How proteins regulate the outer envelope of bacterial cells

How proteins regulate the outer envelope of bacterial cells
The membrane of Bacillus subtilis cells was marked with the dye Laurdan and analysed by fluorescence microscopy. The staining indicates the fluidity of the membrane: The membranes of the blue-stained cells are considerably more rigid than the very fluid membranes of the reference cells (in red). Credit: Marc Bramkamp

Like all cells, bacteria have a membrane that shields them from the outside like a skin. This barrier is not static, but has to allow transport of substances in and out and be flexible so that the bacterial cells can grow. In order to implement these properties, different types of proteins are active in cells, including the so-called flotillins. These proteins are present in cells from bacteria to humans. Until now, scientists assumed that these flotillins mainly help in the formation of other functional protein complexes and confine highly ordered areas of the cell membrane.

A team of international researchers, including researchers from Kiel University, has now found indications of a possible different function of the flotillins: together with colleagues from the Universities of Groningen (the Netherlands) and Bordeaux (France), among others, the Kiel researchers were able to show that flotillin proteins apparently have a direct influence on the structure of the cell and can make it more fluid under certain conditions. The scientists published their findings yesterday in the renowned scientific journal eLife.

Flotillins may work differently than previously assumed

All must be surrounded by a separating barrier that shields them from their environment, but is also permeable for various molecular substances. Various proteins are necessary for the formation of the cell membranes and to equip them with their functions. Until now, researchers assumed that the so-called flotillin proteins serve to contribute to the formation of the necessary functional protein complexes—for example by delimiting certain areas of the membrane.

The work now presented by Professor Marc Bramkamp's Microbial Biochemistry and Cell Biology group at the Institute of General Microbiology at Kiel University contradicts this view: "Together with a group of international colleagues, we have found evidence that the flotillin proteins have a completely different function. Apparently, they regulate the fluidity of bacterial membranes, making them more fluid to a certain extent and thus, changing their properties," says Bramkamp. This assumption might also explain the effect that flotillins have on the synthesis of the cell wall: building blocks for the cell wall are produced inside the and must subsequently be "flipped" outwards, which is easier to do in a more fluid membrane. In addition, the machinery that synthesizes the cell wall moves dynamically through the cell membrane and this movement is significantly reduced in the absence of the flotillins. Consequently, the cells cannot synthesize the cell wall correctly.

How proteins regulate the outer envelope of bacterial cells
Phase-contrast microscopic image of Bacillus subtilis bacteria in which flotillins were made visible with the aid of the green fluorescent protein GFP. Credit: Marc Bramkamp

Without flotilline no stable form

The Kiel research team developed the new hypothesis in cooperation with international colleagues on the basis of experiments with the rod-shaped bacterium Bacillus subtilis. These experiments showed that fast-growing cells are unable to develop their typical shape in the absence of flotillins. However, if the researchers added a chemical substance to fluidize the membranes, the bacteria could maintain their shape even without flotillin proteins. "We therefore assume that they take over a physical role in the bacterial membrane," says Abigail Savietto, Ph.D. student in Bramkamp's group at Kiel University. "The flotillins seem to have an effect on the physical structure of the membrane, conferring the correct fluidity so other membrane-bound processes can function properly."

In further research, the researchers hope to find out what is the exact molecular mechanism between the flotillin proteins and membrane fluidity. One approach might be the investigation of the phospholipid composition of the membrane. These lipids are involved in the formation of many different biomembranes. It is possible that the flotillin proteins are able to bind certain phospholipids that reduce fluidity and thus increase the total fluidity of the cell membrane. The new hypothesis of the Kiel research team thus also holds promising perspectives for application: in the future, it might be possible to specifically influence the physical properties of bacterial cell membranes by disrupting the flotillin function. "My research group has been working on the function of flotillins for many years and we know that cells with altered membrane fluidity are much more sensitive to conventional antibiotics. It might be possible to use this mechanism, for example to specifically alter the membrane of in such a way that they can be killed more easily with antibiotics," Bramkamp says.

Explore further

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More information: Aleksandra Zielińska et al. Flotillin-mediated membrane fluidity controls peptidoglycan synthesis and MreB movement, eLife (2020). DOI: 10.7554/eLife.57179
Journal information: eLife

Provided by Kiel University
Citation: How proteins regulate the outer envelope of bacterial cells (2020, July 16) retrieved 16 June 2021 from
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