Xanthan and Na-hyaluronate (Na-Hy) polysaccharides belong to a class of pol
yelectrolytes that show a maximum in the reduced viscosity as a function of
polyelectrolyte concentration. It is also well documented that xanthan sol
utions present a polyelectrolyte scattering maximum as a function of the wa
vevector q. However, despite considerable expanded experimental efforts, no
scattering peak was observed in Na-Ky systems when using light or neutron
scattering techniques. In this work and far the first time, we report that
only the use of high brilliance of synchrotron radiation at rest and under
shear enables to highlight the expected small-angle scattering peak in the
Na-Hy polyelectrolyte system. At zero shear rate, the scattering profile re
veals a very diffuse and hardly detectable maximum at ideal experimental co
nditions (i.e., semidilute "salt-free" polyelectrolyte concentration-or low
ionic strength- and momentum transfer a). As the shear rate is increased,
this very small maximum is magnified and reveals clearly the expected polye
lectrolyte nature of Na-Hy not yet observed using other radiation (light or
neutrons). The system undergoes a typical and progressive change from isot
ropic to anisotropic phase, when increasing the shear, confirming the origi
n of the peak and the role of the electrostatic interactions on the structu
ral order in polyelectrolyte systems. These results are compared to those o
btained under the same conditions on the xanthan polyelectrolyte system whe
re, in addition to the so-called polyelectrolyte scattering peak, a second-
order peak in the scattering profile is observed as a consequence of the sh
ear.