Novel anaerobic ultramicrobacteria belonging to the Verrucomicrobiales lineage of bacterial descent isolated by dilution culture from anoxic rice paddy soil

The use of dilution culture techniques to cultivate saccharolytic bacteria present in the anoxic soil of flooded rice microcosms allowed the isolation of three new strains of bacteria, typified by their small cell sizes, with culturable numbers estimated at between 1.2 x 10(5) and 7.3 x 10(5) cells per g of dry soil. The average cell volumes of all three strains were 0.03 to 0.04 microns3, and therefore they can be termed ultramicrobacteria or "dwarf cells." The small cell size is a stable characteristic, even when the organisms grow at high substrate concentrations, and thus is not a starvation response. All three strains have genomic DNA with a mol% G+C ratio of about 63, are gram negative, and are motile by means of a single flagellum. The three new isolates utilized only sugars and some sugar polymers as substrates for growth. The metabolism is strictly fermentative, but the new strains are oxygen tolerant. Sugars are metabolized to acetate, propionate, and succinate. Hydrogen production was not significant. In the presence of 0.2 atm of oxygen, the fermentation end products or ratios did not change. The phylogenetic analysis on the basis of 16S ribosomal DNA (rDNA) sequence comparisons indicates that the new isolates belong to a branch of the Verrucomicrobiales lineage and are closely related to a cloned 16S rDNA sequence (PAD7) recovered from rice paddy field soil from Japan. The isolation of these three strains belonging to the order Verrucomicrobiales from a model rice paddy system, in which rice was grown in soil from an Italian rice field, provides some information on the possible physiology and phenotype of the organism represented by the cloned 16S rDNA sequence PAD7. The new isolates also extend our knowledge on the phenotypic and phylogenetic depths of members of the order Verrucomicrobiales, to date acquired mainly from cloned 16S rDNA sequences from soils and other habitats.

[1]  D. Bezdicek,et al.  Estimation of the abundance of an uncultured soil bacterial strain by a competitive quantitative PCR method , 1996, Applied and environmental microbiology.

[2]  E. Stackebrandt,et al.  The genus Nocardiopsis represents a phylogenetically coherent taxon and a distinct actinomycete lineage: proposal of Nocardiopsaceae fam. nov. , 1996, International journal of systematic bacteriology.

[3]  E. Stackebrandt,et al.  Assignment of hitherto unidentified 16S rDNA species to a main line of descent within the domain Bacteria , 1995 .

[4]  T. Ueda,et al.  Molecular phylogenetic analysis of a soil microbial community in a soybean field , 1995 .

[5]  E. Stackebrandt,et al.  Unraveling the extent of diversity within the order Planctomycetales , 1995, Applied and environmental microbiology.

[6]  R. Colwell,et al.  Microbial Diversity and Ecosystem Function. , 1995 .

[7]  B. Griffiths,et al.  Potential application of a community hybridization technique for assessing changes in the population structure of soil microbial communities , 1994 .

[8]  H. Neue Methane emission from rice fields , 1993 .

[9]  Egbert J. de Vries,et al.  Isolation of Typical Marine Bacteria by Dilution Culture: Growth, Maintenance, and Characteristics of Isolates under Laboratory Conditions , 1993, Applied and environmental microbiology.

[10]  J. Mary,et al.  The Most Probable Number estimate and its confidence limits , 1993 .

[11]  D. Button,et al.  Viability and Isolation of Marine Bacteria by Dilution Culture: Theory, Procedures, and Initial Results , 1993, Applied and environmental microbiology.

[12]  W. Liesack,et al.  Occurrence of novel groups of the domain Bacteria as revealed by analysis of genetic material isolated from an Australian terrestrial environment , 1992, Journal of bacteriology.

[13]  R. Conrad,et al.  Metabolism of position-labelled glucose in anoxic methanogenic paddy soil and lake sediment , 1991 .

[14]  F. Bak,et al.  A rapid and sensitive ion chromatographic technique for the determination of sulfate and sulfate reduction rates in freshwater lake sediments , 1991 .

[15]  P. Janssen,et al.  Isolation of a Citrobacter species able to grow on malonate under strictly anaerobic conditions. , 1990, Journal of general microbiology.

[16]  V. Torsvik,et al.  High diversity in DNA of soil bacteria , 1990, Applied and environmental microbiology.

[17]  H. Schlesner Verrucomicrobium spinosum gen. nov., sp. nov.: a Fimbriated Prosthecate Bacterium , 1987 .

[18]  R. Colwell,et al.  Survival strategies of bacteria in the natural environment. , 1987, Microbiological reviews.

[19]  N. Saitou,et al.  The neighbor-joining method: a new method for reconstructing phylogenetic trees. , 1987, Molecular biology and evolution.

[20]  D. Lovley,et al.  Organic Matter Mineralization with Reduction of Ferric Iron in Anaerobic Sediments , 1986, Applied and environmental microbiology.

[21]  J. Felsenstein CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP , 1985, Evolution; international journal of organic evolution.

[22]  R. Cord-Ruwisch A quick method for the determination of dissolved and precipitated sulfides in cultures of sulfate-reducing bacteria , 1985 .

[23]  L. Bakken Separation and Purification of Bacteria from Soil , 1985, Applied and environmental microbiology.

[24]  R. Neihof,et al.  Direct Determination of Activities for Microorganisms of Chesapeake Bay Populations , 1984, Applied and environmental microbiology.

[25]  J. C. Ward,et al.  Microbiology of Wetwood: Importance of Pectin Degradation and Clostridium Species in Living Trees , 1981, Applied and environmental microbiology.

[26]  R. Y. Morita,et al.  Microcultural Study of Bacterial Size Changes and Microcolony and Ultramicrocolony Formation by Heterotrophic Bacteria in Seawater , 1981, Applied and environmental microbiology.

[27]  S. Jeffery Evolution of Protein Molecules , 1979 .

[28]  H. Noller,et al.  Complete nucleotide sequence of a 16S ribosomal RNA gene from Escherichia coli. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[29]  L. Meyer-Reil,et al.  Autoradiography and Epifluorescence Microscopy Combined for the Determination of Number and Spectrum of Actively Metabolizing Bacteria in Natural Waters , 1978, Applied and environmental microbiology.

[30]  N. Pfennig Rhodocyclus purpureus gen. nov. and sp. nov., a Ring-Shaped, Vitamin B12-Requiring Member of the Family Rhodospirillaceae , 1978 .

[31]  L. E. Casida Small cells in pure cultures of Agromyces ramosus and in natural soil. , 1977, Canadian journal of microbiology.

[32]  R. Edlich,et al.  A more reliable gram staining technic for diagnosis of surgical infections. , 1975, American journal of surgery.

[33]  L. E. Casida,et al.  Microflora of Soil as Viewed by Transmission Electron Microscopy , 1972, Applied microbiology.

[34]  A. L. Chaney,et al.  Modified reagents for determination of urea and ammonia. , 1962, Clinical chemistry.

[35]  H. Jannasch,et al.  Bacterial Populations in Sea Water as Determined by Different Methods of Enumeration1 , 1959 .

[36]  N. Larsen,et al.  The Ribosomal Database Project. , 1994, Nucleic acids research.

[37]  R. Conrad Mechanisms Controlling Methane Emission from Wetland Rice Fields , 1993 .

[38]  F. Rainey,et al.  Spirochaeta thermophila sp. nov., an Obligately Anaerobic, Polysaccharolytic, Extremely Thermophilic Bacterium , 1992 .

[39]  H. Schlesner The Genus Verrucomicrobium , 1992 .

[40]  L. Bakken,et al.  DNA-content of soil bacteria of different cell size , 1989 .

[41]  J. Novitsky,et al.  Microautoradiography-based enumeration of bacteria with estimates of thy-midine-specific growth and production rates , 1987 .

[42]  T. Jukes CHAPTER 24 – Evolution of Protein Molecules , 1969 .

[43]  C. H. Werkman Bacterial Metabolism (2nd ed.) , 1940 .

[44]  A. Harden Bacterial Metabolism , 1930, Nature.