Please use this identifier to cite or link to this item: http://repository.ipb.ac.id/handle/123456789/42939
Title: Membrane Topology of Subunit 8 Variant of Yeast Saccharomyces cerevisiae Mitochondrial ATP Synthase
Other Titles: Microbiology Indonesia Vol.3 No.1 Tahun 2009
Authors: Artika, I Made
Issue Date: 2009
Publisher: IPB (Bogor Agricultural University)
Series/Report no.: Vol.3;No.1
Abstract: The yeast mitochondrial F1F0-ATP synthase is a multisubunit complex that contains at least 17 different subunits. Subunit 8 of yeast mitochondrial ATP synthase is a hydrophobic protein of 48 amino acids encoded by the mitochondrial ATP8 gene. There is no homologue of subunit 8 found in bacteria. Subunit 8 has three distinct domains; an N-terminal domain, a central hydrophobic domain and a C-terminal domain. Subunit 8 has been shown to adopt a transmembrane topology with the central hydrophobic domain spans the inner mitochondrial membrane once. In order to elucidate the need of subunit 8 to maintain transmembrane topology for its functioning, a severely functionally defective subunit 8 variant that has been introduced with double-charged residues within the central hydrophobic domain was analysed. A gene encoding this variant was expressed in a yeast strain lacking endogenous subunit 8. The subunit 8 variant was then targeted into mitochondria. Following its assembly into mitochondrial ATP synthase complex, its membrane topology was determined. The results obtained showed that subunit 8 was obligatory to maintain a transmembrane topology for providing proper functioning. The transmembrane topology may be critical for subunit 8’s proposed structural roles as part of the stator stalk of the mitochondrial ATP synthase complex.
URI: http://repository.ipb.ac.id/handle/123456789/42939
ISSN: 1978-3477
Appears in Collections:Journal of Microbiology Indonesia

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