Literature DB >> 2730586

Comparison of glycerolipid biosynthesis in non-green plastids from sycamore (Acer pseudoplatanus) cells and cauliflower (Brassica oleracea) buds.

C Alban1, J Joyard, R Douce.   

Abstract

The availability of methods to fractionate non-green plastids and to prepare their limiting envelope membranes [Alban, Joyard & Douce (1988) Plant Physiol. 88, 709-717] allowed a detailed analysis of the biosynthesis of lysophosphatidic acid, phosphatidic acid, diacylglycerol and monogalactosyl-diacylglycerol (MGDG) in two different types of non-green starch-containing plastids: plastids isolated from cauliflower buds and amyloplasts isolated from sycamore cells. An enzyme [acyl-ACP (acyl carrier protein):sn-glycerol 3-phosphate acyltransferase) recovered in the soluble fraction of non-green plastids transfers oleic acid from oleoyl-ACP to the sn-1 position of sn-glycerol 3-phosphate to form lysophosphatidic acid. Then a membrane-bound enzyme (acyl-ACP:monoacyl-sn-glycerol 3-phosphate acyltransferase), localized in the envelope membrane, catalyses the acylation of the available sn-2 position of 1-oleoyl-sn-glycerol 3-phosphate by palmitic acid from palmitoyl-ACP. Therefore both the soluble phase and the envelope membranes are necessary for acylation of sn-glycerol 3-phosphate. The major difference between cauliflower (Brassica oleracea) and sycamore (Acer pseudoplatanus) membranes is the very low level of phosphatidate phosphatase activity in sycamore envelope membrane. Therefore, very little diacylglycerol is available for MGDG synthesis in sycamore, compared with cauliflower. These findings are consistent with the similarities and differences described in lipid metabolism of mature chloroplasts from 'C18:3' and 'C16:3' plants (those with MGDG containing C18:3 and C16:3 fatty acids). Sycamore contains only C18 fatty acids in MGDG, and the envelope membranes from sycamore amyloplasts have a low phosphatidate phosphatase activity and therefore the enzymes of the Kornberg-Pricer pathway have a low efficiency of incorporation of sn-glycerol 3-phosphate into MGDG. By contrast, cauliflower contains MGDG with C16:3 fatty acid, and the incorporation of sn-glycerol 3-phosphate into MGDG by the enzymes associated with envelope membranes is not limited by the phosphatidate phosphatase. These results demonstrate that: (1) non-green plastids employ the same biosynthetic pathway as that previously established for chloroplasts (the formation of glycerolipids is a general property of all plastids, chloroplasts as well as non-green plastids), (2) the envelope membranes are the major structure responsible for the biosynthesis of phosphatidic acid, diacylglycerol and MGDG, and (3) the enzymes of the envelope Kornberg-Pricer pathway have the same properties in non-green starch-containing plastids as in mature chloroplasts from C16:3 and C18:3 plants.

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Year:  1989        PMID: 2730586      PMCID: PMC1138585          DOI: 10.1042/bj2590775

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  22 in total

1. 

Authors:  R Douce; T Guillot-Salomon
Journal:  FEBS Lett       Date:  1970-11-18       Impact factor: 4.124

2.  Growth of Suspension-cultured Acer pseudoplatanus L. Cells in Automatic Culture Units of Large Volume.

Authors:  R Bligny
Journal:  Plant Physiol       Date:  1977-03       Impact factor: 8.340

3.  Enzymic capacities of purified cauliflower bud plastids for lipid synthesis and carbohydrate metabolism.

Authors:  E P Journet; R Douce
Journal:  Plant Physiol       Date:  1985-10       Impact factor: 8.340

4.  Biochemical changes during sucrose deprivation in higher plant cells.

Authors:  E P Journet; R Bligny; R Douce
Journal:  J Biol Chem       Date:  1986-03-05       Impact factor: 5.157

5.  Characterization of phosphatidate phosphohydrolase activity associated with chloroplast envelope membranes.

Authors:  J Joyard; R Douce
Journal:  FEBS Lett       Date:  1979-06-01       Impact factor: 4.124

6.  Specificities and selectivities of glycerol-3-phosphate acyltransferase and monoacylglycerol-3-phosphate acyltransferase from pea and spinach chloroplasts.

Authors:  M Frentzen; E Heinz; T A McKeon; P K Stumpf
Journal:  Eur J Biochem       Date:  1983-01-01

7.  Enzymes of the Glycolytic and Pentose Phosphate Pathways in Proplastids from the Developing Endosperm of Ricinus communis L.

Authors:  P D Simcox; E E Reid; D T Canvin; D T Dennis
Journal:  Plant Physiol       Date:  1977-06       Impact factor: 8.340

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

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

9.  Site of biosynthesis of galactolipids in spinach chloroplasts.

Authors:  R Douce
Journal:  Science       Date:  1974-03-01       Impact factor: 47.728

10.  Characterization of lipids from chloroplast envelopes.

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

Review 1.  Phosphatidate phosphatases of mammals, yeast, and higher plants.

Authors:  M G Kocsis; R J Weselake
Journal:  Lipids       Date:  1996-08       Impact factor: 1.880

2.  Ratios of carbon isotopes in microbial lipids as an indicator of substrate usage.

Authors:  W R Abraham; C Hesse; O Pelz
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

3.  Characterization of the Glycerolipid Composition and Biosynthetic Capacity of Pea Root Plastids.

Authors:  L. Xue; L. M. McCune; K. F. Kleppinger-Sparace; M. J. Brown; M. K. Pomeroy; S. A. Sparace
Journal:  Plant Physiol       Date:  1997-02       Impact factor: 8.340

4.  Substrate specificities of the membrane-bound and partially purified microsomal acyl-CoA:1-acylglycerol-3-phosphate acyltransferase from etiolated shoots of Pisum sativum (L.).

Authors:  W Hares; M Frentzen
Journal:  Planta       Date:  1991-08       Impact factor: 4.116

  4 in total

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