EXTRACELLULAR-MATRIX ASSEMBLY IN DIATOMS (BACILLARIOPHYCEAE) .1. A MODEL OF ADHESIVES BASED ON CHEMICAL CHARACTERIZATION AND LOCALIZATION OF POLYSACCHARIDES FROM THE MARINE DIATOM ACHNANTHES LONGIPES AND OTHERDIATOMS
Ba. Wustman et al., EXTRACELLULAR-MATRIX ASSEMBLY IN DIATOMS (BACILLARIOPHYCEAE) .1. A MODEL OF ADHESIVES BASED ON CHEMICAL CHARACTERIZATION AND LOCALIZATION OF POLYSACCHARIDES FROM THE MARINE DIATOM ACHNANTHES LONGIPES AND OTHERDIATOMS, Plant physiology, 113(4), 1997, pp. 1059-1069
Extracellular adhesives from the diatoms Achnanthes longipes, Amphora
coffeaeformis, Cymbella cistula, and Cymbella mexicana were characteri
zed by monosaccharide and methylation analysis, lectin-fluorescein iso
thiocyanate localization, and cytochemical staining. Polysaccharide wa
s the major component of adhesives formed during cell motility, synthe
sis of a basal pad, and/or production of a highly organized shaft. Hot
water-insoluble/hot 0.5 M NaHCO3-soluble anionic polysaccharides from
A. longipes and A. coffeaeformis adhesives were primarily composed of
galactosyl (64-70%) and fucosyl (32-42%) residues. In A. longipes pol
ymers, 2,3-, t-, 3-, and 4-linked/substituted galactosyl, t-, 3-, 4-,
and 2-linked fucosyl, and t- and 2-linked glucuronic acid residues pre
dominated. Adhesive polysaccharides from C. cistula were EDTA-soluble,
sulfated, consisted of 83% galactosyl (4-, 4,6-, and 3,4-linked/subst
ituted) and 13% xylosyl (t-, 4(f)/5(p)-, and 3(p)-linked/substituted)
residues, and contained no uronosyl residues. Ulex europaeus agglutini
n uniformly localized alpha(1,2)-L-fucose units in C. cistula and Achn
anthes adhesives formed during motility and in the pads of A. longipes
. D-Galactose residues were localized throughout the shafts of C. cist
ula and capsules of A. coffeaeformis. D-Mannose and/or D-glucose, D-ga
lactose, and alpha(t)-L-fucose residues were uniformly localized in th
e outer layers of A. longipes shafts by Cancavalia ensiformis, Abrus p
recatorius, and Lotos tetragonolobus agglutinin, respectively. A model
for diatom cell adhesive structure was developed from chemical charac
terization, localization, and microscopic observation of extracellular
adhesive components formed during the diatom cell-attachment process.