DOI QR코드

DOI QR Code

Identification and Cloning of the ClpB Gene in Psychromonas arctica by Inverse PCR and Cassette PCR Technology

  • Choi, Ae-Ran (Department of Chemistry, Sejong University) ;
  • Na, Joo-Mi (Department of Chemistry, Sejong University) ;
  • Sung, Min-Sun (Department of Chemistry, Sejong University) ;
  • Im, Ha-Na (Department of Molecular Biology, Sejong University) ;
  • Lee, Kyung-Hee (Department of Chemistry, Sejong University)
  • Published : 2010.04.20

Abstract

The family of ClpB protein is a molecular chaperone which protects cellular proteins from being aggregated upon exposure to severe environmental stresses in association with DnaK/DanJ/GrpE in the ATP-dependent manner. In a psychrophilic bacterium which survives at a subzero temperature, any functional role of cold-active ClpB protein can be rather crucial. In order to identify a ClpB encoding gene from a cold-adapted bacterium whose genome sequence has not been fully discovered, we have employed a series of PCR technologies, including a gradient PCR with homologous primers, an inverse PCR and a cassette PCR. The full sequence of PaclpB gene was successfully identified and compared with those of other psychrophilic species. We have further cloned the gene in E.coli expression systems and were able to induce PaClpB protein expression by IPTG, which help us understand a molecular mechanism for survival against extremely cold environments.

Keywords

References

  1. Patel, S.; Latterich, M. Trends. Cell Biol. 1998, 8, 65. https://doi.org/10.1016/S0962-8924(97)01212-9
  2. Lee, S.; Sowa, M. E.; Watanabe, Y. H.; Sigler, P. B.; Chiu, W.;Yoshida, M.; Tsai, F. T. Cell 2003, 115, 229. https://doi.org/10.1016/S0092-8674(03)00807-9
  3. Mogk, A.; Schlieker, C.; Strub, C.; Rist, W.; Weibezahn, J.; Bukau,B. J. Biol. Chem. 2003, 278, 17815.
  4. Watanabe, Y. H.; Yoshida. M. J. Biol. Chem. 2004, 279, 15723. https://doi.org/10.1074/jbc.M308782200
  5. Chow, I. T.; Barnett, M. E.; Zolkiewski, M.; Baneyx, F. FEBS Lett.2005, 579, 4242. https://doi.org/10.1016/j.febslet.2005.06.055
  6. Schirmer, E. C.; Glover, J. R.; Singer, M. A.; Lindquist, S. Trends Biochem. Sci. 1996, 21, 289. https://doi.org/10.1016/0968-0004(96)10038-4
  7. Feller, G.; Gerday, C. Cell Mol. Life Sci.1997, 53, 830. https://doi.org/10.1007/s000180050103
  8. Liu, S.; Graham, J. E.; Bigelow, L.; Morse, P. D.; Wilkinson, B. J. Appl. Environ. Microbiol. 2002, 8, 1697.
  9. Strocchi, M.; Ferrer, M.; Timmis, K. N.; Golyshin, P. N. Proteomics2006, 6, 193. https://doi.org/10.1002/pmic.200500031
  10. Park, S. K.; Jin, E. S.; Lee, M. Y. Cryo Letters 2008, 29, 351.
  11. Berqholz, P. W.; Bakermans, C.; Tiedje, J. M. J. Bacteriol. 2009,191, 2340. https://doi.org/10.1128/JB.01377-08
  12. Methe, B. A.; Nelson, K. E.; Deming, J. W.; Momen, B.; Melamud,E.; Fraser, C. M. Proc. Natl. Acad. Sci. USA 2005, 102, 10913. https://doi.org/10.1073/pnas.0504766102
  13. Medigue, C.; Krin, E.; Pascal, G.; Barbe, V.; Bernsel, A.; Danchin,A. Genome Res. 2005, 15, 1325. https://doi.org/10.1101/gr.4126905
  14. Ochman, H.; Gerber, A. S.; Hartl, D. L. Genetics 1988, 120, 621.
  15. Isegawa, Y.; Sheng, J.; Sokawa, Y.; Yamanishi, K.; Nakagomi, O.;Ueda, S. Mol. Cell Probes 1992, 6, 467. https://doi.org/10.1016/0890-8508(92)90043-W
  16. Barnett, M. E.; Zolkiewska. A.; Zolkiewski, M. J. Biol. Chem.2000, 275, 37565. https://doi.org/10.1074/jbc.M005211200
  17. Pollastri, G.; Przybylski, D.; Rost, B.; Baldi, P. Proteins 2002, 47,228. https://doi.org/10.1002/prot.10082
  18. Eichelberg, K.; Ginocchio, C.; Galan, J. J. Bacteriology 1994, 176,4501. https://doi.org/10.1128/jb.176.15.4501-4510.1994
  19. Lee, Y. K.; Jung, H. J.; Lee, H. K. J. Microbiol. 2006, 44, 694.
  20. Yoshimune, K.; Galkin, A.; Kulakova, L.; Yoshimura, T.; Esaki, N.Extremophiles 2005, 9, 145. https://doi.org/10.1007/s00792-004-0429-9
  21. Deuerling, E.; Patzelt, H.; Vorderwülbecke, S.; Rauch, T.; Kramer,G.; Bukau, B. Mol. Microbiol. 2003, 47, 1317. https://doi.org/10.1046/j.1365-2958.2003.03370.x

Cited by

  1. PCR Amplification of a Superoxide Dismutase Gene (pasod) from Psychrophilic Bacteria (KOPRI22215) without Genome Information vol.31, pp.8, 2010, https://doi.org/10.5012/bkcs.2010.31.8.2410
  2. Expression and Purification of Recombinant Superoxide Dismutase (PaSOD) from Psychromonas arctica in Escherichia coli vol.32, pp.7, 2010, https://doi.org/10.5012/bkcs.2011.32.7.2405