The structure and monomeric composition of the highly aliphatic and non-sap
onifiable fraction of cutans isolated from the leaf cuticles of Agave ameri
cana L. and Clivia miniata Reg. have been elucidated. Spectroscopic Fourier
transform infrared and C-13-nuclear magnetic resonance, calorimetric and X
-ray diffraction studies, together with biopolymer analysis after exhaustiv
e ozonolysis, showed that the cutan fraction consists of an amorphous three
-dimensional network linked by ether bonds containing double bonds and free
carboxylic acid functions. Data obtained from fatty acid sorption indicate
d that the new biopolymer investigated here has a highly hydrophobic charac
ter constituting an additional barrier biopolymer in those cuticles where i
t is present. Labelled [C-14]linoleic acid was preferentially incorporated
into the non-ester part of C. miniata leaf disks in comparison with the cut
in fraction of the cuticular membrane. This indicates that the cis-pentadie
ne system of polyunsaturated fatty acids is involved in the formation of in
tramolecular linkages, mainly ether bonds, of the aliphatic biopolymer.