Paul J. Janknegt

OXIDATIVE STRESS RESPONSES IN THE MARINE ANTARCTIC DIATOM CHAETOCEROS BREVIS (BACILLARIOPHYCEAE) DURING PHOTOACCLIMATION(1).

The enzyme superoxide dismutase (SOD) holds a key position in the microalgal antioxidant network. The present research focused on oxidative stress responses in the Antarctic diatom Chaetoceros brevis F. Schütt during transition to excess (including ultraviolet radiation [UVR]) and limiting irradiance conditions. Over a 4 d period, cellular responses of thiobarbituric acid reactive substances (TBARS, a general oxidative stress indicator), SOD activity, photosynthetic and xanthophyll cycle pigments, PSII efficiency, and growth were determined. In addition, oxidative responses were measured during a daily cycle. Changing irradiance conditions significantly affected growth rates of C. brevis. PSII efficiency decreased significantly during periodic excess irradiance and increased under low irradiance conditions. Transition to excess irradiance increased the ratio of xanthophyll to light‐harvesting pigments, whereas the opposite was observed for cultures transferred to low irradiance. This acclimation process was completed after 2 d in the new irradiance environment. SOD activity increased significantly after the first day regardless of the new irradiance environment but returned to preexposure values on the fourth day. We hypothesize that SOD activity may be temporarily elevated in C. brevis after irradiance shifts, thereby reducing oxidative stress when photoacclimation is in progress.

Excessive irradiance and antioxidant responses of an Antarctic marine diatom exposed to iron limitation and to dynamic irradiance

The synergistic effects of iron limitation and irradiance dynamics on growth, photosynthesis, antioxidant activity and excessive PAR (400-700 nm) and UV (280-400 nm) sensitivity were investigated for the Antarctic marine diatom Chaetoceros brevis. Iron-limited and iron-replete cultures were exposed to identical daily irradiance levels, supplied as dynamic (20-1350 micromol m(-2) s(-1)) and constant (260 micromol m(-2) s(-1)) irradiance. After acclimation, growth, maximal quantum yield of PSII (F(v)/F(m)), pigment composition, and the activities of the antioxidant enzymes superoxide dismutase (SOD), ascorbate peroxidase (APX) and glutathione reductase (GR) were determined. Then, excessive irradiance sensitivity was assessed by monitoring pigment composition, F(v)/F(m) and viability loss during a single excessive PAR and UV treatment. Iron limitation reduced growth rates, F(v)/F(m) dynamics, and cellular pigments pools. Cellular pigment concentrations were higher under dynamic irradiance than under constant irradiance but this difference was less pronounced under iron limitation compared to iron-replete conditions. SOD and APX activities increased during dynamic irradiance under iron limitation, suggesting increased radical formation around PSII. Despite these physiological differences, no effects on growth were observed between constant and dynamic irradiance cultivation in iron-limited and iron-replete cells. The applied culturing conditions did not affect glutathione reductase activity in C. brevis. F(v)/F(m) and xanthophyll de-epoxidation dynamics during excessive irradiance were not different for iron-limited and replete cells and viability loss was not found during excessive irradiance. This study revealed photoacclimation differences between iron-limited and iron-replete C. brevis cultures that did not affect growth rates and excessive irradiance sensitivity after acclimation to constant and dynamic irradiance.

Short-term antioxidative responses of 15 microalgae exposed to excessive irradiance including ultraviolet radiation

Short-term photosensitivity and oxidative stress responses were compared for three groups of marine microalgae: Antarctic microalgae, temperate diatoms and temperate flagellates. In total, 15 low-light-acclimated species were exposed to simulated surface irradiance including ultraviolet radiation (SSI). Photosensitivity was assessed as the rate of recovery of Fv/Fm in the hours following SSI treatment. Before, during and after the SSI treatment, oxidative stress responses were assessed by following xanthophyll content and cycling, and activities of superoxide dismutase, ascorbate peroxidase and glutathione reductase, and glutathione redox status. When acclimated to low irradiance, antioxidant levels were not group specific. Superoxide dismutase activity was positively correlated with cell size, whereas in general, ascorbate peroxidase activity appeared to be lower and glutathione redox status appeared to be higher in the Antarctic than in the temperate species. After SSI exposure, the strong inhibition of PSII was followed by variable rates of recovery, although four species remained photosynthetically inactive. SSI tolerance appeared unrelated to geographic or taxonomic background, or to cell size. PSII recovery was enhanced in species with decreasing superoxide dismutase activity, glutathione redox status and increased xanthophyll cycle activity. We conclude that antioxidant responses are highly species specific and not related to the geographic or taxonomic background. Furthermore, xanthophyll cycling seems more important than antioxidants. Finally, it can be hypothesized that glutathione could function as a stress sensor and response regulator.

Xanthophyll cycle activity and photosynthesis of Dunaliella tertiolecta (Chlorophyceae) and Thalassiosira weissflogii (Bacillariophyceae) during fluctuating solar radiation

van de Poll W.H., Buma A.G.J., Visser R.J.W., Janknegt P.J., Villafañ V.E. and Helbling E.W. 2010. Xanthophyll cycle activity and photosynthesis of Dunaliella tertiolecta (Chlorophyceae) and Thalassiosira weissflogii (Bacillariophyceae) during fluctuating solar radiation. Phycologia 49: 249–259. DOI: 10.2216/08-83.1 Short-term ultraviolet (UV) radiation (280–400 nm) effects on xanthophyll cycle activity and photosynthesis were assessed during fluctuating irradiance (60- and 10-min cycles – saturating irradiance to near-zero irradiance) for the marine algae Thalassiosira weissflogii (Bacillariophyceae) and Dunaliella tertiolecta (Chlorophyceae). Laboratory cultures were cycled, as above, up and down the water column for 8 h under solar radiation, during which photosystem II (PSII) quantum yield in the light [(Fm′ − Ft)/Fm′] was monitored over 1-min intervals. In addition, pigment composition, xanthophyll de-epoxidation state and carbon assimilation were assessed during the fluctuating irradiance cycles. Although PSII quantum yield in the light of both species mirrored irradiance, the PSII response to irradiance fluctuations changed over time as PSII quantum yield was downregulated at midday. This coincided with maximal xanthophyll de-epoxidation that developed during the course of the day for both species. In contrast to the de-epoxidation levels, nonphotochemical quenching (NPQ) and PSII quantum yield in the light fluctuated with the irradiance dynamics at noon in both species. Maximal xanthophyll de-epoxidation and NPQ at noon was lower under photosynthetically active radiation (PAR) + UV than under PAR exposure for T. weissflogii during the 10-min cycle, whereas this was not found for the 60-min cycle and in D. tertiolecta. Synthesis of xanthophyll cycle pigments occurred in both species, and was faster for D. tertiolecta during PAR + UV than during PAR exposure. Carbon incorporation and on most occasions PSII quantum yield in the light were lower during UV exposure for both species, regardless of xanthophyll de-epoxidation state. UV effects on carbon assimilation were higher during 10-min than during 60-min irradiance fluctuation cycles. However, the 10-min irradiance fluctuation cycle appeared to enhance overall carbon assimilation in D. tertiolecta but depressed productivity of T. weissflogii, as compared with the 60-min cycles.

Wavelength-dependent xanthophyll cycle activity in marine microalgae exposed to natural ultraviolet radiation

The wavelength dependency of xanthophyll cycling in two marine microalgae (Thalassiosira weissflogii and Dunaliella tertiolecta) was studied by establishing biological weighting functions (BWFs) during exposure to natural ultraviolet radiation. High-(HL) and low-(LL) light-acclimated cultures of both species were exposed outdoors for up to 60 min under a series of UVR (280–400 nm) cut-off filters, after which the de-epoxidation state of xanthophyll cycle pigments, radiocarbon assimilation and photochemical quantum yield were measured. Exposures were repeated 4–8 times during the daily cycle to create exposure–response curves for each wavelength condition. UVR affected the three target processes significantly in both species and biological weights increased with decreasing wavelength, particularly in the UVBR region (280–315 nm). Minor wavelength dependency was observed between 315 and 360 nm. After BWF normalization to 300 nm, the LL cultures showed highly similar responses when comparing the three target processes, while the BWFs for the HL cultures differed significantly. The observed enhanced xanthophyll cycling activity in the UVR region implied that xanthophylls had an active role in diminishing UVR stress. However, this enhancement seems to be an indirect effect of damage within the dark reactions of photosynthesis. Hence, another vital target process further downstream in the photosynthetic process, possibly involved in the dark reactions, seems to be responsible for the high similarity in BWFs.

Antioxidative responses of two marine microalgae during acclimation to static and fluctuating natural UV radiation

Photoacclimation properties were investigated in two marine microalgae exposed to four ambient irradiance conditions: static photosynthetically active radiation (PAR: 400–700 nm), static PAR + UVR (280–700 nm), dynamic PAR and dynamic PAR + UVR. High light acclimated cultures of Thalassiosira weissflogii and Dunaliella tertiolecta were exposed outdoors for a maximum of 7 days. Dynamic irradiance was established by computer controlled vertical movement of 2 L bottles in a water filled basin. Immediate (<24 h), short‐term (1–3 days) and long‐term (4–7 days) photoacclimation was followed for antioxidants (superoxide dismutase, ascorbate peroxidase and glutathione cycling), growth and pigment pools. Changes in UVR sensitivity during photoacclimation were monitored by measuring UVR‐induced inhibition of carbon assimilation under standardized UV conditions using an indoor solar simulator. Both species showed immediate antioxidant responses due to their transfer to the outdoor conditions. Furthermore, upon outdoor exposure, carbon assimilation and growth rates were reduced in both species compared with initial conditions; however, these effects were most pronounced in D. tertiolecta. Outdoor UV exposure did not alter antioxidant levels when compared with PAR‐only controls in both species. In contrast, growth was significantly affected in the static UVR cultures, concurrent with significantly enhanced UVR resistance. We conclude that antioxidants play a minor role in the reinforcement of natural UVR resistance in T. weissflogii and D. tertiolecta.