TY - JOUR
T1 - Binding of glycoglycerolipid derived from membranes of Acholeplasma laidlawii PG8 and synthetic analogues to lymphoid cells
AU - Toujima, S.
AU - Kuwano, K.
AU - Zhang, Y.
AU - Fujimoto, N.
AU - Hirama, M.
AU - Oishi, T.
AU - Fukuda, S.
AU - Nagumo, Y.
AU - Imai, H.
AU - Kikuchi, T.
AU - Arai, S.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2000
Y1 - 2000
N2 - A component that binds to human lymphoid cells was isolated from the membranes of Acholeplasma laidlawii PG8. The component was extracted using the Bligh-Dyer method and purified using a silica-gel column and TLC. The active component was identified as 3-O-[2'-O- (α-D-glucopyranosyl)-6'-O-acyl-α-D-glucopyranosyl]-1, 2-di-O-acyl-sn-glycerol (GAGDG) using 1H- and 13C-NMR and GC-MS. The compositions of the major saturated fatty acids were nC14 (17·8%), isoC14 (10·7%) and nC16 (34·9%) as determined by GC-MS. The amounts of unsaturated species were less than 10% of those of the corresponding saturated acids. GAGDGs which have three tetradecanoyl groups were synthesized. These synthetic GAGDGs, as well as GAGDGs derived from A. laidlawii membranes, had a high binding affinity for MOLT-4 and HUT-78 (human T cell lines), Raji (a B cell line), HL-60 (a monoblastoid cell line) and primary cultured human T cells. The binding affinities of GAGDGs with an isoC14 acyl group was higher than those with nC14 and nC16 acyl groups. The binding to lymphoid cells reveals a novel biological activity of GAGDGs.
AB - A component that binds to human lymphoid cells was isolated from the membranes of Acholeplasma laidlawii PG8. The component was extracted using the Bligh-Dyer method and purified using a silica-gel column and TLC. The active component was identified as 3-O-[2'-O- (α-D-glucopyranosyl)-6'-O-acyl-α-D-glucopyranosyl]-1, 2-di-O-acyl-sn-glycerol (GAGDG) using 1H- and 13C-NMR and GC-MS. The compositions of the major saturated fatty acids were nC14 (17·8%), isoC14 (10·7%) and nC16 (34·9%) as determined by GC-MS. The amounts of unsaturated species were less than 10% of those of the corresponding saturated acids. GAGDGs which have three tetradecanoyl groups were synthesized. These synthetic GAGDGs, as well as GAGDGs derived from A. laidlawii membranes, had a high binding affinity for MOLT-4 and HUT-78 (human T cell lines), Raji (a B cell line), HL-60 (a monoblastoid cell line) and primary cultured human T cells. The binding affinities of GAGDGs with an isoC14 acyl group was higher than those with nC14 and nC16 acyl groups. The binding to lymphoid cells reveals a novel biological activity of GAGDGs.
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U2 - 10.1099/00221287-146-9-2317
DO - 10.1099/00221287-146-9-2317
M3 - Article
C2 - 10974119
AN - SCOPUS:0033824667
SN - 1350-0872
VL - 146
SP - 2317
EP - 2323
JO - Microbiology
JF - Microbiology
IS - 9
ER -