Serveur d'exploration sur la glutarédoxine

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Astaxanthin overproduction and proteomic analysis of Phaffia rhodozyma under the oxidative stress induced by TiO2.

Identifieur interne : 000089 ( Main/Exploration ); précédent : 000088; suivant : 000090

Astaxanthin overproduction and proteomic analysis of Phaffia rhodozyma under the oxidative stress induced by TiO2.

Auteurs : Jing Zhang [République populaire de Chine] ; Qingru Li [République populaire de Chine] ; Jiahuan Liu [République populaire de Chine] ; Yanhong Lu [République populaire de Chine] ; Yu Wang [République populaire de Chine] ; Yuhua Wang [République populaire de Chine]

Source :

RBID : pubmed:32447228

Descripteurs français

English descriptors

Abstract

This study analyzed the effect of TiO2 on the growth and astaxanthin yield of P. rhodozyma PR106. Subsequently, proteomics method was used to analyze the proteins changes of the strain under TiO2 treatment, to investigate the metabolic mechanism of the active oxygen generator TiO2 promoting the astaxanthin synthesis in P. rhodozyma. The results showed that TiO2 caused oxidative stress response in P. rhodozyma, and astaxanthin yield was 14.74 mg/L, which was 2 times of the control group; while, TiO2 had no effect on biomass and apoptosis of the cells. Proteomics analysis and parallel reaction monitoring (PRM) technology initially explored that bud-site selection protein (BUD22), ubiquitin-40s ribosomal protein s31 fusion protein, cell cycle control protein, C-4 methyl sterol oxidase and glutaredoxin were associated with astaxanthin synthesis.

DOI: 10.1016/j.biortech.2020.123525
PubMed: 32447228


Affiliations:


Links toward previous steps (curation, corpus...)


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<term>Xanthophylls (MeSH)</term>
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<div type="abstract" xml:lang="en">This study analyzed the effect of TiO
<sub>2</sub>
on the growth and astaxanthin yield of P. rhodozyma PR106. Subsequently, proteomics method was used to analyze the proteins changes of the strain under TiO
<sub>2</sub>
treatment, to investigate the metabolic mechanism of the active oxygen generator TiO
<sub>2</sub>
promoting the astaxanthin synthesis in P. rhodozyma. The results showed that TiO
<sub>2</sub>
caused oxidative stress response in P. rhodozyma, and astaxanthin yield was 14.74 mg/L, which was 2 times of the control group; while, TiO
<sub>2</sub>
had no effect on biomass and apoptosis of the cells. Proteomics analysis and parallel reaction monitoring (PRM) technology initially explored that bud-site selection protein (BUD22), ubiquitin-40s ribosomal protein s31 fusion protein, cell cycle control protein, C-4 methyl sterol oxidase and glutaredoxin were associated with astaxanthin synthesis.</div>
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<sub>2</sub>
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<sub>2</sub>
on the growth and astaxanthin yield of P. rhodozyma PR106. Subsequently, proteomics method was used to analyze the proteins changes of the strain under TiO
<sub>2</sub>
treatment, to investigate the metabolic mechanism of the active oxygen generator TiO
<sub>2</sub>
promoting the astaxanthin synthesis in P. rhodozyma. The results showed that TiO
<sub>2</sub>
caused oxidative stress response in P. rhodozyma, and astaxanthin yield was 14.74 mg/L, which was 2 times of the control group; while, TiO
<sub>2</sub>
had no effect on biomass and apoptosis of the cells. Proteomics analysis and parallel reaction monitoring (PRM) technology initially explored that bud-site selection protein (BUD22), ubiquitin-40s ribosomal protein s31 fusion protein, cell cycle control protein, C-4 methyl sterol oxidase and glutaredoxin were associated with astaxanthin synthesis.</AbstractText>
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<NameOfSubstance UI="D024341">Xanthophylls</NameOfSubstance>
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<Chemical>
<RegistryNumber>15FIX9V2JP</RegistryNumber>
<NameOfSubstance UI="C009495">titanium dioxide</NameOfSubstance>
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<Chemical>
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<CoiStatement>Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.</CoiStatement>
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