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Identification of contaminating fungal DNA sequences in Zymolyase.


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.

SUBMITTER: Rimek D 

PROVIDER: S-EPMC84574 | biostudies-literature | 1999 Mar

REPOSITORIES: biostudies-literature

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Identification of contaminating fungal DNA sequences in Zymolyase.

Rimek D D   Garg A P AP   Haas W H WH   Kappe R R  

Journal of clinical microbiology 19990301 3


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. ...[more]

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