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Forward Genetic Approaches in Chlamydia trachomatis
Published on: October 23, 2013
Characterization of serine hydroxymethyltransferase GlyA as a potential source of D-alanine in Chlamydia pneumoniae
Stefania De Benedetti1, Henrike Bühl1, Ahmed Gaballah1
1Pharmaceutical Microbiology Section, Institute for Medical Microbiology, Immunology and Parasitology, University of Bonn Bonn, Germany.
Abstract:
For intracellular Chlamydiaceae, there is no need to withstand osmotic challenges, and a functional cell wall has not been detected in these pathogens so far. Nevertheless, penicillin inhibits cell division in Chlamydiaceae resulting in enlarged aberrant bodies, a phenomenon known as chlamydial anomaly. D-alanine is a unique and essential component in the biosynthesis of bacterial cell walls. In free-living bacteria like Escherichia coli, penicillin-binding proteins such as monofunctional transpeptidases PBP2 and PBP3, the putative targets of penicillin in Chlamydiaceae, cross-link adjacent peptidoglycan strands via meso-diaminopimelic acid and D-Ala-D-Ala moieties of pentapeptide side chains. In the absence of genes coding for alanine racemase Alr and DadX homologs, the source of D-Ala and thus the presence of substrates for PBP2 and PBP3 activity in Chlamydiaceae has puzzled researchers for years. Interestingly, Chlamydiaceae genomes encode GlyA, a serine hydroxymethyltransferase that has been shown to exhibit slow racemization of D- and L-alanine as a side reaction in E. coli. We show that GlyA from Chlamydia pneumoniae can serve as a source of D-Ala. GlyA partially reversed the D-Ala auxotrophic phenotype of an E. coli racemase double mutant. Moreover, purified chlamydial GlyA had racemase activity on L-Ala in vitro and was inhibited by D-cycloserine, identifying GlyA, besides D-Ala ligase MurC/Ddl, as an additional target of this competitive inhibitor in Chlamydiaceae. Proof of D-Ala biosynthesis in Chlamydiaceae helps to clarify the structure of cell wall precursor lipid II and the role of chlamydial penicillin-binding proteins in the development of non-dividing aberrant chlamydial bodies and persistence in the presence of penicillin.
Insights
Chlamydia pneumoniae utilizes GlyA, a serine hydroxymethyltransferase, for D-alanine biosynthesis, explaining penicillin
Area of Science:
- Microbiology
- Biochemistry
Background:
- Chlamydiaceae lack a detectable cell wall but exhibit penicillin-induced cell division inhibition (chlamydial anomaly).
- Penicillin targets bacterial cell wall synthesis enzymes, requiring D-alanine, whose source in Chlamydiaceae was previously unknown.
- Chlamydiaceae possess GlyA, a serine hydroxymethyltransferase, with potential D-alanine racemase activity.
Purpose of the Study:
- To investigate the source of D-alanine in Chlamydiaceae.
- To determine if Chlamydial GlyA possesses D-alanine racemase activity.
- To elucidate the role of GlyA in chlamydial penicillin response.
Main Methods:
- Complemented an Escherichia coli racemase double mutant with Chlamydia pneumoniae GlyA.
- Purified Chlamydial GlyA and assessed its in vitro racemase activity.
- Tested the inhibitory effect of D-cycloserine on purified GlyA.
Main Results:
- Chlamydial GlyA partially rescued the D-alanine auxotrophic phenotype in E. coli.
- Purified GlyA exhibited L-alanine to D-alanine racemase activity in vitro.
- D-cycloserine inhibited GlyA activity, identifying it as a potential target.
Conclusions:
- Chlamydial GlyA is a source of D-alanine, clarifying its role in cell wall precursor synthesis.
- GlyA activity explains the substrate availability for penicillin-binding proteins in Chlamydiaceae.
- This finding provides insight into chlamydial anomaly and persistence under penicillin treatment.

