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Dive into the research topics where Roger A. Chastain is active.

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Featured researches published by Roger A. Chastain.


Applied and Environmental Microbiology | 2007

The Unique 16S rRNA Genes of Piezophiles Reflect both Phylogeny and Adaptation

Federico M. Lauro; Roger A. Chastain; Lesley E. Blankenship; A. Aristides Yayanos; Douglas H. Bartlett

ABSTRACT In the oceans most extreme depths, pressures of 70 to 110 megapascals prevent the growth of all but the most hyperpiezophilic (pressure-loving) organisms. The physiological adaptations required for growth under these conditions are considered to be substantial. Efforts to determine specific adaptations permitting growth at extreme pressures have thus far focused on relatively few γ-proteobacteria, in part due to the technical difficulties of obtaining piezophilic bacteria in pure culture. Here, we present the molecular phylogenies of several new piezophiles of widely differing geographic origins. Included are results from an analysis of the first deep-trench bacterial isolates recovered from the southern hemisphere (9.9-km depth) and of the first gram-positive piezophilic strains. These new data allowed both phylogenetic and structural 16S rRNA comparisons among deep-ocean trench piezophiles and closely related strains not adapted to high pressure. Our results suggest that (i) the Circumpolar Deep Water acts as repository for hyperpiezophiles and drives their dissemination to deep trenches in the Pacific Ocean and (ii) the occurrence of elongated helices in the 16S rRNA genes increases with the extent of adaptation to growth at elevated pressure. These helix changes are believed to improve ribosome function under deep-sea conditions.


Developmental Dynamics | 2005

Nuclear β-catenin promotes non-neural ectoderm and posterior cell fates in amphioxus embryos

Linda Z. Holland; Kristen A. Panfilio; Roger A. Chastain; Michael Schubert; Nicholas D. Holland

In vertebrate development, Wnt/β‐catenin signaling has an early role in specification of dorsal/anterior identity and a late one in posterior specification. To understand the evolution of these roles, we cloned β‐catenin from the invertebrate chordate amphioxus. The exon/intron organization of β‐catenin is highly conserved between amphioxus and other animals including a cnidarian, but not Drosophila. In development, amphioxus β‐catenin is concentrated in all nuclei from the 16‐cell stage until the onset of gastrulation when it becomes undetectable in presumptive mesendoderm. Li+, which up‐regulates Wnt/β‐catenin signaling, had no detectable effect on axial patterning when applied before the late blastula stage, suggesting that a role for β‐catenin in specification of dorsal/anterior identity may be a vertebrate innovation. From the mid‐gastrula through the neurula stage, the highest levels of nuclear β‐catenin are around the blastopore. In the early neurula, β‐catenin is down‐regulated in the neural plate, but remains high in adjacent non‐neural ectoderm. Embryos treated with Li+ at the late blastula stage are markedly posteriorized and lack a neural plate. These results suggest that in amphioxus, as in vertebrates, down‐regulation of Wnt/β‐catenin signaling in the neural plate is necessary for maintenance of the neuroectoderm and that a major evolutionarily conserved role of Wnt/β‐catenin signaling is to specify posterior identity and pattern the anterior/posterior axis. Developmental Dynamics 233:1430–1443, 2005.


Development Genes and Evolution | 2008

Expression of somite segmentation genes in amphioxus: a clock without a wavefront?

Laura Beaster-Jones; Stacy L. Kaltenbach; Demian Koop; Shaochun Yuan; Roger A. Chastain; Linda Z. Holland

In the basal chordate amphioxus (Branchiostoma), somites extend the full length of the body. The anteriormost somites segment during the gastrula and neurula stages from dorsolateral grooves of the archenteron. The remaining ones pinch off, one at a time, from the tail bud. These posterior somites appear to be homologous to those of vertebrates, even though the latter pinch off from the anterior end of bands of presomitic mesoderm rather than directly from the tail bud. To gain insights into the evolution of mesodermal segmentation in chordates, we determined the expression of ten genes in nascent amphioxus somites. Five (Uncx4.1, NeuroD/atonal-related, IrxA, Pcdhδ2-17/18, and Hey1) are expressed in stripes in the dorsolateral mesoderm at the gastrula stage and in the tail bud while three (Paraxis, Lcx, and Axin) are expressed in the posterior mesendoderm at the gastrula and neurula stages and in the tail bud at later stages. Expression of two genes (Pbx and OligA) suggests roles in the anterior somites that may be unrelated to initial segmentation. Together with previous data, our results indicate that, with the exception that Engrailed is only segmentally expressed in the anterior somites, the genetic mechanisms controlling formation of both the anterior and posterior somites are probably largely identical. Thus, the fundamental pathways for mesodermal segmentation involving Notch–Delta, Wnt/β-catenin, and Fgf signaling were already in place in the common ancestor of amphioxus and vertebrates although budding of somites from bands of presomitic mesoderm exhibiting waves of expression of Notch, Wnt, and Fgf target genes was likely a vertebrate novelty. Given the conservation of segmentation gene expression between amphioxus and vertebrate somites, we propose that the clock mechanism may have been established in the basal chordate, while the wavefront evolved later in the vertebrate lineage.


Applied and Environmental Microbiology | 2014

Novel psychropiezophilic Oceanospirillales species Profundimonas piezophila gen. nov., sp. nov., isolated from the deep-sea environment of the Puerto Rico trench.

Yi Cao; Roger A. Chastain; Emiley A. Eloe; Yuichi Nogi; Chiaki Kato; Douglas H. Bartlett

ABSTRACT The diversity of deep-sea high-pressure-adapted (piezophilic) microbes in isolated monoculture remains low. In this study, a novel obligately psychropiezophilic bacterium was isolated from seawater collected from the Puerto Rico Trench at a depth of ∼6,000 m. This isolate, designated YC-1, grew best in a nutrient-rich marine medium, with an optimal growth hydrostatic pressure of 50 MPa (range, 20 to 70 MPa) at 8°C. Under these conditions, the maximum growth rate was extremely slow, 0.017 h−1, and the maximum yield was 3.51 × 107 cells ml−1. Cell size and shape changed with pressure, shifting from 4.0 to 5.0 μm in length and 0.5 to 0.8 μm in width at 60 MPa to 0.8- to 1.0-μm diameter coccoid cells under 20 MPa, the minimal pressure required for growth. YC-1 is a Gram-negative, facultatively anaerobic heterotroph. Its predominant cellular fatty acids are the monounsaturated fatty acids (MUFAs) C16:1 and C18:1. Unlike many other psychropiezophiles, YC-1 does not synthesize any polyunsaturated fatty acids (PUFAs). Phylogenetic analysis placed YC-1 within the family of Oceanospirillaceae, closely related to the uncultured symbiont of the deep-sea whale bone-eating worms of the genus Osedax. In common with some other members of the Oceanospirillales, including those enriched during the Deepwater Horizon oil spill, YC-1 is capable of hydrocarbon utilization. On the basis of its characteristics, YC-1 appears to represent both a new genus and a new species, which we name Profundimonas piezophila gen. nov., sp. nov.


International Journal of Systematic and Evolutionary Microbiology | 2017

Colwellia marinimaniae sp. nov., a hyperpiezophilic species isolated from an amphipod within the Challenger Deep, Mariana Trench

Masataka Kusube; Than S. Kyaw; Kumiko Tanikawa; Roger A. Chastain; Kevin Hardy; James Cameron; Douglas H. Bartlett

An obligately piezophilic strain was isolated from an amphipod crustacean obtained in the Challenger Deep region of the Mariana Trench during the DEEPSEA CHALLENGE expedition. The strain, MTCD1T, grew at extremely high hydrostatic pressures, with a growth range of 80-140 MPa (optimum, 120 MPa) at 6 °C. Phylogenetic analyses based on the 16S rRNA gene sequence indicate that it is closely affiliated with the genus Colwellia. Comparative 16S rRNA gene sequence analyses revealed 95.7, 95.5 and 95.2 % similarity to Colwellia maris ABE-1T, Colwellia piezophila Y233GT and Colwellia psychrerythraea ATCC 27364T, respectively. The major cellular fatty acids were C16 : 1, C16 : 0 and C22 : 6 (docosahexaenoic acid), and the sole isoprenoid quinone produced was ubiqinone-8. DNA G+C content was 48.6 mol%. The strain was positive for oxidase and catalase activities. Based on the results from this study, strain MTCD1T is a novel Gram-negative species of the genus Colwellia, and the name Colwellia marinimaniae sp. nov. (type strain MTCD1T=ATCC TSD-5T=JCM 30270T) is proposed. It is the most piezophilic organism yet described.


Genome Announcements | 2013

Draft Genome Sequence of the Deep-Sea Bacterium Shewanella benthica Strain KT99

Federico M. Lauro; Roger A. Chastain; Steven Ferriera; Justin Johnson; A. A. Yayanos; Douglas H. Bartlett

ABSTRACT We report the draft genome sequence of the obligately piezophilic Shewanella benthica strain KT99 isolated from the abyssal South Pacific Ocean. Strain KT99 is the first piezophilic isolate from the Tonga-Kermadec trench, and its genome provides many clues on high-pressure adaptation and the evolution of deep-sea piezophilic bacteria.


Genome Announcements | 2013

Complete Genome Sequence of the Deep-Sea Bacterium Psychromonas Strain CNPT3

Federico M. Lauro; T. K. Stratton; Roger A. Chastain; Steven Ferriera; Justin Johnson; S. M. D. Goldberg; A. A. Yayanos; Douglas H. Bartlett

ABSTRACT Members of the genus Psychromonas are commonly found in polar and deep-sea environments. Here we present the genome of Psychromonas strain CNPT3. Historically, it was the first bacterium shown to piezoregulate the composition of its membrane lipids and to have a higher growth rate at 57 megapascals (MPa) than at 0.1 MPa.


Frontiers in Microbiology | 2018

The Effect of Hydrostatic Pressure on Enrichments of Hydrocarbon Degrading Microbes From the Gulf of Mexico Following the Deepwater Horizon Oil Spill

Angeliki Marietou; Roger A. Chastain; Felix Beulig; Alberto Scoma; Terry C. Hazen; Douglas H. Bartlett

The Deepwater Horizon oil spill was one of the largest and deepest oil spills recorded. The wellhead was located at approximately 1500 m below the sea where low temperature and high pressure are key environmental characteristics. Using cells collected 4 months following the Deepwater Horizon oil spill at the Gulf of Mexico, we set up Macondo crude oil enrichments at wellhead temperature and different pressures to determine the effect of increasing depth/pressure to the in situ microbial community and their ability to degrade oil. We observed oil degradation under all pressure conditions tested [0.1, 15, and 30 megapascals (MPa)], although oil degradation profiles, cell numbers, and hydrocarbon degradation gene abundances indicated greatest activity at atmospheric pressure. Under all incubations the growth of psychrophilic bacteria was promoted. Bacteria closely related to Oleispira antarctica RB-8 dominated the communities at all pressures. At 30 MPa we observed a shift toward Photobacterium, a genus that includes piezophiles. Alphaproteobacterial members of the Sulfitobacter, previously associated with oil-degradation, were also highly abundant at 0.1 MPa. Our results suggest that pressure acts synergistically with low temperature to slow microbial growth and thus oil degradation in deep-sea environments.


Frontiers in Microbiology | 2018

Corrigendum: The effect of hydrostatic pressure on enrichments of hydrocarbon degrading microbes from the Gulf of Mexico following the deepwater Horizon Oil Spill [Front. Microbiol., 9, (2018) (808)] doi: 10.3389/fmicb.2018.00808

Angeliki Marietou; Roger A. Chastain; Felix Beulig; Alberto Scoma; Terry C. Hazen; Douglas H. Bartlett

[This corrects the article DOI: 10.3389/fmicb.2018.00808.].


Nature | 1984

Possible artefactual basis for apparent bacterial growth at 250 degrees C.

Jonathan D. Trent; Roger A. Chastain; A. Aristides Yayanos

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A. Aristides Yayanos

Scripps Institution of Oceanography

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Federico M. Lauro

Nanyang Technological University

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A. A. Yayanos

University of California

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Justin Johnson

J. Craig Venter Institute

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Steven Ferriera

J. Craig Venter Institute

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