Sorghum Phytochemicals and Their Potential Impact on Human Health
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Mangifera Indica) Cultivars from the Colombian Caribbean
Vol. 11(7), pp. 144-152, 17 February, 2017 DOI: 10.5897/JMPR2017.6335 Article Number: 94A673D62820 ISSN 1996-0875 Journal of Medicinal Plants Research Copyright © 2017 Author(s) retain the copyright of this article http://www.academicjournals.org/JMPR Full Length Research Paper Mangiferin content, carotenoids, tannins and oxygen radical absorbance capacity (ORAC) values of six mango (Mangifera indica) cultivars from the Colombian Caribbean Marcela Morales1, Santiago Zapata1, Tania R. Jaimes1, Stephania Rosales1, Andrés F. Alzate1, Maria Elena Maldonado2, Pedro Zamorano3 and Benjamín A. Rojano1* 1Laboratorio Ciencia de los Alimentos, Universidad Nacional de Colombia, Medellín, Colombia. 2Escuela de nutrición, Universidad de Antioquia, Medellín, Colombia. 3Graduate School, Facultad de Ciencias Agrarias, Universidad Austral de Chile, Chile. Received 18 January, 2017; Accepted 13 February, 2017 Mango is one of the tropical fruits of greater production and consumption in the world, and a rich source of bioactive compounds, with various functional properties such as antioxidant activity. In Colombia, mango’s market is very broad and diverse. However, there are very few studies that determined the content of bioactive secondary metabolites. The objective of this study was to evaluated the content of different metabolites like Mangiferin, carotenoids, tannins, and the antioxidant capacity by oxygen radical absorbance capacity (ORAC) methodology of six cultivars from the Colombian Caribbean region, with total carotenoid values ranging from 24.67 to 196.15 mg of β-carotene/100 g dry pulp; 84.30 to 161.49 mg Catequine eq./100 g dry pulp for the content of condensed tannins, and 91.80 to 259.23 mg/100 g dry pulp for mangiferin content. -
The Condensed Tannins of Okoume (Aucoumea Klaineana Pierre)
www.nature.com/scientificreports OPEN The condensed tannins of Okoume (Aucoumea klaineana Pierre): A molecular structure and thermal stability study Starlin Péguy Engozogho Anris 1,2*, Arsène Bikoro Bi Athomo1,2, Rodrigue Safou Tchiama2,3, Francisco José Santiago-Medina4, Thomas Cabaret1, Antonio Pizzi4 & Bertrand Charrier1 In order to promote convenient strategies for the valorization of Aucoumea klaineana Pierre (Okoume) plywood and sawmill wastes industry in the felds of adhesives and composites, the total phenolic content of Okoume bark, sapwood and heartwood was measured. The molecular structure of tannins extracted from the bark was determined by Matrix Assisted Laser Desorption/Ionization Time-Of-Flight (Maldi-ToF) mass spectrometry and Fourier transform infrared spectroscopy (FTIR). The total phenolic content displayed signifcant diference (p = 0.001) between the bark, sapwood and heartwood which decreased as follows: 6 ± 0.4, 2 ± 0.8 and 0.7 ± 0.1% respectively. The pro-anthocyanidins content was also signifcantly diferent (p = 0.01) among the three wood wastes, and the bark was the richest in condensed tannins (4.2 ± 0.4%) compared to the sapwood (0.5 ± 0.1%) and heartwood (0.2 ± 0.2%). Liquid chromatography coupled mass spectroscopy (LC-MS) and Maldi-ToF analysis of the bark showed for the frst time that Okoume condensed tannins are fsetinidin, gallocatechin and trihydroxyfavan based monomers and complex polymers obtained with glycosylated units. No free catechin or robitinidin units were detected, whereas distinctive dihydroxy or trihydroxyfavan-3-benzoate dimers were observed in the investigated condensed tannin extracts. FTIR analysis showed the occurrence of glucan- and mannan-like sugars in the condensed tannins, and Maldi-ToF highlighted that these sugars should account for ten glycosylated units chemically bonded with two fsetinidins and one gallocatechin trimer. -
Antioxidant Rich Extracts of Terminalia Ferdinandiana Inhibit the Growth of Foodborne Bacteria
foods Article Antioxidant Rich Extracts of Terminalia ferdinandiana Inhibit the Growth of Foodborne Bacteria Saleha Akter 1 , Michael E. Netzel 1, Ujang Tinggi 2, Simone A. Osborne 3, Mary T. Fletcher 1 and Yasmina Sultanbawa 1,* 1 Queensland Alliance for Agriculture and Food Innovation (QAAFI), The University of Queensland, Health and Food Sciences Precinct, 39 Kessels Rd, Coopers Plains, QLD 4108, Australia 2 Queensland Health Forensic and Scientific Services, 39 Kessels Rd, Coopers Plains, QLD 4108, Australia 3 CSIRO Agriculture and Food, 306 Carmody Road, St Lucia, QLD 4067, Australia * Correspondence: [email protected]; Tel.: +617-344-32471 Received: 26 June 2019; Accepted: 20 July 2019; Published: 24 July 2019 Abstract: Terminalia ferdinandiana (Kakadu plum) is a native Australian plant containing phytochemicals with antioxidant capacity. In the search for alternatives to synthetic preservatives, antioxidants from plants and herbs are increasingly being investigated for the preservation of food. In this study, extracts were prepared from Terminalia ferdinandiana fruit, leaves, seedcoats, and bark using different solvents. Hydrolysable and condensed tannin contents in the extracts were determined, as well as antioxidant capacity, by measuring the total phenolic content (TPC) and free radical scavenging activity using the 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. Total phenolic content was higher in the fruits and barks with methanol extracts, containing the highest TPC, hydrolysable tannins, and DPPH-free radical scavenging capacity (12.2 2.8 g/100 g dry weight ± (DW), 55 2 mg/100 g DW, and 93% respectively). Saponins and condensed tannins were highest in ± bark extracts (7.0 0.2 and 6.5 0.7 g/100 g DW). -
A Biosystematic Study of Allium Amplectens Torr
University of the Pacific Scholarly Commons University of the Pacific Theses and Dissertations Graduate School 1974 A biosystematic study of Allium amplectens Torr Vickie Lynn Cain University of the Pacific Follow this and additional works at: https://scholarlycommons.pacific.edu/uop_etds Part of the Life Sciences Commons Recommended Citation Cain, Vickie Lynn. (1974). A biosystematic study of Allium amplectens Torr. University of the Pacific, Thesis. https://scholarlycommons.pacific.edu/uop_etds/1850 This Thesis is brought to you for free and open access by the Graduate School at Scholarly Commons. It has been accepted for inclusion in University of the Pacific Theses and Dissertations by an authorized administrator of Scholarly Commons. For more information, please contact [email protected]. A BIOSYSTEMI\'l'IC STUDY OF AlHum amplectens Torr. A 'lliesis Presented to The Faculty of the Department of Biological Sciences University of the Pacific In Partial Fulfillment of the Requirewents for the.Degree Master of Science in Biological Sciences by Vickie Lynn Cain August 1974 This thesis, written and submitted by is approved for recommendation to the Committee on Graduate Studies, University of the Pacific. Department Chairman or Dean: Chairman I; /') Date d c.~ cA; lfli ACKUOlvl.EDGSIV!EN'TS 'l'he author_ wishes to tha.'l.k Dr. B. Tdhelton a.YJ.d Dr. P. Gross for their• inva~i uoble advise and donations of time. l\'Iy appreciation to Dr. McNeal> my advisor. Expert assistance in the library vJEts pro:- vlded by Pr·, i:':I. SshaJit. To Vij c.y KJ12nna and Dolores No::..a.n rny ap-- preciatlon for rwraJ. -
3-Deoxyanthocyanins : Chemical Synthesis, Structural Transformations, Affinity for Metal Ions and Serum Albumin, Antioxidant Activity
ACADÉMIE D’AIX-MARSEILLE UNIVERSITÉ D’AVIGNON Ecole Doctorale 536 Agrosciences & Sciences THESE présentée pour l’obtention du Diplôme de Doctorat Spécialité: chimie par Sheiraz AL BITTAR le 17 juin 2016 3-Deoxyanthocyanins : Chemical synthesis, structural transformations, affinity for metal ions and serum albumin, antioxidant activity Composition du jury: Victor DE FREITAS Professeur Rapporteur Faculté des Sciences - Université de Porto Cédric SAUCIER Professeur Rapporteur Faculté de Pharmacie - Université de Montpellier I Hélène FULCRAND Directrice de Recherche à l’INRA Examinatrice Montpellier - SupAgro Olivier DANGLES Professeur Directeur de thèse UFR STS - Université d’Avignon Nathalie MORA- Maître de Conférences Co-Encadrante SOUMILLE UFR STS - Université d’Avignon A Alma & Jana… 2 Remerciements Difficile d’être exhaustive dans ces remerciements tant les rencontres, échanges et soutiens ont été nombreux durant ces cinq années. Tout d’abord, je tiens à remercier l’université d’Avignon pour m’accueillir dans ces locaux et de m’offrir le nécessaire pour acomplir ce travail. Je remercie également l’université Al-Baath en Syrie pour la bourse d’étude qui m’a permis de venir en France et Campus Farnce pour l’accueil et la direction en France. Toute ma gratitude va aux membres du jury Victor DE FREITAS, Cédric SAUCIER et Hélène FULCRAND d’avoir accepté d’évaluer ma thèse. Je remercie encore une fois Hélène FULCRAND tant que membre de mon comité de thèse, pour les discussions constructives et ses conseils pendant ma thèse. Je tiens à remercier infiniment mon directeur de thèse Olivier DANGLES. Merci d’accepter de m’accueillir dans votre équipe sans me connaitre il y a 6 ans. -
EEE M W 24B 24A 27B 27A N Patent Application Publication Dec
US 2009031 1494A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2009/0311494 A1 YAMASHTA et al. (43) Pub. Date: Dec. 17, 2009 (54) RELIEF PRINTING PLATE PRECURSOR FOR (30) Foreign Application Priority Data LASER ENGRAVING, RELIEF PRINTING PLATE, AND PROCESS FOR PRODUCING Jun. 17, 2008 (JP) ................................. 2008-157907 RELEF PRINTING PLATE Feb. 10, 2009 (JP) ................................. 2009-028816 (75) Inventors: Masako YAMASHITA, Publication Classification Shizuoka-ken (JP); Atsushi (51) Int. Cl. SUGASAKI, Shizuoka-ken (JP) B32B 3/00 (2006.01) Correspondence Address: GO3F 7/20 (2006.01) Moss & Burke, PLLC GO3F 7/004 (2006.01) 401 Holland Lane, Suite 407 Alexandria, VA 22314 (US) (52) U.S. Cl. .................... 428/195.1: 430/306: 430/286.1 (73) Assignee: FUJIFILM CORPORATION, (57) ABSTRACT Tokyo (JP) A relief printing plate precursor for laser engraving, including (21) Appl. No.: 12/476,260 a relief forming layer containing (A) a polymerizable com pound having an ethylenic unsaturated bond. (B) a binder (22) Filed: Jun. 2, 2009 polymer, and (C) a compound having deodorizing ability. 11 50 FA - 42 SUB SCANNING DIRECTION -10 - 228 7.s 55 21B EEE m w 24B 24A 27B 27A N Patent Application Publication Dec. 17, 2009 US 2009/0311494 A1 F.G. 1 FA SCANNING DIRECTION 7OA a. CSy ra & 5A - 27WSNS AD 23Ar S3EEASEE21 E-25sagaa EEEEEEEEEEEEEEEEEEEEEEEEE-22s awslighlights fskillsw. 21B 2 TTT "TT". US 2009/031 1494 A1 Dec. 17, 2009 RELEF PRINTING PLATE PRECURSORFOR mask to develop and remove an uncured area, and there is LASER ENGRAVING, RELIEF PRINTING room for improvement since development treatment is nec PLATE, AND PROCESS FOR PRODUCING essary. -
Hydroxylase in Sorghum Mesocotyls Synthesizing 3-Deoxyanthocyanidin Phytoalexins
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Agronomy & Horticulture -- Faculty Publications Agronomy and Horticulture Department 2004 Expression of a putative flavonoid 3'-hydroxylase in sorghum mesocotyls synthesizing 3-deoxyanthocyanidin phytoalexins Jayanand Boddu Pennsylvania State University Catherine Svabek Pennsylvania State University Rajandeep Sekhon Pennsylvania State University Amanda Gevens Michigan State University Ralph L. Nicholson Purdue University See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/agronomyfacpub Part of the Agricultural Science Commons, Agriculture Commons, Agronomy and Crop Sciences Commons, Botany Commons, Horticulture Commons, Other Plant Sciences Commons, and the Plant Biology Commons Boddu, Jayanand; Svabek, Catherine; Sekhon, Rajandeep; Gevens, Amanda; Nicholson, Ralph L.; Jones, A. Daniel; Pedersen, Jeffrey F.; Gustine, David L.; and Chopra, Surinder, "Expression of a putative flavonoid 3'- hydroxylase in sorghum mesocotyls synthesizing 3-deoxyanthocyanidin phytoalexins" (2004). Agronomy & Horticulture -- Faculty Publications. 939. https://digitalcommons.unl.edu/agronomyfacpub/939 This Article is brought to you for free and open access by the Agronomy and Horticulture Department at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Agronomy & Horticulture -- Faculty Publications by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Authors Jayanand -
Datasheet Inhibitors / Agonists / Screening Libraries a DRUG SCREENING EXPERT
Datasheet Inhibitors / Agonists / Screening Libraries A DRUG SCREENING EXPERT Product Name : Malvidin-3-O-glucoside chloride Catalog Number : TN1909 CAS Number : 7228-78-6 Molecular Formula : C23H25ClO12 Molecular Weight : 528.90 Description: Malvidin 3-glucoside has antioxidant activity, alone is not oxidized in the presence of grape polyphenol oxidase. Malvidin 3-glucoside's color stabilization at a higher pH can be explained by self-aggregation of the flavylium cation and copigmentation with the Z-chalcone form. Storage: 2 years -80°C in solvent; 3 years -20°C powder; Receptor (IC50) others In vitro Activity Here we used a gel electrophoresis assay employing supercoiled DNA plasmid to examine the ability of these compounds (1) to intercalate DNA, (2) to inhibit human topoisomerase I through both inhibition of plasmid relaxation activity (catalytic inhibition) and stabilization of the cleavable DNA-topoisomerase complex (poisoning), and (3) to inhibit or enhance oxidative single-strand DNA nicking. We found no evidence of DNA intercalation by anthocyan(id)ins in the physiological pH range for any of the compounds used in this study-cyanidin chloride, cyanidin 3-O-glucoside, cyanidin 3,5-O-diglucoside, Malvidin-3-O-glucoside chloride and luteolinidin chloride. The anthocyanins inhibited topoisomerase relaxation activity only at high concentrations (> 50 muM) and we could find no evidence of topoisomerase I cleavable complex stabilization by these compounds. Reference 1. Anthocyanin Interactions with DNA: Intercalation, Topoisomerase I Inhibition and Oxidative Reactions.J Food Biochem. 2008 Sep 23;32(5):576-596. FOR RESEARCH PURPOSES ONLY. NOT FOR DIAGNOSTIC OR THERAPEUTIC USE. Information for product storage and handling is indicated on the product datasheet. -
Condensed Tannins 7
120 Biochem. J. (1961) 78, 120 Condensed Tannins 7. ISOLATION OF (-)-7:3':4'-TRIHYDROXYFLAVAN-3-OL [(-)-FISETINIDOL], A NATURALLY OCCURRING CATECHIN FROM BLACK-WATTLE HEARTWOOD* By D. G. ROUX AND E. PAULUS Leather Industries Research Institute, Rhodes University, Grahamstown, South Africa (Received 9 May 1960) The interrelated flavonoid compounds (+ )- aqueous phase extracted with ethyl acetate in each in- 7:3':4'-trihydroxyflavan-3:4-diol (Keppler, 1957) stance. The combined organic and ethyl acetate extracts of 2:3-trans:3:4-cis configuration (Clark-Lewis & from each fraction were evaporated to 50 ml. and applied Roux, 1959), (+ )-fustin (2:3-trans) and in bands to sheets (5 ml./sheet) of 221 in. x 18j in. What- 1958, man no. 3 chromatographic paper. The chromatograms fisetin (Roux & Paulus, 1960) have been isolated were developed by upward migration in 2 % acetic acid for from black-wattle-wood tannins. In the present 12 hr. The fustin (RF 0-43 on Whatman no. 3 paper), the study a new catechin, (-)-fisetinidol, correspond- polymeric leuco-fisetinidin and the ( +)-mollisacacidin ing to these substances has been isolated, and their (traces) (RF 0 57) bands were located with toluene-p- biogenesis is discussed. sulphonic acid. Bands in the region Rp 050 which appeared yellowish in ordinary light were cut out and eluted with 70% ethanol. Concentrate of the eluents gave 0-113 g. of EXPERIMENTAL AND RESULTS pale-yellow crystals. The mother liquors were purified by All melting points are uncorrected. Mixed melting running on five sheets, as above, yielding a further 0-05 g. points were on equimolecular mixtures of the substances Pale-yellow crystals of (- )-fisetinidol, m.p. -
Gabon): (Khaya Ivorensis A. Chev
Analysis and valorization of co-products from industrial transformation of Mahogany (Gabon) : (Khaya ivorensis A. Chev) Arsène Bikoro Bi Athomo To cite this version: Arsène Bikoro Bi Athomo. Analysis and valorization of co-products from industrial transformation of Mahogany (Gabon) : (Khaya ivorensis A. Chev). Analytical chemistry. Université de Pau et des Pays de l’Adour, 2020. English. NNT : 2020PAUU3001. tel-02887477 HAL Id: tel-02887477 https://tel.archives-ouvertes.fr/tel-02887477 Submitted on 2 Jul 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. THÈSE Présentée et soutenue publiquement pour l’obtention du grade de DOCTEUR DE L’UNIVERSITÉ DE PAU ET DES PAYS DE L’ADOUR Spécialité : Chimie Analytique et environnement Par Arsène BIKORO BI ATHOMO Analyse et valorisation des coproduits de la transformation industrielle de l’Acajou du Gabon (Khaya ivorensis A. Chev) Sous la direction de Bertrand CHARRIER et Florent EYMA À Mont de Marsan, le 20 Février 2020 Rapporteurs : Pr. Philippe GERARDIN Professeur, Université de Lorraine Dr. Jalel LABIDI Professeur, Université du Pays Basque Examinateurs : Pr. Antonio PIZZI Professeur, Université de Lorraine Maitre assistant, Université des Sciences et Dr. Rodrigue SAFOU TCHIAMA Techniques de Masuku Maitre assistant, Université des Sciences et Dr. -
Effect of Different Levels of Hydrolysable Tannin Intake on The
www.nature.com/scientificreports OPEN Efect of diferent levels of hydrolysable tannin intake on the reproductive hormones and serum biochemical indices in healthy female rats Faiza Manzoor1, Mahr Un Nisa1, Hafz Amjad Hussain2, Nazir Ahmad1* & Huma Umbreen1 The present work aimed to fnd out the efect of diferent levels of hydrolysable tannin (HT) on serum hormonal profle, biochemical indices, lipid profle, apparent digestibility of nutrients and body weight gain in healthy female rats. Forty fve adult healthy female rats of 8 weeks old were randomly divided into fve equal groups. Diferent doses of HT 0, 0.5, 1, 1.5 and 2% were administered daily to each rats group on the body weight basis for 6 weeks. The results had shown the reduction trend (p < 0.05) in the blood glucose, serum cholesterol, low density lipoprotein, testosterone, prolactin, ghrelin, total oxidative stress and serum iron levels; while an improvement (p < 0.05) was seen in serum follicle stimulating hormone, progesterone, luteinizing hormone, high density lipoprotein, IgM and total antioxidant capacity. However, no efect (p > 0.05) was noticed in serum IgG, protein, estrogen and calcium levels. A signifcant reduction (p < 0.05) was seen in the apparent nutrient digestibility and body weight gain. The results had shown improvement in the feed conversion ratio (p < 0.05) but non- signifcant decrease (p > 0.05) in the feed intake. The fndings showed that HT had healthy efects on the serum biochemical indices and reproductive hormonal profle but had a negative impact on the nutrient digestibility. Thus, the study concluded that HT could be used as an herbal medicine for the treatment of leading metabolic and infertility diseases like obesity and polycystic ovarian syndrome in females. -
Different Approaches to Evaluate Tannin Content and Structure of Selected Plant Extracts – Review and New Aspects M
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by JKI Open Journal Systems (Julius Kühn-Institut) Journal of Applied Botany and Food Quality 86, 154 - 166 (2013), DOI:10.5073/JABFQ.2013.086.021 1University of Kiel, Institute of Crop Science and Plant Breeding – Grass and Forage Science / Organic Agriculture, Kiel, Germany 2Institute of Ecological Chemistry, Plant Analysis and Stored Product Protection; Julius Kühn-Institute, Quedlinburg, Germany Different approaches to evaluate tannin content and structure of selected plant extracts – review and new aspects M. Kardel1*, F. Taube1, H. Schulz2, W. Schütze2, M. Gierus1 (Received July 2, 2013) Summary extracts, tannins, salts and derivates was imported to the EU in the year 2011, mainly from Argentina, with a trade value of nearly Tannins occur in many field herbs and legumes, providing an im- 63.5 mio. US Dollar (UN-COMTRADE, 2013). These extracts are pro- mense variability in structure and molecular weight. This leads to duced industrially on a large scale. They could therefore maintain complications when measuring tannin content; comparability of a relatively constant quality and thus provide an advantage in rumi- different methods is problematic. The present investigations aimed at nant feeding. characterizing four different tannin extracts: quebracho (Schinopsis Tannins from different sources can react very diverse regarding lorentzii), mimosa (Acacia mearnsii), tara (Caesalpinia spinosa), protein affinity (MCNABB et al., 1998; BUENO et al., 2008). Diffe- and gambier (Uncaria gambir) and impact of storage conditions. rences in tannin structure can occur even between similar plant Using photometrical methods as well as HPLC-ESI-MS, fundamen- species (OSBORNE and MCNEILL, 2001; HATTAS et al., 2011) and a tal differences could be determined.