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• W1523169438 abstract "Abstract A complex containing 15 to 20% of the lipopolysaccharide, 10 to 15% of the phosphatidylethanolamine, and 10 to 15% of the UDP-galactose-lipopolysaccharide galactosyltransferase of the cell is released from Escherichia coli cells by ethylenediaminetetraacetate. It can be separated from the rest of the released material, which consists mainly of an additional 30 to 35% of the lipopolysaccharide of the cell, by sedimentation in a 10 to 30% sucrose gradient. The ratio of phosphatidylethanolamine phosphate to lipopolysaccharide glucose in the complex is 1.6:1. The enzyme complex is unstable as isolated but can be stabilized in 20% sucrose or glycerol. It has been purified 10-fold over the material released by EDTA and 20-fold over extracts obtained by sonic treatment of whole cells. Varying cell concentration during EDTA treatment does not alter the amount of complex released per cell, and labeled lipopolysaccharide or phosphatidylethanolamine added during EDTA treatment is not incorporated into the complex. These results, as well as additional evidence presented, suggest that the complex is not formed during isolation, but is the biosynthetic unit present in vivo." @default.
• W1523169438 created "2016-06-24" @default.
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• W1523169438 date "1970-02-01" @default.
• W1523169438 modified "2023-09-27" @default.
• W1523169438 title "Release from Escherichia coli of a Galactosyltransferase Complex Active in Lipopolysaccharide Synthesis" @default.
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• W1523169438 doi "https://doi.org/10.1016/s0021-9258(18)63372-1" @default.
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