MICROBIAL PHYTOTOXINS AS POTENTIAL HERBICIDES
Citation
So. Duke et al., MICROBIAL PHYTOTOXINS AS POTENTIAL HERBICIDES, Journal of environmental science and health. Part B. Pesticides, food contaminants, and agricultural wastes, 31(3), 1996, pp. 427-434
Categorie Soggetti
Agriculture,"Environmental Sciences","Public, Environmental & Occupation Heath
SICI code
0360-1234(1996)31:3<427:MPAPH>2.0.ZU;2-M
Abstract
Microbes are sources of a diverse array of phytotoxic compounds. These
compounds are generally structurally different from commercial herbic
ides, targeting different molecular sites of action within the plant.
These novel structures and sites can be excellent leads for the discov
ery and development of safer synthetic herbicides. Microbial phytotoxi
ns are often more environmentally benign than synthetic herbicides. Ex
amples of phytotoxins from fungi (AAL-toxin, cornexistin, cyperin, and
tentoxin) with novel structures and sites of action are discussed. AA
L-toxin is toxic to a wide variety of weeds at very low dose rates. AA
L-toxin and many of its analogues kill plants by inhibiting a ceramide
synthase-like enzyme, causing rapid accumulation of free sphingoid ba
ses that disrupt membranes. Cornexistin appears to be metabolically cn
verted to an inhibitor of certain aspartate amino transferase isoenzym
es. Its activity can be reversed by feeding aspartate and glutamate or
with tricarboxylic acid cycle intermediates. Its activity is much lik
e that of (aminooxy)acetate. Cyperin is a diphenylether phytotoxin tha
t inhibits protoporphyrinogen oxidase, but does not kill plants by thi
s mechanism. It appears to have other effects on porphyrin metabolism.
Tentoxin is toxic by two mechanisms. It disrupts chloroplast developm
ent by inhibiting the processing of a nuclear-coded plastid protein, a
nd it also inhibits photophosphorylation by acting as an energy transf
er inhibitor of coupling factor 1 ATPase. Other examples of phytotoxin
s from microbes with promise as herbicides will be mentioned.