Biotransformations have constructed into a huge instrument of natural synthesis and such a lot artificial sequences will enjoy the use of a biotransformation step. This quantity completes the gathering of biotransformations offered within the Biotechnology sequence. Volumes eight a and b offer a entire consultant to the confirmed and rising makes use of of enzymes, every one bankruptcy is dedicated to a unmarried classification of transformation.
the outline of numerous bond forming reactions is via 4 chapters on structue and catalytic task. Case experiences of significant business and artificial purposes around off the sensible orientation of the ebook.
Chapter 1 Carbon?Carbon Bond Formation, Addition, removing and Substitution Reactions: 1 Carbon?Carbon Bond Formation utilizing Enzymes (pages 4–40): Anthony D. M. Curtis
Chapter 2 Lyases (pages 41–171): Jassem G. Mahdi and David R. Kelly
Chapter three Halocompounds (pages 173–220): Gary ok. Robinson, Simon A. Jackman and Jane Stratford
Chapter four Phosphorylation (pages 221–241): Simon Jones
Chapter five Enzymes in Carbohydrate Chemistry: Formation of Glycosidic Linkages (pages 243–274): Sabine L. Flitsch and Gregory M. Watt
Chapter 6 commercial Biotransformations (pages 276–294): Uwe T. Bornscheuer
Chapter 7 Regioselective Oxidation of Aminosorbitol with Gluconobacter oxydans, Key response within the business 1?Deoxynojirimycin Synthesis (pages 295–311): Michael Schedel
Chapter eight Engineering Microbial Pathways for Amino Acid construction (pages 313–332): Ian G. Fotheringham
Chapter nine Biotechnological construction of common Aroma chemical substances via Fermentation procedures (pages 333–350): Jurgen Rabenhorst
Chapter 10 artificial functions of Enzyme?Catalyzed Reactions (pages 351–400): Jane McGregor?Jones
Chapter eleven Catalytic Antibodies (pages 402–490): George Michael Blackburn and Arnaud Garcon
Chapter 12 man made Enzymes—Artificial Peptides in Stereoselective Synthesis (pages 491–517): Paul A. Bentley
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Extra resources for Biotechnology: Biotransformations II, Volume 8b, Second Edition, Second Edition
Chem. , Chem. , 4424. ,PEDROCCHI- (3S,4S) 4-methyl-3-heptano1, Tetrahedron Lett. FANTONI, G. (1981), Synthesis of the N-benzoyl 23,4269-4272. , PEDROCCHI-FANTONI, G. (L-vancosamine) isomers of 2,3,6-trideoxy-3-C(1983a), Stereospecific synthesis of N-benzoyl-Lmethyl-3-aminohexose from a non-carbohydrate daunosamine and L-ristosamine,J. Org. Chem. 48, 909-910. precursor, Tetrahedron Lett. 22,5073-5076. , SPREAFICO, F. (1982), C. Preparation of (R) y-hexanoacyl derivatives of C-methyl analogs of the amilide, (5R,6S,7S) 6,7-isopropylidendioxy-&octanodeoxy sugar L-acosamine from noncarbohynolide and (+)-exo-brevicomin from (2S,3S,4R) drate precursors, J.
MANZOCCHI, A. , COOPER,J. , RACKER, to the preparation of enantiomerically pure chiral E. (1958), Oxidative pentose phosphate cycle. building blocks, Chem. Rev. 92,1071-1140. I. Preparation of substrates and enzymes, Arch. Biochem. Biophys. 74,295-305. , WHITESIDES, G. M. , FISCHER,P. (1990), Enzyme-catalyzed reactions. 4. Aldolase-cataase (RAMA), J. Am. Chem. 112,9670-9671. , LIDQVIST, Y. (1989), lyzed C-C bond formation for stereoselective Preliminary crystallographic data for transketosynthesis of nitrogen-containing carbohydrates, lase from yeast, J.
Abstr. 45,9004). SHIN,H. , ROGERS, P. L. (1995), Biotransformation Chem. 111,624-627. , SUGIMORI, T. (1984), Purintermediate in L-ephedrine production, by imification and properties of N-acetylneuraminate mobilized Candida utilis, Appl. Microbiol. Biolyase from Escherichia coli, J. Biochem. 96, technol. 44,7-14. 507-522. SHIN,H. , ROGERS,P. L. , SUGIMORI,T. (1985),Distribution of N-acetylneuraminic lyase in bacteria phenylacetylcarbinol (L-PAC) from benzaldeand its production by Escherichia coli,Agric.
Biotechnology: Biotransformations II, Volume 8b, Second Edition, Second Edition