2005
DOI: 10.1002/bit.20347
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Group‐specific primer and probe sets to detect methanogenic communities using quantitative real‐time polymerase chain reaction

Abstract: Real-time polymerase chain reaction (PCR) is a highly sensitive method that can be used for the detection and quantification of microbial populations without cultivating them in anaerobic processes and environmental samples. This work was conducted to design primer and probe sets for the detection of methanogens using a real-time PCR with the TaqMan system. Six group-specific methanogenic primer and probe sets were designed. These sets separately detect four orders (Methanococcales, Methanobacteriales, Methano… Show more

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Cited by 1,350 publications
(767 citation statements)
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“…The V3 and V4 region of the 16S rRNA gene was amplified using forward primer PRK341 and reverse primer PRK806 [20], with further processing for Illumina sequencing as previously described [19]. Finally, quantification of butyric acid in cecum content was performed by GC [21].…”
Section: Methodsmentioning
confidence: 99%
“…The V3 and V4 region of the 16S rRNA gene was amplified using forward primer PRK341 and reverse primer PRK806 [20], with further processing for Illumina sequencing as previously described [19]. Finally, quantification of butyric acid in cecum content was performed by GC [21].…”
Section: Methodsmentioning
confidence: 99%
“…Methanomicrobiales (MMB), Methanosarcinaceae (Msc) and Methanosaetaceae (Mst) were previously described by Yu et al (2005). The reaction mixture of 20µL was prepared by means of the …”
Section: S5 Real-time Pcr Analysismentioning
confidence: 99%
“…Real-time qPCR was performed using Power SYBR® Green PCR Master Mix (Life Technologies). For the total Eubacteria quantification the primers 338F and 805R (Yu et al 2005) were used for the 16S rRNA gene fragment, and cloned 16S rRNA gene from Escherichia coli (JM109) as a standard. Total SRB were quantified using the primers DSR1F (Wagner et al 1998) and DSR500R (Wilms et al 2007) for amplifying the dsrA operon, and cloned dsrAB genes from Desulfotomaculum geothermicum (DSMZ 3669) as a standard.…”
Section: Quantification Of Total Bacterial 16s Rrna Genes and Dsra Gementioning
confidence: 99%