NG-391 (
1) and NG-393 (
2), previously reported fro
m undescribed
Fusarium species as nerve-cellgrowth sti
mulants, were identified fro
m fer
mentation extracts of the ento
mopathogenic fungus
Metarhizium anisopliae. These co
mpounds are 7-des
methyl analogues of fusarin C and (8
Z)-fusarinC,
mutagenic toxins fro
m Fusarium species that conta
minate corn. A
mutant strain of
M. anisopliae(KOB1-3) overproduces
1 and
2 by ca. 10-fold relative to the wild-type strain, ARSEF 2575, fro
mwhich it was derived. Overproduction of these co
mpounds in KOB1-3 i
mparts a yellow pig
mentationto the culture
mediu
m of the fungus. These co
mpounds were inactive at 100
![](/i<font color=)
mages/entities/
mgr.gif">g/disk in anti
microbialdisk diffusion assays. Co
mpound
1 was inactive at 100 pp
m in a
mosquitocidal assay. However, liketheir fusarin analogues,
1 and
2 exhibited potent S9-dependent
mutagenic activity in the
Salmonellamutagenicity test. Discovery of these highly
mutagenic
mycotoxins in
M. anisopliae suggests thatscreening for production of NG-391 and NG-393 in strains that are used as biocontrol agents wouldbe a prudent course of action. The i
mpact of these findings on the use of
M. anisopliae as a biocontrolagent is currently unknown and requires further investigation.