Comparative Proteomic Profiling of Marine and Freshwater Synechocystis Strains Using Liquid Chromatography-Tandem Mass Spectrometry
- Authors
- Kwon, Dami; Park, Jong-Moon; Duong, Van-An; Hong, Seong-Joo; Cho, Byung-Kwan; Lee, Choul-Gyun; Choi, Hyung-Kyoon; Kim, Dong-Myung; Lee, Hookeun
- Issue Date
- Oct-2020
- Publisher
- MDPI
- Keywords
- Data-independent acquisition; Freshwater; Global identification; LC-MS/MS; Marine; Photosynthesis; Proteomics; Synechocystis 6803; Synechocystis 7338
- Citation
- Journal of Marine Science and Engineering, v.8, no.10
- Journal Title
- Journal of Marine Science and Engineering
- Volume
- 8
- Number
- 10
- URI
- https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/78967
- DOI
- 10.3390/jmse8100790
- ISSN
- 2077-1312
- Abstract
- Freshwater Synechocystis sp. PCC 6803 has been considered to be a platform for the production of the next generation of biofuels and is used as a model organism in various fields. Various genomics, transcriptomics, metabolomics, and proteomics studies have been performed on this strain, whereas marine Synechocystis sp. PCC 7338 has not been widely studied despite its wide distribution. This study analyzed the proteome profiles of two Synechocystis strains using a liquid chromatography–tandem mass spectrometry-based bottom-up proteomic approach. Proteomic profiling of Synechocystis sp. PCC 7338 was performed for the first time with a data-dependent acquisition method, revealing 18,779 unique peptides and 1794 protein groups. A data-independent acquisition method was carried out for the comparative quantitation of Synechocystis sp. PCC 6803 and 7338. Among 2049 quantified proteins, 185 up-and 211 down-regulated proteins were defined in Synechocystis sp. PCC 7338. Some characteristics in the proteome of Synechocystis sp. PCC 7338 were revealed, such as its adaptation to living conditions, including the down-regulation of some photosynthesis proteins, the up-regulation of kdpB, and the use of osmolyte glycine as a substrate in C1 metabolism for the regulation of carbon flow. This study will facilitate further studies on Synechocystis 7338 to define in depth the proteomic differences between it and other Synechocystis strains. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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