Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.

Arthrospira (Spirulina) platensis (ASP) is a representative filamentous, non-N2-fixing cyanobacterium that has great potential to enhance the food supply and possesses several valuable physiological features. ASP tolerates high and low temperatures along with highly alkaline and salty environments,...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Wang Huili, Zhao Xiaokai, Lin Meili, Randy A Dahlgren, Chen Wei, Zhou Jaiopeng, Xu Chengyang, Jin Chunlei, Xu Yi, Wang Xuedong, Ding Li, Bao Qiyu
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/e052696018f743458439e81ded94c935
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:e052696018f743458439e81ded94c935
record_format dspace
spelling oai:doaj.org-article:e052696018f743458439e81ded94c9352021-11-18T08:42:08ZProteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.1932-620310.1371/journal.pone.0083485https://doaj.org/article/e052696018f743458439e81ded94c9352013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24349519/?tool=EBIhttps://doaj.org/toc/1932-6203Arthrospira (Spirulina) platensis (ASP) is a representative filamentous, non-N2-fixing cyanobacterium that has great potential to enhance the food supply and possesses several valuable physiological features. ASP tolerates high and low temperatures along with highly alkaline and salty environments, and can strongly resist oxidation and irradiation. Based on genomic sequencing of ASP, we compared the protein expression profiles of this organism under different temperature conditions (15°C, 35°Cand 45°C) using 2-DE and peptide mass fingerprinting techniques. A total of 122 proteins having a significant differential expression response to temperature were retrieved. Of the positively expressed proteins, the homologies of 116 ASP proteins were found in Arthrospira (81 proteins in Arthrospira platensis str. Paraca and 35 in Arthrospira maxima CS-328). The other 6 proteins have high homology with other microorganisms. We classified the 122 differentially expressed positive proteins into 14 functions using the COG database, and characterized their respective KEGG metabolism pathways. The results demonstrated that these differentially expressed proteins are mainly involved in post-translational modification (protein turnover, chaperones), energy metabolism (photosynthesis, respiratory electron transport), translation (ribosomal structure and biogenesis) and carbohydrate transport and metabolism. Others proteins were related to amino acid transport and metabolism, cell envelope biogenesis, coenzyme metabolism and signal transduction mechanisms. Results implied that these proteins can perform predictable roles in rendering ASP resistance against low and high temperatures. Subsequently, we determined the transcription level of 38 genes in vivo in response to temperature and identified them by qRT-PCR. We found that the 26 differentially expressed proteins, representing 68.4% of the total target genes, maintained consistency between transcription and translation levels. The remaining 12 genes showed inconsistent protein expression with transcription level and accounted for 31.6% of the total target genes.Wang HuiliZhao XiaokaiLin MeiliRandy A DahlgrenChen WeiZhou JaiopengXu ChengyangJin ChunleiXu YiWang XuedongDing LiBao QiyuPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 12, p e83485 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Wang Huili
Zhao Xiaokai
Lin Meili
Randy A Dahlgren
Chen Wei
Zhou Jaiopeng
Xu Chengyang
Jin Chunlei
Xu Yi
Wang Xuedong
Ding Li
Bao Qiyu
Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
description Arthrospira (Spirulina) platensis (ASP) is a representative filamentous, non-N2-fixing cyanobacterium that has great potential to enhance the food supply and possesses several valuable physiological features. ASP tolerates high and low temperatures along with highly alkaline and salty environments, and can strongly resist oxidation and irradiation. Based on genomic sequencing of ASP, we compared the protein expression profiles of this organism under different temperature conditions (15°C, 35°Cand 45°C) using 2-DE and peptide mass fingerprinting techniques. A total of 122 proteins having a significant differential expression response to temperature were retrieved. Of the positively expressed proteins, the homologies of 116 ASP proteins were found in Arthrospira (81 proteins in Arthrospira platensis str. Paraca and 35 in Arthrospira maxima CS-328). The other 6 proteins have high homology with other microorganisms. We classified the 122 differentially expressed positive proteins into 14 functions using the COG database, and characterized their respective KEGG metabolism pathways. The results demonstrated that these differentially expressed proteins are mainly involved in post-translational modification (protein turnover, chaperones), energy metabolism (photosynthesis, respiratory electron transport), translation (ribosomal structure and biogenesis) and carbohydrate transport and metabolism. Others proteins were related to amino acid transport and metabolism, cell envelope biogenesis, coenzyme metabolism and signal transduction mechanisms. Results implied that these proteins can perform predictable roles in rendering ASP resistance against low and high temperatures. Subsequently, we determined the transcription level of 38 genes in vivo in response to temperature and identified them by qRT-PCR. We found that the 26 differentially expressed proteins, representing 68.4% of the total target genes, maintained consistency between transcription and translation levels. The remaining 12 genes showed inconsistent protein expression with transcription level and accounted for 31.6% of the total target genes.
format article
author Wang Huili
Zhao Xiaokai
Lin Meili
Randy A Dahlgren
Chen Wei
Zhou Jaiopeng
Xu Chengyang
Jin Chunlei
Xu Yi
Wang Xuedong
Ding Li
Bao Qiyu
author_facet Wang Huili
Zhao Xiaokai
Lin Meili
Randy A Dahlgren
Chen Wei
Zhou Jaiopeng
Xu Chengyang
Jin Chunlei
Xu Yi
Wang Xuedong
Ding Li
Bao Qiyu
author_sort Wang Huili
title Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
title_short Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
title_full Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
title_fullStr Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
title_full_unstemmed Proteomic analysis and qRT-PCR verification of temperature response to Arthrospira (Spirulina) platensis.
title_sort proteomic analysis and qrt-pcr verification of temperature response to arthrospira (spirulina) platensis.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/e052696018f743458439e81ded94c935
work_keys_str_mv AT wanghuili proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT zhaoxiaokai proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT linmeili proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT randyadahlgren proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT chenwei proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT zhoujaiopeng proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT xuchengyang proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT jinchunlei proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT xuyi proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT wangxuedong proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT dingli proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
AT baoqiyu proteomicanalysisandqrtpcrverificationoftemperatureresponsetoarthrospiraspirulinaplatensis
_version_ 1718421474888384512