03215oam 2200685I 450 991045926600332120200520144314.00-429-13297-21-4398-1363-910.1201/EBK1439813621 (CKB)2670000000035599(EBL)566036(OCoLC)664233846(SSID)ssj0000412819(PQKBManifestationID)11306656(PQKBTitleCode)TC0000412819(PQKBWorkID)10381824(PQKB)11633423(MiAaPQ)EBC566036(PPN)154040258(Au-PeEL)EBL566036(CaPaEBR)ebr10405031(CaONFJC)MIL693166(EXLCZ)99267000000003559920180331d2010 uy 0engur|n|---|||||txtccrBioactive peptides applications for improving nutrition and health /Richard Owusu-ApentenBoca Raton :CRC Press,2010.1 online resource (416 p.)Description based upon print version of record.1-4398-5878-0 1-322-61884-4 1-4398-1362-0 Includes bibliographical references and index.Front cover; Contents; Preface; Acknowledgments; Author; Chapter 1: Nutrition and the HostResponse to Infectionand Injury; Chapter 2: Bioactive Peptidesfor Nutrition and Health; Chapter 3: Dietary ProteinRequirements for Health; Chapter 4: Protein Turnoverand Economics within the Body; Chapter 5: Major Processes forMuscle Gain and Loss; Chapter 6: Inflammation and InnateImmune Response; Chapter 7: Infection and Sepsis; Chapter 8: Anabolic Dysfunction; Chapter 9: Bioactive Peptidesfor Alleviating Illness Anorexia; Index; Back coverPresenting data from human studies and trials, along with recent research findings, this work summarizes the applications, and benefits of bioactive peptides used to mitigate major metabolic derangements arising from chronic illnesses and resulting in unwanted weight loss. Recent studies show bioactive peptides to enhance the body's antioxidant status, antisepsis capacity, immune function, anti-inflammatory capacity, mineral absorption, and appetite. This book covers general principles, such as host response, quality factors, protein economics, and muscle loss. It includes case studies on ageing, AIDS, COPD, diabetes, inflammatory bowel disease, kidney failure, and tuberculosis.--Provided by publisher.Peptide drugsDietary supplementsProteinsMetabolismProteins in human nutritionAppetite stimulantsElectronic books.Peptide drugs.Dietary supplements.ProteinsMetabolism.Proteins in human nutrition.Appetite stimulants.572/.65Owusu-Apenten R. K.887420MiAaPQMiAaPQMiAaPQBOOK9910459266003321Bioactive peptides1982491UNINA05418nam 2200673 450 991081857400332120230807204754.01-118-96062-91-118-96055-61-118-96042-4(CKB)2670000000592465(EBL)1895815(SSID)ssj0001420882(PQKBManifestationID)11805037(PQKBTitleCode)TC0001420882(PQKBWorkID)11422675(PQKB)11204673(MiAaPQ)EBC1895815(DLC) 2014023772(Au-PeEL)EBL1895815(CaPaEBR)ebr11015198(CaONFJC)MIL719003(OCoLC)903956521(EXLCZ)99267000000059246520150212h20152015 uy 0engur|n|---|||||txtccrBiosynthesis of heterocycles from isolation to gene cluster /Patrizia Diana, Girolamo CirrincioneHoboken, New Jersey :Wiley,2015.©20151 online resource (783 p.)"A John Wiley & Sons, Inc., publication."1-322-87721-1 1-118-02867-8 Includes bibliographical references at the end of each chapters and index.Cover; Contents; Preface; Acknowledgments; Chapter 1 Introduction; 1.1 Natural Products: Primary and Secondary Metabolites; 1.2 Common Reactions in Secondary Metabolites; 1.2.1 Alkylations; 1.2.2 Wagner-Meerwein Rearrangements; 1.2.3 Aldol and Claisen Reactions; 1.2.4 Schiff Base Formation and Mannich Reactions; 1.2.5 Transaminations; 1.2.6 Decarboxylations; 1.2.7 Oxidation and Reduction Reactions; 1.2.8 Dehalogenation/Halogenation Reactions; 1.2.9 Glycosylation Reactions; References; Chapter 2 Techniques for Biosynthesis; 2.1 Isotopic Labeling; 2.1.1 Stable Isotopes2.1.2 Radioactive Isotopes2.2 Gene Coding for Enzymes; 2.3 Combinatorial Biosynthesis; References; Chapter 3 Three-Membered Heterocyclic Rings and Their Fused Derivatives; 3.1 Aziridines and Azirines; 3.1.1 Azicemicins; 3.1.2 Miraziridine; 3.1.3 Maduropeptin; 3.1.4 Azinomycins; 3.1.5 Ficellomycin; 3.1.6 Mitomycins; 3.1.7 Azirinomycin and Related Azirines; 3.2 Oxiranes and Oxirenes; 3.2.1 Fosfomycin; 3.2.2 AK, HC, and AF toxins; 3.2.3 Cerulenin; 3.2.4 Polyhydroxyalkanoates; 3.2.5 Epoxyrollins; 3.2.6 Asperlactone, Aspyrone, Asperline; 3.2.7 Tajixanthone; 3.2.8 Cyclomarin; 3.2.9 Cyclopenin3.2.10 Ovalicin and Fumagillin3.2.11 Methylenomycin A; 3.2.12 Antibiotic LL-C10037; 3.2.13 Manumycins; 3.2.14 Scopolamine; 3.2.15 Iridoid Glucosides; 3.2.16 Cordiaquinone; 3.2.17 Cyclizidine and Indolizomycin; 3.2.18 Enediyne Antibiotics; 3.2.19 Macrolides; 3.2.20 Epothilones; 3.2.21 Pimaricin; 3.2.22 Hypothemycin; 3.2.23 Radicicol and Monocillin I; 3.2.24 Trichothecenes; 3.2.25 Sporolides A and B; References; Chapter 4 Four-Membered Heterocyclic Rings and Their Fused Derivatives; 4.1 Azetidine and Azetines; 4.1.1 Azetidine-2-carboxylic acid; 4.1.2 Polyoxins; 4.1.3 Mugineic Acids4.1.4 Tabtoxin and Tabtoxinine-β-lactam4.1.5 Nocardicins; 4.1.6 Thienamycin; 4.1.7 Clavulanic Acid and Clavams; 4.1.8 Penicillins and Cephalosporins; 4.2 Oxetanes; 4.2.1 Oxetanocins; 4.2.2 Salinosporamides; 4.2.3 Taxol; 4.3 Dithiethanes; 4.3.1 Tropodithietic acid and Thiotropocin; References; Chapter 5 Five-Membered Heterocyclic Rings and Their Fused Derivatives; 5.1 Pyrroles (Including Tetrapyrroles); 5.1.1 2-Acetyl-1-pyrroline; 5.1.2 Pyrrolnitrin; 5.1.3 Broussonetines; 5.1.4 Prodigiosin and Undecylprodigiosin; 5.1.5 Anatoxin-a and Homoanatoxin-a; 5.1.6 Nostopeptolides A5.1.7 Pyrrolizidine Alkaloids5.1.8 Toyocamycin and Sangivamycin; 5.1.9 Tetrapyrroles; 5.2 Indoles; 5.2.1 Indole-3-acetic acid and Glucobrassicin; 5.2.2 Camalexin; 5.2.3 Cyclomarazines; 5.2.4 Rebeccamycin and Staurosporine; 5.2.5 Paxilline; 5.3 Furans; 5.3.1 Furanomycin; 5.3.2 Xenofuranones A and B; 5.3.3 Acyl α- L-Rhamnopyranosides and Rhamnosyllactones; 5.3.4 Tuscolid and Tuscoron A and B; 5.3.5 Tetronomycin and Tetronasin; 5.3.6 Nonactin and Macrotetrolides; 5.3.7 Furanonaphthoquinone I; 5.4 Thiophenes; 5.5 Pyrazoles; 5.6 Imidazoles; 5.6.1 Histidine; 5.6.2 Amaranzole A; 5.6.3 Oroidin5.6.4 NikkomycinsThis book describes biosynthetic methods to synthesize heterocycliccompounds, offering a guide for the development of new drugs basedon natural products. The authors explain the role of naturalproducts in chemistry and their formation along with importantanalytical methods and techniques for working withheterocycles. Covers methods and techniques: isotopic labelling,enzymes and mutants, and pathway identification Provides a thorough resource of informationspecifically on heterocyclic natural products and their practicalbiosynthetic relevance Explains the role of natural products in chemistry aHeterocyclic compoundsSynthesisBiosynthesisHeterocyclic compoundsSynthesis.Biosynthesis.547/.59Diana Patrizia1642348Cirrincione GirolamoMiAaPQMiAaPQMiAaPQBOOK9910818574003321Biosynthesis of heterocycles3986980UNINA