Four growth-influencing compounds-hydroxyproline, 2,2'-dipyridyl, 2-chloroethylphosphonic acid, and indoleacetic acid-were used to examine the relationship between lignin formation and growth of wheat coleoptile sections. Hydroxyproline and 2-chloroethylphosphonic acid, at low concentrations, inhibited growth and increased lignin content. Dipyridyl, which promoted coleoptile elongation, decreased lignin content. Indoleacetic acid caused a 300% increase in growth at 0.1 mM but resulted in lignin content no different from controls with no auxin. Chemical and anatomical evidence is given which indicates that lignin is present in the epidermal cell walls of the wheat coleoptile. It is thus possible that bonding between lignin and hemicellulose may have some influence on coleoptile growth. Wardrop (20) has hypothesized that lignification may limit enlargement of plant cells by immobilizing the hemicellulose matrix, thereby preventing surface growth. His suggestion pertained to woody cells which undergo secondary wall thickening, and in which lignin forms a major component of the cell wall. Coleoptile cells, however, also have a secondary type of wall layer which is formed at the end of the extension phase (1). Experiments described in this report show that lignin may be synthesized in the epidermal cells of the wheat coleoptile. As a result of bonding between lignin and hemicellulose (5, 7), factors which control lignification may thereby influence the termination of elongation of coleoptile cells. The relationship between lignin biosynthesis and coleoptile elongation was investigated.MATERIALS AND METHODS Incubation and Nitrobenzene Oxidation. Wheat seeds (Triticunz vulgare cultivar Knox or Redcoat) were grown for 72 hr in the dark in vermiculite. Coleoptile sections 9 mm long were cut 3 mm from the tips, and the leaves were removed. The sections were floated in water for 1 to 2 hr before the treatment incubation. Twenty-five to 50 sections were incubated in 50-ml Erlenmeyer flasks in 2-to 4-ml solutions. The basic medium for incubation was 50 mm sucrose; 2.5 mm potassium maleate buffer, pH 4.8; the lignin precursor U-"C-Lphenylalanine, 15