Abstract
The Candidate Phyla Radiation (CPR) encompasses widespread uncultivated bacteria with reduced genomes and limited metabolic capacities. Most CPR bacteria lack the minimal set of enzymes required for peptidoglycan (PG) synthesis, leaving it unclear how these bacteria produce this essential envelope component. In this study, we analysed the distribution of
d
‐amino acid racemases that produce the universal PG components
d
‐glutamate (
d
‐Glu) or
d
‐alanine (
d
‐Ala). We also examined moonlighting enzymes that synthesize
d
‐Glu or
d
‐Ala. Unlike other phyla in the domain Bacteria, CPR bacteria do not exhibit these moonlighting activities and have, at most, one gene encoding either a Glu or Ala racemase. One of these ‘orphan’ racemases is a predicted Glu racemase (MurI
CPR
) from the CPR bacterium
Candidatus Saccharimonas aalborgenesis
. The expression of MurI
CPR
restores the growth of a
Salmonella
d
‐Glu auxotroph lacking its endogenous racemase and results in the substitution of
l
‐Ala by serine as the first residue in a fraction of the PG stem peptides. In vitro, MurI
CPR
exclusively racemizes Glu as a substrate. Therefore,
Ca. Saccharimonas aalborgensis
may couple Glu racemization to serine and
d
‐Glu incorporation into the stem peptide. Our findings provide the first insights into the synthesis of PG by an uncultivated environmental bacterium and illustrate how to experimentally test enzymatic activities from CPR bacteria related to PG metabolism.