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Projects source: E-CRIS

Bioinformatic promoter predictions and theoretical modeling of gene circuits in bacteria

Research activity

Code Science Field
B002  Biomedical sciences  Biophysics 
B110  Biomedical sciences  Bioinformatics, medical informatics, biomathematics biometrics 
B120  Biomedical sciences  Molecular biophysics 
B230  Biomedical sciences  Microbiology, bacteriology, virology, mycology 
P190  Natural sciences and mathematics  Mathematical and general theoretical physics, classical mechanics, quantum mechanics, relativity, gravitation, statistical physics, thermodynamics 
Keywords
modeling biological systems, bioinformatics, biophysics, bacterial promoters, gene circuits
Organisations (2) , Researchers (3)
0022  University of Belgrade, Faculty of Biology
no. Code Name and surname Research area Role Period No. of publicationsNo. of publications
1.  09007  PhD Marko J. Đorđević  Physics  Head  2011 - 2019  18 
2.  11699  PhD Jelena N. Repac  Bioinformatics, medical informatics, biomathematics biometrics  Researcher  2014 - 2019 
3.  11682  Anđela M. Rodić  Bioinformatics, medical informatics, biomathematics biometrics  Researcher  2015 - 2019 
0105  University of Belgrade, Institute of Physics - National Institute of the Republic of Serbia
Abstract
Purpose of the project is to develop novel bioinformatic methods, and to generate fundamental understanding necessary for biotechnology applications. This will be achieved through integration of physical and mathematical modeling with biological experiments. The topic of the project is control of gene expression in bacteria, and we will: i) Develop a novel bioinformatic method for promoter prediction in bacterial genome. The algorithm will be based on our recently developed quantitative model of transcription initiation, and is expected to significantly improve low accuracy of the existing algorithms. This will, in turn, improve our ability to analyze transcription regulation and significantly impact other bioinformatic applications such as gene and operon detection. Our promoter prediction method will be experimentally tested. ii)Theoretically analyze strategies that allow expression of toxic, but otherwise useful, molecules in bacterial cells. Systems to be studied are bacterial gene circuits involved in defense against bacterial viruses: specifically, we will analyze restriction modification systems, and the newly discovered CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) systems. The study will provide guidelines on how to design useful synthetic biology circuits.
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