A nested PCR approach for improved recovery of archaeal 16S rRNA gene fragments from freshwater samples

E.W. Vissers; P.L.E. Bodelier; G. Muyzer; R. Laanbroek

doi:10.1111/j.1574-6968.2009.01718.x

A nested PCR approach for improved recovery of archaeal 16S rRNA gene fragments from freshwater samples

E.W. Vissers, P.L.E. Bodelier, G. Muyzer, R. Laanbroek

Onderzoeksoutput: Bijdrage aan wetenschappelijk tijdschrift/periodieke uitgave › Artikel › Wetenschappelijk › peer review

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In a survey on the presence of archaea in a number of European lakes, it was found that known archaeal primer sets for PCR were not suited for use in freshwater environment, as some lack selectivity, while others were too selective. A nested PCR was developed for denaturing gradient gel electrophoresis (DGGE) with primer sets 21F–958R and Parch519f–Arch915r, respectively. After sequencing of the DGGE bands obtained by this nested method, 93% of the sequences were of archaeal origin. More diverse archaeal DGGE patterns were found as compared with other PCR methods. The nested PCR-DGGE method presented here is therefore a reliable tool to analyze the archaeal diversity in freshwater habitats, revealing even more widespread diversity of the archaea.

Originele taal-2	Engels
Pagina's (van-tot)	193-198
Tijdschrift	FEMS Microbiology Letters
Volume	298
Nummer van het tijdschrift	2
DOI's	https://doi.org/10.1111/j.1574-6968.2009.01718.x
Status	Gepubliceerd - 2009

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10.1111/j.1574-6968.2009.01718.x

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abstract = "In a survey on the presence of archaea in a number of European lakes, it was found that known archaeal primer sets for PCR were not suited for use in freshwater environment, as some lack selectivity, while others were too selective. A nested PCR was developed for denaturing gradient gel electrophoresis (DGGE) with primer sets 21F–958R and Parch519f–Arch915r, respectively. After sequencing of the DGGE bands obtained by this nested method, 93% of the sequences were of archaeal origin. More diverse archaeal DGGE patterns were found as compared with other PCR methods. The nested PCR-DGGE method presented here is therefore a reliable tool to analyze the archaeal diversity in freshwater habitats, revealing even more widespread diversity of the archaea.",

author = "E.W. Vissers and P.L.E. Bodelier and G. Muyzer and R. Laanbroek",

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A nested PCR approach for improved recovery of archaeal 16S rRNA gene fragments from freshwater samples

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