ABSTRACT
Increased consumer awareness for healthier and more sustainable products has driven the search for naturally sourced compounds as substitutes for chemically synthesized counterparts. Research on pigments of natural origin, such as carotenoids, particularly lutein, has been increasing for over three decades. Lutein is recognized for its antioxidant and photoprotective activity. Its ability to cross the blood-brain barrier allows it to act at the eye and brain level and has been linked to benefits for vision, cognitive function and other conditions. While marigold flower is positioned as the only crop from which lutein is extracted from and commercialized, microalgae are proposed as an alternative with several advantages over this terrestrial crop. The main barrier to scaling up lutein production from microalgae to the commercial level is the low productivity compared to the high costs. This review explores strategies to enhance lutein production in microalgae by emphasizing the overall productivity over lutein content alone. Evaluation of how culture parameters, such as light quality, nitrogen sufficiency, temperature and even stress factors, affect lutein content and biomass development in batch phototrophic cultures was performed. Overall, the total lutein production remains low under this metabolic regime due to the low biomass productivity of photosynthetic batch cultures. For this reason, we describe findings on microalgal cultures grown under different metabolic regimes and culture protocols (fed-batch, pulse-feed, semi-batch, semi-continuous, continuous). After a careful literature examination, two-step heterotrophic or mixotrophic cultivation strategies are suggested to surpass the lutein productivity achieved in single-step photosynthetic cultures. Furthermore, this review highlights the urgent need to develop technical feasibility studies at a pilot scale for these cultivation strategies, which will strengthen the necessary techno-economic analyses to drive their commercial production.
Subject(s)
Lutein , Microalgae , Lutein/biosynthesis , Lutein/metabolism , Microalgae/metabolism , Microalgae/growth & development , Heterotrophic Processes , BiomassABSTRACT
3D printing represents a key enabling technology in designing photobioreactors. It allows rapid prototyping of complex geometries at an affordable price. Yet, no study dealt with the biocompatibility of 3D printing material with microalgae. Thus microalga Chlorella vulgaris was cultivated in contact with different 3D printing materials (Acrylonitrile Butadiene Styren - ABS, PolyCarbonate Blend - PC-Blend, PolyLactic acid - PLA, and acrylate methacrylate resin). Cell status was analyzed using flow cytometry, fluorometry, and pigment profiling. Results revealed that acrylate methacrylate resin material inhibits growth, a constant rise in intracellular reactive oxygen species, and a decrease in photosynthetic apparatus functioning. On the contrary, ABS, PC-Blend, and PLA led to nominal perfromances. Nevertheless, PLA was the only material that did not induce an early onset of intracellular reactive oxygen species. Therefore, resin can be ruled out as photobioreactor material, ABS and PC-Blend could be used after a curation period, and PLA induces no detectable perturbations by the means used in this study.
Subject(s)
Chlorella vulgaris , Reactive Oxygen Species , Printing, Three-Dimensional , Polyesters , Acrylates , MethacrylatesABSTRACT
Antioxidant foods represent a potent lever to improve diets while creating value. Yet, their cultivation is often tied to a specific area and climate, limiting availability and increasing market cost. Therefore, microorganism-based antioxidant production emerges as a promising technology to solve these problems. In this view, a novel process was investigated for antioxidant accumulation in yeast culture. S. cerevisiae cells were exposed to various hyperbaric air conditions from 1 to 9 bar (A). Yeast cultures exhibited an increased reactive oxygen species content, which induced oxidative defense expression. After a few hours, reactive oxygen species levels decreased while antioxidant contents remained high, leading to a net increase in antioxidant power. At 6 bar (A), yeast achieved the highest net antioxidant power (phenolics content +48.3 ± 18.6 %, reducing power +120 ± 11.4 %) with an acceptable growth rate (0.27 h-1). Regarding time evolution, a 2 h exposure seems to be the optimum: cells have the lowest reactive oxygen species level while their antioxidant power is increased. From a biotechnological perspective, this finding highlights air pressure as an antioxidant-manipulating stress strategy. Moreover, the proposed process led to a patent that could potentially reduce energy and chemical consumption in such antioxidant accumulation processes.
ABSTRACT
Recently, membrane contactors have gained more popularity in the field of CO2 removal; however, achieving high purity and competitive recovery for poor soluble gas (H2, N2, or CH4) remains elusive. Hence, a novel process for CO2 removal from a mixture of gases using hollow fiber membrane contactors is investigated theoretically and experimentally. A theoretical model is constructed to show that the dissolved residual CO2 hinders the capacity of the absorbent when it is regenerated. This model, backed up by experimental investigation, proves that achieving a purity > 99% without consuming excessive chemicals or energy remains challenging in a closed-loop system. As a solution, a novel strategy is proposed: the pH Swing Absorption which consists of manipulating the acido-basic equilibrium of CO2 in the absorption and desorption stages by injecting moderate acid and base amount. It aims at decreasing CO2 residual content in the regenerated absorbent, by converting CO2 into its ionic counterparts (HCO3- or CO32-) before absorption and improving CO2 degassing before desorption. Therefore, this strategy unlocks the theoretical limitation due to equilibrium with CO2 residual content in the absorbent and increases considerably the maximum achievable purity. Results also show the dependency of the performance on operating conditions such as total gas pressure and liquid flowrate. For N2/CO2 mixture, this process achieved a nitrogen purity of 99.97% with a N2 recovery rate of 94.13%. Similarly, for H2/CO2 mixture, a maximum H2 purity of 99.96% and recovery rate of 93.96% was obtained using this process. Moreover, the proposed patented process could potentially reduce energy or chemicals consumption.
ABSTRACT
Chlorella vulgaris was grown using mixed sources of nitrogen (nitrate and nitrite). Starting from B3N as basal medium, nitrate was substituted by nitrite keeping total nitrogen constant over 7 conditions: 0, 20, 40, 50, 60, 80 and 100% NO2-. Growth rate, nitrogen uptake, photosynthetic apparatus status and pigment contents were monitored. Nitrite addition triggered a growth rate inhibition from early introduction (20% NO2-, 81 mgNO2-/l). Nitrate uptake rate increased with nitrate content in the culture medium (maximum at 5.87 mg/l/Nd, 100% NO3-), while nitrite uptake remained constant around 2.93 mgN/l/d. Photosynthetic apparatus was not impacted by the nitrogen source substitution. Pigments profiles (chlorophyll a, b and total carotenoids) were not statistically different for all the tested conditions. From a biotechnological perspective, this finding rules out the use of nitrite substitution as a pigment manipulating stress strategy.
Subject(s)
Chlorella vulgaris , Nitrates , Chlorophyll A , Nitrites , NitrogenABSTRACT
Flat panels are the most spread type of photobioreactors for studying light effects on a microalgae culture. Their low thickness, usually between 1 and 3 cm, aims at ensuring light homogeneity across the culture. Yet because optical density has to remain very low, studies are still limited to low cell density cultures. To alleviate this problem, even thinner photobioreactors can be designed. Nevertheless, thin flat panel reactors are very prone to induce high shear stress. This work aimed at designing a new millimeter thin panel photobioreactor to study light effects on Chlorella and Scenedesmus genera. We proposed a numerical workflow that is capable of assessing the shear stress intensity in such a reactor. The numerical predictions were validated at three different levels: 2D preliminary simulations were able to reproduce bubble commonly known behaviors; close to the nozzle, the predictions were successfully confronted to shadowgraphy experimental reference; at the mini bioreactor scale, experimental and numerical mixing were found to be close. After these throughout validations, shear stress intensity in the photobioreactor was calculated over 1000 Lagrangian tracers. The experienced shear stress was agglomerated at the population level. From the computed shear stress, it was possible to choose the minimal reactor thickness that would not hinder cell growth.
Subject(s)
Chlorella/growth & development , Microalgae/growth & development , Models, Biological , Photobioreactors , Scenedesmus/growth & development , Stress, MechanicalABSTRACT
This study investigated the impact of oxygen partial pressure on yeast growth. Saccharomyces cerevisiae cells were exposed to various hyperbaric air conditions from 1 bar to 9 bar absolute pressure (A). Batch cultures were grown under continuous airflow in a 750 mL (500 mL culture) bioreactor and monitored through growth rate and specific yields of ethanol and glycerol. In addition, the concentrations of antioxidant metabolites glutathione (reduced state, GSH and oxidized state, GSSG) and the activity of antioxidative enzymes superoxide dismutases (SOD) and catalases (CAT) were monitored. The results demonstrated that the different oxygen partial pressures significantly impacted the key growth parameters monitored. Compared with atmospheric pressure, under 2 to 5 bar (A), yeast cells showed higher growth rates (µ = 0.32 ± 0.01 h-1) and higher catalase (CAT) concentrations (214 ± 5 mU/g). GSH/GSSG ratio (6.36 ± 0.37) maintained until 6 bar (A) and total SOD (240 ± 5 mU/g) level significantly increased compared with 2 bar (A) until 7 bar (A). Under 6 to 9 bar (A), cell growth was inhibited, and a pressure of 9 bar (A) led to excessive GSSG accumulation (GSH/GSSG = 0.31 ± 0.06). The inhibition of t-SOD (160 ± 3 mU/g) and CAT (62.73 ± 0.2 mU/g) was observed under 9 bar (A). A reference experiment (8 bar (A) N2 + 1 bar (A) air) confirmed that the observed behaviors were entirely due to O2. In addition to their utility in biotechnological process design, these results showed that growth impairment was solely due to oxidative stress induced by excessive oxygen pressure. KEY POINTS: ⢠Yeast cells were grown in batch mode under 1 to 9 bar (A) air pressures and up to 5 bar (A) promoted then hindered growth. ⢠The GSH/GSSG ratio was stable up to 5 bar (A) then GSSG accumulated to excess. ⢠Complementary investigations of the activity of SOD and CAT validated growth limitations due to oxidative stress.
Subject(s)
Antioxidants , Saccharomyces cerevisiae , Catalase/metabolism , Glutathione/metabolism , Oxidative Stress , Oxygen , Partial Pressure , Saccharomyces cerevisiae/metabolism , Superoxide Dismutase/metabolismABSTRACT
In this article, a numerical workflow describing the microalgal growth inside of a photobioreactor is proposed. CFD is used to compute reactor internal hydrodynamics taking into account marine impeller rotation and sparged bubbles motion. Lagrangian approach is used to track microalgae motion inside of the culture vessel. The illumination across the reactor is obtained using the classical Beer-Lambert's law. The combination of light field and cell motion allows to reconstruct the light history of each microalgae. These histories are then supplied to Han's model which predicts individual growth rate and experienced photodamages. Once computed, several thousands of trajectories are agglomerated at the population level yielding the photobioreactor performances. After having ensured properties convergence, this procedure is applied to a large range of optical density (0 to 4.0), i.e. cell concentration, and incident light intensities (0 to 2000 µmolPhoton/m2/s). From this exploration, it is possible to determine the photobioreactor response surfaces in terms of growth rate and photodamages. These are latter used to propose an optimal lighting strategy for biomass production - reducing photobioreactor operation time by 16% compared to classical two-step procedure - and assist light induced stress with the aim of triggering secondary metabolites production.
Subject(s)
Microalgae , Photobioreactors , Biomass , Incidence , Population Growth , WorkflowABSTRACT
This work reviews applications of high added value molecules produced from microalgae. Older forms of valorization - health food and quality feed, polyunsaturated fatty acids, pigments, carbohydrates - are currently penetrating their markets. They are driven by desirable properties: texturer and dye for food industry, antioxidant for cosmetics and the appetite of the general public for biosourced compounds. Most recent developments, such as peptides, vitamins, polyphenols, phytosterols and phytohormones, are struggling to meet their market and reach economical competitiveness. Still they are pushed forward by the very powerful driver that is pharmaceutical industry. In addition this work also proposes to link microalgae phyla and related potential applications. This is done through highlighting of which bioactive compounds can be found in which phyla. While some seem to be restricted to aquaculture, Cyanobacteria, Chlorophyta and Rhodophyta show great promises.
Subject(s)
Chlorophyta , Cyanobacteria , Microalgae , Rhodophyta , AntioxidantsABSTRACT
This work reports the design of a light concentrator intended to be used to cast uniform lighting over a photobioreactor. Household aluminum foils was chosen as reflective material to build the concentrator. This choice raised the question of which side to use. Thus measurements of household aluminum foil reflectivity spectra on both bright and matte sides were undergone. These measurements were done using an integrating sphere, over a 250-2500â¯nm range. Diffuse and total reflectivities were acquired, for two samples each time. The obtained results are very repeatable and in good agreement with literature on rolled aluminum sheets, for the bright side at least, as matte side data were not found. Specular reflectivity is higher for the bright side while diffuse reflectivity is higher for the matte one. Furthermore, both sides of the foil have the same total reflectivity, around 86 % in the visible range of the spectrum, 97% in the near infrared. Our measurements are readability usable and available as supplementary materials. Finally, we applied these findings to the in silico design of lab scale light concentrator illuminating a new photobioreactor. A modified version of the raytracing software Soltrace was used to determine which of the two sides of our household aluminum foil was be best suited for our application.
ABSTRACT
This work provides a model and the associated set of parameters allowing for microalgae population growth computation under intermittent lightning. Han's model is coupled with a simple microalgae growth model to yield a relationship between illumination and population growth. The model parameters were obtained by fitting a dataset available in literature using Particle Swarm Optimization method. In their work, authors grew microalgae in excess of nutrients under flashing conditions. Light/dark cycles used for these experimentations are quite close to those found in photobioreactor, i.e. ranging from several seconds to one minute. In this work, in addition to producing the set of parameters, Particle Swarm Optimization robustness was assessed. To do so, two different swarm initialization techniques were used, i.e. uniform and random distribution throughout the search-space. Both yielded the same results. In addition, swarm distribution analysis reveals that the swarm converges to a unique minimum. Thus, the produced set of parameters can be trustfully used to link light intensity to population growth rate. Furthermore, the set is capable to describe photodamages effects on population growth. Hence, accounting for light overexposure effect on algal growth.