L. Scobbie et al., THE NEWLY EXTENDED MAIZE INTERNODE - A MODEL FOR THE STUDY OF SECONDARY CELL-WALL FORMATION AND CONSEQUENCES FOR DIGESTIBILITY, Journal of the Science of Food and Agriculture, 61(2), 1993, pp. 217-225
The upper five internodes were collected from maize (Zea mays L) inbre
d cell lines Co125 and W401 harvested at the same developmental stage,
5 days after silking. Each internode was dissected into ten equal len
gths labelled A (top) to J (base). The youngest cells were found in se
ction J, which contained the intercalary meristem, and the oldest in s
ection A. Internodes 1, 3 and 5 provided material for chemical analysi
s and internodes 2 and 4 for degradability measurements. Cell wall mat
erial accounted for one-third of dry matter in section J, doubling to
two-thirds in the upper half of each internode. Only section J exhibit
ed a polysaccharide profile typical of primary cell walls. In all othe
r sections, 1,4-linked glucose (approximately 46% of cell wall) and xy
lan largely free from side chains (approximately 25% of cell wall) pre
dominated. Net accretion of cell wall polysaccharide reached a maximum
by segment G and thereafter little additional carbohydrate was deposi
ted. Lignification appeared to be separated from the biogenesis of str
uctural carbohydrate and continued over much of each internode reachin
g a maximum in section C. Degradability measurements, made using a mod
ified neutral-detergent cellulase digestibility method, showed substan
tial differences between sections. In line Co125, cell wall degradabil
ity fell from over 95% in the youngest section (J) to approximately 24
% in section B. Internode 4 of line W401 failed to show the same patte
rn of degradabilities, probably because of a sequential rather than si
multaneous pattern of internode elongation. Saponifiable p-coumaric ac
id appeared to provide a more sensitive marker than lignin of the exte
nt of secondary wall development. The inverse relationship between ext
ent of lignification in each section and its degradability confirmed t
he value of the internode model for the study of secondary wall format
ion and its biological consequences.