Emerging knowledge of regulatory roles of d-amino acids in bacteria
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The d-enantiomers of amino acids have been thought to have relatively minor functions in biological processes. While l-amino acids clearly predominate in nature, d-amino acids are sometimes found in proteins that are not synthesized by ribosomes, and d-Ala and d-Glu are routinely found in the peptidoglycan cell wall of bacteria. Here, we review recent findings showing that d-amino acids have previously unappreciated regulatory roles in the bacterial kingdom. Many diverse bacterial phyla synthesize and release d-amino acids, including d-Met and d-Leu, which were not previously known to be made. These noncanonical d-amino acids regulate cell wall remodeling in stationary phase and cause biofilm dispersal in aging bacterial communities. Elucidating the mechanisms by which d-amino acids govern cell wall remodeling and biofilm disassembly will undoubtedly reveal new paradigms for understanding how extracytoplasmic processes are regulated as well as lead to development of novel therapeutics.
Keywordsd-amino acid Racemase Stationary phase Peptidoglycan Biofilm Regulation
Broad spectrum racemase in Vibrio
Objects are described as chiral if their reflected image in a mirror cannot be superimposed on the original. The term chiral is derived from the Greek word for hand, χειρ, as human hands provide a prime example of chirality. While very similar in almost all characteristics, the mirror image of a left hand—the right hand—cannot be superimposed on itself and interacts with other objects in a distinct manner . Natural objects, such as vertebrate appendages, that exhibit chirality are readily apparent. Chirality is also widespread at the molecular level. Remarkably, in 1848 at the age of 25, before he carried out his pioneering studies in microbiology, the great French scientist Louis Pasteur (1822–1895) discovered molecular chirality in mirror-image tartaric acid crystals (revisited in ). Nine years later, while studying the fermentation of tartaric acid by microorganisms, Pasteur discovered that one mirror image of tartaric acid was consumed with greater preference over the other [2, 3]. In the ensuing 150 years, the great importance of molecular chirality in many biochemical processes has become clear.
While chemical synthesis routinely yields both enantiomers, most enzymes display marked substrate selectivity, and as a consequence many biochemical processes generally utilize and yield particular enantiomers. For example, l-amino acids are the predominant building blocks of proteins; d-amino acids cannot be incorporated into proteins via ribosomal synthesis. Similarly, nearly all naturally occurring monosaccharides exist as d-sugars. The origins of enantiospecificity in biological processes are unclear, but it has been proposed that enantiomerically enriched organic compounds were critical for the generation of proto-life forms [5, 6, 7].
Even though l-amino acids are the dominant substrates for ribosome-based protein synthesis, several roles for d-amino acids in other biological processes have been described. For example, d-aspartate is a major regulator of adult neurogenesis  and d-serine acts as a co-agonist of the N-methyl d-aspartate-type glutamate receptors in the brain, which are involved in learning, memory, and behavior in mammals [9, 10, 11]. d-serine is also the most abundant amino acid in human urine and alters gene expression of uropathogenic Escherichia coli (UPEC) .
d-amino acids in eukaryotic peptides
d-amino acid (position)
Phyllomedusa sauvagei (skin secretions of Argentinian tree frog)
Binds to μ-type opiate receptors and acts as an analgesic 1,000 times more powerful than morphine
d-Met or d-Ala (2nd)
Phyllomedusa species (skin secretions)
Binds to δ-type opiate receptors
Bombinins and bombinins H
Bombinatoridae (skin secretions of frogs)
Antimicrobial and hemolytic activity
Achatina fulica (ganglia and atrium of African snail)
Excitatory neurotransmitter controlling muscle contraction
A. fulica (ganglia of African snail)
Excitatory neurotransmitter controlling penis contraction
d-Trp (3rd or 4th)
Conus purpurascens and C. radiatus (venom of cone snail)
Causes tremor and mucous secretions when injected into fish
FRF amide family
Stimulates muscle contraction
Crustacean hyperglycemic hormone
Neurohormone controlling hyperglycemia
Agelenopsis aperta (venom of funnel-web spider)
Blocks voltage-sensitive calcium channels
Three d-amino acid residues including an unusual O-prenyl-d-Tyr
Insect pathogenic fungus Paecilomyces cinnamomeus BCC 9616
Activity against the malarial parasite Plasmodium falciparum K1; cytotoxicity to cancer cell lines (KB and BC)
d-amino acids in bacterial peptides
d-amino acid (position)
d-Phe (4th, 9th)
Bacillus brevis (antimicrobial peptides)
Membrane disruption of lipid bilayer
d-Leu (4th, 10th, 12th, 14th)
B. brevis (antimicrobial peptides)
Permeabilizes lipid membranes by forming ion channels that disrupt ion gradient
d-Val (6th, 8th)
B. brevis (antimicrobial peptides)
Permeabilizes lipid membranes
d-Phe or d-Tyr (4th)
Streptomycetes (S. roseosporus)
Arthrofactin (7 d-amino acids of the 11)
Syringomycin (2 d-amino acids of the 9)
Syringopeptin (about 70% of the sequence is in d-configuration)
Only d-amino acids
Bacterial strains CF-20 (CECT5719) and C-148 (CECT5718), isolated from cultures of larvae of mollusks
Strong antibiotic activity against Vibrio anguillarum
1 d-Ala residue
Lactobacillus gasseri LA39
Antimicrobial activity against Listeria monocytogenes, Bacillus cereus, and S. aureus
Besides being occasionally incorporated in peptides, d-amino acids have been known to be utilized as nutrients to support bacterial growth [24, 25, 26, 27], to regulate bacterial spore germination, and to be components of the bacterial cell wall. We briefly summarize the latter two previously recognized roles of d-amino acids below. Then, we discuss recent findings showing that d-amino acids have previously unappreciated regulatory roles in the bacterial kingdom.
d-amino acids and bacterial spore germination
Bacterial sporulation is an adaptive response to environmental stress, such as starvation, and involves a finely controlled developmental program. Initiation of sporulation leads to asymmetric cell division producing a mother cell and forespore with distinct cell fates. The forespore develops into the spore, whereas the mother cell nurtures the spore but ultimately lyses through programmed cell death .
Bacterial spores are metabolically dormant and resistant to a number of harsh environments including heat, radiation, desiccation, pH extremes, and toxic chemicals . This remarkable resistance is provided by a tough multilayered cell wall . In the presence of specific germinants such as l-alanine or other nutrients, spores can reactivate metabolism and grow vegetatively. In 1949, it was discovered that d-alanine was a potent inhibitor of spore germination in many Bacillus species . Subsequent work since this discovery has revealed that Bacillus species utilize d-alanine as an auto-inhibitor of spore germination at high spore density. This activity is mediated through expression of an alanine racemase in the spore exosporium that converts a spore germinant (l-Ala) to an anti-germinant (d-Ala) . A nutrient receptor is responsible for recognition of l-Ala, and it has been suggested that d-Ala antagonizes l-Ala binding to this receptor . Presumably, this mechanism of auto-inhibition is an evolutionary adaptation to prevent premature germination under low nutrient conditions and high population density, an environmental condition that would lead to rapid nutrient depletion and cell death. Recent work has also suggested that d-Ala alters the kinetics of germination in vivo to enhance the efficiency and timing of infection . d-His has also been implicated as a germination inhibitor of Bacillus anthracis infection in murine macrophages , however its mechanism of action and whether it is physiologically produced by B. anthracis is unknown.
d-amino acids in peptidoglycan
The biosynthesis of PG is divided into three stages (Fig. 2). In the first step, the PG precursors nucleotide sugar-linked UDP-MurNAc-pentapeptide and UDP-GlcNAc are synthesized in the cytoplasm . Second, lipid intermediates of these precursors are formed by transferring the phospho-MurNAc-pentapeptide moiety of UDP-MurNAc-pentapeptide to the membrane acceptor bactoprenyl-P, yielding lipid I. Subsequently, GlcNAc from UDP-GlcNAc is added to lipid I, yielding lipid II. The lipid II intermediate enables the cell to transport the hydrophilic precursors from the aqueous environment of the cytoplasm through the hydrophobic membrane, where they can act as substrates for incorporation into the PG polymer [45, 46]. PG polymerization, the third stage of PG biosynthesis, occurs outside of the cell membrane in the periplasmic space of gram-negative bacteria and outside the cell entirely in gram-positive organisms. Polymerization is carried out by penicillin-binding proteins (PBPs). These enzymes catalyze both the transglycosylation and transpeptidation reactions required to incorporate new muropeptides into the PG polymer [47, 48, 49, 50].
One of the most striking features of PG composition is the presence of d-amino acids in the stem peptides (Fig. 2) . d-amino acids contribute to the architecture of the murein and, more importantly, provide resistance to most known proteases. Thus, the presence of d-amino acids in PG likely constitutes a bacterial adaptation to protect a vital cellular structure. d-Ala and d-Glu are by far the most common d-amino acids present in the bacterial cell wall; however, the PG of some bacteria include other d-amino acids, such as d-Asp in Lactococcus  and Enterococcus , and d-Ser in vancomycin-resistant Staphylococcus aureus [54, 55, 56]. In some cases, such substitutions enable bacteria to tolerate bactericidal agents from the environment .
Production of d-amino acids
Since l-amino acids are the predominant amino acids found in living organisms, typically they act as the substrate for generation of d-amino acids. l- to d-conversion occurs by the action of racemases that change the stereochemistry of the chiral α-carbon atom in amino acids . Amino acid racemases are classified into two groups, pyridoxal-5-phosphate (PLP)-dependent and PLP-independent enzymes, with distinct reaction mechanisms.
PLP-dependent amino acid racemases
Most bacteria encode two different alanine racemases, DadB and Alr. While both racemases use the same reaction mechanism, they are components of distinct molecular pathways. DadB participates in l-Ala catabolism, producing d-Ala to be used as a substrate to form pyruvate via a d-Ala dehydrogenase. In contrast, Alr generates the d-Ala that is utilized in formation of muropeptide precursors for PG synthesis [61, 62].
Bacterial serine racemases are homologues of alanine racemases and play an important role in resistance to vancomycin [54, 56], a glycopeptide antibiotic that inhibits PG synthesis by binding to the d-Ala-d-Ala moiety in muropeptide precursors. In enterococci, vancomycin resistance arises through modification of the vancomycin target site from d-Ala-d-Ala to either d-Ala-d-lactate or d-Ala-d-Ser . d-Ser is generated from l-Ser by VanT, a serine racemase, which, like alanine racemase, is also PLP-dependent and probably uses a two-base catalyzed reaction. The similarity of VanT to alanine racemase suggests that the two enzymes share a common evolutionary history .
PLP-independent amino acid racemases
Like d-Ala, d-Glu is a component of the PG cell wall in bacteria, but this d-amino acid is produced by a PLP-independent racemase. Similar to alanine racemases, glutamate racemases are thought to follow a two-base mechanism, however, two cysteines have been suggested to be involved in the catalysis of the latter [65, 66, 67] (Fig. 3b).
In some organisms, such as E. coli, expression of glutamate racemase is activated 100-fold in the presence of UDP-MurNAc-L-Ala. This intermediate is ligated to d-Glu in generating PG precursor units, lipid I and lipid II. Thus, expression of the glutamate racemase is regulated by the factors that require its presence [68, 69].
Bacillus subtilis encodes two glutamate racemases, Glr and YrpC. Though both proteins have similar biochemical properties, Glr is mainly involved in d-glutamate synthesis for poly-γ-d-glutamate, a structural component of the spore capsule, whereas YrpC is the racemase that creates d-Glu for the cell wall PG [70, 71].
Aspartate and proline racemases
d-Asp occurs in the PG layer of some bacterial cell walls and is produced from l-Asp by an aspartate racemase. The enzyme is present in various gram-positive bacteria, including Lactococcus lactis , Enterococcus faecium , Lactobacillus fermenti , and Streptococcus faecalis , as well as some archea . Like glutamate racemase, aspartate racemase requires no cofactors, contains an essential cysteine residue, and has been proposed to act via a two-base mechanism to remove and return the α-proton of the substrate .
Proline racemase is also a member of the PLP-independent enzyme family. Proline racemases have been identified in Clostridium difficile and Clostridium sticklandii. Currently, it is not known if d-Pro is a component of PG in these spore-forming organisms, but it has been hypothesized that d-Pro may enable these pathogens to evade the host immune response .
Newly appreciated regulatory roles for d-amino acids in bacteria
As outlined above, the roles of d-amino acids in bacteria were thought to be fairly limited. However, recently it has become clear that d-amino acids are synthesized and released by bacteria from diverse phyla, at up to millimolar concentrations . Furthermore, released d-amino acids function to regulate cell wall chemistry and architecture as well as biofilm development in bacteria . These findings and their implications are discussed below.
d-amino acids govern cell wall remodeling in bacteria
Although PG functions as an exoskeleton, bacterial growth and survival depends on PG plasticity [41, 42, 79]. When bacteria grow, covalent bonds in the PG polymer must be cleaved by murein hydrolases and new bonds formed to insert new subunits into the sacculus. Furthermore, new PG synthesis is crucial for the formation of the septum during cell division (with subsequent generation of the new poles in the daughter cells)  and for sporulation/germination PG remodeling [29, 81, 82]. Finally, in times of stress, PG also can be remodeled. For example, many rod-shaped bacteria reorganize their PG in stationary phase, becoming smaller and more coccoid in shape . Currently, there is relatively little understanding of the factors that govern PG remodeling during exponential growth; however, d-amino acids were recently shown to control changes in PG composition and architecture as cells enter stationary phase (see below).
More than six decades ago, high concentrations of exogenous d-amino acids were found to inhibit bacterial growth [84, 85, 86]. This effect, which was attributed to alterations in PG metabolism in the treated cells [87, 88, 89, 90], required addition of seemingly nonphysiological levels of amino acids, and hence was not thought to be biologically meaningful; however, it did inspire the use of exogenously added components to investigate murein segregation. De Pedro and colleagues demonstrated that low concentrations of d-Cys were relatively innocuous to cells but that several bacterial species incorporated this sulfhydryl-bearing amino acid into murein [89, 90]. Immunodetection of the -SH groups in purified sacculi enabled the distribution of d-Cys in PG to be tracked , and such studies have provided valuable insights into cell growth, polarity, and PG synthesis and maintenance [92, 93].
Discovery of production and release of d-amino acids by bacteria
Our group recently made the unexpected discovery that many diverse phyla of bacteria produce types of d-amino acids that were not previously known to be synthesized and release them into the environment . We made this surprising finding while investigating the genetic basis for the curved rod-shape of Vibrio cholerae, the gram-negative bacterium that causes cholera. A genetic screen for V. cholerae with altered cell shape yielded a mutant that exhibited a growth phase-dependent cell morphology defect. We observed that nearly all mrcA mutant cells in stationary phase cultures were spherical, although their morphology did not differ from that of wild-type cells during exponential growth. The mrcA gene encodes PBP1A, an inner membrane-anchored enzyme that elongates the glycan chains and establishes the cross-links between the peptides of the PG . Thus, PBP1A-mediated PG synthesis appears to be required for the maintenance of V. cholerae rod shape in stationary phase. In contrast, deletion of mrcB, which encodes PBP1B, had no effect on V. cholerae morphology suggesting that these two homologous enzymes have clearly separable functions .
We hypothesized that the rod-to-sphere transition of the mrcA cells might be stimulated by an extracellular factor present in stationary phase supernatants, since the morphology of mrcA cells changed as cultures became saturated and entered stationary phase. In fact, exponentially growing rod-shaped mrcA cells rapidly became spherical when incubated in a cell-free supernatant from stationary phase cultures. We purified the sphere-inducing component and identified that the active factors were four amino acids: Met, Leu, Val, and Ile. The d- rather than l-forms of these particular amino acids were the active agents in V. cholerae supernatants that influenced mrcA’s morphology. Remarkably, stationary phase V. cholerae supernatants contained a ~1 mM total concentration of these four d-amino acids, an amount sufficient to account for the sphere-inducing activity in the supernatants. Except for d-Pro and d-Gln, other d-amino acids also had some capacity to stimulate the mrcA mutant’s shape transition from rod to sphere, suggesting that sphere-inducing activity is promoted by the chirality rather than the side chain of the amino acid .
Genomic analysis allowed us to identify a novel V. cholerae racemase that proved to be necessary and sufficient for the synthesis of the unusual d-amino acids in V. cholerae supernatants. Besides the two genes that encode the V. cholerae Glu and Ala racemases, the V. cholerae genome contains an additional gene (vc1312) that encodes a putative PLP-dependent amino acid racemase. A strain with a deletion of this gene was highly defective in the production of d-Met, d-Leu, d-Val, and d-Ile, suggesting that it encodes the principal racemase for the generation of these four d-amino acids. This enzyme, which was named broad spectrum racemase in Vibrio (BsrV) also exhibits in vitro racemase activity for these d-amino acids confirming BsrV as a broad spectrum racemase . Since extracellular d-amino acids were not detected in supernatants from exponential phase cultures of wild-type cells, BsrV is likely only active during stationary phase. In addition, unlike nearly all other bacterial amino acid racemases, which are cytoplasmic, the BsrV racemase was found exclusively in the periplasm, suggesting that d-amino acids produced by BsrV primarily act on periplasmic targets .
Notably, we found that the release of d-amino acids into the media is not limited to V. cholerae and other vibrios; instead, stationary phase supernatants from many species representing diverse phyla including B. subtilis, S. aureus, Pseudomonas aeruginosa, and Deinococcus radiodurans contained different d-amino acids. Consistent with this observation, most bacterial genomes appear to encode one or more amino acid racemases in addition to the enzymes required to generate d-Ala and d-Glu for PG synthesis . This suggests that production of broad spectrum racemases may be a conserved trait amongst diverse bacteria.
d-amino acids regulate peptidoglycan composition, amount, and strength
Even though the morphology of wild-type cells was not altered by d-amino acids, we hypothesized that the production of d-amino acids by wild-type V. cholerae has an important physiological role since their generation represents a significant metabolic expenditure. Several observations supported the idea that release of noncanonical d-amino acids could regulate cell wall remodeling. First, d-amino acids (principally d-Ala and d-Glu) are known to be cell wall components, and thus it seemed reasonable that additional d-amino acids could influence PG metabolism. Second, we observed that wild-type V. cholerae cells became spherical if d-amino acids were supplemented with β-lactam antibiotics. Since PG is the principal determinant of bacterial cell shape, these observations suggested that d-amino acids in combination with either genetic (e.g., deletion of mrcA) or chemical inactivation of PBPs lead to weakened PG that is unable to maintain V. cholerae’s rod shape. Finally, as mentioned above, previous work by de Pedro and colleagues revealed that exogenous d-Cys or d-Met could (at high concentrations) be incorporated into PG [89, 90, 91, 94].
We compared the chemical composition, structure, and amount of PG isolated from stationary phase wild-type and bsrV V. cholerae to ascertain the effects of the physiologic production of d-amino acids on PG metabolism. Remarkably, the bsrV mutant, which fails to produce and release significant amounts of d-Met, d-Leu, d-Val, and d-Ile, but still produces d-Ala and d-Glu, contained twice the amount of PG found in wild-type cells in stationary phase. Furthermore, exogenous addition of d-amino acids reduced the amount of PG in V. cholerae. Thus, d-amino acids negatively regulate the amount of PG produced by V. cholerae in stationary phase. Moreover, because the accumulation of d-amino acids coincides with the transition into stationary phase and appears to downregulate PG synthesis, d-amino acids may enable coordination of metabolic slowing in cell wall and cytoplasmic compartments when resources become scarce .
The noncanonical d-amino acids are incorporated into the PG polymer. HPLC-based analyses of muropeptides from wild-type cells demonstrated that d-Met and d-Leu were present in PG in stationary phase. d-Met and d-Leu replaced d-Ala in the fourth position of the peptide bridge in 3–4% of the stationary phase muropeptides but were not detected in PG from the bsrV mutant. As previously suggested for the incorporation of exogenous d-amino acid into the PG , the incorporation of physiologically released d-Met and d-Leu may occur via the action of a periplasmic, β-lactam-insensitive PG-modifying enzyme.
BsrV-generated d-amino acids also influenced the structure of stationary phase PG. In comparison to wild-type PG, the glycan chains from the bsrV mutant were ~20% shorter, and there was an approximately 50% reduction in the amount of full-length pentapeptides and an increase in the amount of trimer muropeptides. Importantly, the changes in PG structure and abundance in the bsrV mutant appear to reduce PG strength. Wild-type cells were far more resistant to an osmotic challenge, suggesting that the PG in wild-type cells is stronger than that in the bsrV mutant. The osmotic hypersensitivity of bsrV mutant cells was unexpected since the bsrV mutant cells contain twice as much PG as wild-type cells. The “weakness” of the PG in bsrV cells presumably is a consequence of the alterations in cell wall structure that result from the absence of d-amino acids in these cells. In this regard, variations in the proportions of pentapeptides and tetrapeptides should have little, if any, effect on the physical strength of the sacculus (as these peptides do not participate in bridging). However, the decrease in the length of the glycan strands in the bsrV mutant could weaken the PG because the number of covalent bonds closing the net-like peptidoglycan molecule is reduced. Regardless of the chemical changes that weaken the PG in the bsrV mutant, general weakening of the entire sacculus is not required to bestow osmotic sensitivity, only localized weakening of the PG would be sufficient. Together, these observations suggest that d-amino acid production by BsrV as cells enter stationary phase provides an autocrine-like signal for V. cholerae to remodel its PG and decrease PG synthesis in adaptation to stationary phase conditions .
Regulation of PG by d-amino acids is not limited to V. cholerae. We found that B. subtilis produces different d-amino acids than does V. cholerae (mainly d-Phe and d-Tyr) in stationary phase, but these d-amino acids appear to influence PG synthesis and chemistry in similar ways as d-Met and d-Leu in V. cholerae. Thus, evolutionarily distant bacteria have a common strategy to modulate PG synthesis in stationary phase through production and release of d-amino acids. Remarkably, B. subtilis growth was inhibited when cultured in the presence of exogenous physiologic concentrations of d-amino acids produced by B. subtilis in stationary phase. This suggests that d-amino acids may be a mechanism to simultaneously slow down growth and PG synthesis as population density becomes saturating.
Finally, we also found that exogenous physiologic concentrations of d-Met that are produced by V. cholerae were incorporated into E. coli PG at the same position in the peptide bridge. Thus, E. coli is capable of incorporating noncanonical d-amino acid into its murein sacculus even though this bacterium does not produce or release noncanonical d-amino acids. Therefore, d-amino acids can also act as paracrine-like effectors to influence PG physiology in species other than those that produce them.
Mechanisms of d-amino acid cell wall regulation
Consistent with reports in other bacterial species [95, 96], we observed additive effects of exogenous d-amino acids in combination with β-lactam antibiotics on wild-type V. cholerae shape and growth. For example, the combination of d-Met with the cephalosporin cefmetazole or the monobactam aztreonam caused wild-type V. cholerae to become spherical (similar to stationary V. cholerae mrcA), whereas when added independently, only minor morphological changes were induced. These observations support the idea that d-amino acids exert regulatory effects on PG-modifying enzymes.
The challenge of regulating PG composition, amount, and structure
Regulation of PG amount, chemistry, and architecture constitutes a particularly challenging issue for the bacterial cell. This complex polymer as well as the enzymes that assemble and modify it are located beyond the cytoplasmic membrane and thus outside of the carefully controlled milieu of the cytoplasm. d-amino acid production by BsrV in the periplasmic space enables the cell to produce d-amino acids in the cell compartment (the periplasm) where they will act. d-amino acid incorporation into the pre-existing PG polymer in the periplasm can be thought of as cell wall “editing.” Such post-synthetic regulation of PG is analogous to posttranslational modification of proteins by glycosylation and to methylation of DNA, processes that alter the properties/activities of other biopolymers. It is likely that incorporation of noncanonical d-amino acids into PG alters the polymers’ physical properties as well as influences the ability of d-amino acid-modified PG to serve as a substrate for periplasmic PG-modifying enzymes. Controlling the concentration of d-amino acids in the periplasm could constitute a reversible mechanism for inhibiting PBPs, thereby enabling cells to rapidly transition between states of active and inactive PG metabolism under changing environmental conditions.
d-amino acids coordinate cell wall metabolism in bacterial populations
Our work has revealed that noncanonical d-amino acids regulate cell wall metabolism. Because the accumulation of d-amino acids coincides with the transition into stationary phase and appears to downregulate PG synthesis, d-amino acids may couple metabolic slowing in cell wall and cytoplasmic compartments under conditions of stress. Additionally, rapid diffusion of small molecule regulators like d-amino acids in aqueous environments enables a quick and synchronized response from the whole bacterial population. In times of scarce nutrients (and potentially additional undefined cellular stresses) the release of extracellular d-amino acids can signal to the whole population to regulate PG amount, composition, and strength. This mechanism may be crucial in nutrient-depleted environments where secretion of secondary metabolites such as organic acids, antibiotics, or small lipids can put the integrity of the cell at risk. Finally, since bacteria are more likely to grow in polymicrobial communities than in monoculture, d-amino acid control may mediate interspecies regulation among bacteria or other organisms that occupy the same niche. It remains to be seen whether d-amino acids mediate both mutualistic and competitive behaviors among different bacteria that share a niche.
d-amino acids control biofilm dispersal
Many bacteria are able to switch between two different “lifestyles.” They can exist as either single (planktonic) cells or in communities known as biofilms. A biofilm is defined as a sessile microbial community that adheres to a solid surface and is surrounded by a bacterially produced extracellular matrix. This matrix is typically composed of polysaccharides, but it can also include proteins and/or DNA. The transition between planktonic and biofilm growth is regulated by a variety of environmental and physiological cues, including bacterial cell density, nutrient availability, and cellular stress [97, 98].
Biofilms are prevalent both in natural environments and in industrial and hospital settings [99, 100, 101, 102, 103, 104, 105]. Bacterial infections associated with biofilms adherent to medical devices, such as intravascular catheters, are extremely difficult to eradicate, as the extracellular matrices protect biofilm-associated bacteria from antimicrobials and the host immune system. Thus, discovery of new agents to prevent biofilm formation and/or disrupt established biofilms is of considerable interest.
The mechanisms of d-amino acid-regulated biofilm dispersal are being dissected. Koldkin-Gal et al.  showed that d-amino acids can induce the disassembly of matrix-associated amyloid fibers that link B. subtilis cells within the biofilm. Maintenance of these fibers seems likely to contribute to biofilm durability, since mutants that could form biofilms in the presence of d-amino acids contained alterations within yqxM, whose gene product is required for attachment of amyloid fibers to the cell. However, it is likely that disruption of amyloid networks is not the only means by which d-amino acids promote biofilm disassembly, since Koldkin-Gal et al. found that d-amino acids led to biofilm dispersal in additional bacterial species, such as S. aureus and P. aeruginosa, that are not known to produce biofilm matrix-associated amyloid fibers. Thus, a universal mechanism of biofilm dispersal is unlikely. Regardless of the mechanism(s) by which d-amino acids promote biofilm dispersal, use of d-amino acids to combat biofilm-associated infections holds considerable promise, especially since d-amino acids are likely to have favorable pharmacokinetic properties and to lack significant toxicity .
Conclusions and perspectives for future studies
Recent studies have revealed two exciting and unexpected findings regarding d-amino acids in the bacterial kingdom. First, highly diverse bacteria release various d-amino acids into the environment. And second, the released d-amino acids have heretofore unappreciated roles in regulating key processes, including controlling stationary phase cell wall remodeling and biofilm disassembly in aging bacterial communities. Thus, d-amino acids are signaling molecules that control processes that occur at high cell densities, probably when nutrients become limited. However, the conditions that stimulate d-amino acid production have not been thoroughly explored; additional research is needed to define the stimuli that promote the expression and activity of the racemases that generate d-amino acids.
d-amino acid signaling can be regarded as both autocrine and paracrine in nature since released d-amino acids act on both the cells that release them as well as neighboring cells. In many cases, neighboring cells are of the identical bacterial species as the cells that produced them, but d-amino acids can also act on nearby cells that are of different species. For example, we found that d-Met or d-Leu could be incorporated into the PG of E. coli . In addition, in nature, biofilms are thought to often consist of more than one species . Therefore, released d-amino acids in mixed biofilms may be a paracrine signal, which, along with other chemical regulators, control the architecture of the bacterial community. d-amino acids may be considered as a “chemical language” akin to quorum-sensing molecules, such as acyl homoserine-lactones, that mediate interspecies communication. It remains to be seen whether different d-amino acids mediate distinct types of signals in mixed communities. For example, d-Tyr may primarily function as a signal for biofilm disassembly, whereas d-Met may primarily promote cell wall remodeling. Furthermore, d-amino acids are likely mediators of more traditional types of signaling that regulate gene expression, such as the altered gene expression of UPEC by d-serine in human urine .
Many intriguing questions/issues regarding the regulatory roles of d-amino acids in bacterial biology remain to be addressed. Elucidating the mechanisms by which d-amino acids govern cell wall remodeling and biofilm disassembly will undoubtedly reveal new paradigms for understanding how processes outside of the cell membrane are controlled. Finally, application of the regulatory roles of d-amino acids to solve environmental and clinical problems has considerable promise.
This work was supported by Howard Hughes Medical Institute (HHMI), NIH AI-R37-42347 (M.K.W.), MEC Fellowship (F.C.), and Jane Coffin Childs Fellowship (H.L.). We thank Brigid Davis and Simon Ringgaard for helpful comments on this manuscript.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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