Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Mitochondrial adenosine triphosphatase of the fission yeast Schizosaccharomyces pombe 972h-: Changes in inhibitor sensitivities during the cell cycle indicate similarities and differences in binding sites

Lloyd, David ORCID: https://orcid.org/0000-0002-5656-0571 and Edwards, Steven D. 1977. Mitochondrial adenosine triphosphatase of the fission yeast Schizosaccharomyces pombe 972h-: Changes in inhibitor sensitivities during the cell cycle indicate similarities and differences in binding sites. Biochemical Journal 162 (3) , pp. 581-590. 10.1042/bj1620581

Full text not available from this repository.

Abstract

1. We used 11 different inhibitors of energy conservation as inhibitors of ATPase (adenosine triphosphatase) in extracts of Schizosaccharomyces pombe obtained from cells at different stages of the cell cycle. 2. All the inhibitors showed cell-cycle-dependent variations in their I50 values (microng of inhibitor/mg of protein giving 50% inhibition of inhibitor-sensitive ATPase at pH 8.6). 3. From the sensitivity profiles through the cell cycle it was concluded that: (a) oligomycin, venturicidin, triethyltin sulphate and dibutylchloromethyltin chloride all act at closely associated site(s); (b) NN'-dicyclohexylcarbodi-imide and leucinostatin both act at a similar site, which is, however, distinct from that at which other inhibitors of the membrane factor (Fo) act. 4. The variations in I50 values for efrapeptin closely followed changes in specific activity of ATPase, as would be expected for an inhibitor acting at catalytic sites; these fluctuations were different from those for aurovertin, Dio-9, 4-chloro-7-nitrobenzofurazan, quercetin and spegazzinine, all of which show different sensitivity profiles from one another. 5. Anomalous stepwise inhibitor-titration curves were obtained for spegazzinine, NN'-dicyclohexylcarbodiimide, dibutylchloromethyltin chloride and leucinostatin. 6. Possible explanations are proposed for the discontinuous expression of inhibitor-binding sites during the cell cycle.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
ISSN: 0264-6021
Last Modified: 26 Oct 2022 08:37
URI: https://orca.cardiff.ac.uk/id/eprint/127920

Citation Data

Cited 14 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item