Articles, Onomic Units (Otus) of Which Half Were Related to Bacteria Their Numbers Are Highly Variable in Both Time and Space
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Estudio Molecular De Poblaciones De Pseudomonas Ambientales
Universitat de les Illes Balears ESTUDIO MOLECULAR DE POBLACIONES DE PSEUDOMONAS AMBIENTALES T E S I S D O C T O R A L DAVID SÁNCHEZ BERMÚDEZ DIRECTORA: ELENA GARCÍA-VALDÉS PUKKITS Departamento de Biología Universitat de les Illes Balears Palma de Mallorca, Septiembre 2013 Universitat de les Illes Balears ESTUDIO MOLECULAR DE POBLACIONES DE PSEUDOMONAS AMBIENTALES Tesis Doctoral presentada por David Sánchez Bermúdez para optar al título de Doctor en el programa Microbiología Ambiental y Biotecnología, de la Universitat de les Illes Balears, bajo la dirección de la Dra. Elena García-Valdés Pukkits. Vo Bo Director de la Tesis El doctorando DRA. ELENA GARCÍA-VALDÉS PUKKITS DAVID SÁNCHEZ BERMÚDEZ Catedrática de Universidad Universitat de les Illes Balears PALMA DE MALLORCA, SEPTIEMBRE 2013 III IV Index Agradecimientos .................................................................................................... IX Resumen ................................................................................................................ 1 Abstract ................................................................................................................... 3 Introduction ............................................................................................................ 5 I.1. The genus Pseudomonas ............................................................................................ 7 I.1.1. Definition ................................................................................................................ 7 I.1.2. -
Developing a Genetic Manipulation System for the Antarctic Archaeon, Halorubrum Lacusprofundi: Investigating Acetamidase Gene Function
www.nature.com/scientificreports OPEN Developing a genetic manipulation system for the Antarctic archaeon, Halorubrum lacusprofundi: Received: 27 May 2016 Accepted: 16 September 2016 investigating acetamidase gene Published: 06 October 2016 function Y. Liao1, T. J. Williams1, J. C. Walsh2,3, M. Ji1, A. Poljak4, P. M. G. Curmi2, I. G. Duggin3 & R. Cavicchioli1 No systems have been reported for genetic manipulation of cold-adapted Archaea. Halorubrum lacusprofundi is an important member of Deep Lake, Antarctica (~10% of the population), and is amendable to laboratory cultivation. Here we report the development of a shuttle-vector and targeted gene-knockout system for this species. To investigate the function of acetamidase/formamidase genes, a class of genes not experimentally studied in Archaea, the acetamidase gene, amd3, was disrupted. The wild-type grew on acetamide as a sole source of carbon and nitrogen, but the mutant did not. Acetamidase/formamidase genes were found to form three distinct clades within a broad distribution of Archaea and Bacteria. Genes were present within lineages characterized by aerobic growth in low nutrient environments (e.g. haloarchaea, Starkeya) but absent from lineages containing anaerobes or facultative anaerobes (e.g. methanogens, Epsilonproteobacteria) or parasites of animals and plants (e.g. Chlamydiae). While acetamide is not a well characterized natural substrate, the build-up of plastic pollutants in the environment provides a potential source of introduced acetamide. In view of the extent and pattern of distribution of acetamidase/formamidase sequences within Archaea and Bacteria, we speculate that acetamide from plastics may promote the selection of amd/fmd genes in an increasing number of environmental microorganisms. -
Reconstructing the Origin of Oxygenic Photosynthesis: Do Assembly and Photoactivation Recapitulate Evolution?
HYPOTHESIS AND THEORY published: 02 March 2016 doi: 10.3389/fpls.2016.00257 Reconstructing the Origin of Oxygenic Photosynthesis: Do Assembly and Photoactivation Recapitulate Evolution? Tanai Cardona * Department of Life Sciences, Imperial College London, London, UK Due to the great abundance of genomes and protein structures that today span a broad diversity of organisms, now more than ever before, it is possible to reconstruct the molecular evolution of protein complexes at an incredible level of detail. Here, I recount the story of oxygenic photosynthesis or how an ancestral reaction center was transformed into a sophisticated photochemical machine capable of water oxidation. First, I review the evolution of all reaction center proteins in order to highlight that Photosystem II and Photosystem I, today only found in the phylum Cyanobacteria, branched out very early in the history of photosynthesis. Therefore, it is very unlikely that they were acquired via horizontal gene transfer from any of the described phyla of Edited by: anoxygenic phototrophic bacteria. Second, I present a new evolutionary scenario for the Julian Eaton-Rye, origin of the CP43 and CP47 antenna of Photosystem II. I suggest that the antenna University of Otago, New Zealand proteins originated from the remodeling of an entire Type I reaction center protein and Reviewed by: Anthony William Larkum, not from the partial gene duplication of a Type I reaction center gene. Third, I highlight University of Technology, Sydney, how Photosystem II and Photosystem I reaction center proteins interact with small Australia Martin Hohmann-Marriott, peripheral subunits in remarkably similar patterns and hypothesize that some of this Norwegian University of Science and complexity may be traced back to the most ancestral reaction center. -
Cetrimide Agar Base M024
Cetrimide Agar Base M024 Intended use Cetrimide Agar Base is used for the selective isolation of Pseudomonas aeruginosa from clinical specimens. Composition** Ingredients Gms / Litre Gelatin peptone 20.000 Magnesium chloride 1.400 Potassium sulphate 10.000 Cetrimide 0.300 Agar 15.000 Final pH ( at 25°C) 7.2±0.2 **Formula adjusted, standardized to suit performance parameters Directions Suspend 46.7 grams in 1000 ml distilled water containing 10 ml glycerol. Heat, to boiling, to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 45-50°C. If desired, rehydrated contents of 1 vial of Nalidixic Selective Supplement (FD130) may be added aseptically to 1000 ml medium. Mix well and pour into sterile Petri plates. Principle And Interpretation Pseudomonas aeruginosa grows well on all normal laboratory media but specific isolation of the organism, from environmental sites or from human, animal or plant sources, is best carried out on a medium, which contains a selective agent and also constituents to enhance pigment production. Most selective media depend upon the intrinsic resistance of the species to various antibacterial agents. Cetrimide inhibits the growth of many microorganisms whilst allowing Pseudomonas aeruginosa to develop typical colonies. Cetrimide is a quaternary ammonium salt, which acts as a cationic detergent that reduces surface tension in the point of contact and has precipitant, complexing and denaturing effects on bacterial membrane proteins. It exhibits inhibitory actions on a wide variety of microorganisms including Pseudomonas species other than Pseudomonas aeruginosa. King et al developed Medium A for the enhancement of pyocyanin production by Pseudomonas (1). -
Community Structure and Function of High-Temperature Chlorophototrophic Microbial Mats Inhabiting Diverse Geothermal Environments
ORIGINAL RESEARCH ARTICLE published: 03 June 2013 doi: 10.3389/fmicb.2013.00106 Community structure and function of high-temperature chlorophototrophic microbial mats inhabiting diverse geothermal environments Christian G. Klatt 1,2†,William P.Inskeep 1,2*, Markus J. Herrgard 3, Zackary J. Jay 1,2, Douglas B. Rusch4, Susannah G.Tringe 5, M. Niki Parenteau 6,7, David M. Ward 1,2, Sarah M. Boomer 8, Donald A. Bryant 9,10 and Scott R. Miller 11 1 Department of Land Resources and Environmental Sciences, Montana State University, Bozeman, MT, USA 2 Thermal Biology Institute, Montana State University, Bozeman, MT, USA 3 Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Hørsholm, Denmark 4 Center for Genomics and Bioinformatics, Indiana University, Bloomington, IN, USA 5 Department of Energy Joint Genome Institute, Walnut Creek, CA, USA 6 Search for Extraterrestrial Intelligence Institute, Mountain View, CA, USA 7 National Aeronautics and Space Administration Ames Research Center, Mountain View, CA, USA 8 Western Oregon University, Monmouth, OR, USA 9 Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, USA 10 Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT, USA 11 Department of Biological Sciences, University of Montana, Missoula, MT, USA Edited by: Six phototrophic microbial mat communities from different geothermal springs (YNP) were Martin G. Klotz, University of North studied using metagenome sequencing and geochemical analyses. The primary goals of Carolina at Charlotte, USA this work were to determine differences in community composition of high-temperature Reviewed by: Andreas Teske, University of North phototrophic mats distributed across theYellowstone geothermal ecosystem, and to iden- Carolina at Chapel Hill, USA tify metabolic attributes of predominant organisms present in these communities that may Jesse Dillon, California State correlate with environmental attributes important in niche differentiation. -
Cetrimide Agar Plates MPH024
Cetrimide Agar Plates MPH024 For the selection and subculture of Pseudomonas aeruginosa in accordance with the harmonized method of USP/EP/BP/ JP/IP. Composition** Ingredients Gms / Litre Pancreatic digest of gelatin 20.000 Magnesium chloride 1.400 Dipotassium sulphate 10.000 Cetrimide 0.300 Agar 13.600 Glycerol 10 ml **Formula adjusted, standardized to suit performance parameters Directions Either streak, inoculate or surface spread the test inoculum (50-100 CFU) aseptically on the plate. Principle And Interpretation Pseudomonas aeruginosa grows well on all normal laboratory media but specific isolation of the organism, from environmental sites or from human, animal or plant sources, is best carried out on a medium, which contains a selective agent and also constituents to enhance pigment production. Most selective media depend upon the intrinsic resistance of the species to various antibacterial agents. Cetrimide inhibits the growth of many microorganisms whilst allowing Pseudomonas aeruginosa to develop typical colonies. Cetrimide is a quaternary ammonium salt, which acts as a cationic detergent that reduces surface tension in the point of contact and has precipitant, complexing and denaturing effects on bacterial membrane proteins. It exhibits inhibitory actions on a wide variety of microorganisms including Pseudomonas species other than Pseudomonas aeruginosa . King et al developed Medium A for the enhancement of pyocyanin production by Pseudomonas (1). Cetrimide Agar developed by Lowburry (2) is a modification of Tech Agar (Medium A) with addition of 0.1% cetrimide for selective isolation of P. aeruginosa . Later, due to the availability of the highly purified cetrimide, its concentration in the medium was decreased (3). -
Optimization and Characterization of the Growth Of
OPTIMIZATION AND CHARACTERIZATION OF THE GROWTH OF THE PHOTOSYNTHETIC BACTERIUM BLASTOCHLORIS VIRIDIS AND A BRIEF SURVEY OF ITS POTENTIAL AS A REMEDIATIVE TOOL A Dissertation Submitted to the Graduate School of the University of Notre Dame in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy by Darcy Danielle LaClair, B.S. ___________________________________ Agnes E. Ostafin, Director Graduate Program in Chemical and Biomolecular Engineering Notre Dame, Indiana April 2006 OPTIMIZATION AND CHARACTERIZATION OF THE GROWTH OF THE PHOTOSYNTHETIC BACTERIUM BLASTOCHLORIS VIRIDIS AND A BRIEF SURVEY OF THEIR POTENTIAL AS A REMEDIATIVE TOOL Abstract by Darcy Danielle LaClair The growth of B. viridis was characterized in an undefined rich medium and a well-defined medium, which was later selected for further experimentation to insure repeatability. This medium presented a significant problem in obtaining either multigenerational or vigorous growth because of metabolic limitations; therefore optimization of the medium was undertaken. A primary requirement to obtain good growth was a shift in the pH of the medium from 6.9 to 5.9. Once this shift was made, it was possible to obtain growth in subsequent generations, and the media formulation was optimized. A response curve suggested optimum concentrations of 75 mM carbon, supplemented as sodium malate, 12.5 mM nitrogen, supplemented as ammonium sulfate, Darcy Danielle LaClair and 12.7 mM phosphate buffer. In addition, the vitamins p-Aminobenzoic acid, Thiamine, Biotin, B12, and Pantothenate were important to achieving good growth and good pigment formation. Exogenous carbon dioxide, added as 2.5 g sodium bicarbonate per liter media also enhanced growth and reduced the lag time. -
Investigation on the Production of Secondary Metabolites from Anoxygenic Phototrophic Bacteria
Investigation on the production of secondary metabolites from anoxygenic phototrophic bacteria. Dissertation Zur Erlangung des Doktorgrades der Mathematisch-Naturwissenschaftlichen Fakultät der Christian-Albrechts-Universität zu Kiel Vorgelegt von Min Sun Kiel 2015 Referent: Prof. Dr. Johannes F. Imhoff Korreferentin: Prof. Dr. Ute Hentschel-Humeida Tag der mündlichen Prüfung: 19.02.2016 Zum Druck genehmigt: Ja gez. Prof. Dr. Johannes F. Imhoff This present work was carried out at the GEOMAR Helmholtz Centre for Ocean Research Kiel Christian-Albrechts-University of Kiel from August 2011 to August 2015 under the supervision of Prof. Dr. Johannes F. Imhoff. Scientific contribution All the strains used in this studied were offered by Prof. Dr. Johannes F. Imhoff. Allochromatium vinosum strain MT86 was isolated and identified by Dr. Marcus Tank. All bioassays of crude extracts, fractions and pure compounds were done by Arlette Wenzel-Storjohann (Marine Natural Products, GEOMAR). NMR measurement was performed at the Otto-Diels Institute of Organic Chemistry (Christian-Albrechts University of Kiel) and NMR data analysis was analysis by the assistance of Dr. Bin Wu (Zhejiang University, China) and Prof. Dr. Alex Zeeck (BioViotica Naturstoffe GmbH, Götingen). Prof. Dr. Alex Zeeck did the TLC and IR, CD, and polarimetry measurements. All other experiments were done by Min Sun under supervision of Prof. Dr. Johannes F. Imhoff at GEOMAR Marine Microbiology Department. Erklärung Hiermit erkläre ich, dass ich die vorliegende Arbeit unter Einhaltung der Regeln guter wissenschaftlicher Praxis der Deutschen Forschungsgesellschaft verfasst habe, und dass sie nach Form und Inhalt meine eigene Arbeit ist. Außer den angegebenen Quellen und Hilfsmitteln wurden keine weiteren verwendet. -
Metaproteomics Characterization of the Alphaproteobacteria
Avian Pathology ISSN: 0307-9457 (Print) 1465-3338 (Online) Journal homepage: https://www.tandfonline.com/loi/cavp20 Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssus gallinae (De Geer, 1778) José Francisco Lima-Barbero, Sandra Díaz-Sanchez, Olivier Sparagano, Robert D. Finn, José de la Fuente & Margarita Villar To cite this article: José Francisco Lima-Barbero, Sandra Díaz-Sanchez, Olivier Sparagano, Robert D. Finn, José de la Fuente & Margarita Villar (2019) Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssusgallinae (De Geer, 1778), Avian Pathology, 48:sup1, S52-S59, DOI: 10.1080/03079457.2019.1635679 To link to this article: https://doi.org/10.1080/03079457.2019.1635679 © 2019 The Author(s). Published by Informa View supplementary material UK Limited, trading as Taylor & Francis Group Accepted author version posted online: 03 Submit your article to this journal Jul 2019. Published online: 02 Aug 2019. Article views: 694 View related articles View Crossmark data Citing articles: 3 View citing articles Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=cavp20 AVIAN PATHOLOGY 2019, VOL. 48, NO. S1, S52–S59 https://doi.org/10.1080/03079457.2019.1635679 ORIGINAL ARTICLE Metaproteomics characterization of the alphaproteobacteria microbiome in different developmental and feeding stages of the poultry red mite Dermanyssus gallinae (De Geer, 1778) José Francisco Lima-Barbero a,b, Sandra Díaz-Sanchez a, Olivier Sparagano c, Robert D. Finn d, José de la Fuente a,e and Margarita Villar a aSaBio. -
BIODATA 1) Name : Dr. Ch. Sasikala 2) Designation
BIODATA 1) Name : Dr. Ch. Sasikala 2) Designation : Professor and Chairperson, Board of Studies in Environemntal Science and Technology 3) Address a) Official : Centre for Environment, IST, JNT University Hyderabad, Kukatpally, Hyderabad – 500 085 INDIA Phone: 040-23158661 /2/3/4 Extn.3480 Email: [email protected] [email protected] , [email protected] b) Home : 5-3-357, Rashtrapathi Road, Secunderabad 500 003 INDIA Phone: Res. 040-27535462 (R) Mobile : 9000796341 4) Date of Birth : 9 th March 1963 5) Nature of work : Teaching/Research 6) Research experience : 30 years of research experience Including 26 years of post-doctoral experience 7) PG teaching experience : 21 years 8) Field of specialization : Environmental microbiology and biotechnology (Bacterial diversity, Bioprospecting, biodegradation and Bioremediation) 9) Research publications : 191 (Annexure A) (In standard refereed journals) Cumulative impact factor: 440 h index: 28; Number of citations: ~3,000 1 10) Academic qualifications and career record: a) Degrees : B.Sc., B.Ed., M.Sc., Ph.D. b) Details of Educational qualifications : Exam Subjects Board/ Year of Class/ % of passed University passing Division Marks S.S.C Tel. Hindi, Board of 1978 I 70 Eng. Maths, Secondary Ed. Gen. Sci. and Andhra Social studies Pradesh Intermediate Biol. Phy. Board of 1980 I 76.5 Chem. Intermediate Education, A.P B.Sc. Bot. Chem. Osmania 1983 I 83.2 Microbiol University B.Ed. Life Sciences Osmania 1984 I 68 University M.Sc. Applied Bharathiar 1986 I 70 Microbiology University (university second -
A Microbiotic Survey of Lichen-Associated Bacteria Reveals a New Lineage from the Rhizobiales
SYMBIOSIS (2009) 49, 163–180 ©Springer Science+Business Media B.V. 2009 ISSN 0334-5114 A microbiotic survey of lichen-associated bacteria reveals a new lineage from the Rhizobiales Brendan P. Hodkinson* and François Lutzoni Department of Biology, Duke University, Box 90338, Durham, NC 27708, USA, Tel. +1-443-340-0917, Fax. +1-919-660-7293, Email. [email protected] (Received June 10, 2008; Accepted November 5, 2009) Abstract This study uses a set of PCR-based methods to examine the putative microbiota associated with lichen thalli. In initial experiments, generalized oligonucleotide-primers for the 16S rRNA gene resulted in amplicon pools populated almost exclusively with fragments derived from lichen photobionts (i.e., Cyanobacteria or chloroplasts of algae). This effectively masked the presence of other lichen-associated prokaryotes. In order to facilitate the study of the lichen microbiota, 16S ribosomal oligonucleotide-primers were developed to target Bacteria, but exclude sequences derived from chloroplasts and Cyanobacteria. A preliminary microbiotic survey of lichen thalli using these new primers has revealed the identity of several bacterial associates, including representatives of the extremophilic Acidobacteria, bacteria in the families Acetobacteraceae and Brucellaceae, strains belonging to the genus Methylobacterium, and members of an undescribed lineage in the Rhizobiales. This new lineage was investigated and characterized through molecular cloning, and was found to be present in all examined lichens that are associated with green algae. There is evidence to suggest that members of this lineage may both account for a large proportion of the lichen-associated bacterial community and assist in providing the lichen thallus with crucial nutrients such as fixed nitrogen. -
Harmonized Pharmacopeia Dehydrated Media
Harmonised Pharmacopoeia Compliant to Dehydrated Culture Media EP 10th Edition 1. Sterility Testing Sterility testing is required when developing and manufacturing products for pharmaceutical applications as part of a sterilisation validation process as well as routine testing before release. Manufacturers must provide adequate and reliable sterility test data to ensure their product meets strict safety guidelines. Neogen offers the below media for sterility testing, which have been developed in accordance with the European Pharmacopoeia (EP) compliance guidelines: Fluid Thioglycollate Medium NCM0108 This medium has been designed for the detection of aerobic and anaerobic organisms including Clostridia spp., Pseudomonas spp. and Staphylococci. The medium has a nutritionally rich base to support the growth of a wide range of organisms as well as low oxygen reduction potential to prevent any species that may have a negative effect on the recovery and growth of contaminants. NCM0108 Tryptic Soy Broth (Soybean-Casein Digest Broth) NCM0004 This is a highly nutritious medium for the cultivation of a wide range of microorganisms including Aspergillus spp., Bacillus spp. and Candida spp. This versatile medium promotes growth of both fungi and aerobic bacteria, and can also be used as a pre-enrichment broth for non-sterile products. NCM0004 2. Examination of Non-Sterile Products Not all products which are released to market are required to be sterile. Instead, to guarantee that the product meets safety and quality standards, manufacturers are required to evaluate the microbial content of each product and ensure no organisms of concern are present. Neogen’s media range for the examination of non-sterile products has been developed for detection and enumeration of each organism specified within the HP including: Bile-Tolerant Gram-Negative Bacteria Enterobacteriaceae Enrichment (EE) Broth Mossel NCM0057 This is a selective broth for the enrichment of Enterobacteriaceae.