1991
DOI: 10.1099/00207713-41-1-65
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Transfer of Rhodocyclus gelatinosus to Rubrivivax gelatinosus gen. nov., comb. nov., and Phylogenetic Relationships with Leptothrix, Sphaerotilus natans, Pseudomonas saccharophila, and Alcaligenes latus

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Cited by 94 publications
(66 citation statements)
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“…9) Only difference was observed in the use of carbon sources: the KDDS1 could not use butyrate as a carbon source. In addition, 16S rDNA sequence analysis revealed that the KDDS1 has 99.81% high homology to that of the type culture.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…9) Only difference was observed in the use of carbon sources: the KDDS1 could not use butyrate as a carbon source. In addition, 16S rDNA sequence analysis revealed that the KDDS1 has 99.81% high homology to that of the type culture.…”
Section: Resultsmentioning
confidence: 99%
“…gelatinosus has recently been renamed from Rhodocyclus gelatinosus. 9) In addition, the evolutionary tree between Rvi. gelatinosus KDDS1 and other bacteria showed that Rvi.…”
Section: Resultsmentioning
confidence: 99%
“…Data were obtained from Busse & Auling (1992), Kalmbach et al (1999), Malmqvist et al (1994), Moreira et al (2000), Palleroni & Palleroni (1978), Spring et al (1996), Takeda et al (2002) and Willems et al (1991) and Aquabacterium and the species Alcaligenes latus, is the temperature range of growth. Strain N2-680 T differs from species of the genus Leptothrix in the absence of a cell sheath and the inability to produce manganese oxides, as is typical for these organisms (Siering & Ghiorse, 1996).…”
Section: Resultsmentioning
confidence: 99%
“…Bacteriochlorophyll-containing members of this group are represented by the species Rubrivivax gelatinosus (Willems et al, 1991) and Roseateles depolymerans (Suyama et al, 1999). Rubrivivax gelatinosus comprises phototrophic non-sulphur bacteria that occur frequently in sewagetreatment plants and lagoons (Siefert et al, 1978;Pfennig, 1978;Willems et al, 1991). Roseateles depolymerans, isolated from river water in Japan, is an obligately aerobic, heterotrophic organism that produces bacteriochlorophyll a and carotenoid pigments only in the presence of low levels of carbon sources.…”
Section: Introductionmentioning
confidence: 99%
“…For DNA-DNA binding experiments (see below), DNA was extracted from 5 to 10 g (wet weight) of cells grown in Roux flasks containing 130 ml of nutrient agar for 48 h at 30°C by using a slight modification of the method of Marmur (21), as described previously (36). For the amplified rDNA restriction analysis (ARDRA) (see below), total genomic DNA was purified by a method slightly modified from the method of Pitcher et al (26); cells grown in petri dishes containing nutrient agar for 24 to 48 h at 30°C were lysed in an additional step by incubating them with lysozyme at a final concentration of 50 mg/ml of TE buffer (10 mM Tris-HC1, 1 mM EDTA; pH 8.0) for 30 min at 37°C.…”
Section: Methodsmentioning
confidence: 99%