By Bo Mattiasson, Lei Ye
Managed radical polymerization innovations for molecular imprinting, via Mark E. Byrne
From bulk polymers to nanoparticles, via Lei Ye
Post-imprinting and in-cavity functionalization, via Toshifumi Takeuchi
Characterization of MIPs (affinity, selectivity, web site heterogeneity…), through Richard Ansell
Theoretical features and computing device modelling, by way of Ian Nicholls
MIPs in aqueous environments, by means of Bin Lu
MIPs for binding macromolecules, by means of Kenneth J. Shea
Solid section extraction, via Ecevit Yilmaz
Sensors, by way of Sergey A. Piletsky
MIPs for catalysis and synthesis, by means of Marina Resmini
Wastewater therapy, through Bo Mattiasson
MIPs as instruments for bioassays, biotransformation and drug supply, through Meiping Zhao
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Additional resources for Advances In Biochemical Engineering Biotechnology Biotransformations
1 Introduction . . . . . . . . . . . . . . . . 58 2 Deracemization Through Stereoinversion Using Two Microorganisms . . . . . . . . . . . . . . 59 3 Deracemization Through Stereoinversion Using a Single Microorganism . . . . . . . . . . . . . 1 Deracemization of Compounds with One Stereocentre . . . . 2 Deracemization of Compounds with Two Stereocentres . . . . 66 4 Regiospecific Stereoinversions in Sugar Biosynthesis . . . . . 69 5 Conclusions .
53 . . . . . . . . . . . . g. biotransformations [1a–c, 2], will be very advantageous. In this respect, the hydroxynitrile lyases (Hnl) and their catalytic production of chiral cyanohydrins may have a significant role to play. The Hnls catalyse the asymmetric addition of hydrogen cyanide (HCN) to the carbonyl moiety of an aldehyde or ketone (Scheme 1) to yield a chiral cyanohydrin (1) (where R1 and R2 R1 = Alkyl or Aryl and R2 = H or Alkyl). Reflecting their role in nature, the cyanohydrin is also cleaved by the HNL to yield HCN and the parent carbonyl compound.
Becker W, Pfeil E (1966) J Am Chem Soc 88:4299 5. Becker W, Pfeil E (1966) Ger Offen 1,593,260, 25 September 1969 Chem Abstr 1969. 72:P3061t 6. Conn EE (1981) Cyanogenic glycosides. In: Stumpf PK, Conn EE (eds) The biochemistry of plants: a comprehensive treatise. Academic Press, New York, 7:479–500 7. Poulton JE (1990) Plant Physiol 94:401 8. Selmar D, Lieberei R, Biehl B, Conn EE (1989) Physiol Plant 75:97 9. Lieberei R, Selmar D, Biehl B (1985) Pl Syst Evol 150:49 10. Rosenthal GA, Bell EA (1979) Naturally occurring toxic nonprotein amino acids.
Advances In Biochemical Engineering Biotechnology Biotransformations by Bo Mattiasson, Lei Ye