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  • 1
    Keywords: Prokaryotes-Handbooks, manuals, etc. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (1192 pages)
    Edition: 2nd ed.
    ISBN: 9781475721911
    DDC: 589.9
    Language: English
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  • 2
    Keywords: Forschungsbericht
    Description / Table of Contents: Enterococci, drinking water research, hybridization, specific probes, PCR
    Type of Medium: Online Resource
    Pages: 21 p. = 70 kB, text and images
    Edition: [Electronic ed.]
    Language: German , English
    Note: nIndex , Differences between the printed and electronic version of the document are possible
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  • 3
    Online Resource
    Online Resource
    New York, NY :Springer,
    Keywords: Life sciences. ; Electronic books.
    Description / Table of Contents: This text of numerous medically and industrially important taxa offers a revised taxonomic outline of the Firmicutes based upon the SILVA project, including a description of over 1346 species and 235 genera in the Firmicute phylum.
    Type of Medium: Online Resource
    Pages: 1 online resource (1476 pages)
    Edition: 2nd ed.
    ISBN: 9780387684895
    DDC: 579.3012
    Language: English
    Note: Bergeys_FM.pdf -- Bergeys_Ch01.pdf -- Bergeys_Ch02.pdf -- Bergeys_Ch03-5.pdf -- Bergeys_Ch06.pdf -- Bergeys_Ch07.pdf -- Bergeys_Ch08.pdf -- Bergeys_Ch09.pdf -- Bergeys_Ch10.pdf -- Bergeys_Ch11.pdf -- Bergeys_Ch12.pdf -- Bergeys_Ch13.pdf -- Bergeys_Ch14.pdf -- Bergeys_Ch15-18.pdf -- Bergeys_Ch19.pdf -- Bergeys_Ch20.pdf -- Bergeys_Ch21.pdf -- Bergeys_Ch22.pdf -- Bergeys_Ch23.pdf -- Bergeys_Ch25.pdf -- Bergeys_Ch26.pdf -- Bergeys_Ch27.pdf -- Bergeys_Ch28.pdf -- Bergeys_Ch29.pdf -- Bergeys_Ch30.pdf -- Bergeys_Ch31.pdf -- Bergeys_Ch32.pdf -- Bergeys_Ch33.pdf -- Bergeys_Ch34.pdf -- Bergeys_Ch35.pdf -- Bergeys_Ch36.pdf -- Bergeys_Ch37.pdf -- Bergeys_Ch38.pdf -- Bergeys_Ch39-41.pdf -- Bergeys_Ch42-44.pdf -- Bergeys_Ch45.pdf -- Bergeys_Ch46-47.pdf -- Bergeys_Ch48.pdf -- Bergeys_Ch49.pdf -- Bergeys_Ch50.pdf -- Bergeys_Ch51-53.pdf -- Bergeys_Ch54.pdf -- Bergeys_Appendix.pdf.
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  • 4
    Keywords: Microbiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (1415 pages)
    Edition: 2nd ed.
    ISBN: 9780387292984
    DDC: 570
    Language: English
    Note: Intro -- BERGEY'S MANUAL® OFSystematic Bacteriology -- Preface to Volume Two of the Second Edition of Bergey's Manual® of Systematic Bacteriology -- Preface to the First Edition of Bergey's Manual® ofSystematic Bacteriology -- Preface to the First Edition of Bergey's Manual® of Determinative Bacteriology -- Contents -- Contributors -- Class I. Alphaproteobacteria class. nov. -- Class II. Betaproteobacteria class. nov. -- Class IV. Deltaproteobacteria class nov. -- Class V. Epsilonproteobacteria class. nov. -- Bibliography -- Index of Scientific Names of Archaea and Bacteria.
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  • 5
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Refractile inclusion bodies, called R-bodies were observed within the cells of some bacterial strains. They are protein ribbons, which are typically coiled into cylindrical structures. They are produced by members of the genus Caedibacter, gram-negative rod-shaped endosymbionts of paramecia and e.g. the free-living bacteria Hydrogenophaga taeniospiralis and Acidovorax avenae. The phylogenetic relationship even between the members of the genus Caedibacter is quite low: C. taeniospiralis belongs to the Gammaproteobacteria and is related to Francisella tularensis, C. caryophilus is affiliated with the Alphaproteobacteria and clusters with the obligate endosymbiont Holospora. In the case of C. taeniospiralis 51, the genetic determinants of R-body synthesis are located on a plasmid, whereas in other strains like 7 and 562 it looks like phage particles are involved in their production. In the present study, we investigated C. caryophilus, endosymbiont of Paramecium caudatum. Separation of C. caryophilus cells was performed by Percoll™ density gradient centrifugation. The isolated DNA was separated by pulsed-field gel electrophoresis and it was possible to visualize several bands referring to one or more extrachromosomal elements. A small gene library of these extrachromosomal elements was constructed and we already identified transposition-related genes; interestingly, similar genes were reported also on the plasmid of C. taeniospiralis 51.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Up to half of the biomass in the rumen can be represented by ciliates, which play an important role in the digestion processes of their hosts. In the literature, very little information can be found on determination of the diversity of complex rumen ciliate communities. The identification of these fast moving protists is mainly based on live observations and comparisons of their highly variable cell morphologies. It makes accurate identification and quantification of rumen ciliates very difficult if not impossible. The development of fluorescence in situ hybridization (FISH), established as a technique to identify prokaryotes and eukaryotes using ribosomal RNA-targeted fluorescently labeled oligonucleotide probes, is a promising approach to identify and investigate rumen ciliates. The present study, part of CIMES (ciliates as monitors for environmental safety), a project sponsored by the European Commission, shows the problems of applying FISH on rumen ciliates and how to solve them. Tests resulted in a new protocol, which recommends para-formaldehyde and formaldehyde at 1–2% final concentration to preserve the ciliates before applying FISH. Furthermore, seven new oligonucleotide probes could be developed and successfully be tested to identify different rumen ciliate taxa of the order Entodiniomorphida (class Litostomatea) by applying FISH. It is also shown, how FISH together with confocal laser scanning microscopy can improve analyses of ciliate cell morphologies. Thanks to Peter Pristas, Peter Javorsky, Ralf Einspanier, Susanne Ulbrich (providing rumen samples), Seung Yeo Moon-van der Staay, Georg van der Staay (providing unpublished 18S-rDNA sequences), the European Commission (financial support, project QLK3-CT-2002-02151).
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Tubulins are typical eucaryotic genes, which have recently been found in the free-living bacteria Prosthecobacter (Verrucomicrobiales). Nevertheless, microtubule-like structures were never observed in Prostecobacter, whereas they were reported in epixenosomes which are symbiotic Verrucomicrobiales of the ciliate Euplotidium. In the present work, an extensive search for tubulin like genes was performed with several combinations of PCR-primers, designed according to different criteria. Although some combinations of these primers are able to amplify simultaneously eukaryotic α- and β-tubulin as well as Prosthecobacter tubulin genes, no bacterial-like tubulin genes were identified in other Verrucomicrobiales species. Because of host derived contaminations, even a subtractive PCR approach, using microtiter-plate-subtractive-hybridization, was used with the epixenosomes. The characterization of the genomic environment of the Prosthecobacter tubulin genes was performed by gene walking. The sequences obtained from P. debontii revealed a so-far undiscovered gene duplication. The bacterial tubulin operon looks conserved among Prosthecobacter species and includes an α-tubulin, a β-tubulin and a kinesin like protein. Upstream of two operons a repetetive sequence could be found which could be a hint for horizontal gene transfer. The analysis of the genomic environments of the tubulin genes provided open reading frames, which have homology to Verrucomicrobium spinosum genes (ongoing genome project data), whereas up to now the blast search did not reveal tubulin-like genes in this organism. Present results suggest, that the Prosthecobacter tubulin genes are possibly of recent origin, maybe acquired by horizontal gene transfer, or lost by other so far studied Verrucomicrobiales. The origin and nature of microtubular genetic determinants from epixenosomes remains open.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    The @journal of eukaryotic microbiology 52 (2005), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Verrucomicrobiales are a newly proposed, deep branched division of bacteria from which only a handful of cultured isolates are available. Culture-independent analysis of environmental samples shows that members of Verrucomicrobiales are widespread and can be divided into several subdivisions. Symbiotic species of Euplotidium (Ciliophora) and Nematodes, epixenosomes and Xiphinemobacter spp. respectively, are according to the 16S sequences also members of this group. Up to now, only minimal sequence data mainly focused on 16S rRNA gene sequences are available for this group of organisms. The phylogenetic relatives of Verrucomicrobiales are still unclear with Chlamydiales and Planctomycetes being the most probable candidates. The present study describes preliminary results on phylogenetic relationships of Verrucomicrobiales by using protein-coding genes like Hsp70 and RpoC/B. The species which are used for this study are Prosthecobacter vanneervenii, P. debontii, Opitutus sp.VeGlc2, O. terrae and epixenosomes. The genes were amplified with designed consensus-degenerated primers and results are available on the Hsp70. The sequences show several differences within the group. Verrucomicrobium and Prosthecobacter sequences cluster together, but in P. debontii, two sequences were found, and the second one appears quite divergent. Also the two Opitutus genes are quite atypical and cluster together in a deep position. Preliminary attempt was performed on Euplotidium-epixenosome complex. However, amplified and cloned sequences revealed to be closely related to ciliate sequences. Further attempt will be performed applying microtiter-plate-subtractive-hybridization to characterize epixenosome genes.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    The @journal of eukaryotic microbiology 52 (2005), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: We characterized nine macronuclear tubulin gene minichromosomes in the hypotrich ciliate Euplotidium itoi: two α-tubulin genes, five β-tubulin genes, and two γ-tubulin genes. In particular, one peculiar β-tubulin gene was identified. It shows only 81.5% amino acid similarity to the other characterized β-tubulin types and an UAG stop codon in frame. Based on this result we started to analyse stop codon usage in Euplotidium itoi macronuclear tubulin genes and some unrelated macronuclear minichromosomes. Most of the ciliates independently evolved diverse non-canonical genetic codes. Differences to the standard code consist in the reassignment of one or two of the three standard stop codons to encode a particular amino acid. Class Spirotrichea represents a particular case comprising two groups of organisms that do not share any stop codon. In oxytrichids, UAR is translated as glutamine and UGA is the single stop codon. This is in contrast to the genus Euplotes, close relatives of Euplotidium, in which UAR encodes a stop signal and UGA is translated as cysteine. Fourteen complete genes were characterized in Euplotidium itoi; in all cases UAA revealed as the single triplet used to code a stop, UGA was never and UAG rarely observed in frame. The UAG stop codon was observed in the peculiar type 3 β-tubulin gene, in two dynein partial sequences and in some other putative genes. We could confirm the active expression of three of these genes, the unusual β-tubulin, a putative lipase and a possible steroid-binding protein, by RT-PCR. Finally, a detailed analysis on the structure of the macronuclear tubulin genes, including nucleotide and amino acid differences among tubulin gene paralogs, polyadenylation sites, putative chromosome fragmentation sites, ATGC-content in coding and non-coding regions, telomere sequence and length will be presented.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 9 (1980), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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