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In the production of natural sausage casings, three layers of serosa, muscular, and mucosa are removed from gastro-intestinal wall of sheep as waste materials. The submocusa layer is taken for further processing. There is no report about generating added value out of these wastes. In this study, a novel approach was introduced for bioconversion of waste gastro-intestinal wall (WGW) to a value-added product. Alkaline hydrolysis of WGW was investigated and the hydrolysate was utilized for cultivation of Dunaliella salina, a value-added biomass. The hydrolysate that contained the highest total soluble protein was used for three sets of cultivations on different medium compositions, i.e., (1) cultivations on the modified Johnson’s medium enriched with different percentage of hydrolysate (0.5, 1, 2.5, 5, and 10 (%v/v)), (2) cultivations on modified Johnson’s medium which was free of nitrogen and carbon sources and enriched with different percentage of hydrolysate (0.5, 1, 2.5, 5, and 10 (%v/v), and (3) cultivation on modified Johnson’s medium which was free of nitrogen source and enriched with 2.5% hydrolysate. The results showed that WGW contained 60.7, 8.4, 15.8, and 15.2% protein, lipid, moisture, and ash, respectively and the enrichment of the medium with the hydrolysate (2.5%) increased biomass productivity by 20%. Additionally, substitution of 2.5% hydrolysate for nitrogen source (KNO3) resulted in the same biomass productivity. The results of this study revealed the potential of the hydrolysate as an alternative for KNO3 in cultivation of D. salina. Overall, this work proposed a novel approach for converting waste gastro-intestinal wall to value.

Dunaliella salina is a unicellular microalga with the potential of industrial applications. Commercial-scale cultivation of D. salina requires extensive efforts on cost reduction. This can be achieved by minimization of nutrient cost and maximization of specific growth rate and productivity. To this end, in this study, mixotrophic cultivation of D. salina on crude glycerol (by-product of calcinated-fatty acid (CaFA) production process) was investigated in shake flasks and the influences on protein, carotenoid and chlorophyll contents of the cells were studied. The highest maximum specific growth rate and biomass productivity was achieved by cultivation on 2.5 g/L crude glycerol. The protein content was more than two folds and the carotenoid content was more than 60% higher than that of autotrophic cultivation. Subsequently, continuous cultivation of D. salina on crude glycerol in a helical photobioreactor was performed at the dilution rate of 0.52/d. The biomass productivity of 2.3 × 106 cell/(mL d) was achieved which was more than 75% of the values for previously reported autotrophic cultivations. Conclusively, continuous cultivation of D. salina on by-product of CaFA production process could be a potential process technology for production of D. Salina.

The effects of autotrophic, heterotrophic, and mixotrophic conditions were examined on micro green alga Dunaliella salina (UTEX 200) in terms of cell growth, total chlorophyll concentration, and lipid production. Results revealed a minimum growth rate of microalgae in the heterotrophic condition which is not recommended for D. salina. When the cells were cultured in mixotrophic conditions containing different concentrations of acetate or glucose, in 100 mM acetate or 60 mM glucose, the highest levels of growth rate and lipid production were obtained compared with autotrophic culture; however, the chlorophyll concentration decreased. Moreover, a significant correlation between ROS production and lipid synthesis was observed. When the combined acetate and glucose was added to the culture, no increase in growth rate and lipid synthesis was observed. This might be due to substrate inhibition. In the presence of glucose, the acidification of culture and bleaching occurred. Results indicated that lipid production is not affected by acidified conditions. In general, our results confirmed that mixotrophic culture with 100 mM acetate or 60 mM glucose is the most appropriate culture for D. salina concerning high lipid production as well as high growth rate in the shortest period of time.

The development of nanotechnology and the upsurge of interest in titanium dioxide (TiO2) nanoparticles, especially the anatase and rutile crystalline phases, in consumer products such as paint and sunscreen, has polluted the aquatic environment and had adverse effects on living organisms, especially algae. Microalgae help to preserve the aquatic ecosystem. Accordingly, the present study investigated the effects of anatase and rutile TiO2 nanoparticles on the growth, photosynthetic pigment (chlorophyll), photosynthesis, and respiration rate of two algae species, Dunaliella salina (at NaCl concentrations of 1.5 and 0.5 M) and Dunaliella tertiolecta (at NaCl concentrations of 0.5 and 0.17 M). Treatment with 50, 100, 150, and 200 ppm of TiO2 and nano-TiO2 revealed that nano-TiO2 inhibited the growth and decreased the specific growth rate, chlorophyll, and photosynthesis of both algal species. The rate of decrease was significantly lower at higher concentrations of NaCl in both species; however, the greatest significant difference was observed at lower concentrations of NaCl in the anatase phase. The respiration rate increased for 2 weeks but, especially at lower concentrations of NaCl, the rate of increase declined at higher concentrations after exposure to both substances, especially in the anatase phase. The findings reveal that nano-TiO2 has a toxic effect on Dunaliella algae and its effect depends on the concentration of NaCl. The toxic effect was shown to decrease at higher concentrations of NaCl.

Effect of salt stress on biomass, cell number, contents of total lipid, omega-3 fatty acids, including ALA (Alpha Linolenic Acid), EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) and their biosynthetic pathway intermediates (palmitic acid, stearic acid, oleic acid and linoleic acid) of two microalgae Dunaliella salina and Chlorella vulgaris were investigated. Dilution stress from 1.5 to 0.5 M NaCl and salt stress from 1.5 to 3 M NaCl were incorporated into the D. salina medium. Salt stress of 200 mM NaCl was also applied to C. vulgaris culture. Results indicated that increasing salt concentration resulted in the reduced growth rate of C. vulgaris and substantial increase of the total lipid content in both species. Proper growth rate of D. salina observed at 1.5 M of NaCl, but higher and lower concentrations led to the decreased growth rate of D. salina. In addition, considerable increase in the degree of fatty acid unsaturation and thereby the total omega 3 fatty acid content of D. salina was observed under salt stress. Salt stress had little positive effect on the amount of total omega-3 fatty acid of C. vulgaris due to the slight increase of the EPA content. Results showed that salt stress is an effective way for enhancing the total lipid and omega-3 fatty acid production in D. salina.

The ability of two Dunaliella salina strains (AS-B1 and IR-1) and Dunaliella bardawil (UTEX-2538) in the sedimentation of different concentrations (0, 500, 1000, 2000, 3000 and 4000 μM) of aluminum were studied for duration 120 min. In these strains, increase in aluminum concentration was concomitant with the reduction of cell number in supernatant as the index of the sediment aluminum by algal cells-Al 3+ ions binding; cell agglutination and sedimentation caused by presence of aluminum. The ability of D. bardawil was higher in sedimentation of aluminum. The results of adding EDTA to cell suspensions for binding the aluminum confirmed the role of binding algal cells to aluminum in cell agglutination and sedimentation and consequently aluminum bioremediation. In addition, the results imply that the cell agglutination and sedimentation in D. bardawil is higher than Dunaliella salina . It seems this strain has a greater capability for sedimentation of aluminum and can utilize aluminum from aquatic environments for bioremediation.

Electron transport in photosystem II (PSII) and photosystem I (PSI) was estimated in terms of chlorophyll fluorescence and changes in P700 redox, respectively, in the unicellular green alga Dunaliella salina in the presence or absence of a nitrogen source in the culture medium. In a nitrogen-containing medium, the quantum yield of PSII (Φ(II)) and that in PSI (Φ(I)) were at the same level in low light, but cyclic electron transport around photosystem I (CET-PSI) was induced under high light as estimated from an increase in Φ(I)/Φ(II). High light might further enhance the rate of electron transport in PSI by inducing the state 2 transition, in which the distribution of light energy is shifted to PSI at the expense of PSII. Nitrogen deficiency resulted in a decrease in Φ(II) and an increase in Φ(I). As a consequence, the rate of CET-PSI was expected to increase. The high CET-PSI under N deficiency was probably associated with a high level of energy quenching (qE) formation in PSII.

Dunaliella species accumulate carotenoids and their role in protection against photooxidative stress has been investigated extensively. By contrast, the role of other antioxidants in this alga, has received less attention. Therefore, the components of the ascorbate-glutathione cycle, along with superoxide dismutase (E.C. 1.15.1.1) and peroxidase (E.C. 1.11.1.11) activity were compared in two strains of Dunaliella salina. Strain IR-1 had two-fold higher chlorophyll and beta-carotene concentration than Gh-U. IR-1 had around four-fold higher superoxide dismutase, ascorbate peroxidase and pyrogallol peroxidase activities than Gh-U on a protein basis. Ascorbate and glutathione concentrations and redox state did not differ between strains and there was little difference in the activity of ascorbate-glutathione cycle enzymes (monodehydroascorbate reductase [E.C. 1.6.5.4], dehydroascorbate reductase [E.C. 1.8.5.1] and glutathione reductase [E.C. 1.8.1.7]). The response of these antioxidants to high light and low temperature was assessed by transferring cells from normal growth conditions (28 degrees C, photon flux density of 100 micromol m(-2) s(-1))to 28 degrees C/1200 micromol m(-2) s(-1); 13 degrees C/100 micromol m(-2) s(-1); 13 degrees C/1200 micromol m(-2) s(-1) and 28 degrees C/100 micromol m(-2) s(-1) for 24 h. Low temperature and combined high light-low temperature decreased chlorophyll and beta-carotene in both strains indicating that these treatments cause photooxidative stress. High light, low temperature and combined high light-low temperature treatments increased the total ascorbate pool by 10-50% and the total glutathione pool by 20-100% with no consistent effect on their redox state. Activities of ascorbate-glutathione cycle enzymes were not greatly affected but all the treatments increased superoxide dismutase activity. It is concluded that D. salina can partially adjust to photooxidative conditions by increasing superoxide dismutase activity, ascorbate and glutathione.

In this study, carotenoid and glycerol production in two unicellular green algae (Dunaliella salina and D. viridis) isolated from the Gave-Khooni salt marsh grown in media containing five different salt concentrations (0.17, 1, 2, 3, and 4 M NaCl) were evaluated under sterile conditions. Algae growth decreased as the medium salinity increased. Optimum growth of D. salina and D. viridis were obtained at 2 and 1 M NaCl, respectively. As salinity increased, glycerol and carotenoid production were increased in D. salina, whereas lower values for these products were produced in D. viridis under the same conditions. Furthermore, the cell color of D. salina changed from green to orange-red following accumulation of carotenoid, but the color of D. viridis was not changed. Thereby, it seems that the Iranian D. salina may be suitable for carotenoid production (betacarotene) on a large scale. In addition, since carotenoid compounds enhance the efficiency of photosynthesis and glycerol synthesis, it appears that the pathway for glycerol production and mechanisms of salt tolerance in D. viridis are unique from those of D. salina.

Three strains of Dunaliella salina (I, G and A) were cultivated under the climatic conditions of Iran, in open ponds to compare the β-carotene production and the specific rate of growth. The experiments were accomplished in two separate stages. In the first stage, the cells were grown in ponds on nutrient-rich medium containing 2 M NaCl to obtain the necessary biomass. In the second stage, cells were stressed on nutrient-poor medium containing 2.5 M NaCl for β-carotene induction. The results showed that the specific growth rate of strain I was the highest during the first stage, whereas during the second stage, the growth rates of three strains were approximately the same. The overall results indicated that strain G had the highest potential for β-carotene accumulation of the strains tested and hence it was concluded that this strain is more suitable for outdoor cultivation under the climatic conditions of Iran than the other two.

We studied the effects of n-propyl gallate, which is a plastid terminal oxidase inhibitor involved in chlororespiration, on photosynthesis and physiological parameters in Dunaliella salina grown under different salinities and under low or high irradiance using chlorophyll a fluorescence transient measurements and pigment analysis. The inhibitor up to 1 mM had an additive significant effect on the photosynthetic efficiency in the cell suspensions grown under low salinity and irradiance. However, in the presence of high n-propyl gallate concentration (4 mM), there was a negative effect on all physiological aspects. In contrast, this high concentration of the inhibitor could enhance efficiency of electron transport and growth parameters under high irradiance. On the other hand, with salinity increase, the unfavorable effects of high inhibitor concentration on the efficiency of photosystem II were less evident than of low salinity. Interestingly, n-propyl gallate high concentration had a positive effect on fluorescence and on physiological parameters when high salinities-grown cells were exposed to high irradiance. The results suggest that there is a rational correlation between increase of salinity and algae ability to bypass n-propyl gallate inhibited plastid terminal oxidase function and also direct influence of its lethal concentration on photosystem II compartment. The ability is especially substantial when the increase of salinity is accompanying high irradiance. Furthermore, these data show that algal responses to inhibitor concentrations are different under various environmental conditions.

The microalga Dunaliella salina is the best commercial source of natural beta-carotene. Additionally, different species of Dunaliella can accumulate significant amounts of valuable fine chemicals such as carotenoids, glycerol, lipids, vitamins, minerals and proteins. They also have a large potential for biotechnological processes such as expressing of foreign proteins and treatment of wastewater. In this review, we discussed several biotechnological aspects of the mass cultivation of D. salina like strain selection, carotenoid induction, culture conditions, culture systems and downstream processes. We also discuss several traditional and new applications of the genus.