Figure 5 shows that the P60 fraction from cells expressing wag31T73E Mtb produced 7.5-fold more 14C-labeled lipid II, but cells with wag31T73A Mtb yielded 30% less of this product than cells expressing wild-type wag31 Mtb . In a repeated experiment with independently purified P60 fractions,

a similar result was observed (the ratio of reaction BTSA1 cell line product from cells with wild-type wag31 Mtb : wag31T73A Mtb : wag31T73E Mtb were 1 : 0.65 : 5.3) (data not shown). These data suggested that the Wag31 phosphorylation, directly or indirectly, regulates the combined activity of MraY and MurG. Figure 5 Effect of Wag31 phosphorylation on enzymatic activity of MraY and MurG. The three strains used in Fig. 1 were cultured to mid-log phase to purify a cell wall enriched envelope fraction (P60), which was then used as the sources of lipid (polyprenyl phosphate) and enzymes (MraY and MurG). 2 mg of P60 protein https://www.selleckchem.com/products/Rapamycin.html from each strain was incubated with 50 μM UDP-MurNAc-pentapeptide and 100 μM ATP for 5 min at 28°C, and reactions were initiated by adding 1 μCi of UDP-[14C]GlcNAc. After 1 hr, the quantity of radiolabeled lipid II (▶) was determined on TLC plates (inset) by a Phosphoimager. Data shown are from a representative experiment done in duplicate. Consistent

with this finding, we recently found in a Raman spectroscopic analyses that cells click here containing wag31T73E Mtb allele had increased intensity of the Raman peaks that have previously been attributed to D-glutamic acid, D-alanine, and N-acetylglucosamine

triclocarban components of peptidoglycan [23, 24] than cells expressing wild-type wag31 Mtb , which in turn showed higher intensity of the these peaks than cells with wag31T73A Mtb [25]. An increase in the intensity of these peaks suggests an increase in the quantity of these molecules, thus peptidoglycan in the cell. A corresponding pattern in the intensity of these peaks was also seen in the Raman spectra from the P60 cell envelope-enriched fractions, indicating that the increase of these molecules is localized in the membrane. Discussion Our current results provide insights into a novel mechanism for the regulation of polar peptidoglycan synthesis in mycobacteria via differential polar localization of Wag31 depending on its phosphorylation status. This mechanism of the signal transduction system involving the Wag31 phosphorylation may be widespread among Gram-positive bacteria containing DivIVA because recent studies demonstrated that DivIVA in Streptococcus agalactiae and Streptococcus pneumoniae is also phosphorylated even though its function is yet to be discovered [26, 27]. Since some bacteria such as Mycobacterium and Corynebacterium species lack MreB [2, 9] but have a rod-like shape, and insert peptidoglycan at the cell poles instead of the helical pattern that uses actin-like MreB homologues, our data also suggest that Wag31 could serve as a determinant that directs peptidoglycan synthesis to the poles in mycobacterial cells.