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Enzyme Handbook 15

First Supplement Part 1 Class 3: Hydrolases

  • Dietmar Schomburg
  • Dörte Stephan

Table of contents

  1. Front Matter
    Pages I-XIII
  2. Dietmar Schomburg, Dörte Stephan
    Pages 1-3
  3. Dietmar Schomburg, Dörte Stephan
    Pages 5-8
  4. Dietmar Schomburg, Dörte Stephan
    Pages 9-12
  5. Dietmar Schomburg, Dörte Stephan
    Pages 13-15
  6. Dietmar Schomburg, Dörte Stephan
    Pages 17-20
  7. Dietmar Schomburg, Dörte Stephan
    Pages 21-26
  8. Dietmar Schomburg, Dörte Stephan
    Pages 27-29
  9. Dietmar Schomburg, Dörte Stephan
    Pages 31-35
  10. Dietmar Schomburg, Dörte Stephan
    Pages 37-39
  11. Dietmar Schomburg, Dörte Stephan
    Pages 41-43
  12. Dietmar Schomburg, Dörte Stephan
    Pages 45-47
  13. Dietmar Schomburg, Dörte Stephan
    Pages 49-51
  14. Dietmar Schomburg, Dörte Stephan
    Pages 53-56
  15. Dietmar Schomburg, Dörte Stephan
    Pages 57-59
  16. Dietmar Schomburg, Dörte Stephan
    Pages 61-63
  17. Dietmar Schomburg, Dörte Stephan
    Pages 65-67
  18. Dietmar Schomburg, Dörte Stephan
    Pages 69-73
  19. Dietmar Schomburg, Dörte Stephan
    Pages 75-77
  20. Dietmar Schomburg, Dörte Stephan
    Pages 79-81
  21. Dietmar Schomburg, Dörte Stephan
    Pages 83-85
  22. Dietmar Schomburg, Dörte Stephan
    Pages 87-89
  23. Dietmar Schomburg, Dörte Stephan
    Pages 91-96
  24. Dietmar Schomburg, Dörte Stephan
    Pages 97-100
  25. Dietmar Schomburg, Dörte Stephan
    Pages 101-105
  26. Dietmar Schomburg, Dörte Stephan
    Pages 107-110
  27. Dietmar Schomburg, Dörte Stephan
    Pages 111-113
  28. Dietmar Schomburg, Dörte Stephan
    Pages 115-122
  29. Dietmar Schomburg, Dörte Stephan
    Pages 123-126
  30. Dietmar Schomburg, Dörte Stephan
    Pages 127-129
  31. Dietmar Schomburg, Dörte Stephan
    Pages 131-133
  32. Dietmar Schomburg, Dörte Stephan
    Pages 135-138
  33. Dietmar Schomburg, Dörte Stephan
    Pages 139-141
  34. Dietmar Schomburg, Dörte Stephan
    Pages 143-146
  35. Dietmar Schomburg, Dörte Stephan
    Pages 147-150
  36. Dietmar Schomburg, Dörte Stephan
    Pages 151-153
  37. Dietmar Schomburg, Dörte Stephan
    Pages 155-157
  38. Dietmar Schomburg, Dörte Stephan
    Pages 159-161
  39. Dietmar Schomburg, Dörte Stephan
    Pages 163-165
  40. Dietmar Schomburg, Dörte Stephan
    Pages 167-171
  41. Dietmar Schomburg, Dörte Stephan
    Pages 173-175
  42. Dietmar Schomburg, Dörte Stephan
    Pages 177-179
  43. Dietmar Schomburg, Dörte Stephan
    Pages 181-184
  44. Dietmar Schomburg, Dörte Stephan
    Pages 185-187
  45. Dietmar Schomburg, Dörte Stephan
    Pages 189-191
  46. Dietmar Schomburg, Dörte Stephan
    Pages 193-195
  47. Dietmar Schomburg, Dörte Stephan
    Pages 197-200
  48. Dietmar Schomburg, Dörte Stephan
    Pages 201-206
  49. Dietmar Schomburg, Dörte Stephan
    Pages 207-212
  50. Dietmar Schomburg, Dörte Stephan
    Pages 213-215

About this book

Introduction

Today, as the large international genome sequence projects are gaining a great amount of public atte_ntion and huge sequence data bases are created it be­ comes more and more obvious that we are very limited in our ability to access functional data for the gene products - the proteins, in particular for enzymes. Those data are inherently very difficult to collect, interpret and standardize as they are highly distributed among journals from different fields and are often sub­ ject to experimental conditions. Nevertheless a systematic collection is essential for our interpretation of the genome information and more so for possible appli­ cations of this knowledge in the fields of medicine, agriculture, etc .. Recent pro­ gress on enzyme immobilization, enzyme production, enzyme inhibition, coen­ zyme regeneration and enzyme engineering has opened up fascinating new fields for the potential application of enzymes in a large range of different areas. It is the functional profile of an enzyme that enables a biologist or physician to analyse a metabolic pathway and its disturbance; it is the substrate specificity of an enzyme which tells an analytical biochemist how to design an assay; it is the stability, specificity and efficiency of an enzyme which determines its usefulness in the biotechnical transformation of a molecule. And the sum of all these data will have to be considered when the deSigner of artificial biocatalysts has to choose the optimum prototype to start with.

Keywords

Datensammlung Enzym Enzyme Fructose Glutamat Oligosaccharid Oligosaccharide Pyrimidine Subtilisin biotechnology enzymes protein reaction

Editors and affiliations

  • Dietmar Schomburg
    • 1
  • Dörte Stephan
    • 2
  1. 1.Institut für BiochemieUniversität zu KölnKölnGermany
  2. 2.GBF — Gesellschaft für Biotechnologische Forschung mbHBraunschweigGermany

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-642-58948-5
  • Copyright Information Springer-Verlag Berlin Heidelberg 1998
  • Publisher Name Springer, Berlin, Heidelberg
  • eBook Packages Springer Book Archive
  • Print ISBN 978-3-540-64116-2
  • Online ISBN 978-3-642-58948-5
  • Buy this book on publisher's site
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