Organization, Structure, and Assembly of α-Carboxysomes Determined by Electron Cryotomography of Intact Cells
Abstract
Carboxysomes are polyhedral inclusion bodies that play a key role in autotrophic metabolism in many bacteria. Using electron cryotomography, we examined carboxysomes in their native states within intact cells of three chemolithoautotrophic bacteria. We found that carboxysomes generally cluster into distinct groups within the cytoplasm, often in the immediate vicinity of polyphosphate granules, and a regular lattice of density frequently connects granules to nearby carboxysomes. Small granular bodies were also seen within carboxysomes. These observations suggest a functional relationship between carboxysomes and polyphosphate granules. Carboxysomes exhibited greater size, shape, and compositional variability in cells than in purified preparations. Finally, we observed carboxysomes in various stages of assembly, as well as filamentous structures that we attribute to misassembled shell protein. Surprisingly, no more than one partial carboxysome was ever observed per cell. Based on these observations, we propose a model for carboxysome assembly in which the shell and the internal RuBisCO (ribulose-1,5-bisphosphate carboxylase/oxygenase) lattice form simultaneously, likely guided by specific interactions between shell proteins and RuBisCOs.
Additional Information
© 2009 Elsevier Ltd. Received 18 June 2009; received in revised form 6 November 2009; accepted 9 November 2009; available online 17 November 2009. Edited by W. Baumeister. We are indebted to Dr. Raj Menon for culturing T. crunogena cells, Dr. Eric Williams for providing purified H. neapolitanus carboxysomes and initial batches of H. neapolitanus cells, Dr. H. Jane Ding for computational help with generation of phosphorus elemental maps, Dr. William F. Tivol for technical assistance in setting up the spectroscopic imaging experiments, and Dr. Elizabeth R. Wright for freezing grids and imaging several T. intermedia cells. This work was supported in part by NIH grants R01 AI067548 and P50 GM082545 to GJJ, DOE grant DE-FG02-04ER63785 to GJJ, NSF grant MCB-0818680 to GCC and SH, the Beckman Institute at Caltech, and gifts to Caltech from the Gordon and Betty Moore Foundation and Agouron Institute.Attached Files
Accepted Version - nihms-180999.pdf
Supplemental Material - applic1.pdf
Supplemental Material - applic2.pdf
Supplemental Material - applic3.pdf
Supplemental Material - applic4.pdf
Supplemental Material - applic5.pdf
Supplemental Material - applic6.pdf
Supplemental Material - applic7.pdf
Supplemental Material - video1.mov
Supplemental Material - video2.mov
Supplemental Material - video3.mov
Supplemental Material - video4.mov
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Additional details
- PMCID
- PMC2853366
- Eprint ID
- 17694
- Resolver ID
- CaltechAUTHORS:20100308-111110207
- NIH
- R01 AI067548
- NIH
- P50 GM082545
- Department of Energy (DOE)
- DE-FG02-04ER63785
- NSF
- MCB-0818680
- Caltech Beckman Institute
- Gordon and Betty Moore Foundation
- Agouron Institute
- Created
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2010-03-08Created from EPrint's datestamp field
- Updated
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2021-11-08Created from EPrint's last_modified field