Vega 2006 Enzyme Microb Technol: Difference between revisions

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{{Publication
{{Publication
|title=Vega JM, Garbayo I, Dominguez MJ, Vigara JΒ  (2006) Effect of abiotic stress on photosynthesis and respiration in Chlamydomonas reinhardtii. Induction of oxidative stress. Enzyme Microb Technol 40:163-167.
|title=Vega JM, Garbayo I, Dominguez MJ, Vigara JΒ  (2006) Effect of abiotic stress on photosynthesis and respiration in ''Chlamydomonas reinhardtii''. Induction of oxidative stress. Enzyme Microb Technol 40:163-7.
|info=[https://www.sciencedirect.com/science/article/abs/pii/S0141022906003024]
|info=[https://www.sciencedirect.com/science/article/abs/pii/S0141022906003024]
|authors=Vega Jose M, Garbayo Ines, Dominguez Maria J, Vigara A Javier
|authors=Vega Jose M, Garbayo Ines, Dominguez Maria J, Vigara A Javier
|year=2006
|year=2006
|journal=Enzyme Microb Technol
|journal=Enzyme Microb Technol
|abstract=Our results indicate that 200 mM NaCl, 0.2 ΞΌM methyl viologen, 4 mM arsenite or 300 ΞΌM of cadmium in the culture medium are highly toxic for Chlamydomonas reinhardtii productivity. All of them inhibit the photosynthetic-electron flow, while cyanide-sensitive respiration remains high in the alga. The addition of NaCl, 200 mM to the culture medium immediately blocks the photosynthetic activity of the alga which is partially recovered, after 1 h of treatment, remaining high during the following 24 h. At short time (4 h) methyl viologen (MV) inhibits the photosynthetic activity of the alga, while respiration inhibition was only evident at 0.5 ΞΌM of MV. After 24 h treatment, 0.2 ΞΌM MV inhibits drastically the photosynthetic activity of C. reinhardtii, while photosystem I was still functional. At short time, cadmium and arsenite inhibit the alga photosynthetic activity, while only arsenite 4 mM inhibits both photosynthesis and respiration in 24 h-treated C. reinhardtii cells.
|abstract=Our results indicate that 200 mM NaCl, 0.2 ΞΌM methyl viologen, 4 mM arsenite or 300 ΞΌM of cadmium in the culture medium are highly toxic for ''Chlamydomonas reinhardtii'' productivity. All of them inhibit the photosynthetic-electron flow, while cyanide-sensitive respiration remains high in the alga. The addition of NaCl, 200 mM to the culture medium immediately blocks the photosynthetic activity of the alga which is partially recovered, after 1 h of treatment, remaining high during the following 24 h. At short time (4 h) methyl viologen (MV) inhibits the photosynthetic activity of the alga, while respiration inhibition was only evident at 0.5 ΞΌM of MV. After 24 h treatment, 0.2 ΞΌM MV inhibits drastically the photosynthetic activity of C. reinhardtii, while photosystem I was still functional. At short time, cadmium and arsenite inhibit the alga photosynthetic activity, while only arsenite 4 mM inhibits both photosynthesis and respiration in 24 h-treated ''C. reinhardtii'' cells.


Catalase activity of C. reinhardtii was stimulated by abiotic stress, being NaCl the most efficient inductor of the enzyme. After 24 h treatment with NaCl 200 mM, the intracellular catalase activity of the alga reaches 337.5 Β± 2.8 ΞΌmol O2 mgβˆ’1 Chl minβˆ’1, which means a 20-fold higher level than in the control cells. The degree of catalase stimulation correlates the NaCl concentration in the culture medium. These data indicate that abiotic stress induces in C. reinhardtii an increase of intracellular peroxide, which parallel a significant inhibition of the photosynthetic-electron flow.
Catalase activity of ''C. reinhardtii'' was stimulated by abiotic stress, being NaCl the most efficient inductor of the enzyme. After 24 h treatment with NaCl 200 mM, the intracellular catalase activity of the alga reaches 337.5 Β± 2.8 ΞΌmol O2 mgβˆ’1 Chl minβˆ’1, which means a 20-fold higher level than in the control cells. The degree of catalase stimulation correlates the NaCl concentration in the culture medium. These data indicate that abiotic stress induces in ''C. reinhardtii'' an increase of intracellular peroxide, which parallel a significant inhibition of the photosynthetic-electron flow.
|editor=[[Huete-Ortega Maria]]
}}
}}
{{Labeling
{{Labeling
|area=Respiration
|area=Respiration
|additional=Algae, Dark respiration, Photosynthesis, MitoFit 2021 Dark respiration, MitoFit 2021 Photosynthesis
|additional=Algae, Dark respiration, Photosynthesis}}
}}
== Cited by ==
{{Template:Cited by Huete-Ortega M 2021 MitoFit Dark respiration}}
{{Template:Cited by Huete-Ortega M 2021 MitoFit Photosynthesis protocols}}

Revision as of 10:13, 11 September 2021

Publications in the MiPMap
Vega JM, Garbayo I, Dominguez MJ, Vigara J (2006) Effect of abiotic stress on photosynthesis and respiration in Chlamydomonas reinhardtii. Induction of oxidative stress. Enzyme Microb Technol 40:163-7.

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Vega Jose M, Garbayo Ines, Dominguez Maria J, Vigara A Javier (2006) Enzyme Microb Technol

Abstract: Our results indicate that 200 mM NaCl, 0.2 ΞΌM methyl viologen, 4 mM arsenite or 300 ΞΌM of cadmium in the culture medium are highly toxic for Chlamydomonas reinhardtii productivity. All of them inhibit the photosynthetic-electron flow, while cyanide-sensitive respiration remains high in the alga. The addition of NaCl, 200 mM to the culture medium immediately blocks the photosynthetic activity of the alga which is partially recovered, after 1 h of treatment, remaining high during the following 24 h. At short time (4 h) methyl viologen (MV) inhibits the photosynthetic activity of the alga, while respiration inhibition was only evident at 0.5 ΞΌM of MV. After 24 h treatment, 0.2 ΞΌM MV inhibits drastically the photosynthetic activity of C. reinhardtii, while photosystem I was still functional. At short time, cadmium and arsenite inhibit the alga photosynthetic activity, while only arsenite 4 mM inhibits both photosynthesis and respiration in 24 h-treated C. reinhardtii cells.

Catalase activity of C. reinhardtii was stimulated by abiotic stress, being NaCl the most efficient inductor of the enzyme. After 24 h treatment with NaCl 200 mM, the intracellular catalase activity of the alga reaches 337.5 Β± 2.8 ΞΌmol O2 mgβˆ’1 Chl minβˆ’1, which means a 20-fold higher level than in the control cells. The degree of catalase stimulation correlates the NaCl concentration in the culture medium. These data indicate that abiotic stress induces in C. reinhardtii an increase of intracellular peroxide, which parallel a significant inhibition of the photosynthetic-electron flow.


Labels: MiParea: Respiration 






Algae, Dark respiration, Photosynthesis 

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