<p><i>E. coli</i> transformants were cultured and diluted (from left to right) to an OD<sub>580</sub> of 0.25, 0.10, 0.05 and 0.01, representing cell densities of 5.5×10<sup>6</sup>, 1.5×10<sup>6</sup>, 7.7×10<sup>5</sup> and 1.1.×10<sup>5</sup> per mL respectively. Fluorescence was quantified at the following wavelengths: mCherry 587/610 nm, mKat 588/635 nm, mPlum 590/649 nm, tdTomato 554/581 nm, Turbo-635 588/635 nm. Data are the averages and standard deviations from three independent transformants. A value of 1015 corresponds to saturation of the machine. The reporter, promoter and vector backbone are indicated. WT = wild-type oriM; ΔHC – high copy number derivative oriM.</p
<p>Fluorescence is produced solely by <i>E. coli</i> expressing GFP. The strains were cultivated in ...
<p>FbFPs and YFP were expressed in <i>E. coli</i> MG1655 cells using an IPTG-inducible T5 promoter. ...
Additional file 1: Table S1. Growth rates (h−1) of E. coli BW25113 cells carrying pAG032. Table S2. ...
<p>Fluorescent reporters were expressed from P<sub>hps60</sub> or P<sub>smyc</sub> in <i>M. smegmati...
<p>Fluorescent reporters were expressed from P<sub>smyc</sub> in <i>M. marinum</i> and assayed in li...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
<p>Fluorescence was measured after 3(white bars) and with 10 µM (black bars) of chromate. The values...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
<p>Cultures of (A) the MG1655 harboring pPro7(E)-<i>gfp</i> and (B) the JM1012 harboring the 3 plasm...
The use of genetically encoded fluorescent reporters allows speeding up the initial optimization st...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Fluorescence microscopy images corresponding to the Nile Red -stained strains <i>E</i>. <i>co...
Abstract Real-time quantification of recombinant proteins is important in studies on fermentation en...
<p>FbFPs and YFP were expressed in <i>E. coli</i> MG1655 cells using an IPTG-inducible T5 promoter. ...
<p>Fluorescence is produced solely by <i>E. coli</i> expressing GFP. The strains were cultivated in ...
<p>FbFPs and YFP were expressed in <i>E. coli</i> MG1655 cells using an IPTG-inducible T5 promoter. ...
Additional file 1: Table S1. Growth rates (h−1) of E. coli BW25113 cells carrying pAG032. Table S2. ...
<p>Fluorescent reporters were expressed from P<sub>hps60</sub> or P<sub>smyc</sub> in <i>M. smegmati...
<p>Fluorescent reporters were expressed from P<sub>smyc</sub> in <i>M. marinum</i> and assayed in li...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
<p>Fluorescence was measured after 3(white bars) and with 10 µM (black bars) of chromate. The values...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
<p>Cultures of (A) the MG1655 harboring pPro7(E)-<i>gfp</i> and (B) the JM1012 harboring the 3 plasm...
The use of genetically encoded fluorescent reporters allows speeding up the initial optimization st...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Fluorescence microscopy images corresponding to the Nile Red -stained strains <i>E</i>. <i>co...
Abstract Real-time quantification of recombinant proteins is important in studies on fermentation en...
<p>FbFPs and YFP were expressed in <i>E. coli</i> MG1655 cells using an IPTG-inducible T5 promoter. ...
<p>Fluorescence is produced solely by <i>E. coli</i> expressing GFP. The strains were cultivated in ...
<p>FbFPs and YFP were expressed in <i>E. coli</i> MG1655 cells using an IPTG-inducible T5 promoter. ...
Additional file 1: Table S1. Growth rates (h−1) of E. coli BW25113 cells carrying pAG032. Table S2. ...