结果未检出相应的农药残留。该方法为研发建立更快速、准确地检测人参中农药残留的方法提供了思路，也为后续中国国家标准修订人参中农药最大残留限量提供了参考。     

柚木石油醚抽提物成分及其对心边材颜色的影响

为探究国产柚木抽提物对心材和边材颜色差异的影响,采用3种沸程的石油醚溶液分别对国产柚木的心材与边材进行抽提处理,利用气相色谱-质谱法分析抽提液的成分和含量,并以差异较大的抽提物溶液处理柚木边材,通过色度学参数表征柚木边材的变色情况,从而验证影响柚木心材和边材颜色的主要抽提物成分。结果表明:在3种沸程的石油醚抽提液中,柚木心材抽提物在成分种类数量和含量上均显著高于边材;不同沸程的石油醚对柚木心、边材中抽提物成分有一定的影响,其中30~60℃(低沸程)和60~90℃(中沸程)石油醚抽提物成分和含量的差异较小,而90~120℃(高沸程)石油醚抽提物的含量较高,约为中、低沸程抽提物含量的2倍;柚木心材抽提液中酚类、醌类、烯烃类物质的含量较多,但这些物质在边材中含量极低;4-叔丁基-2-苯基苯酚、2-甲基蒽醌(柚木醌)、全反式三十碳六烯(角鲨烯)是柚木心、边材抽提物含量差异最明显的物质。经角鲨烯溶液处理后的柚木边材表面颜色变黄,更接近心材颜色,因此,角鲨烯是导致柚木心边材颜色差异的重要抽提物成分。     

超高效液相色谱串联质谱法对水产品中硝基呋喃代谢物的测定

建立了使用Waters UPLC Xevo TQ超高效液相色谱串联质谱仪检测水产品中4种硝基呋喃代谢物的分析方法。匀浆后的样品在酸性环境下水解,并用2-硝基苯甲醛衍生16h,经磷酸氢二钾提取,LMS固相萃取小柱净化后,在三重四极杆多反应监测模式下进行测定。方法采用同位素内标法定量,四种代谢物的检出限(LOD)均低于0.25μg·kg-1,线性范围在0.5μg·L~(-1)到10μg·L~(-1)间,相关系数大于0.99。在0.5、1.0和5μg·kg-1浓度下分别进行添加回收试验(n=5),回收率在75.2%~123.3%之间,相对标准偏差(RSD)小于9.4%。     

原子吸收光谱法检测大蒜制品中微量元素锗

[目的]研究不同大蒜制品中锗元素含量的差别。[方法]采用马弗炉灰化样品,火焰原子吸收光谱法测定以金乡紫皮蒜为原料加工而成的黑蒜、蒜蓉辣酱、脱水蒜片、蒜粉、糖醋蒜5种制品中锗的含量。[结果]试验表明,黑蒜中锗含量为1.384 mg/g,蒜蓉辣酱中锗含量为0.784 mg/g,脱水蒜片中锗含量为0.913 mg/g,蒜粉中锗含量为0.956 mg/g,糖醋蒜中锗含量为0.827 mg/g。5种蒜制品中均含有锗元素,其含量由多到少依次为黑蒜、蒜粉、脱水蒜片、糖醋蒜、蒜蓉辣酱。[结论]研究可为大蒜及大蒜制品的开发利用提供参考依据。     

浅圆仓膜下氮气气调膜上控温储粮试验

通过改造浅圆仓测温电缆,实现了浅圆仓膜下充氮气调和膜上中央空调控温,提高了卸粮口、大门口、通风口等死角的害虫致死率。将浅圆仓氮气气调杀虫与控温储粮相结合,实现了储粮安全度夏。     

半地下带保温夹套发酵罐的应用

通过对半地下带保温夹套的发酵罐与普通发酵罐24 h的温度变化和6 d的产气量的对比试验分析,结果表明:采用半地下带保温夹套发酵罐发酵,24 h的温度变化缓慢,受外界温度变化影响小,高温持续的时间较长,利于微生物发酵;产气总量多,持续时间长。     

木薯渣与甜菜颗粒粕组合效应对奶牛瘤胃发酵特性的影响

本试验旨在通过体外产气法研究木薯渣与甜菜颗粒粕组合用作泌乳中后期奶牛饲料的可行性及适宜组合比例。试验设计7个处理:木薯渣分别以0%(对照组)、5%、10%、15%、20%、25%和30%与甜菜颗粒粕(风干物质基础)组合,使用AGRS-Ⅲ型微生物发酵产气系统进行体外瘤胃微生物发酵试验,监测体外培养3、6、12、24、48h后的发酵液pH、氨态氮(NH3-N)、微生物蛋白(MCP)含量和体外培养48h后干物质消失率(IVDMD)、累积产气量(GP)及挥发性脂肪酸(VFA)含量等指标。结果表明:体外培养48 h后,GP和底物的最大降解率(RmaxS)随木薯渣占比增加呈线性或二次增加(P<0.05);发酵液各VFA和TVFA含量均随木薯渣占比增加呈线性或二次降低(P<0.05);根据多项组合效应值,以0%组为对照时,5%组和10%组表现为正组合效应,其余组合均表现为负组合效应。在本试验条件下,当木薯渣与甜菜颗粒粕组合使用,且木薯渣为5%~10%较为适宜,但此结果仍需奶牛饲养试验进一步验证。     

Chemical and nutritional characteristics of Cannabis sativa L. co-products

Cannabis sativa L. is an annual herbaceous plant. It was used for centuries to obtain different products. In the last century, hemp cultivation was forbidden due to the psychoactive effects of tetrahydrocannabinol acid (THCA). In the last years, new strains, characterized by high cannabidiolic acid (CBDA) and low THCA level, were developed renewing the interest in hemp cultivation to obtain food or to extract essential oils from flowers. All these processes produce many residues with different chemical–physical characteristics. In order to evaluate their potential use also in animal nutrition, some hemp co-products were evaluated. Two different co-products of seed processes (flour and oil) and two co-products obtained trimming the flowers, differing in granulometry were used. The samples were analysed for chemical composition and evaluated in vitro using the gas production technique with buffaloes' ruminal inoculum. All hemp co-products showed interesting nutritional characteristics, such as crude protein content always higher than 20% on a dry matter basis, and high neutral detergent fibre concentration partially lignified. The in vitro gas production parameters at 120 h of incubation showed quite low fermentability testified by the low organic matter degradability and cumulative gas volume (OMD from 28.09 to 45.64% and OMCV from 110 to 164 ml/g, respectively). Also, the methane produced after 24 h of incubation was particularly low (from 1.78 to 11.73 ml/g dOM). These results could be due to the high lipid and ash amounts or to the CBDA content that probably affected the CH₄ formation processes. According to preliminary results obtained by this study, it is possible to hypothesize that these co-products could be useful to mitigate the methane production into the rumen. Further studies are necessary in order to evaluate the correct inclusion into the diet for ruminants.     

一种利用气相色谱快速检测瘤胃体外发酵液中三甲胺浓度的方法

本试验旨在建立一种利用气相色谱快速检测瘤胃体外发酵液中三甲胺浓度的方法。瘤胃体外发酵试验设置2个组,对照组(n=4)和试验组(n=4),试验组每个发酵瓶中添加0.0414 g三甲胺盐酸盐,发酵24 h。采用10 mol/L氢氧化钾溶液对发酵液样品进行预处理,使用WEL-PEG20M色谱柱和氢火焰离子检测器对三甲胺进行分离和检测。利用无三甲胺背景值的发酵培养基上清液配制不同浓度的三甲胺标准液,制备标准曲线。结果显示:三甲胺的标准曲线在0.1~1.0 mg/mL之间具有较好的线性关系(R 2≥0.993),平均回收率为98.44%~100.27%,三甲胺的最低检出限为0.01 mg/mL。对照组0和24 h发酵液均未检出三甲胺。试验组0 h发酵液三甲胺浓度为0.65 mg/mL,24 h发酵液三甲胺浓度为0.12 mg/mL,说明三甲胺被瘤胃微生物大量利用。综上所述,本试验建立的三甲胺检测方法操作步骤简单,准确度和灵敏度相对较高,能够快速准确监测发酵液中三甲胺浓度的变化,为瘤胃微生物三甲胺代谢研究提供了快捷高效的检测方法。