Deoxyribonucleic acid homology and taxonomy of Agrobacterium, Rhizobium, and Chromobacterium

Hybridization experiments were carried out between high molecular weight, denatured, agar-embedded deoxyribonucleic acid (DNA) and homologous, nonembedded, sheared, denatured (14)C-labeled DNA from a strain of Agrobacterium tumefaciens and Rhizobium leguminosarum (the reference strains) in the presence of sheared, nonembedded, nonlabeled DNA (competing DNA) from the same or different nomen-species of Agrobacterium, Rhizobium, Chromobacterium, and several other organisms. Percentage of DNA homology was calculated from the results. The findings are discussed in relation to previous taximetric studies, present classification schemes, and guanine-cytosine content of the DNA. Strains of A. tumefaciens, A. radiobacter, A. rubi, A. rhizogenes, R. leguminosarum, and R. meliloti exhibited a mean percentage of DNA homology greater than 50 with the two reference strains. A. tumefaciens, A. radiobacter, and A. rubi were indistinguishable on the basis of DNA homology, with strain variations for this group involving up to 30% of their base sequences. The remainder of the organisms studied fall into at least six distinct genetic groups: (i) R. (Agrobacterium) rhizogenes, which is more homologous to R. leguminosarum than to the A. tumefaciens-A. radiobacter group; (ii) R. leguminosarum; (iii) R. meliloti; (iv) R. japonicum, which has a mean DNA homology of some 38 to 45% with the reference strains; (v) Chromobacterium, which is as genetically remote from the reference strains as, for example, Pseudomonas; and (vi) A. pseudotsugae strain 180, which has a DNA homology with A. tumefaciens and R. leguminosarum of only about 10%. Since this latter homology value is similar to what was found after hybridizations between the reference strains and organisms such as Escherichia coli and Bacillus subtilis, A. pseudotsugae should definitely be removed from the genus.     

Deoxyribonucleic acid reassociation in the taxonomy of the genus Chlorella

Four species of the unicellular green alga Chlorella, C. vulgaris, C. luteoviridis, C. minutissima, and C. zofingiensis, were characterized with respect to DNA similarities as determined by quantitative DNA hybridization procedures. In contrast to previous DNA hybridization procedures. In contrast to previous results, C. vulgaris turned out to be a homogeneous species with the exception of strain 211-11c of the Göttingen collection, which was shown to belong to C. kessleri. Similary, C. luteoviridis and C. minutissima represent well defined species in terms of phenotypic and genotypic features. Whitin C. zofingiensis on strain is clearly different with respect to DNA base composition and DNA hybridization data even though it shares phenotypic characteristics with the other strains of C. zofingiensis.     

Deoxyribonucleic acid base composition and taxonomy of violet-pigmented cocci

The content of guanine and cytosine in DNA of the violet-pigmented micrococci designated asStaphylococcus flavocyaneus andMicrococcus flavocyaneus varies within the range of 70.8 – 72.0%. These species have similar deoxyribonucleic acid base compositions and do not differ physiologically and morphologically: they both produce yellow and violet pigments, hydrolyse gelatin and casein, reduce nitrates and do not form lipase. Therefore we consider them in accordance with Kocur and Martinec (1962, 1963) identical. They do not, however, seem to be identical withMicrococcus luteus (Schroeter, 1872) Cohn 1872 because the content of guanine and cytosine in DNA of the neotype culture of this species was found to be 66.3%.Micrococcus luteus differs from the violet pigmented micrococci also physiologically. It does not produce violet pigment, does not hydrolyse gelatin and casein and does not produce urease. For the violet pigmented strainMicrococcus cyaneus the use of the original designation is recommended:Micrococcus cyaneus (Schroeter) Cohn 1872, as it differs from the other violet cocci not only physiologically — it does not produce yellow pigment, oxidises mannitol, dulcitol and sorbitol, produces lipase and does not hydrolyse casein — but also in its DNA base composition.     

Deoxyribonucleic acid reassociation in the taxonomy of the genus Chlorella

The genetic relationships of nine strains of Chlorella saccharophila were determined by DNA hybridization techniques. Four strains are closely related to the type strain 211-9a and one strain seems to be moderately related, whereas the taxonomic position of the remaining three strains is not clear. C. saccharophila, like C. sorokiniana, is another species of Chlorella containing strains which are heterogeneous in their overall DNA base sequence and partly also in morphological, biochemical and physiological characters.     

Deoxyribonucleic acid reassociation in the taxonomy of the genus Chlorella

DNA homologies of 14 strains of Chlorella protothecoides were determined. All strains are related by a high degree of DNA similarity (96–102% D) with the exception of strain 211-11 a which proved to belong to C. kessleri. There is, however, no detectable DNA homology with strains of the genus Prototheca which is supposed to have evolved from C. protothecoides by loss of photosynthetic pigments. Even within Prototheca the low degree of DNA similarity indicates a heterogeneity similar to that observed in the genus Chlorella.     

Deoxyribonucleic acid reassociation in the taxonomy of the genus Chlorella

DNA hybridization techniques showed Chlorella fusca var. vacuolata and C. kessleri to be homogeneous species with DNA homologies of 90–100% C. fusca var. fusca and var. rubescens, however, have only about 15% DNA homology with C. fusca var. vacuolata and should no longer be regarded as varieties. A good correlation was found so far between biochemical and physiological characters used in the taxonomy of Chlorella and DNA relatedness. Mutant strains of Chlorella were tested for DNA homologies to prove the reliability of the taxonomical interpretation.     

Deoxyribonucleic acid base composition and taxonomy in the genus Geotrichum Link

The molar percentage of guanine + cytosine (% GC) in the DNA from 25 yeast-like fungi related to the genus Geotrichum has been measured. This criterion together with the biochemical characteristics allow the division of the species into 3 groups: one group resembling G. candidum (% GC: 31.5–42) and containing 8 imperfect and 6 perfect forms. In this group only G. capitatum has a lower % GC (31.5). A second group of 6 species resembling the genus Trichosporon (57–60%) and a third intermediate category of 4 species (42–53.5%) were observed. The GC-values correlate well with biochemical characters, e.g. the presence of urease, the number of organic substrates assimilated, and also with the presence of characters typical of the Ascomycetes or the Basidiomycetes.This work was supported by I.N.S.E.R.M. (Institut National de la Santé et de la Recherche Médicale) C.R.L. n^o 76 1 153 8.     

Deoxyribonucleic acid base composition and taxonomy of Moniliella and allied genera

DNA base compositions of representative (type) strains of Moniliella, Trichosporonoides and Hyalodendron were determined. Within Trichosporonoides over 16% variance was found. Most species separated well, but M. suaveolens showed considerable heterogeneity. The standard 2% G+C differences for species distinction is probably not applicable to these yeasts. The new combination M. pollinis is proposed for M. tomentosa var. pollinis on the basis of slight ecological, morphological and physiological differences, supported by a marked difference in % G+C.     

Some applications of deoxyribonucleic acid base composition in bacterial taxonomy

The melting pointT _m, the mean molar (guanine+cytosine) composition and the compositional distribution of purified DNA from several strains ofXanthomonas, Chromobacterium and yellow-pigmented marine bacteria have been determined. These groups were selected because they had been analyzed adansonially. Ten strains ofXanthomonas had an average molar (guanine+cytosine) composition within the range 66.0–68.2%, which was very close to that ofPseudomonas (60–68%), as expected. All strains ofChromobacterium (six of theviolaceum biotype and three of thelividum biotype) had mean molar (guanine+cytosine) compositions within the range 63.4–71.4%. The yellow-pigmented marine flavobacteria had mean molar (guanine+cytosine) compositions of 35.6–40.6%. This suggests that they would not be genetically related to the yellow-pigmentedXanthomonas, nor to facultative aerobic organisms, such asAeromonas and theEnterobacteriaceae. The yellow-pigmented marine swarming bacteria, which resembleCytophaga, fell into two separate groups: some had a mean molar (guanine+cytosine) composition of about 34%, others were around 63%. This suggests genetic heterogeneity. The compositional distribution of DNA molecules was on the whole more narrow in polarly flagellated than in peritrichous organisms.     

Deoxyribonucleic acid homology among the species of the genus Bifidobacterium isolated from animals

Summary Representatives of the species of the genus Bifidobacterium isolated from bovine rumen, intestinal content of honey bees and pig feces were studied for their deoxyribonucleic acid similarities with DNA-DNA filter hybridization-competition experiments. The species were: B. asteroides, B. indicum and B. coryneforme from honey bees; B. ruminale and B. globosum from rumen; B. suis from pig feces; Mitsuoka's species B. thermophilum and B. pseudolongum. Strains of B. bifidum, B. infantis, B. longum and B. breve from human sources were included in some comparative experiments. The group of bacteria investigated is largely heterogeneous: virtually no homology exists among the species from rumen and pig feces; the species or types from bees, although unrelated with rumen and pig types, share with these a significant portion of the genome; the competitor DNA's from human strains did not at all react with any of the homologous systems. The annealing reaction was carried out under stringent conditions to ensure against mismatching of nucleotide sequences (70°C in Denhardt's reactive mixture). The separation within the genus Bifidobacterium of several specific entities is fully substantiated.This investigation was supported by a research grant of C. N. R. (Consiglio Nazionale delle Ricerche, Roma).