Abstract
The mechanisms of metal resistance of a cadmium-resistant Alcaligenes sp. were studied. Growth in a defined medium was unaffected by cadmium at concentrations up to 0.1 mM, while at concentrations up to 2.5 mM, growth occurred after an extended lag phase. The increase in length of the lag phase was abolished by repeated subculturing at these higher concentrations. However, subculture in the absence of cadmium reversed the adaptation process. Plasmid DNA was not detected in adapted cells, suggesting that adaptation is not plasmid mediated. Increased sulfide production in response to cadmium was observed, although the levels were too low to account fully for cadmium resistance. Adaptation of cells to cadmium resulted in the appearance of a major new membrane protein (molecular weight, 34,500) whose presence was not dependent upon the method of membrane preparation. This protein was induced at cadmium concentrations of 0.1 mM and above, but below this level the protein was absent. The onset of growth at concentrations above 0.1 mM was coincident with the appearance of this protein, which was also induced by zinc (0.4 mM) but not by manganese or nickel. The protein was only solubilized by a sodium dodecyl sulfate-2-mercaptoethanol mixture. Similar solubility properties were shown by a second major membrane protein (molecular weight, 33,000). These two proteins proved to be similar by peptide-mapping experiments and amino acid analysis. The appearance of the 34,500-molecular-weight protein and its possible role in cadmium resistance are discussed.
Full text
PDF





Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aiking H., Kok K., van Heerikhuizen H., van 't Riet J. Adaptation to Cadmium by Klebsiella aerogenes Growing in Continuous Culture Proceeds Mainly via Formation of Cadmium Sulfide. Appl Environ Microbiol. 1982 Oct;44(4):938–944. doi: 10.1128/aem.44.4.938-944.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aiking H., Stijnman A., van Garderen C., van Heerikhuizen H., van 't Riet J. Inorganic phosphate accumulation and cadmium detoxification in Klebsiella aerogenes NCTC 418 growing in continuous culture. Appl Environ Microbiol. 1984 Feb;47(2):374–377. doi: 10.1128/aem.47.2.374-377.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chopra I. Mechanism of plasmic-mediated resistance to cadmium in Staphylococcus aureus. Antimicrob Agents Chemother. 1975 Jan;7(1):8–14. doi: 10.1128/aac.7.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eckhardt T. A rapid method for the identification of plasmid desoxyribonucleic acid in bacteria. Plasmid. 1978 Sep;1(4):584–588. doi: 10.1016/0147-619x(78)90016-1. [DOI] [PubMed] [Google Scholar]
- Ehrlich H. L., Fox S. I. Copper sulfide precipitation by yeasts from Acid mine-waters. Appl Microbiol. 1967 Jan;15(1):135–139. doi: 10.1128/am.15.1.135-139.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hansen J. B., Olsen R. H. Isolation of large bacterial plasmids and characterization of the P2 incompatibility group plasmids pMG1 and pMG5. J Bacteriol. 1978 Jul;135(1):227–238. doi: 10.1128/jb.135.1.227-238.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holmes D. S., Quigley M. A rapid boiling method for the preparation of bacterial plasmids. Anal Biochem. 1981 Jun;114(1):193–197. doi: 10.1016/0003-2697(81)90473-5. [DOI] [PubMed] [Google Scholar]
- Hunkapiller M. W., Lujan E., Ostrander F., Hood L. E. Isolation of microgram quantities of proteins from polyacrylamide gels for amino acid sequence analysis. Methods Enzymol. 1983;91:227–236. doi: 10.1016/s0076-6879(83)91019-4. [DOI] [PubMed] [Google Scholar]
- Jones J. G. Studies on freshwater bacteria: effect of medium composition and method on estimates of bacterial population. J Appl Bacteriol. 1970 Dec;33(4):679–686. doi: 10.1111/j.1365-2672.1970.tb02250.x. [DOI] [PubMed] [Google Scholar]
- Khazaeli M. B., Mitra R. S. Cadmium-binding component in Escherichia coli during accommodation to low levels of this ion. Appl Environ Microbiol. 1981 Jan;41(1):46–50. doi: 10.1128/aem.41.1.46-50.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lischwe M. A., Ochs D. A new method for partial peptide mapping using N-chlorosuccinimide/urea and peptide silver staining in sodium dodecyl sulfate-polyacrylamide gels. Anal Biochem. 1982 Dec;127(2):453–457. doi: 10.1016/0003-2697(82)90203-2. [DOI] [PubMed] [Google Scholar]
- Macaskie L. E., Dean A. C. Cadmium accumulation by a Citrobacter sp. J Gen Microbiol. 1984 Jan;130(1):53–62. doi: 10.1099/00221287-130-1-53. [DOI] [PubMed] [Google Scholar]
- Minney S. F., Quirk A. V. Growth and adaptation of Saccharomyces cerevisiae at different cadmium concentrations. Microbios. 1985;42(167):37–44. [PubMed] [Google Scholar]
- Mitra R. S., Bernstein I. A. Nature of the repair process associated with the recovery of Escherichia coli after exposure to Cd2+. Biochem Biophys Res Commun. 1977 Feb 21;74(4):1450–1455. doi: 10.1016/0006-291x(77)90604-0. [DOI] [PubMed] [Google Scholar]
- Mitra R. S., Bernstein I. A. Single-strand breakage in DNA of Escherichia coli exposed to Cd2+. J Bacteriol. 1978 Jan;133(1):75–80. doi: 10.1128/jb.133.1.75-80.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mitra R. S., Gray R. H., Chin B., Bernstein I. A. Molecular mechanisms of accommodation in Escherichia coli to toxic levels of Cd2+. J Bacteriol. 1975 Mar;121(3):1180–1188. doi: 10.1128/jb.121.3.1180-1188.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morrissey J. H. Silver stain for proteins in polyacrylamide gels: a modified procedure with enhanced uniform sensitivity. Anal Biochem. 1981 Nov 1;117(2):307–310. doi: 10.1016/0003-2697(81)90783-1. [DOI] [PubMed] [Google Scholar]
- Nikodem V., Fresco J. R. Protein fingerprinting by SDS-gel electrophoresis after partial fragmentation with CNBr. Anal Biochem. 1979 Sep 1;97(2):382–386. doi: 10.1016/0003-2697(79)90089-7. [DOI] [PubMed] [Google Scholar]
- Novick R. P. Penicillinase plasmids of Staphylococcus aureus. Fed Proc. 1967 Jan-Feb;26(1):29–38. [PubMed] [Google Scholar]
- Tijssen P., Kurstak E. A simple and sensitive method for the purification and peptide mapping of proteins solubilized from densonucleosis virus with sodium dodecyl sulfate. Anal Biochem. 1979 Oct 15;99(1):97–104. doi: 10.1016/0003-2697(79)90048-4. [DOI] [PubMed] [Google Scholar]
- Tynecka Z., Gos Z., Zajac J. Energy-dependent efflux of cadmium coded by a plasmid resistance determinant in Staphylococcus aureus. J Bacteriol. 1981 Aug;147(2):313–319. doi: 10.1128/jb.147.2.313-319.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tynecka Z., Gos Z., Zajac J. Reduced cadmium transport determined by a resistance plasmid in Staphylococcus aureus. J Bacteriol. 1981 Aug;147(2):305–312. doi: 10.1128/jb.147.2.305-312.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tynecka Z., Zajac J., Goś Z. Plasmid dependent impermeability barrier to cadmium ions in Staphylococcus aureus. Acta Microbiol Pol A. 1975;7(1):11–20. [PubMed] [Google Scholar]
- Vallee B. L., Ulmer D. D. Biochemical effects of mercury, cadmium, and lead. Annu Rev Biochem. 1972;41(10):91–128. doi: 10.1146/annurev.bi.41.070172.000515. [DOI] [PubMed] [Google Scholar]
- Weiss A. A., Silver S., Kinscherf T. G. Cation transport alteration associated with plasmid-determined resistance to cadmium in Staphylococcus aureus. Antimicrob Agents Chemother. 1978 Dec;14(6):856–865. doi: 10.1128/aac.14.6.856. [DOI] [PMC free article] [PubMed] [Google Scholar]


