Abstract
Air-dried cells of Hansenula nonfermentans AKU 4332 catalyzed the production of (S)-3-pentyn-2-ol from (RS)-3- pentyn-2-ol acetate ester at 10% (v/v). The product was formed at 96.6% e.e. with a molar yield of 45% in 24 h. © Rapid Science Ltd. 1998
Similar content being viewed by others
References
Burgess, K., and Jennings, L.D. (1991). J. Am. Chem. Soc., 113, 6129–6139.
Gluanzer, B. I., Faber, L. and Griengl, H. (1987). Tetrahedron, 43, 5791–5796.
Gluanzer, B. I., Faber, K., and Griengl, H. (1988). Enzyme Microb. Technol., 10, 744–749.
Gluanzer, B.I., Konigsberger, B., Berger, B., Faber, K., and Griengl, H. (1990). Chem. Phys. Lipids, 54, 43–48.
Kamezawa, M., Raku, T., Tachibana, H., Ohtani, T., and Naoshima, Y. (1995). Biosci. Biotech. Biochem., 59, 549–551.
Kawashima, M., and Hasegawa, T. (1992). Biotech. Lett., 14, 1135–1136.
Midland, M. M. (1989). Chem. Rev., 89, 1553–1561.
Mori, K., and Akao, H. (1990). Tetrahedron, 36, 91–96.
Ogawa, J., Xie, S.-X., and Shimizu, S. (1998) Appl. Microbiol. Biotechnol. in press.
Ohta H., and Tetsukawa, H. (1980). Agric. Biol. Chem., 44, 863–867.
Oritani, T., and Yamashita, K. (1980). Agric. Biol. Chem., 44, 2407–2411.
Shimizu, M., Kawanami, H., and Fujisawa, T. (1992). Chemistry Letters, 107–110.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Xie, SX., Ogawa, J. & Shimizu, S. (S)-3-Pentyn-2-ol production through microbial enzyme-catalyzed, highly enantioselective hydrolysis of racemic 3-pentyn-2-ol esters. Biotechnology Letters 20, 935–938 (1998). https://doi.org/10.1023/A:1005497825103
Issue Date:
DOI: https://doi.org/10.1023/A:1005497825103