Genome organization of the linear cytoplasmic element pPE1B from Pichia etchellsii

Klassen R, Tontsidou L, Larsen M, Meinhardt F

Research article (journal)

Abstract

The linear cytoplasmic element pPE1B from Pichia etchellsii CBS2011 (synonym Debaryomyces etchellsii) mas totally sequenced. It consists of 12835 bp and has a remarkable high A + T content of 77.3%, The termini of pPE1B were found to consist of inversely orientated identical nucleotide repetitions 161 base pairs long, to which proteins are probably covalently linked at the 5 ' ends. Ten putative genes (open reading frames, ORFs) were identified, covering 96.5% of the total sequence. The predicted polypeptides correspond to proteins encoded by ORFs 2-11 of the linear plasmids pGKL2 of Kluyveromyces lactis and pSKL of Saccharomyces kluyveri. ORF1, existing on both latter elements, is lacking on pPE1B, An upstream conserved sequence motif (UCS) is located at the expected distance from the start codon of each of the 10 ORFs. As the arbitrarily chosen UCS6 was able to drive expression of a reporter gene in the heterologous pGKL-encoded killer system of K. lactis, extranuclear promoter function is probable. The almost congruent genome organization of pPE1B and other autonomous linear yeast plasmids sequenced so far, i.e. pGKL2 and pSKL, suggests a common, presumably viral, ancestor. The sequence of pPE1B has been submitted to the EMBL data library under Accession No. AJ278986, Copyright (C) 2001 John Wiley & Sons, Ltd.

Details about the publication

JournalYeast
Volume18
Issue10
Page range953-961
StatusPublished
Release year2001 (31/07/2001)
Language in which the publication is writtenEnglish
KeywordsPichia Debaryomyces linear plasmid UCS terminal inverted repeats kluyveromyces-lactis toxin killer plasmids saccharomyces-cerevisiae extranuclear expression nucleotide-sequence dna plasmids yeast system pgkl2 promoters

Authors from the University of Münster

Meinhardt, Friedhelm

Projects the publication originates from

Duration: since 01/01/2000
Type of project: Own resources project