Literature DB >> 11732909

Effects of phospholipid headgroup and phase on the activity of diacylglycerol kinase of Escherichia coli.

J D Pilot1, J M East, A G Lee.   

Abstract

Diacylglycerol kinase (DGK) of Escherichia coli has been reconstituted into a variety of phospholipid bilayers and its activity determined as a function of lipid headgroup structure and phase preference. The anionic phospholipids dioleoylphosphatidic acid, dioleoylphosphatidylserine, and cardiolipin were all found to support activities lower than that supported by dioleoylphosphatidylcholine. In mixtures of dioleoylphosphatidylcholine and 20 mol % anionic phospholipids, the presence of anionic phospholipids all resulted in lower activities than in dioleoylphosphatidylcholine, except for dioleoylphosphatidylglycerol whose presence had little effect on activity. In some cases, the low activity in the presence of anionic phospholipid followed from a decrease in v(max); in some cases, it followed from an increase in the K(m) for diacylglycerol, and in the case of dioleoylphosphatidic acid, it followed from both. Activities in mixtures containing 80 mol % dioleoylphosphatidylethanolamine were lower than in dioleoylphosphatidylcholine at temperatures where both lipids adopted a bilayer phase; at higher temperatures where dioleoylphosphatidylethanolamine preferred a hexagonal H(II) phase, the differences in activity were greater. These experiments suggest that the presence of lipids preferring a hexagonal H(II) phase leads to low activities. Activities of DGK are low in a gel phase lipid.

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Year:  2001        PMID: 11732909     DOI: 10.1021/bi011333r

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  9 in total

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7.  Insulin receptor activation and down-regulation by cationic lipid transfection reagents.

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8.  Droplet interface bilayer reconstitution and activity measurement of the mechanosensitive channel of large conductance from Escherichia coli.

Authors:  Hanna M G Barriga; Paula Booth; Stuart Haylock; Richard Bazin; Richard H Templer; Oscar Ces
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9.  Lipid binding attenuates channel closure of the outer membrane protein OmpF.

Authors:  Idlir Liko; Matteo T Degiacomi; Sejeong Lee; Thomas D Newport; Joseph Gault; Eamonn Reading; Jonathan T S Hopper; Nicholas G Housden; Paul White; Matthew Colledge; Altin Sula; B A Wallace; Colin Kleanthous; Phillip J Stansfeld; Hagan Bayley; Justin L P Benesch; Timothy M Allison; Carol V Robinson
Journal:  Proc Natl Acad Sci U S A       Date:  2018-06-11       Impact factor: 11.205

  9 in total

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