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High copy number integration into the ribosomal DNA of the yeast Phaffia rhodozyma.

J. Wery, D. Gutker, A.C.H.M. Renniers, J.C. Verdoes, A.J.J. van Ooyen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

This report describes a transformation system leading to stable high copy number integration into the ribosomal DNA (rDNA) of the astaxanthin-producing yeast Phaffia rhodozyma. A plasmid was constructed that contains the transposon Tn5 encoded kanamycin resistance gene (KmR) fused in frame to the 5'-terminal portion of the Phaffia actin gene. This marker, driven by the Phaffia actin promoter, confers resistance to G418 (Geneticin). The plasmid also contains a rDNA portion that comprises the 18S rDNA and promotes high copy integration leading to stable Phaffia transformants that maintained the plasmid at high copy number after 15 generations of non-selective growth. Phaffia, strain CBS 6938, was found to contain the rDNA units in clusters distributed over three chromosomes with a total copy number of 61. Phaffia transformants were shown to have over 50 copies of pGB-Ph9 integrated in tandem in chromosomes that contain rDNA loci. The chromosomal shifts that occur as a result of these integrations as shown by pulsed field electrophoresis strongly suggest that Phaffia is haploid.
Original languageEnglish
Pages (from-to)89-97
JournalGene
Volume184
DOIs
Publication statusPublished - 1997

Keywords

  • Astaxanthin
  • Geneticin
  • Genomic organization
  • Homologous integration
  • Mitotic stability
  • Transformation

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