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The import of proteins into isolated higher plant mitochondria

Investigations of plant mitochondrial protein import have been very limited and few reports exist in the literature. The work presented in this thesis describes the development of an <i>in vitro Zea mays</i> mitochondrial protein import system, which has enabled the import of plant nuclear-encoded mitochondrial proteins to be examined. This <i>Z.mays</i> import system was characterised and partially optimised with the <i>Nicotiana plumbaginifolia</i> manganese superoxide dismutase (MnSOD). Results suggest that the energy requirements for protein import into plant mitochondria are similar to those of <i>Saccharomyces cerevisiae</i> and <i>Neurospora crassa</i>, requiring both an energised inner mitochondrial membrane and ATP. The inclusion of 1,10-phenanthroline inhibited the processing, but not the import of MnSOD and indicated that the processing activity within <i>Z.mays</i> mitochondria was dependent upon the presence of metal ions. The plant mitochondrial processing protease may therefore be similar to the characterised <i>S.cerevisiae</i> and <i>N.crassa</i> matrix processing protease. The import of the <i>Z.mays</i> adenine nucleotide translocator (ANT) protein was then investigated. Unlike the ANT of <i>S.cerevisiae</i> and <i>N. crassa</i>, this plant ANT was synthesised as a precursor protein, which was processed upon import into mitochondria isolated from both <i>Z.mays</i> and <i>Solanum tuberosum</i>. The subsequent isolation of an <i>S.tuberosum</i> ANT cDNA clone <i>PANT-1</i>, enabled the import of a second plant ANT to be investigated. Results corroborated the findings previously obtained with the <i>Z.mays</i> ANT and it was therefore concluded that the import of plant ANT proteins are distinctly different from those of <i>S.cerevisiae</i> and <i>N.crassa</i>.

Identiferoai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:661587
Date January 1991
CreatorsSarah, Caroline J.
PublisherUniversity of Edinburgh
Source SetsEthos UK
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Sourcehttp://hdl.handle.net/1842/12898

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