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Table 1 PCR primers used in the various culture-dependent and culture-independent approaches

From: Mapping of wine yeast and fungal diversity in the Small Carpathian wine-producing region (Slovakia): evaluation of phenotypic, genotypic and culture-independent approaches

Method

Designation

Sequence

Target

Reference

Real-time PCR

Hauf 2 L

CCCTTTGCCTAAGGTACG

Hanseniaspora sp.

Zott et al. 2010

Hauf 2R

CGCTGTTCTCGCTGTGATG

MPL3

CTCTCAAACCTCCGGTTTG

Metschnikowia pulcherrima

Zott et al. 2010

MPR3

GATATGCTTAAGTTCAGCGGG

SC1

GAAAACTCCACAGTGTGTTG

Saccharomyces sp.

Zott et al. 2010

SC2

GCTTAAGTGCGCGGTCTTG

Tods L2

CAAAGTCATCCAAGCCAGC

Torulaspora delbrueckii

Zott et al. 2010

Tods R2

TTCTCAAACAATCATGTTTGGTAG

TR03

TCTGCCCTATCAACTTTCGATGGA

Universal eukaryotic

Allmann et al. 1993

TR04

AATTTGCGCGCCTGCTGCCTTCCTT

Culture-independent approach and ITS sequencing

ITS1

TCCGTAGGTGAACCTGCGG

18S rRNA

White et al. 1990

ITS3

GCATCGATGAAGAACGCAGC

5.8S rRNA

White et al. 1990

ITS4

TCCTCCGCTTATTGATATGC

26S rRNA

White et al. 1990

ITS4-FAM

FAM-TCCTCCGCTTATTGATATGC

26S rRNA

Brežná et al. 2010

M13F-40

GTTTTCCCAGTCACGAC

pDrive vector

Qiagena

M13R

AACAGCTATGACCATG

  1. ITS, Internal transcribed spacer
  2. aSequences of these primers were obtained from the Qiagen PCR cloning handbook (Qiagen, Hilden, Germany)