Yuelu Jiang

PHOTOSYNTHETIC PERFORMANCE, LIPID PRODUCTION AND BIOMASS COMPOSITION IN RESPONSE TO NITROGEN LIMITATION IN MARINE MICROALGAE

Increasing energy prices demand a renewable, carbon neutral, transport fuel that is environmentally and commercially sustainable. The interest in the production of microalgae as biofuels is increasing due to their high oil content, rapid biomass production and small foot print. In this research, marine microalgae Dunaliella tertiolecta (Chlorophyceae) and Thalassiosira pseudonana (Bacillariophyceae) were incubated in nitrogen (N)-replete medium, and then transferred to N-free medium for 15 and 11 days, respectively. Fluorescence induction and relaxation (FIRe) fluorometry and Fourier transform infrared spectroscopy (FTIR) were used to monitor the photosynthetic performance, lipid production and metabolic responses to changing N availability. Growth rates of D. tertiolecta and T. pseudonana were 0.84 ± 0.16 d(-1) and 1.21 ± 0.09 d(-), respectively in N-replete medium. Upon transfer to N-free medium. The growth rates of T. pseudonana declined rapidly, while D. tertiolecta continued to grow for 5 days in N-free medium before growth declined slowly. The maximum quantum yield of photochemistry (F(v)/F(m)) remained high initially for D. tertiolecta but decreased immediately after transfer to N-free media for T. pseudonana. The functional absorption cross section for PSII (σ(PSII)) increased, the time constant for Q(A) reoxidation (τ(Qa)) and connectivity factor (p) decreased in parallel to the nutritional status of the microalgae. The relative protein and lipid content varied in response to N limitation, but carbohydrates did not change. Based on FTIR, D. tertiolecta and T. pseudonana produced 20-26% lipid when most stressed. The combination of photosynthetic efficiency and biomass composition monitoring provided evidence that metabolic strategies to changing nutrient status are species-specific.

Aggregation, Dissolution, and Stability of Quantum Dots in Marine Environments: Importance of Extracellular Polymeric Substances

There is an increasing concern that a considerable fraction of engineered nanoparticles (ENs), including quantum dots (QDs), will eventually find their way into the marine environment and have negative impacts on plankton. As ENs enter the ocean, they will encounter extracellular polymeric substances (EPS) from microbial sources before directly interacting with plankton cells. In this study, EPS harvested from four phytoplankton species, Amphora sp., Dunaliella tertiolecta, Phaeocystis globosa, and Thalassiosira pseudonana, were examined for potential interactions with CdSe nonfunctionalized and functionalized (carboxyl- and amine-) QDs in artificial seawater. Our results show that EPS do not reduce the solubility of QDs but rather decrease their stability. The degradation rate of QDs was positively correlated to the protein composition of EPS (defined by the ratio of protein/carbohydrate). Two approaches showed significant inhibition to the degradation of carboxyl-functionalized QDs: (1) the presence of an antioxidant, such as N-acetyl cysteine, and (2) absence of light. Owing to the complexity in evaluating integrated effects of QDs intrinsic properties and the external environmental factors that control the stability of QDs, conclusions must be based on a careful consideration of all these factors when attempting to evaluate the bioavailability of QDs and other ENs in the marine environments.

Effects of Engineered Nanoparticles on the Assembly of Exopolymeric Substances from Phytoplankton

The unique properties of engineered nanoparticles (ENs) that make their industrial applications so attractive simultaneously raise questions regarding their environmental safety. ENs exhibit behaviors different from bulk materials with identical chemical compositions. Though the nanotoxicity of ENs has been studied intensively, their unintended environmental impacts remain largely unknown. Herein we report experimental results of EN interactions with exopolymeric substances (EPS) from three marine phytoplankton species: Amphora sp., Ankistrodesmus angustus and Phaeodactylum tricornutum. EPS are polysaccharide-rich anionic colloid polymers released by various microorganisms that can assemble into microgels, possibly by means of hydrophobic and ionic mechanisms. Polystyrene nanoparticles (23 nm) were used in our study as model ENs. The effects of ENs on EPS assembly were monitored with dynamic laser scattering (DLS). We found that ENs can induce significant acceleration in Amphora sp. EPS assembly; after 72 hours EN-EPS aggregation reached equilibrium, forming microscopic gels of ∼4–6 µm in size. In contrast, ENs only cause moderate assembly kinetic acceleration for A. angustus and P. tricornutum EPS samples. Our results indicate that the effects of ENs on EPS assembly kinetics mainly depend on the hydrophobic interactions of ENs with EPS polymers. The cycling mechanism of EPS is complex. Nonetheless, the change of EPS assembly kinetics induced by ENs can be considered as one potential disturbance to the marine carbon cycle.

Effects of fluctuating temperature and silicate supply on the growth, biochemical composition and lipid accumulation of Nitzschia sp.

Nitzschia sp. (Bacillariophyceae) was grown under temperature and photoperiods mimicking those, typical during summer, spring/fall and winter conditions in the southern United States, and using five silicate (Si) concentrations. In general, higher Si concentrations resulted in higher growth rates in summer and spring/fall conditions and lower organic content. Si-deficient Nitzschia sp. had higher levels of neutral lipid compared to those growing in Si replete media. Under summer conditions, the proportion of saturated fatty acids (SFA) and monounsaturated fatty acids (MUFA) was relatively stable compared with spring/fall and winter conditions, and the proportion of polyunsaturated fatty acids (PUFA) was low. In the winter condition, SFA and MUFA showed a gradient of decreasing abundance while PUFA gradients increased with increasing Si concentrations in the medium. Cumulative productivity (optimization of growth and lipid content) would be best in the spring/fall but less so in the other conditions for this strain of Nitzschia sp.

Molecular level characterization of diatom‐associated biopolymers that bind 234Th, 233Pa, 210Pb, and 7Be in seawater: A case study with Phaeodactylum tricornutum

In order to investigate the importance of biogenic silica associated biopolymers on the scavenging of radionuclides, the diatom Phaeodactylum tricornutum was incubated together with the radionuclides 234Th, 233Pa, 210Pb, and 7Be during their growth phase. Normalized affinity coefficients were determined for the radionuclides bound with different organic compound classes (i.e., proteins, total carbohydrates, uronic acids) in extracellular (nonattached and attached exopolymeric substances), intracellular (ethylene diamine tetraacetic acid and sodium dodecyl sulfate extractable), and frustule embedded biopolymeric fractions (BF). Results indicated that radionuclides were mostly concentrated in frustule BF. Among three measured organic components, Uronic acids showed the strongest affinities to all tested radionuclides. Confirmed by spectrophotometry and two-dimensional heteronuclear single quantum coherence-nuclear magnetic resonance analyses, the frustule BF were mainly composed of carboxyl-rich, aliphatic-phosphoproteins, which were likely responsible for the strong binding of many of the radionuclides. Results from this study provide evidence for selective absorption of radionuclides with different kinds of diatom-associated biopolymers acting in concert rather than as a single compound. This clearly indicates the importance of these diatom-related biopolymers, especially frustule biopolymers, in the scavenging and fractionation of radionuclides used as particle tracers in the ocean.