LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 12

Search options

  1. Article ; Online: Temporal dynamics in microbial soil communities at anthrax carcass sites.

    Valseth, Karoline / Nesbø, Camilla L / Easterday, W Ryan / Turner, Wendy C / Olsen, Jaran S / Stenseth, Nils Chr / Haverkamp, Thomas H A

    BMC microbiology

    2017  Volume 17, Issue 1, Page(s) 206

    Abstract: Background: Anthrax is a globally distributed disease affecting primarily herbivorous mammals. It is caused by the soil-dwelling and spore-forming bacterium Bacillus anthracis. The dormant B. anthracis spores become vegetative after ingestion by grazing ...

    Abstract Background: Anthrax is a globally distributed disease affecting primarily herbivorous mammals. It is caused by the soil-dwelling and spore-forming bacterium Bacillus anthracis. The dormant B. anthracis spores become vegetative after ingestion by grazing mammals. After killing the host, B. anthracis cells return to the soil where they sporulate, completing the lifecycle of the bacterium. Here we present the first study describing temporal microbial soil community changes in Etosha National Park, Namibia, after decomposition of two plains zebra (Equus quagga) anthrax carcasses. To circumvent state-associated-challenges (i.e. vegetative cells/spores) we monitored B. anthracis throughout the period using cultivation, qPCR and shotgun metagenomic sequencing.
    Results: The combined results suggest that abundance estimation of spore-forming bacteria in their natural habitat by DNA-based approaches alone is insufficient due to poor recovery of DNA from spores. However, our combined approached allowed us to follow B. anthracis population dynamics (vegetative cells and spores) in the soil, along with closely related organisms from the B. cereus group, despite their high sequence similarity. Vegetative B. anthracis abundance peaked early in the time-series and then dropped when cells either sporulated or died. The time-series revealed that after carcass deposition, the typical semi-arid soil community (e.g. Frankiales and Rhizobiales species) becomes temporarily dominated by the orders Bacillales and Pseudomonadales, known to contain plant growth-promoting species.
    Conclusion: Our work indicates that complementing DNA based approaches with cultivation may give a more complete picture of the ecology of spore forming pathogens. Furthermore, the results suggests that the increased vegetation biomass production found at carcass sites is due to both added nutrients and the proliferation of microbial taxa that can be beneficial for plant growth. Thus, future B. anthracis transmission events at carcass sites may be indirectly facilitated by the recruitment of plant-beneficial bacteria.
    Language English
    Publishing date 2017-09-26
    Publishing country England
    Document type Journal Article
    ISSN 1471-2180
    ISSN (online) 1471-2180
    DOI 10.1186/s12866-017-1111-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Genotyping of B. licheniformis based on a novel multi-locus sequence typing (MLST) scheme.

    Madslien, Elisabeth H / Olsen, Jaran S / Granum, Per E / Blatny, Janet M

    BMC microbiology

    2012  Volume 12, Page(s) 230

    Abstract: Background: Bacillus licheniformis has for many years been used in the industrial production of enzymes, antibiotics and detergents. However, as a producer of dormant heat-resistant endospores B. licheniformis might contaminate semi-preserved foods. The ...

    Abstract Background: Bacillus licheniformis has for many years been used in the industrial production of enzymes, antibiotics and detergents. However, as a producer of dormant heat-resistant endospores B. licheniformis might contaminate semi-preserved foods. The aim of this study was to establish a robust and novel genotyping scheme for B. licheniformis in order to reveal the evolutionary history of 53 strains of this species. Furthermore, the genotyping scheme was also investigated for its use to detect food-contaminating strains.
    Results: A multi-locus sequence typing (MLST) scheme, based on the sequence of six house-keeping genes (adk, ccpA, recF, rpoB, spo0A and sucC) of 53 B. licheniformis strains from different sources was established. The result of the MLST analysis supported previous findings of two different subgroups (lineages) within this species, named "A" and "B" Statistical analysis of the MLST data indicated a higher rate of recombination within group "A". Food isolates were widely dispersed in the MLST tree and could not be distinguished from the other strains. However, the food contaminating strain B. licheniformis NVH1032, represented by a unique sequence type (ST8), was distantly related to all other strains.
    Conclusions: In this study, a novel and robust genotyping scheme for B. licheniformis was established, separating the species into two subgroups. This scheme could be used for further studies of evolution and population genetics in B. licheniformis.
    MeSH term(s) Bacillus/classification ; Bacillus/genetics ; Bacterial Proteins/genetics ; Cluster Analysis ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; Genotype ; Humans ; Industrial Microbiology ; Multilocus Sequence Typing/methods
    Chemical Substances Bacterial Proteins ; DNA, Bacterial
    Language English
    Publishing date 2012-10-10
    Publishing country England
    Document type Evaluation Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2041505-9
    ISSN 1471-2180 ; 1471-2180
    ISSN (online) 1471-2180
    ISSN 1471-2180
    DOI 10.1186/1471-2180-12-230
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Genotyping of B. licheniformis based on a novel multi-locus sequence typing (MLST) scheme

    Madslien Elisabeth H / Olsen Jaran S / Granum Per E / Blatny Janet M

    BMC Microbiology, Vol 12, Iss 1, p

    2012  Volume 230

    Abstract: Abstract Background Bacillus licheniformis has for many years been used in the industrial production of enzymes, antibiotics and detergents. However, as a producer of dormant heat-resistant endospores B. licheniformis might contaminate semi-preserved ... ...

    Abstract Abstract Background Bacillus licheniformis has for many years been used in the industrial production of enzymes, antibiotics and detergents. However, as a producer of dormant heat-resistant endospores B. licheniformis might contaminate semi-preserved foods. The aim of this study was to establish a robust and novel genotyping scheme for B. licheniformis in order to reveal the evolutionary history of 53 strains of this species. Furthermore, the genotyping scheme was also investigated for its use to detect food-contaminating strains. Results A multi-locus sequence typing (MLST) scheme, based on the sequence of six house-keeping genes ( adk, ccpA, recF, rpoB, spo0A and sucC ) of 53 B. licheniformis strains from different sources was established. The result of the MLST analysis supported previous findings of two different subgroups (lineages) within this species, named “A” and “B” Statistical analysis of the MLST data indicated a higher rate of recombination within group “A”. Food isolates were widely dispersed in the MLST tree and could not be distinguished from the other strains. However, the food contaminating strain B. licheniformis NVH1032, represented by a unique sequence type (ST8), was distantly related to all other strains. Conclusions In this study, a novel and robust genotyping scheme for B. licheniformis was established, separating the species into two subgroups. This scheme could be used for further studies of evolution and population genetics in B. licheniformis.
    Keywords Microbiology ; QR1-502 ; Science ; Q ; DOAJ:Microbiology ; DOAJ:Biology ; DOAJ:Biology and Life Sciences
    Subject code 590
    Language English
    Publishing date 2012-10-01T00:00:00Z
    Publisher BioMed Central
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    More links

    Kategorien

  4. Article: Draft Genome Sequences of Two Bacillus anthracis Strains from Etosha National Park, Namibia.

    Valseth, Karoline / Nesbø, Camilla L / Easterday, W Ryan / Turner, Wendy C / Olsen, Jaran S / Stenseth, Nils C / Haverkamp, Thomas H A

    Genome announcements

    2016  Volume 4, Issue 4

    Abstract: Bacillus anthracis strains K1 and K2 were isolated from two plains zebra anthrax carcasses in Etosha National Park, Namibia. These are draft genomes obtained by Illumina MiSeq sequencing of isolates collected from culture of blood-soaked soil from each ... ...

    Abstract Bacillus anthracis strains K1 and K2 were isolated from two plains zebra anthrax carcasses in Etosha National Park, Namibia. These are draft genomes obtained by Illumina MiSeq sequencing of isolates collected from culture of blood-soaked soil from each carcass.
    Language English
    Publishing date 2016-08-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2704277-7
    ISSN 2169-8287
    ISSN 2169-8287
    DOI 10.1128/genomeA.00861-16
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article: Genetic characterization of trh positive Vibrio spp. isolated from Norway.

    Ellingsen, Anette B / Olsen, Jaran S / Granum, Per E / Rørvik, Liv M / González-Escalona, Narjol

    Frontiers in cellular and infection microbiology

    2013  Volume 3, Page(s) 107

    Abstract: The thermostable direct hemolysin (TDH) and/or TDH-related hemolysin (TRH) genes are carried by most virulent Vibrio parahaemolyticus serovars. In Norway, trh+ V. parahaemolyticus constitute 4.4 and 4.5% of the total number of V. parahaemolyticus ... ...

    Abstract The thermostable direct hemolysin (TDH) and/or TDH-related hemolysin (TRH) genes are carried by most virulent Vibrio parahaemolyticus serovars. In Norway, trh+ V. parahaemolyticus constitute 4.4 and 4.5% of the total number of V. parahaemolyticus isolated from blue mussel (Mytilus edulis) and water, respectively. The trh gene is located in a region close to the gene cluster for urease production (ure). This region was characterized in V. parahaemolyticus strain TH3996 and it was found that a nickel transport operon (nik) was located between the first gene (ureR) and the rest of the ure cluster genes. The organization of the trh-ureR-nik-ure gene cluster in the Norwegian trh+ isolates was unknown. In this study, we explore the gene organization within the trh-ureR-nik-ure cluster for these isolates. PCR analyses revealed that the genes within the trh-ureR-nik-ure gene cluster of Norwegian trh+ isolates were organized in a similar fashion as reported previously for TH33996. Additionally, the phylogenetic relationship among these trh+ isolates was investigated using Multilocus Sequence Typing (MLST). Analysis by MLST or ureR-trh sequences generated two different phylogenetic trees for the same strains analyzed, suggesting that ureR-trh genes have been acquired at different times in Norwegian V. parahaemolyticus isolates. MLST results revealed that some pathogenic and non-pathogenic V. parahaemolyticus isolates in Norway appear to be highly genetically related.
    MeSH term(s) Animals ; Bacterial Proteins/genetics ; Cluster Analysis ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; Gene Order ; Hemolysin Proteins/genetics ; Molecular Sequence Data ; Multigene Family ; Multilocus Sequence Typing ; Mytilus edulis/microbiology ; Norway ; Phylogeny ; Polymerase Chain Reaction ; Sequence Homology ; Vibrio parahaemolyticus/genetics ; Vibrio parahaemolyticus/isolation & purification
    Chemical Substances Bacterial Proteins ; DNA, Bacterial ; Hemolysin Proteins ; thermostable direct hemolysin-related hemolysin protein, Vibrio parahaemolyticus
    Language English
    Publishing date 2013-12-25
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2619676-1
    ISSN 2235-2988
    ISSN 2235-2988
    DOI 10.3389/fcimb.2013.00107
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Analysis of the genetic distribution among members of Clostridium botulinum group I using a novel multilocus sequence typing (MLST) assay.

    Olsen, Jaran S / Scholz, Holger / Fillo, Silvia / Ramisse, Vincent / Lista, Florigio / Trømborg, Anette K / Aarskaug, Tone / Thrane, Ingjerd / Blatny, Janet M

    Journal of microbiological methods

    2014  Volume 96, Page(s) 84–91

    Abstract: Clostridium botulinum is the etiological agent of botulism. Due to food-borne poisoning and the potential use of the extremely toxic botulinum neurotoxin (BoNT) from C. botulinum in bioterror or biocrime related actions, reliable high resolution typing ... ...

    Abstract Clostridium botulinum is the etiological agent of botulism. Due to food-borne poisoning and the potential use of the extremely toxic botulinum neurotoxin (BoNT) from C. botulinum in bioterror or biocrime related actions, reliable high resolution typing methods for discriminating C. botulinum strains are needed. Partial sequencing of the adk, atpH, gyrB, proC, rpoD and spo0A genes from 51 various C. botulinum/sporogenes isolates was performed, resulting in 37 different sequence types (STs). Analysis of the sequence data revealed a genetic distribution in five larger clusters with a loose correlation to the BoNT serotypes. The developed MLST assay had a slightly lower resolution ability when compared to the MLVA (multilocus variable number of tandem repeat analysis), but the two methods resulted in similar subclusters of the strains possessing the BoNT serotypes A, B and F. The current work presents the development of a novel MLST assay useful for genotyping C. botulinum related to basic phylogenetic research and trace-back analysis in microbial forensic studies.
    MeSH term(s) Bacterial Proteins/genetics ; Clostridium botulinum/classification ; Clostridium botulinum/genetics ; Cluster Analysis ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; Genotype ; Humans ; Molecular Sequence Data ; Multilocus Sequence Typing/methods ; Phylogeny ; Sequence Analysis, DNA ; Sequence Homology ; Serotyping
    Chemical Substances Bacterial Proteins ; DNA, Bacterial
    Language English
    Publishing date 2014-01
    Publishing country Netherlands
    Document type Comparative Study ; Evaluation Studies ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604916-3
    ISSN 1872-8359 ; 0167-7012
    ISSN (online) 1872-8359
    ISSN 0167-7012
    DOI 10.1016/j.mimet.2013.11.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article: Analysis of the genetic distribution among members of Clostridium botulinum group I using a novel multilocus sequence typing (MLST) assay

    Olsen, Jaran S / Anette K. Trømborg / Florigio Lista / Holger Scholz / Ingjerd Thrane / Janet M. Blatny / Silvia Fillo / Tone Aarskaug / Vincent Ramisse

    Journal of microbiological methods. 2014 Jan., v. 96

    2014  

    Abstract: Clostridium botulinum is the etiological agent of botulism. Due to food-borne poisoning and the potential use of the extremely toxic botulinum neurotoxin (BoNT) from C. botulinum in bioterror or biocrime related actions, reliable high resolution typing ... ...

    Abstract Clostridium botulinum is the etiological agent of botulism. Due to food-borne poisoning and the potential use of the extremely toxic botulinum neurotoxin (BoNT) from C. botulinum in bioterror or biocrime related actions, reliable high resolution typing methods for discriminating C. botulinum strains are needed. Partial sequencing of the adk, atpH, gyrB, proC, rpoD and spo0A genes from 51 various C. botulinum/sporogenes isolates was performed, resulting in 37 different sequence types (STs). Analysis of the sequence data revealed a genetic distribution in five larger clusters with a loose correlation to the BoNT serotypes. The developed MLST assay had a slightly lower resolution ability when compared to the MLVA (multilocus variable number of tandem repeat analysis), but the two methods resulted in similar subclusters of the strains possessing the BoNT serotypes A, B and F. The current work presents the development of a novel MLST assay useful for genotyping C. botulinum related to basic phylogenetic research and trace-back analysis in microbial forensic studies.
    Keywords botulinum toxin ; botulism ; Clostridium botulinum ; etiological agents ; forensic sciences ; genes ; multilocus sequence typing ; multiple-locus variable number tandem-repeat analysis ; phylogeny ; serotypes ; toxicity
    Language English
    Dates of publication 2014-01
    Size p. 84-91.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 604916-3
    ISSN 1872-8359 ; 0167-7012
    ISSN (online) 1872-8359
    ISSN 0167-7012
    DOI 10.1016/j.mimet.2013.11.003
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  8. Article ; Online: Evaluation of a highly discriminating multiplex multi-locus variable-number of tandem-repeats (MLVA) analysis for Vibrio cholerae.

    Olsen, Jaran S / Aarskaug, Tone / Skogan, Gunnar / Fykse, Else Marie / Ellingsen, Anette Bauer / Blatny, Janet M

    Journal of microbiological methods

    2009  Volume 78, Issue 3, Page(s) 271–285

    Abstract: Vibrio cholerae is the etiological agent of cholera and may be used in bioterror actions due to the easiness of its dissemination, and the public fear for acquiring the cholera disease. A simple and highly discriminating method for connecting clinical ... ...

    Abstract Vibrio cholerae is the etiological agent of cholera and may be used in bioterror actions due to the easiness of its dissemination, and the public fear for acquiring the cholera disease. A simple and highly discriminating method for connecting clinical and environmental isolates of V. cholerae is needed in microbial forensics. Twelve different loci containing variable numbers of tandem-repeats (VNTRs) were evaluated in which six loci were polymorphic. Two multiplex reactions containing PCR primers targeting these six VNTRs resulted in successful DNA amplification of 142 various environmental and clinical V. cholerae isolates. The genetic distribution inside the V. cholerae strain collection was used to evaluate the discriminating power (Simpsons Diversity Index=0.99) of this new MLVA analysis, showing that the assay have a potential to differentiate between various strains, but also to identify those isolates which are collected from a common V. cholerae outbreak. This work has established a rapid and highly discriminating MLVA assay useful for track back analyses and/or forensic studies of V. cholerae infections.
    MeSH term(s) Bacterial Typing Techniques/methods ; Cholera/diagnosis ; Cholera/microbiology ; DNA Fingerprinting/methods ; DNA Primers/genetics ; DNA, Bacterial/genetics ; Environmental Microbiology ; Genotype ; Humans ; Minisatellite Repeats ; Polymerase Chain Reaction/methods ; Polymorphism, Genetic ; Sensitivity and Specificity ; Vibrio cholerae/classification ; Vibrio cholerae/genetics
    Chemical Substances DNA Primers ; DNA, Bacterial
    Language English
    Publishing date 2009-09
    Publishing country Netherlands
    Document type Evaluation Studies ; Journal Article
    ZDB-ID 604916-3
    ISSN 1872-8359 ; 0167-7012
    ISSN (online) 1872-8359
    ISSN 0167-7012
    DOI 10.1016/j.mimet.2009.06.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: OmpU as a biomarker for rapid discrimination between toxigenic and epidemic Vibrio cholerae O1/O139 and non-epidemic Vibrio cholerae in a modified MALDI-TOF MS assay.

    Paauw, Armand / Trip, Hein / Niemcewicz, Marcin / Sellek, Ricela / Heng, Jonathan Me / Mars-Groenendijk, Roos H / de Jong, Ad L / Majchrzykiewicz-Koehorst, Joanna A / Olsen, Jaran S / Tsivtsivadze, Evgeni

    BMC microbiology

    2014  Volume 14, Page(s) 158

    Abstract: Background: Cholera is an acute diarrheal disease caused by Vibrio cholerae. Outbreaks are caused by a genetically homogenous group of strains from serogroup O1 or O139 that are able to produce the cholera toxin. Rapid detection and identification of ... ...

    Abstract Background: Cholera is an acute diarrheal disease caused by Vibrio cholerae. Outbreaks are caused by a genetically homogenous group of strains from serogroup O1 or O139 that are able to produce the cholera toxin. Rapid detection and identification of these epidemic strains is essential for an effective response to cholera outbreaks.
    Results: The use of ferulic acid as a matrix in a new MALDI-TOF MS assay increased the measurable mass range of existing MALDI-TOF MS protocols for bacterial identification. The assay enabled rapid discrimination between epidemic V. cholerae O1/O139 strains and other less pathogenic V. cholerae strains. OmpU, an outer membrane protein whose amino acid sequence is highly conserved among epidemic strains of V. cholerae, appeared as a discriminatory marker in the novel MALDI-TOF MS assay.
    Conclusions: The extended mass range of MALDI-TOF MS measurements obtained by using ferulic acid improved the screening for biomarkers in complex protein mixtures. Differences in the mass of abundant homologous proteins due to variation in amino acid sequences can rapidly be examined in multiple samples. Here, a rapid MALDI-TOF MS assay was developed that could discriminate between epidemic O1/O139 strains and other less pathogenic V. cholerae strains based on differences in mass of the OmpU protein. It appeared that the amino acid sequence of OmpU from epidemic V. cholerae O1/O139 strains is unique and highly conserved.
    MeSH term(s) Adhesins, Bacterial/analysis ; Bacteriological Techniques/methods ; Cholera/diagnosis ; DNA, Bacterial/chemistry ; DNA, Bacterial/genetics ; Humans ; Molecular Sequence Data ; Sequence Analysis, DNA ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods ; Vibrio cholerae/chemistry ; Vibrio cholerae/classification ; Vibrio cholerae/isolation & purification
    Chemical Substances Adhesins, Bacterial ; DNA, Bacterial ; OmpU protein, Vibrio cholerae
    Language English
    Publishing date 2014-06-18
    Publishing country England
    Document type Evaluation Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1471-2180
    ISSN (online) 1471-2180
    DOI 10.1186/1471-2180-14-158
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Development and validation of a real-time quantitative PCR assay for rapid identification of Bacillus anthracis in environmental samples.

    Irenge, Léonid M / Durant, Jean-François / Tomaso, Herbert / Pilo, Paola / Olsen, Jaran S / Ramisse, Vincent / Mahillon, Jacques / Gala, Jean-Luc

    Applied microbiology and biotechnology

    2010  Volume 88, Issue 5, Page(s) 1179–1192

    Abstract: A real-time polymerase chain reaction (PCR) assay was developed for rapid identification of Bacillus anthracis in environmental samples. These samples often harbor Bacillus cereus bacteria closely related to B. anthracis, which may hinder its specific ... ...

    Abstract A real-time polymerase chain reaction (PCR) assay was developed for rapid identification of Bacillus anthracis in environmental samples. These samples often harbor Bacillus cereus bacteria closely related to B. anthracis, which may hinder its specific identification by resulting in false positive signals. The assay consists of two duplex real-time PCR: the first PCR allows amplification of a sequence specific of the B. cereus group (B. anthracis, B. cereus, Bacillus thuringiensis, Bacillus weihenstephanensis, Bacillus pseudomycoides, and Bacillus mycoides) within the phosphoenolpyruvate/sugar phosphotransferase system I gene and a B. anthracis specific single nucleotide polymorphism within the adenylosuccinate synthetase gene. The second real-time PCR assay targets the lethal factor gene from virulence plasmid pXO1 and the capsule synthesis gene from virulence plasmid pXO2. Specificity of the assay is enhanced by the use of minor groove binding probes and/or locked nucleic acids probes. The assay was validated on 304 bacterial strains including 37 B. anthracis, 67 B. cereus group, 54 strains of non-cereus group Bacillus, and 146 Gram-positive and Gram-negative bacteria strains. The assay was performed on various environmental samples spiked with B. anthracis or B. cereus spores. The assay allowed an accurate identification of B. anthracis in environmental samples. This study provides a rapid and reliable method for improving rapid identification of B. anthracis in field operational conditions.
    MeSH term(s) Adenylosuccinate Synthase/genetics ; Bacillus/genetics ; Bacillus anthracis/classification ; Bacillus anthracis/genetics ; Bacillus anthracis/isolation & purification ; Bacillus anthracis/pathogenicity ; Bacterial Typing Techniques ; Bacteriological Techniques ; Base Sequence ; DNA, Bacterial/analysis ; DNA, Bacterial/genetics ; Genes, Bacterial ; Nucleotides/genetics ; Phosphotransferases/genetics ; Phylogeny ; Plasmids ; Polymerase Chain Reaction/methods ; Polymorphism, Single Nucleotide ; Ribose/analogs & derivatives ; Ribose/genetics ; Sensitivity and Specificity ; Sequence Alignment ; Sequence Analysis, DNA ; Virulence/genetics
    Chemical Substances 2'-O-4'-C-methylene-ribofuranosyl nucleotide ; DNA, Bacterial ; Nucleotides ; Ribose (681HV46001) ; Phosphotransferases (EC 2.7.-) ; Adenylosuccinate Synthase (EC 6.3.4.4)
    Language English
    Publishing date 2010-11
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Validation Studies
    ZDB-ID 392453-1
    ISSN 1432-0614 ; 0171-1741 ; 0175-7598
    ISSN (online) 1432-0614
    ISSN 0171-1741 ; 0175-7598
    DOI 10.1007/s00253-010-2848-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top