POST. MIKROBIOL.,
2000, 39, 3, 291-301 |
FILOGENEZA
BAKTERII
Z RODZAJU ACINETOBACTER |
Józef Kur, Krzysztof
Lewandowski,
Beata Krawczyk, Alfred Samet
1. Molekularne systemy odtwarzania
drzew filogenetycznych.
2. Drzewo filogenetyczne odtwarzane w oparciu o sekwencję nukleotydową genu
kodującego 16S rRNA.
3. Drzewo filogenetyczne odtwarzane w oparciu o sekwencję nukleotydową genu gyrB.
4. Gen recA w badaniach filogenetycznych bakterii.
5. Amplifikacja fragmentu genu recA Acinetobacter sp. i sekwencjonowanie.
6. Molekularne drzewo filogenetyczne rodzaju Acinetobacter w oparciu o sekwencję
nukleotydową fragmentu genu recA.
7. Podsumowanie |
Phylogeny of Acinetobacter genus
Abstract: The genomic
species is one of the major concepts of a bacterial species and is based on quantitative
similarities between chromosomal DNAs of bacteria (DNA reassociation values) as determined
by DNA-DNA hybridization. This method is one of the recommended standards for delineating
bacterial species and a genomic species is defined as a group of bacterial strains that
have DNA-DNA reassociation values of approximately 70% or more. The similarity of small
subunit rRNA (16S rRNA) sequences is increasingly being used for the classification of
bacteria. However, the resolution of 16S rRNA sequence analysis is insufficient to
distinguish closely related genomic species because of the extremely slow rate of base
substitution in 16S rDNAs. On the other hand, phylogenetic analysis based on
protein-encoding genes provides a greater degree of resolution than that based on 16S rRNA
genes since the former genes evolve faster than the latter. Various protein-encoding genes
such as recA, groEL, hsp75, rpoB, rpoD and gyrB have been used for the
classification of bacteria at the intragenic level. It has been reported that the grouping
of Acinetobacter strains based on 1 6S rRNA sequence analysis, DNA-DNA
hybridization analysis and phenotypic methods is inconsistent and therefore the
establishment of reliable methods for unambiguous identification of these strains is quite
urgent. We are interested in examining the possibility that phylogenetic analysis using
protein-encoding recA genes could be used for the identification of Acinetobacter
strains and to provide information equivalent to that of DNA-DNA hybridization
analysis. |
1. Molecular systems for
reproducing phylogenetic trees.
2. Phylogenetic tree reproduced based on nucleotide sequence of 16S rRNA gene.
3. Phylogenetic tree reproduced based on nucleotide sequence of gyrB gene.
4. recA gene in phylogenetic studies of bacteria.
5. Amplification of Acinetobacter sp. recA gene fragment and sequencing.
6. Molecular phylogenetic tree of Acinetobacter genus based on nucleotide sequences
of
recA gene fragment.
7. Summary |
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