Team:Goettingen/Project/Outlook
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Worldwide, the number of antibiotic resistant bacteria is increasing, while the development of new antibiotics is still stumbling. Therefore, we intended to build a reporter system to screen for antibiotics directed against cyclic di-AMP, an essential signaling nucleotide found in many Gram-positive bacteria. | Worldwide, the number of antibiotic resistant bacteria is increasing, while the development of new antibiotics is still stumbling. Therefore, we intended to build a reporter system to screen for antibiotics directed against cyclic di-AMP, an essential signaling nucleotide found in many Gram-positive bacteria. | ||
- | We applied the Gram-negative bacterium ''E. coli'' , which has no endogenous c-di-AMP, as a carrier organism. We used several existing Biobricks and recently discovered c-di-AMP sensors from ''Bacillus subtilis'' or ''Mycobacterium smegmatis'', We managed to construct two ''in vivo'' screening systems based on different | + | We applied the Gram-negative bacterium ''E. coli'' , which has no endogenous c-di-AMP, as a carrier organism. We used several existing Biobricks and recently discovered c-di-AMP sensors from ''Bacillus subtilis'' or ''Mycobacterium smegmatis'', We managed to construct two ''in vivo'' screening systems based on different principles. Though these systems still need improvement, they were active and partially functional in ''E. coli''. Thus, we plan to optimize these systems for further development. Once these systems are fully functional, one could provide ''E. coli'' with c-di-AMP by co-expressing its biosynthesis enzyme, a diadenylate cyclase(Fig. 1). Such an ''in vivo'' screening system could be used to screen effectively for novel antibiotics. |
As c-di-AMP homeostasis plays a vital role in many Gram-positive bacteria, its biosynthesis enzyme, diadenylate cyclase (DAC), becomes a very promising target for novel antibacterial substances. We worked on the characterization of one DAC from ''Listeria monocytogenes''. We were able to obtain the crystal structure with the help of the department of Structural Biology and determined a 3D-structure out of it. With this structure known, ''in silico'' screenings for novel antibiotics which could disturb this enzyme could start. The purified DAC could also be employed for ''in vitro'' screenings. | As c-di-AMP homeostasis plays a vital role in many Gram-positive bacteria, its biosynthesis enzyme, diadenylate cyclase (DAC), becomes a very promising target for novel antibacterial substances. We worked on the characterization of one DAC from ''Listeria monocytogenes''. We were able to obtain the crystal structure with the help of the department of Structural Biology and determined a 3D-structure out of it. With this structure known, ''in silico'' screenings for novel antibiotics which could disturb this enzyme could start. The purified DAC could also be employed for ''in vitro'' screenings. |
Revision as of 21:44, 4 October 2013