Freshwater Cyanobacteria Research Articles

Temperature effects on growth rates and fatty acid content in freshwater algae and cyanobacteria

Mass cultivation of algae for biofuel and other bioproduct production in outdoor, open raceway ponds has some considerable economic advantages. However, these systems would be subject to fluctuations in temperature (among other environmental factors), which can have dramatic effects on the growth rates of algal species and impact the overall productivity and quality of targeted algal crops. This study sought to elucidate the effects of temperature on algal growth rates, biomass accumulation, fatty acid production and composition. We surveyed 26 algal species from 5 different functional groups, growing them at 6 different temperatures between 9 and 32 °C. For each surveyed species, we collected eco-physiological trait data including maximum growth rate, thermal optimum (Topt), thermal niche width, and lower and upper temperature limits for growth (CTmin and CTmax, respectively); these data were also pooled for analysis at the functional group level. Responses to temperature varied among species, but at the functional group level we determined that the cyanobacteria have the highest thermal optimum (30.6 ± 2.3 °C), followed by chlorophytes (25.7 ± 0.1 °C) and diatoms (24.0 ± 0.4 °C). Temperature-specific fatty acid (FA) production was mostly controlled by growth rates, though some change in production was attributable to modification of intracellular FA stores. Temperature affected FA profiles in diverse ways, with no consistent trends across species or functional groups. In sum, temperature significantly impacts the overall productivity of algal biofuel systems by influencing species growth rates and fatty acid production. While algal growth rates varied predictably with temperature, we did not find the generalizable trends in temperature dependence of FA composition, suggesting that some aspects of algal cultivation for bioproducts in outdoor, open-air systems may be less predictable. However, a compilation of algal growth and FA composition responses to temperature, such as ours, may be useful for choosing appropriate species for given temperature regimes.

Calothrixamides A and B from the Cultured Cyanobacterium Calothrix sp. UIC 10520.

Cyanobacteria are a source of chemically diverse metabolites with potential medicinal and biotechnological applications. Rapid identification of compounds is central to expedite the natural product discovery process. Mass spectrometry has been shown to be an important tool for dereplication of complex natural product samples. In addition, chromatographic separation and complementary spectroscopic analysis (e.g., UV) can enhance the confidence of the dereplication process. Here, we applied a droplet-liquid microjunction-surface sampling probe (droplet probe) coupled with UPLC-PDA-HRMS-MS/MS to identify two new natural products in situ from the freshwater strain Calothrix sp. UIC 10520. This allowed us to prioritize this strain for chemical investigation based on the presence of new metabolites very early in our discovery process, saving both time and resources. Subsequently, calothrixamides A (1) and B (2) were isolated from large-scale cultures, and the structures were elucidated by 1D and 2D NMR spectroscopy and mass spectrometry. The absolute configurations were determined by a combination of chemical degradation reactions, derivatization methods (Mosher's, Marfey's, and phenylglycine methyl ester), and J-based configurational analysis. Calothrixamides showed no cytotoxic activity against the MDA-MB-435, MDA-MB-231, and OVCAR3 cancer cell lines. They represent the first functionalized long-chain fatty acid amides reported from the Calothrix genus and from a freshwater cyanobacterium.

ACUTE TOXICITY OF THE ETHANOL EXTRACT AND ETHYL ACETATE FRACTION OF EUPATORIUM FORTUNEI TO DAPHNIA MAGNA

Previous studies have shown that the crude ethanol extract and its ethylacetate fraction of the plant Eupatorium fortunei Turcz strongly inhibited the growth of a harmful freshwater cyanobacterium Microcystis aeruginosa. However, the perspective of using these plant extracts as alternative algicides takes into account their potential risks to other species in aquatic ecosystems, including Daphnia magna. The current study presents the acute toxicity of the extracts to D. magna. The median lethal concentrations, immobilizing 50 % of D. magna, (LC50) after 24 and 48 h of the ethanol extract were 247 and 183 mg L-1, respectively. In the exposure to ethyl acetate fraction, the values of 24h-LC50 and 48h-LC50 were 47 and 13 mg L-1, respectively. The values of dissolved oxygen (DO) and pH in the control and treatments had little change during the 48-hour experiment period, fluctuating from 6.44 ÷ 7.90 and 6.07 ÷ 7.78 mg L-1, respectively, and they were still good conditions for D.magna growth. Finally, these results prove clearly that the ethyl acetate fraction is more toxic to the freshwater cladoceran than the ethanol extract. To our knowledge, it is the first report of the acute toxic estimation of E. fortunei extracts to zooplankton species, D. magna. Chronic toxicity of these extracts to D. magna needs to be studied in next step.

Requirement of alkanes for salt tolerance of Cyanobacteria: characterization of alkane synthesis genes from salt-sensitive Synechococcus elongatus PCC7942 and salt-tolerant Aphanothece halophytica

Cyanobacteria have been attracting great interest in the research area of biofuel production. All Cyanobacteria contain C15 -C19 hydrocarbons, but physiological roles of hydrocarbons remain to be clarified. In this study, it was found that the deletion mutant of alkane synthesis genes in fresh water cyanobacterium Synechococcus elongates PCC 7942 was incapable to produce alkanes and salt sensitive. The alkane synthesis gene from halotolerant cyanobacterium Aphanothece halophytica was salt induced and produced a significant amount of alkanes at high salinity. These results demonstrate the alkane synthesis genes from A.halophytica could be a promising candidate for future biofuel application.

Physiological properties and genetic analysis related to exopolysaccharide (EPS) production in the fresh-water unicellular cyanobacterium Aphanothece sacrum (Suizenji Nori).

The clonal strains, phycoerythrin(PE)-rich- and PE-poor strains, of the unicellular, fresh water cyanobacterium Aphanothece sacrum (Suringar) Okada (Suizenji Nori, in Japanese) were isolated from traditional open-air aquafarms in Japan. A. sacrum appeared to be oligotrophic on the basis of its growth characteristics. The optimum temperature for growth was around 20°C. Maximum growth and biomass increase at 20°C was obtained under light intensities between 40 to 80 μmol m-2 s-1 (fluorescent lamps, 12 h light/12 h dark cycles) and between 40 to 120 μmol m-2 s-1 for PE-rich and PE-poor strains, respectively, of A. sacrum . Purified exopolysaccharide (EPS) of A. sacrum has a molecular weight of ca. 104 kDa with five major monosaccharides (glucose, xylose, rhamnose, galactose and mannose; ≥85 mol%). We also deciphered the whole genome sequence of the two strains of A. sacrum. The putative genes involved in the polymerization, chain length control, and export of EPS would contribute to understand the biosynthetic process of their extremely high molecular weight EPS. The putative genes encoding Wzx-Wzy-Wzz- and Wza-Wzb-Wzc were conserved in the A. sacrum strains FPU1 and FPU3. This result suggests that the Wzy-dependent pathway participates in the EPS production of A. sacrum.

Physiological sensitivity of Haematococcus pluvialis (Chlorophyta) to environmental pollutants: a comparison with Microcystis wesenbergii (cyanobacteria) and Pseudokirchneriella subcapitata (Chlorophyta)

Haematococcus pluvialis is beneficial to human health and is important for commercial use. However, it seldom prevails in permanent freshwater bodies. Increasing environmental pollutants from anthropogenic activity may threaten the wide distribution of H. pluvialis. Here, we quantified and compared the adverse effects of the common pesticides atrazine, pentachlorophenol, malathion, and 3,5-dichlorophenol and the heavy metals Cu(II), Cr(VI), and Cd(II) on H. pluvialis, Microcystis wesenbergii (a freshwater bloom-forming cyanobacterium), and Pseudokirchneriella subcapitata (a standard toxicity test species). We found that H. pluvialis was the species most sensitive to 3,5-dichlorophenol and Cr(VI) exposure and the most tolerant to pentachlorophenol exposure according to IC50, changes in chlorophyll a content, maximum electron transport rates (ETRmax), the quantum efficiency of photosystem II (Fv/Fm), and esterase activity. Haematococcus pluvialis was also the species most sensitive to atrazine according to IC50, chlorophyll a, and ETRmax. Overall, our findings suggest that atrazine, 3,5-dichlorophenol, and Cr(VI) are potential factors limiting the distribution of H. pluvialis. We suggest that H. pluvialis can be a potentially useful bioindicator for evaluating pollutants. Furthermore, ETRmax, FDA assay, and flow cytometry can be combined with Haematococcus to test for toxicity.

The influence of sigma factors and ribosomal recognition elements on heterologous expression of cyanobacterial gene clusters in Escherichia coli.

Cyanobacterial natural products offer new possibilities for drugs and lead compounds but many factors can inhibit the production of sufficient yields for pharmaceutical processes. While Escherichia coli and Streptomyces sp. have been used as heterologous expression hosts to produce cyanobacterial natural products, they have not met with resounding success largely due to their inability to recognize cyanobacterial promoter regions. Recent work has shown that the filamentous freshwater cyanobacterium Anabaena sp. strain PCC 7120 recognizes various cyanobacterial promoter regions and can produce lyngbyatoxin A from the native promoter. Introduction of Anabaena sigma factors into E. coli might allow the native transcriptional machinery to recognize cyanobacterial promoters. Here, all 12 Anabaena sigma factors were expressed in E. coli and subsets were found to initiate transcription from several cyanobacterial promoters based on transcriptional fusions to the chloramphenicol acetyltransferase (CAT) reporter. Expression of individual Anabaena sigma factors in E. coli did not result in lyngbyatoxin A production from its native cyanobacterial gene cluster, possibly hindered by deficiencies in recognition of cyanobacterial ribosomal binding sites by native E. coli translational machinery. This represents an important step toward engineering E. coli into a general heterologous expression host for cyanobacterial biosynthetic gene cluster expression.

4-Oxo-β-apo-13-carotenone from the Cyanobacterium Anabaena cylindrica PCC 7122.

Apocarotenoids are widely distributed among living organisms (bacteria, fungi, algae, plants and even animals) and have been associated with several signaling functions. These compounds are generated by the activity of carotenoid cleavage dioxygenases (CCDs), whose diversity greatly contributes to the large number of apocarotenoids that have been described so far. It is nevertheless expected that a considerable diversity of these molecules is yet to be discovered. In this work, we describe the isolation and structural elucidation of the apocarotenoid 4-oxo-β-apo-13-carotenone from the cultured freshwater cyanobacterium Anabaena cylindrica PCC 7122, corresponding to the first report of this compound from natural sources.

Adaptation of the Freshwater Bloom-Forming Cyanobacterium Microcystis aeruginosa to Brackish Water Is Driven by Recent Horizontal Transfer of Sucrose Genes

Microcystis aeruginosa is a bloom-forming cyanobacterium found in eutrophic water bodies worldwide. M. aeruginosa blooms usually occur in freshwater; however, they have also been reported to occur in brackish water. Because M. aeruginosa often produces the cyanotoxin microcystin, they are a major concern to public health and environment. Despite this, the ecology, genomic basis, and evolutionary process underlying the M. aeruginosa bloom invasion from fresh to brackish water have been poorly investigated. Hence, in the present study, we have sequenced and characterized genomes of two newly discovered salt-tolerant M. aeruginosa strains obtained from Japanese brackish water lakes (Lakes Shinji and Tofutsu). Both genomes contain a set of genes for the synthesis of osmolyte sucrose (sppA, spsA, and susA), hitherto identified in only one strain (PCC 7806) of M. aeruginosa. Chemical and gene expression analyses confirmed sucrose accumulation induced by salt. A comprehensive genetic survey of >200 strains indicated that sucrose genes are extremely rare in M. aeruginosa. Most surprisingly, comparative genome analyses of the three strains indicated extremely low genetic diversity in the sucrose genes compared with other core genome genes, suggesting very recent acquisitions via horizontal transfer. Invasion of M. aeruginosa blooms into brackish water may be a recent event triggered by anthropogenic eutrophication of brackish water.

A Cluster of Five Genes Essential for the Utilization of Dihydroxamate Xenosiderophores in Synechocystis sp. PCC 6803.

The unicellular freshwater cyanobacterium Synechocystis sp. PCC 6803 is capable of using dihydroxamate xenosiderophores, either ferric schizokinen (FeSK) or a siderophore of the filamentous cyanobacterium Anabaena variabilis ATCC 29413 (SAV), as the sole source of iron in the TonB-dependent manner. The fecCDEB1-schT gene cluster encoding a siderophore transport system that is involved in the utilization of FeSK and SAV in Synechocystis sp. PCC 6803 was identified. The gene schT encodes TonB-dependent outer membrane transporter, whereas the remaining four genes encode the ABC-type transporter FecB1CDE formed by the periplasmic binding protein FecB1, the transmembrane permease proteins FecC and FecD, and the ATPase FecE. Inactivation of any of these genes resulted in the inability of cells to utilize FeSK and SAV. Our data strongly suggest that Synechocystis sp. PCC 6803 can readily internalize Fe-siderophores via the classic TonB-dependent transport system.

Solar Photocatalysis Using Fixed-Film TiO2 for Microcystins from Colonial Microcystis aeruginosa

Microcystins (MCs) are endotoxins produced by cyanobacteria in freshwaters globally. With known potential for human health risks, rapid and effective treatment methods are needed for MCs. Previous studies have shown photocatalysis can achieve rapid half-lives with UV lamps and slurries of TiO2. In this experiment, rates and extents of solar photocatalysis of MCs were measured using bench-scale reactors with fixed films of TiO2 for solutions with a range of cellular:aqueous MC ratios. Since cellular MCs can be removed physically, photocatalysis rates were measured following sand filtration to discern the extent of MC removal post-filtration. Since UV energy drives photocatalysis using TiO2, rates of removal were calculated as a function of cumulative UV insolation and time. For water containing 90% aqueous MC treatment, filtration removed 0% MCs, and the photocatalysis half-life for MCs was 0.37 MJ/m2 (or 135 min). Previous studies have used clarified waters; however, results from this study are likely representative of scenarios with waters containing confounding water characteristics and use of solar light for UV, as anticipated in developing countries with less advanced water treatment methods. Photocatalysis is a rapid and effective process for decreasing concentrations of MCs and could be useful for mitigating risks from MC exposures in drinking water.

Post-Translational Tyrosine Geranylation in Cyanobactin Biosynthesis.

Prenylation is a widespread modification that improves the biological activities of secondary metabolites. This reaction also represents a key modification step in biosyntheses of cyanobactins, a family of ribosomally synthesized and post-translationally modified peptides (RiPPs) produced by cyanobacteria. In cyanobactins, amino acids are commonly isoprenylated by ABBA prenyltransferases that use C5 donors. Notably, mass spectral analysis of piricyclamides from a fresh-water cyanobacterium suggested that they may instead have a C10 geranyl group. Here we characterize a novel geranyltransferase involved in piricyclamide biosynthesis. Using the purified enzyme, we show that the enzyme PirF catalyzes Tyr O-geranylation, which is an unprecedented post-translational modification. In addition, the combination of enzymology and analytical chemistry revealed the structure of the final natural product, piricyclamide 7005E1, and the regioselectivity of PirF, which has potential as a synthetic biological tool providing drug-like properties to diverse small molecules.

A report of Cylindrospermopsis raciborskii and other cyanobacteria in the water reservoirs of power plants in Ukraine

The occurrence of cyanobacteria in freshwaters attracts much attention due to its associated health threats and ecological implications. Yet data on the composition of cyanobacteria taxa and toxigenicity in some regions is still scarce. Here, we explored the occurrence of cyanobacteria and cyanotoxins in three locations in Ukraine (reservoir for Kasperivtsi Hydrothermal Power Plant and outflowing River Seret, and cooling pond of Khmelnytsky Atomic Power Plant) in summer 2017. Cyanobacteria were a dominant fraction at all stations. A number of potent-toxin producers were identified including Cylindrospermopsis raciborskii, Aphanizomenon gracile, Dolichospermum flos-aquae, and Planktothrix agardhii. Screening for the presence of dissolved and particulate content of microcystins (-LR, -YR, and -RR), cylindrospermopsin, and anatoxin-a yielded negative results. The studied waters displayed no toxicity in human platelets in vitro. Further toxicological and ecological studies are necessary to evaluate the potential presence of cyanotoxin producers in Ukraine.

Comparative effects of ammonium, nitrate and urea on growth and photosynthetic efficiency of three bloom‐forming cyanobacteria

Abstract Urea‐based fertilisers have grown in popularity over the past half‐century and are now the dominant nitrogen (N) form applied to agricultural landscapes. The widespread use of urea fertilisers has favoured its export to local waterways, and urea pollution may be contributing to the propagation and maintenance of cyanobacteria harmful algal blooms in fresh waters. The relative success of cyanobacteria in response to urea and inorganic N additions was studied to understand whether the recent changes in the magnitude and composition of N loading have created a scenario that now favours the dominance of cyanobacteria in fresh waters. Growth and photosynthetic efficiency of three bloom‐forming freshwater cyanobacteria (Microcystis, Dolichospermum and Synechococcus) grown on nitrate (), ammonium () and urea (CO(NH2)2) as the sole N form were monitored. We hypothesised that N substrates that require the lowest energetic investment or offer the highest energetic return would favour optimal growth and photosynthetic performance. We predicted that urea would result in higher cellular growth and pigment production relative to or , as urea provides twice the amount N and an additional carbon (C) source making it more energetically efficient. Cyanobacteria biomass was not significantly enhanced on urea relative to inorganic N forms. Growth on urea was matched by for all species, whereas growth on was halved compared urea or . However, cyanobacteria cells had higher pigment concentrations when grown on urea relative to inorganic N sources. These findings suggest that the additional nutrient building blocks supplied from the hydrolysis of urea were not directed towards active growth, but rather accumulated in secondary pools to increase production of N‐rich compounds, such as pigments. Although urea did not influence cyanobacteria quantity “(i.e. biomass)” compared to inorganic N sources, it produced higher “quality” cells by enhancing pigment synthesis and potentially giving cyanobacteria a competitive advantage in light‐limiting conditions. Furthermore, when supplied in excess, cyanobacteria rapidly consumed urea in excess of their biosynthetic requirements suggesting a form of urea “gluttony.” These results demonstrate the importance of N speciation on cyanobacteria physiological responses and reinforce the emerging links between urea and cyanobacteria harmful algal blooms in inland waters.

A Rhamnose-Inducible System for Precise and Temporal Control of Gene Expression in Cyanobacteria

Cyanobacteria are important for fundamental studies of photosynthesis and have great biotechnological potential. In order to better study and fully exploit these organisms, the limited repertoire of genetic tools and parts must be expanded. A small number of inducible promoters have been used in cyanobacteria, allowing dynamic external control of gene expression through the addition of specific inducer molecules. However, the inducible promoters used to date suffer from various drawbacks including toxicity of inducers, leaky expression in the absence of inducer and inducer photolability, the latter being particularly relevant to cyanobacteria, which, as photoautotrophs, are grown under light. Here we introduce the rhamnose-inducible rhaBAD promoter of Escherichia coli into the model freshwater cyanobacterium Synechocystis sp. PCC 6803 and demonstrate it has superior properties to previously reported cyanobacterial inducible promoter systems, such as a non-toxic, photostable, non-metabolizable inducer, a linear response to inducer concentration and crucially no basal transcription in the absence of inducer.

Incomplete Selective Sweeps of Microcystis Population Detected by the Leader-End CRISPR Fragment Analysis in a Natural Pond.

The freshwater cyanobacterium Microcystis aeruginosa frequently forms toxic massive blooms and exists in an arms race with its infectious phages in aquatic natural environments, and as a result, has evolved extremely diverse and elaborate antiviral defense systems, including the clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated genes (Cas) system. Here, to assess Microcystis population dynamics associated with exogenous mobile genetic elements such as phages and plasmids, we examined the temporal variation in CRISPR genotypes (CTs) by analyzing spacer sequences detected in a natural pond between June and October 2013 when a cyanobacterial bloom occurred. A total of 463,954 high-quality leader-end CRISPR sequences were obtained and the sequences containing spacers were classified into 31 previously reported CTs and 68 new CTs based on the shared order of the leader-end spacers. CT19 was the most dominant genotype (32%) among the 16 most common CTs, followed by CT52 (14%) and CT58 (9%). Spacer repertoires of CT19 showed mainly two different types; CT19origin, which was identical to the CT19 spacer repertoire of previously isolated strains, and CT19new+, which contained a new spacer at the leader-end of the CRISPR region of CT19origin, which were present in almost equal abundance, accounting for up to 99.94% of CT19 sequences. Surprisingly, we observed the spacer repertoires of the second to tenth spacers of CT19origin at the most leader-end of proto-genotype sequences of CT19origin. These were observed during the sampling in this study and our previous study at the same ecosystem in 2010 and 2011, suggesting these CTs persisted from 2011 to 2013 in spite of phage pressure. The leader-end variants were observed in other CT genotypes. These findings indicated an incomplete selective sweep of Microcystis populations. We explained the phenomenon as follow; the abundance of Microcystis varied seasonally and drastically, resulting that Microcystis populations experience a bottleneck once a year, and thereby founder effects following a bottleneck mean that older CTs have an equal chance of increasing in prevalence as the CTs generated following acquisition of newer spacers.

Isolation Purification and Structure Elucidation of Antibacterial Active Compounds from Freshwater Cyanobacterium Lyngbya sp.

Cyanobacteria are considered as a rich source of bioactive compounds as they are able to produce a great variety of secondary metabolites characterized by a broad spectrum of biological activities including antiviral, antibacterial, antifungal, and anticancer properties. In the present study, freshwater cyanobacterium Lyngbya sp. was isolated from the Sennayaka samudraya and methanol crude extract was selected based on the previous antibacterial study (Agar disc diffusion method and Broth Microdialution method (Minimum Inhibition Concentration) to isolate and purify antibacterial active compounds. The antimicrobial activity of the methanol crude extract of Lynbya sp. was tested against two human pathogenic Gram-positive bacteria (Bacillus sp., Staphylococcus aureus-ATCC 2593), two human pathogenic Gram-negative bacteria (Escherichia coli-ATCC 25922, 2785 and Salmonella typhi) using bioautochromatography. Ciprofloxacin (5 μg/disc) was used as a positive control whereas DMSO (100%) used as negative control. The antioxidant property in the crude extract was evaluated using DPPH (2,2-diphenyl-1-picrylhydrazyl) scavenging test (Inhibitory Concentration, IC50 = 120.042 ppm). Thin Layer Chromatography (TLC), Column chromatography (CC), Preparative Thin Layer Chromatography (PTLC), Solid Phase Extraction (SPE) and finally High Performance Liquid Chromatography (HPLC) was carried out to purify the antibacterial active ingredient in methanol crude extract. Secondary phytochemical screening was done using TLC spray reagents to identify the antibacterial active chemical compound class. Structure elucidation of isolated compound was carried out using Gas Chromatography Mass Spectrometry (GCMS) and Fourier-Transform InfraRed spectroscopy (FTIR). Two solvent systems, Ethyl acetate: methanol: deionized water (100:13.5:10) and Toluene, ethyl acetate (93:7) were optimised to separate and purify the active compounds in the crude extract by thin layer chromatography plates. One clear band with antibacterial active compounds was detected on the TLC plates, which were developed using Toluene, ethyl acetate (93:7) solvent system by bioautochromatography test and that band was named as A1 (Rf =0.108). A1 showed antibacterial activity against Bacillus sp, E. coli and S.aureus. Three clear bands with antibacterial active compounds were detected on the TLC plates, which were developed using Ethyl acetate: Methanol: Water (100:13.5:10) solvent system by bioautochromatography test and that bands were named as B1 (Rf=0.361), B2 (Rf=0.326), B3 (Rf=0.035). B1 showed antibacterial activity against Bacillus sp, E. coli and S. aureus. B2 showed antibacterial activity against E. coli and Bacillus sp. B3 showed antibacterial activity against Bacillus sp, E. coli and S.aureus. The three main fractions namely fraction 1, 2, 3 were obtained by PTLC and antibacterial activity of each fraction was verified using bioautochromatography and fraction 1 showed potential antibacterial activity whereas fraction 2 and 3 were not shown any activity against test organisms. Secondary chemical screening was given positive result for Arbutin Anthraquinone glycoside and Alkaloid. According to the GC-MS analysis was revealed that fraction 1 contain 3,5-bis (1-1-dimethylethyl)-4-hydroxy-octadecyl ester, 1- Hexadecene and 1-Heptadecanol. These results of the present study revealed that the cyanobacterium Lyngbya sp. had antibacterial activity against the tested human pathogenic bacteria and the Lyngbya sp. is a potential candidate to utilize as a natural source to produce antibiotics. Keywords: Antibacterial activity, PTLC, TLC, HPLC

ATP-binding cassette transporters of the multicellular cyanobacterium Anabaena sp. PCC 7120: a wide variety for a complex lifestyle.

Two hundred genes or 3% of the known or putative protein-coding genes of the filamentous freshwater cyanobacterium Anabaena sp. PCC 7120 encode domains of ATP-binding cassette (ABC) transporters. Detailed characterization of some of these transporters (14-15 importers and 5 exporters) has revealed their crucial roles in the complex lifestyle of this multicellular photoautotroph, which is able to differentiate specialized cells for nitrogen fixation. This review summarizes the characteristics of the ABC transporters of Anabaena sp. PCC 7120 known to date.

Coping with iron limitation: a metabolomic study of Synechocystis sp. PCC 6803

Iron (Fe) is a key element for all living systems, especially for photosynthetic organisms because of its important role in the photosynthetic electron transport chain. Fe limitation in cyanobacteria leads to several physiological and morphological changes. However, the overall metabolic responses to Fe limitation are still poorly understood. In this study, we integrated elemental, stoichiometric, macromolecular, and metabolomic data to shed light on the responses of Synechocystis sp. PCC 6803, a non-N2-fixing freshwater cyanobacterium, to Fe limitation. Compared to Synechocystis growing at nutrient replete conditions, Fe-limited cultures had lower growth rates and amounts of chlorophyll a, RNA, RNA:DNA, C, N, and P, and higher ratios of protein:RNA, C:N, C:P, and N:P, in accordance with the growth rate hypothesis which predicts faster growing organisms will have decreased biomass RNA contents and C:P and N:P ratios. Fe-limited Synechocystis had lower amounts Fe, Mn, and Mo, and higher amount of Cu. Several changes in amino acids of cultures growing under Fe limitation suggest nitrogen limitation. In addition, we found substantial increases in stress-related metabolites in Fe-limited cyanobacteria such antioxidants. This study represents an advance in understanding the stoichiometric, macromolecular, and metabolic strategies that cyanobacteria use to cope with Fe limitation. This information, moreover, may further understanding of changes in cyanobacterial functions under scenarios of Fe limitation in aquatic ecosystems.

Low temperatures can promote cyanobacterial bloom formation by providing refuge from microbial antagonists.

Freshwater cyanobacteria are prone to a wide range of highly potent microbial antagonists. Most of these exploit their prey in a frequency-dependent manner and are therefore particularly well suited to prevent any accumulation of cyanobacteria. Mass developments of cyanobacteria, the so-called blooms, should therefore be rare events, which is in striking contrast to what we actually see in nature. Laboratory experiments of the present study showed that the temperature range 5.8–10 °C forms a thermal refuge, inside which the cyanobacterium Planktothrix can grow without being exploited by two otherwise highly potent microbial antagonists. In nature, access of Planktothrix to this refuge was associated with positive net growth and a high probability of bloom formation, confirming that refuge temperatures indeed allow Planktothrix to grow with a minimum of biomass loss caused by microbial antagonists. Contact to higher temperatures, in contrast, was associated with decreases in net growth rate and in probability of bloom formation, with population collapses and with the occurrence of parasite infection. This is in agreement with the finding of laboratory experiments that above 10 °C exploitation of Planktothrix by multiple microbes increases in a temperature-dependent manner. Taken together, above findings suggest that temperature modulates the microbial control of natural Planktothrix populations. Low temperatures form a thermal refuge that may promote Planktothrix bloom formation by shielding the cyanobacterium from otherwise highly potent microbial antagonists.