Front Matter

12.5 Examples of application 245

Table 3.continued.

Head group
introduced

Educt^1 Source of PLD Solvent system Reference

2,5,7,8-Tetramethyl-
6-hydroxy-2-
(hydroxy-
ethyl)chroman
(Figure 13G)

PC (egg) Streptomyces

lydicus

buffer/diethyl

ether

Koga et al., 1994

Diverse aromatic
compounds
(Figure 13H)

DPPC Streptomycessp. acetate buffer/

benzene or other

Takami et al., 1994a

4-Methoxyphenol DPPC Streptomycessp.
(PLD immobilized)

acetate buffer/

benzene

Takami and Suzuki,

1995

Arsenocholine
(Figure 13I)

DOPC Cabbage,

Streptomycessp.

acetate buffer/

diethyl ether

Hirche et al., 1997b

N-heterocyclic
alcohols

PC Streptomycessp. acetate buffer/ethyl

acetate, methylene

chloride

D’Arrigo et al.,

1996b

(Figure 13J) DOPC Cabbage,
Streptomycessp.

acetate buffer/

diethyl ether

Hirche et al., 1997b

(^1) DEPC, 1,2-dielaidoyl-sn-glycero-3-phosphocholine; DHPC, 1,2-dihexanoyl-sn-glycero-3-phosphati-
dylcholine; DHePC, dihexadecyl-sn-phosphatidylcholine; DMPC, 1,2-dimyristoyl-sn-glycero-3-
phosphocholine; DOPC, 1,2-dioleoyl-sn-glycero-3-phosphocholine; DPPC, 1,2-dipalmitoyl-sn-gly-
cero-3-phosphocholine; DSPC, 1,2-distearoyl-sn-glycero-3-phosphocholine; SM, sphingomyelin.
Figure 11. Synthesis ofO-alkyl inositol 1-phosphates by PI–PLC. XOH: alkanols, alkandiols, glyce-
rol, sugar alcohols, aminoalcohols, serine, uridine, peptides, pentaethylene glycol.