Identification of steroleosin in oil bodies of pine megagametophytes
Three classes of integral proteins termed oleosin, caleosin and steroleosin have been identified in seed oil bodies of diverse angiosperm species. Recently, two oleosin isoforms and one caleosin were identified in megagametophyte oil bodies of pine (Pinus massoniana), a representative gymnosperm spe...
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Veröffentlicht in: | Plant physiology and biochemistry 2016-04, Vol.101, p.173-181 |
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Sprache: | eng |
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Zusammenfassung: | Three classes of integral proteins termed oleosin, caleosin and steroleosin have been identified in seed oil bodies of diverse angiosperm species. Recently, two oleosin isoforms and one caleosin were identified in megagametophyte oil bodies of pine (Pinus massoniana), a representative gymnosperm species. In this study, a putative steroleosin of approximately 41 kDa was observed in isolated oil bodies of pine megagametophytes, and its corresponding cDNA fragment was obtained by PCR cloning and further confirmed by mass spectrometric analysis. Phylogenetic tree analysis showed that pine steroleosin was evolutionarily more closely-related to steroleosin-B than steroleosin-A found in angiosperm seed oil bodies. As expected, artificial oil bodies constituted with recombinant steroleosin over-expressed in Escherichia coli were less stable and larger than native pine oil bodies. Filipin staining of artificial oil bodies sheltered by recombinant steroleosin with or without its sterol binding domain showed that the sterol binding domain was responsible for the sterol binding capability of steroleosin. Sterol-coupling dehydrogenase activity was demonstrated in artificial oil bodies constituted with recombinant steroleosin as well as in purified pine oil bodies.
•Steroleosin was identified in oil bodies of pine megagametophytes.•Pine steroleosin was evolutionarily close to angiosperm seed steroleosin-B.•Artificial oil bodies constituted with steroleosin were relatively unstable.•The sterol binding domain was responsible for the sterol binding of steroleosin.•Dehydrogenase activity was detected for steroleosin in artificial oil bodies. |
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ISSN: | 0981-9428 1873-2690 |
DOI: | 10.1016/j.plaphy.2016.02.008 |