From the nisZ gene sequence, a non-radioactive digoxigenin-labeled DNA prob
e, was tested for detection of nisin-producing strains using polymerase cha
in reaction amplification. The digoxigenin-labeled DNA probe clearly discri
minated between nisin-producing and non-producing strains with a high degre
e of sensitivity and specificity. By agarose gel electrophoresis, 1.4 ng of
nisin DNA was detected using the digoxigenin-labeled DNA probe compared wi
th 11 ng using direct polymerase chain reaction amplification. A colony hyb
ridization method using digoxigenin-labeled DNA to selectively detect nisin
ogenic bacteria showed that the nis-probe was specific and did not react wi
th any other non-bacteriocinogenic and non-nisinogenic strains. (C) 1999 Fe
deration of European Microbiological Societies. Published by Elsevier Scien
ce B.V. All rights reserved.