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Escherichia coli Arabinose Isomerase and Staphylococcus aureus Tagatose-6-Phosphate Isomerase: Which is a Better Template for Directed Evolution of Non-Natural Substrate Isomerization?

  • Kim, Hye-Jung (Department of Biotechnology, Catholic University of Korea) ;
  • Uhm, Tae-Guk (Department of Biotechnology, Catholic University of Korea) ;
  • Kim, Seong-Bo (Food Ingredient Center, Food R&D, CJ Cheiljedang Corp.) ;
  • Kim, Pil (Department of Biotechnology, Catholic University of Korea)
  • Received : 2010.01.29
  • Accepted : 2010.02.10
  • Published : 2010.06.28

Abstract

Metallic and non-metallic isomerases can be used to produce commercially important monosaccharides. To determine which category of isomerase is more suitable as a template for directed evolution to improve enzymes for galactose isomerization, L-arabinose isomerase from Escherichia coli (ECAI; E.C. 5.3.1.4) and tagatose-6-phosphate isomerase from Staphylococcus aureus (SATI; E.C. 5.3.1.26) were chosen as models of a metallic and non-metallic isomerase, respectively. Random mutations were introduced into the genes encoding ECAI and SATI at the same rate, resulting in the generation of 515 mutants of each isomerase. The isomerization activity of each of the mutants toward a non-natural substrate (galactose) was then measured. With an average mutation rate of 0.2 mutations/kb, 47.5% of the mutated ECAIs showed an increase in activity compared with wild-type ECAI, and the remaining 52.5% showed a decrease in activity. Among the mutated SATIs, 58.6% showed an increase in activity, whereas 41.4% showed a decrease in activity. Mutant clones showing a significant change in relative activity were sequenced and specific increases in activity were measured. The maximum increase in activity achieved by mutation of ECAI was 130%, and that for SATI was 190%. Based on these results, the characteristics of the different isomerases are discussed in terms of their usefulness for directed evolution of non-natural substrate isomerization.

Keywords

References

  1. Asboth, B. and G. Naray-Szabo. 2000. Mechanism of action of D-xylose isomerase. Curr. Protein Pept. Sci. 1: 237-254. https://doi.org/10.2174/1389203003381333
  2. Bhosale, S. H., M. B. Rao, and V. V. Deshpande. 1996. Molecular and industrial aspects of glucose isomerase. Microbiol. Rev. 60: 280-300.
  3. Choi, K. W., K. M. Park, S. Y. Jun, C. S. Park, K. H. Park, and J. Cha. 2008. Modulation of the regioselectivity of a Thermotoga neapolitana beta-glucosidase by site-directed mutagenesis. J. Microbiol. Biotechnol. 18: 901-907.
  4. Dische, Z. and E. Borenfreund. 1951. A new spectrophotometric method for the detection and determination of keto sugars and trioses. J. Biol. Chem. 192: 583-587.
  5. Kim, P. 2004. Current studies on biological tagatose production using L-arabinose isomerase: A review and future perspective. Appl. Microbiol. Biotechnol. 65: 243-249.
  6. Kim, P., S. H. Yoon, M. J. Seo, D. K. Oh, and J. H. Choi. 2001. Improvement of tagatose conversion rate by genetic evolution of thermostable galactose isomerase. Biotechnol. Appl. Biochem. 34: 99-102. https://doi.org/10.1042/BA20010025
  7. Kobayashi, M. and S. Shimizu. 1999. Cobalt proteins. Eur. J. Biochem. 261: 1-9. https://doi.org/10.1046/j.1432-1327.1999.00186.x
  8. Lee, D. W., E. A. Choe, S. B. Kim, S. H. Eom, Y. H. Hong, S. J. Lee, H. S. Lee, D. Y. Lee, and Y. R. Pyun. 2005. Distinct metal dependence for catalytic and structural functions in the L-arabinose isomerases from the mesophilic Bacillus halodurans and the thermophilic Geobacillus stearothermophilus. Arch. Biochem. Biophys. 434: 333-343. https://doi.org/10.1016/j.abb.2004.11.004
  9. Manjasetty, B. A. and M. R. Chance. 2006. Crystal structure of Escherichia coli L-arabinose isomerase (ECAI), the putative target of biological tagatose production. J. Mol. Biol. 360: 297-309. https://doi.org/10.1016/j.jmb.2006.04.040
  10. Oh, D. K., E. S. Ji, Y. D. Kwon, H. J. Kim, and P. Kim. 2005. Substrate variety of a non-metal dependent tagatose-6-phosphate isomerase from Staphylococcus aureus. Kor. J. Microbiol. Biotechnol. 33: 106-111.
  11. Oh, D. K., H. J. Oh, H. J. Kim, J. Cheon, and P. Kim. 2006. Modification of optimal pH in L-arabinose isomerase from Geobacillus stearothermophilus for D-galactose isomerization. J. Mol. Cat. B Enz. 43: 108-112. https://doi.org/10.1016/j.molcatb.2006.06.015
  12. Rhimi, M., M. Juy, N. Aghajari, R. Haser, and S. Bejar. 2007. Probing the essential catalytic residues and substrate affinity in the thermoactive Bacillus stearothermophilus US100 L-arabinose isomerase by site-directed mutagenesis. J. Bacteriol. 189: 3556-3563. https://doi.org/10.1128/JB.01826-06
  13. Roh, H. J., P. Kim, Y. C. Park, and J. H. Choi. 2000. Bioconversion of D-galactose into D-tagatose by expression of L-arabinose isomerase. Biotechnol. Appl. Biochem. 31 (Pt 1): 1-4. https://doi.org/10.1042/BA19990065
  14. Seeholzer, S. H. 1993. Phosphoglucose isomerase: A ketol isomerase with aldol C2-epimerase activity. Proc. Natl. Acad. Sci. U.S.A. 90: 1237-1241. https://doi.org/10.1073/pnas.90.4.1237
  15. Sriprapundh, D., C. Vieille, and J. G. Zeikus. 2000. Molecular determinants of xylose isomerase thermal stability and activity: Analysis of thermozymes by site-directed mutagenesis. Protein Eng. 13: 259-265. https://doi.org/10.1093/protein/13.4.259
  16. Zhu, G. P., C. Xu, M. K. Teng, L. M. Tao, X. Y. Zhu, C. J. Wu, J. Hang, L. W. Niu, and Y. Z. Wang. 1999. Increasing the thermostability of D-xylose isomerase by introduction of a proline into the turn of a random coil. Protein Eng. 12: 635-638. https://doi.org/10.1093/protein/12.8.635

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