Dunaliella salina: Difference between revisions

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===Higher order Taxa===
===Higher order Taxa===
Bacteria (Domain);  Chlorophyta (Phylum); Chlorophyceae (Class);  Volvocales (Order);  Dunaliellaceae  (Family);  Dunaliella (Genus).
Eukaryota (Domain); Viridiplantae (Kingdom);  Chlorophyta (Phylum); Chlorophyceae (Class);  Volvocales (Order);  Dunaliellaceae  (Family);  Dunaliella (Genus).


===Species===
===Species===
''Dunaliella salina''
''Dunaliella salina''
=Description and Significance=
[[File:LMDsalina.jpeg|300px|thumb|right|Figure 1A. ''Dunaliella salina'' under light microscope [[#Reference|[17]]].]]
[[File:Dunaliella salina.png|300px|thumb|right|Figure 1B. ''Dunaliella salina'' modified from Shariati and Hadi[[#References|[6]]] and Heakel, Hefny and El-Tawab[[#References|[16]]] ]]




=Description and Significance=


''Dunaliella salina'' is a unicellular green alga found in environments with high salt concentration [[#References|[1]]]. It produces a distinct pink and red colour often characteristic of [http://en.wikipedia.org/wiki/Salt_evaporation_pond saltern] ponds [[#References|[2]]]. Michel Felix Dunal first discovered "D. salina" in 1838 in the south of France occupying; however, it was not named until 1905 by Teodoresco [[#References|[1]]].  
''Dunaliella salina'' is a unicellular green alga found in environments with high salt concentration [[#References|[1]]]. It produces a distinct pink and red colour often characteristic of [http://en.wikipedia.org/wiki/Salt_evaporation_pond saltern] ponds [[#References|[2]]]. Michel Felix Dunal first discovered "D. salina" in 1838 in the south of France occupying; however, it was not named until 1905 by Teodoresco [[#References|[1]]].  
''Dunaliella'' species are able to tolerate varying NaCl concentrations, ranging from 0.2% to approximately 35% [[#References|[3]]]. Thus,  ''Dunaliella salina'' is a hyper-halotolerant organism found in high densities in saline lakes. ''D. salina'' has adapted to survive in high salinity environments by accumulating [http://en.wikipedia.org/wiki/Glycerol glycerol] to balance osmotic pressure. ''D. salina'' is also adapted to solar radiation using [http://en.wikipedia.org/wiki/Beta-Carotene β-carotene] to protect against ionizing energy. This combination offers potential in biotechnological applications for the purpose of commercial products such as lipstick due to β-carotene production [[#References|[4]]].  ''Dunaliella salina'' is a model organism to study the effects of saline adaptation in algae [[#References|[1]]]. In addition, the role of glycerol in ''D. salina'' as a key organic compatible solute has been used as a research model [[#References|[1]]].  
''Dunaliella'' species are able to tolerate varying NaCl concentrations, ranging from 0.2% to approximately 35% [[#References|[3]]]. Thus,  ''Dunaliella salina'' is a hyper-halotolerant organism found in high densities in saline lakes. ''D. salina'' has adapted to survive in high salinity environments by accumulating [http://en.wikipedia.org/wiki/Glycerol glycerol] to balance osmotic pressure. ''D. salina'' is also adapted to solar radiation using [http://en.wikipedia.org/wiki/Beta-Carotene β-carotene] to protect against ionizing energy. This combination offers potential in biotechnological applications for the purpose of commercial products such as lipstick due to β-carotene production [[#References|[4]]].  ''Dunaliella salina'' is a model organism to study the effects of saline adaptation in algae [[#References|[1]]]. In addition, the role of glycerol in ''D. salina'' as a key organic compatible solute has been used as a research model [[#References|[1]]].  


[[File:LMDsalina.jpeg|500px|thumb|Figure 1A. ''Dunaliella salina'' under light microscope [[#Reference|[17]]].]]


[[File:Dunaliella salina.png|300px|thumb|Figure 1B. ''Dunaliella salina'' modified from Shariati and Hadi[[#References|[6]]] and Heakel, Hefny and El-Tawab[[#References|[16]]] ]]
 
 




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=Ecology=
=Ecology=
[[File:hypersaline.jpeg|300px|thumb|left|Figure 2. Hypersaline Lake [[#Reference|[5]]]. ]]


''Dunaliella salina'' are found in high salinity environments such as salted brines, salt evaporation ponds, and [http://en.wikipedia.org/wiki/Hypersaline_lake hypersaline lakes] [[#References|[7]]]. The ability to tolerate high salt concentrations is advantageous, since competition is minimal as salt high salt concentrations. ''Dunaliella salina'' was thought to be responsible for the red colouring of salted brines [[#References|[1]]]. However, carotenoids responsible for the red colouration in ''D. salina'' are found in algal chloroplasts, whereas halophilic archaea also occupying hypersaline lakes have red pigments dispersed throughout the cell membrane [2]. Although there is a much greater abundance of ''D. salina'', the red pigments on the cell membrane of archaea are more visibly accessible. Therefore, ''D. salina'' has a much less overall impact to colouration and archaeal communities contribute more to the red colouration of hypersaline lakes.
''Dunaliella salina'' are found in high salinity environments such as salted brines, salt evaporation ponds, and [http://en.wikipedia.org/wiki/Hypersaline_lake hypersaline lakes] [[#References|[7]]]. The ability to tolerate high salt concentrations is advantageous, since competition is minimal as salt high salt concentrations. ''Dunaliella salina'' was thought to be responsible for the red colouring of salted brines [[#References|[1]]]. However, carotenoids responsible for the red colouration in ''D. salina'' are found in algal chloroplasts, whereas halophilic archaea also occupying hypersaline lakes have red pigments dispersed throughout the cell membrane [2]. Although there is a much greater abundance of ''D. salina'', the red pigments on the cell membrane of archaea are more visibly accessible. Therefore, ''D. salina'' has a much less overall impact to colouration and archaeal communities contribute more to the red colouration of hypersaline lakes.


[[File:hypersaline.jpeg|300px|thumb|Figure 2. Hypersaline Lake [[#Reference|[5]]]. ]]
 
 


=Life Cycle=
=Life Cycle=
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=Genome Structure=
=Genome Structure=


[[File:Dsalinamitochondria.jpeg|150px|thumb|right|Figure 3A. Complete ''Dunaliella salina'' mitochondrial genome map[[#References|[9]]]. ]]
[[File:Dsalinamitochondria.jpeg|350px|thumb|left|Figure 3A. Complete ''Dunaliella salina'' mitochondrial genome map[[#References|[9]]]. ]]
 
[[File:Dsalinaplastid.jpeg|350px|thumb|left|Figure 3B. Complete ''Dunaliella salina'' plastid genome map [[#References|[9]]]. ]]
 
The sequencing of ''Dunaliella species'' is important to isolate different species for commercial purposes. Olmos et al. [[#References|[8]]] sequenced five species of ''Dunaliella'' using their 18S ribosomal RNA genes.  The ''D. salina'' organelle genome sequence are circular and large with approximately 60% non-coding DNA [[#References|[9]]]. Although the biochemistry and physiology of ''D. salina'' has been researched, much about the genome was unknown until Smith ''et al.'' [[#References|[9]]] studied the mitochondrial and plastid genome of ''D. salina''. The mitochondrial and plastid genome contains 28.3 (12 genes) and 269 kb (102 genes) respectively [[#References|[9]]].  In addition, Smith ''et al.'' [[#References|[9]]] found that both genomes are highly occupied with introns: mitochondrial DNA (58%) and plastid DNA (65.5%). The GC content of "D. salina" is relatively low compared to other Chlamydomonadales at 34.4% for mitochondrial DNA and 32.1% for plastid DNA[[#References|[9]]].
 
=β-carotene=
 
[[File:saltgrowth.png|300px|thumb|left|Figure 4.Cell density of Dunaliella salina cells grown in media containing wide range of salt concentrations[[#Reference|[6]]]. ]]  


[[File:Dsalinaplastid.jpeg|150px|thumb|right|Figure 3B. Complete ''Dunaliella salina'' plastid map [[#References|[9]]]. ]]
β-carotene is a type of pro-vitamin A, responsible for inhibiting the production of [http://en.wikipedia.org/wiki/Radical_(chemistry) free radicals] from ultraviolet light [[#References|[3]]].  They are contained in the chloroplasts in lipid globules[[#References|[9]]]. Among various carotenoid-rich microalgae, ''D. salina'' has the greatest carotene concentration making up  ~10% algal dry weight[[#References|[6]]]. Due to its ability to produce red pigmentation, β-carotene, the natural food colouring is highly demanded for cosmetic products[1]. β-carotene also contributes to the [http://en.wikipedia.org/wiki/Antioxidant anti-oxidant] effects of ''D. salina''[[#References|[11]]] and is used as an additive in human and animal nutrition for sources of vitamin A [[#References|[3]]]. However, despite the positive contributions of ''D. salina'', commercial production is limited due to the low productivity of β-carotene [[#References|[3]]]. Farhat et al. [[#References|[3]]] studied the effects of salinity to maximize β-carotene production and found carotenoid concentration increases with increasing salinity. In order to maximize β-carotene production, ''D. salina'' should be grown in 1.5M to 3.0 M NaCl concentration until a stable cell density is reached then increased to 4.4 – 5.0 M NaCl concentration for maximum carotenoid production [[#References|[3]]].


The sequencing of ''Dunaliella species'' is important to isolate different species for commercial purposes. Olmos et al. [[#References|[8]]] sequenced five species of ''Dunaliella'' using their 18S ribosomal RNA genes.  The ''D. salina'' organelle genome sequence are circular and large with approximately 60% non-coding DNA [[#References|[9]]]. Although the biochemistry and physiology of ''D. salina'' has been researched, much about the genome was unknown until Smith ''et al.'' [[#References|[9]]] studied the mitochondrial and plastid genome of ''D. salina''. The mitochondrial and plastid genome contains 28.3 (12 genes) and 269 kb (102 genes) respectively [[#References|[9]]].  In addition, Smith ''et al.'' [[#References|[9]]] found that both genomes are highly occupied with introns: mitochondrial DNA (58%) and plasmid DNA (65.5%). The GC content of "D. salina" is relatively low compared to other Chlamydomonadales at 34.4% for mitochondrial DNA and 32.1% for plasmid DNA[[#References|[9]]].




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=β-carotene=
β-carotene is a type of pro-vitamin A, responsible for inhibiting the production of [http://en.wikipedia.org/wiki/Radical_(chemistry) free radicals] from ultraviolet light [[#References|[3]]].  They are contained in the chloroplasts in lipid globules[[#References|[9]]]. Among various carotenoid-rich microalgae, ''D. salina'' has the greatest carotene concentration making up  ~10% algal dry weight[[#References|[6]]]. Due to its ability to produce red pigmentation, β-carotene, the natural food colouring is highly demanded for cosmetic products[1]. β-carotene also contributes to the [http://en.wikipedia.org/wiki/Antioxidant anti-oxidant] effects of ''D. salina''[[#References|[11]]] and is used as an additive in human and animal nutrition for sources of vitamin A [[#References|[3]]].  However, despite the positive contributions of ''D. salina'', commercial production is limited due to the low productivity of β-carotene [[#References|[3]]]. Farhat et al. [[#References|[3]]] studied the effects of salinity to maximize β-carotene production and found carotenoid concentration increases with increasing salinity. In order to maximize β-carotene production, ''D. salina'' should be grown in 1.5M to 3.0 M NaCl concentration until a stable cell density is reached then increased to 4.4 – 5.0 M NaCl concentration for maximum carotenoid production [[#References|[3]]].


=Glycerol and Osmotic behaviour=
=Glycerol and Osmotic behaviour=
[[File:glycerolshock.jpeg|300px|thumb|left|Figure 5. Intracellular glycerol content as a function of extracellular NaCl concentrations in Dunaliella salina[[#Reference|[6]]]. ]]
''Dunaliella salina'' lacks a rigid wall, and the plasma membrane alone makes the cell susceptible to [http://en.wikipedia.org/wiki/Osmotic_pressure osmotic pressure] [[#References|[1]]]. Glycerol is a compatible solute in which not only contributes to osmotic balance of the cell but also maintains enzyme activity (Brown as stated in Oren[[#References|[1]]]). Glycerol is produced through two metabolic processes: intracellular synthesis through a photosynthetic product and metabolism of starch in the cell [[#References|[15]]]. The cell membrane of ''D. salina'' has low permeability to glycerol to prevent glycerol from leaving the cell [[#References|[13]]], accounting for the high concentration inside the cell. Glycerol synthesis from starch is regulated through osmotic changes as shown in Figure 5. High extracellular salt concentration drives the synthesis of glucose. Osmotic stress affects enzyme activity of key enzymes of the glycerol metabolic pathway: glycerol-3-phosphate dehydrogenase, glycerol-3-phosphate phosphatase, dihydroxyacetone reductase, and dihydroxyacetone kinase[[#References|[15]]]. These enzymes regulate glycerol requirements of the cell by responding to osmotic stresses. Johnson et al. [[#References|[14]]] found that high salt concentration inside cells decrease enzymatic activity. Thus, while ''D. salina'' live in high salt concentrations, they maintain a relatively low concentration of sodium inside [[#References|[15]]].  
''Dunaliella salina'' lacks a rigid wall, and the plasma membrane alone makes the cell susceptible to [http://en.wikipedia.org/wiki/Osmotic_pressure osmotic pressure] [[#References|[1]]]. Glycerol is a compatible solute in which not only contributes to osmotic balance of the cell but also maintains enzyme activity (Brown as stated in Oren[[#References|[1]]]). Glycerol is produced through two metabolic processes: intracellular synthesis through a photosynthetic product and metabolism of starch in the cell [[#References|[15]]]. The cell membrane of ''D. salina'' has low permeability to glycerol to prevent glycerol from leaving the cell [[#References|[13]]], accounting for the high concentration inside the cell. Glycerol synthesis from starch is regulated through osmotic changes as shown in Figure 5. High extracellular salt concentration drives the synthesis of glucose. Osmotic stress affects enzyme activity of key enzymes of the glycerol metabolic pathway: glycerol-3-phosphate dehydrogenase, glycerol-3-phosphate phosphatase, dihydroxyacetone reductase, and dihydroxyacetone kinase[[#References|[15]]]. These enzymes regulate glycerol requirements of the cell by responding to osmotic stresses. Johnson et al. [[#References|[14]]] found that high salt concentration inside cells decrease enzymatic activity. Thus, while ''D. salina'' live in high salt concentrations, they maintain a relatively low concentration of sodium inside [[#References|[15]]].  




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Edited by Saki Konomura, student of MICB 301 at the University of British Columbia


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Latest revision as of 19:54, 7 June 2020

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Classification

Higher order Taxa

Eukaryota (Domain); Viridiplantae (Kingdom); Chlorophyta (Phylum); Chlorophyceae (Class); Volvocales (Order); Dunaliellaceae (Family); Dunaliella (Genus).

Species

Dunaliella salina

Description and Significance

Figure 1A. Dunaliella salina under light microscope [17].
Figure 1B. Dunaliella salina modified from Shariati and Hadi[6] and Heakel, Hefny and El-Tawab[16]


Dunaliella salina is a unicellular green alga found in environments with high salt concentration [1]. It produces a distinct pink and red colour often characteristic of saltern ponds [2]. Michel Felix Dunal first discovered "D. salina" in 1838 in the south of France occupying; however, it was not named until 1905 by Teodoresco [1]. Dunaliella species are able to tolerate varying NaCl concentrations, ranging from 0.2% to approximately 35% [3]. Thus, Dunaliella salina is a hyper-halotolerant organism found in high densities in saline lakes. D. salina has adapted to survive in high salinity environments by accumulating glycerol to balance osmotic pressure. D. salina is also adapted to solar radiation using β-carotene to protect against ionizing energy. This combination offers potential in biotechnological applications for the purpose of commercial products such as lipstick due to β-carotene production [4]. Dunaliella salina is a model organism to study the effects of saline adaptation in algae [1]. In addition, the role of glycerol in D. salina as a key organic compatible solute has been used as a research model [1].






Ecology

Figure 2. Hypersaline Lake [5].

Dunaliella salina are found in high salinity environments such as salted brines, salt evaporation ponds, and hypersaline lakes [7]. The ability to tolerate high salt concentrations is advantageous, since competition is minimal as salt high salt concentrations. Dunaliella salina was thought to be responsible for the red colouring of salted brines [1]. However, carotenoids responsible for the red colouration in D. salina are found in algal chloroplasts, whereas halophilic archaea also occupying hypersaline lakes have red pigments dispersed throughout the cell membrane [2]. Although there is a much greater abundance of D. salina, the red pigments on the cell membrane of archaea are more visibly accessible. Therefore, D. salina has a much less overall impact to colouration and archaeal communities contribute more to the red colouration of hypersaline lakes.



Life Cycle

Dunaliella salina can reproduce asexually, sexually and through division of motile vegetative cells[1]. Sexual reproduction, the formation of two gametes into a zygospore, is affected by salt concentrations[1]. Martinez et al. [10] determined the sexual activity of "D. salina" from evaluating ratio of zygotes and zygospores to total cells observed in culture. Low salt concentrations of 2% and 5% induced sexual activity, whereas higher salt concentration of 30% decreases sexual reproduction[10].

Genome Structure

Figure 3A. Complete Dunaliella salina mitochondrial genome map[9].
Figure 3B. Complete Dunaliella salina plastid genome map [9].

The sequencing of Dunaliella species is important to isolate different species for commercial purposes. Olmos et al. [8] sequenced five species of Dunaliella using their 18S ribosomal RNA genes. The D. salina organelle genome sequence are circular and large with approximately 60% non-coding DNA [9]. Although the biochemistry and physiology of D. salina has been researched, much about the genome was unknown until Smith et al. [9] studied the mitochondrial and plastid genome of D. salina. The mitochondrial and plastid genome contains 28.3 (12 genes) and 269 kb (102 genes) respectively [9]. In addition, Smith et al. [9] found that both genomes are highly occupied with introns: mitochondrial DNA (58%) and plastid DNA (65.5%). The GC content of "D. salina" is relatively low compared to other Chlamydomonadales at 34.4% for mitochondrial DNA and 32.1% for plastid DNA[9].

β-carotene

Figure 4.Cell density of Dunaliella salina cells grown in media containing wide range of salt concentrations[6].

β-carotene is a type of pro-vitamin A, responsible for inhibiting the production of free radicals from ultraviolet light [3]. They are contained in the chloroplasts in lipid globules[9]. Among various carotenoid-rich microalgae, D. salina has the greatest carotene concentration making up ~10% algal dry weight[6]. Due to its ability to produce red pigmentation, β-carotene, the natural food colouring is highly demanded for cosmetic products[1]. β-carotene also contributes to the anti-oxidant effects of D. salina[11] and is used as an additive in human and animal nutrition for sources of vitamin A [3]. However, despite the positive contributions of D. salina, commercial production is limited due to the low productivity of β-carotene [3]. Farhat et al. [3] studied the effects of salinity to maximize β-carotene production and found carotenoid concentration increases with increasing salinity. In order to maximize β-carotene production, D. salina should be grown in 1.5M to 3.0 M NaCl concentration until a stable cell density is reached then increased to 4.4 – 5.0 M NaCl concentration for maximum carotenoid production [3].





Glycerol and Osmotic behaviour

Figure 5. Intracellular glycerol content as a function of extracellular NaCl concentrations in Dunaliella salina[6].

Dunaliella salina lacks a rigid wall, and the plasma membrane alone makes the cell susceptible to osmotic pressure [1]. Glycerol is a compatible solute in which not only contributes to osmotic balance of the cell but also maintains enzyme activity (Brown as stated in Oren[1]). Glycerol is produced through two metabolic processes: intracellular synthesis through a photosynthetic product and metabolism of starch in the cell [15]. The cell membrane of D. salina has low permeability to glycerol to prevent glycerol from leaving the cell [13], accounting for the high concentration inside the cell. Glycerol synthesis from starch is regulated through osmotic changes as shown in Figure 5. High extracellular salt concentration drives the synthesis of glucose. Osmotic stress affects enzyme activity of key enzymes of the glycerol metabolic pathway: glycerol-3-phosphate dehydrogenase, glycerol-3-phosphate phosphatase, dihydroxyacetone reductase, and dihydroxyacetone kinase[15]. These enzymes regulate glycerol requirements of the cell by responding to osmotic stresses. Johnson et al. [14] found that high salt concentration inside cells decrease enzymatic activity. Thus, while D. salina live in high salt concentrations, they maintain a relatively low concentration of sodium inside [15].






References

1. Oren A. “A century years of Dunaliella research: 1905-2005.” Saline Systems, 2005.

2. Oren A. and Rodriguez-Valera F. “The contribution of halophilic Bacteria to the red coloration of saltern crystallizer ponds.” FEMS Microbiology Ecology, 2001.

3. Farahat N., Rabhi M., Falleh H., Jouini J., Abdelly C. and Smaoui A. “Optimization of salt concentrations for a higher carotenoid production in Dunaliella salina (Chlorophyceae).” Phycological Society of America, 2011. DOI: 10.1111/j.1529-8817.2011.01036.x

4. Schilipaulis L. “The Extensive Commercial Cultivation of Dunaliella.” Bioresource Technology, 1991. DOI: 10.1016/0960-8524(91)90162-D

5. What is Dunaliella salina? n.d. Web. 22 Nov. 2012. <http://blog.recoverye21.com/dunaliella-salina/>

6. Shariati M., Hadi M.R. “Microalgal Biotechnology and Bioenergy in Dunaliella” Biomedical Engineering, 2011. DOI: 10.5772/19046

7. Brock T. “Salinity and the Ecology of Dunaliella from Great Salt Lake.” Journal of General Microbiology, 1975.

8. Olmos J., Paniagua J. and Contreras R. “Molecular identification of Dunaliella sp. utilizing the 18S rDNA gene.” Letters in Applied Microbiology, 2000.

9. Smith D., Lee R., Cushman J., Magnuson J., Tran D. and Polle J.” The Dunaliella salina organelle genomes: large sequences, inflated with intronic and intergenic DNA.” BMA Plant Biology, 2010. DOI: 10.1186/1471-2229-10-83

10. Martinez G., Cifuentes A., Gonzalez M. and Parra O. “Effect of salinity on sexual activity of Dunaliella salina (Dunal) Teodoresco, strain CONC-006.” Revista Chilena de Historia Natural, 1995.

11. Tammam A., Fakhry E. and El-Sheekh M. “Effect of salt stress on antioxidant system and the metabolism of the reactive oxygen species in Dunaliella saline and Dunaliella tertiolecta.” African Journal of Biotechnology, 2011. DOI: 10.5897/AJB10.2392

12. Wengmann K. “Osmotic Regulation of photosynthetic Glycerol Production in Dunaliella.” Biochimica et biophysica acta, 1971.

13. Gimmler H. and Hartung W. “Low Permeability of the Plasma Membrane of Dunaliella parva for Solutes.” Journal of Plant Physiology, 1988. DOI: 10.1016/S0176-1617(88)80132-9

14. Johnson M., Johnson E., MacElroy R., Speer H. and Bruff B. “Effects of Salts on Halophilic Alga Dunaliella viridis.” Journal of Bacteriology, 1968.

15. Chen H., Lu Y. and Jiang J. “Comparative Analysis on the Key Enzymes of the Glycerol Cycle Metabolic Pathway in Dunaliella salina under Osmotic Stresses.” PLoS ONE, 2012, DOI: 10.1371/journal.pone.0037578

16. Heakal F., Hefny M., El-Tawab A., “Electrochemical behaviour of 340L stainless steel in high saline and sulphate solutions containing alga Dunaliella salina and β-carotene. Journal of Alloys and Compounds, 2010, DOI: 10.1016/j.jallcom.2009.11.028

17. Mixed Carotenoids. Rejuvenal healthy aging, n.d. Web. 22 Nov 2012.