| Old | New | Caption |
| Fig. 2 | Fig. 1 | Nucleoside phosphotransferase reaction with pyrophosphate as a substrate |
| Fig. 3 | Fig. 2 | Conformational flexibility of subtilisin on enantiorecognition |
| Fig. 4 | Fig. 3 | Synthesis of R-(-)-2-phenylpropionic acid by N. diaphanozonaria resting cells |
| Fig. 6 | Fig. 4 | Schematic representation of the reaction and ultrasound frequency dependence of activity of b-N-acetylglucosaminidases. |
| Fig. 7 | Fig. 5 | Conformational flexibility of subtilisin |
| Fig. 8 | Fig. 6 | Schematic representation of xylanse-catalyzed glycoside synthesis |
| Fig. 9 | Fig. 7 | Microbial deracemization of 2-substituted propanoic acids |
| Fig. 10 | Fig. 8 | Enzymatic asymmetric protonation of enol esters in organic solvents |
| Fig. 11 | Fig. 9 | Synthesis of (R)-flurbiprofen via enzymatic asymmetric decarboxylation |
| Fig. 12 | Fig. 10 | Inversion of the enantioselectivity of arylmalonate decarboxylase by point mutation |
| Fig. 13 | Fig. 11 | Novel compounds which possess gem-difluorocyclopropane moieties |
| Fig. 14 | Fig. 12 | Lipase-catalyzed enantioselective acylation under reduced pressure conditions in an ionic liquid solvent system |
| Fig. 15 | Fig. 13 | Enantioselective acylation of mandelic acid methyl ester catalyzed by immobilized-lipase PS in an ionic liquid solvent system |
| Fig. 17 | Fig. 14 | Protease-catalyzed regioselective polymerization of diethyl L-glutamate hydrochloride |
| Fig. 18 | Fig. 15 | Reduction of ketones with Cyanobacteria |
| Fig. 19 | Fig. 16 | Carboxylation of pyrrole in supercritical CO2 |
| Fig. 20 | Fig. 17 | The exploitation of 'P6C Ｗorld'using biotransformation |
| Fig. 21 | Fig. 18 | Glucosylation of gentisic acid with a glucosyltransferase from C. roseus |
| Fig. 22 | Fig. 19 | Enzymatic coupling of inverse substrates with dipeptide esters |
| Fig. 23 | Fig. 20 | Lipase-catalyzed trans esterification of 1,1,1-trifluoro-2-alkanoles |
| Fig. 24 | Fig. 21 | The oxidative modification of Trp-43 in the mutant |
| Fig. 25 | Fig. 22 | The reduction of a-keto esters by SCKER |
| Fig. 26 | Fig. 23 | Chemoenzymatic synthesis of 1 |
| Fig. 27 | Fig. 24 | Substrate specificity of Pfω-III toward various amino donors |
| Fig. 29 | Fig. 25 | Preparation of 'Toyonites'with silane coupling agents |
| Fig. 30 | Fig. 26 | Substrate analogs studied in this work |
| Fig. 31 | Fig. 27 | FPS reaction of epoxygeranyl diphosphate with IPP-homologs |
| Fig. 32 | Fig. 28 | Synthsis of biologically active compounds |
| Fig. 33 | Fig. 29 | Cyclo(Gly-Leu) hydrolysis by Agrobacterium radiobacter NM5-3 |
| Fig. 34 | Fig. 30 | Cyclo(Leu-Phe) dehydrogenation by Streptomyces albulus KO23 |
| Fig. 35 | Fig. 31 | Kinetic resolution of 2,3-difluorohomoalylalcohols |
| Fig. 36 | Fig. 32 | The direct glycosylation of capsaicin by Eucalyptus cultured suspension cells |
| Fig. 37 | Fig. 33 | Enzyme-catalyzed resolution of racemic prolines and prolinols |
| Fig. 38 | Fig. 34 | Substrate specificity of Torulaspora delbrueckii-mediated reduction on bicyclic substrates |
| Fig. 39 | Fig. 35 | Synthetic route to sporochnols |
| Fig. 40 | Fig. 36 | Synthesis of macrosphelide A based on enzymatic hydrolysis of triester |
| Fig. 41 | Fig. 37 | Synthesis of (+)-ambrein based on the coupling of enzymatic reaction products |
| Fig. 42 | Fig. 38 | Lactonization along with trans-cis isomerization from enzymatic reaction products |
| Fig. 43 | Fig. 39 | Asymmetric reduction of a nitroalkene by novel nitroalkane reductases |
| Fig. 44 | Fig. 40 | Inversion temperatures in the lipase-catalyzed kinetic resolutions |
| Fig. 45 | Fig. 41 | Organic bridges used for immobilization of a lipase |
| Fig. 46 | Fig. 42 | Optically active azirines as the chiral building block |
| Fig. 47 | Fig. 43 | Enantioselective and regioselective glucosidation of 1,2-diols by CGTase |
| Fig. 48 | Fig. 44 | Asymmetric reduction of ketones using a reductase isolated from bakers' yeast |
| Fig. 49 | Fig. 45 | In vitro evolution of E. coli sialic acid aldolase |
| Fig. 50 | Fig. 46 | Polymerization of phenol catalyzed by crude peroxidase from horseradish |
| Fig. 51 | Fig. 47 | Enantioselective acetylation of 2-octanol by lipases immobilized on mesoporous silica FMS. |
| Fig. 52 | Fig. 48 | Dynamic kinetic resolution of hemiaminals using Lipase PS |
| Fig. 53 | Fig. 49 | Bio-catalyzed resolution of cis- and trans-indandiol diacetate mixture |
| Fig. 54 | Fig. 50 | Enantioselective esterification in supercritical CO2 |
| Fig. 56 | Fig. 51 | Lipase-catalyzed polymerization of diethoxydimethylsilane |
| Fig. 57 | Fig. 52 | A specific use for each enantiomer with food proteins |
| Fig. 58 | Fig. 53 | Biotransformation of Nobiletin (1) by S. litura |
| Fig. 59 | Fig. 54 | Synthetic route to 2-docosahexaenoyl-1-tetracosahexaenoyl-sn glycerophosphocholine |
| Fig. 1 | Table 1 | Increase of enantioselectivity by mutant esterases |
| Fig. 5 | Table 2 | Feasibility study for synthesis of single-enantiomer compounds in industry |
| Fig. 16 | Table 3 | LPS-catalyzed acetylations of 2-substituted cyclohexanols |
| Table 1 | Table 4 | Comparison of MsATs with an aminotransferase belonging to subfamily Ig |
| Fig. 28 | Table 5 | Stereoselectivity to acetates of primary and secondary aryl or aryloxy alcohol by Candida antarctica lipase |
| Table 2 | Table 6 | The characteristics of chitinase inhibiors from 5 fungal strains |
| Fig. 55 | Table 7 | The reduction of a-keto esters by SCKER |