The following article is of interest: "Vanillin Formation by Microbial Amine Oxidases from Vanillylamine" Yoshida, A; Takenaka, Y.; Tamaki, H.; Frebort, I.; Adachi, O.; and Kumagai, H. in Journal of Fermentation and Bioengineering (published in Japan in English) Vol. 84, No. 6 pp 603-605 It discusses testing of amine oxidase from Aspergillus niger and monoamine oxidase from Escherichia coli to produce vanillin from vanillylamine. Most of the vanillin of commerce is synthetically produced from eugenol (clove), ferulic acid or guaiacol with only 20 tons of 12,000 tons used annually being extracted from vanilla beans. One quote from the article is interesting: "Vanillylamine (4-hydroxy-3-methoxy phenyl methylamine) is one of the possible precursors of vanillin. It can be isolated from CAPSAICIN (N-[(4-hydroxy-3-methoxy-phenyl)methyl]-8-methyl-6-nonenamide) by cleavage of its amide bond. Capsaicin, a natural pungent ingredient of peppers and capsicums, can be easily obtained at low cost." Well, for those of us who toil in gardens and watch our seedlings, the capsaicin is obtained at a relatively dear price. Further, it ought to be a bit disturbing that the researchers suggest breaking our favorite molecule to use a piece of it. However, I suppose there is enough in commerce to act as starting material to make some vanillin. It might mean planting more and hotter chiles, so the research could lead to some good after all! George Nelson 70431.3065@compuserve.com