|
|
||||||||
Research Paper |
Microbiology (BIOSI 1, Main Building), Cardiff University, PO Box 915, Cardiff CF10 3TL, Wales, UK1
School of Applied Science, University of the South Bank, 103 Borough Road, London SET 0AA, UK2
Author for correspondence: David Lloyd. Tel: +44 29 20874772. Fax: +44 29 20874305. e-mail: Lloydd{at}cf.ac.uk
A continuous culture of Saccharomyces cerevisiae IFO 0233, growing with glucose as the major carbon and energy source, shows oscillations of respiration with a period of 48 min. Samples taken at maxima and minima indicate that (i) periodic changes do not occur as a result of carbon depletion, (ii) intrinsic differences in respiratory activity occur in washed organisms and (iii) a respiratory inhibitor accumulates during respiratory oscillations. Plasma membrane and inner mitochondrial membranes generate transmembrane electrochemical potentials; changes in these can be respectively assessed using anionic or cationic fluorophores. Thus flow cytometric analyses indicated that an oxonol dye [DiBAC4(3); bis(1,3-dibutylbarbituric acid)trimethine oxonol] was excluded from yeasts to a similar extent (in >98% of the population) at all stages, showing that the plasma membrane potential was maintained at a steady value. However, uptake of Rhodamine 123 was greatest at that phase characterized by a low respiratory rate. Addition of uncouplers of energy conservation [CCCP (m-chlorocarbonylcyanide phenylhydrazone) or S-13(5-chloro-3-t-butyl-2-chloro-41-nitrosalicylanilide)] to the continuous cultures increased the respiration, but had only a transient effect on the period of the oscillation. Electron microscopy showed changes in mitochondrial ultrastructure during the respiratory oscillation. At low respiration the cristae were more clearly defined due to swelling of the matrix; this corresponds to the orthodox conformation. When respiration was high the mitochondrial configuration was condensed. It has been shown previously that a temperature-compensated ultradian clock operates in S. cerevisiae. It is proposed that mitochondria undergo cycles of energization in response to energetic demands driven by this ultradian clock output.
Keywords: mitochondria, redox regulation, NADH, cytochrome, ultradian clock
Abbreviations: CCCP, m-chlorocarbonylcyanide phenylhydrazone; DiBAC4(3), bis(1,3-dibutylbarbituric acid)trimethine oxonol; S-13, 5-chloro-3-t-butyl-2-chloro-41-nitrosalicylanilide; DOT, dissolved O2 tension; SHAM, salicylhydroxamic acid
This article has been cited by other articles:
![]() |
W. J. H. Koopman, F. Distelmaier, M. A. Hink, S. Verkaart, M. Wijers, J. Fransen, J. A. M. Smeitink, and P. H. G. M. Willems Inherited complex I deficiency is associated with faster protein diffusion in the matrix of moving mitochondria Am J Physiol Cell Physiol, May 1, 2008; 294(5): C1124 - C1132. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. B. Murray, M. Beckmann, and H. Kitano Regulation of yeast oscillatory dynamics PNAS, February 13, 2007; 104(7): 2241 - 2246. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Li and R. R. Klevecz From the Cover: A rapid genome-scale response of the transcriptional oscillator to perturbation reveals a period-doubling path to phenotypic change PNAS, October 31, 2006; 103(44): 16254 - 16259. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. R. Klevecz, J. Bolen, G. Forrest, and D. B. Murray From the Cover: A genomewide oscillation in transcription gates DNA replication and cell cycle PNAS, February 3, 2004; 101(5): 1200 - 1205. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |