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Fig. 11.8 Elution profile
of etiolated corn leaves
following a 2.5 ms flash
of light at room
temperature followed by
immediate precipitation
with ammoniacal acetone.
Separations were performed
on a PE Pecosphere
3
3C, C-18 reversed
phase, 4
0.5 cm column.
Elution was with an
isocratic, solvent system
that consisted of H2O:
acetone:methanol
(5:20:75 v/v/v. P Pchlide
a
,
PE Pchlide
a
ester, CE
Chlide
a
ester, RT retention
time) (Adapted from Rebeiz
et al.
2003
)
Formation of the latter implied the involvement of a light-independent Chlide
a
E
biosynthetic step in higher plants during dark germination which is depicted by
biosynthetic route 16D (Fig.
11.8
). Recently, the detection of Chlide
a
E has also
been reported by others in etiolated plant tissues (Skribanek et al.
2000
) (Fig.
11.9
).
Photoconversion of DV Pchlide
a
E to DV Chlide
a
E
In Fig.
11.9
, (see below) the photoconversion of DV Pchlide
a
ester to DV Chl
a
is
assigned to a fully esterified DV Chl
a
biosynthetic route. This assignment is based
on the detection of DV Chl
a
formation immediately following a 47 ms actinic
white light
treatment of etiolated cucumber cotyledons, at room temperature
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