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How bacteria change movement direction in response to oxygen: Molecular interactions unravelled

Date:
June 25, 2012
Source:
Ruhr-Universitaet-Bochum
Summary:
How single cell organisms like bacteria manage to react to their environment is not yet completely understood. Scientists have now gained new insights into the molecular interactions during aerotaxis of Bacillus subtilis, i.e., the dependence of the movement direction on the oxygen concentration in the environment. The research team investigated the conformational changes within the protein HemAT. Via a signal transduction chain, this protein sends a command to the flagellar motor which controls the movement direction.

Conformational changes within HemAT: When oxygen binds to the sensor domain (for methodological reasons, the experiment was carried out with carbon monoxide, CO, instead of oxygen), the protein conformation in the vicinity of the sensor domain changes. Thus, helices B and G are displaced. This affects the neighboring H-helix which is continuous with the signalling domain.
Credit: Illustration: Samir El-Mashtoly

How single cell organisms like bacteria manage to react to their environment is not yet completely understood. Together with colleagues from Japan, Dr. Samir El-Mashtoly from the RUB Department of Biophysics, led by Prof. Dr. Klaus Gerwert, has gained new insights into the molecular interactions during aerotaxis of Bacillus subtilis, i.e., the dependence of the movement direction on the oxygen concentration in the environment. The research team investigated the conformational changes within the protein HemAT. Via a signal transduction chain, this protein sends a command to the flagellar motor which controls the movement direction.

They report in the Journal of Biological Chemistry.

Signal transduction chain

The signal transduction chain starts with binding of oxygen to HemAT's heme domain, which is also known from haemoglobin in the red blood cells and is called the sensor domain of HemAT. Oxygen binding leads to a conformational change in the sensor domain. This in turn provokes several further conformational changes within HemAT that finally affect the signalling domain of the protein. The signalling domain then transmits the information about a rise in oxygen concentration to other proteins within the cell. These proteins forward the message to the motor of the flagellum. The research team investigated how the information travels from the sensor domain of HemAT to its signalling domain.

Protein helices forward the information

For that purpose, Dr. El-Mashtoly used the time-resolved ultraviolet resonance Raman spectroscopic facilities in the Picobiology Institute in Japan. This method provides, for instance, structural information about the conformation of the protein and hydrogen bonding interactions on a nanosecond to microsecond time scale. The results suggest that the conformational change in the sensor domain, i.e., the heme structure, induces the displacement of two protein helices within HemAT. This displacement affects another helix which is continuous with the structure of the signalling domain. Due to a series of conformational changes, the information about oxygen binding thus reaches the signalling domain of the protein.


Story Source:

The above story is based on materials provided by Ruhr-Universitaet-Bochum. Note: Materials may be edited for content and length.


Journal Reference:

  1. S. F. El-Mashtoly, M. Kubo, Y. Gu, H. Sawai, S. Nakashima, T. Ogura, S. Aono, T. Kitagawa. Site-specific Protein Dynamics in Communication Pathway from Sensor to Signaling Domain of Oxygen Sensor Protein, HemAT-Bs: TIME-RESOLVED ULTRAVIOLET RESONANCE RAMAN STUDY. Journal of Biological Chemistry, 2012; 287 (24): 19973 DOI: 10.1074/jbc.M112.357855

Cite This Page:

Ruhr-Universitaet-Bochum. "How bacteria change movement direction in response to oxygen: Molecular interactions unravelled." ScienceDaily. ScienceDaily, 25 June 2012. <www.sciencedaily.com/releases/2012/06/120625064448.htm>.
Ruhr-Universitaet-Bochum. (2012, June 25). How bacteria change movement direction in response to oxygen: Molecular interactions unravelled. ScienceDaily. Retrieved September 16, 2014 from www.sciencedaily.com/releases/2012/06/120625064448.htm
Ruhr-Universitaet-Bochum. "How bacteria change movement direction in response to oxygen: Molecular interactions unravelled." ScienceDaily. www.sciencedaily.com/releases/2012/06/120625064448.htm (accessed September 16, 2014).

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