This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Adams, L. F.
Right arrow Articles by Ghiorse, W. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Adams, L. F.
Right arrow Articles by Ghiorse, W. C.
Agricola
Right arrow Articles by Adams, L. F.
Right arrow Articles by Ghiorse, W. C.

 Previous Article  |  Next Article 

Appl Environ Microbiol. 1985 March; 49(3): 556-562
Copyright © 1985, American Society for Microbiology. All Rights Reserved.

Influence of Manganese on Growth of a Sheathless Strain of Leptothrix discophora

Lee F. Adams and William C. Ghiorse*

Department of Microbiology, Cornell University, Ithaca, New York 14853

ABSTRACT

Mn2+ exerted various effects on the growth of Leptothrix discophora strain SS-1 in batch cultures depending on the concentration added to the medium. Concentrations of 0.55 to 5.5 µM Mn2+, comparable to those in the environment from which strain SS-1 was isolated, decreased cell yield and prolonged stationary-phase survival, but did not affect growth rate. Elevated concentrations of 55 to 910 µM Mn2+ also decreased cell yield and prolonged survival, but growth rate was decreased as well. The addition of 1,820 µM Mn2+ caused a decline in cell numbers followed by an exponential rise after 80 h of incubation, indicating the development of a population of cells resistant to Mn2+ toxicity. When 360 µM Mn2+ or less was added to growth flasks, Mn2+ was oxidized to manganese oxide (MnOx, where x is ~2), which appeared as brown particles in the medium. Quantification of Mn oxidation during growth of cultures to which 55 µM Mn2+ was added showed that nearly all of the Mn2+ was oxidized by the beginning of the stationary phase of growth (15 to 25 h). This result suggested that the decrease in cell yield observed at low and moderate concentrations of Mn2+ was related to the formation of MnOx, which may have bound cationic nutrients essential to the growth of SS-1. The addition of excess Fe3+ to cultures containing 55 µM Mn2+ increased cell yield to levels near those found in cultures with no added Mn2+, indicating that iron deprivation by MnOx was at least partly responsible for the decreased cell yield.


FOOTNOTES

* Corresponding author.


Appl Environ Microbiol. 1985 March; 49(3): 556-562
Copyright © 1985, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Wang, W., Shao, Z., Liu, Y., Wang, G. (2009). Removal of multi-heavy metals using biogenic manganese oxides generated by a deep-sea sedimentary bacterium - Brachybacterium sp. strain Mn32. Microbiology 155: 1989-1996 [Abstract] [Full Text]  
  • El Gheriany, I. A., Bocioaga, D., Hay, A. G., Ghiorse, W. C., Shuler, M. L., Lion, L. W. (2009). Iron Requirement for Mn(II) Oxidation by Leptothrix discophora SS-1. Appl. Environ. Microbiol. 75: 1229-1235 [Abstract] [Full Text]  
  • Webb, S. M., Dick, G. J., Bargar, J. R., Tebo, B. M. (2005). Evidence for the presence of Mn(III) intermediates in the bacterial oxidation of Mn(II). Proc. Natl. Acad. Sci. USA 102: 5558-5563 [Abstract] [Full Text]  
  • Emerson, D., Moyer, C. L. (2002). Neutrophilic Fe-Oxidizing Bacteria Are Abundant at the Loihi Seamount Hydrothermal Vents and Play a Major Role in Fe Oxide Deposition. Appl. Environ. Microbiol. 68: 3085-3093 [Abstract] [Full Text]  
  • Brouwers, G.-J., de Vrind, J. P. M., Corstjens, P. L. A. M., Cornelis, P., Baysse, C., de Vrind-de Jong, E. W. (1999). cumA, a Gene Encoding a Multicopper Oxidase, Is Involved in Mn2+ Oxidation in Pseudomonas putida GB-1. Appl. Environ. Microbiol. 65: 1762-1768 [Abstract] [Full Text]