Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 350, Issue 13, Pages 1954-1958Publisher
WILEY-BLACKWELL
DOI: 10.1002/adsc.200800382
Keywords
acceleration; enhanced enantioselectivity; enzyme catalysis; lipase; transesterification
Categories
Funding
- Ministry of Educatio, Culture, Sports, Science and Technology of Japan
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The chiral pyrrolidine-substituted imidazolium cetyl-PEG10-sulfate (D-ProMe) derived from D-proline worked as an excellent activating agent of Burkholderia cepacia lipase; it is particularly interesting that the D-isomer of the imidazolium salt worked better than the L-isomer. This suggests that the imidazolium cation group directly interacts with the enzyme protein and causes preferable modification of the reactivity.
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