Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1997 May;63(5):2089–2091. doi: 10.1128/aem.63.5.2089-2091.1997

Transformation of Escherichia coli with a large plasmid of Acidiphilium multivorum AIU 301 encoding arsenic resistance.

K Suzuki 1, N Wakao 1, Y Sakurai 1, T Kimura 1, K Sakka 1, K Ohmiya 1
PMCID: PMC168498  PMID: 9143138

Abstract

Acidiphilium multivorum AIU 301 isolated from acid mineral water had strong arsenic resistance. This bacterium harbored a number of plasmids with different molecular sizes. A plasmid of 56 kbp, named pKW301, was isolated from A. multivorum AIU 301. When pKW301 was transferred into Escherichia coli JM109 by electroporation, an E. coli transformant carrying pKW301 exhibited resistance to sodium arsenite, sodium arsenate, and mercuric (II) chloride.

Full Text

The Full Text of this article is available as a PDF (796.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Datta N., Hedges R. W., Shaw E. J., Sykes R. B., Richmond M. H. Properties of an R factor from Pseudomonas aeruginosa. J Bacteriol. 1971 Dec;108(3):1244–1249. doi: 10.1128/jb.108.3.1244-1249.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Guay R., Silver M. Thiobacillus acidophilus sp. nov.; isolation and some physiological characteristics. Can J Microbiol. 1975 Mar;21(3):281–288. doi: 10.1139/m75-040. [DOI] [PubMed] [Google Scholar]
  3. Götz F., Zabielski J., Philipson L., Lindberg M. DNA homology between the arsenate resistance plasmid pSX267 from Staphylococcus xylosus and the penicillinase plasmid pI258 from Staphylococcus aureus. Plasmid. 1983 Mar;9(2):126–137. doi: 10.1016/0147-619x(83)90015-x. [DOI] [PubMed] [Google Scholar]
  4. Harrison A. P., Jr, Jarvis B. W., Johnson J. L. Heterotrophic bacteria from cultures of autotrophic Thiobacillus ferrooxidans: relationships as studied by means of deoxyribonucleic acid homology. J Bacteriol. 1980 Jul;143(1):448–454. doi: 10.1128/jb.143.1.448-454.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Harrison A. P., Jr Microbial succession and mineral leaching in an artificial coal spoil. Appl Environ Microbiol. 1978 Dec;36(6):861–869. doi: 10.1128/aem.36.6.861-869.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Harrison A. P., Jr The acidophilic thiobacilli and other acidophilic bacteria that share their habitat. Annu Rev Microbiol. 1984;38:265–292. doi: 10.1146/annurev.mi.38.100184.001405. [DOI] [PubMed] [Google Scholar]
  7. Hedges R. W., Baumberg S. Resistance to arsenic compounds conferred by a plasmid transmissible between strains of Escherichia coli. J Bacteriol. 1973 Jul;115(1):459–460. doi: 10.1128/jb.115.1.459-460.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Inoue C., Sugawara K., Kusano T. Thiobacillus ferrooxidans mer operon: sequence analysis of the promoter and adjacent genes. Gene. 1990 Nov 30;96(1):115–120. doi: 10.1016/0378-1119(90)90349-v. [DOI] [PubMed] [Google Scholar]
  9. Inoue C., Sugawara K., Shiratori T., Kusano T., Kitagawa Y. Nucleotide sequence of the Thiobacillus ferrooxidans chromosomal gene encoding mercuric reductase. Gene. 1989 Dec 7;84(1):47–54. doi: 10.1016/0378-1119(89)90138-8. [DOI] [PubMed] [Google Scholar]
  10. Kado C. I., Liu S. T. Rapid procedure for detection and isolation of large and small plasmids. J Bacteriol. 1981 Mar;145(3):1365–1373. doi: 10.1128/jb.145.3.1365-1373.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Manning H. L. New medium for isolating iron-oxidizing and heterotrophic acidophilic bacteria from acid mine drainage. Appl Microbiol. 1975 Dec;30(6):1010–1016. doi: 10.1128/am.30.6.1010-1016.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Novick R. P., Roth C. Plasmid-linked resistance to inorganic salts in Staphylococcus aureus. J Bacteriol. 1968 Apr;95(4):1335–1342. doi: 10.1128/jb.95.4.1335-1342.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Rosen B. P., Borbolla M. G. A plasmid-encoded arsenite pump produces arsenite resistance in Escherichia coli. Biochem Biophys Res Commun. 1984 Nov 14;124(3):760–765. doi: 10.1016/0006-291x(84)91023-4. [DOI] [PubMed] [Google Scholar]
  14. Sheng Y., Mancino V., Birren B. Transformation of Escherichia coli with large DNA molecules by electroporation. Nucleic Acids Res. 1995 Jun 11;23(11):1990–1996. doi: 10.1093/nar/23.11.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Silver S., Budd K., Leahy K. M., Shaw W. V., Hammond D., Novick R. P., Willsky G. R., Malamy M. H., Rosenberg H. Inducible plasmid-determined resistance to arsenate, arsenite, and antimony (III) in escherichia coli and Staphylococcus aureus. J Bacteriol. 1981 Jun;146(3):983–996. doi: 10.1128/jb.146.3.983-996.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Summers A. O., Silver S. Microbial transformations of metals. Annu Rev Microbiol. 1978;32:637–672. doi: 10.1146/annurev.mi.32.100178.003225. [DOI] [PubMed] [Google Scholar]
  17. Tuttle J. H., Randles C. I., Dugan P. R. Activity of microorganisms in acid mine water. I. Influence of acid water on aerobic heterotrophs of a normal stream. J Bacteriol. 1968 May;95(5):1495–1503. doi: 10.1128/jb.95.5.1495-1503.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Wichlacz P. L., Unz R. F. Acidophilic, heterotrophic bacteria of acidic mine waters. Appl Environ Microbiol. 1981 May;41(5):1254–1261. doi: 10.1128/aem.41.5.1254-1261.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Yano K., Nishi T. pKJ1, a naturally occurring conjugative plasmid coding for toluene degradation and resistance to streptomycin and sulfonamides. J Bacteriol. 1980 Aug;143(2):552–560. doi: 10.1128/jb.143.2.552-560.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES