Dense winter bloom of the dinoflagellate Heterocapsa triquetra below the thick surface ice of brackish Lake Shihwa,Korea

We investigated the seasonal abundance of the dinoflagellate Heterocapsa triquetra (Ehrenberg) F. Stein, as well as the relevant in situ environmental factors, in brackish Lake Shihwa, Korea. We also examined the growth rates and morphological characteristics of the species in laboratory cultures. In the field, the population densities of H. triquetra remained at low levels from late spring to early summer, and then completely disappeared from August to November 2007. Interestingly, a dense bloom of H. triquetra appeared below the ice surface on 17 January 2008; identities of the cells were confirmed by rDNA sequence comparisons. The second peak reached a density of 672 × 10³ cells L^?1 on 28 March 2008, at a water temperature of 9.1°C. Laboratory experiments showed that growth rates of H. triquetra increased with incremental temperature increases within the range of 10 and 20°C. The highest growth rate reached by H. triquetra was 0.62 d^?1 at 20°C with a salinity of 30. Above 25°C, the dinoflagellate was unable to grow between salinities of 10 and 15, and reached only relatively low growth rates (<0.12 d^?1) under other salinity conditions. However, under continuous cultures at 5°C and 8°C, H. triquetra cells retained its growth capability for more than 12 days, implying that H. triquetra can survive and grows even at very low temperatures. The equivalent spherical diameter (ESD) of H. triquetra did not change markedly between 10 and 25°C, but the equivalent spherical diameter was significantly different at 5°C. The cell volume buildup of H. triquetra at low temperatures is one of the important survival strategies to overcome the harsh environmental conditions. These characteristics make H. triquetra a consistently dominant dinoflagellate in Lake Shihwa during the cold winter season.     

Constant Proportionality in the Female Segment of a Roosevelt Elk Population

Abstract: Incomplete population counts indicate change in population sizes when constant proportionality holds, a condition that is rarely met. However, researchers have not explored whether constant proportionality holds for a segment of a population. I examined whether the female segment (juv, subadult M, subadult and ad F) of a Roosevelt elk (Cervus elaphus roosevelti) population displayed constant proportionality. When most food is in particular habitats, females of polygynous species should use that habitat frequently, even when food is limited, because they are more familiar with food distribution and abundance than males. I obtained counts of elk and tallies of naturally marked animals from vehicle surveys of a population inhabiting a landscape where forage was in meadows that were interspersed in closed-canopied forest. I conducted population surveys in January or February and estimated population size with Bowden's mark-resight estimator. Population size estimates declined from 130 in 1997 to 37 in 2006. The proportion of the population counted during surveys was inversely related to population size estimates. Estimated population sizes were inversely related to male (r² = 0.56) but not female sighting probabilities (r² = 0.004), which were ≥0.9. Constant proportionality in counts held for only the female segment of the population. Counts of the female segment of the population can inform managers about changes in this segment of the population over time.     

Physiological function of soluble cytochrome <Emphasis Type="Italic">c</Emphasis>-552 from alkaliphilic <Emphasis Type="Italic">Pseudomonas alcaliphila</Emphasis> AL15-21<Superscript>T</Superscript>

It has been found that the alkaliphilic Gram-negative bacterium Pseudomonas alcaliphila AL15-21^T produces a larger amount of soluble c-type cytochromes at pH 10.0 under air-limited condition than at pH 7.0 under high aeration. Cytochrome c-552 was confirmed as the major c-type cytochrome among three soluble c-type cytochromes in the strain. To understand the physiological function of cytochrome c-552, a P. alcaliphila AL15-21^T cytochrome c-552 gene deletion mutant without a marker gene was constructed by electrotransformation adjusted in this study for the strain. The maximum specific growth rate and maximum cell turbidity of cells grown at pHs 7.0 and 10.0 under the high-aeration condition did not differ significantly between the wild-type and cytochrome c-552 deletion mutant strains. In the mutant grown at pH 10.0 under low-aeration condition, marked decreases in the maximum specific growth rate (40%) and maximum cell turbidity (25%) compared with the wild type were observed. On the other hand, the oxygen consumption rates of cell suspensions of the mutant obtained by the growth at pH 10 under low-aeration condition were slightly higher than that of the wild type. Considering the high electron-retaining ability of cytochrome c-552, the above observations could be accounted for by cytochrome c-552 acting as an electron sink in the periplasmic space. This may facilitate terminal oxidation in the respiratory system at high pH under air-limited conditions.     

The use of the chemostat to study the relationship between cell growth rate, viability, and the effect of interferon on L 1210 cells

Mouse leukemia L 1210 cells were cultivated in the chemostat at growth rates ranging from 0.1 day⁻¹ (population doubling time (T_d) 166.3 h) to 2.0 day⁻¹ (T_d 8.3 h). At growth rates of 1.0 day⁻¹ and above, the viability of the steady-state culture was greater than 99%. However, below 1.0 day⁻¹ there was a progressive decrease in the viability of the culture with decreasing growth rate until a minimum growth rate (0.1 day⁻¹) was reached below which steady-state cultures of L 1210 cells could not be established. Interferon treatment had no effect on the viability (>99%) of L 1210 cells cultivated at fast growth rates in the chemostat, whereas at slow growth rates (0.35 day⁻¹) interferon treatment markedly reduced the viability of the culture, even though the percentage increase in the doubling time of interferon-treated cultures was the same for cells cultivated at both fast and slow growth rates. Thus, although interferon is not directly cytotoxic, it can cause cell death by reducing the rate of cell multiplication below the minimum value compatible with viability.     

Establishment and Growth Kinetics of the Mutant Ehrlich-Lettré Ascites Cell Strain Hd33 In Permanent Suspension Culture1,2

Cells of a mutant in vivo subline of the Ehrlich-Lettré mouse ascites tumour (ELAT) were converted to growth in suspension culture. Kinetic analysis revealed the selective character of the conversion process; without a detectable adaptation period, a fraction of about 2 × 10^-5 of the explanted cells continued to grow in vitro. the resulting, mutant Ehrlich-Lettré ascites cell strain was designated HD33 and propagated uninterruptedly from 1974 on. the corresponding in vivo ELAT subline HD33 was derived from the HD33 ascites cell strain by intraperitoneal retransplantation. In HD33 cell suspension cultures, the population doubling time, the average intermitotic interval, as determined by videomonitoring, and the average duration of the cell cycle, as determined from percentage of labelled mitoses (PLM) data, were all measured at 15 hr. Cell loss and quiescent compartments were insignificant. the duration of the G₁ phase was effectively zero. Both PLM data and [³H]/[¹⁴C] thymidine double-labetling measurements revealed an S-phase duration of between 11 and 12 hr. the G₂ phase lasted 3–5 hr. The HD33 strain differs from comparable suspension strains of wild-type Ehrlich ascites cells in the insignificant role of density-dependent inhibition in growth, and the striking prolongation of the S phase which is associated with an excessive, cytoplasmic storage of glycogen by the mutant cells.     

Crop growth,water-use efficiency and carbon isotope discrimination in groundnut (Arachis hypogaea L.) genotypes under end-of season drought conditions*

Ten groundnut genotypes were grown under adequately irrigated conditions or subjected to drought during the pod filling phase (83–113 days after sowing) in a medium deep Alfisol at the ICRISAT Centre during the 1986–1987 post-rainy season. Crop growth was measured in both treatments, but transpiration (7) and water-use efficiency (W) were quantified only in the drought treatment. Leaf samples from both treatments were assayed for discrimination against ¹³CO₂ fixed in leaves (Δ) to examine the relationships between Δ, crop growth, and W under field conditions. The shoot dry matter accumulated during the period of drought (Y) ranged from 72–150 g m^-2 and was closely related to transpiration. This indicates scope for selection of traits and practices to increase T. Water-use efficiencies ranged from 1.38–2.50 g kg^-1 and were inversely related to Δ in eight out of the 10 genotypes. For the other two genotypes, there was evidence that T was underestimated by field measurements. Water-use efficiency and transpiration were not correlated suggesting that these two traits might be combined through breeding. Variation between genotypes was greatest for the partitioning of total dry matter to pods (73%), followed by water-use efficiency (31%) and transpiration (29%). Crop growth rates were negatively related to Δ under irrigated conditions but not under drought.     

Characterization of Microaerobacter geothermalis gen. nov., sp. nov., a novel microaerophilic, nitrate- and nitrite-reducing thermophilic bacterium isolated from a terrestrial hot spring in Tunisia

A novel thermophilic anaerobic and microaerophilic bacterium (optimal growth in the presence of 5–10% O₂), strain Nad S1^T was isolated from the terrestrial hot spring of Hammam Sidi Jdidi, Nabeul, Tunisia. Cells were motile rods having a Gram-positive cell wall structure. Strain Nad S1^T grew optimally at 55°C (range 37–70°C). Optimum pH for growth was 6.5–7.0. It was halotolerant growing with NaCl up to 7% (optimum concentration 1.5–3.0%). It grew chemoorganotrophically on various carbohydrates, organic-acids and amino-acids as energy sources, or chemolithotrophically on H₂ using nitrate, as terminal electron acceptor. Beside oxygen (under microaerobic conditions) and nitrate, nitrite was also used. Nitrate was completely reduced to N₂. No fermentation occurred. The genomic DNA G + C content was 41.8 mol%. Based on 16S rRNA gene sequence analysis, strain Nad S1^T belongs to the Bacillaceae family within the class ‘Bacilli’. Because of its phylogenetic and phenotypic characteristics, we propose this isolate to be assigned as a novel genus and a novel species within the domain Bacteria, Microaerobacter geothermalis gen. nov., sp. nov. The type strain is Nad S1^T (=DSM 22679^T =JCM 16213^T).     

Description of the novel perchlorate-reducing bacteria Dechlorobacter hydrogenophilus gen. nov., sp. nov. and Propionivibrio militaris, sp. nov.

Novel dissimilatory perchlorate-reducing bacteria (DPRB) were isolated from enrichments conducted under conditions different from those of all previously described DPRB. Strain LT-1^T was enriched using medium buffered at pH 6.6 with 2-(N-morpholino)ethanesulfonic acid (MES) and had only 95% 16S rRNA gene identity with its closest relative, Azonexus caeni. Strain MP^T was enriched in the cathodic chamber of a perchlorate-reducing bioelectrical reactor (BER) and together with an additional strain, CR (99% 16S rRNA gene identity), had 97% 16S rRNA gene identity with Propionivibrio limicola. The use of perchlorate and other electron acceptors distinguished strains MP^T and CR from P. limicola physiologically. Strain LT-1^T had differences in electron donor utilization and optimum growth temperatures from A. caeni. Strains LT-1^T and MP^T are the first DPRB to be described in the Betaproteobacteria outside of the Dechloromonas and Azospira genera. On the basis of phylogenetic and physiological features, strain LT-1^T represents a novel genus in the Rhodocyclaceae; strain MP^T represents a novel species within the genus Propionivibrio. The names Dechlorobacter hydrogenophilus gen. nov., sp. nov and Propionivibrio militaris sp. nov. are proposed.     

Oxidation of arsenite by Thiomonas strains and characterization of Thiomonas arsenivorans sp. nov.

A novel bacterium, strain b6^T (T=type strain), was isolated from a disused mine site by growth using arsenite [As(III)] as energy source in a simple mineral medium. Cells of strain b6^T were rod-shaped, Gram-negative, non-sporulating and motile. Optimum growth occurred at temperatures between 20 and 30 °C, and at pH between 4.0 and 7.5. Strain b6^T grew chemoautotrophically on As(III), sulphur and thiosulphate, and also heterotrophically on yeast extract and a variety of defined organic compounds. Several other Thiomonas strains, including the type species Thiomonas (Tm.) intermedia, were able to oxidize As(III), though only strain b6^T and strain NO115 could grow using As(III) as sole energy source in the absence of any organic compound. The G+C content of the DNA of strain b6^T was 65.1 mol %. Comparative small subunit (SSU) ribosomal RNA (rRNA) analysis indicated that strain b6^T belongs to the genus Thiomonas in the β-subdivision of the Proteobacteria. It was closely related to an unnamed Thiomonas strain (NO115) isolated from a Norwegian mining site, though sequence identities between strain b6^T and characterized Thiomonas species were less than 95%. DNA–DNA hybridization between strain b6^T and the type species of the genus Tm. intermedia showed less than 50% homology. On the basis of phylogenetic and phenotypic characteristics, strain b6^T (DSM 16361^T, LMG 22795^T) is proposed as the type strain of the new species Thiomonas arsenivorans, sp. nov.     

A comparative kinetic analysis of proliferation in vitro of Con-A-treated splenocytes and syngeneic leukaemia cells

Abstract. The growth kinetics of Con-A-treated mouse splenocytes and syngeneic leukaemia cells cultured in vitro were compared with respect to (i) the total cell number, (ii) the rate of [¹⁴C]thymidine incorporation (measured by pulse-labelling the cells at various times of incubation), and (iii) the labelling index of the cell populations. By correlating the thymidine incorporation, labelling index and cell number data, it has been established that, for both types of cells, the rate of [¹⁴C]thymidine incorporation is directly proportional to the number of cells synthesizing DNA. A new approach to cytokinetic analysis has been developed, showing that important information can be obtained by determining the cumulative kinetics of [¹⁴C]thymidine incorporation. The latter has been calculated by integrating the area underneath the time course of the rate of thymidine incorporation, and was directly proportional to the overall growth of both leukaemia cells and Con-A-stimulated splenocytes. Based on this proportionality, an estimate of the average duration of the S phase for both types of cells was calculated, suggesting that normal and neoplastic blasts maintain this parameter at a constant value (7.6 and 5.9 hr, respectively) throughout different stages of growth. The percentage of Con-A-responsive cells within the initial splenocyte population and their overall proliferation in vitro have been determined by a procedure which measures the cumulative kinetics of thymidine incorporation and the kinetics of cell total number in the presence or in the absence of the lectin, as well as in the presence of Con-A plus colcemid. A minor fraction (11%) of the initial splenocytes is recruited into cycle by Con-A, proliferating with similar kinetics to that of leukaemia cells in the same conditions. The great majority of the initial splenocyte population is unaffected by Con-A, decaying exponentially throughout the incubation with the same half-life (28 hr), both in the presence or in the absence of the lectin.     

Synergistic effects of food shortage and an insecticide on a <Emphasis Type="Italic">Daphnia</Emphasis> population: rapid decline of food density at the peak of population density reduces tolerance to the chemical and induces a large population crash

Laboratory populations of cloned Daphnia magna were exposed at different population phases (growing phase, density peak, stable phase) to the insecticide carbaryl at 15 μg 1⁻¹, which was harmful to juveniles but not to adults, and their population dynamics were analyzed. The population declined most at the density peak, when not only juveniles but also many adult individuals died. To analyze the factors affecting population vulnerability to carbaryl, acute toxicity tests were conducted using Daphnia individuals of different body sizes under different food conditions. The test revealed that daphnid sensitivity to carbaryl increased greatly when food density was changed from a high food level to a low level. This food condition, of low availability, might be the condition to which the Daphnia populations were exposed at their density peak. The synergism of the negative impacts of anthropogenic and natural stresses such as insecticides and food shortage may control aquatic populations.     

A model for growth of Artemia franciscana cultures based on food ration-dependent gross growth efficiencies

Laboratory cultures of Artemia franciscana grown under batch regimes at constant temperatures (28 °C) and salinity (35 g l^–1), three initial food concentrations (0.1, 0.4 and 1 M cells ml^–1), various daily food rations (0.1–9M Dunaliella tertiolecta cells Artemia ^–1), and different population densities (1–16 ind ml^–1) were used to develop a model of population growth. Growth rates and gross growth efficiencies (K ₁) were largely independent of population densities and initial food concentrations but determined by age and daily amount of food ingested. While maximum growth rates were found with the highest rations, K _{1 max} peaked at rations of 0.5 million cells d^–1 and decreased at feeding levels above this. A contour plot showing the trend relating K ₁ to Artemia size and ingestion rate in combination and was used to model growth in analogous controlled feeding conditions. Computer simulations using this model paralleled published results of final 15-day average individual sizes of Artemia. Optimal results for near constant food utilization are predicted for high initial population densities (100 Artemia nauplii ml ^–1) and daily culls of enough animals to equilibrate food demand with food availability. This strategy could permit a range of Artemia sizes harvested, maximize final individual sizes and retain high total yields (> 1.2 kg dry wt 1^–1). Effects of different culture strategies are discussed.     

Kinetics of bacteriophage lambda deoxyribonucleic acid infection of Escherichia coli

Barnhart, Benjamin J. (Los Alamos Scientific Laboratory, University of California, Los Alamos, N.M.). Kinetics of bacteriophage lambda deoxyribonucleic acid infection of Escherichia coli. J. Bacteriol. 90:1617-1623. 1965.-The kinetics of Escherichia coli K-12 infection by phage lambda deoxyribonucleic acid (DNA) were determined. An initial lag of 55 to 80 sec was found to be the time required for infecting DNA to become deoxyribonuclease-insensitive at 33 C. When cell-DNA interactions were stopped by washing away unbound DNA, the already bound DNA continued to infect the cell at rates described by linear kinetics with no apparent lag. Whereas the lag period was relatively insensitive to DNA and cell concentrations, both the lag and the subsequent linear portions of the rate curves were temperature-sensitive. Cell and DNA dose-response curves prescribed hyperbolic functions. Similarities between lambda DNA infection of E. coli and bacterial transformation systems are discussed.     

HYBRID BREAKDOWN IN DEVELOPMENTAL TIME IN THE COPEPOD TIGRIOPUS CALIFORNICUS

Laboratory crosses were carried out among three genetically differentiated Los Angeles populations (all located within approximately 15 km) and one San Diego population (approximately 150 km away) of the intertidal copepod Tigriopus californicus. Despite high levels of allozyme differentiation, all crosses produced viable F₁ progeny. Most F₁ progeny had shorter developmental times and reduced variance in developmental times compared to the parental populations. Only one pair of populations failed to produce viable F₂ progeny; when the central Los Angeles population (AB) was crossed to the San Diego (SD) population, most larvae died during the late naupliar stages. Developmental times in the F₂ generation of the other Los Angeles × San Diego crosses were typically 40% longer than developmental times of the parental populations. Among the Los Angeles populations, only one cross (and not its reciprocal) showed a similarly large increase in developmental time. Variance in F₂ developmental times was greater than the parental variance in 5 of 10 crosses. These results are discussed with regard to the evolution of coadapted gene complexes and population differentiation in T. californicus.     

An alphaproteobacterium capable of both aerobic and anaerobic anoxygenic photosynthesis but incapable of photoautotrophy: <Emphasis Type="Italic">Charonomicrobium ambiphototrophicum</Emphasis>, gen. nov., sp. nov.

A facultatively aerobic deep brown coccoid to ovoid bacterium, strain EG17^T, was isolated from a saline effluent stream in the NaCl-dominated brine spring system known as East German Creek in the province of Manitoba, Canada. The strain produced BChl a incorporated into a functional reaction center and two light-harvesting complexes with absorption peaks at 802, 850, and 879 nm. EG17^T is the first reported anoxygenic phototroph capable of photoheterotrophic growth under both oxic and anoxic conditions. It yielded proportionally the greatest aerobic photosynthetic biomass under oligotrophic conditions. The results of 16S rRNA gene sequence comparisons revealed that EG17^T was related most closely to the aerobic anoxygenic phototrophs Roseibacterium elongatum (98.3%) and quite distantly to both Dinoroseobacter shibae (95.2%) and Roseicyclus mahoneyensis (94.7%). The DNA G + C content was 65.6 mol%. On the basis of the unique dual aerobic/anaerobic photosynthetic capability, the distinctive spectrophotometric absorption of the photosynthetic apparatus, diagnostic physiological and biochemical traits, and the moderate phylogenetic separation between EG17^T and its nearest relatives, it is concluded that this microorganism should be classified as a novel genus and species, Charonomicrobium ambiphototrophicum gen. nov., sp. nov., with EG17^T as the type strain.     

SYNCHRONOUS GROWTH IN THE COLONIAL EUDORINA ELEGANS (CHLOROPHYCEAE)1,2

Eudorina elegans Ehrenberg has been synchronized by growing the organisms at 32 C in an enriched medium on a 16:8 LD cycle. Nuclear division occurred during the light period and 2–4 h was required, for the population to complete the sequence of 4 or 5 divisions each cell normally undergoes. Each cell division required 2–3 min with ca. 15 min as the intermitotic time. The sequence was repealed, every 24 h as long as synchrony was maintained.     

PERTURBED CELL PROLIFERATION KINETICS OF THE EMT6/M/AC TUMOUR IN MICE TREATED WITH ANTI-MOUSE LYMPHOCYTE SERUM

The cell proliferation kinetics of the EMT6/M/AC tumour were determined at two volumes, 6-3 mm³ and 180 mm³, in mice treated with anti-mouse lymphocyte serum, AMLS. Comparison of the growth curve with that obtained in non-AMLS treated animals showed a marked increase in the growth rate at all volumes in the treated group. In contrast, the cell cycle time and the intermitotic phase times were not significantly different in the treated and untreated groups at comparable volumes. The increase in the growth rate in AMLS treated mice was obtained in spite of decreases in both the rate constant for cell production and the growth fraction, and was due to a marked decrease in the rate constant for cell loss.     

Cell yield and bioenergetics of Thiomicrospira denitrificans compared with Thiobacillus denitrificans

From cell yields of Thiomicrospira denitrificans grown in the chemostat at different growth rates under anaerobic conditions a value of 1.4mm S₂O _inf3 ^sup= per g dry wt and per h could be calculated for maintenance energy requirements, and of 5.65 g dry wt per mole S₂O _inf3 ^sup= for the true growth yield.Cell yields of Thiomicrospira denitrificans appeared to be almost half of those of Thiobacillus denitrificans. Though in Thiobacillus denitrificans at D=0.03 h^-1 under anaerobic conditions a value was found of 11.60 g dry wt per mole of thiosulphate used for energetic purposes, a value of 5.72 g dry wt per mole of thiosulphate was found under comparable conditions in Thiomicrospira denitrificans. Under aerobic conditions at D=0.03 h^-1 values of 18.54 g dry wt per mole of thiosulphate were found in Thiobacillus denitrificans whereas Thiomicrospira denitrificans yielded only 9.38 g dry wt per mole of thiosulphate.As in Thiobacillus denitrificans anaerobic cell yields on sulphide were comparable to those on thiosulphate.Calculations have been made which indicate that the biosynthetic efficiency of Thiomicrospira denitrificans is lower than that of Thiobacillus denitrificans. This can only partly be explained by the absence of adenosine-phosphosulphate (APS) reductase.     

New insights into the energy metabolism and taxonomy of Deferribacteres revealed by the characterization of a new isolate from a hypersaline microbial mat

Strain L21-Ace-BES^T, isolated from a lithifying cyanobacterial mat, could be assigned to a novel species and genus within the class Deferribacteres. It is an important model organism for the study of anaerobic acetate degradation under hypersaline conditions. The metabolism of strain L21-Ace-BES^T was characterized by biochemical studies, comparative genome analyses, and the evaluation of gene expression patterns. The central metabolic pathway is the citric acid cycle, which is mainly controlled by the enzyme succinyl-CoA:acetate-CoA transferase. The potential use of a reversed oxidative citric acid cycle to fix CO₂ has been revealed through genome analysis. However, no autotrophic growth was detected in this strain, whereas sulfide and H₂ can be used mixotrophically. Preferred electron acceptors for the anaerobic oxidation of acetate are nitrate, fumarate and dimethyl sulfoxide, while oxygen can be utilized only under microoxic conditions. Aerotolerant growth by fermentation was observed at higher oxygen concentrations. The redox cycling of sulfur/sulfide enables the generation of reducing power for the assimilation of acetate during growth and could prevent the over-reduction of cells in stationary phase. Extracellular electron transfer appears to be an essential component of the respiratory metabolism in this clade of Deferribacteres and may be involved in the reduction of nitrite to ammonium.     

Vibrio nitrifigilis sp. nov., a marine nitrogen-fixing bacterium isolated from the lagoon sediment of an islet inside an atoll

A nitrogen-fixing isolate of facultatively anaerobic, marine bacterium, designated strain NFV-1^T, was recovered from the lagoon sediment of Dongsha Island, Taiwan. It was a Gram-negative rod which exhibited motility with monotrichous flagellation in broth cultures. The strain required NaCl for growth and grew optimally at about 25–35 °C, 3% NaCl and pH 7–8. It grew aerobically and could achieve anaerobic growth by fermenting d-glucose or other carbohydrates as substrates. NH₄Cl could serve as a sole nitrogen source for growth aerobically and anaerobically, whereas growth with N₂ as the sole nitrogen source was observed only under anaerobic conditions. Cellular fatty acids were predominated by C_16:1 ω7c, C_16:0, and C_18:1 ω7c. The major polar lipids consisted of phosphatidylethanolamine and phosphatidylserine. Strain NFV-1^T had a DNA G?+?C content of 42.5 mol%, as evaluated according to the chromosomal DNA sequencing data. Analyses of sequence similarities and phylogeny based on the 16S rRNA genes, together with the housekeeping genes, gyrB, ftsZ, mreB, topA and gapA, indicated that the strain formed a distinct species-level lineage in the genus Vibrio of the family Vibrionaceae. These phylogenetic data and those from genomic and phenotypic characterisations support the establishment of a novel Vibrio species, for which the name Vibrio nitrifigilis sp. nov. (type strain NFV-1^T?=?BCRC 81211^T?=?JCM 33628^T) is proposed.