Native architecture of the Chlamydomonas chloroplast revealed by in situ cryo-electron tomography

被引:246
作者
Engel, Benjamin D. [1 ]
Schaffer, Miroslava [1 ]
Cuellar, Luis Kuhn [1 ]
Villa, Elizabeth [1 ]
Plitzko, Juergen M. [1 ]
Baumeister, Wolfgang [1 ]
机构
[1] Max Planck Inst Biochem, Dept Mol Struct Biol, D-82152 Martinsried, Germany
来源
ELIFE | 2015年 / 4卷
关键词
CARBONIC-ANHYDRASE; THYLAKOID MEMBRANE; PHOTOSYSTEM-II; RIBULOSE-1,5-BISPHOSPHATE CARBOXYLASE; VITREOUS SECTIONS; CO2-CONCENTRATING MECHANISMS; 3-DIMENSIONAL ARCHITECTURE; ELECTRON CRYOTOMOGRAPHY; CONCENTRATING MECHANISM; REINHARDTII MUTANTS;
D O I
10.7554/eLife.04889
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chloroplast function is orchestrated by the organelle's intricate architecture. By combining cryo-focused ion beam milling of vitreous Chlamydomonas cells with cryo-electron tomography, we acquired three-dimensional structures of the chloroplast in its native state within the cell. Chloroplast envelope inner membrane invaginations were frequently found in close association with thylakoid tips, and the tips of multiple thylakoid stacks converged at dynamic sites on the chloroplast envelope, implicating lipid transport in thylakoid biogenesis. Subtomogram averaging and nearest neighbor analysis revealed that RuBisCO complexes were hexagonally packed within the pyrenoid, with similar to 15 nm between their centers. Thylakoid stacks and the pyrenoid were connected by cylindrical pyrenoid tubules, physically bridging the sites of light-dependent photosynthesis and light-independent carbon fixation. Multiple parallel minitubules were bundled within each pyrenoid tubule, possibly serving as conduits for the targeted one-dimensional diffusion of small molecules such as ATP and sugars between the chloroplast stroma and the pyrenoid matrix.
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页数:29
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