Enzymes in Lipid Modification 2000
DOI: 10.1002/3527606033.ch12
|View full text |Cite
|
Sign up to set email alerts
|

Phospholipases Used in Lipid Transformations

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
14
0

Year Published

2001
2001
2012
2012

Publication Types

Select...
4
2

Relationship

2
4

Authors

Journals

citations
Cited by 19 publications
(15 citation statements)
references
References 131 publications
1
14
0
Order By: Relevance
“…As several examples show, the catalytic potential of PLDs is not restricted to the phosphatidyl backbone but allows also modifications in the nonpolar residue. In addition to the head group exchange in lysophosphocholine [13], the transesterification in ether glycerophospholipids was reported (review in [1]). Interestingly, even alkylphosphocholines lacking the glycerol backbone [14] and -still more surprisingly -alkylphosphonocholines [15] can be transesterified by means of PLD.…”
Section: Microbial Contra Plant Phospholipases Dmentioning
confidence: 97%
See 2 more Smart Citations
“…As several examples show, the catalytic potential of PLDs is not restricted to the phosphatidyl backbone but allows also modifications in the nonpolar residue. In addition to the head group exchange in lysophosphocholine [13], the transesterification in ether glycerophospholipids was reported (review in [1]). Interestingly, even alkylphosphocholines lacking the glycerol backbone [14] and -still more surprisingly -alkylphosphonocholines [15] can be transesterified by means of PLD.…”
Section: Microbial Contra Plant Phospholipases Dmentioning
confidence: 97%
“…The spectrum of chemical structures of alcohols, which can be introduced as head group, is wide and comprises in addition to the natural components of phospholipids (glycerol, choline, ethanolamine, serine, inositides) nucleosides, peptides, arsenocholine, N-heterocyclic alcohols, and aromatic compounds (reviewed in [1]). In general, primary alcohols are better acceptors than secondary ones, while no tertiary alcohol is known to be introduced.…”
Section: Microbial Contra Plant Phospholipases Dmentioning
confidence: 99%
See 1 more Smart Citation
“…In industry and chemical laboratories, secretory PLA 2 s have been exploited for the synthesis of lysophospholipids, which are widely used as emulgators in food and dietary industry or as drug carriers in pharmaceutical industry. More recently, PLA 2 s have been probed as catalyst for the synthesis of phospholipids with defined fatty acids by reesterification of lysophospholipids (review in Ulbrich-Hofmann, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…In glycerophospholipids, they catalyze the hydrolysis of the two acyl ester (phospholipases A 1 and A 2 ) and the two phosphate ester bonds (phospholipase C and PLD). In biocatalysis, phospholipases have been exploited for a number of phospholipid-transforming reactions in the laboratory as well as on an industrial scale (Servi 1999, Ulbrich-Hofmann 2000. PLD has an outstanding position by its transphosphatidylation potential.…”
Section: Introductionmentioning
confidence: 99%