Mycobacteria and Corynebacteria are diderm Gram positive bacteria with a very impermeable cell envelope composed of a very thick complex of peptidoglycan arabinogalactan and mycolic acids.
Our group is focused on the structure, organization and mechanism of assembly of this unique envelope whose function is essential for viability.
Project
Corynebacteriales are an order of actinomycetes that includes corynebacteria, mycobacteria, nocardia, rhodococci and other related microorganisms. Some species, e.g. Mycobacterium tuberculosis, Mycobacterium leprae, are known to cause severe infectious diseases in humans, while others are of considerable economic benefit like Corynebacterium glutamicum, the world’s largest producer of glutamate and lysine.
Organisation of {Corynebacteriales} cell envelope
The cell envelope of Corynebacteriales has a complex and unusual structure that possesses features of both Gram-positive and Gram-negative bacteria. The cell wall core of these bacteria is made up of a specific matrix composed of cross-linked peptidoglycan (PG) covalently bound to arabinogalactan chains (AG), which in turn are linked to long chain fatty acids (up to 90 carbon atoms in mycobacteria) and named mycolic acids (MA), allowing the attached lipids to form with other trehalose mycolates an outer membrane (mycomembrane). Our group played a significant role in the identification and biochemical characterization of this mycomembrane in C. glutamicum during the last decade (for example: Zuber et al. 2008, Marchand et al. 2012).
The biosynthesis of individual MA and AG cell wall compounds has been studied for a long time primarily because the production of these compounds is essential for mycobacterial survival. As a matter of fact, the AG and MA synthesis is the target of several known antituberculous drugs, e.g. isoniazid, ethionamide, ethambutol. In the last few years, many progresses have been made using C. glutamicum as a model microorganism, because, in contrast to mycobacteria we and others showed that viable mutants totally or severely deprived of mycolates or synthesizing a truncated AG could be obtained. Despite the fact that a large part of the cytoplasmic steps of these biosynthetic pathways has been elucidated, only little information is available regarding the trafficking of these cell wall components across the whole cell envelope and their final assembly to yield this very complex and fascinating architecture.
Currently, our group is focused on different projects using C. glutamicum and M. smegmatis as model organisms:
Structure and function of Mycoloyltransferases and their role during cell elongation and division
Protein mycoloylation: an atypical post translationnal modification
team
BAYAN Nicolas Group Leader Professor
CONSTANTINESCO-BECKER Florence Lecturer
LABARRE Cécile Lecturer
REGEARD Christophe Lecturer
DE SOUSA-D'AURIA Célia Engineer
DIETRICH Christiane Engineer
MERABISHVILI Khatia PhD student
ROBERT Guillaume PhD student
ZHANG Yijie PhD student
team
Nicolas BAYAN
Group Leader
Professor
Christophe REGEARD
Associate Professor
Florence CONSTANTINESCO-BECKER
Associate Professor
Cécile LABARRE
Associate Professor
Célia DE SOUSA-D'AURIA
Engineer
Christiane DIETRICH
Assistant Engineer
Yijie ZHANG
PhD student
Tianyue WEI
PhD student
Guillaume ROBERT
Engineer
Latest publications
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