Buoyancy Regulation in a Strain of Microcystis

Регуляция плавучести у штамма Microcystis
Ranjeny Thomas, A. E. Walsby
1985-04-01

Microcystiscell turgor pressurecyanobacterial buoyancygas vesiclesphoton flux density
A strain of the gas-vacuolate cyanobacterium Microcystis was found to float in cultures grown at low light intensities and to sink in those grown at high intensities. The loss of buoyancy that occurred within 1 to 5 h on increasing the photon flux density from 10 to l00 μmol m–2 s–1 was investigated by centrifuging the cell suspensions in a horizontally placed capillary with a rectangular cross-section, and then separately counting the floating cells under the upper tube surface and sinking cells on the lower surface. Buoyancy loss was not accompanied by loss of gas vesicles, as occurs in some other planktonic cyanobacteria, but was caused by a relative increase in dry matter, principally carbohydrate, without a corresponding increase in gas vesicles. The increase in light intensity gave an increase in cell turgor pressure but this was insufficient to collapse the strong gas vesicles present in this strain, which had a median critical pressure of 0·75 MPa (7·5 bar).
1
Higher light intensity increased cellular turgor pressure, but this pressure was insufficient to collapse the strain’s strong gas vesicles.
2
Light-induced sinking was not caused by gas-vesicle loss; instead, cells accumulated dry matter, principally carbohydrate, without a corresponding increase in gas vesicles.
3
Microcystis floated under low light but sank under high light, with buoyancy loss occurring within 1–5 hours after increasing photon flux density from 10 to 100 μmol m⁻² s⁻¹.
4
The gas vesicles had a median critical collapse pressure of 0.75 MPa (7.5 bar).

a gas-vacuolate strain of the cyanobacterium Microcystis

light-intensity-dependent buoyancy regulation and its mechanism through changes in cellular dry matter, carbohydrate content, turgor pressure, and gas-vesicle stability

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1985-04-01
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Ranjeny Thomas
A. E. Walsby
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