LEADER 05510nam 2200697Ia 450 001 9910141395103321 005 20200520144314.0 010 $a1-118-40932-9 010 $a1-283-64617-X 010 $a1-118-40934-5 010 $a1-118-40929-9 035 $a(CKB)2670000000242714 035 $a(EBL)918272 035 $a(SSID)ssj0000721607 035 $a(PQKBManifestationID)11398121 035 $a(PQKBTitleCode)TC0000721607 035 $a(PQKBWorkID)10688718 035 $a(PQKB)10578404 035 $a(DLC) 2012034366 035 $a(Au-PeEL)EBL918272 035 $a(CaPaEBR)ebr10605288 035 $a(CaONFJC)MIL395867 035 $a(MiAaPQ)EBC918272 035 $a(OCoLC)808108828 035 $a(EXLCZ)992670000000242714 100 $a20120820d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aRedox biocatalysis$b[electronic resource] $efundamentals and applications /$fDaniela Gamenara ... [et al.] 210 $aHoboken, N.J. $cWiley$d2012 215 $a1 online resource (549 p.) 300 $aDescription based upon print version of record. 311 $a0-470-87420-1 320 $aIncludes bibliographical references and index. 327 $aREDOX BIOCATALYSIS; CONTENTS; PREFACE; 1. Enzymes Involved in Redox Reactions: Natural Sources and Mechanistic Overview; 1.1 Motivation: Green Chemistry and Biocatalysis; 1.2 Sources of Biocatalysts; 1.2.1 Plants and Animals as Sources of Redox Biocatalysts; 1.2.2 Wild-Type Microorganisms; 1.2.2.1 Yeasts; 1.2.2.2 Fungi; 1.2.2.3 Bacteria; 1.2.3 Metagenomic Assessments; 1.3 Overview of Redox Enzymes; 1.3.1 Dehydrogenases; 1.3.1.1 Zn-Dependent Dehydrogenases; 1.3.1.2 Flavin-Dependent Dehydrogenases; 1.3.1.3 Pterin-Dependent Dehydrogenases; 1.3.1.4 Quinoprotein Dehydrogenases 327 $a1.3.1.5 Dehydrogenases without Prosthetic Group1.3.2 Oxygenases; 1.3.2.1 Monooxygenases; 1.3.2.2 Dioxygenases; 1.3.3 Oxidases; 1.3.3.1 Iron-Containing Oxidases; 1.3.3.2 Copper-Containing Oxidases; 1.3.3.3 Flavin-Dependent Oxidases; 1.3.4 Peroxidases; 1.4 Concluding Remarks; References; 2. Natural Cofactors and Their Regeneration Strategies; 2.1 Types of Natural Cofactors-Mechanisms; 2.2 Cofactor Regeneration; 2.2.1 Enzymatic Regeneration of Reduced Cofactors; 2.2.1.1 Substrate-Assisted Method; 2.2.1.2 Enzyme-Assisted Method; 2.2.2 Enzymatic Regeneration of Oxidized Cofactors 327 $a2.2.3 Chemical Regeneration of Cofactors2.2.4 Electrochemical Regeneration of Cofactors; 2.2.5 Photochemical Regeneration of Cofactors; 2.3 Concluding Remarks; References; 3. Reactions Involving Dehydrogenases; 3.1 General Considerations; 3.2 Reduction of Carbonyl Groups; 3.2.1 Reduction of Aliphatic and Aromatic Ketones; 3.2.2 Reduction of ?- and ?-keto Esters and Derivatives; 3.2.3 Reduction of Diketones; 3.2.4 Reduction of Aldehydes; 3.3 Racemization and Deracemization Reactions; 3.4 Preparation of Amines; 3.5 Reduction of C-C Double Bonds; 3.6 Oxidation Reactions 327 $a3.7 Dehydrogenase-Catalyzed Redox Reactions in Natural Products3.8 Concluding Remarks; References; 4. Reactions Involving Oxygenases; 4.1 Monooxygenase-Catalyzed Reactions; 4.1.1 Hydroxylation of Aliphatic Compounds; 4.1.2 Hydroxylation of Aromatic Compounds; 4.1.3 Baeyer-Villiger Reactions; 4.1.3.1 Classification and Metabolic Role of BVMOs; 4.1.3.2 Isolated Enzymes versus Whole-Cell Systems (Wild-Type and Recombinant Microorganisms); 4.1.3.3 Substrate Profile of Available Baeyer-Villiger Monooxygenases; 4.1.3.4 Synthetic Applications of BVMOs; 4.1.4 Epoxidation of Alkenes 327 $a4.2 Dioxygenase-Catalyzed Reactions4.2.1 Aromatic Dioxygenases; 4.2.1.1 Dihydroxylation of Aromatic Compounds; 4.2.1.2 Other Oxidation Reactions Performed by Aromatic Dioxygenases; 4.2.2 Miscellaneous Dioxygenases; 4.2.2.1 Lipoxygenase; 4.3 Concluding Remarks; References; 5. Reactions Involving Oxidases and Peroxidases; 5.1 Oxidase-Catalyzed Reactions; 5.1.1 Oxidases Acting on C-O Bonds; 5.1.1.1 Galactose Oxidase; 5.1.1.2 Pyranose Oxidase; 5.1.1.3 Alcohol Oxidase; 5.1.1.4 Glucose Oxidase; 5.1.1.5 Glycolate Oxidase; 5.1.2 Laccases and Tyrosinases (Phenol Oxidases); 5.1.2.1 Laccase 327 $a5.1.2.2 Tyrosinase and Other Polyphenol Oxidases 330 $a Paves the way for new industrial applications using redox biocatalysis Increasingly, researchers rely on the use of enzymes to perform redox processes as they search for novel industrial synthetic routes. In order to support and advance their investigations, this book provides a comprehensive and current overview of the use of redox enzymes and enzyme-mediated oxidative processes, with an emphasis on the role of redox enzymes in chemical transformations. The authors examine the full range of topics in the field, from basic principles to new and emerging research and application 606 $aEnvironmental chemistry$xIndustrial applications 606 $aEnvironmental chemistry 606 $aEnzymes 606 $aOxidation-reduction reaction 615 0$aEnvironmental chemistry$xIndustrial applications. 615 0$aEnvironmental chemistry. 615 0$aEnzymes. 615 0$aOxidation-reduction reaction. 676 $a660.6/34 701 $aGamenara$b Daniela$f1964-$0968786 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910141395103321 996 $aRedox biocatalysis$92200895 997 $aUNINA LEADER 02094nam 2200601 450 001 9910814919603321 005 20230721020013.0 010 $a1-282-71003-6 010 $a9786612710032 010 $a1-4411-1475-0 035 $a(CKB)2670000000034315 035 $a(EBL)564312 035 $a(OCoLC)650310420 035 $a(SSID)ssj0000411828 035 $a(PQKBManifestationID)11306578 035 $a(PQKBTitleCode)TC0000411828 035 $a(PQKBWorkID)10356245 035 $a(PQKB)10792210 035 $a(MiAaPQ)EBC564312 035 $a(MiAaPQ)EBC5309764 035 $a(Au-PeEL)EBL5309764 035 $a(CaPaEBR)ebr11518730 035 $a(OCoLC)1027161903 035 $a(MiAaPQ)EBC3002971 035 $a(Au-PeEL)EBL3002971 035 $a(OCoLC)928191416 035 $a(EXLCZ)992670000000034315 100 $a20180315h20072007 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aAnglican and Evangelical? /$fRichard Turnbull 210 1$aLondon, [England] ;$aNew York, New York :$cContinuum,$d2007. 210 4$dİ2007 215 $a1 online resource (191 p.) 300 $aDescription based upon print version of record. 311 $a0-8264-8164-7 320 $aIncludes bibliographical references and index. 327 $aContents; Abbreviations; Introduction; 1 Understanding Anglican identity; 2 Understanding Evangelical identity; 3 Anglican Evangelicalism; 4 Church, culture and society; Conclusion; Bibliography; Index of names and subjects 330 $aAt a time when Anglicans and Evangelicals seem to be increasingly polarized rather than part of the same tradition, an Evangelical Anglican takes a fre 606 $aEvangelicalism$xChurch of England 615 0$aEvangelicalism$xChurch of England. 676 $a283.42 700 $aTurnbull$b R. D$g(Richard D.),$01683606 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910814919603321 996 $aAnglican and Evangelical$94054485 997 $aUNINA