Humic substances (HS) act as biostimulants for terrestrial photosynthetic organisms. Their effects on plants are related to specific HS features: pH and redox buffering activities, (pseudo)emulsifying and surfactant characteristics, capacity to bind metallic ions and to encapsulate labile hydrophobic molecules, ability to adsorb to the wall structures of cells. The specific properties of HS result from the complexity of their supramolecular structure. This structure is more dynamic in aqueous solutions/suspensions than in soil, which enhances the specific characteristics of HS. Therefore, HS effects on microalgae are more pronounced than on terrestrial plants. The reported HS effects on microalgae include increased ionic nutrient availability, improved protection against abiotic stress, including against various chemical pollutants and ionic species of potentially toxic elements, higher accumulation of value-added ingredients, and enhanced bio-flocculation. These HS effects are similar to those on terrestrial plants and could be considered microalgal biostimulant effects. Such biostimulant effects are underutilized in current microalgal biotechnology. This review presents knowledge related to interactions between microalgae and humic substances and analyzes the potential of HS to enhance the productivity and profitability of microalgal biotechnology.

In this study, we investigated the use of functionalized deep eutectic solvents (DESs) as a medium for CO₂ capture integrated with CO₂ desorption and biofixation in microalgal culture, as an approach for carbon capture, utilization, and storage (CCUS). The newly devised DES formulation—comprising choline chloride, ethylene glycol, and monoethanolamine—demonstrated a significant advancement in CO₂ absorption capacity compared with conventional solvents. Effective CO₂ desorption from the solvent was also achieved, recovering nearly 90% of the captured CO₂. We then examined the application of the functionalized DESs to promote microalgal cultivation using a Chlorella sp. strain. The experimental results indicated that microalgae exposed to DES-desorbed CO₂ exhibited heightened growth rates and enhanced biomass production, signifying the potential of DES-driven CO₂ capture for sustainable microalgal biomass cultivation. This research contributes to the growing field of CCUS strategies, offering an avenue for efficient CO₂ capture and conversion into valuable biomasses, thereby contributing to both environmental sustainability and bioresource use.

In terrestrial plants, strigolactones act as multifunctional endo- and exo-signals. On microalgae, the strigolactones determine akin effects: induce symbiosis formation with fungi and bacteria and enhance photosynthesis efficiency and accumulation of biomass. This work aims to synthesize and identify strigolactone mimics that promote photosynthesis and biomass accumulation in microalgae with biotechnological potential. Novel strigolactone mimics easily accessible in significant amounts were prepared and fully characterized. The first two novel compounds contain 3,5-disubstituted aryloxy moieties connected to the bioactive furan-2-one ring. In the second group of compounds, a benzothiazole ring is connected directly through the cyclic nitrogen atom to the bioactive furan-2-one ring. The novel strigolactone mimics were tested on Chlorella sorokiniana NIVA-CHL 176. All tested strigolactones increased the accumulation of chlorophyll b in microalgae biomass. The SL-F3 mimic, 3-(4-methyl-5-oxo-2,5-dihydrofuran-2-yl)-3H-benzothiazol-2-one (7), proved the most efficient. This compound, applied at a concentration of 10⁻⁷ M, determined a significant biomass accumulation, higher by more than 15% compared to untreated control, and improved the quantum yield efficiency of photosystem II. SL-F2 mimic, 5-(3,5-dibromophenoxy)-3-methyl-5H-furan-2-one (4), applied at a concentration of 10⁻⁹ M, improved protein production and slightly stimulated biomass accumulation. Potential utilization of the new strigolactone mimics as microalgae biostimulants is discussed.

This study aimed to evaluate the impact of a more cost-efficient strigolactone mimic SL-6 on Chlorella sorokiniana NIVA-CHL 176 growth in comparison with the strigolactone analog GR24 and the plant biostimulant functions of microalgal extracts. Three molar SL-6 concentrations were tested: 10⁻⁷ M, 10⁻⁸ M, and 10⁻⁹ M, respectively. Five parameters of microalgal growth were assessed: optical density, turbidity, biomass production, chlorophyll fluorescence, and pigment concentration. Results after 15 days of culturing revealed that the SL-6 treatments significantly enhanced biomass production (13.53% at 10⁻⁹ M), pigment synthesis, and photosystem II activity (14.38% at 10⁻⁹ M). The highest increases in pigments induced by SL-6 were 15.7% for chlorophyll a (at 10⁻⁸ M SL-6), 12.87% for chlorophyll b (at 10⁻⁹ M SL-6), 2.3% for carotenoids (at 10⁻⁸ M SL-6), and 10.78% for total pigments (at 10⁻⁸ M SL-6) per gram biomass compared to the solvent control (DMSO). Higher doses of GR24 and SL-6 (10⁻⁷ M) inhibited microalgal growth, reducing cell density, biomass production, and pigment synthesis. The microalgal extracts acted as plant biostimulants, stimulating root and shoot elongation and proton pump functioning of mung seedlings in the presence and absence of salt stress. The extracts from SL-6 biostimulated C. sorokiniana were more active as plant biostimulants than the extracts from the non-stimulated C. sorokiniana.

In this work, HAs were obtained by humification of lignin that was extracted from beer spent grain (BSG) obtained from beer fabrication with deep eutectic solvents (DESs). The humification process used in this case was reacting the BSG-extracted lignin with hydrogen peroxide in the presence of ferric sulphate heptahydrate. The biostimulant effect of HAs was tested on the Chlorella Sorokiniana microalgae species. Additionally, biostimulant tests were conducted using a commercial product containing HAs (BlackJak, BJK) and a coal-extracted lignosulphonate (LsNa).

Fungi are known for their capacity to produce two main categories of enzymes, cellulolytic and lignolytic, both valuable for biodegradation of lignocellulosic biomass