Abstract
The mechanisms by which the dissimilatory Fe(III)-reducing bacterium Shewanella alga adheres to amorphous Fe(III) oxide were examined through comparative analysis of S. alga BrY and an adhesion-deficient strain of this species, S. alga RAD20. Approximately 100% of S. alga BrY cells typically adhered to amorphous Fe(III) oxide, while less than 50% of S. alga RAD20 cells adhered. Bulk chemical analysis, isoelectric point analysis, and cell surface analysis by time-of-flight secondary-ion mass spectrometry and electron spectroscopy for chemical analysis demonstrated that the surfaces of S. alga BrY cells were predominantly protein but that the surfaces of S. alga RAD20 cells were predominantly exopolysaccharide. Physicochemical analyses and hydrophobic interaction assays demonstrated that S. alga BrY cells were more hydrophobic than S. alga RAD20 cells. This study represents the first quantitative analysis of the adhesion of a dissimilatory Fe(III)-reducing bacterium to amorphous Fe(III) oxide, and the results collectively suggest that hydrophobic interactions are a factor in controlling the adhesion of this bacterium to amorphous Fe(III) oxide. Despite having a reduced ability to adhere, S. alga RAD20 reduced Fe(III) oxide at a rate identical to that of S. alga BrY. This result contrasts with results of previous studies by demonstrating that irreversible cell adhesion is not requisite for microbial reduction of amorphous Fe(III) oxide. These results suggest that the interaction between dissimilatory Fe(III)-reducing bacteria and amorphous Fe(III) oxide is more complex than previously believed.
Full Text
The Full Text of this article is available as a PDF (200.8 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Baddiley J., Hancock I. C., Sherwood P. M. X-ray photoelectron studies of magnesium ions bound to the cell walls of gram-positive bacteria. Nature. 1973 May 4;243(5401):43–45. doi: 10.1038/243043a0. [DOI] [PubMed] [Google Scholar]
- Balch W. E., Fox G. E., Magrum L. J., Woese C. R., Wolfe R. S. Methanogens: reevaluation of a unique biological group. Microbiol Rev. 1979 Jun;43(2):260–296. doi: 10.1128/mr.43.2.260-296.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balch W. E., Wolfe R. S. New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressureized atmosphere. Appl Environ Microbiol. 1976 Dec;32(6):781–791. doi: 10.1128/aem.32.6.781-791.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bendinger B., Rijnaarts H. H., Altendorf K., Zehnder A. J. Physicochemical cell surface and adhesive properties of coryneform bacteria related to the presence and chain length of mycolic acids. Appl Environ Microbiol. 1993 Nov;59(11):3973–3977. doi: 10.1128/aem.59.11.3973-3977.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blumenkrantz N., Asboe-Hansen G. New method for quantitative determination of uronic acids. Anal Biochem. 1973 Aug;54(2):484–489. doi: 10.1016/0003-2697(73)90377-1. [DOI] [PubMed] [Google Scholar]
- Bryant M. P. Commentary on the Hungate technique for culture of anaerobic bacteria. Am J Clin Nutr. 1972 Dec;25(12):1324–1328. doi: 10.1093/ajcn/25.12.1324. [DOI] [PubMed] [Google Scholar]
- Caccavo F., Blakemore R. P., Lovley D. R. A Hydrogen-Oxidizing, Fe(III)-Reducing Microorganism from the Great Bay Estuary, New Hampshire. Appl Environ Microbiol. 1992 Oct;58(10):3211–3216. doi: 10.1128/aem.58.10.3211-3216.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Caccavo F., Frolund B., Van Ommen K. F., Nielsen P. H. Deflocculation of Activated Sludge by the Dissimilatory Fe(III)-Reducing Bacterium Shewanella alga BrY. Appl Environ Microbiol. 1996 Apr;62(4):1487–1490. doi: 10.1128/aem.62.4.1487-1490.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deflaun M. F., Tanzer A. S., McAteer A. L., Marshall B., Levy S. B. Development of an Adhesion Assay and Characterization of an Adhesion-Deficient Mutant of Pseudomonas fluorescens. Appl Environ Microbiol. 1990 Jan;56(1):112–119. doi: 10.1128/aem.56.1.112-119.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hobbie J. E., Daley R. J., Jasper S. Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977 May;33(5):1225–1228. doi: 10.1128/aem.33.5.1225-1228.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lovley D. R. Bioremediation of organic and metal contaminants with dissimilatory metal reduction. J Ind Microbiol. 1995 Feb;14(2):85–93. doi: 10.1007/BF01569889. [DOI] [PubMed] [Google Scholar]
- Lovley D. R. Dissimilatory Fe(III) and Mn(IV) reduction. Microbiol Rev. 1991 Jun;55(2):259–287. doi: 10.1128/mr.55.2.259-287.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lovley D. R., Phillips E. J. Novel mode of microbial energy metabolism: organic carbon oxidation coupled to dissimilatory reduction of iron or manganese. Appl Environ Microbiol. 1988 Jun;54(6):1472–1480. doi: 10.1128/aem.54.6.1472-1480.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lovley D. R., Phillips E. J. Rapid assay for microbially reducible ferric iron in aquatic sediments. Appl Environ Microbiol. 1987 Jul;53(7):1536–1540. doi: 10.1128/aem.53.7.1536-1540.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Millard M. M., Bartholomew J. C. Surface studies of mammalian cells grown in culture by X-ray photoelectron spectroscopy. Anal Chem. 1977 Aug;49(9):1290–1296. doi: 10.1021/ac50017a004. [DOI] [PubMed] [Google Scholar]
- Nikaido H., Vaara M. Molecular basis of bacterial outer membrane permeability. Microbiol Rev. 1985 Mar;49(1):1–32. doi: 10.1128/mr.49.1.1-32.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Obuekwe C. O., Westlake D. W., Cook F. D., William Costerton J. Surface changes in mild steel coupons from the action of corrosion-causing bacteria. Appl Environ Microbiol. 1981 Mar;41(3):766–774. doi: 10.1128/aem.41.3.766-774.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tugel J. B., Hines M. E., Jones G. E. Microbial iron reduction by enrichment cultures isolated from estuarine sediments. Appl Environ Microbiol. 1986 Nov;52(5):1167–1172. doi: 10.1128/aem.52.5.1167-1172.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weerkamp A. H., van der Mei H. C., Slot J. W. Relationship of cell surface morphology and composition of Streptococcus salivarius K+ to adherence and hydrophobicity. Infect Immun. 1987 Feb;55(2):438–445. doi: 10.1128/iai.55.2.438-445.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Williams V., Fletcher M. Pseudomonas fluorescens adhesion and transport through porous media are affected by lipopolysaccharide composition. Appl Environ Microbiol. 1996 Jan;62(1):100–104. doi: 10.1128/aem.62.1.100-104.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van der Mei H. C., Léonard A. J., Weerkamp A. H., Rouxhet P. G., Busscher H. J. Surface properties of Streptococcus salivarius HB and nonfibrillar mutants: measurement of zeta potential and elemental composition with X-ray photoelectron spectroscopy. J Bacteriol. 1988 Jun;170(6):2462–2466. doi: 10.1128/jb.170.6.2462-2466.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van der Mei H. C., Noordmans J., Busscher H. J. Molecular surface characterization of oral streptococci by Fourier transform infrared spectroscopy. Biochim Biophys Acta. 1989 Jun 27;991(3):395–398. doi: 10.1016/0304-4165(89)90063-9. [DOI] [PubMed] [Google Scholar]