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Published on: December 17, 2021
The hydrolase LpqI primes mycobacterial peptidoglycan recycling
Patrick J Moynihan1, Ian T Cadby2, Natacha Veerapen2
1Institute of Microbiology and Infection, School of Biological Sciences, University of Birmingham, Birmingham, B15 2TT, UK. p.j.moynihan@bham.ac.uk.
Abstract:
Growth and division by most bacteria requires remodelling and cleavage of their cell wall. A byproduct of this process is the generation of free peptidoglycan (PG) fragments known as muropeptides, which are recycled in many model organisms. Bacteria and hosts can harness the unique nature of muropeptides as a signal for cell wall damage and infection, respectively. Despite this critical role for muropeptides, it has long been thought that pathogenic mycobacteria such as Mycobacterium tuberculosis do not recycle their PG. Herein we show that M. tuberculosis and Mycobacterium bovis BCG are able to recycle components of their PG. We demonstrate that the core mycobacterial gene lpqI, encodes an authentic NagZ β-N-acetylglucosaminidase and that it is essential for PG-derived amino sugar recycling via an unusual pathway. Together these data provide a critical first step in understanding how mycobacteria recycle their peptidoglycan.
Insights
Pathogenic mycobacteria, including Mycobacterium tuberculosis, can recycle peptidoglycan (PG) components. The gene lpqI encodes an essential enzyme for this PG-derived amino sugar recycling pathway.
Area of Science:
- Microbiology
- Cell Biology
- Biochemistry
Background:
- Bacterial growth and division necessitate cell wall remodeling and cleavage.
- This process releases peptidoglycan (PG) fragments called muropeptides, which are recycled by many bacteria.
- Muropeptides serve as signals for cell wall damage in bacteria and infection detection in hosts.
Purpose of the Study:
- To investigate whether pathogenic mycobacteria, specifically Mycobacterium tuberculosis and Mycobacterium bovis BCG, recycle their peptidoglycan.
- To identify the molecular mechanisms underlying peptidoglycan recycling in mycobacteria.
Main Methods:
- Genetic analysis of the mycobacterial gene lpqI.
- Biochemical characterization of the enzyme encoded by lpqI.
- Investigation of peptidoglycan-derived amino sugar recycling pathways.
Main Results:
- Mycobacterium tuberculosis and Mycobacterium bovis BCG were shown to recycle PG components.
- The gene lpqI encodes a functional NagZ β-N-acetylglucosaminidase.
- This enzyme is essential for an atypical pathway of PG-derived amino sugar recycling.
Conclusions:
- Contrary to previous assumptions, pathogenic mycobacteria do recycle peptidoglycan.
- The lpqI gene and its encoded NagZ enzyme are critical for this recycling process.
- This study provides foundational insights into mycobacterial peptidoglycan recycling mechanisms.
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