Pleiotrohpic Effect of a Gene Fragment Conferring H$_{2}$O$_{2}$ resistance in Streptomyces coelicolor

  • Um, Tae-Han (Research Center for Molecular Microbiology, Seoul National University) ;
  • Oh, chung-Hun (Research Center for Molecular Microbiology, Seoul National University) ;
  • Lee, Jong-Soo (Department of Microbiology, Seoul National University) ;
  • Park, Yong-Doo (Department of Microbiology, Seoul National University) ;
  • Roe, Jung-Hye (Department of Microbiology, Seoul National University) ;
  • Kim, Jae-Heon (Research Center for Molecular Microbiology, Seoul National University)
  • Published : 1995.12.01

Abstract

We isolated a 10 kb Bam HI fragment originated from the chromosome of a $H_2O$$^2$-resistant mutant strain of Streptomyces coelicolor, which confer $H_2O$$^2$-resistance to S. lividance upon transformation. Among various subclones ot 10kb Bam HI fragment tested for their $H_2O$$^2$-resistant phenotype in S. lividans, a subclone containing 5.2 kb Bam HI-BglII fragment was found to be responsible for $H_2O$$^2$-resistance. The plasmid containing this 5.2 kb fragment was then transformed into S. coellicolor A3(2) at early and tested for their phenotype of $H_2O$$^2$-resistance and the change in various enzymes whose activity can be stained in the gel. We found out that the 5.2 kb insert DNA conferred $H_2O$$^2$-resisstance in S. coelicolor A3(2) at early phase of cell growth. The presence of this DNA also resulted in higher level of peroxidase compared with the wild type cell containing parental vector (pIJ702) only. Esterase activity was also higher in this clone. However, alcohol dehydrogenase activity decreased compared with the wild type. These results suggest that the presence of a gene in 5.2 kb BamHI-BglII DNA fragment causes multiple changes in S. coelicolor related to its response against hydrogen peroxide. The result also implies that not only peroxidase but also esterase may function in the defencse meahsnism agianst $H_2O$$^2$-.

Keywords

References

  1. J. Bact. v.172 Characterization of an inducible oxidative stress system in Bacillus subtilis Bol,K.D.;R.E.Yasbin
  2. J. Bact. v.169 Relationship among oxidative stress, growth cycle, and sporulation in Bacillus subtilis Dowds,B.C.A.;P.Murphy;D.J.McConnel;K.M.Devine
  3. Physiological regulation of sporulation of Streptomyces griseus In Biology of actinomycetes '88 Ensign,J.C.;Y.Okami(eds.);T.Beppu(eds.);H.Ogawara(eds.)
  4. Micobiol. Rev. v.55 Oxidative stress responses in Escherichia coli and Salmonella typhimurium Farr,B.S.;T.Kogoma
  5. Free radicals in biology and medicine Halliwell,B.;J.M.C.Gutteridge
  6. Gel electrophoresis of proteins Hames,B.D.;D.Rickwood
  7. Genetic manipulation of Streptomyces, a Laboratory manual Hopwood,D.A.;M.J.Bibb;K.F.Chater;T.Kieser;C.J.Bruton;D.J.Lydiate;C.P.Smith;J.M.Ward;h.Schrempf
  8. Ph.D. Thesis, Seoul National University The response of Streptomyces coelicolor (Muller) against hydrogen peroxide stress Lee,J.S.
  9. J. Gen. Micro. v.139 The induction of oxidative enzymes in Sterpomyces coelicolor upon hydrogen peroxide treatment Lee,J.S.;Y.C.Hah;J.H.Roe
  10. J. Bact. v.169 Oxidative stress and growth temperature in Bacillus subtilis Murphy,P.;B.C.A.Dowds;D.J.McConnel;K.M.Devine
  11. Practical isozyme genetics Pasteur,N.;G.Pasteur;F.Bonhomme;J.Catalan;J.Britton-Davidian
  12. Appl. Environ. Microbiol. v.51 Methods of multilocus enzyme electrophoresis for bacterial population genetics and systematics Selander,R.K.;D.A.Caugant;H.Ochman;J.M.Musser;M.N.Gilmour;T.S.Whittam
  13. Trends Genet. v.6 Bacterial defecses against oxidative stress Storz,G.;L.A.Tartaglia;S.B.Farr;B.N.Ames
  14. Primary and secondary metabolism In Biology of actinomycetes '88 Vanek,Z.;j.Novak;V.Jechova;Y.Okami(eds.);T.Beppu(eds.);H.Ogawara(eds.)