Phylogenetic Analysis by 16S rRNA Gene Sequencing of Obligate Oligotrophs Isolated from the Northern Basin of Lake Biwa (Mesotrophic Lake)
スポンサーリンク
概要
- 論文の詳細を見る
We determined the number of total oligotrophs (obligate and facultative) in the northern basin of Lake Biwa (mesotrophic lake) on May 9th and June 7th, 1995,using the MPN (most probable number) method with two nutrient-poor media; a filter-sterilized lake water medium (LW-medium; ca. 1.7 mg C/l) and a diluted peptone medium (LT10^<-3>; ca. 2 mg C/1). The number of oligotrophs was generally 300-fold higher than the number of colony forming units on LT10^<-1> agar plates containing 0.5 g of peptone per liter (ca. 200 mg C/1), and corresponded to more than 25% of the total bacterial count determined by a direct counting method with DAPI staining. Most oligotrophs (97.5%; average) were obligate oligotrophs (OO), growing only at low nutrient concentrations with no growth on LT10^<-1> solid or liquid media. Five OO strains were isolated from LT10^<-3> and LW-medium in May, and approximately sequences of a region of 500 nucleotides of their 16S rRNA gene (16S rDNA) were determined. Phylogenetic analysis of 16S rDNA showed that the OO isolates were clearly distinguishable from the six strains of platable bacteria, which were isolated from the LT10^<-1> agar plate medium at the same time. Moreover, all platable bacteria were closely related to Comamonas testosteroni (β-proteobacteria subgroup), while all OO isolates with the exception of LO-52 were phylogenetically distant from every wellknown bacteria in the database and were widely distributed into proteobacterial subgroups. These results strongly suggest that there are many unknown OO living in freshwater environments, and that OO isolates will provide important information regarding microbial ecology.
- 日本微生物生態学会の論文
- 1997-06-30
著者
-
Ishida Y
Fukuyama Univ. Hiroshima Jpn
-
Ishida Yuzaburo
The Center For Environmental Research Ritsumeikan University
-
UCHIDA Aritsune
Laboratory of Marine Microbiology, Department of Applied Bioscience, Graduate School of Agriculture,
-
Shin Mi-sun
Laboratory Of Microbiology Department Of Applied Bioscience Graduate School Of Agriculture Kyoto Uni
-
Yoshinaga Ikuo
Laboratory Of Microbiology Department Of Applied Bioscience Graduate School Of Agriculture Kyoto Uni
-
Yoshinaga Ikuo
Laboratory Of Marine Microbiology Department Of Applied Biosciences Graduate School Of Agriculture K
-
Uchida A
Graduate School Of Agriculture Kyoto University
-
Uchida Aritsune
Laboratory Of Marine Microbiology Department Of Applied Bioscience Graduate School Of Agriculture Ky
-
KATANOZAKA NORIAKI
Laboratory of Microbiology, Department of Applied Bioscience, Graduate School of Agriculture, Kyoto
-
Katanozaka Noriaki
Laboratory Of Microbiology Department Of Applied Bioscience Graduate School Of Agriculture Kyoto Uni
関連論文
- Cloning, Sequence Analysis, and Expression in Escherichia coli of a Gene Coding for an Enzyme from Bacillus circulans K-1 that Degrades Guar Gum
- Purification, Properties, and N-Terminal Amino Acid Sequences of Guar Gum-degrading Enzyme from Bacillus circulans K-1
- Molecular Cloning and Nucleotide Sequence Analysis of the Gene Coding for Chloroplast-type Ferredoxin from the Dinoflagellates Peridinium bipes and Alexandrium tamarense
- There Are 4 Introns in the Gene Coding the DNA-binding Protein HCc of Crypthecodinium cohnii (Dinophyceae)
- Phylogenetic Analysis by 16S rRNA Gene Sequencing of Obligate Oligotrophs Isolated from the Northern Basin of Lake Biwa (Mesotrophic Lake)
- Post-replication Repair of the Heat-induced DNA Injury in Deinococcus radiodurans
- A Molecular View of Microbial Diversity in Marine and Rerrestrial Hot Water Environments.
- Extrinsic Thermostabilization Factors and Thermodenaturation Mechanisms for Phosphoenolpyruvate Carboxylase (PEPC)from an Extremely Thermophilic Bacterium Phodothermus obanensis
- Extremely Thermostable Phosphoenolpyruvate Carboxylase from an Extreme Thermophile, Rhodothermus obamensis^1
- Contribution of Anammox Bacteria to Benthic Nitrogen Cycling in a Mangrove Forest and Shrimp Ponds, Haiphong, Vietnam
- Detection of Anammox Activity and Diversity of Anammox Bacteria-Related 16S rRNA Genes in Coastal Marine Sediment in Japan
- Purification and characterization of sulfotransferase specific to O-22 of 11-hydroxy saxitoxin from the toxic dinoflagellate Gymnodinium catenatum (dinophyceae)
- Origin of the plastid in the anomalously pigmented dinoflagellate Gymnodinium mikimotoi (Gymnodiniales, Dinophyta) as inferred from phylogenetic analysis based on the gene encoding the large subunit of form I-type RuBisCO
- Preliminary phylogenetic analysis of plastid-encoded genes from an anomalously pigmented dinoflagellate Gymnodinium mikimotoi (Gymnodiniales, Dinophyta)
- Ribotype Analysis of HAKB (Heterosigma akashiwo-Killing Bacteria) Strains Isolated During Termination Period of a H.akashiwo Bloom Occurred in Osaka Bay
- Contribution of Anammox Bacteria to Benthic Nitrogen Cycling in a Mangrove Forest and Shrimp Ponds, Haiphong, Vietnam
- Evidence of Exponential Growth of an Anammox Population in an Anaerobic Batch Culture
- Occurrence of Blue-green Algae and Algal Lytic Bacteria in Lake Biwa
- Geographic differences in paralytic shellfish poisoning toxin profiles among Japanese populations of Alexandrium tamarense and A. catenella (Dinophyceae)
- Reevaluation of the Phylogenetic Depth of the Marine Aerobic Hyperthermophilic Archaeon Aeropyrum pernix Based on Comparative Analysis of 23S rRNA Sequences
- Molecular cloning and nucleotide sequence analysis of psbA from the dinoflagellates: Origin of the dinoflagellate plastid
- Evidence of Exponential Growth of an Anammox Population in an Anaerobic Batch Culture
- Distribution and Diversity of Anaerobic Ammonium Oxidation (Anammox) Bacteria in the Sediment of a Eutrophic Freshwater Lake, Lake Kitaura, Japan
- Detection of Anammox Activity and 16S rRNA Genes in Ravine Paddy Field Soil
- Detection of Anammox Activity and 16S rRNA Genes in Ravine Paddy Field Soil
- Apurinic/Apyrimidinic Endodeoxyribonuclease Level during the Life Cycle of Bacillus subtilis