Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1980 Aug;66(2):238–241. doi: 10.1104/pp.66.2.238

Membrane Phospholipid Phase Separations in Plants Adapted to or Acclimated to Different Thermal Regimes 1

Carl S Pike 1,2,3, Joseph A Berry 1,4
PMCID: PMC440573  PMID: 16661412

Abstract

The phase separation temperatures of total leaf phospholipids from warm and cool climate plants were determined in order to explore the relationship of lipid physical properties to a species' thermal habitat. The separation temperatures were determined by measuring the fluorescence intensity and fluorescence polarization of liposomes labeled with the polyene fatty acid probe trans-parinaric acid. To focus on a single climatic region, Mojave Desert dicots (chiefly ephemeral annuals) were examined, with plants grown under identical conditions whenever possible. Winter active species showed lower phase separation temperatures than the summer active species. A group of warm climate annual grasses showed separation temperatures distinctly higher than those of a group of cool climate grasses, all grown from seed under the same conditions. Growth at low temperature seems correlated with (and may require) a low phase separation temperature. Winter active ephemerals appear genetically programmed to synthesize a mixture of phospholipids which will not phase separate in the usual growth conditions. When the lipids of desert perennials were examined in cool and warm seasons, there was a pronounced seasonal shift in the phase separation temperature, implying environmental influences on lipid physical properties. The relationship of these results to high and low temperature tolerance is discussed.

Full text

PDF
238

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Armond P. A., Schreiber U., Björkman O. Photosynthetic Acclimation to Temperature in the Desert Shrub, Larrea divaricata: II. Light-harvesting Efficiency and Electron Transport. Plant Physiol. 1978 Mar;61(3):411–415. doi: 10.1104/pp.61.3.411. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Mooney H. A., Björkman O., Collatz G. J. Photosynthetic Acclimation to Temperature in the Desert Shrub, Larrea divaricata: I. Carbon Dioxide Exchange Characteristics of Intact Leaves. Plant Physiol. 1978 Mar;61(3):406–410. doi: 10.1104/pp.61.3.406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Pearcy R. W. Effect of Growth Temperature on the Fatty Acid Composition of the Leaf Lipids in Atriplex lentiformis (Torr.) Wats. Plant Physiol. 1978 Apr;61(4):484–486. doi: 10.1104/pp.61.4.484. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Pearcy R. W. Effects of Growth Temperature on the Thermal Stability of the Photosynthetic Apparatus of Atriplex lentiformis (Torr.) Wats. Plant Physiol. 1977 May;59(5):873–878. doi: 10.1104/pp.59.5.873. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Sinensky M. Homeoviscous adaptation--a homeostatic process that regulates the viscosity of membrane lipids in Escherichia coli. Proc Natl Acad Sci U S A. 1974 Feb;71(2):522–525. doi: 10.1073/pnas.71.2.522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Sklar L. A., Hudson B. S., Simoni R. D. Conjugated polyene fatty acids as membrane probes: preliminary characterization. Proc Natl Acad Sci U S A. 1975 May;72(5):1649–1653. doi: 10.1073/pnas.72.5.1649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Sklar L. A., Miljanich G. P., Dratz E. A. Phospholipid lateral phase separation and the partition of cis-parinaric acid and trans-parinaric acid among aqueous, solid lipid, and fluid lipid phases. Biochemistry. 1979 May 1;18(9):1707–1716. doi: 10.1021/bi00576a012. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES