红曲色素提取条件及结构表证

以乙醇为溶剂,从红曲中提取红曲色素。探讨了提取条件对提取率的影响,并用FTIR和UV对色素结构进行了表征。结果表明,最佳乙醇浓度为70％～80％,在此条件下提取5次,提取率可达到90％。在提取的头一小时内,浸出速率较高,提高温度有利于提高提取液浓度和降低乙醇用量。增大乙醇对红曲的用量比例,虽然有利于提高浸出率,但是会明显增加乙醇耗量。     

玫瑰茄花色素的提取工艺研究

通过单因素和正交实验对玫瑰茄花色素提取工艺条件进行了比较筛选和优化。结果表明:玫瑰茄花色素提取的适宜溶剂为乙醇,适宜的酸碱度为p H 2.0;影响提取效果因素依次是提取时间、乙醇浓度、温度、料液比;最佳提取工艺条件为粉碎粒度40目、乙醇浓度70%(V∶V)、提取温度40℃、提取时间1.5 h、最佳料液比1∶20,在此优化条件下,玫瑰茄花色素的提取率可达0.485%。     

注射用高纯度蛋黄卵磷脂制备新工艺的研究

本文探索建立了一条以新鲜蛋黄为原料,以乙醇为唯一提取溶剂,制备高纯度注射用蛋黄卵磷脂的新工艺。首先,用4倍重量的96%(v/v)乙醇作为沉淀剂将新鲜蛋黄中的蛋白质沉淀为滤饼,得到初级提取液;然后,再用4倍重量的96%(v/v)乙醇对滤饼抽提3次,提取残余卵磷脂,得到次级提取液。合并提取液,置9℃下静置分层,除去大部分蛋黄油。所得上清液上硅胶柱,用86%(v/v)的乙醇作为洗脱剂,纯化蛋黄卵磷脂,经高效液相色谱检测纯度达98%。并对提取过程进行了优化,得到最佳工艺条件:35℃的96%乙醇溶液,添加量为1∶4(w/w)提取蛋黄液,180 rpm转速下搅拌10 min。抽滤后,用60℃的96%乙醇提取滤饼3次,料液比为1∶4,静置15 min。最佳工艺条件下,蛋黄卵磷脂的提取率可达93.38%。     

黑米中花青苷色素的测定方法研究

以 4种黑米为实验材料 ,用酸性乙醇作为提取溶剂 ,以色价值为色素含量的评价依据 ,研究了时间、温度、提取批次和脱脂对黑米中花青苷色素提取的影响。结果表明 :80℃ ,酸性乙醇 ,6 0min重复提取 2次 ,可实现 90 %以上的色素溶出。在最大吸收峰 5 35nm处测定提取液的ABS值 ,计算色价 ,作为黑米中花青苷色素的测定方法 ,可用于黑米品质分析     

超声法提取虎杖色素及其稳定性的研究

用乙醇作为提取溶剂,以提取得率和色价为评价指标,通过单因素实验,探讨料液比、提取温度、超声功率、提取时间、乙醇体积分数对色素提取效果的影响;通过正交实验优化提取条件,并对提取的色素进行了稳定性考察。实验结果表明:虎杖色素的最佳提取工艺条件为乙醇体积分数80%,料液比1∶30,超声温度25℃,超声功率50 W,超声时间20 min,其中料液比为显著影响因素;虎杖色素对热、光、蔗糖、NaCl、维生素C(Vc)等因素的影响较稳定,而pH、H2O2、柠檬酸对虎杖色素稳定性影响较大。     

真眼点藻类色素的提取与测定方法

分别采用甲醇、乙醇和丙酮3种有机溶剂提取7种真眼点藻的色素,比较3种有机溶剂提取色素的效果,测定3种有机溶剂色素提取液的吸收光谱,利用分光光度法计算藻的叶绿素a和类胡萝卜素的含量,并比较甲醇和乙醇色素提取液在A₄₇₀和A₆₆₆的最大吸收峰。结果表明:使用乙醇比甲醇和90%丙酮操作更简便、快捷并且毒害低。3种有机溶剂色素提取液的叶绿素a和类胡萝卜素的含量均无显著性差异(P>0.05),提取率基本一致。色素在3种有机溶剂中的吸收光谱相似,甲醇和乙醇的色素提取液在A₄₇₀和A₆₆₆的最大吸收峰并无显著性差异(P>0.05)。乙醇色素提取液可使用Lichtenthaler的公式计算色素含量。     

老龙皮总氨基酸的提取工艺研究

通过单因素选择和正交设计法,以老龙皮总氨基酸含量为指标,分别对乙醇浓度、料液比、提取温度、提取时间等因素进行考查,优选老龙皮总氨基酸的最佳提取条件。结果显示料液比对总氨基酸提取率影响最大,最佳提取条件为60%乙醇作提取液,料液比(W/V)为1∶20,在70℃提取3 h。     

紫山药色素的提取工艺及抗氧化性能研究

研究紫山药色素的最佳提取工艺及其抗氧化性能。在单因素试验的基础上,采用L9(34)正交试验法,以pH示差法测定花色苷得率为考察指标,优化了溶剂提取法提取紫山药色素的工艺参数。通过DPPH体系测定该色素清除自由基能力。试验结果表明:紫山药色素属于花色苷类物质,优化的紫山药色素提取条件为:提取温度60℃,提取时间80 min,料液比1∶30,提取溶剂为0.5%盐酸乙醇溶液,提取液花色苷含量可达2.075mg/鲜紫山药g。紫山药色素提取液清除DPPH自由基的IC50为98.14μg/mL。紫山药具有开发功能性色素的潜力。     

醇沉条件和干燥方式对毛头鬼伞子实体多糖品质的影响

为改善毛头鬼伞子实体多糖的性状,以粗多糖得率、多糖含量、吸潮性及色素含量为指标,对乙醇沉淀制备多糖的参数进行了优化。结果表明:子实体经提取后浓缩至浓缩比为1∶2,即m(物料干质量/g)∶V(提取液/m L)=1∶2时以60%乙醇沉淀,再以60%乙醇洗涤1次,经冷冻干燥所得粗多糖产品多糖含量较高、色浅,且吸潮性降低,性状得到明显改善。     

正交试验法优选超声提取知母皂甙的研究

用正交实验法对知母(Anemarrhena asphodeloides Bge.)中总皂甙的超声提取工艺进行了研究,采用正交表L9(34),以提取剂的体积分数、料液比(mA∶VB)、提取时间以及提取次数为因素,以知母总皂甙元的含量为指标,用紫外分光光度计法进行检测,所得提取液经大孔树脂纯化,得到的最佳提取参数和结果为:以φ(乙醇)=75%的水溶液为提取剂、提取料液比mA∶VB=1∶8、提取次数2次、每次30min,提取率92.8%,纯度91.0%。结果证明了对知母而言,超声提取法是一种提取效率高、操作简便、省时的方法。     

辣椒红色素稳定性研究

本文对辣椒红色素的稳定性进行了研究。结果表明,色素样品的耐热、耐酸碱性较好;室内光线下,放置四周不褪色。但置于室外强阳光下曝晒,两小时后即褪色;常见金属离子中,Ｃｕ２＋可使色素立即褪色,而Ｆｅ３＋、Ａｌ３＋、Ｓｎ２＋对色素影响较小     

A novel system for separation and purification of egg pigments from the nondiapause red-egg mutant Re-nd in the silkworm,Bombyx mori

Re-nd, which was induced from the wild-type C108 by the chemical mutagen N-methane-N-methylnitrourea, is a nondiapause red-egg mutant of silkworm Bombyx mori. The special significance of the Re-nd mutant is that it is an independent dominant mutant. The aim of this study was to establish the type of pigment responsible for the red coloration in the Re-nd mutant eggs in silkworm. We compared the eggs of Re-nd mutants with those of the other B. mori egg color strains and confirmed that the Re-nd mutant is the only strain with red color and red pigment granules in nondiapause, showing this mutant belongs to the pigmentation in the serosa. We speculated that the red substance, which contributed to the bright red pigmentation for nondiapause eggs of the Re-nd mutant, could potentially be a novel pigment according to its solubility, optimum absorption peak, and oxidation–reduction reaction. Moreover, we have successfully constituted the system for enrichment, extraction, and purification of the red substance responsible for the Re-nd mutant, providing a new method for the separation and purification of other known and unknown pigments or substances.     

栀子色素研究的进展

从栀子果中可提制出黄色、蓝色、天蓝色、红色等色素。本文详尽评述了栀子黄和栀子蓝的提制和纯化分离的各种技术,并指出了今后的发展方向。     

Copepod feeding behavior and the measurement of grazing rates in vivo and in vitro

In this paper some aspects of the use of the gut fluorescence method for estimating ingestion rates have been, examined. One assumption is that gut turnover time in feeding copepods is equal to the gut clearance time in filtered seawater. When arctic Pseudocalanus were pre-fed on Thalassiosira weisflogii, and then given a trace addition of the same C¹⁴-labelled culture, or were transferred to filtered seawater, results suggested that this assumption was probably justified. In another experiment in which Pseudocalanus were fed at the same concentration of either melted ice algae, or pelagic under ice algae, there were significant differences in both gut clearance times and gut pigment levels in the two cases.Pigment: biogenic silica ratios in epontic algae were higher than those in faecal pellets produced by Pseudocalanus feeding on the algae, suggesting that pigment destruction was occurring during grazing. In a 28 hr time course experiment ingestion rates determined by rate of disappearance of particulate chlorophyll were higher than those simultaneously determined by the gut fluorescence method, which also supports the idea of pigment destruction in copepods guts.     

我国植物食用色素资源开发利用评价

古代人们使用的着色剂都是天然产品,除少数矿物颜料外,主要是植物源色素。我国古代就有以红曲米作为着色剂利用的习惯;在高等植物方面,生产蓝色、黄色、绿色的颜料的高等植物种类不少,大多沿用至今。自19世纪中叶以后,人工合成色素以着色牢固、鲜艳、成本低廉等特点,迅速占领了印染、食品等许多行业,但20世纪60年代以后,许多研究表明,一般合成色素都有程度不等的毒性,特别是化学结构含偶氮型的色素有可能在人体内成为致癌物。同时,在色素合成的过程中,还有可能污染有重金属及其他有害物质。因此,合成色素越来越使人们感到不安全。从20世纪50年代的100多种人工合成色素用于食品着色,到20世纪末,已有60~70余种被禁用了,而植物食用色素在食品行业中成为主要着色剂。近年来又涌现出多种有价值的高等植物源色素,我们选择其主要一些植物种类做些介绍,供有关方面参考。     

禽类蛋壳颜色及其基因的遗传研究进展

禽类的蛋壳具有白色、青色及褐色３种颜色, 特别是鸡和鸭的青壳蛋因外观美观, 口感好, 营养价值高, 蛋壳硬度和强度高于白壳蛋而具有较好的市场前景。但依据表型培育青壳鸡或鸭品系存在误选, 因而研究蛋壳颜色的形成及控制机理具有重要的理论及现实意义。文章主要介绍了禽类蛋壳颜色的种类、色素组成及其合成, 它的可遗传性、遗传力大小、遗传模式, 控制蛋壳颜色的基因数量及其相互之间的显隐性关系, 以期为揭示蛋壳颜色的形成机理提供参考。     

Phototrophic pigment production with microalgae: biological constraints and opportunities

There is increasing interest in naturally produced colorants, and microalgae represent a bio‐technologically interesting source due to their wide range of colored pigments, including chlorophylls (green), carotenoids (red, orange and yellow), and phycobiliproteins (red and blue). However, the concentration of these pigments, under optimal growth conditions, is often too low to make microalgal‐based pigment production economically feasible. In some Chlorophyta (green algae), specific process conditions such as oversaturating light intensities or a high salt concentration induce the overproduction of secondary carotenoids (β‐carotene in Dunaliella salina (Dunal) Teodoresco and astaxanthin in Haematococcus pluvialis (Flotow)). Overproduction of all other pigments (including lutein, fucoxanthin, and phycocyanin) requires modification in gene expression or enzyme activity, most likely combined with the creation of storage space outside of the photosystems. The success of such modification strategies depends on an adequate understanding of the metabolic pathways and the functional roles of all the pigments involved. In this review, the distribution of commercially interesting pigments across the most common microalgal groups, the roles of these pigments in vivo and their biosynthesis routes are reviewed, and constraints and opportunities for overproduction of both primary and secondary pigments are presented.     

Isolation of two novel purple naphthoquinone pigments concomitant with the bioactive red bikaverin and derivates thereof produced by Fusarium oxysporum

Filamentous fungi have gained growing interest as sources of diverse pigmented secondary metabolites. Some specific polyketides from Ascomycetous species have demonstrated a wide range of industrial applications in food, cosmetic, textile, and in the design of pharmaceutical products. The formulation of recipes containing fungal polyketides has increased over recent years. Fusarium strains were proven useful to mankind in a variety of technologies. Nevertheless, there is still need of new isolates of Fusarium for use in emerging and already existing fields. In this article, we report the concomitant production of the bioactive red bikaverin along with two novel purple pigments by the phytopathogenic Fusarium oxysporum LCP531 strain isolated from soil. In literature, the production of purple pigment had only been described in cultures of Fusarium Fujikuroi, Fusarium verticillioides, and Fusarium graminearum. The production of these naphthoquinonic pigments, their distribution (either produced in mycelia or excreted in liquid medium) and their chemical profiles were investigated with respect to nutrient composition. The pigments were extracted by using a pressurized liquid extraction method, monitored by colorimetric analysis and characterized by HPLC-DAD chromatography. To our knowledge, this is the first report of these two novel wild-type purple naphtoquinones pigments along with bikaverin, where additionally, the culture conditions were put into perspective to optimize fermentation cultures and extraction process accordingly to the pigment/biomolecule desired. These colored naphthoquinones should be promising fungal functional compounds which could be expected to have a place of choice, along with other antibacterial, antifungal, antiviral, anticancer, and antineoplastic derivatives. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 35: e2738, 2019     

Autofluorescence method to measure macular pigment optical densities fluorometry and autofluorescence imaging

Non-invasive measurement of the optical density of the human macular pigment by the autofluorescence method takes advantage of the fluorescence of lipofuscin in the human retinal pigment epithelium. Measuring the intensity of fluorescence above 550 nm, where macular pigment has essentially zero absorption, and stimulating the fluorescence with two wavelengths, one well absorbed by macular pigment and the other minimally absorbed by macular pigment, provides a single-pass measurement of the macular pigment optical density. The method is implemented either by fluorometry of lipofuscin to yield the optical density of the macular pigment in a 2 degrees diameter central area, or by autofluorescence imaging to yield a high-resolution map of the macular pigment distribution.     

山蓝色素前体的分子组成和化学变化

山蓝色素前体是很不稳定的化合物。用液相色谱-核磁共振谱联用的技术,结合紫外光谱的变化,研究山蓝色素前体的分子组成及化学变化。表明山蓝色素前体分子有由2个紫蓝氨酸残基和1个氨基酚残基键合而成的片段,在室温下放置后,氨基酚结构转变为醌结构。研究结果为山蓝色素前体、山蓝色素及其相关化合物的结构测定提供了重要数据,为山蓝色素的化学、山蓝色素形成机理的阐明起到了关键作用。