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Identification of a Major Lipid Droplet Protein in a Marine DiatomPhaeodactylum tricornutum
- Source :
- Plant and Cell Physiology. 57:397-406
- Publication Year :
- 2016
- Publisher :
- Oxford University Press (OUP), 2016.
-
Abstract
- Various kinds of organisms, including microalgae, accumulate neutral lipids in distinct intracellular compartments called lipid droplets. Generally, lipid droplets are generated from the endoplasmic reticulum, and particular proteins localize on their surface. Some of these proteins function as structural proteins to prevent fusion between the lipid droplets, and the others could have an enzymatic role or might be involved in intracellular membrane trafficking. However, information about lipid droplet proteins in microalgae is scarce as compared with that in animals and land plants. We focused on the oil-producing, marine, pennate diatom Phaeodactylum tricornutum that forms lipid droplets during nitrogen deprivation and we investigated the proteins located on the lipid droplets. After 6 d of cultivation in a nitrate-deficient medium, the mature lipid droplets were isolated by sucrose density gradient centrifugation. Proteomic analyses revealed five proteins, with Stramenopile-type lipid droplet protein (StLDP) being the most abundant protein in the lipid droplet fraction. Although the primary sequence of StLDP did not have homology to any known lipid droplet proteins, StLDP had a central hydrophobic domain. This structural feature is also detected in oleosin of land plants and in lipid droplet surface protein (LDSP) of Nannochloropsis species. As a proline knot motif of oleosin, conservative proline residues existed in the hydrophobic domain. StLDP was up-regulated during nitrate deprivation, and fluctuations of StLDP expression levels corresponded to the size of the lipid droplets.
- Subjects :
- 0301 basic medicine
Aquatic Organisms
endocrine system
Physiology
Molecular Sequence Data
Plant Science
complex mixtures
03 medical and health sciences
Lipid droplet
Amino Acid Sequence
RNA, Messenger
Phaeodactylum tricornutum
Proline
Peptide sequence
Diatoms
Sequence Homology, Amino Acid
biology
Chemistry
Endoplasmic reticulum
technology, industry, and agriculture
Membrane Proteins
Lipid Droplets
Cell Biology
General Medicine
biology.organism_classification
eye diseases
030104 developmental biology
Gene Expression Regulation
Membrane protein
Biochemistry
Electrophoresis, Polyacrylamide Gel
lipids (amino acids, peptides, and proteins)
Oleosin
Sequence Alignment
Nannochloropsis
Subjects
Details
- ISSN :
- 14719053 and 00320781
- Volume :
- 57
- Database :
- OpenAIRE
- Journal :
- Plant and Cell Physiology
- Accession number :
- edsair.doi.dedup.....0f55b2619a5ca36543ebec67369dfd76
- Full Text :
- https://doi.org/10.1093/pcp/pcv204