ABSTRACIThe composition of the aliphatic components of suberin in the stele and cortex of young corn (Zea mays L.) roots was determined by combined gas-liquid chromatography/mass spectrometry of the LiAID4 depolymerization products. u.-Hydroxy acids were shown to be the major clss of the aliphatic components of both the hypodermal (35%) and endodermal (28%) polymeric materials with the dominant chain length being C24 in the former and C16 in the latter. Suberin, which is thought to be a polymer composed of aliphatic and aromatic domains, serves as the structural component of certain diffusion barriers in the plant (15). Electron micrographs of suberin reveal a lamellar structure composed of light and dark bands probably representing alternating layers of wax and polymer (23,24). Suberin, which has been ultrastructurally identified, has been examined chemically from only a few sources (5,8,9), but in these cases the composition of the aliphatic components agreed well with an early generalization that long chain (C,6-C26) w-hydroxy and dicarboxylic acids are very often the major aliphatic components of suberin (16 cells (19,20), suberin in roots has been examined chemically in only a few cases (7,14,18). Suberization in the plant may frequently be a response to certain types of stress, but there have been no combined chemical and ultrastructural studies on the effects of such stress upon suberization in roots. In this paper, we report the suberin composition of the hypodermis and endodermis of young corn roots and show chemically and ultrastructurally that Mg deficiency causes an increase in the suberization of corn roots.
MATERIALS AND METHODSDetermination of the Composition of the Aliphatic Components of the Hypodermal and Endodermal Suberin. Seeds of Zea mays L. cv Golden Cross were germinated on moist filter paper in the dark for 6 d at room temperature. The tip of the root (approximately 1 cm) was removed, and the remainder of the root (approximately 5 cm) was manually separated into hypodermal and endodermal fractions with the tissue being retained only when it was clear that the separation had been complete (7). The two fractions were frozen, lyophilized, ground to a powder (Wig-L-Bug amalgamator), and $oxhlet extracted (72 h with CHC13 and 72 h with CH30H). Portions (500 mg) of these powders were depolymerized with LiAlD4, fractionated on TLC, and analyzed by combined GC-MS with a Varian gas chromatograph attached to a Perkin-Elmer-Hitachi RMU6D mass spectrometer with a Biemann separator interphase (26