共查询到20条相似文献,搜索用时 15 毫秒
1.
基于固定化酶的化学发光停流法测定D-氨基酸 总被引:2,自引:0,他引:2
基于固定化酶的化学发光停流法测定D-氨基酸封满良,黄玉文,宫志龙,章竹君(陕西师范大学化学系,西安,710062)关键词固定化酶,化学发光,甲壳质,D-氨基酸自从发现人体有关组织及血桨中D-氨基酸的水平与某些疾病有关以来,已报道了许多测定D-氨基酸的... 相似文献
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应用等速电泳法分离并测定了人齿菌斑培养液中的乳酸,测定回收率在94.2%-102.2%之间,相对标准偏差小于4.5%,比较了抗龋者与易感龋者的菌斑在相同培养条件下的乳酸产量,并对不同饥饿时间下菌斑所产的乳酸进行了测定与比较。 相似文献
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研究了高锰酸钾氧化叶酸荧光体系的形成条件,并建立了测定叶酸含量的间接荧光法。在pH为4.0,80℃水浴中,高锰酸钾可将叶酸氧化为蝶呤-6-羧酸,氧化产物的荧光值较叶酸的荧光值大大增强。荧光强度与叶酸浓度在0~1.6 mg.L-1范围内呈线性关系,方法的检出限为51μg.L-1,将此方法应用到孕妇强化奶粉中叶酸含量的测定,RSD为2.52%(n=6)。 相似文献
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甲醛-三氯乙酸沉淀-凯氏定氮法测定牛奶中真蛋白质 总被引:1,自引:0,他引:1
提出了一种有效去除三聚氰胺等非蛋白氮干扰的凯氏定氮法测定牛奶中真蛋白质的含量的方法。在5mL样品中加入甲醛3 mL,漩涡混匀1 min,于70℃水浴加热10 min后,加入150g·L-1三氯乙酸溶液5mL沉淀蛋白质,抽滤分离后,应用自动凯氏定氮仪测定沉淀中的蛋白质含量。经配对t检验分析,本法与国家标准方法测定牛血清白蛋白标准溶液中蛋白质含量、与考马斯亮蓝G-250法测定牛奶中真蛋白质含量以及干扰试验中各干扰物添加组与对照组中蛋白质含量的测定结果均无显著性差异。被分离的滤液中干扰物的回收率在98.4%~100%之间。 相似文献
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MALIK Maqsood Ahmad KHAN Zaheer 《物理化学学报》2007,23(7):1013-1017
The kinetics and mechanism of lactic acid oxidation in the presence of Mn(II)and Ce(IV)ions by chromic acid were studied spectrophotometrically.The oxidation of lactic acid by Cr(VI)was found to proceed in two measurable steps,both of which gave pyruvic acid as the primary product in the absence of Mn(II).2Cr(VI) 2CH3CHOHCOOH→2CH3COCOOH Cr(V) Cr(III)Cr(V) CH3CHOHCOOH→Cr(III) CH3COCOOH The observed kinetics was explained due to the catalytic and inhibitory effects of Mn(II)and Ce(IV)on the lactic acid oxidation by Cr(VI).The reactivity of lactic acid depends upon the experimental conditions.It acts as a two-or three-equivalent reducing agent in the absence or presence of Mn(II).It was examined that Cr(III)products resulting from the direct reduction of Cr(VI)by three-equivalent reducing agents.The oxidation of lactic acid follows the complex order kinetics with respect to [lactic acid].The activation parameters Ea,ΔH#,and ΔS# were calculated and discussed. 相似文献
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Exopolysaccharides (EPSs), produced by lactic acid bacteria (LAB), have been used primarily to improve the quality and taste of food, also possess a variety of unique biological functions, such as immunoregulation and anti-tumor activities. The diversity of molecular structural characteristics of LAB-generated EPSs represents one of the main factors responsible for this plethora of functions. Accordingly, the structural analysis of the EPSs produced by LAB is the prerequisite and basis for examining its functional and structure-activity relationships. In this report, we summarized the current progress of key methodologies involved in the structural analysis of LAB-generated EPSs, including their isolation, purification, primary structure and advances in structural research. A comprehensive discussion regarding the application of chemical analysis, instrument analysis and computer aided technology in the structure analysis of LAB-generated EPSs was provided. Further, the future development of the research on the structure of LAB-generated EPSs was also presented. 相似文献
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Because fossil fuels are continuously depleted, valorization of biomass into valuable liquid products and chemicals is of great significance yet it remains challenging. Among many biomass-derived products, lactic acid is one of the most important renewable monomers for preparing the degradable polymer polylactic acid. The use of raw biomass to produce lactic acid through catalytic conversion is an attractive approach. In this work, the catalytic reaction performance and mechanism of different Lewis acids (Y3+, Sc3+, and Al3+) for the production of lactic acid from cellulose were investigated in detail by isotopic nuclear magnetic resonance (NMR) and mass spectrometry. The production of lactic acid from cellulose includes tandem and competing reactions. The order of catalytic activity for the one-pot conversion of cellulose into lactic acid is as follows: Y3+ > Al3+ > Sc3+. The main tandem reactions involve the hydrolysis of cellulose into glucose, the isomerization of glucose into fructose (the order of catalytic activity, the same below: Y3+ > Al3+, Y3+ > Sc3+), the cleavage of fructose via a retro-aldol reaction to glyceraldehyde (GLY) and 1, 3-dihydroxyacetone (DHA) (Sc3+ > Y3+ > Al3+), and the conversion of DHA or GLY to the final product lactic acid (Al3+ > Y3+ > Sc3+). It was found that the process of glucose isomerization to fructose was the key step to the final selectivity of the tandem reaction of cellulose conversion to lactic acid, and it was clarified that the production of lactic acid from DHA underwent a keto-enol (K-E) tautomerization process rather than a classical 1, 2-shift process. First, DHA was transformed into GLY via the isomerization process, then the adjacent hydroxyl group of GLY was removed in the form of water to produce an α, β-unsaturated species. After that, the α, β-unsaturated species underwent K-E tautomerization to generate unsaturated aldehyde-ketone intermediates. Meanwhile, a molecule of water was added to aldehyde-ketone intermediates to obtain a diol product, the hydrogen atom at the methine position was transferred and the lactic acid was finally obtained through the K-E tautomerization process. The in-depth understanding of the reaction mechanism presented in this work will help to design more selective catalysts for cellulose conversion into value-added oxygen-containing small molecule chemicals.
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Janina Lulek Katarzyna Szyrwińska Barbara Szafran Anna Pachcińska ElżBieta Nowak 《International journal of environmental analytical chemistry》2013,93(6):487-494
A method for determination of trace concentrations of individual PCB congeners in human milk was validated. The analytical procedure included the following steps: acetone : hexane extraction, clean-up of extracts with concentrated sulfuric acid and solid phase extraction (SPE) on Florisil. The identification and quantification of analytes in purified extracts were carried out by high-resolution gas chromatography (HRGC) with electron capture detection (ECD) and/or with low-resolution mass spectrometry (LRMS). Recoveries of 14 PCB congeners from spiked cow milk samples, based on HRGC-ECD were between 87.3 and 93.6%. The precision of analyte determination was established as close to or less than 10%. The detection limits ranged between 0.14 and 0.26 ng/g fat and the quantification limits between 0.57 and 0.86 ng/g fat. The method was linear and characterized by good correlation coefficients (>0.99) for most of the compounds studied. The quality of the method under validation was verified by the analysis of Standard Reference Material (CRM-450) and interlaboratory exercise. 相似文献
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荧光分光光度法测定奶粉及尿液中叶酸——基于同时高锰酸钾氧化及光化学反应 总被引:1,自引:0,他引:1
对基于同时用高锰酸钾氧化及光化学反应的荧光分光光度法测定复杂试品如奶粉及人尿中叶酸的条件作了系统的试验并予以优化.对奶粉试样的预处理方法也作了详细叙述.试样溶液在作荧光光度检测之前,须经硅藻土填充的层析柱进行纯化.含有叶酸的试液在0.01 mol·L-1盐酸介质中,用1×10-3 mol·L-1高锰酸钾溶液氧化,并置于波长为254 nm的紫外灯下照射30 min,经如此处理后叶酸的荧光强度明显增大,并测得其激发波长及发射波长分别为280 nm及448 nm.在5.0×10-8~2.0×10-6 mol·L-1叶酸浓度范围内,与相应的荧光强度之间保持线性关系,相关系数为0.999 1.方法的检出限为6.5×10-9 mol·L-1,所提出的方法曾用于奶粉及人尿中叶酸的测定.测定结果的RSD值(n=7)为3.2%~4.9%,方法的回收率为97.0%~102.0%. 相似文献
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Marek Kieliszek Katarzyna Pobiega Kamil Piwowarek Anna M. Kot 《Molecules (Basel, Switzerland)》2021,26(7)
Over the past several decades, we have observed a very rapid development in the biotechnological use of lactic acid bacteria (LAB) in various branches of the food industry. All such areas of activity of these bacteria are very important and promise enormous economic and industrial successes. LAB are a numerous group of microorganisms that have the ability to ferment sugars into lactic acid and to produce proteolytic enzymes. LAB proteolytic enzymes play an important role in supplying cells with the nitrogen compounds necessary for their growth. Their nutritional requirements in this regard are very high. Lactic acid bacteria require many free amino acids to grow. The available amount of such compounds in the natural environment is usually small, hence the main function of these enzymes is the hydrolysis of proteins to components absorbed by bacterial cells. Enzymes are synthesized inside bacterial cells and are mostly secreted outside the cell. This type of proteinase remains linked to the cell wall structure by covalent bonds. Thanks to advances in enzymology, it is possible to obtain and design new enzymes and their preparations that can be widely used in various biotechnological processes. This article characterizes the proteolytic activity, describes LAB nitrogen metabolism and details the characteristics of the peptide transport system. Potential applications of proteolytic enzymes in many industries are also presented, including the food industry. 相似文献
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脱氧核糖核酸电化学传感器的原理及其应用 总被引:5,自引:0,他引:5
对电化学DNA传感器的组成及其在DNA损伤研究、环境污染监控、病原基因检测、基因疾病诊断和药物机理分析等方面的进行了总结,并对其发展趋势进行了评述。 相似文献
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《Electroanalysis》2018,30(3):543-550
Electrochemical sensors have been developed by modifying a glassy carbon electrode with organo‐kaolinite hybrid materials. These materials were obtained by the grafting of four ionic liquids (1‐(2‐hydroxyethyl)‐4‐benzylpyridinium chloride, 1‐(2‐hydroxyethyl)‐4‐(tert‐butyl)pyridinium chloride, 1‐(2‐hydroxyethyl)‐4‐ethylpyridinium chloride and 1‐(2‐hydroxyethyl)‐4‐methylpyridinium chloride) on the interlayer aluminol surfaces of kaolinite. With the presence of ionic liquids in the interlayer space of kaolinite, the hybrid materials acquired anion exchange properties and were successfully applied as electrode modifier for the electroanalysis of thiocyanate (SCN−), an anion of medical and environmental concern. A pre‐concentration/detection strategy was used to overcome the interfering effect of the electrolytic solution. After the optimisation of some key experimental parameters (sodium nitrate as electrolyte, 5 min of accumulation time) calibration curves were plotted. Excellent linearity was obtained in the low concentration region (1×10−6 M to 4×10−5 M). The lowest detection limit (15 nM) was obtained with the benzylpyridinium functionalized kaolinite and the highest (60 nM) with the methylpyridinium functionalized kaolinite. Interfering anions (NO3−, Cl−, SO42− and CH3COO−) present in the pre‐concentration solution were found to interfere with SCN− but the sensors remained stable and produced reproducible signals. The most sensitive sensor was successfully applied for the amperometric determination of SCN− in human saliva samples. 相似文献
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In this study,the disposable facial tissues derived carbon aerogels(DFTs-CAs)were synthesized using disposable facial tissues as the raw material for fabricating a sensitive amperometric ascorbic acid(AA)sensor.The experimental results indicated that compared to glassy carbon electrode(GCE)and the popular carbon nanotubes modified GCE(CNTs/GCE),DFTs-CAs modified GCE(DFTs-CAs/GCE)exhibited better electrocatalytic activity(i.e.,lower peak potential and higher peak current)for AA electrooxidation and higher analytical performance for AA determination(i.e.,wider linear range,higher sensitivity and lower detection limit),which could be most likely due to the high density of defective sites and large specific surface area of DFTs-CAs.Especially,the DFTs-CAs/GCE was used for evaluating the AA level in real samples(i.e.,medical injection dose,vitamin C tablets,fresh orange juice and human urine)and the results are satisfactory. 相似文献
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高效阴离子交换色谱-脉冲安培检测法测定牛乳及制品中的唾液酸 总被引:1,自引:0,他引:1
建立了高效阴离子交换色谱分离-脉冲安培检测法检测常见唾液酸N-乙酰神经氨酸(Neu5AC)和N-羟乙酰神经氨酸(Neu5Gc)的方法,对影响分离和检测的条件进行了优化。以NaOH和NaAc为淋洗液,在CarboPac PA20阴离子交换柱上梯度分离,在30℃柱温,0.5 mL/min的流速下,20 min内可完成两种唾液酸的分析。使用脉冲安培检测法测定Neu5AC和Neu5Gc的线性范围为5~500μg/L;检出限为3.0和1.8μg/L(25.0μL进样,以3倍信噪比计算检出限)。将该方法用于15个牛乳及制品中Neu5AC和Neu5Gc的测定,两种唾液酸的标准加入回收率为88%~115%。方法具有灵敏、简便和环境友好的特点,样品前处理方法简单,方法适用性好。 相似文献
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提出了同时测定环境样品中挥发性有机酸及乳酸的离子排斥色谱法(IEC法)。考察了流动相浓度、流速对有机酸分离的影响。实验结果表明,乳酸、甲酸、乙酸、丙酸、正丁酸和正戊酸可达到完全分离,被测组分的浓度与其峰高在一定的范围呈良好的线性关系,检出限均低于0.10 mg/L。测定了糖蜜酒精废水和消化污泥中有机酸的含量,结果满足检... 相似文献
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《Electroanalysis》2005,17(23):2156-2162
In this work an automated flow methodology based on a tubular amperometric detector coupled to a multicommutated flow system was developed and applied in the determination of uric acid in urine. The exploitation of the analytical potential of multicommutated flow systems allowed the implementation of an expeditious and easily controlled on‐line sample dilution, based on the zone sampling approach. The dilution capability exhibited by the developed methodology allowed a direct insertion of the samples in the flow system, without any pretreatment, assuring faster, simpler and less expensive analyses when compared to the enzymatic based methods with spectrophotometric detection commonly used in clinical analyses. The results obtained with the developed system in the determination of uric acid in urine were compared with those obtained by the enzymatic method used in clinical analysis laboratories, and no statistical difference between both methods (for a confidence level of 95%) was found. The proposed system showed good repeatability (RSD<3%, n=10) and a detection limit of 4×10?7 mol L?1. 相似文献
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The processes of lactic acid production include two key stages, which are (a) fermentation and (b) product recovery. In this
study, free cell of Bifidobacterium longum was used to produce lactic acid from cheese whey. The produced lactic acid was then separated and purified from the fermentation
broth using combination of nanofiltration and reverse osmosis membranes. Nanofiltration membrane with a molecular weight cutoff
of 100–400 Da was used to separate lactic acid from lactose and cells in the cheese whey fermentation broth in the first step.
The obtained permeate from the above nanofiltration is mainly composed of lactic acid and water, which was then concentrated
with a reverse osmosis membrane in the second step. Among the tested nanofiltration membranes, HL membrane from GE Osmonics
has the highest lactose retention (97 ± 1%). In the reverse osmosis process, the ADF membrane could retain 100% of lactic
acid to obtain permeate with water only. The effect of membrane and pressure on permeate flux and retention of lactose/lactic
acid was also reported in this paper. 相似文献