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- Publisher Website: 10.1104/pp.15.01174
- Scopus: eid_2-s2.0-84949571274
- PMID: 26486592
- WOS: WOS:000368472700009
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Article: Genomic foundation of starch-to-lipid switch in oleaginous chlorella spp.
Title | Genomic foundation of starch-to-lipid switch in oleaginous chlorella spp. |
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Authors | |
Issue Date | 2015 |
Citation | Plant Physiology, 2015, v. 169, n. 4, p. 2444-2461 How to Cite? |
Abstract | The ability to rapidly switch the intracellular energy storage form from starch to lipids is an advantageous trait for microalgae feedstock. To probe this mechanism, we sequenced the 56.8-Mbp genome of Chlorella pyrenoidosa FACHB-9, an industrial production strain for protein, starch, and lipids. The genome exhibits positive selection and gene family expansion in lipid and carbohydrate metabolism and genes related to cell cycle and stress response. Moreover, 10 lipid metabolism genes might beoriginated from bacteria via horizontal gene transfer. Transcriptomic dynamics tracked via messenger RNA sequencing over six time points during metabolic switch from starch-rich heterotrophy to lipid-rich photoautotrophy revealed that under heterotrophy, genes most strongly expressed were from the tricarboxylic acid cycle, respiratory chain, oxidative phosphorylation, gluconeogenesis, glyoxylate cycle, and amino acid metabolisms, whereas those most down-regulated were from fatty acid and oxidative pentose phosphate metabolism. The shift from heterotrophy into photoautotrophy highlights up-regulation of genes from carbon fixation, photosynthesis, fatty acid biosynthesis, the oxidative pentose phosphate pathway, and starch catabolism, which resulted in a marked redirection of metabolism, where the primary carbon source of glycine is no longer supplied to cell building blocks by the tricarboxylic acid cycle and gluconeogenesis, whereas carbon skeletons from photosynthesis and starch degradation may be directly channeled into fatty acid and protein biosynthesis. By establishing the first genetic transformation in industrial oleaginous C. pyrenoidosa, we further showed that overexpression of an NAD(H) kinase from Arabidopsis (Arabidopsis thaliana) increased cellular lipid content by 110.4%, yet without reducing growth rate. These findings provide a foundation for exploiting the metabolic switch in microalgae for improved photosynthetic production of food and fuels. |
Persistent Identifier | http://hdl.handle.net/10722/311403 |
ISSN | 2023 Impact Factor: 6.5 2023 SCImago Journal Rankings: 2.101 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Fan, Jianhua | - |
dc.contributor.author | Ning, Kang | - |
dc.contributor.author | Zeng, Xiaowei | - |
dc.contributor.author | Luo, Yuanchan | - |
dc.contributor.author | Wang, Dongmei | - |
dc.contributor.author | Hu, Jianqiang | - |
dc.contributor.author | Li, Jing | - |
dc.contributor.author | Xu, Hui | - |
dc.contributor.author | Huang, Jianke | - |
dc.contributor.author | Wan, Minxi | - |
dc.contributor.author | Wang, Weiliang | - |
dc.contributor.author | Zhang, Daojing | - |
dc.contributor.author | Shen, Guomin | - |
dc.contributor.author | Run, Conglin | - |
dc.contributor.author | Liao, Junjie | - |
dc.contributor.author | Fang, Lei | - |
dc.contributor.author | Huang, Shi | - |
dc.contributor.author | Jing, Xiaoyan | - |
dc.contributor.author | Su, Xiaoquan | - |
dc.contributor.author | Wang, Anhui | - |
dc.contributor.author | Bai, Lili | - |
dc.contributor.author | Hu, Zanmin | - |
dc.contributor.author | Xu, Jian | - |
dc.contributor.author | Li, Yuanguang | - |
dc.date.accessioned | 2022-03-22T11:53:51Z | - |
dc.date.available | 2022-03-22T11:53:51Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Plant Physiology, 2015, v. 169, n. 4, p. 2444-2461 | - |
dc.identifier.issn | 0032-0889 | - |
dc.identifier.uri | http://hdl.handle.net/10722/311403 | - |
dc.description.abstract | The ability to rapidly switch the intracellular energy storage form from starch to lipids is an advantageous trait for microalgae feedstock. To probe this mechanism, we sequenced the 56.8-Mbp genome of Chlorella pyrenoidosa FACHB-9, an industrial production strain for protein, starch, and lipids. The genome exhibits positive selection and gene family expansion in lipid and carbohydrate metabolism and genes related to cell cycle and stress response. Moreover, 10 lipid metabolism genes might beoriginated from bacteria via horizontal gene transfer. Transcriptomic dynamics tracked via messenger RNA sequencing over six time points during metabolic switch from starch-rich heterotrophy to lipid-rich photoautotrophy revealed that under heterotrophy, genes most strongly expressed were from the tricarboxylic acid cycle, respiratory chain, oxidative phosphorylation, gluconeogenesis, glyoxylate cycle, and amino acid metabolisms, whereas those most down-regulated were from fatty acid and oxidative pentose phosphate metabolism. The shift from heterotrophy into photoautotrophy highlights up-regulation of genes from carbon fixation, photosynthesis, fatty acid biosynthesis, the oxidative pentose phosphate pathway, and starch catabolism, which resulted in a marked redirection of metabolism, where the primary carbon source of glycine is no longer supplied to cell building blocks by the tricarboxylic acid cycle and gluconeogenesis, whereas carbon skeletons from photosynthesis and starch degradation may be directly channeled into fatty acid and protein biosynthesis. By establishing the first genetic transformation in industrial oleaginous C. pyrenoidosa, we further showed that overexpression of an NAD(H) kinase from Arabidopsis (Arabidopsis thaliana) increased cellular lipid content by 110.4%, yet without reducing growth rate. These findings provide a foundation for exploiting the metabolic switch in microalgae for improved photosynthetic production of food and fuels. | - |
dc.language | eng | - |
dc.relation.ispartof | Plant Physiology | - |
dc.title | Genomic foundation of starch-to-lipid switch in oleaginous chlorella spp. | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1104/pp.15.01174 | - |
dc.identifier.pmid | 26486592 | - |
dc.identifier.pmcid | PMC4677908 | - |
dc.identifier.scopus | eid_2-s2.0-84949571274 | - |
dc.identifier.volume | 169 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | 2444 | - |
dc.identifier.epage | 2461 | - |
dc.identifier.eissn | 1532-2548 | - |
dc.identifier.isi | WOS:000368472700009 | - |