615.954Foo3rded.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

615.954Foo3rded.Pdf Index Acquired immunodeficiency syndrome pinnipeds (seals, sea lions, walruses), 47ll-1 (AIDS), 451-3, 474, 475 second intermediate hosts, 471 Acromelic acids, 605 Arcobacterspp., 272-3 Acute non-bacterial gastroenteritis see Arizona spp., 344 Noroviruses Ascaris suum, 476 Adenoviruses,404 Aspergillusflavus, A. parasiticus see Aeromonas spp., 342-3 Aflatoxin Aeramonas hydrophile, 342-3 Aspergillus mycotoxins (nitropropionic acid, Aflatoxin, 586--9, 609-12 territrems, sterigmatocystin), 597--8 Aspergillusjlavus, A. parasiticus, 586 Astroviruses, 402-3 biosynthesis, 587-8 carcinogenesis in humans, 588-9 Bacillary dysentery, 359-60 ebselen, 625 Bacillus cereus gastroenteritis, 563-77, hepatitis B virus and carcinogenesis, contemporary problems, 564 588-9 historical aspects, 563--4 human foods (com, cotton seeds, peanuts, outbreaks, 57ll-1 tree nuts), 588 treatment and prevention. 577 Agaricus bisporus, 606 Bacillus cereus, 56&-75 AIDS see Acquired immunodeficiency antibodies, 574-5 syndrome characteristics, 564-5 Alcaligenes[aecalis, 343--4 chemical preservatives, 572 Allyl isothiocyanates, 694 detection, 573--4 Alternaria mycotoxins, 600 growth and survival, 572 Amanita spp. toxins (amanitins, growth temperature, 568 phallotoxins, virotoxins). 602-3 isolation, 573 ibotenic acid (lBA), 604 peR test, 574 isoxazoles, 605 prevalence in foods. 571-2 muscarine (MUS), 604-5 spore antibodies, 574-5 Amnesic shellfish poisoning (domoic acid), spores, germination, 572 676,682--4 spores, heat resistance of, 572 Pseudo-nitzschia spp., 682-3 virulence mechanism, 569 Ancylostoma spp., 476 Bacillus cereus typing, 575-6 Anisakis simplex & Pseudoterranova amplified fragment length polymorphism, decipiens, 470-1 575 cetaceans (whales, dolphins, porpoises), automated ribotyping, 575 47ll-1 fatty acid analysis foods (ceviche, sashimi, sushi), 471 phage typing, 575 886 Index Bacillus cereus typing (Continued) saxitoxin in the rumen, 699 poly random amplified polymorphic DNA Brucella spp., 346-7 poul test, 575 Botulism, 493-8 poul Bacillus cereus toxin detection, 576 adult infectious botulism, 497-8 proc boar spermatozoa bioassay, 576 animal botulism, 499-500 reac ELISA, 576 birds, 500 2J reversed passive latex agglutination, 576 case fatality rate, 495 risk vera cell cytotoxicity, 576 cattle, 499 SUTV Bacillus cereus diarrheal syndrome, 566--9 diagnosis, 494 treat incubation time, 568,569 dog, 499 typir infective dose, 568,569 fish, 499 wate pathogenesis, 566-9 foodbome, 495-ll wildl sign, & symptom" 566 foods associated with, 503--4 zoon treatment & prevention, 577 historical aspects, 486 Campy. Bacillus cereus enterotoxin. 567-9 incidence in humans, 502 C.co enzyme inactivation, 568 incidence in USA, 494 Cfe, in foods, 571-2 incubation time, 495 Ch> mode of action, 569 infant botulism, 496-7 c. la. pH resistance, 568 mink,499 Cup Bacillus cereus emetic syndrome, 569-70 signs and symptoms, 495 Canava cereulide, 570 treatment, 494-5, 497 alfaU emetic toxin. 570 wound botulism, 496 lathy pathogenesis, 570 Botulinum toxin, 492--508 Capillai signs & symptoms, 569 detection, 506-8 Carcinc toxin detection, 576 enzyme-linked coagulation assay, 507 Case-cc Bacillus spp., 344-{i, 670-1 enzyme-linked immunosorbent assay, 507 Cassava B. anthracis. 345 hemagglutination inhibition, 507 Cestode B. cereus, 670 hemagglutination, 493 Ceviche B. subtilis, 346 molecular size, 493 Chemic toxins. 670 molecular structure, 493 Bacil. Bacilli other than B. cereus, 576 mouse test, 506-7 Bacil, Bacterial growth in canned foods offensive weapon, 498-9 Clost. Bacterial toxins, 669-73 plasmids, 493 Clost, endotoxins, 672 therapeutic use of, 498 Lister Enterobacteriaceae, 672 typing, 507 nitriu enterococci, 672 Botulinum toxin formation, 503--4 parat streptococci, group B, 672 anaerobiosis, 503-4 phenr Bayliascaris procyonts. 476 foods associated with, 503--4 phos; Biofilm,,792-5 pH effects, 503 Salmc accumulation, 793 temperature, 503--4 Staph benefits, 798-9 water activity, 504 sulfiu biological removal, 798 Ciguate chemical removal, 797 Campyiobacterjejuni, 259-270 dinofl detachment, 795 cattle, pigs & sheep, 266 etc. development, 793 classification, 260 Citreovi formation, 794-5 culturing, 267 Citrinin physical removal, 797 farm-level controls. 268-9 Citrobac structure, 795-7 fluoroquinolones. ze'i Clavicep Bonkrekic toxin & toxoflavin, 669-70 food,267 Cleanin, Burkholderia cocovenenans, 669-70 Guillain-Barre syndrome, 259, 261-2 acidc Bovine paraplegic syndrome, 699-700 Infection in humans, 261-5 alkali Clostridium perfringens type D, 700 milk, unpasteurized, 264, 267 chlori Lactobacillus vitulinum, 700 pathogenesis, 260 c1eani Index 887 polymerase chain reaction (PCR), 268 enzyme-based cleaners, 751 poultry reservoirs, 266 soaps, 749 poultry consumption, 263-4 syntheticdetergents, 750-1 processingcontrols. 269 Cluocybe spp. toxins, 604-5 reactive arthritis (Reiter's syndrome), Clonorchis sinensis, 471-2 259,262 adult worms,471 risk factors, 263-5 cyprinid fish, 471 survival in environment, 260-1 snail host, 471 treatment of acutecarnpylobacteriosis., 262 Clostridium bifermentans, 348 typing, 268 Clostridium perfringens, [37-163 water, 264-5, 267 alpha toxin method, 163 wildlife reservoirs, 265--6 bacteriocintyping, 159 zoonotic transmission, 265, 270 butylated hydroxyanisole (BHA), 146 Campy/abaeter spp., other thanjejuni, 270-2 confirmatory tests, ]61-2 C coli, 261 cooling, low temperatures., 144-5 Cc fetus subspeciesjeres, 271 curedmeat products, 147 C. hvointesunalis. 27L description, 138 C lari,271 diseasesassociated, ]48 C. upsaliensis, 271-2 enterotoxin (CPE), 139-42, 147-52, Canavanine, 697-8 156-7,162 alfalfa sprouts, Jackbean, 697 enterotoxin activation, 156 lathyrism, 698 enterotoxin assays., serological. 162 Capillaria philipiensis. 469-70 enterotoxin biochemicalcharacteristics, Carcinogenic poisonous mushrooms,605-6 156 Case-control study, 18-24, 105-S enterotoxinmode of action, 150-2 Cassava (Man/hal esculentas, 690-1, 694 enterotoxin purification, 157 Cestode in fish, 473 enumeration, )60 Ceviche, 470, 471 environmental reservoirs, 154 Chemicalantimicrobials, 746-9 fecal shedding, 153-4 Bacillus spp., 747 feeding studies, 149 Bacillus cereus, 748 foodbome illness symptoms, 148-9 Clostridium botulinum, 747 food reservoirs, 154-5 Clostridium perfringens, 747 gene probes for enterotoxigenicity, 163 Lister/a, 747, 748, 749 generation times, 143 nitrites, 747 germination of spores, 142-3 parabens, 748-9 heat resistance of spores., 142 phenolicantioxidants, 749 hemorrhagic necrosisof thejejunum phosphates, 748 ('pig-bel'), 149 Salmonella, 747 incidence of food poisoning, 152-3 Staphylococcus aureus. 748, 749 irradiation, gamma, ]43 sulfites, 747-8 isolation, 160-2 Ciguatera fish poisoning, 675, 677-8 moleculargenetics, 147--8 dinoflagellates tGambierdiscus toxicus, outbreakcriteria, ]57 etc.), 678 oxidation-reduction potential (~), 145-.Q Citreoviridin see Penicillium mycoroxins pH, 146 Citrinin see Penicillium mycotoxins plating media, 160 Citrobacter spp., 347-8 prevention. 155 Ctaviceps purpurea, C. paspali.601 pulsed field gel electrophoresis, (PFGE), Cleaning media, 749--51 159 acid compounds, 750 randomamplified polymorphic DNA alkaline compounds, 750 (RAPD) analysis, 159 chlorinecleaners, 750 ribotyping, 159-.Q0 cleaningauxiliaries., 75] serotyping, 158 888 Index Clostridium perfringens (Continued) Cortine//us shitake, 606 anti sodium chloride, sodium nitrite, 146 Corynebacterium diphtheriae. 348-9 dete sporulation, 138-42 Colton seeds, 588 dial temperature effect on vegetative cell Coumarin, 693 dise growth, 143-5 Coxiella burnetii, 349-50 fooc thermal injury, recovery of spores, 143 Coxsackieviruses see Enteroviruses grOl toxin typing, 157-8 Cryplosporidiwn hominis, C. parvum. 474-5 hem vehicles, food, 153 AIDS patients, 475 o water activity, 146 Cyanobacterial intoxications, 685-7 info Western immunoblots, enterotoxin, 162 Anabena, Aphanazomenom. Nodularia, locu Clostridium botulinum, 485-508 Osctllatoria, 686 non antibiotic resistance, 505-6 anatoxin-a(s),686 2' characteristics, 487-92 drinking water, 685--6 015 classification, 487-9 Mytilus edulis. 686-7 015 detection. 504-6 Cyanogenic glycosldes, 396-4 path DNA homology, 487-8 cassava. Lima beans, bitter almonds, 694 qUOI enrichment, 504-5 seeds of fruits, 693 Shig geographic distribution, 501-2 Cyclochloritine see Penicillium mycotoxins surv germination. 489-91 Cyclopiazonic acid (PA) see Penicillium treat groups of, 487--1l mycotoxins vacc growth, 491 Cyclospora cayetanensis, 474 virul heat activation, 489~90, 505 Cysticercosis see Taenia sagtnata Entero identification, 506 Entero isclaton, 505-6 DANMAP,67 22 metabolism, 487-8 Deoxynivalenol (DON) see Trichothecene dete oxidation-reduction potential, 491 (TCTC) mycotoxins EAS pH requirements, 491 Diarrhetic shellfish poisoning (DSP), 675, locus plasmids, 488-93 684 patb polymerase chain reaction Dinophysis spp., 684 Enteroi proteolysis, 487--1l okadaic acid, pectenctoxins, yessotoxin, color random amplified polymorphic DNA 684 dera analysis, 508 Dietary supplements, toxicology & safety, food' salt resistance, 487-8 700 imrm sporulation, 491-2 Diffusely adherent E. coli (DAEC), 206,210 LTe' temperature requirements, 487-8, 492 Diphyllobothrium latum, 473 path. toxin production, 492-3 vitaminBl2,473 STe, toxin types, 487-8 Dose-response assessment, 42-3 Enterrr Closridium botulinum B in sous vide See also chapters on individual agents eel products, 720 dera Clostridium butyricum, 488, 496 Echinosstoma spp., 472-3 food Clostridium barati, 488,
Recommended publications
  • Solanum Alkaloids and Their Pharmaceutical Roles: a Review
    Journal of Analytical & Pharmaceutical Research Solanum Alkaloids and their Pharmaceutical Roles: A Review Abstract Review Article The genus Solanum is treated to be one of the hypergenus among the flowering epithets. The genus is well represented in the tropical and warmer temperate Volume 3 Issue 6 - 2016 families and is comprised of about 1500 species with at least 5000 published Solanum species are endemic to the northeastern region. 1Department of Botany, India Many Solanum species are widely used in popular medicine or as vegetables. The 2Department of Botany, Trivandrum University College, India presenceregions. About of the 20 steroidal of these alkaloid solasodine, which is potentially an important starting material for the synthesis of steroid hormones, is characteristic of *Corresponding author: Murugan K, Plant Biochemistry the genus Solanum. Soladodine, and its glocosylated forms like solamargine, and Molecular Biology Lab, Department of Botany, solosonine and other compounds of potential therapeutic values. India, Email: Keywords: Solanum; Steroidal alkaloid; Solasodine; Hypergenus; Glocosylated; Trivandrum University College, Trivandrum 695 034, Kerala, Injuries; Infections Received: | Published: October 21, 2016 December 15, 2016 Abbreviations: TGA: Total Glycoalkaloid; SGA: Steroidal range of biological activities such as antimicrobial, antirheumatics, Glycoalkaloid; SGT: Sergeant; HMG: Hydroxy Methylglutaryl; LDL: Low Density Lipoprotein; ACAT: Assistive Context Aware Further, these alkaloids are of paramount importance in drug Toolkit; HMDM: Human Monocyte Derived Macrophage; industriesanticonvulsants, as they anti-inflammatory, serve as precursors antioxidant or lead molecules and anticancer. for the synthesis of many of the steroidal drugs which have been used CE: Cholesterol Ester; CCl4: Carbon Tetrachloride; 6-OHDA: 6-hydroxydopamine; IL: Interleukin; TNF: Tumor Necrosis Factor; DPPH: Diphenyl-2-Picryl Hydrazyl; FRAP: Fluorescence treatments.
    [Show full text]
  • Plant Secondary Metabolites: an Opportunity for Circular Economy
    molecules Review Plant Secondary Metabolites: An Opportunity for Circular Economy Ilaria Chiocchio , Manuela Mandrone * , Paola Tomasi, Lorenzo Marincich and Ferruccio Poli Department of Pharmacy and Biotechnology, Alma Mater Studiorum—University of Bologna, Via Irnerio 42, 40126 Bologna, Italy; [email protected] (I.C.); [email protected] (P.T.); [email protected] (L.M.); [email protected] (F.P.) * Correspondence: [email protected]; Tel.: +39-0512091294 Abstract: Moving toward a more sustainable development, a pivotal role is played by circular economy and a smarter waste management. Industrial wastes from plants offer a wide spectrum of possibilities for their valorization, still being enriched in high added-value molecules, such as secondary metabolites (SMs). The current review provides an overview of the most common SM classes (chemical structures, classification, biological activities) present in different plant waste/by- products and their potential use in various fields. A bibliographic survey was carried out, taking into account 99 research articles (from 2006 to 2020), summarizing all the information about waste type, its plant source, industrial sector of provenience, contained SMs, reported bioactivities, and proposals for its valorization. This survey highlighted that a great deal of the current publications are focused on the exploitation of plant wastes in human healthcare and food (including cosmetic, pharmaceutical, nutraceutical and food additives). However, as summarized in this review, plant SMs also possess an enormous potential for further uses. Accordingly, an increasing number of investigations on Citation: Chiocchio, I.; Mandrone, neglected plant matrices and their use in areas such as veterinary science or agriculture are expected, M.; Tomasi, P.; Marincich, L.; Poli, F.
    [Show full text]
  • Natural Toxins
    Lecture Material - Food Safety 2013/2014 Inneke Hantoro FOOD AND TOXICITY: Natural Toxins Hazards in food • Physical: glass, stone, metal, wood, etc • Chemical: - natural toxins - residues - metals - toxins formed during food processing • Microbiological: pathogenic microorganisms (bacteria, viruses, parasites, etc) Foodborne Diseases Infections Intoxications Toxicoinfection Invasive Infection Chemical Poisonous Poisonous Microbial Other Neurotoxins Enterotoxins Poisoning Plant Animal Intoxications Tissues Tissues Intestinal Systemic Other Mucosa Tissues or Organs (Muscle, Mycotoxins Algal Toxins Bacterial Liver, Joints, (Fungal Toxins Fetus, Other) Toxins) Diarrhogenic Emetic Enterotoxins Neurotoxins Other 1 Natural Toxins • They are naturally present in plants & animals. • The long term ingestion of natural toxins in commonly eaten foods the risks to human health? • Usually, natural toxins are not acutely toxic, except in a few cases in animals. • Most of the natural toxins, particularly those occurring in plant-derived foods, induce adverse effects only after chronic ingestion or by allergic reactions. Risks of toxins in food • General toxicity (instant death or illness) • Carcinogenic • Mutagenic • Teratogenic • Endocrine disrupters (hormones) • Microbial pathogens Natural Toxins in Foods • Endogenous toxins of plant origin Toxic phenolic substances: flavonoids, tannins, coumarin, safrole, and myristicin Cyanogenic glycosides Glucosinolates Acetylcholinesterase inhibitors Biogenic amines Central stimulants • Natural contaminants Mixing of edible plants with toxic plants Contamination resulting from intake of toxic substances by animals Microbial toxins 2 Endogenous toxins of plant origin Flavonoids • A class of plant pigments that are widely present in human food, are the flavonoids. • These pigments are polyhydroxy-2-phenylbenzo-γ- pyrone derivatives, occurring as aglycones, glycosides and methyl ethers. A group of yellow pigments that occurs abundantly is the flavones.
    [Show full text]
  • Toxins and Signalling Evelyne Benoit, Françoise Goudey-Perriere, P
    Toxins and Signalling Evelyne Benoit, Françoise Goudey-Perriere, P. Marchot, Denis Servent To cite this version: Evelyne Benoit, Françoise Goudey-Perriere, P. Marchot, Denis Servent. Toxins and Signalling. SFET Publications, Châtenay-Malabry, France, pp.204, 2009. hal-00738643 HAL Id: hal-00738643 https://hal.archives-ouvertes.fr/hal-00738643 Submitted on 21 May 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. Collection Rencontres en Toxinologie © E. JOVER et al. TTooxxiinneess eett SSiiggnnaalliissaattiioonn -- TTooxxiinnss aanndd SSiiggnnaalllliinngg © B.J. LAVENTIE et al. Comité d’édition – Editorial committee : Evelyne BENOIT, Françoise GOUDEY-PERRIERE, Pascale MARCHOT, Denis SERVENT Société Française pour l'Etude des Toxines French Society of Toxinology Illustrations de couverture – Cover pictures : En haut – Top : Les effets intracellulaires multiples des toxines botuliques et de la toxine tétanique - The multiple intracellular effects of the BoNTs and TeNT. (Copyright Emmanuel JOVER, Fréderic DOUSSAU, Etienne LONCHAMP, Laetitia WIOLAND, Jean-Luc DUPONT, Jordi MOLGÓ, Michel POPOFF, Bernard POULAIN) En bas - Bottom : Structure tridimensionnelle de l’alpha-toxine staphylocoque - Tridimensional structure of staphylococcal alpha-toxin. (Copyright Benoit-Joseph LAVENTIE, Daniel KELLER, Emmanuel JOVER, Gilles PREVOST) Collection Rencontres en Toxinologie La collection « Rencontres en Toxinologie » est publiée à l’occasion des Colloques annuels « Rencontres en Toxinologie » organisés par la Société Française pour l’Etude des Toxines (SFET).
    [Show full text]
  • Review of the Inhibition of Biological Activities of Food-Related Selected Toxins by Natural Compounds
    Toxins 2013, 5, 743-775; doi:10.3390/toxins5040743 OPEN ACCESS toxins ISSN 2072-6651 www.mdpi.com/journal/toxins Review Review of the Inhibition of Biological Activities of Food-Related Selected Toxins by Natural Compounds Mendel Friedman 1,* and Reuven Rasooly 2 1 Produce Safety and Microbiology Research Unit, Agricultural Research Service, USDA, Albany, CA 94710, USA 2 Foodborne Contaminants Research Unit, Agricultural Research Service, USDA, Albany, CA 94710, USA; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-510-559-5615; Fax: +1-51-559-6162. Received: 27 March 2013; in revised form: 5 April 2013 / Accepted: 16 April 2013 / Published: 23 April 2013 Abstract: There is a need to develop food-compatible conditions to alter the structures of fungal, bacterial, and plant toxins, thus transforming toxins to nontoxic molecules. The term ‘chemical genetics’ has been used to describe this approach. This overview attempts to survey and consolidate the widely scattered literature on the inhibition by natural compounds and plant extracts of the biological (toxicological) activity of the following food-related toxins: aflatoxin B1, fumonisins, and ochratoxin A produced by fungi; cholera toxin produced by Vibrio cholerae bacteria; Shiga toxins produced by E. coli bacteria; staphylococcal enterotoxins produced by Staphylococcus aureus bacteria; ricin produced by seeds of the castor plant Ricinus communis; and the glycoalkaloid α-chaconine synthesized in potato tubers and leaves. The reduction of biological activity has been achieved by one or more of the following approaches: inhibition of the release of the toxin into the environment, especially food; an alteration of the structural integrity of the toxin molecules; changes in the optimum microenvironment, especially pH, for toxin activity; and protection against adverse effects of the toxins in cells, animals, and humans (chemoprevention).
    [Show full text]
  • Abstracts from the 3Rd ECFG
    Fungal Genetics Reports Volume 43 Article 34 Abstracts from the 3rd ECFG European Congress on Fungal Genetics Follow this and additional works at: https://newprairiepress.org/fgr This work is licensed under a Creative Commons Attribution-Share Alike 4.0 License. Recommended Citation European Congress on Fungal Genetics. (1996) "Abstracts from the 3rd ECFG," Fungal Genetics Reports: Vol. 43, Article 34. https://doi.org/10.4148/1941-4765.1330 This Supplementary Material is brought to you for free and open access by New Prairie Press. It has been accepted for inclusion in Fungal Genetics Reports by an authorized administrator of New Prairie Press. For more information, please contact [email protected]. Abstracts from the 3rd ECFG Abstract Abstracts from the European Congress on Fungal Genetics #3, held March 27-30, 1996, Munster, Germany This supplementary material is available in Fungal Genetics Reports: https://newprairiepress.org/fgr/vol43/iss1/34 : Abstracts from the 3rd ECFG European Congress on Fungal Genetics #3 Held March 27-30, 1996 Munster, Germany Table of Contents Lecture Abstracts ...................................................................................................................... 1 Poster Abstracts, Differentiation ..................................................................................... 20 Poster Abstracts, Biotechnology ...................................................................................... 49 Poster Abstracts, Fungal-host- interaction and signal transduction .................. 81
    [Show full text]
  • HT29) and Liver (Hepg2) Cancer Cells
    2832 J. Agric. Food Chem. 2004, 52, 2832−2839 Glycoalkaloids and Metabolites Inhibit the Growth of Human Colon (HT29) and Liver (HepG2) Cancer Cells KAP-RANG LEE,† NOBUYUKI KOZUKUE,† JAE-SOOK HAN,† JOON-HONG PARK,† EUN-YOUNG CHANG,† EUN-JUNG BAEK,† JONG-SUN CHANG,† AND MENDEL FRIEDMAN*,§ College of Human Ecology and Kinesiology, Yeungnam University, Gyongsan 712-749, Korea, and Western Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, 800 Buchanan Street, Albany, California 94710 As part of an effort to improve plant-derived foods such as potatoes, eggplants, and tomatoes, the antiproliferative activities against human colon (HT29) and liver (HepG2) cancer cells of a series of structurally related individual compounds were examined using a microculture tetrazolium (MTT) assay. The objective was to assess the roles of the carbohydrate side chain and aglycon part of Solanum glycosides in influencing inhibitory activities of these compounds. Evaluations were carried out with four concentrations each (0.1, 1, 10, and 100 µg/mL) of the the potato trisaccharide glycoalkaloids R-chaconine and R-solanine; the disaccharides â1-chaconine, â2-chaconine, and â2-solanine; the monosaccharide γ-chaconine and their common aglycon solanidine; the tetrasaccharide potato glycoalkaloid dehydrocommersonine; the potato aglycon demissidine; the tetrasaccharide tomato glycoalkaloid R-tomatine, the trisaccharide â1-tomatine, the disaccharide γ-tomatine, the monosac- charide δ-tomatine, and their common aglycon tomatidine; the eggplant glycoalkaloids solamargine and solasonine and their common aglycon solasodine; and the nonsteroidal alkaloid jervine. All compounds were active in the assay, with the glycoalkaloids being the most active and the hydrolysis products less so.
    [Show full text]
  • Supplementary Material
    Supplementary Material Figure S1. Coomassie bright blue staining of purified protein, SETDB1 (23 kD), Lane 1, 2 and 3 are liquid flow outs 1, 2 and 3 times from the column Table S1. Cell viability percentages of 502 natural compounds against U251 glioma cells Compound Name Cell viability (%) Compound Name Cell viability (%) Emetine 34.46 Bicuculline, (+)- 75.80 Methyllycaconitine citrate 44.15 Butein 76.09 Streptonigrin 49.91 Rauwolscine 76.29 Brefeldin A 49.94 Deltaline 76.93 Harringtonine 50.79 Eburnamonine, (-)- 77.05 Echinomycin 57.97 Salsolinol HBr 77.21 Dehydroandrographolide 58.25 Pseudopelletierin HCl 78.16 Nonactin 60.74 Quinidine HCl 78.87 Vinblastine sulfate 63.91 Rotenone 79.18 Antimycin A1 66.14 Delcorine 79.19 Thapsigargin 66.72 Brucine n-oxide 79.31 Taxol 67.43 Strychnine HCl 79.34 Radicicol 67.80 Rottlerin 79.98 Vincristine sulfate 69.39 Resveratrol 80.08 Phorbol 12-myristate 13-acetate, 4-a - 73.81 Eriodictyol 80.38 Tunicamycin B 74.38 Sterigmatocystin 81.05 Sitosterol, b - 74.46 Arecoline HBr 81.16 Kaempferol 74.61 Emodin 81.39 Anisomycin 75.32 Gramine 81.52 Rosmarinic acid 75.79 Veratridine 81.59 Veratramine 81.71 Condelphine 84.56 Eriocitrin 81.71 Robinetine 84.58 Narasin 82.20 Quassin 84.80 Bavachinin A 82.27 Quercetin 84.86 Actinomycin D 82.39 Diacetylkorseveriline 84.94 Harmaline HCl 82.48 Cotinine, (-)- 85.01 Chrysoeriol 82.67 Chaetomellic acid A 85.07 Lysergol 82.69 Rhamnetine 85.14 Desoxypeganine HCl 83.13 Austricin 85.48 Datiscetin 83.15 Phytosphingosine 85.74 Harmine HCl 83.42 Rifampicin 85.76 Compound Name
    [Show full text]
  • INSECTICIDES from PLANTS a Review of the Literature, 1954-1971
    /■■, INSECTICIDES FROM PLANTS A Review of the Literature, 1954-1971 Agriculture Handbook No. 461 >. M. r-ii cr- -•-.X €*0 ., ••> «H fTI 5:> ^':UA "X> ..; pn 1 2 Ci) :, ^'2 cr : .> oO > 5 Ç? o :í::;:'. or Agricultural Research Service UNITED STATES DEPARTMENT OF AGRICULTURE USDA, National Agricultural Library NALBldg 10301 Baltimore Blvd BeltsviHô, MD 20705-2351 Washington, D.C. Issued January 197Î For sale by the Superintendent of Documents, U.S. Government Printing Office ' Washington, D.C. 20402—Price $2 Stock Number 0100-03197 CONTENTS Page Page Cryptogams 2 Cyrillaceae 26 Agaricaceae 2 Datiscaceae 26 Dematiaceae 2 Diapensiaceae 26 Entomophthoraceae 2 Dichapetalaceae 26 Equsetaceae 2 Dioscoreaceae 26 Moniliaceae 2 Dipsacaceae___ 27 Osmundaceae 3 Dipterocarpaceae 27 Polypodiaceae 3 Ebenaceae 28 Rhodomelaceae 3 Elaeagnaceae 28 Phanerogams and spermatophytes 3 Elaeocarpaceae 28 Acanthaceae 3 Ericaceae :-. 28 Aceraceae 4 Eriocaulaceae 29 Aizoaceae 4 Erythroxylaceae 29 Alismataceae 4 Euphorbiaceae 29 Amaranthaceae 4 Fagaceae 31 Amaryllidaceae 4 Flacourtiaceae 32 Anacardiaceae 4 Gentianaceae 32 Annonaceae 6 Geraniaceae 32 Apocynaceae 7 Gesneriaceae 32 Aquifoliaceae 8 Ginkgoaceae 32 Araceae 8 Gramineae 32 Araliaceae 9 Guttiferae __. 35 Aristolochiaceae 10 Halorrhagidaceae 37 Asclepiadaceae 10 Hamamelidaceae 37 Balsaminaceae 10 Hemandiaceae 37 Begoniaceae 11 Hippocastanaceae 37 Berberidaceae 11 Humiriaceae 37 Betulaceae 11 Hypericaceae 37 Bignoniaceae 12 Icacinaceae 37 Bombacaceae 13 Juglandaceae 37 Boraginaceae 13 Labiatae 38 Burseraceae
    [Show full text]
  • Pour Sonder La Bioaffinité Et Les Interactions Biocatalytiques De Petits Xénobiotiques
    d’ordre: 2007-12 Année 2007 THESE EN COCO----TUTELLETUTELLE entre l’Ecole Centrale de Lyon, France (Ecole doctorale Electronique, Electrotechnique, Automatique ) et l’Institut de Biologie Moléculaire et Génétique, Kyiv, Ukraine (Discipline : Biotechnologie) présentée devant Ecole Centrale de Lyon pour obtenir le grade de DOCTEUR d’ECOLE CENTRALE DE LYON soutenue publiquement le 15 juin 2007 par Iryna BENILOVA née SKSKRYSHEVSKARYSHEVSKA AppApprocheroche « biocapteur » pour sonder la bioaffinité et les interactions biocatalytiques de petits xénobiotiques Jury: Dr. Nicole JAFFREZIC-RENAULT Présidente Pr. Roland SALESSE Rapporteur Dr. Alexandr KUKLA Rapporteur Pr. Claude MARTELET Directeur de thèse (France) Pr. Alexey SOLDATKIN Directeur de thèse (Ukraine) Dr. Sergey DZYADEVYCH Examinateur AcknowledAcknowledggggmentsments The present work was carried out in the former laboratory CEGELY (now AMPERE) of Ecole Centrale de Lyon (ECL) in collaboration with the Laboratory of Biomolecular Electronics (LBME) in the Institute of Molecular Biology and Genetics (IMBG) of National Academy of Sciences of Ukraine (NASU). These institutions are gratefully acknowledged. My work in French laboratories was financially supported by EGIDE (France). I wish to thank my French supervisors, Professor Claude Martelet and Professor Nicole Jaffrezic-Renault for accepting me in CEGELY for my “co- tutelle” thesis. I am infinitely grateful for their confidence in me, their priceless help and generosity and, of course, for our fruitful scientific discussions during these years. I warmly thank Academician Anna V. El’skaya, the Director of IMBG NASU, and my Ukrainian supervisor, Professor Alexey P. Soldatkin, the Head of LBME, for giving me the chance to start my research work in the LBME and to continue it in the Ecole Centrale de Lyon.
    [Show full text]
  • Natural Toxins: Risks, Regulations and the Analytical Situation in Europe
    Anal Bioanal Chem (2004) 378 : 1152–1160 1152 DOI 10.1007/s00216-003-2373-4 REVIEW Hans P. van Egmond Natural toxins: risks, regulations and the analytical situation in Europe Received: 25 July 2003 / Revised: 15 October 2003 / Accepted: 27 October 2003 / Published online: 13 December 2003 © Springer-Verlag 2003 Abstract Natural toxins in food and feed are considered pean context are now directed towards significantly im- important food safety issues of growing concern, in par- proving this situation, and techniques such as liquid chro- ticular mycotoxins, phycotoxins and plant toxins. Most matography–mass spectroscopy offer promise in this re- scientific developments have occurred in the past few spect. Both the working group on biotoxins of the Euro- decades in the area of mycotoxins. Formal health risk as- pean Standardization Committee and the network of Na- sessments have been carried out by the Joint Expert Com- tional Reference Laboratories for Marine Biotoxins have mittee on Food Additives of the World Health Organiza- taken up responsibilities here. The plant toxins are a cate- tion and the Food and Agriculture Organization. Limits gory of natural toxins, where the situation is the least de- and regulations for mycotoxins in food and feed have veloped with respect to regulations, validated methods of been established in many countries, including practically analysis and reference materials. Yet, their occurrence in a all European countries. An array of (formally validated) wide range of consumable plant species demands the at- analytical methods and (certified) reference materials have tention of the analytical community. become available. Several European research projects, funded by the European Commission and supported by the Keywords Natural toxin · Mycotoxin · Phycotoxin · European Standardization Committee, have significantly Plant toxin · Analysis · Reference material contributed to this development.
    [Show full text]
  • Chemistry, Biochemistry, and Safety of Acrylamide. a Review Mendel Friedman J
    Subscriber access provided by DigiTop | USDA's Digital Desktop Library Review Chemistry, Biochemistry, and Safety of Acrylamide. A Review Mendel Friedman J. Agric. Food Chem., 2003, 51 (16), 4504-4526• DOI: 10.1021/jf030204+ • Publication Date (Web): 03 July 2003 Downloaded from http://pubs.acs.org on February 12, 2009 More About This Article Additional resources and features associated with this article are available within the HTML version: • Supporting Information • Links to the 35 articles that cite this article, as of the time of this article download • Access to high resolution figures • Links to articles and content related to this article • Copyright permission to reproduce figures and/or text from this article Journal of Agricultural and Food Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 4504 J. Agric. Food Chem. 2003, 51, 4504−4526 Chemistry, Biochemistry, and Safety of Acrylamide. A Review MENDEL FRIEDMAN* Western Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, 800 Buchanan Street, Albany, California 94710 Acrylamide (CH2dCHsCONH2), an industrially produced R,â-unsaturated (conjugated) reactive molecule, is used worldwide to synthesize polyacrylamide. Polyacrylamide has found numerous applications as a soil conditioner, in wastewater treatment, in the cosmetic, paper, and textile industries, and in the laboratory as a solid support for the separation of proteins by electrophoresis. Because of the potential of exposure to acrylamide, effects of acrylamide in cells, tissues, animals, and humans have been extensively studied. Reports that acrylamide is present in foods formed during their processing under conditions that also induce the formation of Maillard browning products heightened interest in the chemistry, biochemistry, and safety of this vinyl compound.
    [Show full text]