scholarly journals Quantitative Proteomic Analysis Reveals Novel Insights into Intracellular Silicate Stress-Responsive Mechanisms in the Diatom Skeletonema dohrnii

2019 ◽  
Vol 20 (10) ◽  
pp. 2540 ◽  
Author(s):  
Satheeswaran Thangaraj ◽  
Xiaomei Shang ◽  
Jun Sun ◽  
Haijiao Liu
Keyword(s):  
Oxidative Stress ◽  
Stress Responses ◽  
Carbon Fixation ◽  
Marine Phytoplankton ◽  
Silicate Concentration ◽  
Light Harvesting Complex ◽  
Photosynthetic Carbon Fixation ◽  
Ros Accumulation ◽  
Successful Group ◽  
Insight Into

Diatoms are a successful group of marine phytoplankton that often thrives under adverse environmental stress conditions. Members of the Skeletonema genus are ecologically important which may subsist during silicate stress and form a dense bloom following higher silicate concentration. However, our understanding of diatoms’ underlying molecular mechanism involved in these intracellular silicate stress-responses are limited. Here an iTRAQ-based proteomic method was coupled with multiple physiological techniques to explore distinct cellular responses associated with oxidative stress in the diatom Skeletonema dohrnii to the silicate limitation. In total, 1768 proteins were detected; 594 proteins were identified as differentially expressed (greater than a two-fold change; p < 0.05). In Si-limited cells, downregulated proteins were mainly related to photosynthesis metabolism, light-harvesting complex, and oxidative phosphorylation, corresponding to inducing oxidative stress, and ROS accumulation. None of these responses were identified in Si-limited cells; in comparing with other literature, Si-stress cells showed that ATP-limited diatoms are unable to rely on photosynthesis, which will break down and reshuffle carbon metabolism to compensate for photosynthetic carbon fixation losses. Our findings have a good correlation with earlier reports and provides a new molecular level insight into the systematic intracellular responses employed by diatoms in response to silicate stress in the marine environment.

Ultraviolet radiation stimulated activity of extracellular carbonic anhydrase in the marine diatom Skeletonema costatum

2009 ◽  
Vol 36 (2) ◽  
pp. 137 ◽  
Author(s):  
Hongyan Wu ◽  
Kunshan Gao
Keyword(s):  
Carbonic Anhydrase ◽  
Ultraviolet Radiation ◽  
Uv Radiation ◽  
Carbon Fixation ◽  
Skeletonema Costatum ◽  
Marine Phytoplankton ◽  
Marine Diatom ◽  
Redox Activity ◽  
Photosynthetic Carbon Fixation ◽  
Photosynthetic Carbon

Previous studies have shown that reduced levels of solar UV radiation (280–400 nm) can enhance photosynthetic carbon fixation of marine phytoplankton, but the mechanisms are not known. The supply of CO2 for photosynthesis is facilitated by extracellular (periplasmic) carbonic anhydrase (CAe) in most marine phytoplankton species. The present study showed that the CAe activity of Skeletonema costatum (Greville) Cleve was stimulated when treated with UV-A (320–395 nm) or UV-A + UV-B (295–320 nm) in addition to visible radiation. The presence of UV-A and UV-B enhanced the activity by 28% and 24%, respectively, at a low irradiance (PAR 161, UV-A 28, UV-B 0.9 W m−2) and by 21% and 19%, respectively, at a high irradiance (PAR 328, UV-A 58, UV-B 1.9 W m−2) level after exposure for 1 h. Ultraviolet radiation stimulated CAe activity contributed up to 6% of the photosynthetic carbon fixation as a result of the enhanced supply of CO2, as revealed using the CAe inhibitor (acetazolamide). As a result, there was less inhibition of photosynthetic carbon fixation compared with the apparent quantum yield of PSII. The UV radiation stimulated CAe activity coincided with the enhanced redox activity at the plasma membrane in the presence of UV-A and/or UV-B. The present study showed that UV radiation can enhance CAe activity, which plays an important role in counteracting UV inhibition of photosynthesis.

scholarly journals Physiological and biochemical responses of <i>Emiliania huxleyi</i> to ocean acidification and warming are modulated by UV radiation

2017 ◽  
Author(s):  
Shanying Tong ◽  
David A. Hutchins ◽  
Kunshan Gao
Keyword(s):  
Ocean Acidification ◽  
Uv Radiation ◽  
Carbon Fixation ◽  
Co2 Concentration ◽  
Emiliania Huxleyi ◽  
Marine Phytoplankton ◽  
Negative Effects ◽  
Photosynthetic Carbon Fixation ◽  
Photosynthetic Carbon ◽  
Increasing Temperature

Abstract. Marine phytoplankton such as bloom-forming, calcite-producing coccolithophores, are naturally exposed to solar UV radiation (UVR, 280–400 nm) in the ocean's upper mixed layers. Nevertheless, effects of increasing CO2-induced ocean acidification and warming have rarely been investigated in the presence of UVR. We examined calcification and photosynthetic carbon fixation performance in the most cosmopolitan coccolithophorid, Emiliania huxleyi, grown under high (1000 μatm, HC; pHT: 7.70) and low (400 μatm, LC; pHT: 8.02) CO2 levels, at 15 °C (LT), 20 °C (MT) and 24 °C (HT) with or without UVR. The HC treatment didn't affect photosynthetic carbon fixation at 15 °C, but significantly enhanced it with increasing temperature. Exposure to UVR inhibited photosynthesis, with higher inhibition by UVA (320–395 nm) than UVB (295–320 nm), except in the HC and 24 °C-grown cells, in which UVB caused more inhibition than UVA. Reduced thickness of the coccolith layer in the HC-grown cells appeared to be responsible for the UV-induced inhibition, and an increased repair rate of UVA-derived damage in the HCHT-grown cells could be responsible for lowered UVA-induced inhibition. While calcification was reduced with the elevated CO2 concentration, exposure to UVB or UVA affected it differentially, with the former inhibiting and the latter enhancing it. UVA-induced stimulation of calcification was higher in the HC-grown cells at 15 and 20 °C, whereas at 24 °C, observed enhancement was not significant. The calcification to photosynthesis ratio (Cal / Pho ratio) was lower in the HC treatment, and increasing temperature also lowered the value. However, at 20 and 24 °C, exposures to UVR significantly increased the Cal / Pho ratio, especially in HC-grown cells, by up to 100 %. This implies that UVR can counteract the negative effects of the greenhouse treatment on the Cal / Pho ratio, and so may be a key stressor when considering the impacts of future greenhouse conditions on E. huxleyi.

T-2 Toxin Induces Oxidative Stress at Low Doses Via ATF3∆Zip2a/2b-Mediated Ubiquitination and Degradation of Nrf2

2021 ◽  
Author(s):  
Xiaoxuan Chen ◽  
Peiqiang Mu ◽  
Lang Zhu ◽  
Xiaoxiao Mao ◽  
Shuang Chen ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Cell Viability ◽  
Target Gene ◽  
Antioxidant Defense ◽  
Low Doses ◽  
Antioxidant Genes ◽  
Defense Gene ◽  
Ros Accumulation ◽  
Insight Into ◽  
Mcf 7

Abstract Background: T-2 toxin is mainly produced by Fusarium species, which is an extremely toxic mycotoxin to humans and animals. It is well known that T-2 toxin induces oxidative stress, but the molecular mechanism is still unknown. Results: In this study, we found that T-2 toxin significantly promoted ROS accumulation in MCF-7 cells at low doses which maintains cell viability at least 80%. Further analysis showed that T-2 toxin downregulated the expression of the master regulator of antioxidant defense gene, Nrf2, and its targeted antioxidant genes. Overexpression of Nrf2 or its target gene HO1 significantly blocked the ROS accumulation in MCF-7 cells under T-2 toxin treatment. Moreover, we found that T-2 toxin downregulated the antioxidant genes via inducing the expression of ATF3∆Zip2a/2b. Importantly, overexpression of ATF3∆Zip2a/2b promoted the ubiquitination and degradation of Nrf2. Conclusions: This work demonstrated that T-2 toxin induced ROS accumulation via ATF3∆Zip2a/2b mediated ubiquitination and degradation of Nrf2, which provided a new insight into the mechanism of T-2 toxin-induced oxidative stress.

scholarly journals Diurnal regulation of photosynthetic light absorption, electron transport and carbon fixation in two contrasting oceanic environments

2019 ◽  
Vol 16 (7) ◽  
pp. 1381-1399 ◽  
Author(s):  
Nina Schuback ◽  
Philippe D. Tortell
Keyword(s):  
Electron Transport ◽  
Light Absorption ◽  
Carbon Fixation ◽  
Spatial Scales ◽  
Marine Phytoplankton ◽  
Optical Data ◽  
Reaction Centre ◽  
Phytoplankton Productivity ◽  
Ne Pacific ◽  
Insight Into

Abstract. Understanding the dynamics of marine phytoplankton productivity requires mechanistic insight into the non-linear coupling of light absorption, photosynthetic electron transport and carbon fixation in response to environmental variability. In the present study, we examined the variability of phytoplankton light absorption characteristics, light-dependent electron transport and 14C-uptake rates over a 48 h period in the coastal subarctic north-east (NE) Pacific. We observed an intricately coordinated response of the different components of the photosynthetic process to diurnal irradiance cycles, which acted to maximize carbon fixation, while simultaneously preventing damage by excess absorbed light energy. In particular, we found diurnal adjustments in pigment ratios, excitation energy transfer to reaction centre II (RCII), the capacity for non-photochemical quenching (NPQ), and the light efficiency (α) and maximum rates (Pmax) of RCII electron transport (ETRRCII) and 14C uptake. Comparison of these results from coastal waters to previous observations in offshore waters of the subarctic NE Pacific provides insight into the effects of iron limitation on the optimization of photosynthesis. Under iron-limited, low-biomass conditions, there was a significant reduction of iron-rich photosynthetic units per chlorophyll a, which was partly offset by higher light absorption and electron transport per photosystem II (PSII). Iron deficiency limited the capacity of phytoplankton to utilize peak midday irradiance for carbon fixation and caused an upregulation of photoprotective mechanisms, including NPQ, and the decoupling of light absorption, electron transport and carbon fixation. Such decoupling resulted in an increased electron requirement (Φe,C) and decreased quantum efficiency (ΦC) of carbon fixation at the iron-limited station. In both coastal and offshore waters, Φe,C and ΦC correlated strongly to NPQ, albeit with a significantly different slope. We discuss the implications of our results for the interpretation of bio-optical data and the parameterization of numerical productivity models, both of which are vital tools in monitoring marine photosynthesis over large temporal and spatial scales.

scholarly journals Physiological and biochemical responses of <i>Emiliania huxleyi</i> to ocean acidification and warming are modulated by UV radiation

2019 ◽  
Vol 16 (2) ◽  
pp. 561-572 ◽  
Author(s):  
Shanying Tong ◽  
David A. Hutchins ◽  
Kunshan Gao
Keyword(s):  
Ocean Acidification ◽  
Carbon Fixation ◽  
Co2 Concentration ◽  
Emiliania Huxleyi ◽  
Marine Phytoplankton ◽  
Negative Effects ◽  
Solar Ultraviolet Radiation ◽  
Photosynthetic Carbon Fixation ◽  
Photosynthetic Carbon ◽  
Increasing Temperature

Abstract. Marine phytoplankton such as bloom-forming, calcite-producing coccolithophores, are naturally exposed to solar ultraviolet radiation (UVR, 280–400 nm) in the ocean's upper mixed layers. Nevertheless, the effects of increasing carbon dioxide (CO2)-induced ocean acidification and warming have rarely been investigated in the presence of UVR. We examined calcification and photosynthetic carbon fixation performance in the most cosmopolitan coccolithophorid, Emiliania huxleyi, grown under high (1000 µatm, HC; pHT: 7.70) and low (400 µatm, LC; pHT: 8.02) CO2 levels, at 15 ∘C, 20 ∘C and 24 ∘C with or without UVR. The HC treatment did not affect photosynthetic carbon fixation at 15 ∘C, but significantly enhanced it with increasing temperature. Exposure to UVR inhibited photosynthesis, with higher inhibition by UVA (320–395 nm) than UVB (295–320 nm), except in the HC and 24 ∘C-grown cells, in which UVB caused more inhibition than UVA. A reduced thickness of the coccolith layer in the HC-grown cells appeared to be responsible for the UV-induced inhibition, and an increased repair rate of UVA-derived damage in the HC–high-temperature grown cells could be responsible for lowered UVA-induced inhibition. While calcification was reduced with elevated CO2 concentration, exposure to UVB or UVA affected the process differentially, with the former inhibiting it and the latter enhancing it. UVA-induced stimulation of calcification was higher in the HC-grown cells at 15 and 20 ∘C, whereas at 24 ∘C observed enhancement was not significant. The calcification to photosynthesis ratio (Cal ∕ Pho ratio) was lower in the HC treatment, and increasing temperature also lowered the value. However, at 20 and 24 ∘C, exposure to UVR significantly increased the Cal ∕ Pho ratio, especially in HC-grown cells, by up to 100 %. This implies that UVR can counteract the negative effects of the “greenhouse” treatment on the Cal ∕ Pho ratio; hence, UVR may be a key stressor when considering the impacts of future greenhouse conditions on E. huxleyi.

scholarly journals T-2 Toxin Induces Oxidative Stress at Low Doses via Atf3ΔZip2a/2b-Mediated Ubiquitination and Degradation of Nrf2

2021 ◽  
Vol 22 (15) ◽  
pp. 7936
Author(s):  
Xiaoxuan Chen ◽  
Peiqiang Mu ◽  
Lang Zhu ◽  
Xiaoxiao Mao ◽  
Shuang Chen ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Fusarium Species ◽  
Heme Oxygenase 1 ◽  
Related Factor ◽  
Low Doses ◽  
Antioxidant Genes ◽  
Defense Gene ◽  
Ros Accumulation ◽  
Insight Into ◽  
Mcf 7

T-2 toxin is mainly produced by Fusarium species, which is an extremely toxic mycotoxin to humans and animals. It is well known that T-2 toxin induces oxidative stress, but the molecular mechanism is still unknown. In this study, we found that T-2 toxin significantly promoted reactive oxygen species (ROS) accumulation in MCF-7 cells at low doses which maintains cell viability at least 80%. Further analysis showed that T-2 toxin downregulated the expression of the master regulator of antioxidant defense gene, nuclear factor erythroid 2-related factor (Nrf2), and its targeted antioxidant genes. Overexpression of Nrf2 or its target gene heme oxygenase 1 (HO1) significantly blocked the ROS accumulation in MCF-7 cells under T-2 toxin treatment. Moreover, we found that T-2 toxin downregulated the antioxidant genes via inducing the expression of ATF3ΔZip2a/2b. Importantly, overexpression of ATF3ΔZip2a/2b promoted the ubiquitination and degradation of Nrf2. Altogether, our results demonstrated that T-2 toxin-induced ROS accumulation via ATF3ΔZip2a/2b mediated ubiquitination and degradation of Nrf2, which provided a new insight into the mechanism of T-2 toxin-induced oxidative stress.

scholarly journals Diurnal regulation of photosynthetic light absorption, electron transport and carbon fixation in two contrasting oceanic environments

2019 ◽  
Author(s):  
Nina Schuback ◽  
Phillipe D. Tortell
Keyword(s):  
Electron Transport ◽  
Light Absorption ◽  
Carbon Fixation ◽  
Spatial Scales ◽  
Marine Phytoplankton ◽  
Optical Data ◽  
Photochemical Quenching ◽  
Phytoplankton Productivity ◽  
Ne Pacific ◽  
Insight Into

Abstract. Understanding the dynamics of marine phytoplankton productivity requires mechanistic insight into the non-linear coupling of light absorption, photosynthetic electron transport and carbon fixation in response to environmental variability. In the present study, we examined the variability of phytoplankton light absorption characteristics, light-dependent electron transport and 14C-uptake rates over a 48 hour period in the coastal Subarctic NE Pacific. We observed an intricately coordinated response of the different components of the photosynthetic process to diurnal irradiance cycles, which acted to maximise carbon fixation while simultaneously preventing damage by excess absorbed light energy. In particular, we found diurnal adjustments in pigment ratios, excitation energy transfer to reaction center II (RCII), the capacity for non-photochemical quenching (NPQ), and the light efficiency (α) and maximum rates (Pmax) of RCII electron transport (ETRRCII) and 14C-uptake. Comparison of these results from coastal waters to previous observations in offshore waters of the Subarctic NE Pacific provided insight into the effects of iron limitation on the optimization of photosynthesis. Under iron-limiting conditions, there was a significant reduction of iron-rich photosynthetic units per chlorophyll a, which was partly offset by higher light absorption and electron transport per photosystem II. Iron deficiency limited the capacity of phytoplankton to utilize peak mid-day irradiance for carbon fixation, and caused an upregulation of photo-protective mechanisms, including NPQ, and the decoupling of light absorption, electron transport and carbon fixation. Such decoupling resulted in an increased electron requirement (Φe,C) and decreased quantum efficiency (ΦC) of carbon fixation at the iron-limited station. In both coastal and off-shore waters, Φe,C and ΦC correlated strongly to NPQ. We discuss the implications of our results for the interpretation of bio-optical data, and the parameterization of numerical productivity models, both of which are vital tools in monitoring marine photosynthesis over large temporal and spatial scales.

Sectioned rubisco crystals in TEM

1990 ◽  
Vol 48 (3) ◽  
pp. 664-665
Author(s):  
Gunnel Karlsson ◽  
Jan-Olov Bovin ◽  
Michael Bosma
Keyword(s):  
Plant Cell ◽  
Carbon Fixation ◽  
Unit Cell ◽  
Protein Crystals ◽  
Unit Cell Parameters ◽  
Cell Parameters ◽  
Photosynthetic Carbon Fixation ◽  
Photosynthetic Carbon

RuBisCO (D-ribulose-l,5-biphosphate carboxylase/oxygenase) is the most aboundant enzyme in the plant cell and it catalyses the key carboxylation reaction of photosynthetic carbon fixation, but also the competing oxygenase reaction of photorespiation. In vitro crystallized RuBisCO has been studied earlier but this investigation concerns in vivo existance of RuBisCO crystals in anthers and leaves ofsugarbeets. For the identification of in vivo protein crystals it is important to be able to determinethe unit cell of cytochemically identified crystals in the same image. In order to obtain the best combination of optimal contrast and resolution we have studied different staining and electron accelerating voltages. It is known that embedding and sectioning can cause deformation and obscure the unit cell parameters.

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