Protein (Fig. 4), confirming that the first 10 amino acids of Wze were

Protein (Fig. 4), confirming that the first 10 amino acids of Wze were necessary and sufficient for expression of Citrine in S. pneumoniae. We have named this 10 amino acid tag, which improved protein expression in pneumococcal bacteria, “i-tag”. The increased fluorescence due to the presence of the i-tag fused to Citrine could be the result of higher mRNA or higher protein levels. We therefore quantified, by real-time PCR, the levels of mRNA encoding untagged Citrine, Wze-Citrine fusion and the various truncated forms of this fusion, in exponentially growing bacteria, relatively to the mRNA for the tetracycline resistance marker, encoded in the plasmid backbone. Fig. 5A shows that levels of the different mRNAs were not sufficiently different to explain the variability in fluorescence expression. However, analysis of Citrine protein levels in the same strains showed a correlation between strains in which Citrine protein could be detected and strains which were fluorescent, namely those encoding for Wze-Citrine (strain BCSMH007) and all that included the first 10 amino acids of the Wze fused to Citrine (strains BCSJC001, BCSJC002, BCSJC004 and BCSJC005). Taken together these results show that fusion of the i-tag to Citrine increased fluorescence levels due to increased protein levels and not increased mRNA levels. To 16985061 determine if increased protein levels resulted from higher translation rates or increased protein stability, we generated a silent MedChemExpress TA-01 mutation in the sequence encoding the i-tag, fused to Citrine, and analyzed the fluorescence of the resulting constructs. We were able to identify mutations that did not alter the amino acid sequence of the tag, but resulted in loss of fluorescence, namely the substitution of UUA leucine codon by CUC (Fig. 6). Given that protein sequence was not altered, we can rule out the hypothesis that the itag acted by increasing stability of the fusion proteins. We also do not think that increased expression is due to the introduction of an additional ribosome-binding site, as previously GHRH (1-29) web reported by Halfmann and colleagues [22], as we did not introduce any additional sequence upstream of the starting codon. Therefore the presence of the nucleotide sequence encoding the i-tag results in increased translation rates, possibly by destabilizing the mRNA structure of this region and thus facilitating ribosome binding to the mRNA molecule.Construction of plasmids for the expression of fluorescent protein fusions in S. pneumoniaeWe have redesigned plasmids pBCSMH001, pBCSMH002, pBCSMH018 and pBCSMH020, expressing untagged fluorescent proteins (Fig. 2) to improve expression of mCherry (pBCSMH030), Citrine (pBCSJC001), CFP (pBCSMH031) and GFP (pBCSMH032) by including the “i-tag” upstream of the fluorescent proteins (Fig. 7A). Additionally, we have introduced unique restriction sites flanking the genes encoding for the fluorescent proteins, so that the resulting plasmids can be used to express both N- and C-terminal fluorescent fusions of S. pneumoniae proteins, under the control of a constitutive consensus S. pneumoniae SigA promoter [23]. Analysis of strains containing these new plasmids showed that expression of i-tagged fluorescent proteins generates cells with fluorescence levels comparable to the ones expressing the Wze-fusions (Fig. 7B). Importantly, the itagged fluorescent proteins were dispersed throughout the cytoplasm of the encapsulated pneumococcal cells (Fig. S2) indicating that the i-tag did not int.Protein (Fig. 4), confirming that the first 10 amino acids of Wze were necessary and sufficient for expression of Citrine in S. pneumoniae. We have named this 10 amino acid tag, which improved protein expression in pneumococcal bacteria, “i-tag”. The increased fluorescence due to the presence of the i-tag fused to Citrine could be the result of higher mRNA or higher protein levels. We therefore quantified, by real-time PCR, the levels of mRNA encoding untagged Citrine, Wze-Citrine fusion and the various truncated forms of this fusion, in exponentially growing bacteria, relatively to the mRNA for the tetracycline resistance marker, encoded in the plasmid backbone. Fig. 5A shows that levels of the different mRNAs were not sufficiently different to explain the variability in fluorescence expression. However, analysis of Citrine protein levels in the same strains showed a correlation between strains in which Citrine protein could be detected and strains which were fluorescent, namely those encoding for Wze-Citrine (strain BCSMH007) and all that included the first 10 amino acids of the Wze fused to Citrine (strains BCSJC001, BCSJC002, BCSJC004 and BCSJC005). Taken together these results show that fusion of the i-tag to Citrine increased fluorescence levels due to increased protein levels and not increased mRNA levels. To 16985061 determine if increased protein levels resulted from higher translation rates or increased protein stability, we generated a silent mutation in the sequence encoding the i-tag, fused to Citrine, and analyzed the fluorescence of the resulting constructs. We were able to identify mutations that did not alter the amino acid sequence of the tag, but resulted in loss of fluorescence, namely the substitution of UUA leucine codon by CUC (Fig. 6). Given that protein sequence was not altered, we can rule out the hypothesis that the itag acted by increasing stability of the fusion proteins. We also do not think that increased expression is due to the introduction of an additional ribosome-binding site, as previously reported by Halfmann and colleagues [22], as we did not introduce any additional sequence upstream of the starting codon. Therefore the presence of the nucleotide sequence encoding the i-tag results in increased translation rates, possibly by destabilizing the mRNA structure of this region and thus facilitating ribosome binding to the mRNA molecule.Construction of plasmids for the expression of fluorescent protein fusions in S. pneumoniaeWe have redesigned plasmids pBCSMH001, pBCSMH002, pBCSMH018 and pBCSMH020, expressing untagged fluorescent proteins (Fig. 2) to improve expression of mCherry (pBCSMH030), Citrine (pBCSJC001), CFP (pBCSMH031) and GFP (pBCSMH032) by including the “i-tag” upstream of the fluorescent proteins (Fig. 7A). Additionally, we have introduced unique restriction sites flanking the genes encoding for the fluorescent proteins, so that the resulting plasmids can be used to express both N- and C-terminal fluorescent fusions of S. pneumoniae proteins, under the control of a constitutive consensus S. pneumoniae SigA promoter [23]. Analysis of strains containing these new plasmids showed that expression of i-tagged fluorescent proteins generates cells with fluorescence levels comparable to the ones expressing the Wze-fusions (Fig. 7B). Importantly, the itagged fluorescent proteins were dispersed throughout the cytoplasm of the encapsulated pneumococcal cells (Fig. S2) indicating that the i-tag did not int.