scispace - formally typeset
R

Rupert De Wachter

Researcher at University of Antwerp

Publications -  92
Citations -  11570

Rupert De Wachter is an academic researcher from University of Antwerp. The author has contributed to research in topics: Ribosomal RNA & Phylogenetic tree. The author has an hindex of 44, co-authored 92 publications receiving 11365 citations. Previous affiliations of Rupert De Wachter include Laboratory of Molecular Biology.

Papers
More filters
Journal ArticleDOI

Identification of the bacterial endosymbionts in leaf galls of Psychotria (Rubiaceae, angiosperms) and proposal of 'Candidatus Burkholderia kirkii' sp. nov.

TL;DR: This paper reports the identification of bacterial endosymbionts inhabiting the leaf galls of Psychotria kirkii and proposes a provisional name for this as yet uncultivable bacterial endophytes in the genus Burkholderia.
Journal ArticleDOI

About the Order of Divergence of the Major Bacterial Taxa During Evolution

TL;DR: An evolutionary tree, reconstructed from 1232 bacterial small ribosomal subunit RNA sequences by a distance method, reflects the existence of 11 divisions and a number of subdivisions, but the order of divergence that gave rise to these taxa remains indeterminate.
Journal ArticleDOI

Evolution of Basidiomycetous Yeasts As Deduced From Small Ribosomal-subunit Rna Sequences

TL;DR: Complete small ribosomal subunit RNA sequences were used to infer the relationship between several basidiomycetous yeasts, and to resolve the evolutionary position of the basidiologycetes among the fungi.
Journal ArticleDOI

Phylogenetic analysis of five medically important candida species as deduced on the basis of small ribosomal subunit rna sequences

TL;DR: The small ribosomal subunit RNA (srRNA) sequences of the type strains of three human pathogenic Candida species; Candida krusei, C. lusitaniae and C. albicans were determined and showed that the yeasts diverge rather late in the course of eukaryote evolution, namely at the same depth as green plants, ciliates and some smaller taxa.
Journal ArticleDOI

Specific detection of campylobacter-concisus by pcr amplification of 23s rdna areas.

TL;DR: A simple Campylobacter concisus-specific PCR assay was developed, based on a target sequence which comprises the most variable areas of 23S rDNA, which was successfully evaluated on a broad selection of C. Concisus strains and phylogenetically related bacteria.