Ethanolamine in phosphatidylethanolamine

FIGURE 21-28 Pathway for phosphatidylcholine synthesis from choline in mammals. The same strategy shown here (strategy 2 in Fig. 21-24) is also used for salvaging ethanolamine in phosphatidylethanolamine synthesis. 

Synthesis of phosphatidylcholine and phosphatidylethanolamine begins with activation of choline (or ethanolamine) with ATP via choline kinase to yield phosphocholine (phosphoethanolamine) + ADP the activated base is transferred via CTP and phosphocholine cytidyl transferase to form CDP-choline (CDP-ethanolamine) and PPi. The base is then transferred to the sn-3 of diacylglycerol via phosphocholine diacylglycerol transferase to yield phosphatidylcholine (phosphatidylethanolamine) + CMP. The cytidyl transferase is believed to be the rate-limiting or regulatory step in the pathway. Phospha-tidylserine is formed by a direct transfer and substitution of serine for ethanolamine in phosphatidylethanolamine. Phosphatidyl serine can be dec-arboxylated to form phosphatidylethanolamine. 

If SIP is not secreted or dephosphorylated by specific SIP phosphatases, as well as by more general lipid phosphatases, it is cleaved irreversibly to ethanolamine phosphate and rrans-2-hexadecenal by SIP lyase (J. Zhou, 1998 P.P. Van Veldhoven, 20(X)). As shown first in the 1970s by W. Stoffel and coworkers, the phosphoethanolamine can be utilized for the synthesis of phosphatidylethanolamine (Chapter 8), and fran5-2-hexadecenal can be reduced to the alcohol and incorporated into alkyl ether lipids. Under certain conditions, degradation of sphingoid bases can account for as much as one-third of the ethanolamine in phosphatidylethanolamine (E.R. Smith, 1995). It is interesting that both the first enzyme of sphingoid base metabolism (SPT) and the last enzyme, the lyase, are pyridoxal 5 -phosphate-dependent. 

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See also in sourсe #XX -- [ ]

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