Sodium pyrithione and zinc pyrithione (NaPT and ZnPT, respectively) ar
e antimicrobial agents widely used in both the cosmetics and fuel indu
stries. They are also utilized in the mining industry because of their
metal chelating properties. They have been shown to depolarize membra
ne electropotential in fungi and are also known to inhibit fungal and
bacterial substrate transport processes. Recent work has shown that bo
th pyrithiones cause the leakage of intracellular material (potassium
ions and O.D.(260nm) absorbing material) from exposed bacterial cells.
The work here reports studies on the interactions between the pyrithi
ones and the bacterial phospholipid head group structures, at both a p
ractical and a theoretical level, utilizing tube dilution neutralizer
studies, scanning spectrophotometry and molecular modelling. The tube
dilution neutralizer studies exhibited a decrease in minimum inhibitor
y concentration (MIC) for both pyrithiones in the presence of extracel
lular phosphatidylethanolamine and EDTA. Scanning spectrophotometry ex
hibited the chelation of the central zinc atom from the ZnPT chelate b
y the addition of EDTA. Molecular modelling studies exhibited the chel
ation of the phosphatidyl-ethanolamine head group by ZnPT. Zinc pyrith
ione also exhibited an interaction with the ammonium tail of the head
group structures. Sodium pyrithione exhibited electrostatic interactio
ns with the phospholipid head groups in the molecular modelling studie
s.