Identification of contaminating fungal DNA sequences in Zymolyase

J Clin Microbiol. 1999 Mar;37(3):830-1. doi: 10.1128/JCM.37.3.830-831.1999.

Abstract

When different preparations of Zymolyase were included in the pretreatment protocol of a panfungal PCR assay using a primer system for the 18S rRNA gene, an amplification product occurred in negative controls. The amplified fragment showed 100.0% sequence identity to the Saccharomyces sensu stricto complex and Kluyveromyces lodderae. Lyticase, lysing enzymes, and proteinase K appeared to be free from fungal DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Primers
  • DNA, Fungal / genetics
  • DNA, Fungal / isolation & purification*
  • DNA, Ribosomal / genetics
  • DNA, Ribosomal / isolation & purification
  • Drug Contamination*
  • Glucan Endo-1,3-beta-D-Glucosidase*
  • Kluyveromyces / genetics
  • Kluyveromyces / isolation & purification*
  • Polymerase Chain Reaction / methods
  • RNA, Ribosomal, 16S / genetics
  • Saccharomyces / genetics
  • Saccharomyces / isolation & purification*

Substances

  • DNA Primers
  • DNA, Fungal
  • DNA, Ribosomal
  • RNA, Ribosomal, 16S
  • Glucan Endo-1,3-beta-D-Glucosidase