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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Science. Author manuscript; available in PMC Nov 1, 2010.
Published in final edited form as:
PMCID: PMC2921573
NIHMSID: NIHMS226057

D-Amino Acids Trigger Biofilm Disassembly

Abstract

Bacteria form communities known as biofilms, which disassemble over time. Here we found that prior to biofilm disassembly Bacillus subtilis produced a factor that prevented biofilm formation and could break down existing biofilms. The factor was shown to be a mixture of D-leucine, D-methionine, D-tyrosine and D-tryptophan that could act at nanomolar concentrations. D-amino acid treatment caused the release of amyloid fibers that linked cells in the biofilm together. Mutants able to form biofilms in the presence of D-amino acids contained alterations in a protein (YqxM) required for the formation and anchoring of the fibers to the cell. D-amino acids also prevented biofilm formation by Staphylococcus aureus and Pseudomonas aeruginosa. D-amino acids are produced by many bacteria and thus may be a widespread signal for biofilm disassembly.

Most bacteria form multicellular communities known as biofilms in which cells are protected from environmental insults (12). However, as biofilms age, nutrients become limiting, waste products accumulate, and it is advantageous for the biofilm-associated bacteria to return to a planktonic existence (2). Thus, biofilms have a finite life time, characterized by eventual disassembly. Bacillus subtilis forms communities on semi-solid surfaces and thick pellicles at the air-liquid interface of standing cultures (1, 35). Cells in the biofilms are held together by an extracellular matrix consisting of exopolysaccharide and amyloid fibers composed of TasA (57). The exopolysaccharide is produced by the epsA-O operon and the TasA protein is encoded by the yqxM-sipW-tasA operon (8).

After three days of incubation in biofilm-inducing medium, B. subtilis formed thick pellicles at the air/liquid interface of standing cultures (Fig. 1A). Upon incubation for an additional three to five days, however, the pellicle lost its integrity (Fig. 1B). To investigate whether mature biofilms produce a factor that triggers biofilm disassembly, we asked whether conditioned medium would prevent pellicle formation when added to fresh medium. Medium from an eight-day-old culture was applied to a C18 Sep Pak column, and concentrated eluate from the column was added to a freshly inoculated culture. The eluate was sufficient to prevent pellicle formation (Fig. 1C). Concentrated eluate from a three-day-old culture had little effect on pellicle formation (Fig. 1D). Further purification of the factor was achieved by eluting the cartridge step-wise with methanol. Elution with 40% methanol resulted in a fraction that was active in inhibiting pellicle formation (Fig. 1E), but had little effect on cell growth (Fig. S1). The activity was resistant to heating at 100 °C for 2 hours and proteinase K treatment (Fig. 1F).

Figure 1
Conditioned medium blocks pellicle formation

Bacteria produce D-amino acids in stationary phase (9). We asked whether the biofilm-inhibiting factor was composed of one or more D-amino acids. Indeed, D-tyrosine, D-leucine, D-tryptophan, and D-methionine were active in inhibiting biofilm formation both in liquid and on solid medium (Figures 1G–H, Figures S2–3). In contrast, the corresponding L-isomers and D-isomers of other amino acids, such as D-alanine and D-phenylalanine, were inert in our biofilm-inhibition assay. Next, we determined the minimum concentration needed to prevent biofilm formation. Individual D-amino acids varied in their activity, with D-tyrosine being more effective (3 µM) than D-methionine (2 mM), D-tryptophan (5 mM) or D-leucine (8.5 mM). A mixture of all four D-amino acids was particularly potent, with a minimum inhibitory concentration of ~10 nM. Thus, D-amino acids could act synergistically. The D-amino acids not only prevented biofilm formation, but also disrupted existing biofilms. The addition of D-tyrosine or a mixture of the four D-amino acids (but not the corresponding L-amino acids) caused pellicle breakdown (Fig. 2A).

Figure 2
D-amino acids mimic the effect of conditioned medium

D-amino acids are generated by racemases (10). Genetic evidence consistent with the idea that the biofilm-inhibiting factor is D-amino acids came from mutants of ylmE and racX, genes whose predicted products exhibit sequence similarity to known racemases. Strains mutant for ylmE or racX alone showed a modest delay in pellicle disassembly (Fig. S4). However, pellicles formed by cells doubly mutant for the putative racemases were significantly delayed in disassembly (Fig. S4). Conversely, cells engineered to overexpress ylmE were blocked in biofilm formation (Fig. S5). Conditioned medium from the double mutant was also ineffective in inhibiting biofilm formation, in contrast to conditioned medium from the wild type (Fig. 2B). Next, we asked whether D-amino acids are produced in sufficient abundance to account for disassembly of mature biofilms. Accordingly, we carried out liquid chromatography-mass spectrometry followed by the identification of the D-amino acids using derivatization with Nα-(2,4-dinitro-5-fluorophenyl)-L-alaninamide (L-FDAA) on conditioned medium collected at early and late times after pellicle formation. D-tyrosine (6 µM), D-leucine (23 µM), and D-methionine (5 µM) were present at concentrations at or above those needed to inhibit biofilm formation by day 6 but at concentrations of <10 nM at day 3. In contrast, the ylmE racX double mutant was blocked in D-tyrosine production and impaired in D-leucine production at day 6 (Table S1).

How do D-amino acids disassemble biofilms? D-amino acids did not inhibit growth (Fig. S6), nor did they inhibit the expression of the matrix operons epsA-O and yqxM-sipW-tasA (Fig. S7). D-amino acids are incorporated into the peptide side chains of peptidoglycan in place of the terminal D-alanine (9). Using 14C -D-tyrosine, we confirmed that the D-tyrosine (but not 14C -L-proline) was incorporated into the cell wall (Fig. S8), with incorporation commencing at day 3 (Fig. S9). Finally, and in keeping with the idea D-amino acids act via their incorporation into the wall, the effects of D-tyrosine and the D-amino acid mixture were prevented by D-alanine (Fig. 1K–L).

We hypothesized that TasA fibers are anchored to the cell wall and that the incorporation of biofilm-disassembling D-amino acids into the cell wall might disengage the fibers from their anchor. To investigate this possibility, we examined the localization of a functional fusion of TasA with the fluorescent reporter mCherry. Treatment with D-tyrosine had little effect on the accumulation of TasA-mCherry (Fig. S10). In contrast, when the cells were washed by centrifugation, resuspended and then examined by fluorescence microscopy, untreated cells, which were often in clumps, were intensely decorated with TasA-mCherry (Fig. 3A). In contrast, D-tyrosine-treated cells, which were largely unclumped, showed only low levels of fluorescence (17-fold lower; Table S2). Similar results were obtained with D-leucine and with the D-amino acid mixture. We also carried out electron microscopy with gold-labeled anti-TasA antibodies to visualize unmodified TasA. TasA fibers were anchored to the cells of untreated pellicles (Fig. 3B, images 1 and 2). In contrast, cells treated with D-tyrosine consisted of a mixture of cells that were largely undecorated with TasA fibers and free TasA fibers or aggregates of fibers that were not anchored to cells (Fig. 3B, images 3–6).

Figure 3
D-tyrosine causes the release of TasA fibers

Next, we isolated D-amino acid resistant mutants (Fig. 4A). Wrinkled papillae appeared spontaneously on the flat colonies formed during growth on solid medium containing D-tyrosine (Fig. 4A) or D-leucine (Fig S2). When purified, these spontaneous mutants gave rise to wrinkled colonies and pellicles in the presence of individual D-amino acids. We isolated several such mutants and found that they contained mutations in the 3’ region of yqxM. Two mutations that conferred resistance to D-tyrosine were examined in detail. yqxM2 was an insertion of G:C at base pair 728 and yqxM6 was a deletion of A:T at base pair 569 (Fig. 4B). The presence of yqxM2 and yqxM6 restored clumping and cell decoration by TasA-mCherry to cells treated with D-tryosine (Fig. 3D, Fig. S12, see above). Because YqxM is required for the association of TasA with cells (6), the discovery that the biofilm-inhibiting effect of D-amino acids could be overcome by mutants of YqxM reinforces the view that the effect of D-amino acid incorporation into the cell wall is to impair the anchoring of the TasA fibers to the cell. A domain near the C-terminus of YqxM could trigger the release of TasA in response to the presence of D-amino acids in the cell wall.

Figure 4
Biofilm formation by YqxM mutants resistant to D-tyrosine

Finally, we wondered whether D-amino acids would inhibit biofilm formation by other bacteria. The pathogens Staphylococcus aureus and Pseudomonas aeruginosa form biofilms on plastic surfaces (11), which can be detected by washing away unbound cells and staining the bound cells with Crystal Violet. D-tyrosine and the D-amino acid mixture were effective in preventing biofilm formation (Fig. S13), whereas L-tyrosine and L-amino acids had no effect. Furthermore, the effect of D-amino acids was prevented by the presence of D-alanine (Fig. S13), suggesting that D-amino acids acted to block biofilm formation by replacement of D-alanine in the peptide side chain. Given that many bacteria produce D-amino acids, D-amino acids may provide a general strategy for biofilm disassembly. If so, then D-amino acids might prove widely useful in medical and industrial applications for the prevention or eradication of biofilms.

Supplementary Material

supplemental

References and Notes

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12. We thank T. Norman for the analysis of Table S2. I.K. and D.R. are postdoctoral fellows of the HFSP and Fullbright/MEC(Spain), respectively. This work was funded by NIH grants to R.K. (GM58213), J.C. (GM086258 and CA24487) and R.L. (GM18546), and grants from BASF to R.K. and R.L.
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