Microcystis and Nodularia species produce cyclic hepta- and pentapepti
des, microcystins and nodularin, respectively, both containing the sam
e unusual C20 amino acid, abbreviated Adda. Biosynthesis of nodularin
from Nodularia and especially of Adda employs a pathway similar to tha
t employed by Microcystis for producting microcystins. Nearly 30 new m
icrocystins have been isolated in our laboratory from cyanobacteria sp
ecies and their structures assigned, largely employing tandem FAB mass
spectrometry (FABMS/CID/MS). Acyclic peptides, some of them presumed
precursors of nodularin and microcystins, have now been isolated and c
haracterized. The numerous analogs identified or synthesized allow the
identification of important parameters in a structure-activity relati
onship study.