1992
DOI: 10.1094/phyto-82-828
|View full text |Cite
|
Sign up to set email alerts
|

Detection of DNA of Plant Pathogenic Mycoplasmalike Organisms by a Polymerase Chain Reaction that Amplifies a Sequence of the 16S rRNA Gene

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

6
278
1
5

Year Published

1997
1997
2021
2021

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 508 publications
(290 citation statements)
references
References 0 publications
6
278
1
5
Order By: Relevance
“…Phloem was removed with a knife from the bark. DNA extraction and PCR amplification were done according to Ahrens & Seemüller (1992). For the DNA amplification phytoplasma universal primer pairs (U5/U3, amplifying a fragment of about 880 bp in length) (Seemüller et al, 1994) and more specific pome-fruit phytoplasma primer pairs (fPD/rO1, amplifying a fragment of about 930 bp in length) (Lorenz et al, 1995) were used.…”
Section: Detection and Characterization Of The Pathogenmentioning
confidence: 99%
“…Phloem was removed with a knife from the bark. DNA extraction and PCR amplification were done according to Ahrens & Seemüller (1992). For the DNA amplification phytoplasma universal primer pairs (U5/U3, amplifying a fragment of about 880 bp in length) (Seemüller et al, 1994) and more specific pome-fruit phytoplasma primer pairs (fPD/rO1, amplifying a fragment of about 930 bp in length) (Lorenz et al, 1995) were used.…”
Section: Detection and Characterization Of The Pathogenmentioning
confidence: 99%
“…The development of universal PCR primer pairs designed to amplify all known phytoplasma 16S rDNA has facilitated this approach significantly (Ahrens & Seemu$ ller, 1992 ;Deng & Hiruki, 1991 ;Gundersen & Lee, 1996 ;Namba et al, 1993a). Moreover, nucleotide sequence analyses of the amplified 16S rDNA fragments have made phylogenetic analysis of phytoplasma isolates possible, and the information obtained has been used as the basis for delineating phytoplasmas into several groups (Kuske & Kirkpatrick, 1992 ;Schneider et al, 1995 ;Seemu$ ller et al, 1998 ;White et al, 1998).…”
Section: Introductionmentioning
confidence: 99%
“…For PCR, total DNA was isolated from 1g of fresh plant material (leaf midribs, buds and stems) following the phytoplasma-enrichment procedure of Ahrens and Seemüller (1992) and stored at -20°C until processing. Samples from both affected and symptomless plants were analysed for phytoplasma infection by two PCR methods: Nested PCR and real-time PCR.…”
Section: Nested Pcr and Real-time Pcrmentioning
confidence: 99%