2008
DOI: 10.1016/j.hydromet.2008.01.012
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Rapid and specific detection of Acidithiobacillus ferrooxidans and Leptospirillum ferrooxidans by PCR

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Cited by 22 publications
(11 citation statements)
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“…To quantify the abundance of Acidithiobacillus ferrooxidans at all sites, qPCR was performed with species‐specific primers F1_Thio (ATGCGTAGGAATCTGTCTTT) and R1_Thio (GGACTTAACCCAACATCTCA) and universal bacterial primers 1108F (ATGGYTGTCGTCAGCTCGTG) and 1132R (GGGTTGCGCTCGTTGC) as described previously (Escobar et al ., 2008; Větrovský et al ., 2010). Amplifications were performed on a StepOne Plus cycler (Applied Biosystems) using optical grade 96‐well plates.…”
Section: Methodsmentioning
confidence: 99%
“…To quantify the abundance of Acidithiobacillus ferrooxidans at all sites, qPCR was performed with species‐specific primers F1_Thio (ATGCGTAGGAATCTGTCTTT) and R1_Thio (GGACTTAACCCAACATCTCA) and universal bacterial primers 1108F (ATGGYTGTCGTCAGCTCGTG) and 1132R (GGGTTGCGCTCGTTGC) as described previously (Escobar et al ., 2008; Větrovský et al ., 2010). Amplifications were performed on a StepOne Plus cycler (Applied Biosystems) using optical grade 96‐well plates.…”
Section: Methodsmentioning
confidence: 99%
“…A. ferrooxidans was isolated by streak plating from AMD in the Jiguan Mountain Cu‐Au sulfide mine in Anhui Province, eastern China. The strain was identified by 16S rDNA using existing methods . After amplification of 16S rDNA by PCR, the sequence of this strain was determined by Invitrogen, Inc. (Shanghai, China) and was compared with the known sequence A. ferrooxidans ATCC23270 using the Basic Local Alignment Search Tool.…”
Section: Methodsmentioning
confidence: 99%
“…Conventional plate count methods and biochemical identification methods described previously could not circumvent the problems linked to the long wait for the colony to develop and/or the inability of some bacteria to grow on solid media (Johnson, 1991;Ahmad, 1993). In recent years, various nucleic acid-based molecular methods, such as Polymerase chain reaction (PCR) method (Feng et al, 2012;Escobar et al, 2008;Kamimura et al, 2001;DeWulfDurand et al, 1997) and fluorescent in situ hybridization (FISH) (Mahmoud et al, 2005), have been developed for the rapid detection and identification of Acidithiobacillus strains because of simplicity in operation, stable detection results, and savings in time. A high level of marker specificity is crucial for various nucleic acid-based molecular methods.…”
Section: Atc_1903mentioning
confidence: 99%