ON STRUCTURE OF CARDIOLIPIN
ON STRUCTURE OF CARDIOLIPIN
复制标题
DOI:
10.1021/bi00895a023
复制
发表时间:
1964-01-01
期刊:
影响因子:
2.9
通讯作者:
BALLOU, CE
中科院分区:
文献类型:
--
作者:
LECOCQ, J;BALLOU, CE
Cardiolipin (diphos-phatidylglycerol) from beef heart and from Mycobacterium phlei has been deacylated and degraded to glycerol-l,3-diphosphate by the action of sodium metaperiodate and 1,1-dimethylhydrazine. The results establish that the lipid has the 1,3-diphosphatidyl-glycerol structure, a point that was still open to question. For references, crystalline cyclo-hexylamine salts of glycerol-l,3-diphosphate and L-glycerol-1,2-diphosphate have been prepared. The reported optical activity of the triglyceroldiphosphate obtained by deacylation of cardiolipin has been confirmed, and is found to be identical with that of synthetic 1,3-di-O-(L-glycerol-3[image]-phosphoryl)-glycerol synthesized by P. Plackett (Australian J. Chem. 17, 101, 1964), thus establishing the over-all absolute configuration of the cardiolipin molecule.