The Journal of General Physiology
Axon Instruments microelectrode amplifiers
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow PDF (Full Text)
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JGP
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sanders, D.
Right arrow Articles by Slayman, C. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sanders, D.
Right arrow Articles by Slayman, C. L.
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  
What's this?

The Journal of General Physiology, Vol 80, 377-402, Copyright © 1982 by The Rockefeller University Press


ARTICLES

Control of intracellular pH. Predominant role of oxidative metabolism, not proton transport, in the eukaryotic microorganism Neurospora

D Sanders and CL Slayman

Recessed-tip microelectrodes were used to measure internal pH (pHi) in the fungus Neurospora, and to examine the response of pHi to several kinds of stress: changes of extracellular pH (pHo), inhibition of the principal proton pump in the plasma membrane, and inhibition of respiration. Under control conditions, at pHo = 5.8, pHi in Neurospora is 7.19 +/- 0.04. Changes of pHo between 3.9 and 9.3 affect pHi linearly but with a slope of only approximately 0.1 unit pHi per unit pHo, stable pHi being reached within 3 min of changed pHo. Despite a postulated high passive permeability of the Neurospora membrane to protons (Slayman, 1970), neither active nor passive H+ transport appears critical to pHi because (alpha) specific inhibition of the proton pump by orthovanadate has little effect on pHi, and (b) cytoplasmic acidification produced by respiratory blockade is unaffected by the size or direction of proton gradient. To convert measured changes in pHi into net proton fluxes, intracellular buffering capacity (beta i) was measured by the weak acid/weak base technique. At pHi = 7.2, beta i was (-) 35 mmol H+ (liter cell water)-1 (pH unit)-1, but beta i increased substantially in both the acid and alkaline directions, which suggests that amino acid side chains are the principal source of buffer.
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    What's this?


This article has been cited by other articles:


Home page
ANN BOT (LOND)Home page
H. H. FELLE
Apoplastic pH During Low-oxygen Stress in Barley
Ann. Bot., November 1, 2006; 98(5): 1085 - 1093.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
J. B. Hafke, J.-K. van Amerongen, F. Kelling, A. C.U. Furch, F. Gaupels, and A. J.E. van Bel
Thermodynamic Battle for Photosynthate Acquisition between Sieve Tubes and Adjoining Parenchyma in Transport Phloem
Plant Physiology, July 1, 2005; 138(3): 1527 - 1537.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
S. J. Cookson, L. E. Williams, and A. J. Miller
Light-Dark Changes in Cytosolic Nitrate Pools Depend on Nitrate Reductase Activity in Arabidopsis Leaf Cells
Plant Physiology, June 1, 2005; 138(2): 1097 - 1105.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
H. H. Felle and S. Hanstein
The apoplastic pH of the substomatal cavity of Vicia faba leaves and its regulation responding to different stress factors
J. Exp. Bot., January 1, 2002; 53(366): 73 - 82.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. J. Bowman, F. J. O'Neill, and B. J. Bowman
Mutations of pma-1, the Gene Encoding the Plasma Membrane H+-ATPase of Neurospora crassa, Suppress Inhibition of Growth by Concanamycin A, a Specific Inhibitor of Vacuolar ATPases
J. Biol. Chem., June 6, 1997; 272(23): 14776 - 14786.
[Abstract] [Full Text] [PDF]



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents