Molecular Cloning and Functional Expression of esf Gene Encoding Enantioselective Lipase from Serratia marcescens ES-2 for Kinetic Resolution of Optically Active (S)-Flurbiprofen

  • Lee, Kwang-Woo (Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University) ;
  • Bae, Hyun-Ae (Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University) ;
  • Lee, Yong-Hyun (Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University)
  • Published : 2007.01.31

Abstract

An enantioselective lipase gene (esf) for the kinetic resolution of optically active (S)-flurbiprofen was cloned from the new strain Serratia marcescens ES-2. The esf gene was composed of a 1,845-bp open reading frame encoding 614 amino acid residues with a calculated molecular mass of 64,978 Da. The lipase expressed in E. coli was purified by a three-step procedure, and it showed preferential substrate specificity toward the medium-chain-length fatty acids. The esf gene encoding the enantioselective lipase was reintroduced into the parent strain S. marcescens ES-2 for secretory overexpression. The transformant S. marcescens BESF secreted up to 217kU/ml of the enantioselective lipase, about 54-fold more than the parent strain, after supplementing 3.0% Triton X-207. The kinetic resolution of (S)-flurbiprofen was carried out even at an extremely high (R,S)-flurbiprofen ethyl ester [(R,S)-FEE] concentration of 500 mM, 130 kU of the S. marcescens ES-2 lipase per mmol of (R,S)-FEE, and 1,000 mM of succinyl ${\beta}-cyclodextrin$ as the dispenser at $37^{\circ}C$ for 12h, achieving the high enantiomeric excess and conversion yield of 98% and 48%, respectively.

Keywords

References

  1. Akatsuka, H., E. Kawai, K. Omori, S. Komatsubara, T. Shibatani, and T. Tosa. 1994. The lipA gene of Serratia marcescens which encodes an extracellular lipase having no N-terminal signal peptide. J. Bacteriol. 176: 1949-1956 https://doi.org/10.1128/jb.176.7.1949-1956.1994
  2. Akatsuka, H., E. Kawai, K. Omori, and T. Shibatani. 1995. The three genes lipB, lipC, and lipD involved in the extracellular secretion of the Serratia marcescens lipase which lacks an N-terminal signal peptide. J. Bacteriol. 177: 6381-6389 https://doi.org/10.1128/jb.177.22.6381-6389.1995
  3. Amada, K., K. Haruki, T. Imanaka, M. Morikawa, and S. Kanaya. 2000. Overproduction in E. coli, purification, and characterization of a family I.3 lipase from Pseudomonas sp. MIS38. Biochim. Biophys. Acta 1478: 201-210 https://doi.org/10.1016/S0167-4838(00)00046-7
  4. Arpigny, J. L. and K. E. Jaeger. 1999. Bacterial lipolytic enzymes: Classification and properties. Biochem. J. 343: 177-183 https://doi.org/10.1042/0264-6021:3430177
  5. Bae, H. A., K. W. Lee, and Y. H. Lee. 2006. Enantioselective properties of extracellular lipase from Serratia marcescens ES-2 for kinetic resolution of (S)-flurbiprofen. J. Mol. Catal. B Enzyme 40: 24-29 https://doi.org/10.1016/j.molcatb.2006.02.004
  6. Binet, R., S. Letoffe, J. M. Ghigo, P. Delepelaire, and C. Wandersman. 1997. Protein secretion by Gram-negative bacterial ABC exporters - a review. Gene 192: 7-11 https://doi.org/10.1016/S0378-1119(96)00829-3
  7. Carabaza, A., F. Cabre, E. Rotllan, M. Gomez, M. Gutierrez, M. L. Garcia, and D. Mauleon. 1996. Stereoselective inhibition of inducible cyclooxygenase by chiral nonsteroidal antiinflammatory drugs. J. Clin. Pharmacol. 36: 505-512 https://doi.org/10.1002/j.1552-4604.1996.tb05040.x
  8. Chabeaun, P., A. de Groot, W. Bitter, J. Tommassen, T. Heulin, and W. Achouak. 2001. Phase-variable expression of an operon encoding extracellular alkaline protease, a serine protease homolog, and lipase in Pseudomonas brassicacearum. J. Bacteriol. 183: 2117-2120 https://doi.org/10.1128/JB.183.6.2117-2120.2001
  9. Duong, F., C. Soscia, A. Lazdunski, and M. Murgier. 1994. The Pseudomonas fluorescens lipase has a C-terminal secretion signal and is secreted by a three-component bacterial ABCexporter system. Mol. Microbiol. 11: 1117-1126 https://doi.org/10.1111/j.1365-2958.1994.tb00388.x
  10. Hayball, P. J. 1996. Chirality and nonsteroidal anti-inflammatory drugs. Drugs 52: 47-58
  11. Idei, A., H. Matsumae, E. Kawai, R. Yoshioka, T. Shibatani, H. Akatsuka, and K. Omori. 2002. Utilization of ATP-binding cassette exporter for hyperproduction of an exoprotein: Construction of lipase-hyperproducing recombinant strains of Serratia marcescens. Appl. Microbiol. Biotechnol. 58: 322-329 https://doi.org/10.1007/s00253-001-0896-1
  12. Jaeger, K. E. and M. T. Reetz. 1998. Microbial lipases from versatile tools for biotechnology. Trends Biotechnol. 16: 396-403 https://doi.org/10.1016/S0167-7799(98)01195-0
  13. Jaeger, K. E. and T. Eggert. 2002. Lipases for biotechnology. Curr. Opin. Biotechnol. 13: 390-397 https://doi.org/10.1016/S0958-1669(02)00341-5
  14. Jung, Y. J., H. K. Kim, J. F. Kim, S. H. Park, T. K. Oh, and J. K. Lee. 2005. A direct approach for finding functional lipolytic enzymes from the Paenibacillus polymyxa genome. J. Microbiol. Biotechnol. 15: 155-160
  15. Kovach, M. E., P. H. Elzer, D. S. Hill, G. T. Robertson, M. A. Farris, R. M. Roop II, and K. M. Peterson. 1995. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene 166: 175-176 https://doi.org/10.1016/0378-1119(95)00584-1
  16. Kwon, H. J., M. Haruki, M. Morikawa, K. Omori, and S. Kanaya. 2002. Role of repetitive nine-residue sequence motifs in secretion, enzymatic activity, and protein conformation of a family I.3 lipase. J. Biosci. Bioeng. 93: 157-164 https://doi.org/10.1263/jbb.93.157
  17. Li, X., S. Tetling, U. K. Winkler, K. E. Jaeger, and M. J. Benedik. 1995. Gene cloning, sequence analysis, purification, and secretion by Escherichia coli of an extracellular lipase from Serratia marcescens. Appl. Environ. Microbiol. 61: 2764-2680
  18. Li, G., J. H. Xu, X. J. Li, and Z. Z. Liu. 2004. Optimization of Serratia marcescens lipase production for enantioselective hydrolysis of 3-phenylglycidic acid ester. J. Ind. Microbiol. Biotechnol. 31: 525-530 https://doi.org/10.1007/s10295-004-0182-1
  19. Margolin, A. L. 1993. Enzymes in the synthesis of chiral drugs. Enzyme Microb. Technol. 15: 266-280 https://doi.org/10.1016/0141-0229(93)90149-V
  20. Matsumae, H. and T. Shibatani. 1994. Purification and characterization of the lipase from Serratia marcescens Sr41 8000 responsible for asymmetric hydrolysis of 3- phenylglycidic acid esters. J. Ferment. Bioeng. 77: 152- 158 https://doi.org/10.1016/0922-338X(94)90315-8
  21. Omori, K., A. Idei, and H. Akatsuka. 2001. Serratia ATPbinding cassette protein exporter, Lip, recognizes a protein region upstream of the C terminus for specific secretion. J. Biol. Chem. 276: 27111-27119 https://doi.org/10.1074/jbc.M101410200
  22. Rhys-Williams, W., F. McCarthy, J. Baker, Y. F. Hung, M. J. Thomason, A. W. Lloyd, and G. W. Hanlon. 1998. A mechanistic investigation into the microbial chiral inversion of 2-arylpropionic acids using deuterated derivatives of 2- phenylpropionic acid. Enzyme Microb. Technol. 22: 281- 287 https://doi.org/10.1016/S0141-0229(97)00185-3
  23. Reetz, M. T. 2002. Lipases as practical biocatalysts. Curr. Opin. Chem. Biol. 6: 145-150 https://doi.org/10.1016/S1367-5931(02)00297-1
  24. Shibatani, T., K. Omori, H. Akatsuka, F. Kawai, and H. Matsumae. 2000. Enzymatic resolution of diltiazem intermediate by Serratia marcescens lipase: Molecular mechanism of lipase secretion and its industrial application. J. Mol. Catal. B Enzyme 10: 141-149 https://doi.org/10.1016/S1381-1177(00)00122-3
  25. Shin, G. S., K. W. Lee, T. K. Kim, H. D. Shin, and Y. H. Lee. 2005. Lipase-catalyzed production of optically active (S)- flurbiprofen in aqueous phase reaction system containing chiral succinyl $\beta$-cyclodextrin. J. Mol. Catal. B Enzyme 33: 93-98 https://doi.org/10.1016/j.molcatb.2005.02.005
  26. Shin, G. S., K. W. Lee, and Y. H. Lee. 2005. Fed-batch production of (S)-flurbiprofen in lipase-catalyzed dispersed aqueous phase reaction system induced by succinyl $\beta$- cyclodextrin and its extractive purification. J. Mol. Catal. B Enzyme 37: 109-111 https://doi.org/10.1016/j.molcatb.2005.08.006
  27. Young, J. and I. B. Holland. 1999. ABC transporters: Bacterial exporters revisited five years on. Biochim. Biophys. Acta 1461: 177-200 https://doi.org/10.1016/S0005-2736(99)00158-3
  28. Yoon, M. Y., P. K. Shin, Y. S. Han, S. H. Lee, J. K. Park, and C. S. Cheong. 2004. Isolation of an Acinetobacter junii SY-01 strain producing an extracellular lipase enantioselectively hydrolyzing itraconazole precursor, and some properties of the lipase. J. Microbiol. Biotechnol. 14: 97-104