Microalgae have garnered scientific interest for their potential to produce bioactive compounds. However, the large-scale industrial utilization of microalgae faces challenges related to production costs and achieving optimal growth conditions. Thus, this study aimed to investigate the potential role of exogenous indole-3-acetic acid (IAA) application in improving the growth and production of bioactive metabolites in microalgae. To this end, the study employed different concentrations of exogenously administered IAA ranging from 0.36 µM to 5.69 µM to assess its influence on the growth and biochemical composition of Synechocystis and Chlorella. IAA exposure significantly increased IAA levels in both strains. Consequentially, improved biomass accumulation in parallel with increased total pigment content by approximately eleven-fold in both strains was observed. Furthermore, the application of IAA stimulated the accumulation of primary metabolites. Sugar levels were augmented, providing a carbon source that facilitated amino acid and fatty acid biosynthesis. As a result, amino acid levels were enhanced as well, leading to a 1.55-fold increase in total amino acid content in Synechocystis and a 1.42-fold increase in Chlorella. Total fatty acids content increased by 1.92-fold in Synechocystis and by 2.16-fold in Chlorella. Overall, the study demonstrated the effectiveness of exogenously adding IAA as a strategy for enhancing the accumulation of microalgae biomass and biomolecules. These findings contribute to the advancement of microalgae-based technologies, opening new avenues to produce economically important compounds derived from microalgae.

Background: Biofuels produced from trans-esterification of high lipid content in microalgae represent a promising alternative renewable source of energy to the limited and depleted global fossil fuel reservoir. The most critical step in such a process is the harvesting of algal cells. Objective: We aimed to improve the current methodology for microalgae harvesting via utilizing biosynthesized silver nanoparticles (AgNPs) from Synechocystis sp. ElfSCS31 as an eco-friendly, stable, and affordable flocculant agent. Methods: AgNPs were prepared by the green synthesis method using the alcoholic extract of Synechocystis sp. ElfSCS31. The synthesized nanoparticles were characterized by Zeta sizer, X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), and UV-Vis Spectroscopy. Biosynthesised AgNPs were applied for harvesting 20 microalgae strains, and then, harvesting efficiency was determined by UV Spectrophotometry. Results: Our results revealed an average size of polydispersed nanoparticles ranging from 10 to 100 nm for prepared AgNPs and the potential of 1.78 mV, with an average crystallite size of 22 nm. Biosynthesised AgNPs exhibited harvesting efficiency towards different strains of microalgae, which reached 97% in some strains as in Chlorella lobophora and Chlorococcum oleofaciens. Conclusion: The presented study introduces a feasible strategy using biosynthesized AgNPs as a flocculant agent to harvest different strains of microalgae at normal growth conditions of light and temperature. Our developed method could replace the classical high-cost step of harvesting that leads to unravelling the full potential of microalgae as a promising and fascinating source for biofuels production.

The contamination resulting from heavy metals present in industrial effluents represents a critical global challenge, posing profound risks to aquatic ecosystems and human health. Industrial activities worldwide release wastewater laden with toxic metals, prominently cadmium (Cd), into rivers, lakes, and oceans, frequently surpassing permissible limits. Current treatment technologies are costly and may produce secondary pollutants, thereby necessitating the urgent development of sustainable and cost-effective alternatives. This study investigates the efficacy of the microalga Chlamydomonas sp. as a natural biosorbent for the phycoremediation of cadmium from industrial effluent. Critical parameters affecting cadmium biosorption, including pH, contact time, Cd concentration, and biomass dosage, were optimized. Under optimal conditions of 25°C, pH 4, Cd concentration of 50 mg/L, a contact time of 60 min, and a biomass dosage of 0.8 g/L, Chlamydomonas demonstrated a cadmium adsorption capacity of 44.75 mg/g, achieving a removal efficiency of 95.6%. Analytical techniques such as SEM, XRD, FTIR, DLS, and zeta potential analysis confirmed cadmium binding to the algal biomass. Kinetic modeling suggested a pseudo-second-order process, while isotherm analysis adhered to the Langmuir model, indicating considerable adsorption capacity and efficiency under optimal conditions. These results support using Chlamydomonas as an effective biosorbent for integration into global industrial wastewater treatment systems. This biological approach offers a sustainable and cost-efficient method for heavy metal removal, reducing secondary pollution and aligning with international efforts to mitigate water contamination. Implementing bioremediation strategies could greatly decrease the release of toxic metals into aquatic ecosystems, providing a scalable and environmentally friendly solution for industrial applications globally.

The potential of microalgae to produce valuable compounds has garnered considerable attention. However, there are various challenges that hinder their large-scale industrial utilization, such as high production costs and the complexities associated with achieving optimal growth conditions. Therefore, we investigated the effects of glycine at different concentrations on the growth and bioactive compounds production of Synechocystis sp. PAK13 and Chlorella variabilis cultivated under nitrogen availability. Glycine supplementation resulted in increased biomass and bioactive primary metabolites accumulation in both species. Sugar production, particularly glucose content, significantly improved in Synechocystis at 3.33 mM glycine (1.4 mg/g). This led to enhanced organic acid, particularly malic acid, and amino acids production. Glycine stress also influenced the concentration of indole-3-acetic acid, which was significantly higher in both species compared to the control. Furthermore, fatty acids content increased by 2.5-fold in Synechocystis and by 1.36-fold in Chlorella. Overall, the exogenous application of glycine is a cheap, safe, and effective approach to enhancing sustainable microalgal biomass and bioproducts production.

In the realm of applied phycology, algal physiology, and biochemistry publications, the absence of proper identification and documentation of microalgae is a common concern. This poses a significant challenge for non-specialists who struggle to identify numerous eukaryotic microalgae. However, a promising solution lies in employing an appropriate DNA barcoding technique and establishing comprehensive databases of reference sequences. To address this issue, we conducted a study focusing on the molecular characterization and strain identification of Tetraselmis and Chlorella species, utilizing the internal transcribed spacer (ITS) barcode approach. By analyzing the full nuclear ITS region through the Sanger sequencing approach, we obtained ITS barcodes that were subsequently compared with other ITS sequences of various Tetraselmis and Chlorella species. To ensure the reliability of our identification procedure, we conducted a meticulous comparison of the DNA alignment, constructed a phylogenetic tree, and determined the percentage of identical nucleotides. The findings of our study reveal the significant value of the ITS genomic region as a tool for distinguishing and identifying morphologically similar chlorophyta. Moreover, our results demonstrate that both the ITS1 and ITS2 regions are capable of effectively discriminating isolates from one another; however, ITS2 is preferred due to its greater intraspecific variation. These results underscore the indispensability of employing ITS barcoding in microalgae identification, highlighting the limitations of relying solely on morphological characterization.