2013
DOI: 10.1590/s1516-89132013005000004
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Polymerase chain reaction (PCR) identification of terverticillate Penicillium species isolated from agricultural soils in eskişehir province

Abstract: In the present study, nine terverticillate Penicillium isolates (P. griseofulfum, P. puberulum, P. crustosum, P. aurantiogriseum, P. chrysogenum, P. primulinum, P. expansum, P. viridicatum, Eupenicillium egyptiacum) from 56 soil samples were characterized genetically by a PCR method. The DNAs of the strains were isolated using the glass beads and vortexing extraction method and then used for PCR amplification with the internal transcribed spacer 1 (ITS1) and ITS4 universal fungal specific primers. The ITS regi… Show more

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Cited by 18 publications
(16 citation statements)
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“…PCR product was separated by agarose gel electrophoresis (1% W/v in 1xTAE) and visualized by GelRed staining. PCR products were purified using EXOSAP-IT (Affimetrix) and sequenced using primers ITS1 (5'-TCCGTAGGTGAACCTGCGG-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3') with a CEQ 8000 Genetic Analysis System (Beckman Coulter, Fullerton, CA, USA) following the method of Demirel et al (2013).…”
Section: Identificationmentioning
confidence: 99%
“…PCR product was separated by agarose gel electrophoresis (1% W/v in 1xTAE) and visualized by GelRed staining. PCR products were purified using EXOSAP-IT (Affimetrix) and sequenced using primers ITS1 (5'-TCCGTAGGTGAACCTGCGG-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3') with a CEQ 8000 Genetic Analysis System (Beckman Coulter, Fullerton, CA, USA) following the method of Demirel et al (2013).…”
Section: Identificationmentioning
confidence: 99%
“…Compared to the first sampling, the amount of bacterial contamination in pools number 1 and 2 was reduced which might be due to the increase in the level of remaining free chlorine in water. In average, the level of free chlorine and pH in the water in these pools was in an acceptable range [21][22][23][24].…”
Section: Bacteriummentioning
confidence: 99%
“…Molecular identification: DNA were extracted from the mycelium of the isolated Penicillium digitatum and Penicillium italicum according to Demirel et al, 2013 and the Internal Transcribed Spacer (IST1) region of the ribosomal nuclear DNA (rnDNA) was amplified using PCR. Standard methods were used to get the ITS1 sequencing and was carried out at a commercial facility (Macrogen Inc., Seoul, South Korea).…”
Section: Methodsmentioning
confidence: 99%