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
|