Ester, aldehyde and alcohol analogues were all shown to be incapable of inducing the decarboxylase system. However, a low level of apparent decarboxylation of these compounds was detected using pre-induced enzyme suggesting that they may be poor, indirect substrates, probably following a low level of oxidation to the corresponding carboxylic acid. Sorbic acid and

cinnamic acid both contain an alkenyl bond between carbons 2 and 3, which has the trans (E)-configuration ( Table 1). This bond is essential. Removal of this alkenyl bond in either of the carboxylic ABT-888 nmr acids abolished all activities as decarboxylase inducer or substrate. The structures of these acids are shown in Table 2. The effect learn more of the C2–C3 alkenyl bond may simply be due to its unsaturation or its geometry, or a combination of both. Analogues of the alkenyl fragment between C2 and C3, such as a triple bond or a cyclopropane ring (e.g. phenylpropiolic acid and 2-phenylcyclopropanecarboxylic acid, SD entries 44,62), did not substitute for the alkene bond. The importance of the trans (E)-configuration of the C2–C3 alkene bond was examined by comparing cis (Z)-2,4-methoxycinnamic acid with its trans (E)-isomer. The trans (E)-isomer was active

both as an inducer and as a substrate while the cis (Z)-isomer was inactive (SD entries 79,82). Sorbic acid also contains alkene unsaturation between Adenosine C4 and C5 and cinnamic acid is substituted by a phenyl ring at C3. Removal of the C4–C5 unsaturation in sorbic acid again abolished all activity as inducer or substrate for Pad-decarboxylation (Table 2; 2-hexenoic acid). While the trans (E)-configuration at C4–C5 in sorbic acid is important for activity, cinnamic acid, together with the furan and thiophene analogues shown in Table 2, contain additional or extended unsaturation at C3. This extended unsaturation, however, allows the molecules to assume a similar shape to that found in sorbic acid, which presumably is one reason why the furan and thiophene analogues are successfully decarboxylated as Pad substrates and inducers in whole conidia.

All of the compounds that were found to decarboxylate with high activity carried substituents beyond C5 in their structures. In cinnamic acid, this extension formed part of the aromatic ring and sorbic acid accommodated a methyl group at C5. Removal of this additional substitution at C5 resulted in substantial loss of decarboxylation activity, as demonstrated by the low level of activity against trans (E)-2,4-pentadienoic acid (SD entry 10). This carboxylic acid contains all of the significant features mentioned previously, and would seem to fit into a site that would accommodate sorbic acid, yet it was decarboxylated poorly, and is particularly poor as an inducer. This feature strongly indicates that a carbon substituent at C5 in sorbic acid is a pre-requisite for induction.