Harmful algal blooms caused huge ecological damage and economic losses around the world. Controlling algal blooms by algicidal bacteria is expected to be an effective biological control method. The current study investigated the molecular mechanism of harmful cyanobacteria disrupted by algicidal bacteria. Microcystis aeruginosa was co-cultured with Brevibacillus laterosporus Bl-zj, and RNA-seq based transcriptomic analysis was performed compared to M. aeruginosa, which was cultivated separately. A total of 1706 differentially expressed genes were identified, which were mainly involved in carbohydrate metabolism, energy metabolism and amino acid metabolism. In the co-cultured group, the expression of genes mainly enriched in photosynthesis and oxidative phosphorylation were significantly inhibited. However, the expression of the genes related to fatty acid synthesis increased. In addition, the expression of the antioxidant enzymes, such as 2-Cys peroxiredoxin, was increased. These results suggested that B. laterosporus could block the electron transport by attacking the PSI system and complex I of M. aeruginosa, affecting the energy acquisition and causing oxidative damage. This further led to the lipid peroxidation of the microalgal cell membrane, resulting in algal death. The transcriptional analysis of algicidal bacteria in the interaction process can be combined to explain the algicidal mechanism in the future.

Natural astaxanthin helps reduce the negative effects caused by oxidative stress and other related factors, thereby minimizing oxidative damage. Therefore, it has considerable potential and broad application prospects in human health and animal nutrition. Haematococcus pluvialis is considered to be the most promising cell factory for the production of natural astaxanthin. Previous studies have confirmed that nonmotile cells of H. pluvialis are more tolerant to high intensity of light than motile cells. Cultivating nonmotile cells as the dominant cell type in the red stage can significantly increase the overall astaxanthin productivity. However, we know very little about how to induce nonmotile cell formation. In this work, we first investigated the effect of phosphorus deficiency on the formation of nonmotile cells of H. pluvialis, and then investigated the effect of NaCl on the formation of nonmotile cells under the conditions of phosphorus deficiency. The results showed that, after three days of treatment with 0.1% NaCl under phosphorus deficiency, more than 80% of motile cells had been transformed into nonmotile cells. The work provides the most efficient method for the cultivation of H. pluvialis nonmotile cells so far, and it significantly improves the production of H. pluvialis astaxanthin.

In recent years, bisphenol AF (BPAF) in aquatic environments has drawn attention to its ecological risks. This study aims to investigate the toxic effects of BPAF (188.33 μg/L) exposure for 30 days on female marine medaka (Oryzias melastigma). On the 10th and 30th day of exposure, the toxicity was evaluated using histological analysis of the liver and ovaries and the transcription levels of genes related to the antioxidant system, immune system, and hypothalamic-pituitary-gonadal (HPG) axis. Findings revealed that (1) BPAF exposure caused vacuolation, karyopyknosis and karyolysis in the liver of marine medaka, and the toxic impact augmented with duration; (2) exposure to BPAF for 10 days facilitated the growth and maturation of primary ova, and this exposure had a comparatively inhibitory effect after 30 days; (3) exposure to BPAF resulted in a biphasic regulation of the transcriptional abundance of genes involved in antioxidant and inflammatory response (e.g., il-8, cat), with an initial up-regulation followed by down-regulation. Additionally, it disrupted the transcriptional pattern of HPG axis-related genes (e.g., 3βhsd, arα). In conclusion, 188.33 μg/L BPAF can alter the expression levels of functionally related genes, impair the structural integrity of marine organisms, and pose a threat to their overall health.

To enhance the nutrient removal efficiency of Oocystis borgei for mariculture wastewater (MW), the effects and processes of three phytohormones on nitrogen and phosphorus removal from synthetic mariculture wastewater (SMW) by O. borgei under sequential batch operation were compared. The findings revealed that the supplementation with 10⁻⁶ M 3-indoleacetic acid (IAA), gibberellic acid (GA3), and zeatin (ZT) resulted in the most effective elimination, while there was no appreciable difference among them. The nitrogen and phosphorus indices of the effluent dramatically reduced (p < 0.01) upon the supplementation of phytohormones, and the removal effects were ranked as NO₃⁻-N > PO₄³⁻-P > NH₄⁺-N > NO₂⁻-N. The removal rates for NH₄⁺-N and PO₄³⁻-P were 0.72–0.74 mg·L⁻¹·d⁻¹ and 1.26–1.30 mg·L⁻¹·d⁻¹, respectively. According to physiological studies, phytohormones enhanced the levels of photosynthetic pigments and chlorophyll fluorescence parameters (Fv/Fm and φPSII), thereby improving photosynthetic activity. Additionally, they stimulated Nitrate Reductase (NR) and Glutamine Synthetase (GS) activities to promote nitrogen metabolism and increased Superoxide Dismutase (SOD), Catalase (CAT), and carotenoid contents to mitigate oxidative stress damage caused by abiotic stress. These activities contribute to the proliferation of O. borgei, which in turn resulted in an increase in the assimilation of nitrogen and phosphorus from SMW. In conclusion, phytohormone supplementation significantly increased nutrient removal from SMW by O. borgei in a sequential batch reactor, which has potential application in MW treatment.