SYNTHESIS AND ENZYMATIC CONVERSION OF AN ETHER ANALOG OF MONOGALACTOSYL DIACYLGLYCEROL

被引：10

作者：

HEINZ, E ^{[1
]}

SIEBERTZ, HP ^{[1
]}

LINSCHEID, M ^{[1
]}

机构：

[1] UNIV COLOGNE,INST ORGAN CHEM,D-5000 COLOGNE 41,FED REP GER

来源：

CHEMISTRY AND PHYSICS OF LIPIDS | 1979年 / 24卷 / 03期

关键词：

D O I：

10.1016/0009-3084(79)90032-X

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The synthesis of 1,2-di-O-9′-octadecenyl-3-O-β-D-galactopyranosyl-sn-glycerol is described, including a detailed discussion of mass spectrometric fragmentation patterns of this and related substances. Enzymatic experiments showed that this compound is converted by plant enzymes to the 6-O-acyl derivative. The availability of the di-9-octadecynyl compound for tritium reduction will provide a substrate for studies on direct desaturation of lipid-linked acyl or alkyl chains. © 1979.

引用

页码：265 / 276

页数：12

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