Complete Genome Sequence of Flavisolibacter Tropicus LCS9 , A
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Kaistella Soli Sp. Nov., Isolated from Oil-Contaminated Soil
A001 Kaistella soli sp. nov., Isolated from Oil-contaminated Soil Dhiraj Kumar Chaudhary1, Ram Hari Dahal2, Dong-Uk Kim3, and Yongseok Hong1* 1Department of Environmental Engineering, Korea University Sejong Campus, 2Department of Microbiology, School of Medicine, Kyungpook National University, 3Department of Biological Science, College of Science and Engineering, Sangji University A light yellow-colored, rod-shaped bacterial strain DKR-2T was isolated from oil-contaminated experimental soil. The strain was Gram-stain-negative, catalase and oxidase positive, and grew at temperature 10–35°C, at pH 6.0– 9.0, and at 0–1.5% (w/v) NaCl concentration. The phylogenetic analysis and 16S rRNA gene sequence analysis suggested that the strain DKR-2T was affiliated to the genus Kaistella, with the closest species being Kaistella haifensis H38T (97.6% sequence similarity). The chemotaxonomic profiles revealed the presence of phosphatidylethanolamine as the principal polar lipids;iso-C15:0, antiso-C15:0, and summed feature 9 (iso-C17:1 9c and/or C16:0 10-methyl) as the main fatty acids; and menaquinone-6 as a major menaquinone. The DNA G + C content was 39.5%. In addition, the average nucleotide identity (ANIu) and in silico DNA–DNA hybridization (dDDH) relatedness values between strain DKR-2T and phylogenically closest members were below the threshold values for species delineation. The polyphasic taxonomic features illustrated in this study clearly implied that strain DKR-2T represents a novel species in the genus Kaistella, for which the name Kaistella soli sp. nov. is proposed with the type strain DKR-2T (= KACC 22070T = NBRC 114725T). [This study was supported by Creative Challenge Research Foundation Support Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF- 2020R1I1A1A01071920).] A002 Chitinibacter bivalviorum sp. -
Complete Genome Sequence of Flavisolibacter Ginsenosidimutans T Gsoil 636 , a Ginsenoside-Converting Bacterium, Isolated from Soil Used for Cultivating Ginseng
Korean Journal of Microbiology (2019) Vol. 55, No. 4, pp. 459-461 pISSN 0440-2413 DOI https://doi.org/10.7845/kjm.2019.9131 eISSN 2383-9902 Copyright ⓒ 2019, The Microbiological Society of Korea Complete genome sequence of Flavisolibacter ginsenosidimutans T Gsoil 636 , a ginsenoside-converting bacterium, isolated from soil used for cultivating ginseng 1 2 2 1 1,3 Dong-Ho Keum , Byoung Hee Lee , Ki-Eun Lee , Soon Youl Lee , and Wan-Taek Im * 1 Department of Biotechnology, Hankyong National University, Gyeonggi-do 17579, Republic of Korea 2 Microorganism Resources Division, National Institute of Biological Resources, Incheon 22689, Republic of Korea 3 AceEMzyme Co., Ltd., Academic Industry Cooperation, Gyeonggi-do 17579, Republic of Korea 인삼 재배 토양에서 분리한 진세노사이드 전환능력이 있는 T Flavisolibacter ginsenosidimutans Gsoil 636 의 유전체 서열 분석 금동호1 ・ 이병희2 ・ 이기은2 ・ 이순열1 ・ 임완택1,3* 1 2 3 국립한경대학교 농업생명과학대학 생명공학과, 국림생물자원관 미생물자원과, (주)에이스엠자임 (Received October 30, 2019; Revised December 9, 2019; Accepted December 9, 2019) T A yellow-colored, circular, convex, rod-shaped baterial strain Im, 2007). Strain Gsoil 636 is Gram-negative-bacterium, rod- T designated Flavisolibacter ginsenosidimutans Gsoil 636 was shaped, non-motile, non-spore-forming, yellow-pigmented and isolated from soil of a ginseng cultivation field in Pocheon T is allocated to the family Chitinophagaceae. Within the genus Province, South Korea. Gsoil 636 showed the ability to con- Flavisolibacter, the genomic DNA G + C content range is from vert Rb1 (one of the dominant active components of ginseng) to 42.7 to 46.4 mol%. Based on recent studies, this genus consists F2, and its whole genome was sequenced. -
Metagenomic Insights Into the Uncultured Diversity and Physiology of Microbes in Four Hypersaline Soda Lake Brines
Lawrence Berkeley National Laboratory Recent Work Title Metagenomic Insights into the Uncultured Diversity and Physiology of Microbes in Four Hypersaline Soda Lake Brines. Permalink https://escholarship.org/uc/item/9xc5s0v5 Journal Frontiers in microbiology, 7(FEB) ISSN 1664-302X Authors Vavourakis, Charlotte D Ghai, Rohit Rodriguez-Valera, Francisco et al. Publication Date 2016 DOI 10.3389/fmicb.2016.00211 Peer reviewed eScholarship.org Powered by the California Digital Library University of California ORIGINAL RESEARCH published: 25 February 2016 doi: 10.3389/fmicb.2016.00211 Metagenomic Insights into the Uncultured Diversity and Physiology of Microbes in Four Hypersaline Soda Lake Brines Charlotte D. Vavourakis 1, Rohit Ghai 2, 3, Francisco Rodriguez-Valera 2, Dimitry Y. Sorokin 4, 5, Susannah G. Tringe 6, Philip Hugenholtz 7 and Gerard Muyzer 1* 1 Microbial Systems Ecology, Department of Aquatic Microbiology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, Netherlands, 2 Evolutionary Genomics Group, Departamento de Producción Vegetal y Microbiología, Universidad Miguel Hernández, San Juan de Alicante, Spain, 3 Department of Aquatic Microbial Ecology, Biology Centre of the Czech Academy of Sciences, Institute of Hydrobiology, Ceskéˇ Budejovice,ˇ Czech Republic, 4 Research Centre of Biotechnology, Winogradsky Institute of Microbiology, Russian Academy of Sciences, Moscow, Russia, 5 Department of Biotechnology, Delft University of Technology, Delft, Netherlands, 6 The Department of Energy Joint Genome Institute, Walnut Creek, CA, USA, 7 Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences and Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia Soda lakes are salt lakes with a naturally alkaline pH due to evaporative concentration Edited by: of sodium carbonates in the absence of major divalent cations. -
Functional Structure of the Bromeliad Tank Microbiome Is Strongly Shaped by Local Geochemical Conditions
Environmental Microbiology (2017) 19(8), 3132–3151 doi:10.1111/1462-2920.13788 Functional structure of the bromeliad tank microbiome is strongly shaped by local geochemical conditions Stilianos Louca,1,2* Saulo M. S. Jacques,3,4 denitrification steps, ammonification, sulfate respira- Aliny P. F. Pires,3 Juliana S. Leal,3,5 tion, methanogenesis, reductive acetogenesis and 6 1,2,7 Angelica L. Gonzalez, Michael Doebeli and anoxygenic phototrophy. Overall, CO2 reducers domi- Vinicius F. Farjalla3 nated in abundance over sulfate reducers, and 1Biodiversity Research Centre, University of British anoxygenic phototrophs largely outnumbered oxy- Columbia, Vancouver, BC, Canada. genic photoautotrophs. Functional community 2Department of Zoology, University of British Columbia, structure correlated strongly with environmental vari- Vancouver, BC, Canada. ables, between and within a single bromeliad species. 3Department of Ecology, Biology Institute, Universidade Methanogens and reductive acetogens correlated Federal do Rio de Janeiro, Rio de Janeiro, Brazil. with detrital volume and canopy coverage, and exhib- 4Programa de Pos-Graduac ¸ao~ em Ecologia e ited higher relative abundances in N. cruenta.A Evoluc¸ao,~ Universidade Estadual do Rio de Janeiro, Rio comparison of bromeliads to freshwater lake sedi- de Janeiro, Brazil. ments and soil from around the world, revealed stark differences in terms of taxonomic as well as func- 5Programa de Pos-Graduac ¸ao~ em Ecologia, tional microbial community structure. Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. 6Biology Department & Center for Computational & Introduction Integrative Biology, Rutgers University, Camden, NJ, USA. Bromeliads (fam. Bromeliaceae) are plants found through- 7Department of Mathematics, University of British out the neotropics, with many species having rosette-like Columbia, Vancouver, BC, Canada. -
2018 Issn: 2456-8643
International Journal of Agriculture, Environment and Bioresearch Vol. 3, No. 05; 2018 ISSN: 2456-8643 METAGENOMIC ANALYSIS OF BACTERIAL COMMUNITIES IN THE RHIZOSPHERE OF STIPA CAPILLATA AND CENTAUREA DIFFUSA Oleg Zhurlov and Nataliya Nemtseva Institute For Cellular And Intracellular Symbiosis, Ural Branch Russian Academy Of Sciences, Pio-nerskaya St.11, 46000, Orenburg, Russia. ABSTRACT The effectiveness of bioremediation of unproductive agricultural lands and marginal lands, not only on the zonal climatic conditions and physico-chemical parameters of soil, but also on the used plants and rhizosphere microorganisms. The use of xerophytic perennial grasses, adapted to the regional climatic conditions and physico-chemical parameters of soils, will improve the efficiency of bioremediation of unproductive agricultural lands and marginal lands. The article presents the results of a comparative analysis of the prokaryotic communities of the rhizosphere of the two representatives of the xerophytes herbs - Stipa capillata and Centaurea diffusa. We have shown that the dominant position in the prokaryotic communities of the rhizosphere of Stipa capillata and Centaurea diffusa is the phyla Proteobacteria, Actinobacteria, Firmicutes, Bacteroidetes, Verrucomicrobia, Planctomycetes and Chloroflexi. The microorganisms with cellulolytic activity and the destructors of aromatic compounds included in the composition of prokaryotic communities in the rhizosphere of Stipa capillata and Centaurea diffusa. Keywords: Stipa capillata, Centaurea diffusa, 16s rRNA gene, bioremediation 1. INTRODUCTION Soil is not only the main means of agricultural production, but also an important component of terrestrial biocenoses, a regulator of the composition of the atmosphere, hydrosphere and a reliable barrier to the migration of pollutants. However, this irreplaceable component of the biosphere undergoes significant degradation as a result of anthropogenic impact. -
Taxonomy JN869023
Species that differentiate periods of high vs. low species richness in unattached communities Species Taxonomy JN869023 Bacteria; Actinobacteria; Actinobacteria; Actinomycetales; ACK-M1 JN674641 Bacteria; Bacteroidetes; [Saprospirae]; [Saprospirales]; Chitinophagaceae; Sediminibacterium JN869030 Bacteria; Actinobacteria; Actinobacteria; Actinomycetales; ACK-M1 U51104 Bacteria; Proteobacteria; Betaproteobacteria; Burkholderiales; Comamonadaceae; Limnohabitans JN868812 Bacteria; Proteobacteria; Betaproteobacteria; Burkholderiales; Comamonadaceae JN391888 Bacteria; Planctomycetes; Planctomycetia; Planctomycetales; Planctomycetaceae; Planctomyces HM856408 Bacteria; Planctomycetes; Phycisphaerae; Phycisphaerales GQ347385 Bacteria; Verrucomicrobia; [Methylacidiphilae]; Methylacidiphilales; LD19 GU305856 Bacteria; Proteobacteria; Alphaproteobacteria; Rickettsiales; Pelagibacteraceae GQ340302 Bacteria; Actinobacteria; Actinobacteria; Actinomycetales JN869125 Bacteria; Proteobacteria; Betaproteobacteria; Burkholderiales; Comamonadaceae New.ReferenceOTU470 Bacteria; Cyanobacteria; ML635J-21 JN679119 Bacteria; Proteobacteria; Betaproteobacteria; Burkholderiales; Comamonadaceae HM141858 Bacteria; Acidobacteria; Holophagae; Holophagales; Holophagaceae; Geothrix FQ659340 Bacteria; Verrucomicrobia; [Pedosphaerae]; [Pedosphaerales]; auto67_4W AY133074 Bacteria; Elusimicrobia; Elusimicrobia; Elusimicrobiales FJ800541 Bacteria; Verrucomicrobia; [Pedosphaerae]; [Pedosphaerales]; R4-41B JQ346769 Bacteria; Acidobacteria; [Chloracidobacteria]; RB41; Ellin6075 -
Characterization of the Dominant Bacterial Communities Associated with Terrestrial Isopod Species Based on 16S Rdna Analysis by PCR-DGGE
Open Journal of Ecology, 2018, 8, 495-509 http://www.scirp.org/journal/oje ISSN Online: 2162-1993 ISSN Print: 2162-1985 Characterization of the Dominant Bacterial Communities Associated with Terrestrial Isopod Species Based on 16S rDNA Analysis by PCR-DGGE Delhoumi Majed, Zaabar Wahiba, Bouslama Mohamed Fadhel, Achouri Mohamed Sghaier* Laboratory of Bio-Ecology and Evolutionary Systematics, Department of Biology, Faculty of Sciences of Tunis, University of Tunis El Manar, Tunis, Tunisia How to cite this paper: Majed, D., Wahi- Abstract ba, Z., Fadhel, B.M. and Sghaier, A.M. (2018) Characterization of the Dominant Bacterial From the marine environment, woodlice gradually colonized terrestrial areas Communities Associated with Terrestrial benefiting from the symbiotic relationship with the bacterial community that Isopod Species Based on 16S rDNA Analy- they host. Indeed, they constitute the only group of Oniscidea suborder that sis by PCR-DGGE. Open Journal of Ecolo- gy, 8, 495-509. has succeed to accomplish their lives in terrestrial even desert surfaces. Here- https://doi.org/10.4236/oje.2018.89030 in they play an important role in the dynamic of ecosystems and the decom- position of litter. So to enhance our understanding of the sea-land transition Received: January 30, 2018 and other process like decomposition and digestion of detritus, we studied Accepted: September 15, 2018 Published: September 18, 2018 the bacterial community associated with 11 specimens of terrestrial isopods belonging to six species using a Culture independent approach (DGGE). Copyright © 2018 by authors and Bands sequencing showed that the cosmopolitan species Porcellionides prui- Scientific Research Publishing Inc. nosus has the most microbial diversity. -
Ice-Nucleating Particles Impact the Severity of Precipitations in West Texas
Ice-nucleating particles impact the severity of precipitations in West Texas Hemanth S. K. Vepuri1,*, Cheyanne A. Rodriguez1, Dimitri G. Georgakopoulos4, Dustin Hume2, James Webb2, Greg D. Mayer3, and Naruki Hiranuma1,* 5 1Department of Life, Earth and Environmental Sciences, West Texas A&M University, Canyon, TX, USA 2Office of Information Technology, West Texas A&M University, Canyon, TX, USA 3Department of Environmental Toxicology, Texas Tech University, Lubbock, TX, USA 4Department of Crop Science, Agricultural University of Athens, Athens, Greece 10 *Corresponding authors: [email protected] and [email protected] Supplemental Information 15 S1. Precipitation and Particulate Matter Properties S1.1 Precipitation Categorization In this study, we have segregated our precipitation samples into four different categories, such as (1) snows, (2) hails/thunderstorms, (3) long-lasted rains, and (4) weak rains. For this categorization, we have considered both our observation-based as well as the disdrometer-assigned National Weather Service (NWS) 20 code. Initially, the precipitation samples had been assigned one of the four categories based on our manual observation. In the next step, we have used each NWS code and its occurrence in each precipitation sample to finalize the precipitation category. During this step, a precipitation sample was categorized into snow, only when we identified a snow type NWS code (Snow: S-, S, S+ and/or Snow Grains: SG). Likewise, a precipitation sample was categorized into hail/thunderstorm, only when the cumulative sum of NWS codes for hail was 25 counted more than five times (i.e., A + SP ≥ 5; where A and SP are the codes for soft hail and hail, respectively). -
The Antarctic Mite, Alaskozetes Antarcticus, Shares Bacterial Microbiome Community Membership but Not Abundance Between Adults and Tritonymphs
Polar Biology (2019) 42:2075–2085 https://doi.org/10.1007/s00300-019-02582-5 ORIGINAL PAPER The Antarctic mite, Alaskozetes antarcticus, shares bacterial microbiome community membership but not abundance between adults and tritonymphs Christopher J. Holmes1 · Emily C. Jennings1 · J. D. Gantz2,3 · Drew Spacht4 · Austin A. Spangler1 · David L. Denlinger4 · Richard E. Lee Jr.3 · Trinity L. Hamilton5 · Joshua B. Benoit1 Received: 14 January 2019 / Revised: 3 September 2019 / Accepted: 4 September 2019 / Published online: 16 September 2019 © Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract The Antarctic mite (Alaskozetes antarcticus) is widely distributed on sub-Antarctic islands and throughout the Antarctic Peninsula, making it one of the most abundant terrestrial arthropods in the region. Despite the impressive ability of A. ant- arcticus to thrive in harsh Antarctic conditions, little is known about the biology of this species. In this study, we performed 16S rRNA gene sequencing to examine the microbiome of the fnal immature instar (tritonymph) and both male and female adults. The microbiome included a limited number of microbial classes and genera, with few diferences in community membership noted among the diferent stages. However, the abundances of taxa that composed the microbial community difered between adults and tritonymphs. Five classes—Actinobacteria, Flavobacteriia, Sphingobacteriia, Gammaproteobac- teria, and Betaproteobacteria—comprised ~ 82.0% of the microbial composition, and fve (identifed) genera—Dermacoccus, Pedobacter, Chryseobacterium, Pseudomonas, and Flavobacterium—accounted for ~ 68.0% of the total composition. The core microbiome present in all surveyed A. antarcticus was dominated by the families Flavobacteriaceae, Comamonadaceae, Sphingobacteriaceae, Chitinophagaceae and Cytophagaceae, but the majority of the core consisted of operational taxonomic units of low abundance. -
The Nasal Microbiome Mirrors and Potentially Shapes Olfactory Function Received: 10 August 2017 Kaisa Koskinen 1,2, Johanna L
www.nature.com/scientificreports OPEN The nasal microbiome mirrors and potentially shapes olfactory function Received: 10 August 2017 Kaisa Koskinen 1,2, Johanna L. Reichert2,3, Stefan Hoier4, Jochen Schachenreiter5, Accepted: 29 December 2017 Stefanie Duller1, Christine Moissl-Eichinger1,2 & Veronika Schöpf 2,3 Published: xx xx xxxx Olfactory function is a key sense for human well-being and health, with olfactory dysfunction having been linked to serious diseases. As the microbiome is involved in normal olfactory epithelium development, we explored the relationship between olfactory function (odor threshold, discrimination, identifcation) and nasal microbiome in 67 healthy volunteers. Twenty-eight subjects were found to have normal olfactory function, 29 had a particularly good sense of smell (“good normosmics”) and 10 were hyposmic. Microbial community composition difered signifcantly between the three olfactory groups. In particular, butyric acid-producing microorganisms were found to be associated with impaired olfactory function. We describe the frst insights of the potential interplay between the olfactory epithelium microbial community and olfactory function, and suggest that the microbiome composition is able to mirror and potentially shape olfactory function by producing strong odor compounds. Te human olfactory system is able to discriminate a vast number of odors1. Tis function is mediated by olfac- tory receptors situated within the olfactory epithelium. Te sense of smell shapes our perception of our external environment and is essential in decision-making and in guiding behavior, including eating behavior, and detec- tion of danger, as well as contributing signifcantly to the hedonic component of everyday life (e.g. favor and fragrance perception2,3). Anosmia (complete loss of olfactory function) and hyposmia (decreased olfactory function) together afect approximately 20% of the population3. -
Culture Independent Analysis of Microbiota in the Gut of Pine Weevils
Culture independent analysis of microbiota in the gut of pine weevils KTH Biotechnology 2013-January-13 Diploma work by: Tobias B. Ölander Environmental Microbiology, KTH Supervisor: Associate prof. Gunaratna K. Rajarao Examinator: Prof. Stefan Ståhl 1 Abstract In Sweden, the pine weevil causes damages for several hundreds of millions kronor annually. The discouraged use of insecticides has resulted in that other methods to prevent pine weevil feeding needs to be found. Antifeedants found in the pine weevil own feces is one such alternative. The source of the most active antifeedants in the feces is probably from bacterial or fungal lignin degrading symbionts in the pine weevil gut. The aim of the project was to analyze the pine weevil gut microbiota with the help of culture independent methods. DNA (including bacterial DNA) was extracted from both midgut and egg cells. The extracted DNA was amplified with PCR. A clone library was created by cloning the amplified DNA into plasmid vectors and transforming the vector constructs with chemically competent cells. The clones were amplified again with either colony PCR or plasmid extraction followed by PCR, and used for RFLP (Restriction Fragment Length Polymorphism) and sequencing. Species found in the midgut sample included Acinetobacter sp., Ramlibacter sp., Chryseobacterium sp., Flavisolibacter sp. and Wolbachia sp. Species found in the egg sample included Wolbachia sp. and Halomonas sp. Wolbachia sp. and Halomonas sp. were found to be the dominant members of the midgut and egg cells respectively. -
Proposal of Vibrionimonas Magnilacihabitans Gen. Nov., Sp
Marquette University e-Publications@Marquette Civil and Environmental Engineering Faculty Civil and Environmental Engineering, Department Research and Publications of 2-1-2014 Proposal of Vibrionimonas magnilacihabitans gen. nov., sp. nov., a Curved Gram Negative Bacterium Isolated From Lake Michigan Water Richard A. Albert Marquette University, [email protected] Daniel Zitomer Marquette University, [email protected] Michael Dollhopf Marquette University, [email protected] Anne Schauer-Gimenez Marquette University Craig Struble Marquette University, [email protected] See next page for additional authors Accepted version. International Journal of Systematic and Evolutionary Microbiology, Vol. 64, No. 2 (February 2014): 613-620. DOI. © 2014 Society for General Microbiology. Used with permission. Authors Richard A. Albert, Daniel Zitomer, Michael Dollhopf, Anne Schauer-Gimenez, Craig Struble, Michael King, Sona Son, Stefan Langer, and Hans-Jürgen Busse This article is available at e-Publications@Marquette: https://epublications.marquette.edu/civengin_fac/8 NOT THE PUBLISHED VERSION; this is the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation at the bottom of the page. Proposal of Vibrionimonas magnilacihabitans gen. nov., sp. nov., a Curved Gram-Stain-Negative Bacterium Isolated from Lake Water Richard A. Albert Water Quality Center, Marquette University, Milwaukee, WI Daniel Zitomer Water Quality Center, Marquette University, Milwaukee, WI Michael Dollhopf Water Quality Center, Marquette University, Milwaukee, WI A.E. Schauer-Gimenez Water Quality Center, Marquette University, Milwaukee, WI Craig Struble Department of Mathematics, Statistics and Computer Science, Marquette University, Milwaukee, WI International Journal of Systematic and Evolutionary Microbiology, Vol. 64, No. 2 (February 2014): pg.