A rapid method for direct extraction of RNA from soil was developed. I
t is based on cell lysis by a bead beater procedure that optimizes ext
raction efficiency and minimizes shearing of RNA. The RNA was extracte
d from three very different soils and was free of DNA contamination. T
he extracted RNA was sufficiently pure to permit amplification by RT-P
CR. Intact rRNA molecules of both prokaryotic and eukaryotic origin we
re extracted by this method and were of sufficient yield to visualize
these molecules on agarose gels. (C) 1997 Elsevier Science Ltd.