Cfb. Sene et al., FOURIER-TRANSFORM RAMAN AND FOURIER-TRANSFORM INFRARED-SPECTROSCOPY -AN INVESTIGATION OF 5 HIGHER-PLANT CELL-WALLS AND THEIR COMPONENTS, Plant physiology, 106(4), 1994, pp. 1623-1631
Infrared and Raman spectra of sequentially extracted primary cell welt
s and their pectic polymers were obtained from five angiosperm plants.
Fourier-transform Raman spectrometry was shown to be a powerful tool
for the investigation of primary cell-wall architecture at a molecular
level, providing complementary information to that obtained by Fourie
r-transform infrared microspectroscopy. The use of an extraction proce
dure using imidazole instead of cyclohexane trans-1,2-N,N,N',N'-diamin
otetraacetate allows the extension of the infrared spectral window for
data interpretation from 1300 to 800 cm(-1), to 2000 to 800 cm(-1), a
nd allows us to obtain Raman spectra from extracted cell-wall material
. Wall constituents such as pectins, proteins, aromatic phenolics, cel
lulose, and hemicellulose have characteristic spectral features that c
an be used to identify and/or fingerprint these polymers without, in m
ost cases, the need for any physical separation. The Gramineae (rice [
Oryza sativa], polypogon [Polypogon fugax steud], and sweet corn [Zee
mays]) are spectroscopically very different from the nongraminaceous m
onocotyledon (onion [Allium cepa]) and the dicotyledon (carrot [Daucus
carota]); this reflects differences in chemical composition and cross
-linking of the walls. The possibility of a taxonomic classification o
f plant cell walls based on infrared and Raman spectroscopies and the
use of spectral fingerprinting for authentication and detection of adu
lteration of products rich in cell-wall materials are discussed.