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Biochemistry |
Department of Bacteriology, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830-0011, Japan1
Department of Chemistry, Graduate School of Science, Tohoku University Aoba, Aramaki aza, Aoba-ku, Sendai 980-8578, Japan2
Author for correspondence: Sumio Arai. Tel: +81 942 31 7548. Fax: +81 942 31 0343. e-mail: sumiyuku{at}mx2.tiki.ne.jp
A component that binds to human lymphoid cells was isolated from the membranes of Acholeplasma laidlawii PG8. The component was extracted using the BlighDyer method and purified using a silica-gel column and TLC. The active component was identified as 3-O-[2'-O-(
-D-glucopyranosyl)- 6'-O-acyl-
-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 nC 14 (17·8%), isoC14 (10·7%) and nC 16 (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.
Keywords: Acholeplasma laidlawii, adherence, glycoglycerolipids, lymphoid cells
Abbreviations: GAGDG, 3-O-[2'-O-(
-D-glucopyranosyl)- 6'-O-acyl-
-D-glucopyranosyl]-1,2-di-O- acyl-sn-glycerol
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