Enhancement of pigment extraction from B. braunii pretreated using CO2 rapid depressurization

Abstract Extraction of compounds from microalgae requires cell disruption as a pretreatment to increase extraction yield. Botryococcus braunii is a microalga with a significant content of carotenoids and other antioxidant compounds, such as chlorophylls. Cell disruption of B. braunii using CO2 rapid depressurization was studied as a pretreatment for the extraction of carotenoid and chlorophyll pigments. We studied the effect of temperature (21–49 °C) and pressure (6–13 MPa) during static compression on pigment recovery with supercritical CO2 at 40 °C, 30 MPa and solvent flow of 4.7 L NPT/min. Within the experimental region, the extraction yield of carotenoids and chlorophylls increased by 2.4- and 2.2-fold respectively. Static compression conditions of high pressure and low temperature increased the extraction of carotenoids and especially chlorophylls. We selected 21 °C and 13 MPa as the cell disruption condition, which produced 1.91 g/kg d.s. of carotenoids and 14.03 mg/kg d.s. of chlorophylls. Pretreated microalga gave a 10-fold higher chlorophyll extraction yield compared to the untreated sample. While for carotenoids and tocopherols were 1.25 and 1.14-fold higher, respectively. Additionally, antioxidant activity of pretreated microalga (33.22 mmol TE/kg oil) was significantly higher than the value for the untreated samples (29.11 mmol TE/kg oil) (p ≤ 0.05). Confocal microscopy images showed morphological differences between micro-colonies with and without disruption treatment, suggesting that partial cell disruption by rapid depressurization improved the extraction of microalga compounds.

Hydrogen production by photosynthetic green algae.

Oxygenic photosynthetic organisms such as cyanobacteria, green algae and diatoms are capable of absorbing light and storing up to 10-13% of its energy into the H-H bond of hydrogen gas. This process, which takes advantage of the photosynthetic apparatus of these organisms to convert sunlight into chemical energy, could conceivably be harnessed for production of significant amounts of energy from a renewable resource, water. The harnessed energy could then be coupled to a fuel cell for electricity generation and recycling of water molecules. In this review, current biochemical understanding of this reaction in green algae, and some of the major challenges facing the development of future commercial algal photobiological systems for H2 production have been discussed.

Carotenogénesis de cinco cepas del alga Dunaliella sp. (Chlorophyceae) aisladas de lagunas hipersalinas de Venezuela / Carotenogenesis of five strains of the algae Dunaliella sp. (Chlorophyceae) isolated from Venezuelan hypersaline lagoons

Se realizaron cultivos discontinuos (medio Algal con 0.5 mM de NaNO3 y 27% de NaCl) de cinco cepas de Dunaliella sp., aisladas de diferentes lagunas hipersalinas de Venezuela (Araya, Coche, Peonía, Cumaraguas y Boca Chica) y una cepa de referencia (Dunaliella salina LB1644). Los bioensayos se mantuvieron a 25 ± 1 °C con aireación constante, fotoperiodo 12:12 y dos intensidades luminosas (195 y 390 µE.m-2.s-1) durante 30 días. El crecimiento celular se determinó diariamente mediante conteo celular en cámara de Neubaüer. La clorofila a y los carotenoides totales se analizaron al final del ensayo. Las mayores densidades celulares correspondieron a los ensayos de menor intensidad luminosa. La cepa que alcanzó la mayor densidad celular fue la aislada de Boca Chica (8 x106 y 2.5 x106 cel.ml-1 a 195 y 390 µE.m-2.s-1, respectivamente). El incremento de la intensidad luminosa en los cultivos produjo una disminución significativa de las tasas de crecimiento en todas las cepas. Los carotenoides totales por volumen fueron mayores a 390 µE.m-2 .s-1; siendo las cepas de referencia LB1644, Coche y Araya las que produjeron mayor cantidad (38.4; 32.8 y 21.0 µg.ml-1, respectivamente). El contenido de carotenoides totales por célula en los dos tratamientos fue significativamente diferente, obteniéndose la mayor concentración a 390 µE.m-2.s-1. Las cepas LB1644 y Coche fueron las que produjeron los valores más altos de carotenos (137.14 y 106.06 pg.cel-1, respectivamente). La cepa LB1644 presentó la mayor relación carotenoides totales:clorofila a (20:1) a 195 µE.m-2.s-1, mientras que en la cepa Coche no se evidenciaron diferencias significativas entre las dos intensidades (15:1). El resto de las cepas mostraron relaciones inferiores a uno. Nuestros resultados sugieren que las cepas Coche y Araya pueden ser potencialmente utilizadas en la biotecnología de producción de carotenoides

We evaluated discontinuous cultures (Algal medium at 0.5 mM of NaNO3 , and 27% NaCl) of five strains of Dunaliella sp. isolated from Venezuelan hypersaline lagoons (Araya, Coche, Peonía, Cumaraguas, and Boca Chica) and one strain from a reference collection (Dunaliella salina, LB1644). Cultures were maintained to 25±1 °C, with constant aeration, photoperiod 12:12, and two light intensities (195 and 390 µE.m-2 .s-1) during 30 days. Cell count was recorded on a daily basis using a Neubaüer camera. Totals of chlorophyll a and carotenoids were measured at the end of the experiment. The largest cellular densities were measured during the smallest light intensities. The strain with the largest cellular density was isolated from Boca Chica (8 x106 and 2.5 x106 cel.ml-1 a 390 and 195µE.m-2 .s-1, respectively). The increment of light intensity produced a significant reduction of growth rates in all strains. Totals of carotenoids by volume were as large as 390 µE.m-2 .s-1. Strains LB1644, from Coche and Araya were those that produced the largest amount of carotenoids (38.4; 32.8 and 21.0 µg.ml-1 , respectively). Differences total carotenoids by cell between treatments were significant. The largest concentration was 390 µE.m-2 .s-1 . The strains LB1644 and Coche produced the highest values of carotenes (137.14 and 106.06 pg.cel-1, respectively). Differences in the relation carotenoid:chlorophyll a between the strains at various light intensities was significant. Strains LB1644 presented the largest value of the relation carotenoids:chlorophyll a (20:1) at 195 µE.m-2 .s-1. No significant differences were detected in the strain Coche (15:1). All the other strains showed relations lower than one. Our results suggest that the strains of Coche and Araya show potential to be used in the biotechnology of carotenoids production

Biosorption of zinc (II) using Spirogyra species from electroplating effluent.

Zinc was removed from the metal plating effluent with the biosorbent consisting of filamentous algae Spirogyra sp. The sorption was pH dependent with best adsorption at pH 2.5. The metal uptake increased from 3.9% (for no dilution) to 36.8% (for 10 times dilution), indicating that sorption increased with dilution of sample. The adsorption was faster at initial contact time, gradually decreased and remains constant after certain optimum time. Percentage removal of zinc increased from 20.3% to 63.6% with increase in the temperature from 25 degrees C to 35 degrees C but further increase resulted in the decrease in adsorption. Freundlich isotherm was applied and it holds good for the adsorption data.

Carbon concentration mechanisms in photosynthetic microorganisms.

Unicellular green algae and cyanobacteria have mechanism to actively concentrate dissolved inorganic carbon into the cells, only if they are grown with air levels of CO2. The carbon concentration mechanisms are commonly known as "CCM" or "DIC-pumps". The DIC-pumps are environmental adaptation that function to actively transport and accumulate inorganic carbon (HCO3- and CO2; Ci) within the cell and then uses this Ci pool to actively increase the concentration of CO2 at the site of ribulose bisphosphate carboxylase-oxygenase (Rubisco), the primary CO2-fixing enzyme. The current working model for dissolved inorganic carbon concentration mechanism in unicellular green algae includes several isoforms of carbonic anhydrase (CA), and ATPase driven active transporters at the plasmalemma and at the inner chloroplast envelopes. In the past fifteen years, significant progress has been made in isolating and characterizing the various isoforms of carbonic anhydrase at the biochemical and molecular level. However, we have an inadequate understanding of active transporters that are located on the plasmalemma and at the chloroplast envelopes. In this mini-review we focus on certain aspects of the induction, function and significance of the dissolved inorganic carbon concentration mechanisms in aquatic photosynthetic microorganisms.