Cyanobacteria and microalgae help reduce the environmental impact of human energy consumption by playing a vital role in carbon and nitrogen cycling. They are also used in various applications like biofuel production, food, medicine, and bioremediation. Understanding how these organisms respond to stress is important for efficient recovery strategies and sustainable outcomes. This study investigated the effects of low-level bleaching and thermal stress on cyanobacteria and microalgae, specifically Synechocystis, Chlorella, and Scenedesmus. The role of ferroptosis, an iron-dependent form of cell death, in the degradation of cellular components under these stressors was examined. Flow cytometry and spectrophotometry were used to measure changes in cellular health and viability. The results showed that temperature influences the type of cell death mechanism and can impact photosynthetic organisms. When treated with Liproxstatin-1, an inhibitor of ferroptosis, both Synechocystis and Chlorella experienced a decrease in oxidative damage, suggesting a potential protective role for the compound. Further investigation into ferroptosis and other forms of cell death, as well as identifying additional inhibitory molecules, could lead to strategies for mitigating oxidative stress and enhancing the resilience of cyanobacteria and microalgae.

In order for microalgae to be a cost-effective renewable energy source, a high CO2-transfer efficiency (CTE) is necessary. Using hollow-fiber membranes (HFM), membrane carbonation (MC) in microalgal cultivation can be used to achieve a CTE near 100%. Due to the diurnal cycle in outdoor algal cultivation, an inconsistent CO2 demand with temperature fluctuations can cause pore wetting of the inner and outer fiber layers in composite HFMs. In addition, the presence of supersaturated O2 during high algal growth may change the gas transfer dynamics of the fibers, which can be critical when trying to selectively remove CO2 from a valuable gas such as biogas. This study evaluated fiber performance under conditions that mimic these effects by analyzing the carbon transfer efficiency (CTE), CO2 flux (JCO2), and outlet CO2 concentration compared to baseline values. Wetting of the interior fiber macropores resulted in an average 32% ± 8.3% decrease in flux, which was greater than for flooding of the outer macropores, which showed no significant change. All tests resulted in a decrease in CTE and an increase in outlet CO2. The presence of elevated O2 levels did not decrease the CO2 flux compared to baseline values, but it increased the O2 concentration and decreased the CH4 concentration at the distal end of the fibers. These findings highlight that liquid accumulation can decrease HFM performance during MC for microalgal cultivation, while the presence of supersaturated O2 can reduce separation efficiency.

Cocoamidopropyl betaine (CAPB), which is a biodegradable ampholytic surfactant, has recently been found to dramatically enhance the aerobic digestion of waste activated sludge (WAS) in short-time aerobic digestion (STAD) systems. Therefore, it is important to understand the mechanisms in which CAPB enhances WAS aerobic digestion performance. Results showed that CAPB could dramatically enhance the solubilization of soluble proteins (PN), polysaccharides (PS), nucleic acids (NA) and humic-like substances (HS) in the STAD system within the initial 2 h. Then PN, PS and NA gradually decreased, while HS showed only minor decease. In addition, CAPB increased the proportion of low MW fractions (<20 kDa) from 4.22% to 39.4%, which are more biodegradable. Specific oxygen uptake rates and dehydrogenase enzyme activity results indicated that CAPB markedly improved the aerobic microorganism activities. Microbial community analyses and principle coordinate analyses (PCoA) revealed that CAPB increased the proportion of some functional microorganisms, including Proteobacteria, Planctomycetales, Acinetobacter, Pseudomonas and Aeromonas. The changes driven by CAPB could explain the enhanced performance of the STAD system for WAS aerobic treatment.