1999
DOI: 10.1016/s0168-1656(99)00154-6
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Design of a primer for ribosomal DNA internal transcribed spacer with enhanced specificity for ascomycetes

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Cited by 248 publications
(137 citation statements)
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“…The primers ITS1 and ITS4 (White et al 1990) or ITS4A and ITS5 (Larena et al 1999) were used to amplify and sequence the ITS region. The largest subunit of RNA polymerase II (RPB1) was amplified and sequenced with RPB1-Af and RPB1-6Rlasc (Stiller andHall 1997, Hofstetter et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…The primers ITS1 and ITS4 (White et al 1990) or ITS4A and ITS5 (Larena et al 1999) were used to amplify and sequence the ITS region. The largest subunit of RNA polymerase II (RPB1) was amplified and sequenced with RPB1-Af and RPB1-6Rlasc (Stiller andHall 1997, Hofstetter et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…Ascomycete isolates were PCR-amplified with the primers ITS 1-F (5′ CTT GGT CAT TTA GAG GAA GTA A 3′; Gardes and Bruns 1993) and ITS 4-A (5′ CGC CGT TAC TGG GGC AAT CCC TG 3′; Larena et al 1999). PCR conditions were as follows: initial denaturation at 95°C for 3 min, 35 cycles of denaturation at 95°C for 1 min, annealing at 52°C for 30 s, extension at 72°C for 1 min, followed by a final extension at 72°C for 10 min (Walker and Campbell 2010) in a Thermo Electron Px2 thermocycler (Thermo Electron Corp., Waltham, MA, USA) and a Peltier Thermal Cycler PTC-100 (Bio-Rad Laboratories, Hercules, CA, USA).…”
Section: Molecular Identification Of Fungal Isolatesmentioning
confidence: 99%
“…ITS rDNA was PCRamplified in triplicate reactions for each sample using the fungal primers ITS 1-F (Gardes and Bruns 1993) and ITS 4-A (Larena et al 1999) -as most fungi reported from marine environments belong to the phylum Ascomycota (Shearer et al 2007) -with ITS 1-F labelled on the 5′ end with the fluorescent dye FAM (6-carboxyfluorescein) and PCR conditions as previously stated. All PCR products were combined and purified using a QIAquick PCR purification kit (Qiagen, Valencia, CA, USA).…”
Section: Optimization Of Dna Extraction From Biofilms In Preparationmentioning
confidence: 99%
“…Samples with d a o2.1 mm were not included for the analyses owing to no or weak PCR amplification. Universal fungal primers ITS1F and ITS4 (Larena et al, 1999;Manter and Vivanco, 2007) along with adaptor, key and multiplex identifier sequences were used to amplify the ITS region of fungal rDNA (Supplementary Table 2 DNA sequence processing and analyses Sequence FASTA and QUAL files were extracted from the machine output file, trimmed and parsed by sequence tag using the Ribosomal Database Project pyrosequencing pipeline (Cole et al, 2005). Trimming removed primers, sequences with one or more undefined base, sequences below a minimum machine quality score of 20 and sequences with a trimmed read length of fewer than 300 bp.…”
Section: Dna Extractionmentioning
confidence: 99%