Food Additives - Numerical List
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The Synthesis and Biological Evaluation of Potential ABA-Like Analogues: Prospective Substrates to Control Berry Ripening of Wine Grapes
The Synthesis and Biological Evaluation of Potential ABA-Like Analogues: Prospective Substrates to Control Berry Ripening of Wine Grapes. A thesis presented in fulfilment of the requirements for the degree of Doctor of Philosophy Ruyi Li BSc (Bio-Eng), MSc (Vit./Oen.) Northwest A&F University The University of Adelaide School of Agriculture, Food and Wine July 2012 Table of Contents Abstract........................................................................................................................... iii Declaration...................................................................................................................... vi Acknowledgements......................................................................................................... vii Abbreviations.................................................................................................................. ix Figures, Schemes and Tables......................................................................................... xi CHAPTER 1: INTRODUCTION................................................................................ 1 1.1 General Introduction................................................................................................... 1 1.2 Carotenoids................................................................................................................. 3 1.2.1 Definition, types and identification of carotenoids................................................. 3 1.2.2 Factors influencing the concentration of carotenoids -
CALCIUM STABILITY in a Nutshell ESSENTIAL CHEMISTRY
CALCIUM STABILITY in a nutshell ESSENTIAL CHEMISTRY Precipitation of calcium tartrate is becoming more frequent all over the world and causing both economic and brand damage that companies should be aware of. The cause of the problem is still unknown but may be found in climate change, viticultural and enological practices or the use of untreated concrete tanks. Whatever the origin, it is important to know how to identify wines that are potentially calcium unstable and how to treat them. Calcium content (0.04 - 0.15 g/L) of wine is 10-20 times lower than potassium. Calcium precipitates mainly as calcium tartrate (CaT). CaT solubility is only 3 times lower at -4°C than at 20°C: cooling has little effect on the rate of CaT precipitation. Potassium bitartrate precipitation does not induce that of CaT. Low calcium content and the presence of inhibiting factors in wine makes the formation of CaT germs that start the crystallization process unpredictable. WINE COMPOUNDS THAT HAVE AN INHIBITING EFFECT ON CALCIUM PRECIPITATION GLUCONIC ACID MALIC ACID CITRIC ACID COLLOIDS POTASSIUM MAGNESIUM MAIN FACTORS PROMOTING CaT PRECIPITATION CALCIUM LOW HIGH INSTABILITY TARTARIC ACID INSTABILITY pH The main factors promoting calcium precipitation are calcium, pH and tartaric acid. In particular, pH has a tremendous impact. The increase of only 0.1 points has a dramatic effect on the speed and intensity of precipitation. HOW TO RECOGNIZE CALCIUM TARTRATE PRECIPITATE Both CaT and potassium bitartrate form white (or red in the case of red wine) crystals and a sandy precipitate. To distinguish one salt from the other, perform the following trial put some crystals in a flask or beaker add some clean water warm the solution between 80-100°C stir occasionally If crystals do not dissolve, it is calcium tartrate ENARTIS SOLUTION FOR CALCIUM STABILITY HOW TO CHECK IF WINE IS CALCIUM UNSTABLE Analyze wine calcium content (Ca1). -
Notices Federal Register Vol
28416 Notices Federal Register Vol. 62, No. 100 Friday, May 23, 1997 This section of the FEDERAL REGISTER 1255 22nd Street, NW, Room 311, West interests of consumers. Through contains documents other than rules or End Court Building, Washington, DC adoption of food standards, codes of proposed rules that are applicable to the 20250±3700; (202) 418±8852. For practice, and other guidelines public. Notices of hearings and investigations, information pertaining to particular developed by its committees and by committee meetings, agency decisions and committees, the delegate of that promoting their adoption and rulings, delegations of authority, filing of petitions and applications and agency committee may be contacted. (A implementation by governments, Codex statements of organization and functions are complete list of U.S. delegates and seeks to ensure that the world's food examples of documents appearing in this alternate delegates can be found in supply is sound, wholesome, free from section. Appendix 1 to this notice.) adulteration, and correctly labeled. In SUPPLEMENTARY INFORMATION: the United States, the United States Department of Agriculture (USDA); the DEPARTMENT OF AGRICULTURE Background Food and Drug Administration (FDA), The World Trade Organization (WTO) Department of Health and Human Food Safety and Inspection Service was established on January 1, 1995, as Services (HHS), and the Environmental [Docket No. 97±026N] the common international institutional Protection Agency (EPA) manage and framework for the conduct of trade carry out U.S. Codex activities. International Standard-Setting relations among its members in matters As the agency responsible for Activities related to the Uruguay Round informing the public of the sanitary and Agreements. -
Ricinus Cell Cultures. I. Identification of Rhodoxanthin
Hormone Induced Changes in Carotenoid Composition in Ricinus Cell Cultures. I. Identification of Rhodoxanthin Hartmut Kayser Abteilung für Allgemeine Zoologie and Armin R. Gemmrich Abteilung für Allgemeine Botanik, Universität Ulm, Postfach 40 66. D-7900 Ulm/Donau Z. Naturforsch. 39c, 50-54 (1984); received November 10. 1983 Rhodoxanthin. Carotenoids, Plant Cell Cultures, Plant Hormones, Ricinus communis When cell cultures of Ricinus communis are grown in light and with kinetin as the sole growth factor red cells are formed. The red pigmentation is due to the accumulation o f rhodoxanthin which is the major carotenoid in these cultures. The identification of this retro-type carotenoid is based on electronic and mass spectra, on chemical transformation to zeaxanthin, and on comparison with an authentic sample. Rhodoxanthin is not present in any part of the intact plant. The major yellow carotenoid in the red cultures is lutein. Introduction Materials and Methods Chloroplasts of higher plants contain a fairly Plant material constant pattern of carotenoids which function as accessory pigments in photosynthesis and protect The callus cultures are derived from the endo the chlorophylls and chloroplast enzymes against sperm of the castor bean. Ricinus communis; only photodestruction [1]. In contrast to this type of strain A, as characterized elsewhere [5]H was used. plastids, chromoplasts contain a great variety of The cells were cultivated under fluorescent white carotenoids, some of which are not found in other light (Osram L65W/32, 5 W /m 2) at 20 °C On a solid types of plastids. These pigments are responsible for Gamborg B5 medium [7] supplemented with 2% the bright red. -
Method for Producting L-Aspartic Acid
Europiisches Patentamt (19) J European Patent Office © Publication number: 0 129 119 Office europeen des brevets A2 © EUROPEAN PATENT APPLICATION © Application number: 84106218.5 ©Int CI.3: C 12 N 15/00 C 12 P 13/20, C 12 N 1/20 @ Date of filing: 30.05.84 C 12 N 9/88 //(C12N1/20,C12R1/19), (C12P13/20,C12R1/19) © Priority: 15.06.83 JP 107573/83 © Applicant: Tanabe Seiyaku Co., Ltd. No. 21 Dosho-machi 3-chome Higashi-ku Osaka-shi Osaka-fu(JP) © Date of publication of application: 27.12.84 Bulletin 84/52 © Inventor: KisumLMasahiko No. 12-20, Morikitacho4-chome Higashinada-ku © Designated Contracting States: Kobe-shi Hyogo-ken(JP) CH DE FR GB U SE © Inventor: Komatsubara,Saburo No. 385-10, Kamigasacho Kusatsu-shi Shiga-ken(JP) © Inventor: Taniguchi, Tomoyasu No. 12-22, Kawaharacho Izumiotsu-shi Osaka-fu(JP) © Representative: Kraus, Walter, Dr. et al, Patentanwalte Kraus, Weisert & Partner Irmgardstrasse 15 D-8000 Munchen 71 (DE) © Method for producing L-aspartic acid. A novel microorganism of the genus Escherichia contain- ing a hybrid plasmid prepared by integrating a plasmid with a deoxyribonucleic acid carrying the gene for aspartase which is obtained from a microorganism of the genus Escherichia. An industrially advantageous method for producing L-aspartic acid comprising contacting a culture of the novel microorganism, microbial cells collected from the culture or a processed material of the microbial cells with fumaric acid and ammonia to produce L-aspartic acid and then collecting L-aspartic acid thus produced is also disclosed. < 0> FIELD OF THE INVENTION The present invention relates to a novel micro- organism of the genus Escherichia having high aspartase activity and a method for producing L-aspartic acid using the microorganism. -
Analysis of Chemical Composition of Cowpea Floral Volatiles and Nectar
i ANALYSIS OF CHEMICAL COMPOSITION OF COWPEA FLORAL VOLATILES AND NECTAR BY CONSOLATA ATIENO AGER, B.Ed (Kenyatta) I56/7423/2001 THESIS SUBMITTED IN PARTIAL FULFILLMENT FOR THE REQUIREMENTS OF THE DEGREE OF MASTER OF SCIENCE IN THE SCHOOL OF PURE AND APPLIED SCIENCES, KENYATTA UNIVERSITY NOVEMBER 2009 1 DECLARATION I hereby declare that this is my own original work and it has not been presented for award of a degree in any other university. Signed………………………..Date……………………… Consolata Atieno Ager Department of Chemistry Kenyatta University We confirm that the work reported in this thesis was carried out by the candidate under our supervision. Signed……………………..Date……………………… Prof. Isaiah O. Ndiege Department of Chemistry Kenyatta University Signed……………………..Date……………………… Dr. Sauda Swaleh Department of Chemistry Kenyatta University Signed……………………..Date……………………… Prof. Ahmed Hassanali Behavioral and Chemical Ecology Department (BCED) International Center of Insect Physiology and Ecology (ICIPE) Signed……………………..Date……………………… Dr. Remmy Pasquet Molecular Biology and Biochemistry Department (MBBD) 1 2 International Center of Insect Physiology and Ecology (ICIPE) DEDICATION To my husband Godfrey Isaac Ochieng‟ and my children Mercy, Humphrey and Jeffrey 2 3 ACKNOWLEDGEMENTS Above all, I want to glorify and exalt the Almighty God for giving me sound health and mind during the entire research period. I register my sincere appreciation to my research supervisors: Prof. Isaiah Ndiege, Prof. Ahmed Hassanali, Dr. Remmy Pasquet and Dr. Sauda Swaleh for the guidance, comments, discussions, supervision, advice, support and encouragement they gave me during my research. Special thanks to all the staff of BCED and MBBD departments at ICIPE for technical assistance and cooperation during my stay at the center. -
Characterization of the Novel Role of Ninab Orthologs from Bombyx Mori and Tribolium Castaneum T
Insect Biochemistry and Molecular Biology 109 (2019) 106–115 Contents lists available at ScienceDirect Insect Biochemistry and Molecular Biology journal homepage: www.elsevier.com/locate/ibmb Characterization of the novel role of NinaB orthologs from Bombyx mori and Tribolium castaneum T Chunli Chaia, Xin Xua, Weizhong Sunb, Fang Zhanga, Chuan Yea, Guangshu Dinga, Jiantao Lia, ∗ Guoxuan Zhonga,c, Wei Xiaod, Binbin Liue, Johannes von Lintigf, Cheng Lua, a State Key Laboratory of Silkworm Genome Biology, Key Laboratory of Sericultural Biology and Genetic Breeding, Ministry of Agriculture and Rural Affairs, College of Biotechnology, Southwest University, Chongqing 400715, China b College of Animal Science and Technology, Southwest University, Chongqing 400715, China c Life Sciences Institute and the Innovation Center for Cell Signaling Network, Zhejiang University, Hangzhou 310058, China d College of Plant Protection, Southwest University, Chongqing 400715, China e Sericulture Research Institute, Sichuan Academy of Agricultural Science, Chengdu 610066, China f Department of Pharmacology, Case Western Reserve University, School of Medicine, Cleveland, OH 44106, USA ABSTRACT Carotenoids can be enzymatically converted to apocarotenoids by carotenoid cleavage dioxygenases. Insect genomes encode only one member of this ancestral enzyme family. We cloned and characterized the ninaB genes from the silk worm (Bombyx mori) and the flour beetle (Tribolium castaneum). We expressed BmNinaB and TcNinaB in E. coli and analyzed their biochemical properties. Both enzymes catalyzed a conversion of carotenoids into cis-retinoids. The enzymes catalyzed a combined trans to cis isomerization at the C11, C12 double bond and oxidative cleavage reaction at the C15, C15′ bond of the carotenoid carbon backbone. Analyses of the spatial and temporal expression patterns revealed that ninaB genes were differentially expressed during the beetle and moth life cycles with high expression in reproductive organs. -
Pigment Palette by Dr
Tree Leaf Color Series WSFNR08-34 Sept. 2008 Pigment Palette by Dr. Kim D. Coder, Warnell School of Forestry & Natural Resources, University of Georgia Autumn tree colors grace our landscapes. The palette of potential colors is as diverse as the natural world. The climate-induced senescence process that trees use to pass into their Winter rest period can present many colors to the eye. The colored pigments produced by trees can be generally divided into the green drapes of tree life, bright oil paints, subtle water colors, and sullen earth tones. Unveiling Overpowering greens of summer foliage come from chlorophyll pigments. Green colors can hide and dilute other colors. As chlorophyll contents decline in fall, other pigments are revealed or produced in tree leaves. As different pigments are fading, being produced, or changing inside leaves, a host of dynamic color changes result. Taken altogether, the various coloring agents can yield an almost infinite combination of leaf colors. The primary colorants of fall tree leaves are carotenoid and flavonoid pigments mixed over a variable brown background. There are many tree colors. The bright, long lasting oil paints-like colors are carotene pigments produc- ing intense red, orange, and yellow. A chemical associate of the carotenes are xanthophylls which produce yellow and tan colors. The short-lived, highly variable watercolor-like colors are anthocyanin pigments produc- ing soft red, pink, purple and blue. Tannins are common water soluble colorants that produce medium and dark browns. The base color of tree leaf components are light brown. In some tree leaves there are pale cream colors and blueing agents which impact color expression. -
STB046 1939 the Carotenoid Pigments
THE CAROTENOID PIGMENTS Occurrence, Properties, Methods of Determination, and Metabolism by the Hen FOREWORD This bulletin has been written as a brief review of the carotenoid pigments. The occurrence, properties, and methods of determina- tion of this interesting class of compounds are considered, and special consideration is given to their utilization by the hen. The work has been done in the departments of Chemistry and Poultry Husbandry, cooperating, on Project No. 193. The project was started in 1932 and several workers have aided in the accumulation of information. The following should be men- tioned for their contributions: Mr. Wilbor Owens Wilson, Mr. C. L. Gish, Mr. H. F. Freeman, Mr. Ben Kropp, and Mr. William Proudfit. We are also greatly indebted to Dr. H. D. Branion of the Depart- ment of Animal Nutrition, Ontario Agricultural College, Guelph, Canada, for his fine coöperative studies on the vitamin A potency of corn. A number of unpublished observations from these laboratories and others have been organized and included in this bulletin. Extensive use has also been made of the material presented in Zechmeister’s “Carotenoide,” and “Leaf Xanthophylls” by Strain. It is hoped that this work be considered in no way a complete story of the metab- olism of carotenoid pigments in the fowl, but rather an interpreta- tion of the information which is available at this time. The wide range of distribution of the carotenoid pigments in such a wide variety of organisms points strongly to the importance of these materials biologically. In recent years chemical and physio- logical studies of the carotenoids have revealed numerous relation- ships to other classes of substances in the plant and animal world. -
Identifying Anatomical Sites of Carotenoid Metabolism in Birds
Naturwissenschaften (2009) 96:987–988 DOI 10.1007/s00114-009-0544-7 COMMENTS & REPLIES Identifying anatomical sites of carotenoid metabolism in birds Kevin J. McGraw Received: 8 April 2009 /Accepted: 9 April 2009 /Published online: 20 May 2009 # Springer-Verlag 2009 Carotenoid metabolism has long interested plant and animal identification (Wyss 2004), isotope labeling of precursors biochemists (Goodwin 1986; Lu and Li 2008). Identifying (Burri and Clifford 2004), and by inference from ex vivo tissue sites and enzymes responsible for carotenoid trans- chemical reactions (Khachik et al. 1998) or where caroten- formations (e.g., β-carotene to vitamin A) has been oid types exist in no other tissue type (McGraw 2004). challenging. Colorful birds have recently become a model del Val et al. (2009) undertook none of these types of for studying carotenoid nutrition and metabolism, in the investigation. The first step in such research is to rule out a context of sexual selection and honest signaling (McGraw dietary source to the pigment, but the authors did not study 2006). In a recent paper published in Naturwissenschaften, food carotenoids in crossbills; they sampled only liver, del Val et al. (2009) described carotenoid profiles in tissues skin, and feathers from accidentally field-killed animals and of male common crossbills (Loxia curvirostra), with the drew blood from molting birds. While red carotenoids are aim of localizing metabolic site(s) for a ketocarotenoid not currently thought to be common in diets of herbivorous pigment—3-hydroxy-echinenone (3HE)—present in red land birds (e.g., rubixanthin in rose hips, rhodoxanthin in feathers. They found 3HE in blood and liver, unlike Taxus berries), this is a key assumption to biochemically previous studies of colorful songbirds where metabolized validate for any species, given the paucity of information integumentary carotenoids were found only at peripheral on avian food carotenoids. -
Things We're Dwelling on Now… Cold Stabilization
Grape Resources www.fruit.cornell.edu/grapes Things We’re Dwelling on Now… Cold Stabilization Chris Gerling, Enology Extension Associate, Cornell University - NYSAES First published in Cellar Dweller - January 2010. Cold stabilization time is here for many of us. When you think about it, cold stabilization shares with all winemaking the principle that bad results are unlikely to hurt anyone, but you can definitely upset people. Here are some tips to keep in mind when attempting to get the “wine diamonds” out before they show up at a dinner party. Faster chilling is better. For quicker and more complete precipitation, changing the temperature drastically is the best way to shake those crystals loose. Seeding with potassium bitartrate and agitating the wine can speed up the process further. Stabilization can still take place with traditional chilling and higher temperatures, but the process will take more time. Chilling is only effective on potassium bitartrate. In a year where a lot of deacidification took place, a fair amount of calcium carbonate was most likely used. Calcium tartrate is NOT responsive to temperature like potassium bitartrate is. The standard conductivity and freeze tests are also not effective in determining stability. What conditions do affect calcium tartrate? Alcohol, pH and the presence of sugars and acids all play a role in both potassium and calcium tartrate precipitation. As a general rule, higher alcohol and higher pH will favor precipitation, while organic acids and sugars seem to inhibit it. Malic acid seems more inhibitory than lactic, however, so malolactic fermentation can be considered as a step towards precipitation, especially when the pH bump is considered. -
Tartaric Acid Handling 1 2 Identification of Petitioned Substance
Tartaric Acid Handling 1 2 Identification of Petitioned Substance 3 Chemical Names: 14 4 2,3-dihydroxybutanedioic acid CAS Numbers: 5 L(+) tartaric acid: 87-69-4 6 Other Name: D(-) tartaric acid: 147-71-7 7 2,3-dihydroxysuccinic acid Mesotartaric acid: 147-73-9 8 Thearic acid Racemic acid: 133-37-9 9 Uvic acid 10 L(+) tartaric acid Other Codes: D(-) tartaric acid L(+) tartaric acid: 205-695-6 Mesotartaric acid D(-) tartaric acid: 201-766-0 Racemic acid Mesotartaric acid: 205-696-1 Racemic acid: 205-105-7 11 Trade Names: 12 None 1513 Characterization of Petitioned Substance 16 17 Composition of the Substance: 18 Tartaric acid [HOOCCH(OH)CH(OH)COOH; C4H6O6] is a four-carbon, organic acid with two OH groups 19 on the second and third carbon atoms, and two carboxylic acid (COOH) groups involving the first and 20 fourth carbons. The chemical structure of L(+) tartaric acid is shown below: 21 22 Source: Reusch, 1999 23 24 Tartaric acid exists in three distinct isomeric forms, as shown in the Fisher projection formulas below. Two 25 forms are chiral isomers, which means that the molecules are non-superimposable on their mirror images. 26 The form of tartaric acid found naturally in grapes and often produced synthetically for use in handling is 27 the L(+) tartaric acid isomer. This form is generally referred to as the ‘dextro form’ (Church and Blumberg, 28 1951). The D(-) form of tartaric acid is less common in nature and has almost no practical uses. The third 29 form is an achiral isomer, mesotartaric acid, that also can be manufactured (Reusch, 1999).