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. 2009 Dec;8(12):1856-68.
doi: 10.1128/EC.00272-09. Epub 2009 Oct 30.

Algal lipid bodies: stress induction, purification, and biochemical characterization in wild-type and starchless Chlamydomonas reinhardtii

Affiliations

Algal lipid bodies: stress induction, purification, and biochemical characterization in wild-type and starchless Chlamydomonas reinhardtii

Zi Teng Wang et al. Eukaryot Cell. 2009 Dec.

Abstract

When the unicellular green soil alga Chlamydomonas reinhardtii is deprived of nitrogen after entering stationary phase in liquid culture, the cells produce abundant cytoplasmic lipid bodies (LBs), as well as abundant starch, via a pathway that accompanies a regulated autophagy program. After 48 h of N starvation in the presence of acetate, the wild-type LB content has increased 15-fold. When starch biosynthesis is blocked in the sta6 mutant, the LB content increases 30-fold, demonstrating that genetic manipulation can enhance LB production. The use of cell wall-less strains permitted development of a rapid "popped-cell" microscopic assay to quantitate the LB content per cell and permitted gentle cell breakage and LB isolation. The highly purified LBs contain 90% triacylglycerol (TAG) and 10% free fatty acids (FFA). The fatty acids associated with the TAGs are approximately 50% saturated (C(16) and C(18)) fatty acids and approximately 50% unsaturated fatty acids, half of which are in the form of oleic acid (C(18:1)). The FFA are approximately 50% C(16) and approximately 50% C(18). The LB-derived TAG yield from a liter of sta6 cells at 10(7) cells/ml after starvation for 48 h is calculated to approach 400 mg. The LB fraction also contains low levels of charged glycerolipids, with the same profile as whole-cell charged glycerolipids, that presumably form LB membranes; chloroplast-specific neutral glycerolipids (galactolipids) are absent. Very low levels of protein are also present, but all matrix-assisted laser desorption ionization-identified species are apparent contaminants. Nitrogen stress-induced LB production in C. reinhardtii has the hallmarks of a discrete pathway that should be amenable to additional genetic and culture condition manipulation.

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Figures

FIG. 1.
FIG. 1.
Confocal microscopy surveys of cw15 (A) and cw15 sta6 (B) cell samples starved for N for 24 h. Red, chlorophyll autofluorescence; yellow, Nile Red fluorescence.
FIG. 2.
FIG. 2.
(A) Optical sections of cw15 cells (top) and cw15 sta6 cells (bottom) starved for N for 24 h. (B) Three-dimensional reconstructions of through-focal optical sections of cw15 cells (top) and cw15 sta6 cells (bottom) starved for N for 24 h. Red, chlorophyll autofluorescence; yellow, Nile Red fluorescence.
FIG. 3.
FIG. 3.
Size distributions of LBs from the following samples: through-focal optical sections of cw15 cells starved for N for 24 h and cw15 sta6 cells starved for N for 24 and 48 h (A), popped cells after 24 h of N starvation (B), and washed LBs after 18 h of N starvation (C). Frequency indicates number of LBs having a given size.
FIG. 4.
FIG. 4.
Confocal fluorescence microscopy images of cw15 sta6 cells popped in situ. Red, chlorophyll autofluorescence; yellow, Nile Red fluorescence.
FIG. 5.
FIG. 5.
Popped cw15 and cw15 sta6 cells stained with Nile Red after 24 and 48 h of N starvation. Values give the total area of fluorescent pixels per cell in μm2. Each sample displays three images with mean values, three images with values one SD above the mean, and three images with values one SD below the mean.
FIG. 6.
FIG. 6.
Pooled distributions of LB contents in popped cw15 and cw15 sta6 cells after 0, 24, and 48 h of N starvation. Arrows indicate median values. Data for individual experiments are given in Table SA1 in the supplemental material. Frequency indicates number of cells having a given lipid area.
FIG. 7.
FIG. 7.
Washed LB preparation. (A) Survey view. (B) Phase contrast versus Nile Red fluorescence.
FIG. 8.
FIG. 8.
(A and B) MS-GC spectra of FA derived from TAG in washed LB preparations from cw15 (A) and cw15 sta6 (B) cells. (C) Relative amounts of TAG-derived FA (light gray, cw15 cells; dark gray, cw15 sta6 cells).
FIG. 9.
FIG. 9.
(A and B) MS-GC spectra of FA standards (A) and FFA (B) from purified cw15 cell LBs. (C) Relative amounts of FFA (light gray, cw15 cells; dark gray, cw15 sta6 cells).
FIG. 10.
FIG. 10.
Thin-layer chromatographs (TLC) of NGLs and CGLs from cw15 cells and from initial LB preparations from cw15 sta6 cells. (A) TLC of a plate sprayed with Dragendorff reagent to detect tertiary amines in DGTS [1,2-diacylglyceryl-3-O-4′-(N,N,N-trimethylhomoserine)]. (B) TLC of a plate sprayed with sulfuric acid. M, monogalactosyldiacylglycerol; D, digalactosyldiacylglycerol; 1, sulfoquinovosyldiacylglycerol; 2, phosphatidylglycerol; 3, phosphatidylethanolamine; 4, DGTS.
FIG. 11.
FIG. 11.
TAG contents of five independent washed LB preparations from cw15 sta6 and cw15 cells after 18 h of N starvation. Black, results from glycerol assay; gray, results from dry weight analysis.

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