Characterization of the Fad 12 mutant of Synechocystis that is defective in Δ12 acyl-lipid desaturase activity

Zoltan Gombos, Hajime Wada, Zsuzsanna Varkonyi, Dmitry A. Los, Norio Murata

Research output: Article

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The Fad 12 mutant of Synechocystis sp. PCC 6803 has a defect in the desA gene for A12 acyl-lipid desaturase. We identified a change in the nucleotide sequence of the structural gene for the desaturase, in which a leucine codon has been converted to a stop codon. Western blot analysis revealed that the Δ12 acyl-lipid desaturase was localized in both plasma membranes and thylakoid membranes of wild-type cells but was absent from both types of membrane in Fad12 cells. These findings suggest that the desaturation of fatty acids takes place in both types of membrane in Synechocystis sp. PCC 6803. The mutation in the Δ12 desaturase did not affect the lipid composition of thylakoid and plasma membranes, but it changed the fatty acid composition of lipids in similar ways in both types of membrane. 0

Original languageEnglish
Pages (from-to)117-123
Number of pages7
JournalBiochimica et Biophysica Acta - Lipids and Lipid Metabolism
Issue number1
Publication statusPublished - jan. 1 1996


ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Endocrinology

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