spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Figures Only
Right arrow Full Text
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 Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Doeller, J. E.
Right arrow Articles by Kraus, D. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Doeller, J. E.
Right arrow Articles by Kraus, D. W.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
The Journal of Experimental Biology 204, 3755-3764 (2001)
© 2001 The Company of Biologists Limited

Chemolithoheterotrophy in a metazoan tissue: thiosulfate production matches ATP demand in ciliated mussel gills

Jeannette E. Doeller1,*, Manfred K. Grieshaber2 and David W. Kraus1

1 Department of Biology, University of Alabama at Birmingham, 1300 University Boulevard, Birmingham, AL 35294-1170, USA and
2 Institut für Zoophysiologie, Heinrich-Heine-Universität, Universitätsstraße 1, 40225 Düsseldorf, Germany

*e-mail: doeller{at}uab.edu

Accepted August 10, 2001

The ribbed mussel Geukensia demissa inhabits sulfide-rich coastal sediments with a distribution that suggests a preference for exposure to sulfide. Although sulfide is a respiratory poison, it is also a potent reductant. Geukensia demissa gill mitochondria can use sulfide as a respiratory substrate for ATP production, and the gills of this species exhibit sulfide-supported oxygen consumption that matches the energy demand of ciliary beating. Here, we demonstrate (i) that the major product of G. demissa gill sulfide oxidation is thiosulfate and (ii) that the rate of sulfide oxidation also matches the cellular energy demand, resulting in a ratio near unity of oxygen consumed to sulfide oxidized at both low and high ciliary beat frequencies. A value for this ratio of unity is consistent with electrons from sulfide oxidation entering the mitochondrial electron transport chain. In the gills of the blue mussel Mytilus edulis from sulfide-free conditions, this ratio is 3–5 times higher, indicating an uncoupling of oxygen consumption from sulfide oxidation. Whereas M. edulis gills exhibit anaerobic metabolism during sulfide exposure, G. demissa gills do not, indicating a difference in sulfide tolerance between the two mussel species.

Key words: sulphide, gills, sulphide oxidation, bromobimane HPLC, succinate, mussel, Geukensia demissa, Mytilus edulis.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Phil Trans R Soc BHome page
M. Mentel and W. Martin
Energy metabolism among eukaryotic anaerobes in light of Proterozoic ocean chemistry
Phil Trans R Soc B, August 27, 2008; 363(1504): 2717 - 2729.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
M. Goubern, M. Andriamihaja, T. Nubel, F. Blachier, and F. Bouillaud
Sulfide, the first inorganic substrate for human cells
FASEB J, June 1, 2007; 21(8): 1699 - 1706.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
J. R. Koenitzer, T. S. Isbell, H. D. Patel, G. A. Benavides, D. A. Dickinson, R. P. Patel, V. M. Darley-Usmar, J. R. Lancaster Jr, J. E. Doeller, and D. W. Kraus
Hydrogen sulfide mediates vasoactivity in an O2-dependent manner
Am J Physiol Heart Circ Physiol, April 1, 2007; 292(4): H1953 - H1960.
[Abstract] [Full Text] [PDF]


Home page
Biol. Bull.Home page
L. F. Gainey Jr. and M. J. Greenberg
Hydrogen Sulfide Is Synthesized in the Gills of the Clam Mercenaria mercenaria and Acts Seasonally to Modulate Branchial Muscle Contraction
Biol. Bull., August 1, 2005; 209(1): 11 - 20.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. W. Kraus and J. E. Doeller
Sulfide consumption by mussel gill mitochondria is not strictly tied to oxygen reduction: measurements using a novel polarographic sulfide sensor
J. Exp. Biol., October 1, 2004; 207(21): 3667 - 3679.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Hoffmeister, A. van der Klei, C. Rotte, K. W. A. van Grinsven, J. J. van Hellemond, K. Henze, A. G. M. Tielens, and W. Martin
Euglena gracilis Rhodoquinone:Ubiquinone Ratio and Mitochondrial Proteome Differ under Aerobic and Anaerobic Conditions
J. Biol. Chem., May 21, 2004; 279(21): 22422 - 22429.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
U. Theissen, M. Hoffmeister, M. Grieshaber, and W. Martin
Single Eubacterial Origin of Eukaryotic Sulfide:Quinone Oxidoreductase, a Mitochondrial Enzyme Conserved from the Early Evolution of Eukaryotes During Anoxic and Sulfidic Times
Mol. Biol. Evol., September 1, 2003; 20(9): 1564 - 1574.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2001