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Plant lipid transfer proteins, also known as plant LTPs or PLTPs, are a group of highly-conserved proteins of about 7-9kDa found in higher plant tissues. [ 1 ] [ 2 ] As its name implies, lipid transfer proteins facilitate the shuttling of phospholipids and other fatty acid groups between cell membranes . [ 3 ]
Lipid metabolism is the synthesis and degradation of lipids in cells, involving the breakdown and storage of fats for energy and the synthesis of structural and functional lipids, such as those involved in the construction of cell membranes. In animals, these fats are obtained from food and are synthesized by the liver. [1]
Like most leucoplasts, elaioplasts are non-pigmented organelles capable of alternating between the different forms of plastids.The elaioplast specifically is primarily responsible for the storage and metabolism of lipids, [5] among these roles, recent studies have shown that these organelles participate in the formation of terpenes and fatty acids.
Lacking photosynthetic pigments, leucoplasts are located in non-photosynthetic tissues of plants, such as roots, bulbs and seeds. They may be specialized for bulk storage of starch , lipid or protein and are then known as amyloplasts , elaioplasts , or proteinoplasts (also called aleuroplasts) respectively.
Osmium tetroxide binds to lipids, consequently staining and fixing them, making the lipids then visible during electron scanning. [5] In the staining of plasma membrane like structures, such as spherosomes, osmium tetroxide binds to the phospholipid regions, thus creating a contrast with the surrounding cytoplasm making it easy to identify the ...
In biochemistry, lipogenesis is the conversion of fatty acids and glycerol into fats, or a metabolic process through which acetyl-CoA is converted to triglyceride for storage in fat. [1] Lipogenesis encompasses both fatty acid and triglyceride synthesis , with the latter being the process by which fatty acids are esterified to glycerol before ...
These disorders may be described as fatty acid oxidation disorders or as a lipid storage disorders, and are any one of several inborn errors of metabolism that result from enzyme or transport protein defects affecting the ability of the body to oxidize fatty acids in order to produce energy within muscles, liver, and other cell types.
One lipid-cholesterol system that has recently been studied intently is the lipid raft. Lipid rafts are cholesterol-enriched gel domains that have been potentially implicated in certain cell signaling processes, [ 12 ] but the subject remains controversial, with some researchers doubting even their existence in vivo.