Literature DB >> 3988805

Localization of phosphatidylcholine in outer envelope membrane of spinach chloroplasts.

A J Dorne, J Joyard, M A Block, R Douce.   

Abstract

We have examined the effects of phospholipase C from Bacillus cereus on the extent of phospholipid hydrolysis in envelope membrane vesicles and in intact chloroplasts. When isolated envelope vesicles were incubated in presence of phospholipase C, phosphatidylcholine and phosphatidylglycerol, but not phosphatidylinositol, were totally converted into diacylglycerol if they were available to the enzyme (i.e., when the vesicles were sonicated in presence of phospholipase C). These experiments demonstrate that phospholipase C can be used to probe the availability of phosphatidylcholine and phosphatidylglycerol in the cytosolic leaflet of the outer envelope membrane from spinach chloroplasts. When isolated, purified, intact chloroplasts were incubated with low amounts of phospholipase C (0.3 U/mg chlorophyll) under very mild conditions (12 degrees C for 1 min), greater than 80% of phosphatidylcholine molecules and almost none of phosphatidylglycerol molecules were hydrolyzed. Since we have also demonstrated, by using several different methods (phase-contrast and electron microscopy, immunochemical and electrophoretic analyses) that isolated spinach chloroplasts, and especially their outer envelope membrane, remained intact after mild treatment with phospholipase C, we can conclude that there is a marked asymmetric distribution of phospholipids across the outer envelope membrane of spinach chloroplasts. Phosphatidylcholine, the major polar lipid of the outer envelope membrane, is almost entirely accessible from the cytosolic side of the membrane and therefore is probably localized in the outer leaflet of the outer envelope bilayer. On the contrary, phosphatidylglycerol, the major polar lipid in the inner envelope membrane and the thylakoids, is probably not accessible to phospholipase C from the cytosol and therefore is probably localized mostly in the inner leaflet of the outer envelope membrane and in the other chloroplast membranes.

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Year:  1985        PMID: 3988805      PMCID: PMC2113847          DOI: 10.1083/jcb.100.5.1690

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


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Journal:  FEBS Lett       Date:  1970-11-18       Impact factor: 4.124

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5.  Separation and characterization of inner and outer envelope membranes of pea chloroplasts.

Authors:  K Cline; J Andrews; B Mersey; E H Newcomb; K Keegstra
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

6.  Site of synthesis of phosphatidic acid and diacyglycerol in spinach chloroplasts.

Authors:  J Joyard; R Douce
Journal:  Biochim Biophys Acta       Date:  1977-02-23

Review 7.  Membrane asymmetry. A survey and critical appraisal of the methodology. II. Methods for assessing the unequal distribution of lipids.

Authors:  A H Etemadi
Journal:  Biochim Biophys Acta       Date:  1980-12-31

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Authors:  H P Siebertz; E Heinz; M Linscheid; J Joyard; R Douce
Journal:  Eur J Biochem       Date:  1979-11

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Authors:  S J Singer; G L Nicolson
Journal:  Science       Date:  1972-02-18       Impact factor: 47.728

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Authors:  A Rawyler; P A Siegenthaler
Journal:  Biochim Biophys Acta       Date:  1981-04-13
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Journal:  Mol Biol Cell       Date:  2001-12       Impact factor: 4.138

6.  Rapid kinetic labeling of Arabidopsis cell suspension cultures: implications for models of lipid export from plastids.

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7.  Import of lyso-phosphatidylcholine into chloroplasts likely at the origin of eukaryotic plastidial lipids.

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8.  In situ incorporation of Fatty acids into lipids of the outer and inner envelope membranes of pea chloroplasts.

Authors:  M Miquel; J P Dubacq
Journal:  Plant Physiol       Date:  1992-09       Impact factor: 8.340

9.  Do thylakoids really contain phosphatidylcholine?

Authors:  A J Dorne; J Joyard; R Douce
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

10.  The Arabidopsis P4-ATPase ALA3 localizes to the golgi and requires a beta-subunit to function in lipid translocation and secretory vesicle formation.

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