nted in
TEIN
cacia erioi~ba
ATES~
DAVID W. GAMMON, ALISTAIRM. STEPHEN.AND SHIRLEYC. CHURMS
De~arcmeni of Organic Che~~t~,
~nive~i~
of Cape Town,
ptcd for publication, Au
alactose occ~
~nted, in part, at the Int , and the 8th Int~mational 62151
03.50
rides,
U.S.
in three
15
MON. A. M. STEPHEN. S. C. CHURMS
cia e
~LYCOP
s of concanavalin
D. W. GA
N, A. M. STEP
1 Elu
L)
aphy of A8OP on DEAE-~~1~10~: carbo
STEPHEN,
Elut
1
-
l5
-0.
1
-
5
-
(x5
(mL) &ion with proteinase K: (a) st
eluted ~th M NaCI:
RESULT
S. C. CHURMS
ab~rbance at 220 nm, ----; amino
AND DISCUSSION
ical locations. Since
ucts of 2 su~essive
AC
eriolo 1
G~~COP 2
Fig. 3. SDS-PAGE o (channels 4 and 7), a b, (b) albumin, (c) Channels l-5 were st
a
S 4
s
D. W. GAMMON, A. M. SIPHON, lb)
(a)
A‘ 60%
Amberiite IR- 120 tH+)
Insoluble
SOlUble
Al
saturated
Insoluble
Soluble
A2
eo *I. saturated
(i) dialysed (ii)~reeze-dried
(i 1 dialysed (ii) l~eeze-dried
Scheme
1.
A8305
(i) diolysed (ii)
freeze-dried
ABOP
Scheme 1. Fractionation of gum samp!es A and A’ from A. erioloba.
onents (“a continuous s
S. C. C
Fig. 4. Chromate c~bohydrate, -;
y, on a ~lumn (10 x 0.5 cm) of byd~xyapatite, of (a) A, (b) Al, and (c) A2: ate buffer (pH 7.4), --.-a-. ante at 220 nm, -----; ph
CH20Ac
I
Scheme 2. O~gin of the si
ent ions in the mass 5pectNm of 1.
1
~ETHY~TION
2,3,4,62,3,4,6-
. STEPHEN, S. C. CHU
Al (
ANALYSES FOR MENDED
1) AND PRODU~S
DERIVED ~ERE~OM
5”
1
23h
-
2,3,4,~Gal-
6
2,3,6-Gal 2,3,4-Gal 2,4-Gal Uroni~ acid
14 12 6 21”
39 4 5 -
8 11 11 8 -
30 27 31 12 n.d.
I 8
J1.2”
l~tegrated interim
5. 4. 4.
2.8 3.4 7.3
0.33 1 0.
S
J1.2
integrated interim
5.07
3.4
1
protons not included.
ata insistent
~th th
S
JI,2
integrated interim
5.25
3.4
0.5
4.56 4.54
7.1 7.4
1.5
of Pear
et al.%. cP.p.m. do~fieid
8
J12
l~t~grated i~te~~~
4.52
7.2
1
Assignment
. eJ,,5value is tentative.
1
D. W. GAMMON, A.
STEPHEN, S. C. CHUR
-- ??-I -- 96-l ---------------
(b)
--------
143-==108~ 190-155
J
237--,202J
--=-216---l&31
Scheme
3.
entat rved. mentationz7 in each arises, as expectedz8, from abJ, fragmentation,
not react~~31 in
(b) acid II; m/z val is from te~inal u he de~vative of I includes an ion m/z 314
cac~a erioloba GLYCOPRO~INS
io-Gel P-2) of the pro cts of hydrol~is of PA1 with ba~um hy yproline, ------; optics rotation at 365 nm, -.-.--.-.
17
ON, A. M. STEPHEN.
S. C. C
S
After removal oft
ACKNO
~DGMENTS
RENCES
LLEN, A. NEVBERGER, Fkw~,
Carbo~ydr.
C. L. GILL, C. G. A.
C. L. GILL, A. M.
Poiym., 5 (1985) 251-273. CNAB. AND
G. DE PINTO, Phytochemistry, 23
JEFFREY. AND F. J. MCDOUGALL,
F~ytochemistry, 24
Phytochemist~, 22 (1983) 2481-
171
a GLYCOPRO~INS
BERS, AND
F. Stmw, Anal. Chem.,