Marine Cyanobacterium Trichodesmium Research Articles

Structure and Mechanism of Iron Translocation by a Dps Protein from Microbacterium arborescens

Dps (DNA protection during starvation) enzymes are a major class of dodecameric proteins that bacteria use to detoxify their cytosol through the uptake of reactive iron species. In the stationary growth phase of bacteria, Dps enzymes are primarily used to protect DNA by biocrystallization. To characterize the wild type Dps protein from Microbacterium arborescens that displays additional catalytic functions (amide hydrolysis and synthesis), we determined the crystal structure to a resolution of 2.05 Å at low iron content. The structure shows a single iron at the ferroxidase center coordinated by an oxo atom, one water molecule, and three ligating residues. An iron-enriched protein structure was obtained at 2 Å and shows the stepwise uptake of two hexahydrated iron atoms moving along channels at the 3-fold axis before a restriction site inside the channels requires removal of the hydration sphere. Supporting biochemical data provide insight into the regulation of this acylamino acid hydrolase. Moreover, the peroxidase activity of the protein was determined. The influence of iron and siderophores on the expression of acylamino acid hydrolase was monitored during several stages of cell growth. Altogether our data provide an interesting view of an unusual Dps-like enzyme evolutionarily located apart from the large Dps sequence clusters.

Decoupling of ammonium regulation and ntcA transcription in the diazotrophic marine cyanobacterium Trichodesmium sp. IMS101.

Nitrogen (N) physiology in the marine cyanobacterium Trichodesmium IMS101 was studied along with transcript accumulation of the N-regulatory gene ntcA and of two of its target genes: napA (nitrate assimilation) and nifH (N(2) fixation). N(2) fixation was impaired in the presence of nitrite, nitrate and urea. Strain IMS101 was capable of growth on these combined N sources at <2 μM but growth rates declined at elevated concentrations. Assimilation of nitrate and urea was impaired in the presence of ammonium. Whereas ecologically relevant N concentrations (2-20 μM) suppressed growth and assimilation, much higher concentrations were required to affect transcript levels. Transcripts of nifH accumulated under nitrogen-fixing conditions; these transcript levels were maintained in the presence of nitrate (100 μM) and ammonium (20 μM). However, nifH transcript levels were below detection at ammonium concentrations >20 μM. napA mRNA was found at low levels in both N(2)-fixing and ammonium-utilizing filaments, and it accumulated in filaments grown with nitrate. The positive effect of nitrate on napA transcription was abolished by ammonium additions of >200 μM. This effect was restored upon addition of the glutamine synthetase inhibitor L-methionin-DL-sulfoximine. Surprisingly, ntcA transcript levels remained high in the presence of ammonium, even at elevated concentrations. These findings indicate that ammonium repression is decoupled from transcriptional activation of ntcA in Trichodesmium IMS101.

First Evidence of Palytoxin and 42-Hydroxy-palytoxin in the Marine Cyanobacterium Trichodesmium

Marine pelagic diazotrophic cyanobacteria of the genus Trichodesmium (Oscillatoriales) are widespread throughout the tropics and subtropics, and are particularly common in the waters of New Caledonia. Blooms of Trichodesmium are suspected to be a potential source of toxins in the ciguatera food chain and were previously reported to contain several types of paralyzing toxins. The toxicity of water-soluble extracts of Trichodesmium spp. were analyzed by mouse bioassay and Neuroblastoma assay and their toxic compounds characterized using liquid chromatography coupled with tandem mass spectrometry techniques. Here, we report the first identification of palytoxin and one of its derivatives, 42-hydroxy-palytoxin, in field samples of Trichodesmium collected in the New Caledonian lagoon. The possible role played by Trichodesmium blooms in the development of clupeotoxism, this human intoxication following the ingestion of plankton-eating fish and classically associated with Ostreopsis blooms, is also discussed.

A historical analysis of the potential nutrient supply from the N2 fixing marine cyanobacterium Trichodesmium spp. to Karenia brevis blooms in the eastern Gulf of Mexico

Blooms of Karenia brevis co-occur with populations of the N2 fixing cyanobacterium Trichodesmium on the West Florida shelf where iron (Fe) and phosphorus (P) supplies have been shown to control the growth potential of these cyanophytes. Historical data records of Trichodesmium presence and abundance (1960–2008) were analyzed in relation to the nutrient requirements of annually coincident K. brevis blooms, focusing on the potential direct supply of nitrogen (N) via N2-fixation with subsequent excretion of recently fixed N2 as NH4+ and dissolved organic nitrogen and indirect transfer from Trichodesmium biomass (as particulate N and P) during cell death. While release of “new” N from biological N2-fixation can supply up to 40% of the 2001 large red tide (9.5 × 106 cells L−1), estimates of the total N available, including the regeneration of additional nutrients supplied from particulate stocks aggregated within surface populations of observed Trichodesmium biomass during cell death, suggest that up to 100% of N and P requirements of such large blooms can be met from N2-fixation sources.

Two flavodoxin genes in Trichodesmium (Oscillatoriales, Cyanophyceae): Remarkable sequence divergence and possible functional diversification

We analyzed flavodoxin gene sequences and transcription patterns in the marine nitrogen-fixing cyanobacterium Trichodesmium Ehrenberg ex Gomont 1892. While a typical cyanobacterial flavodoxin ortholog ( fld1) was identified from cultured (strain IMS101) and environmental Trichodesmium by PCR and Southern blot hybridization, a second flavodoxin ( fld2) was identified in the genome sequence. BLAST and phylogenetic analyses indicated that the two fld genes were highly divergent: fld1 was most closely related to fld common in cyanobacteria, wheras fld2 formed a distinct cluster with a fld so far only found in the unicellular diazotrophic cyanobacteria Cyanothece and Crocosphaera (in which fld2 was the only fld). The fld2 cluster was more closely allied with a fld in non-cyanobacterial diazotrophs such as Azotobacter and Azoarcus than fld1 in other cyanobacteria. This result suggests different evolutionary history of these two genes. Real-Time RT–PCR analysis on iron-replete and iron-deplete Trichodesmium cultures revealed remarkable diel dynamics in transcription of both flds but surprisingly failed to show induction under iron stress. Addition of nitrate to these cultures depressed nifH and fld2 transcription while elevating the transcription of fld1 in iron-stressed cultures. A positive correlation between fld and nifH transcript abundances was found, which was stronger in the case of fld2 than fld1. Our data suggest that these two flavodoxins in Trichodesmium may be functionally diversified and that use of flavodoxin as an iron stress indicator needs to be validated for each organism with consideration of diel dynamics of gene expression.

Reversible coupling of individual phycobiliprotein isoforms during state transitions in the cyanobacterium Trichodesmium analysed by single-cell fluorescence kinetic measurements

In the non-heterocyst, marine cyanobacterium Trichodesmium nitrogen fixation is confined to the photoperiod and occurs coevally with oxygenic photosynthesis although nitrogenase is irreversibly inactivated by oxygen. In previous studies it was found that regulation of photosynthesis for nitrogen fixation involves Mehler reaction and various activity states with reversible coupling of photosynthetic components. We now investigated these activity states in more detail. Spectrally resolved fluorescence kinetic measurements of single cells revealed that they were related to alternate uncoupling and coupling of phycobilisomes from and to the photosystems, changing the effective cross-section of PSII. Therefore, we isolated and purified the phycobiliproteins of Trichodesmium via ion exchange chromatography and recorded their UV/VIS absorption, fluorescence excitation and fluorescence emission spectra. After describing these spectra by mathematical equations via the Gauss-Peak-Spectra method, we used them to deconvolute the in vivo fluorescence spectra of Trichodesmium cells. This revealed that the contribution of different parts of the phycobilisome antenna to fluorescence quenching changed during the daily activity cycle, and that individual phycobiliproteins can be reversibly coupled to the photosystems, while the expression levels of these proteins did not change much during the daily activity cycle. Thus we propose that variable phycobilisome coupling plays a key role in the regulation of photosynthesis for nitrogen fixation in Trichodesmium.

Aerobic hydrogen production and dinitrogen fixation in the marine cyanobacterium Trichodesmium erythraeum IMS101

Rates of hydrogen production and acetylene reduction were measured in aerobic cultures of the marine cyanobacterium Trichodesmium erythraeum IMS101 grown in a supplemented seawater medium low in combined inorganic nitrogen. Both hydrogen production and acetylene reduction conformed to a circadian pattern with maximum activity in the afternoon. Normalized hydrogen production rates ranged from 0.06 to 0.71 nmol H2 [g chlorophyll a (Chl a)‐1 h‐1, while nitrogen fixation rates, calculated using an assumed ratio of 4 mol acetylene to 1 mol dinitrogen, ranged from 0.12 to 4.71 nmol N2 Chl a−1 h−1. Yields of hydrogen from nitrogen fixation were in the range 0.15–0.48 mol H2 evolved per mol N2 reduced. A comparatively low net rate of H2 uptake was observed in one culture during the dark period (20.01 nmol H2 [g Chl a−1 h−1). These measurements suggest that T. erythraeum is potentially a net source of hydrogen to the low‐latitude surface ocean.

Saharan dust and phosphatic fidelity: A three-dimensional biogeochemical model of Trichodesmium as a nutrient source for red tides on the West Florida Shelf

The availability of iron within the surface waters of the broad, oligotrophic West Florida Shelf (WFS) controls periodic blooms of the pelagic marine cyanobacterium Trichodesmium. Summer delivery of Saharan dust provided adequate iron (Fe) to shift limitation of growth to the availability of phosphorus (P). Florida's rivers drain Miocene phosphorus deposits to provide the WFS with freshwater nutrient supplies at molar dissolved inorganic nitrogen/phosphate (DIN/PO 4) ratios of <6. These diazotrophs draw upon ubiquitous stocks of dissolved nitrogen gas, once stimulated by Fe-deposition within P-replete waters of the WFS. An extensive in situ data set collected between 1998 and 2001 (NEGOM/ECOHAB) provided plankton taxonomy, hydrographic, nutrient, dissolved organic matter (DOM), pigment, and optical properties on the shelf. We constructed a three-dimensional numerical model to analyze the impact of iron fertilization of the diazotroph Trichodesmium and the resultant effect upon the elemental cycles of N, P, and Fe. The coupled physical and ecological models show that the wet deposition of Fe-rich Saharan dust was necessary to stimulate enough nitrogen fixation to initialize the toxic red tide ( Karenia brevis) of ∼20 μg chl a l −1 that occurred in October 1999. The simulation suggests that the magnitude and longevity of the Trichodesmium population, and therefore this source of ‘new’ nitrogen, was controlled by both phosphorus and iron availability.

Structure of Trichamide, a Cyclic Peptide from the Bloom-Forming Cyanobacterium Trichodesmium erythraeum , Predicted from the Genome Sequence

A gene cluster for the biosynthesis of a new small cyclic peptide, dubbed trichamide, was discovered in the genome of the global, bloom-forming marine cyanobacterium Trichodesmium erythraeum ISM101 because of striking similarities to the previously characterized patellamide biosynthesis cluster. The tri cluster consists of a precursor peptide gene containing the amino acid sequence for mature trichamide, a putative heterocyclization gene, an oxidase, two proteases, and hypothetical genes. Based upon detailed sequence analysis, a structure was predicted for trichamide and confirmed by Fourier transform mass spectrometry. Trichamide consists of 11 amino acids, including two cysteine-derived thiazole groups, and is cyclized by an N C terminal amide bond. As the first natural product reported from T. erythraeum, trichamide shows the power of genome mining in the prediction and discovery of new natural products.

Modeling the dynamic regulation of nitrogen fixation in the cyanobacterium Trichodesmium sp.

A physiological, unbalanced model is presented that explicitly describes growth of the marine cyanobacterium Trichodesmium sp. at the expense of N(2) (diazotrophy). The model involves the dynamics of intracellular reserves of carbon and nitrogen and allows the uncoupling of the metabolism of these elements. The results show the transient dynamics of N(2) fixation when combined nitrogen (NO(3)(-), NH(4)(+)) is available and the increased rate of N(2) fixation when combined nitrogen is insufficient to cover the demand. The daily N(2) fixation pattern that emerges from the model agrees with measurements of rates of nitrogenase activity in laboratory cultures of Trichodesmium sp. Model simulations explored the influence of irradiance levels and the length of the light period on fixation activity and cellular carbon and nitrogen stoichiometry. Changes in the cellular C/N ratio resulted from allocations of carbon to different cell compartments as demanded by the growth of the organism. The model shows that carbon availability is a simple and efficient mechanism to regulate the balance of carbon and nitrogen fixed (C/N ratio) in filaments of cells. The lowest C/N ratios were obtained when the light regime closely matched nitrogenase dynamics.

Overexpression and Characterization of an Iron Storage and DNA-Binding Dps Protein from Trichodesmium erythraeum

Although the role of iron in marine productivity has received a great deal of attention, no iron storage protein has been isolated from a marine microorganism previously. We describe an Fe-binding protein belonging to the Dps family (DNA binding protein from starved cells) in the N(2)-fixing marine cyanobacterium Trichodesmium erythraeum. A dps gene encoding a protein with significant levels of identity to members of the Dps family was identified in the genome of T. erythraeum. This gene codes for a putative Dps(T. erythraeurm) protein (Dps(tery)) with 69% primary amino acid sequence similarity to Synechococcus DpsA. We expressed and purified Dps(tery), and we found that Dps(tery), like other Dps proteins, is able to bind Fe and DNA and protect DNA from degradation by DNase. We also found that Dps(tery) binds phosphate, like other ferritin family proteins. Fe K near-edge X-ray absorption of Dps(tery) indicated that it has an iron core that resembles that of horse spleen ferritin.

Plasticity of N:P ratios in laboratory and field populations of Trichodesmium spp.

AME Aquatic Microbial Ecology Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout the JournalEditorsSpecials AME 42:243-253 (2006) - doi:10.3354/ame042243 Plasticity of N:P ratios in laboratory and field populations of Trichodesmium spp. Jamie M. Krauk1,5, Tracy A. Villareal2, Jill A. Sohm3, Joseph P. Montoya4, Douglas G. Capone3,* 1Chesapeake Biological Laboratory, University of Maryland Center for Environmental Sciences, Solomons, Maryland 20615, USA 2Marine Science Institute, The University of Texas at Austin, 750 Channel View Dr., Port Aransas, Texas 78373, USA 3Wrigley Institute for Environmental Studies and Department of Biological Sciences University of Southern California, Los Angeles, California 90089, USA 4School of Biology, Georgia Institute of Technology, Atlanta, Georgia 30332, USA 5Present address: National Sea Grant Office, Department of Commerce, National Oceanic and Atmospheric Administration, 1315 East West Highway, R/SG, SSMC 3 room 11853, Silver Spring, Maryland 20910, USA *Corresponding author. Email: capone@usc.edu ABSTRACT: We followed changes in N:P ratios in batch cultures of the planktonic marine cyanobacterium Trichodesmium (IMS 101) grown in 2 different media and in field populations from 4 different oceanic regions. Cultures grown on low P media showed a rapid rise in N:P ratio upon depletion of phosphate. Ratios exceeding 125 were reached in 1 experiment before attaining stationary phase. A transect across the North Atlantic Ocean along 32°N showed a monotonic decrease in the N:P ratio of field collected colonies, dropping from about 60:1 on the western side of the basin to about 30:1 on the eastern side. A second cruise sampled colonies and surface slicks in waters along the north coast of Australia, where ratios of N:P were generally lower than in the North Atlantic, ranging from 11:1 to 47:1 with an average of 22:1. A comparison of rising and sinking colonies collected at 8 stations in the Gulf of Mexico shows a higher mean N:P ratio among sinking colonies than floating colonies. Overall, the average N:P in the Gulf of Mexico was about 68:1. N:P ratios of Trichodesmium around the Hawaiian Islands were very consistent between 2 consecutive years of sampling, with an average colony N:P for both years of about 38:1. Our research demonstrates high variability in the cellular N:P in Trichodesmium both in the laboratory and in the field. Trichodesmium N:P ratio may provide an index to the relative severity of P limitation in these diazotrophs. Geochemical and ecological modeling efforts which rely on using the N:P ratio of diazotrophs in deriving nitrogen fixation rates should account for the variability of these ratios in situ. KEY WORDS: Trichodesmium · N:P ratio · Nitrogen fixation · Diazotroph · Cyanobacteria Full text in pdf format PreviousNextExport citation RSS - Facebook - Tweet - linkedIn Cited by Published in AME Vol. 42, No. 3. Online publication date: March 29, 2006 Print ISSN: 0948-3055; Online ISSN: 1616-1564 Copyright © 2006 Inter-Research.

Traffic lights in trichodesmium. Regulation of photosynthesis for nitrogen fixation studied by chlorophyll fluorescence kinetic microscopy.

We investigated interactions between photosynthesis and nitrogen fixation in the non-heterocystous marine cyanobacterium Trichodesmium IMS101 at the single-cell level by two-dimensional (imaging) microscopic measurements of chlorophyll fluorescence kinetics. Nitrogen fixation was closely associated with the appearance of cells with high basic fluorescence yield (F(0)), termed bright cells. In cultures aerated with normal air, both nitrogen fixation and bright cells appeared in the middle of the light phase. In cultures aerated with 5% oxygen, both processes occurred at a low level throughout most of the day. Under 50% oxygen, nitrogen fixation commenced at the beginning of the light phase but declined soon afterwards. Rapid reversible switches between fluorescence levels were observed, which indicated that the elevated F(0) of the bright cells originates from reversible uncoupling of the photosystem II (PSII) antenna from the PSII reaction center. Two physiologically distinct types of bright cells were observed. Type I had about double F(0) compared to the normal F(0) in the dark phase and a PSII activity, measured as variable fluorescence (F(v) = F(m) - F(0)), similar to normal non-diazotrophic cells. Correlation of type I cells with nitrogen fixation, oxygen concentration, and light suggests that this physiological state is connected to an up-regulation of the Mehler reaction, resulting in oxygen consumption despite functional PSII. Type II cells had more than three times the normal F(0) and hardly any PSII activity measurable by variable fluorescence. They did not occur under low-oxygen concentrations, but appeared under high-oxygen levels outside the diazotrophic period, suggesting that this state represents a reaction to oxidative stress not necessarily connected to nitrogen fixation. In addition to the two high-fluorescence states, cells were observed to reversibly enter a low-fluorescence state. This occurred mainly after a cell went through its bright phase and may represent a fluorescence-quenching recovery phase.

CHARACTERIZATION OF MICROBIALITE‐FORMING CYANOBACTERIA IN A TROPICAL LAGOON: TIKEHAU ATOLL, TUAMOTU, FRENCH POLYNESIA

Natural populations of benthic cyanobacteria in the lagoon of Tikehau Atoll in French Polynesia were studied using a polyphasic approach that combined field observations, LM, culturing, and molecular sequencing. The approach assessed their phenotypic (morphotypic and ecological) and genotypic diversity. Partial sequences (approximately 450 bp long) of the PCR‐amplified 16S rRNA gene were obtained from both natural and cultured populations using cyanobacteria‐specific primers. The sequences obtained clustered into six separate phylogenetic clusters in relation to the complete set of 16S rRNA sequences available in public databases. Phylogenetic clustering correlated in many cases with some morphological characteristics. For example, Spirulina subsalsa could be identified to the morphospecies level using both molecular and microscopic approaches. Morphotypes identified as Symploca hydnoides (Kütz. ex Gomont) TK22, Phormidium sp. TK1, and P. laysanense (Lemmerman) TK14 formed a distinct cluster. The morphogenus Hydrocoleum (Blennothrix) clustered interestingly close to the morphologically similar, but planktonic, marine cyanobacterium Trichodesmium, suggesting a relationship. Other sequences belonging to morphotaxa with very narrow trichomes were found to be polyphyletic. Enrichment cultures, with inoculum obtained from field populations, were followed over a period of 18 months. Dominance in all cultures shifted over time in favor of a set of cyanobacterial strains with narrow trichomes, which were phenotypically and phylogenetically different from natural populations dominating the original samples. Sequences from strains enriched by cultivation clustered into two well‐defined phylogenetic groups, possibly identifying new taxa. These clusters may represent a niche of opportunistic species, evolved to exploit short‐term nutrient spikes in the environment.

Phosphorus limitation of nitrogen fixation by Trichodesmium in the central Atlantic Ocean.

Marine fixation of atmospheric nitrogen is believed to be an important source of biologically useful nitrogen to ocean surface waters, stimulating productivity of phytoplankton and so influencing the global carbon cycle. The majority of nitrogen fixation in tropical waters is carried out by the marine cyanobacterium Trichodesmium, which supplies more than half of the new nitrogen used for primary production. Although the factors controlling marine nitrogen fixation remain poorly understood, it has been thought that nitrogen fixation is limited by iron availability in the ocean. This was inferred from the high iron requirement estimated for growth of nitrogen fixing organisms and the higher apparent densities of Trichodesmium where aeolian iron inputs are plentiful. Here we report that nitrogen fixation rates in the central Atlantic appear to be independent of both dissolved iron levels in sea water and iron content in Trichodesmium colonies. Nitrogen fixation was, instead, highly correlated to the phosphorus content of Trichodesmium and was enhanced at higher irradiance. Furthermore, our calculations suggest that the structural iron requirement for the growth of nitrogen-fixing organisms is much lower than previously calculated. Although iron deficiency could still potentially limit growth of nitrogen-fixing organisms in regions of low iron availability-for example, in the subtropical North Pacific Ocean-our observations suggest that marine nitrogen fixation is not solely regulated by iron supply.

ALKALINE PHOSPHATASE ACTIVITIES AMONG POPULATIONS OF THE COLONY‐FORMING DIAZOTROPHIC CYANOBACTERIUM TRICHODESMIUM SPP. (CYANOBACTERIA) IN THE RED SEA

Alkaline phosphatase activities of the diazotrophic marine cyanobacterium Trichodesmium were studied among natural populations in the northern Red Sea and in laboratory cultures of Trichodesmium sp. strain WH9601. Open‐water tuft‐shaped colonies of Trichodesmium showed high alkaline phosphatase activities with 2.4–11.7 μmol p‐nitrophenylphosphate (PNPP) hydrolyzed·μg chl a−1·h−1, irrespective of date or origin of the sample. Coastal populations of the Trichodesmium tuft colonies had low alkaline phosphatase activities with 0.2–0.5 μmol PNPP·μg chl a−1·h−1. An exception was the Trichodesmium fall maximum, when both tuft colonies and the plankton community (&lt;100 μm) had alkaline phosphatase activities of 0.6–7.4 μmol PNPP·μg chl a−1·h−1. Likewise, the more rare puff and bow‐tie colonies of Trichodesmium spp. in coastal waters had elevated alkaline phosphatase activities (0.8–1.6 μmol PNPP·μg chl a−1·h−1) as compared with tuft colonies coinhabiting the same waters. Intact filaments of tuft‐forming Trichodesmium sp. strain WH9601 from phosphate‐replete cultures had a base alkaline phosphatase activity of 0.5 μmol PNPP·μg chl a−1·h−1. This activity underwent a 10‐fold increase in phosphate‐deplete cultures and in cultures supplied with glycerophosphate as the sole P source. The elevated level of alkaline phosphatase activity was sustained in P‐deplete cultures, but it declined in cultures with glycerophosphate. The decline is suggested to result from feedback repression of alkaline phosphatase synthesis by the phosphate generated in the glycerophosphate hydrolysis. The enhanced alkaline phosphatase activities of Trichodesmium spp. populations provide evidence that P stress is an important factor in the ecology of Trichodesmium in the northern Red Sea.

Temporal Variability in Nitrogenase Gene Expression in Natural Populations of the Marine Cyanobacterium Trichodesmium thiebautii

We report a distinct diel periodicity in the abundance of nifH (dinitrogenase reductase) mRNA in natural populations of the nonheterocystous marine cyanobacterium Trichodesmium thiebautii. Our observations show that in addition to translational and posttranslational controls, Trichodesmium nitrogenase expression is also regulated at the transcriptional and/or posttranscriptional level.

Isolation of nifH and part of nifD by modified capture polymerase chain reaction from a natural population of the marine cyanobacterium Trichodesmium sp.

A modified capture polymerase chain reaction (CPCR) technique was used to isolate the entire sequence of the nifH gene and its flanking regions from a natural population of Trichodesmium sp. A set of specific CPCR primers derived from a known 72-bp DNA segment of the nifH sequence permitted isolation of both the upstream and the downstream region of Trichodesmium sp. nifH. The 882-bp nifH gene presented here is the first full-length gene isolated from Trichodesmium sp. A sequence similar to a nif-like promoter was found in front of nifH. The nifH open reading frame of Trichodesmium sp. encoded 294 amino acids. Comparative analysis of the Trichodesmium sp. NifH sequence revealed strong similarity with 23 known NifH proteins. Amino acids postulated to be involved in binding of the 4Fe:4S cluster and those subjected to ADP-ribosylation were present. An open reading frame for the nifD gene was identified 189 bp downstream of nifH. A sequence similar to the consensus of the nif-like promoter was also found in front of nifD.

SeaWiFS potential for remote sensing of marine Trichodesmium at sub-bloom concentration

Abstract The SeaWiFS potential for identifying the marine cyanobacterium Trichodesmium, at low concentration in oligotrophic case I waters, has been investigated by numerical simulations using a three-component model of sea colour. The results obtained indicate that simple algorithms, which operate on data recorded by SeaWiFS bands 2, 3. and 5, should have the capability to discriminate pixels containing Trichodesmium at concentrations as low as 0·1–0·3 mgm-3 chlorophyll a, as well as to yield an estimate of the concentration. The validity range of the procedure has been explored by a sensitivity analysis, assuming realistic variations in the input data to the optical model.

Toxic effect of the bloom-forming Trichodesmium sp. (Cyanophyta) to the copepod Acartia tonsa.

The toxicity of the marine cyanobacterium Trichodesmium sp. to the copepod Acartia tonsa was assessed in a series of experiments during a Trichodesmium bloom off the North Carolina coast in late October 1992. Healthy intact cells of Trichodesmium sp. were not toxic to A. tonsa and were ingested by A. tonsa when no other foods were available. However, homogenized Trichodesmium cells were toxic to A. tonsa, suggesting that Trichodesmium sp. contains certain type(s) of intracellular biotoxins. This hypothesis was consistent with the observed high mortality when A. tonsa was treated with aging Trichodesmium sp. cells or with filtered cell homogenate. The affected copepods showed weakness, recumbency, and reduced responsiveness. Many were observed to have distended intestines. Bioassays using aged Trichodesmium sp. cells and filtered homogenate demonstrated a dose-dependent effect on A. tonsa survival.