Antioxidant activity and free radical scavenging activities of Streptomyces sp.strain MJM 10778

Objective:To investigate the antioxidant activity of soil-borne aetinobacteria.Methods:The total phenolic contents,the level of antioxidant potential by DPPH radical scavenging activity,MO scavenging activity,and ABTS radical scavenging activity in ethyl acelale extract were determined.Results:The 16 S rDNA sequencing analysis revealed that Streptomyces sp.strain MJM 10778.which was isolated from Hambak Mountain.Korea,has 99.9% similarity to Streptomyces misionensis(S.misionenis) NBRC 13063.The physiological and the morphological test revealed that the strain MJM 10778 has different characteristics from the strain NBRC.13063.The entire antioxidant assay with the ethyl acelale extract displayed good radical scavenging activity.The IC_(50) values of the strain MJM 10778 extract on DPPH,.NO.and ABTS radicals were identified to he 92.8 μg/mL,0.02 μg/ml,and 134.9 μg/mL,respectively.The ethyl acetate extract of the strain MJM 10778 showed an 81.500% of cell viability at 100 μg/mL in Raw264.7cell viability assay.Conclusions:The results obtained suggesl that the ethyl acetate extract of Streptomyces sp.strain MJM 10778 could be considered as a potential source of drug for the diseases that is caused by free radicals with its anti-oxidant activities and low cytotoxicity.

STUDIES ON FREE RADICAL SCAVENGING ACTIVITY IN CHINESE SEAWEEDS PART I. SCREENING RESULTS

Antioxidants have attracted the attention of researchers due to their beneficial effects as free radical scavengers. Application of a stable free radical named 1,1 diphenyl 2 picrylhydrazyl(DPPH) to screen the free radical scavenging activity in 27 species of Chinese seaweed showed that 15 of them had significant activity in at least one of the organic solvent extracts. The most interesting seaweed species were Gelidium amansii, Gloiosiphonia capillaris, Polysiphonia urceolata, Sargassum kjellmanianum, Desmarestia viridis, and Rhodomela teres.

Antioxidant Activity of Pigment Extracted from Green-Wheat-Bran

The anthocyanin pigment extracted from green-wheat-bran was studied to identify its antioxidant activity.The antioxidant activities of the pigment were evaluated by anti-lipid peroxidation,total antioxidant activity （TAA）,superoxide anion radical scavenging activity （SARSA）,active oxygen scavenging activity （AOSA）,and DPPH （1,1-diphenyl-2 picrylhydrazyl free radical） radical scavenging activity.The results showed that the pigment had higher antioxidant activity and TAA,SARSA,AOSA and DPPH.scavenging activities at a certain concentration than Vc （antiscorbutic vitamin,vitamin C）,and the capacity increased with the increase of pigment concentration.Its TAA was 51.06 U mL-1,1.73 times of Vc,and SARSA 18 025.21 U mL-1,2.26% higher than Vc,and AOSA 3 776.31 U mL-1,1.24 times of Vc.As to the DPPH.scavenging activity of the pigment,there was a trend that higher concentration performed higher activity significantly improved with the company of Vc.The pigment showed significant antioxidant activities evaluated by different assays.Results will provide a better understanding on antioxidant activity of green wheat and allow the screening or breeding of green wheat varieties with higher antioxidant activity for food processing.

Phytochemical composition and in vitro antioxidant activity of aqueous extract of Aerva lanata(L.) Juss.ex Schult.Stem(Amaranthaceae)

Objective:To analyze the phytochemical composition and in vitro antioxidant properties of aqueous extract of Aerva Lanata（A.lanata） stem.Methods:During the preliminary phytochemical analysis,the aqueous extract of A.Ianata was screened for the presence of carbohydrates,proteins,phenolic compounds,oil and fats,saponins,flavonoids,alkaloids. tannins and phytosterols.Antioxidant activity of the extract was determined by 2.2-dipbenyl- 1-picrylhydrazyl radical scavenging activity,metal chelating activity,reducing power activity and DNA damage inhibition activity.Analysis of phenolic compounds was performed by FolinCiocaiteau reagent method and gradient high performance liquid chromatography technique. Results:Preliminary phytochemical analysis exhibited the presence of phenolic compounds, saponins.flavonoids.tannins and phytosterols as major phytochemical groups.The extract exhibited high 2.2—diphenyl-1-picrylhydrazyl radical scavenging activity(IC50= 110.74μg/ mL).metal chelating activity(IC50= 758.17μg/mL).reducing power activity and DIA damage inhibition efficiency.The extract was reported to possess a high amount of total phenolic content and some of them were identified as gallic acid（3,4,3-OH）,apigenin-7—O-glucoside tapigetrin), quercetin-3—O-rutinoside（rutin） and myricetin（3,5,7,3,4,5-OH）by high performance liquid chromatography analysis.The extract was found non toxic towards human erythrocytes in the hemolytic assay(IC50= 24.89 mg/mL).Conclusions:These results conclud that A.lanata stem possesses high antioxidant activity and can he used for the development of natural and sale antioxidant compounds.

Study on the Antioxidant Activity of Grape Stems (<i>Vitis vinifera</i>). A Preliminary Assessment of Crude Extracts

The antioxidant activity of 80% ethanol and 70% acetone extracts of stems from red and white grapes (Vitis vinifera) used in wine industry were evaluated to determine their feasibility as natural antioxidants. The results showed that all grape stem extracts were rich in total polyphenolic compounds and flavanols and had clear antioxidant activities. The free radical-scavenging capacity of the extracts was determined using the DPPH (2,2-diphenyl-1-picrylhydrazyl) method. The extracts obtained from red grape stem present EC50 values of 0.14 g dm/g DPPH (acetone extract) and 0.20 g dm/g DPPH (ethanol extract) while the extracts obtained from white grape stem present EC50 values of 0.26 g dm/g DPPH (acetone extract) and 0.37 g dm/g DPPH (ethanol extract). There are significant correlations between the total content of polyphenols and the antioxidant activity (R2 = 0.9352) and between the flavanols content and the antioxidant activity (R2 = 0.9404) of the grape stem extracts obtained.

Comparison of Antioxidant and Antimicrobial Activities of Acetone and Water Extracts of <i>Theobroma cacao</i>Beans

This present study compared antioxidant and antimicrobial activities of acetone and water extracts of Theobroma cacao beans against Escherichia coli. Total phenolic content (TPC) in both extracts was estimated by the Folin-Denis reagent. The present study showed that the 70% (v/v) acetone extract had a higher extraction yield and TPC (37% and 109 mg TAE g-1 dry weight) than the water extract (33% and 76 mg TAE g-1 dry weight). The antioxidant activities of both extracts were estimated by the DPPH Scavenging Assay. The extract obtained using 70% (v/v) acetone showed higher antioxidant activity (54%) compared to the antioxidant activity obtained using water (34%). Antimicrobial activities of acetone and water extracts from Theobroma cacao were measured against Escherichia coli and were screened by agar well diffusion method and further confirmed with the disc diffusion method. The bacterial growth was measured in Mueller Hinton agar. The extracts inhibited the growth of the Escherichia coli cultured, and the acetone extracts showed antimicrobial capacity comparable or equivalent, as seen in commercial ampicillin.

Antioxidant and Antibacterial Activities in the Leaf Extracts of Indian Borage (<i>Plectranthus amboinicus</i>)

The different solvent extracts of the leaves of Plectranthus amboinicus were evaluated for their antioxidant and anti-bacterial properties. The ethyl acetate extract of the leaves which had the highest polyphenolic content showed an appreciable DPPH radical scavenging activity as well as total antioxidant capacity as compared with extracts obtained using hexane, acetone, methanol, hydroalcohol and freeze dried form. The acetone extract of the leaves which had the second highest polyphenolic content showed appreciable antibacterial activity with least MIC values against the tested foodborne pathogens namely Staphylococcus aureus, Bacillus cereus, Escherichia coli and Yersinia enterocolitica. The findings indicated the potentiality of ethyl acetate and acetone extract of the leaves of Indian borage for use as biopreservatives as they showed high antioxidant and antibacterial activities.

Effect of pH on Antioxidant and Phytochemical Activities of Mulhatti Roots (Glycyrrhiza glabra L.)

Glycyrrhiza glabra L.is the most widely used herb in the ancient history of Ayurvedic medicine,as a medicinal value as well as an aromatic herb,and it is commonly known as Mulhatti.Mulhatti roots are useful for medically and are also a good source of phytoproducts and secondary metabolites present in Mulhatti roots are triterpenoid saponin,glycosides,glycyrrhizin,prenylated biaurone,licoaagrone,7-acetoxy-2-methylisoflavone,4-methylcoumarin,liqcoumarin,glycyrrhetinic acid,quercetin,liquiritigenin,isoliquiritigenin,etc.This study was carried out to study the evaluation of phenolic compounds,2,2-diphenyl-1-picrylhydrazyl(DPPH)free radical activity and general antioxidant capacity of water extracts of Mulhatti roots prepared at different pH values,namely 2,4,7 and 9.Data have shown great differences in terms of results.Most of the phenolic compounds are at pH 7(19.25),followed by pH 9(17.25),pH 2(14.62)and pH 4(8.89 mg GAE/g),respectively.Similarly,the flavonoid data also showed variations,the maximum has been present in pH 2(5.39),then pH 7(3.02),pH 9(1.79)and pH 4(1.40 mg CE/g),respectively.The value for DPPH IC50 free radical scavenging activity was the lowest at pH 7(82.22),followed by pH 2(110.40),pH 4(111.99)and pH 9(146.24μg/mL)and IC50 reference standard(ascorbic acid)was 59.52μg/mL in distilled water.The total capacity of the antioxidant was the highest at pH 2(9.93)followed by pH 4(5.54),pH 7(5.34)and pH 9(4.23 mg AAE/g).According to current research,pH 7 is the best for phytochemicals as well as antioxidants that catch harmful radicals.

Antioxidant activities of different extracts from Amomum longiligulare Fruits

Objective:To study the antioxidant activities of five extracts ofAmomi longiligulare (A. longiligulare) to determine the antioxidant fraction.Methods: The ethanol extract ofA. longiligulare was extracted by systematic solvent extraction to obtain the petroleum ether, dichloromethane, ethyl acetate, n-butanol fractions successively. Thein vitro antioxidant activities of the five extracts were evaluated by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical and hydroxyl radical (OH-) scavenging assay methods.Results: The five extracts showed different extent of antioxidant activities in vitro, especially the ethyl acetate and dichloromethane fractions.Conclusion: The difference of antioxidant activity of different extracts may be associated with the type and structure of antioxidant components in each fraction of A. longiligulare fruits.

Antioxidant phenanthrenes and lignans from Dendrobium nobile

To study the antioxidant constituents from the stems of Dendrobium nobile, and to discuss theft structure-activity relationship. Compounds were isolated from a 60% ethanolic extract by various chromatographic techniques and were identified by spectral analysis. The antioxidant activities of compounds were evaluated by DPPH free radical scavenging assay. Five phenanthrenes and four lignans were obtained from the active fractions ofD. nobile. Their structures were identified as fimbriatone （1）, confusarin （2）, flavanthrinin （3）, 2,5-dihydroxy-4,9-dimethoxyphenanthrene （4）, 3,7-dihydroxy-2,4-dimethoxyphenanthrene （5）, syringaresinol （6）, pinoresinol （7）, medioresinol （8） and lirioresinol-A （9）, respectively. Compounds 2 and 6 exhibited more potent DPPH scavenging activities than vitamin C. All the above compounds were reported from this plant for the first time, and compounds 3, 4 and 9 were reported for the first time from the genus of Dendrobiurn. For all phenanthrenes and lignans, an electron-donating methoxyl group in the ortho position to the phenolic hydroxyl group exhibits enhanced antioxidant activities.

玫瑰茄粗多糖清除DPPH自由基活性研究

以玫瑰茄干花萼为原料,利用水浸醇析法提取玫瑰茄粗多糖,其抗氧化活性用清除1,1-二苯基苦基苯肼(DPPH)自由基的能力进行评价。结果表明,玫瑰茄粗多糖具有良好的抗氧化活性,其浓度在0.551～2.150mg/mL范围内,与清除率呈较好的线性关系:y=28.7684x+39.43208,R=0.973。

葡萄状枝瑚菌粗多糖的提取及其清除DPPH自由基活性

利用水浸法提取珊瑚菌(Ramaria botrytis)中的粗多糖,以苯酚-硫酸法测定粗多糖含量,采用单因素和正交试验对浸提参数温度、时间、料液比进行优化,并在此基础上制备粗多糖,以清除DPPH自由基测定其抗氧化能力。结果表明:珊瑚菌粗多糖的最佳提取条件为浸提温度90℃、浸提时间2h、料液比1∶20,平均得率为5.64%。另外,当粗多糖的浓度大于7mg/mL时,对DPPH自由基的清除率保持在78%～84%之间。

苯并呋喃酮衍生物结构对其DPPH捕获能力的影响

采用自由基比色法考察苯并呋喃酮衍生物结构对其DPPH捕获能力的影响。结果发现,母体苯环5,7位上甲基和叔丁基的改变以及取代苯环上强供电子取代基的存在对苯并呋喃酮衍生物的DPPH捕获能力没有明显影响。苯环2′位存在明显的位阻作用,对苯并呋喃酮衍生物的DPPH捕获能力具有明显的抑制作用;并且当此位为不含活泼氢的氢键受体取代基时,苯并呋喃酮衍生物的DPPH捕获能力会由于取代基与3位活泼氢的氢键作用而被进一步削弱;但此位为含有活泼氢的氢键受体取代基时,此取代基的氢将会由于3位活泼氢与取代基的氢键作用而活化,从而使其位阻作用得到一定程度的抑制。

响应面法优化樱桃籽清除DPPH自由基物质的提取工艺(英文)

优化樱桃籽抗氧化物质的提取工艺。以DPPH自由基清除法检测提取物的抗氧化能力,考察3个变量(乙醇体积分数、提取温度和提取时间)对樱桃籽清除DPPH自由基的影响,并通过响应面分析法确定樱桃籽抗氧化物质提取的最佳工艺条件。结果表明:最佳工艺条件为液料比20:1(mL/g)、乙醇溶液体积分数33%、提取温度60℃、提取时间31min。在最佳提取条件下,DPPH自由基实际清除率达到92.58%,与理论预测值非常接近,说明采用响应面法优化樱桃籽抗氧化物质的提取工艺可行。

9种傣药提取物对DPPH自由基清除作用的研究

对9种傣药用甲醇进行提取,得到的甲醇提取物依次用石油醚、乙酸乙酯、正丁醇进行萃取,这样每一种傣药得到4种提取物,并用DPPH法测定了不同溶剂提取物清除DPPH自由基的能力,结果表明:不同傣药显示出不同的清除自由基的能力,在9种傣药中以黑皮跌打藤茎正丁醇提取物清除自由基的能力最强.同一种傣药不同溶剂提取物显示出不同的活性,通常其活性成分存在于乙酸乙酯和正丁醇提取物中,相比而言,石油醚提取物的活性最差.

DPPH自由基比色法测定番石榴叶提取物抗氧化活性的研究(英文)

本文用2,2-联苯-1-三硝基苯肼(DPPH·)比色法测定了番石榴叶(PsidiumguajavaL.)的抗氧化活性,并使用了三个不同参数抑制率、EC50和AE来评价其抗氧化活性。结果表明,浓度越高,番石榴叶提取物清除自由基的能力越强,其中AE是表示抗氧化活性的最有效的能数。本研究表明番石榴叶提取物是一种有效的、有开发价值的天然抗氧化剂。

基于体外抗氧化DPPH法优化生地抗氧化活性工艺

以生地为原料,DPPH自由基清除率为指标,同时监测提取液中地黄苷D、梓醇、毛蕊花糖苷组分含量,通过正交实验法优化生地抗氧化活性并探讨抗其氧化活性与其抗氧化成分的量效关系;结果表明:最佳工艺条件为浸泡时间13 h、煎煮次数3次、煎煮时间30 min,生地抗氧化活性大大增强,同时发现生地抗氧化活性与其抗氧化成分含量正向相关。该工艺能很好地提高生地抗氧化活性,且设计稳定可行。

八角莲中两对新的双黄酮对应异构体

采用硅胶柱色谱、Sephadex LH-20柱色谱和制备型高效液相色谱法,从八角莲乙醇提取物中分离得到5个双黄酮类化合物。通过波谱数据分析(MS、UV、IR、NMR)与电子圆二色谱(ECD)技术,分别鉴定为(+)-八角莲双黄酮H(1a)、(-)-八角莲双黄酮H(1b)、(+)-八角莲双黄酮I(2a)、(-)-八角莲双黄酮I(2b)、podoverine F(3),其中,1a与1b、2a与2b为2对新的双黄酮对应异构体。DPPH自由基清除实验结果显示,化合物2、2a、2b对DPPH自由基具有较强的清除能力,IC 50值分别为8.87、10.18、11.35μmol/L,且强于阳性药trolox(14.95μmol/L)。化合物2、2a、2b对DPPH自由基的清除能力分别强于化合物1、1a、1b,进一步的构效关系研究表明,B环上邻二酚羟基是黄酮类化合物具有DPPH自由基清除活性的必需结构基团。

基于均匀试验设计的3种浆果花色苷体外协同抗氧化研究

本研究旨在探究3种浆果花色苷的协同抗氧化活性,以DPPH自由基清除率为评价指标,采用均匀试验设计法优化3种浆果花色苷协同抗氧化组合。经过统计分析和数学回归模型拟合得到最优组合:笃斯越橘花色苷(DP)、黑加仑花色苷(HP)、蓝靛果花色苷(LP)最佳浓度分别为0.08 mg/mL、0.14 mg/mL和0.18 mg/mL,对DPPH自由基的实际清除率为(97.67±0.51)%,接近理论期望值100%,说明模型优选的组合具有可行性。通过协同效应分析,优选组合清除DPPH自由基和羟自由基的协同效应指数CI值分别为0.297和0.651,进一步说明DP、HP、LP3种浆果花色苷具有显著协同抗氧化效果。研究成果可为天然抗氧剂及小浆果功能产品研发提供依据。

红曲糟源酶解蛋白肽的功能性评价

【目的】研究不同蛋白酶对红曲糟酶解的效果,并对其酶解液进行功能性评价,为红曲糟源蛋白肽的研发制备提供理论支持。【方法】以提高蛋白含量后的红曲糟为原料,利用碱性蛋白酶、胰蛋白酶、动物蛋白酶、木瓜蛋白酶、菠萝蛋白酶、胃蛋白酶、复配酶制剂F106、酵母抽提酶等不同蛋白酶进行酶解,考察其酶解率、1,1-二苯基-2-三硝基苯肼(DPPH)和2,2-联氮-二(3-乙基-苯并噻唑-6-磺酸)二铵盐(ABTS)自由基清除抗氧化能力、黄嘌呤氧化酶(Xanthine oxidase,XOD)和血管紧张素转化酶(Angiotensin converting enzyme,ACE)抑制活性等生物活性功能。【结果】蛋白酶解率最高的为动物蛋白酶和胰蛋白酶酶解处理,分别为(71.43±1.03)%和(70.20±0.32)%。DPPH自由基清除抗氧化能力最优的是胃蛋白酶、碱性蛋白酶和酵母抽提酶酶解处理,蛋白肽的半数效应浓度(Median effective concentration,EC50)分别为(2.78±0.34)mg·mL^(-1)、(3.02±0.03)mg·mL^(-1)、(3.24±0.65)mg·mL^(-1);ABTS自由基清除抗氧化能力、XOD抑制活性能力最优的均为胃蛋白酶和碱性蛋白酶酶解液,其蛋白肽的EC50值分别为(1.54±0.07)mg·mL^(-1)、(6.45±0.27)mg·mL^(-1)和(10.71±0.06)mg·mL^(-1)、(17.68±0.04)mg·mL^(-1),二者的XOD半数抑制指数分别为(1.28±0.01)、(1.78±0.03);ACE抑制活性最优的为碱性蛋白酶酶解液和木瓜蛋白酶酶解液,蛋白肽的EC50值均为(0.27±0.01)mg·mL^(-1),半数抑制指数分别为(118.40±3.53)、(98.35±1.95)。【结论】红曲糟源蛋白经不同蛋白酶酶解后的肽段具有不同的生物活性,其中以胃蛋白酶酶解的XOD抑制活性能力较强,碱性蛋白酶和木瓜蛋白酶酶解的ACE抑制活性较优。