CELL-WALL METABOLISM IN RIPENING FRUIT .8. CELL-WALL COMPOSITION AND SYNTHETIC CAPACITY OF 2 REGIONS OF THE OUTER PERICARP OF MATURE GREEN AND RED RIPE CV JACKPOT TOMATOES
M. Huysamer et al., CELL-WALL METABOLISM IN RIPENING FRUIT .8. CELL-WALL COMPOSITION AND SYNTHETIC CAPACITY OF 2 REGIONS OF THE OUTER PERICARP OF MATURE GREEN AND RED RIPE CV JACKPOT TOMATOES, Physiologia Plantarum, 101(2), 1997, pp. 314-322
Pericarp discs were excised from mature green and red ripe tomato (Lyc
opersicon esculentum Mill. cv. Jackpot) fruit and kept in sterile tiss
ue culture plates for 4 days, in eluding 2 days of incubation with D-[
U-C-13]-glucose, Cell walls were prepared and differentially extracted
with dimethylsulfoxide (DMSO), trans-1,2-diaminocyclohexane-N,N,N',N'
-tetraacetic acid (CDTA), Na2CO3, 4 M KOH and 8 M KOH. Cell wall nonce
llulosic neutral sugar (NS) composition and cell wall synthetic capaci
ty (i.e. incorporation of density label into cell wall sugars) were de
termined by using a gas chromatograph coupled to a flame ionization de
tector and a mass spectrometer, respectively. In the crude cell wall,
there was significantly less galactose (Gal) and glucose (Glc) in the
''outer'' 2-mm pericarp region, including the cuticle, compared to the
''inner'' 2-mm region immediately below it (closer to the locules). I
n the CDTA-soluble pectin, rhamnose (Rha), arabinose (Ara) and Gal acc
ounted for approximately 90% of the total NS. The ratios of these suga
rs were very similar in the total (C-12 plus C-13) sugars, and also in
the newly synthesized ([C-13]-labeled) sugars, suggesting that newly
synthesized NS associated with the chelator-extractable pectic fractio
n has a composition very similar to that of preexisting NS, In the 4 M
KOH-soluble material, xylose (Xyl) and Glc accounted for approximatel
y 70% of the total NS, The ratio of these sugars was very similar in t
he total sugars, but much lower in the newly synthesized portion. This
suggests that the hemicellulosic polymers synthesized during the ripe
ning process are different in type and/or proportion from those presen
t in the developing fruit. Because the outer pericarp of tomatoes cont
ains at least two distinct tissue types and these have a distinct cell
wall composition, analysis of tomato cell wall polysaccharide composi
tion by homogenization of the entire outer pericarp will obscure subtl
e changes associated with ripening/softening within specific tissue ty
pes.