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
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Research Support, Non-U.S. Gov't
MeSH terms
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DNA Primers
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DNA, Fungal / genetics
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DNA, Fungal / isolation & purification*
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DNA, Ribosomal / genetics
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DNA, Ribosomal / isolation & purification
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Drug Contamination*
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Glucan Endo-1,3-beta-D-Glucosidase*
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Kluyveromyces / genetics
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Kluyveromyces / isolation & purification*
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Polymerase Chain Reaction / methods
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RNA, Ribosomal, 16S / genetics
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Saccharomyces / genetics
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Saccharomyces / isolation & purification*
Substances
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DNA Primers
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DNA, Fungal
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DNA, Ribosomal
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RNA, Ribosomal, 16S
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Glucan Endo-1,3-beta-D-Glucosidase