Suppression of Alkalization in Rainwater Regulating Reservoir by Shading on a Pilot Scale

As water in a rainwater regulating reservoir at the Sankyo landfill site in Nagasaki City tends to be alkalized and to exceed the pH upper limit of 7.5, measures to suppress the alkalization should be implemented. Inhibiting photosynthesis in algae is required to suppress the alkalization. Shading is one of the methods for inhibiting algal photosynthesis. In this study, we evaluated the pH reduction effect of shading on a pilot scale. pH decreased from 7.28 to 7.15 when 3% of the total area of the rainwater regulating reservoir was shaded. In addition, a clear decrease in pH was observed with more than 60% shading.

Combining SIMS and mechanistic modelling to reveal nutrient kinetics in an algal-bacterial mutualism

Microbial communities are of considerable significance for biogeochemical processes, for the health of both animals and plants, and for biotechnological purposes. A key feature of microbial interactions is the exchange of nutrients between cells. Isotope labelling followed by analysis with secondary ion mass spectrometry (SIMS) can identify nutrient fluxes and heterogeneity of substrate utilisation on a single cell level. Here we present a novel approach that combines SIMS experiments with mechanistic modelling to reveal otherwise inaccessible nutrient kinetics. The method is applied to study the onset of a synthetic mutualistic partnership between a vitamin B12-dependent mutant of the alga Chlamydomonas reinhardtii and the B12-producing, heterotrophic bacterium Mesorhizobium japonicum, which is supported by algal photosynthesis. Results suggest that an initial pool of fixed carbon delays the onset of mutualistic cross-feeding; significantly, our approach allows the first quantification of this expected delay. Our method is widely applicable to other microbial systems, and will contribute to furthering a mechanistic understanding of microbial interactions.

Determination of Fucoxanthin in Bloom-Forming Macroalgae by HPLC–UV

Fucoxanthin is a carotenoid natural product with extensive biological activities and offers a variety of health benefits. Brown algae and diatoms are known producers of this compound as an important component of their light-harvesting complexes. Considering its important function in algal photosynthesis, we assume that the massive biomass from macroalgal blooms is potential bioresources of this compound. Accordingly, a high-performance liquid chromatography–ultra-violet (HPLC–UV) method was developed and validated for quantitation of fucoxanthin in bloom-forming macroalgal species from coastal waters of north China. The linear regression was acquired with r = 0.9991. The precisions were evaluated by intra- and inter-day tests, and the relative standard deviation (RSD) values were within the range of 0.59 and 2.30%, respectively. The recoveries for the method were observed over the range of 99.3–100.4% with RSD values < 2.6%. Our results showed that fucoxanthin occurs in all the tested algae including red and green algal species, which are not generally considered as fucoxanthin producers. Application of HPLC–time-of-flight mass spectrometry for the qualitative analysis further confirmed the production of fucoxanthin in these species. The developed method provided an insight into the potential of the macroalgal biomass commercial production of fucoxanthin.

Alternative electron pathways of photosynthesis drive the algal CO2 concentrating mechanism

Global photosynthesis consumes ten times more CO2 than net anthropogenic emissions, and microalgae account for nearly half of this consumption1. The great efficiency of algal photosynthesis relies on a mechanism concentrating CO2 (CCM) at the catalytic site of the carboxylating enzyme RuBisCO, thus enhancing CO2 fixation2. While many cellular components involved in the transport and sequestration of inorganic carbon (Ci) have been uncovered3,4, the way microalgae supply energy to concentrate CO2 against a thermodynamic gradient remains elusive4-6. Here, by monitoring dissolved CO2 consumption, unidirectional O2 exchange and the chlorophyll fluorescence parameter NPQ in the green alga Chlamydomonas, we show that the complementary effects of cyclic electron flow and O2 photoreduction, respectively mediated by PGRL1 and flavodiiron proteins, generate the proton motive force (pmf) required by Ci transport across thylakoid membranes. We demonstrate that the trans-thylakoid pmf is used by bestrophin-like Ci transporters and further establish that a chloroplast-to-mitochondria electron flow contributes to energize non-thylakoid Ci transporters, most likely by supplying ATP. We propose an integrated view of the CCM energy supply network, describing how algal cells distribute photosynthesis energy to power different Ci transporters, thus paving the way to the transfer of a functional algal CCM in plants towards improving crop productivity.One sentence summaryPhotosynthetic alternative electron flows and mitochondrial respiration drive the algal CO2 concentrating mechanism

Allelopathic effect of rhubarb extracts on the growth of Microcystis aeruginosa

With its advantages of ecological safety, environmental affinity, and high selectivity, allelopathic technology has been widely developed for algae inhibition. However, obtaining effective allelochemicals and realizing their mechanism are difficult. In this paper, a Chinese herbal medicine, namely, Rheum palmatum L. (Chinese rhubarb), was utilized as a source of allelopathic substances for the first time. Four units of rhubarb organic extracts were collected to study the inhibition of growth, photosynthesis, proteins, and algal toxin of Microcystis aeruginosa. Results showed that the ethyl acetate, n-butanol, and aqueous phases of the rhubarb extracts have notable inhibitory effects. After a 16-day treatment, the four extracts reduced M. aeruginosa by 64.1%, 59.3%, 61.9%, and 7.2% with disruption of algal photosynthesis and protein synthesis and reduction of algal toxin.

Observations of late-winter marine microbial activity in an ice-covered fjord, west Greenland

Direct observations of marine microbial metabolism are sparse in the Arctic, particularly under sea ice during winter. This paper presents the first observations of Arctic winter microbial activity under sea ice in a west Greenland fjord (Lillefjord, ∼ 70∘ N). Here, measured changes in dissolved oxygen (DO) content in light and dark in situ incubations were used to calculate net community productivity, respiration and photosynthesis rates. Data were collected at two fully ice covered sites during February 2013, shortly after the end of the polar night. Averaged over the full study period, dark incubations showed statistically significant decreases in DO of -0.36±0.24 (near shore) and -0.09±0.07 g O2 m−3 d−1 (fjord centre), indicating respiration rates that were 2–20 times greater than rates previously reported under sea ice in the Arctic. Meanwhile, a lack of significant evidence for photosynthesis suggests that the rate of photosynthesis – if it was occurring – was much lower than that of respiration. The data also show no significant evidence of a temporal trend in metabolism rates over the study period; however, ambient seawater DO increased significantly at the fjord centre (0.023±0.013 g O2 m−3 d−1), possibly attributable to processes not occurring in the incubations (such as sea ice algal photosynthesis). These data may improve our understanding of microbial activity in the fjord during winter, and its contribution to Arctic ecosystems under present and future conditions. The data are archived at PANGAEA (https://doi.org/10.1594/PANGAEA.906332, Chandler and Mackie, 2019; https://doi.org/10.1594/PANGAEA.912677, Chandler and Mackie, 2020).

Algal photosynthesis converts nitric oxide into nitrous oxide

Nitrous oxide (N2O), a potent greenhouse gas in the atmosphere, is produced mostly from aquatic ecosystems, to which algae substantially contribute. However, mechanisms of N2O production by photosynthetic organisms are poorly described. Here we show that the green microalga Chlamydomonas reinhardtii reduces NO into N2O using the photosynthetic electron transport. Through the study of C. reinhardtii mutants deficient in flavodiiron proteins (FLVs) or in a cytochrome p450 (CYP55), we show that FLVs contribute to NO reduction in the light, while CYP55 operates in the dark. Both pathways are active when NO is produced in vivo during the reduction of nitrites and participate in NO homeostasis. Furthermore, NO reduction by both pathways is restricted to chlorophytes, organisms particularly abundant in ocean N2O-producing hot spots. Our results provide a mechanistic understanding of N2O production in eukaryotic phototrophs and represent an important step toward a comprehensive assessment of greenhouse gas emission by aquatic ecosystems.

Symbiosis extended: exchange of photosynthetic O2 and fungal-respired CO2 mutually power metabolism of lichen symbionts

Lichens are a symbiosis between a fungus and one or more photosynthetic microorganisms that enables the symbionts to thrive in places and conditions they could not compete independently. Exchanges of water and sugars between the symbionts are the established mechanisms that support lichen symbiosis. Herein, we present a new linkage between algal photosynthesis and fungal respiration in lichen Flavoparmelia caperata that extends the physiological nature of symbiotic co-dependent metabolisms, mutually boosting energy conversion rates in both symbionts. Measurements of electron transport by oximetry show that photosynthetic O2 is consumed internally by fungal respiration. At low light intensity, very low levels of O2 are released, while photosynthetic electron transport from water oxidation is normal as shown by intrinsic chlorophyll variable fluorescence yield (period-4 oscillations in flash-induced Fv/Fm). The rate of algal O2 production increases following consecutive series of illumination periods, at low and with limited saturation at high light intensities, in contrast to light saturation in free-living algae. We attribute this effect to arise from the availability of more CO2 produced by fungal respiration of photosynthetically generated sugars. We conclude that the lichen symbionts are metabolically coupled by energy conversion through exchange of terminal electron donors and acceptors used in both photosynthesis and fungal respiration. Algal sugars and O2 are consumed by the fungal symbiont, while fungal delivered CO2 is consumed by the alga.