Literature DB >> 15927962

Phosphate-limited oat. The plasma membrane and the tonoplast as major targets for phospholipid-to-glycolipid replacement and stimulation of phospholipases in the plasma membrane.

Mats X Andersson1, Karin E Larsson, Henrik Tjellström, Conny Liljenberg, Anna Stina Sandelius.   

Abstract

We recently reported that cultivation of oat (Avena sativa L.) without phosphate resulted in plasma membrane phosphoglycerolipids being replaced to a large extent by digalactosyldiacylglycerol (DGDG) (Andersson, M. X., Stridh, M. H., Larsson, K. E., Liljenberg, C., and Sandelius, A. S. (2003) FEBS Lett. 537, 128-132). We report here that DGDG is not the only non-phosphorous-containing lipid that replaces phospholipids but that also the content of glucosylceramides and sterolglycosides increased in plasma membranes as a response to phosphate starvation. In addition, phosphate deficiency induced similar changes in lipid composition in the tonoplast. The phospholipid-to-glycolipid replacement apparently did not occur to any greater extent in endoplasmic reticulum, Golgi apparatus, or mitochondrial inner membranes. In contrast to the marked effects on lipid composition, the polypeptide patterns were largely similar between root plasma membranes from well-fertilized and phosphate-limited oat, although the latter condition induced at least four polypeptides, including a chaperone of the HSP80 or HSP90 family, a phosphate transporter, and a bacterial-type phosphoesterase. The latter polypeptide reacted with an antibody raised against a phosphate deficiency-induced phospholipase C from Arabidopsis thaliana (Nakamura, Y., Awai, K., Masuda, T., Yoshioka, Y., Takamiya, K., and Ohta, H. (2005) J. Biol. Chem. 280, 7469-7476). In plasma membranes from oat, however, a phospholipase D-type activity and a phosphatidic acid phosphatase were the dominant lipase activities induced by phosphate deficiency. Our results reflect a highly developed plasticity in the lipid composition of the plasma membrane and the tonoplast. In addition, phosphate deficiency-induced alterations in plasma membrane lipid composition may involve different sets of lipid-metabolizing enzymes in different plant tissues or species, at different stages of plant development and/or at different stages of stress adjustments.

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Year:  2005        PMID: 15927962     DOI: 10.1074/jbc.M503273200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  65 in total

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Journal:  Plant Signal Behav       Date:  2007-05

5.  The Arabidopsis thaliana non-specific phospholipase C2 is involved in the response to Pseudomonas syringae attack.

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6.  The Arabidopsis hit1-1 mutant has a plasma membrane profile distinct from that of wild-type plants at optimal growing temperature.

Authors:  Lian-Chin Wang; Kai-Yu Chang; Yi-Ting Ke; Hao-Yu Huang; Shaw-Jye Wu
Journal:  Plant Signal Behav       Date:  2011-08-01

7.  Rice and chickpea GDPDs are preferentially influenced by low phosphate and CaGDPD1 encodes an active glycerophosphodiester phosphodiesterase enzyme.

Authors:  P Mehra; J Giri
Journal:  Plant Cell Rep       Date:  2016-04-23       Impact factor: 4.570

8.  The plasma membrane proteome of Medicago truncatula roots as modified by arbuscular mycorrhizal symbiosis.

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9.  Membrane glycerolipid remodeling triggered by nitrogen and phosphorus starvation in Phaeodactylum tricornutum.

Authors:  Heni Abida; Lina-Juana Dolch; Coline Meï; Valeria Villanova; Melissa Conte; Maryse A Block; Giovanni Finazzi; Olivier Bastien; Leïla Tirichine; Chris Bowler; Fabrice Rébeillé; Dimitris Petroutsos; Juliette Jouhet; Eric Maréchal
Journal:  Plant Physiol       Date:  2014-12-08       Impact factor: 8.340

10.  ACYL-LIPID DESATURASE2 is required for chilling and freezing tolerance in Arabidopsis.

Authors:  Mingjie Chen; Jay J Thelen
Journal:  Plant Cell       Date:  2013-04-12       Impact factor: 11.277

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