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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 219 (2003), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A polymerase chain reaction-based method was used to isolate a Nostoc sp. PCC 9229 cDNA from infected glands of Gunnera chilensis. The complete gene sequence was isolated from a genomic Nostoc sp. PCC 9229 library. Sequence analysis showed 84% amino acid similarity to a putative cyclodextrin glycosyltransferase from Nostoc sp. PCC 7120 and the gene was therefore termed cgt. Southern blot revealed that the cgt gene was present in symbiotically competent cyanobacteria. The cgt gene was expressed in free-living nitrogen-fixing cultures in light or in darkness when supplemented with fructose. This is the first expression analysis of a cgt gene from a cyanobacterium.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 168 (1998), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The filamentous cyanobacteria Symploca PCC 8002 (Symploca) and Trichodesmium spp. fix nitrogen aerobically in the light in a light/dark cycle, without forming specialized thick-walled cells (heterocysts). Even though they do not form heterocysts, we amplified and sequenced a segment of a key regulatory gene in heterocyst differentiation, the hetR gene, from Symploca, Trichodesmium erythraeum and Leptolyngbya PCC 73110 (which fixes nitrogen anaerobically) using degenerate oligonucleotides. The transcriptional level of hetR in Symploca PCC 8002 was examined in relation to nifH expression during nitrogen step-down. The expression pattern of hetR suggests that it was not induced during removal of combined nitrogen, as is the case with the heterocystous cyanobacteria. This is the first report of sequences corresponding to a portion of hetR from within the group of non-heterocystous cyanobacteria.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 30 (1999), S. 0 
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The genetic diversity of Trichodesmium, a marine nitrogen-fixing non-heterocystous cyanobacterium of great ecological importance, was examined using the partial gene sequences of the small subunit ribosomal RNA (16S rDNA) gene and the regulatory gene hetR. Different species and morphotypes (fusiform and spherical colonies) of Trichodesmium were collected in the northern Caribbean Sea, the central Atlantic Ocean and southern Pacific Ocean. The trichome morphologies were observed with light microscopy before DNA extraction and PCR amplification. Phylogenetic analysis of 16S rDNA revealed that all cyanobacterial sequences from the colonies of Trichodesmium spp. were very closely related to the laboratory culture of Trichodesmium sp. NIBB 1067. The overall results from the hetR analysis were congruent with that of 16S rDNA, but the variation in nucleotide sequence between different species was higher within the hetR gene. The sequence data showed that three main clades were represented. One clade comprised sequences from Trichodesmium hildebrandtii Gomont and Trichodesmium thiebautii Gomont (including both its fusiform and spherical colony forms). Sequences from Trichodesmium contortum Wille and Trichodesmium tenue Wille constituted a second clade. The third clade contained Trichodesmium erythraeum Ehrenberg together with the two laboratory strains of this species, Trichodesmium sp. NIBB 1067 and Trichodesmium sp. IMS 101.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 118 (1994), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract In Trichodesmium contortum, nitrogenase was detected in only a limited number (about 10%) of microscopically distinguishable, consecutively arranged cells in central regions of the trichomes. Cells with nitrogenase also contained the photosystem II associated pigment phycoerythrin. These cells were not distinguishable from other cells on a structural basis, but were clearly visible at low magnification microscopy as all in the zone were more compact and shorter than those on either side. The compartmentalisation of nitrogenase into a chain of cells and in a possibly photosynthetic environment represents a previously undescribed phenomenon. The nitrogenase containing cells apparently perform the O2 protective function of heterocysts yet are different in several aspects.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Parasitism within the group of dinoflagellates is a widespread phenomenon. Whether the parasitic dinoflagellates exhibit specificity in their infection is not well known, but this possibility has become an important issue in the development of biological control of harmful algal blooms. The 18S rDNA sequences from the parasite Amoebophrya sp. and its dinoflagellate host Dinophysis norvegica were determined and compared with the published sequence of Amoebophrya sp. infecting Gymnodinium sanguineum and other dinoflagellates. The results showed that the sequence from the parasite within D. norvegica was clustered with that of the one from G. sanguineum with 100% bootstrap support in a maximum-likelihood analysis. The observed identity between these two sequences was 93%, which indicates that they are not identical species. The two sequences from Amoebophrya sp. were deeply branched within the group of dinoflagellate sequences and represent the earliest diverging dinoflagellates. The sequence from the parasite Parvilucifera infectans, also infecting D. norvegica, was not closely related to the Amoebophrya sp. sequences. The sequence from D. norvegica appeared as a sister group to a cluster containing Prorocentrum lima and Alexandrium spp. without significant bootstrap support. The data presented herein support the hypothesis that A. ceratii comprises more than one species, and this opens the possibility that infections of harmful algal species might involve more than one Amoebophrya species.
    Type of Medium: Electronic Resource
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  • 6
    Publication Date: 2018-08-15
    Description: Observations of the dinoflagellate Dinophysis norvegica in the Baltic Sea during the summers of 1991–1993 indicate that maximal abundances (c 40–150 × 103 cells l-1) were found at the thermocline, typically at 12°C. Maximum densities were usually between 12 and 15 m where 2·9% and 1·5% of surface photon irradiances, respectively, were measured. No diel vertical migration was observed, and cell densities in the mixed layer were always low. Photosynthesis versus irradiance measurements with an oxygen electrode indicated that these populations had a P max of 2·47 [coefficient of variation (CV) 7·3%] and 3·4 (CV 4·7%) mg O2 mg Chl a -1 h-1, and compensation values of photon irradiance were 16·5 and 83 μmol m-2 s-1 in 1992 and 1993, respectively. Both oxygen electrode and 14C light/dark bottle measurements indicated that D. norvegica had very little net photosynthesis at the depths where it was most abundant; it would have had about 2·5-fold greater capacity at photon irradiances present closer to the surface. Calculated carbon doubling times via photosynthesis averaged 4–11 months. There was no observable diel rhythym of DNA synthesis, suggesting that either D. norvegica was not dividing synchronously (asynchronous division is common in heterotrophs) or not dividing at all. Electron microscopy did not reveal the presence of food vacuoles, but feeding and digestion could have been extracellular. The data suggest that this species is a mixotroph which received its primary nutrition via heterotrophic means during our observation periods in the summers of 1991–1993.
    Type: Article , PeerReviewed
    Format: text
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