a, Synthetic gene circuits that couple curli subunit secretion to
external inducer signals, when combined with a spatial inducer gradient, enable
patterning across multiple length scales. We used an agar plate with opposing
concentration gradients of AHL and aTc to achieve control at the macroscale
(Supplementary Fig.
12). This was combined with regulation of nanoscale patterning to
achieve multiscale patterning. Embedded in top agar were equal numbers of
AHLReceiver/CsgA, aTcReceiver/CsgAHis,
AHLReceiver/GFP, and aTcReceiver/mCherry cells.
b, By combining synthetic gene regulation with spatial inducer
gradients, we created a change in the nanoscale structure of fibrils across a
distance of millimetres. This nanoscale and macroscale patterning was shown by
changes in segment lengths of unlabelled and NiNTA-AuNP-labelled fibril segments
at different locations across the agar plate. Inducer concentration gradients
were demonstrated by overlaid GFP and mCherry fluorescence images of embedded
AHLReceiver/GFP and and aTcReceiver/mCherry reporter
cells. Scale bars are 200nm. c, We also achieved patterning at the
nanoscale by protein engineering of curli subunits. Concatenating eight tandem
repeats of CsgA and adding one histidine tag to the C-terminus
(8XCsgAHis) resulted in fibrils that were labelled by a
syncopated pattern of NiNTA-AuNPs, with clusters of particles separated by
33.3±27.1 (s.e.m.) nm. Scale bars are 100nm. d, Synthetic
gene circuits that couple curli subunit secretion to external inducer signals,
when combined with subunit engineering, enable patterning across multiple length
scales (nanometres to micrometres). We used AHL to induce production of
8XCsgAHis from AHLReceiver/8XCsgAHis and
then used aTc to induce production of CsgAHis from
aTcReceiver/CsgAHis. In the TEM images, dashed brown
lines refer to syncopated 8XCsgAHis segments while the solid amethyst
lines indicate CsgAHis segments. Detailed histograms for data shown
here can be found in Supplementary Figure 11. Scale bars are 100nm.