Maize stem tissues: cell wall concentration and composition during development

Grass maturation results in reduced cell wall degradability by ruminant livestock. Using a specific internode of maize (Zea mays L.) stems as a model, the pattern of grass stem tissue and cell wall development was characterized. The fourth elongated internode above ground level from three maize hybrids was sampled at 10 stages of development beginning when the internodewas about 10 mm in length through physiological maturity from a 2-yr, replicated field trial at St. Paul, MN. Tissue development was characterized by light microscopy. Cell wall concentration and composition (polysaccharide sugar residues, lignin, ferulates, and p-coumarates) were determined. Internode length and cross-sectional area increased from Sampling Date 1 until the interval between Sampling Dates 5 and 6. During elongation only protoxylem vessels stained positive for lignin. After elongation, parenchyma, sclerenchyma, and metaxylem tissues lignified, but phloem did not. Cell wall concentration increased until shortly after elongation ended. Cell wall lignin concentration declined over the first four samples, with an increase in glucose and xylose polysaccharide residues, before rising sharply until after elongation was complete. Ferulate cross-links of lignin to arabinoxylan increased 12-fold during elongation. Our results indicated that post-elongation development of sclerenchyma and rind-region parenchyma accounted for the majority of cell wall accumulation and lignification in maize stems.

[1]  Richard F. Helm,et al.  Pathway of p-Coumaric Acid Incorporation into Maize Lignin As Revealed by NMR , 1994 .

[2]  R. Andersson,et al.  Total dietary fiber determined as neutral sugar residues, uronic acid residues, and Klason lignin (the Uppsala method): collaborative study. , 1995, Journal of AOAC International.

[3]  J. Hanway How a corn plant develops , 1966 .

[4]  Hansang Jung,et al.  Forage quality variation among maize inbreds: Relationships of cell‐wall composition and in‐vitro degradability for stem internodes , 1994 .

[5]  R. Hatfield,et al.  Isolates of cell types from sorghum stems: Digestion, cell wall and anatomical characteristics , 1993 .

[6]  D. R. Buxton,et al.  Cell‐Wall Composition of Maize Internodes of Varying Maturity , 1998 .

[7]  A. Chesson,et al.  The newly extended maize internode: A model for the study of secondary cell wall formation and consequences for digestibility , 1993 .

[8]  F. M. Engels,et al.  Alfalfa Stem Tissues: Cell Wall Deposition, Composition, and Degradability , 2002 .

[9]  Hansang Jung,et al.  Maize Stem Tissues , 2006 .

[10]  A. Chesson Mechanistic Models of Forage Cell Wall Degradation , 1993 .

[11]  I. Morrison Changes in the hemicellulosic polysaccharides of rye-grass with increasing maturity. , 1974, Carbohydrate research.

[12]  J. Ralph,et al.  Diferulate cross-links impede the enzymatic degradation of non-lignified maize walls , 1998 .

[13]  F. M. Engels,et al.  Alfalfa stem tissues: cell-wall development and lignification. , 1998 .

[14]  D. W. Stewart,et al.  Carbohydrate levels in field-grown leafy and normal maize genotypes , 1995 .

[15]  J. Ralph,et al.  Ferulate Cross-Links Limit the Enzymatic Degradation of Synthetically Lignified Primary Walls of Maize , 1998 .

[16]  Zengyu Wang,et al.  Lignin deposition and associated changes in anatomy, enzyme activity, gene expression, and ruminal degradability in stems of tall fescue at different developmental stages. , 2002, Journal of agricultural and food chemistry.

[17]  C. Chapple,et al.  Impact of lignin composition on cell‐wall degradability in an Arabidopsis mutant , 1999 .

[18]  Bruce A. Stone,et al.  Phenolic acid bridges between polysaccharides and lignin in wheat internodes , 1990 .

[19]  Hansang Jung,et al.  Maize stem tissues: ferulate deposition in developing internode cell walls. , 2003, Phytochemistry.

[20]  Michael D. Casler,et al.  Maize Stem Tissues: Impact of Development on Cell Wall Degradability , 2006 .

[21]  F. M. Engels,et al.  Alfalfa stem tissues: rate and extent of cell-wall thinning during ruminal degradation , 2001 .

[22]  R. Helm,et al.  Cell Wall Cross-Linking in Grasses by Ferulates and Diferulates , 1998 .

[23]  Peter B. Kaufman,et al.  On Nature of Intercalary Growth and Cellular Differentiation in Internodes of Avena sativa , 1965, Botanical Gazette.

[24]  R. Smith,et al.  Cell wall composition and degradability of stem tissue from lucerne divergently selected for lignin and in vitro dry‐matter disappearance , 1994 .

[25]  G. A. Jung,et al.  Chemical Composition of Parenchyma and Sclerenchyma Cell Walls Isolated from Orchardgrass and Switchgrass , 1991 .

[26]  D. E. Akin Histological and Physical Factors Affecting Digestibility of Forages , 1989 .

[27]  J. Ralph,et al.  Pyrolysis-GC-MS characterization of forage materials , 1991 .

[28]  J. Labavitch,et al.  A SIMPLIFIED METHOD FOR ACCURATE DETERMINATION OF CELL WALL URONIDE CONTENT , 1978 .

[29]  D. Buxton,et al.  Maize Internode Elongation Patterns , 1994 .

[30]  D. Buxton,et al.  Forage Cell Wall Structure and Digestibility , 1993 .

[31]  I. Morrison Changes in the lignin and hemicellulose concentrations of ten varieties of temperate grasses with increasing maturity , 1980 .

[32]  J. Wilson Organization of Forage Plant Tissues , 1993 .

[33]  Ronald D. Hatfield,et al.  Composition of cell walls isolated from cell types of grain sorghum stems , 1999 .

[34]  Hansang Jung,et al.  Variation in the extractability of esterified p-coumaric and ferulic acids from forage cell walls. , 1990 .

[35]  G. A. Jung,et al.  Isolation of parenchyma and sclerenchyma cell types from the plant parts of grasses , 1991 .