Biotransformations have built into a big device of natural synthesis and such a lot man made sequences will enjoy the use of a biotransformation step. This quantity completes the gathering of biotransformations awarded within the Biotechnology sequence. Volumes eight a and b offer a finished advisor to the confirmed and rising makes use of of enzymes, every one bankruptcy is dedicated to a unmarried classification of transformation.
the outline of a number of bond forming reactions is by way of 4 chapters on structue and catalytic job. Case experiences of vital commercial and artificial functions around off the sensible orientation of the ebook.
Chapter 1 Carbon?Carbon Bond Formation, Addition, removal 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 okay. 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 ordinary Aroma chemical substances by way of Fermentation strategies (pages 333–350): Jurgen Rabenhorst
Chapter 10 artificial purposes 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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Additional resources for Biotechnology: Biotransformations II, Volume 8b, Second Edition, Second Edition
C. (1995), Synthesis of enantiomerically pure a-hydroxyaldehydes from the corresponding a-hydroxycarboxylic acids: novel substrates for Escherichia coli transketolase, J. Chem. , Chem. , 2475-2476. G. M. HUNG,R. , STRAUB,J. , WHITESIDES, (1991), a-Aminoaldehyde equivalents as substrates for rabbit muscle aldolase - synthesis of 1,4-dideoxy-~-arabitinol and 2(R),S(R)-bis(hy- 8 References droxymethyl)-3(R),4(R)-dihydroxypyrrolidine, J. Org. Chem. 56,3849-3855. , OIKAWA, H. (1997), Biosynthesis of phytotoxins from Alternaria solani, Biosci.
1993), Chemoenzymatic carbon+arbon bond formation leading to noncarbohydrate derivative TURNER, N. J. (1994), Recent advances in the use of - stereoselective synthesis of pentamycin C-llenzyme-catalyzed reactions in organic synthesis, C-16 fragment, Chem. Pharm. Bull. 41,282-286. Nut. Prod. Rep. 11,l-15. SHIMAZU, Y. (1950), Formation and decomposition TURNER, N. , WHITESIDES, G. M. (1989), A comof D-( -)-phenylacetylcarbinol by yeast, J. Chem. bined chemical-enzymatic synthesis of 2-deoxyD-arabino-heptulosonic acid 7-phosphate, J.
Enzymic condensation of ybenzyloxybutanal(67) (Fig. , 1996). , 1997). , 1993,1994). Transaldolase catalyzes in vivo the transfer of a dihydroxyacetone unit between phosphorylated metabolites; for example, the C-1-C-3 aldol unit is transferred from D-sedoheptulose 7-phosphate (69) to D-glyceraldehyde 3-phosphate, delivering D-erythrose 4phosphate (70) and D-fructose 6-phosphate (71)(Fig. 28). However, despite its availability and potentially low acceptor substrate specificity, transaldolase has not been fully exploited in organic synthesis.