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WANG Xiuxiu,HUANG Bangqin,ZHANG Huan. 2014. Phosphorus deficiency affects multiple macromolecular biosynthesis pathways of Thalassiosira weissflogii. Acta Oceanologica Sinica, 33(4):85-91
Phosphorus deficiency affects multiple macromolecular biosynthesis pathways of Thalassiosira weissflogii
Phosphorus deficiency affects multiple macromolecular biosynthesis pathways of Thalassiosira weissflogii
Received:September 23, 2012  Revised:December 31, 2012
DOI:10.1007/s13131-014-0413-x
Key words:phosphorus deficiency  Thalassiosira weissflogii  LFQ-LC-MS/MS  sulfolipid biosynthesis protein
中文关键词:  phosphorus deficiency  Thalassiosira weissflogii  LFQ-LC-MS/MS  sulfolipid biosynthesis protein
基金项目:The National Natural Science Foundation of China (NSFC) under contract No. 40925018; the National Basic Research Program (973 Program) under contract No. 2011CB403603.
Author NameAffiliationE-mail
WANG Xiuxiu Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, Xiamen University, Xiamen 361005, China
State Key Laboratory of Marine Environmental Science, Xiamen University, Xiamen 361005, China 
 
HUANG Bangqin Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystem, Xiamen University, Xiamen 361005, China
State Key Laboratory of Marine Environmental Science, Xiamen University, Xiamen 361005, China 
bqhuang@xmu.edu.cn 
ZHANG Huan Department of Marine Sciences, University of Connecticut, Groton 06340, USA  
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Abstract:
      Phosphorus (P) is one of the key nutrients for the growth of phytoplankton. In this study, we used a method coupling label-free quantitation with liquid chromatography-mass spectrometry (LFQ-LC-MS/MS) to track the change of relative protein abundance between P-replete and P-deficient treatments in a non-model diatom, Thalassiosira weissflogii. Out of the 631 proteins identified, 132 were found to have significant changes in abundance (>1.5 folds) between the two treatments, especially those proteins involved in macromolecular biosynthesis pathways. For example, the up-regulation of sulfolipid biosynthesis protein in the P-deficient culture suggested a switch from using phospholipids to sulfolipids. In addition, the ribosome subunits and tRNA synthetases were down-regulated, which might explain the decrease in protein content in the P-deficient culture. A vacuolar sorting receptor homologous protein was found to be 9.2-folds up-regulated under P-deficiency, indicating an enhancement in the vacuolar sorting pathway for protein degradation. Our results show that T. weissflogii has sophisticated responses in multiple macromolecular metabolism pathways under P-deficiency, a mechanism which can be critical for this species to survive under various levels of P availability in the environment.
中文摘要:
      Phosphorus (P) is one of the key nutrients for the growth of phytoplankton. In this study, we used a method coupling label-free quantitation with liquid chromatography-mass spectrometry (LFQ-LC-MS/MS) to track the change of relative protein abundance between P-replete and P-deficient treatments in a non-model diatom, Thalassiosira weissflogii. Out of the 631 proteins identified, 132 were found to have significant changes in abundance (>1.5 folds) between the two treatments, especially those proteins involved in macromolecular biosynthesis pathways. For example, the up-regulation of sulfolipid biosynthesis protein in the P-deficient culture suggested a switch from using phospholipids to sulfolipids. In addition, the ribosome subunits and tRNA synthetases were down-regulated, which might explain the decrease in protein content in the P-deficient culture. A vacuolar sorting receptor homologous protein was found to be 9.2-folds up-regulated under P-deficiency, indicating an enhancement in the vacuolar sorting pathway for protein degradation. Our results show that T. weissflogii has sophisticated responses in multiple macromolecular metabolism pathways under P-deficiency, a mechanism which can be critical for this species to survive under various levels of P availability in the environment.
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