A new staining method for the examination of active regions of hyphae is pr
esented. Using a simple protocol, application of the fluorescent stain Mag
fura (tetra-potassium salt) in low pH buffer to two filamentous fungi resul
ted in bright responses to active hyphal regions. Not only were active apic
es delineated, but more distal compartments were also found to respond to t
he stain. Some apices did not stain, presumably because they were inactive.
It is believed that all stained regions retained cell membrane integrity a
nd are thought to have had high membrane ATPase activity. All showed high n
uclear and mitochondrial complements. The stain was apparently held within
the cell wall structure, close to the cell membrane. It is hypothesized tha
t it was responding to a localized flux of divalent cations from the cell m
embrane. With non-active regions, only a low level of response to the stain
remained, at the exterior of the cell wall. This low emission is thought t
o be a response to contaminating ions in the buffer. It could be clearly di
stinguished from the bright response associated with the active regions. Co
unter-staining with other commonly used fluorescent probes showed these reg
ions of low response (unless they were completely degenerated) still contai
ned nuclear material and mitochondria.
The fluorescent signal from active regions of fungal hyphae was sufficientl
y bright and persistent for visualization by a conventional CCD camera. Thi
s will allow the development of image analysis protocols to measure the eff
ects of environmental conditions on fungal physiology, using commonly avail
able equipment.