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Planta

, Volume 208, Issue 4, pp 503–511 | Cite as

Cloning and functional analysis of a cDNA encoding a starch synthase from potato (Solanum tuberosum L.) that is predominantly expressed in leaf tissue

  • Jens Kossmann
  • Gernot J. W. Abel
  • Franziska Springer
  • James R. Lloyd
  • Lothar Willmitzer
Article

Abstract.

Three isoforms of starch synthase (SS) were shown to be present in soluble potato tuber extracts by activity staining after native gel electrophoresis. A cDNA encoding SSI from rice was used as a probe to clone a corresponding cDNA from potato. The deduced amino acid sequence identified the protein as an SS from potato with an Mr of 70.6 kDa for the immature enzyme including its transit peptide. This novel isoform was designated SSI. An analysis of the expression pattern of the gene indicated that SSI is predominantly expressed in sink and source leaves, and, to a lower extent in tubers. In several independent transgenic potato lines, where the expression of SSI was repressed using the antisense approach, the activity of a specific SS isoform was reduced to non-detectable levels as determined through activity staining after native gel electrophoresis. The reduction in the amount of this isoform of SS did not lead to any detectable changes in starch structure, probably due to the fact that this isoform only represents a minor activity in potato tubers.

Key words: Antisense potato Isoform (starch synthase) Solanum (starch synthase) Starch structure Transgenic potato Tuber 

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Copyright information

© Springer-Verlag Berlin Heidelberg 1999

Authors and Affiliations

  • Jens Kossmann
    • 1
  • Gernot J. W. Abel
    • 1
  • Franziska Springer
    • 1
  • James R. Lloyd
    • 1
  • Lothar Willmitzer
    • 1
  1. 1.Max-Planck-Institut für molekulare Pflanzenphysiologie, Karl-Liebknecht-Str. 24-25, D-14476 Golm, GermanyDE

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