Reserve lipid accumulation and translocation of 14 C in the photosynthetically active and senescent shoot parts of Dicranum elongatum

Lipid metabolism of the subarctic moss Dicranum elongatum was studied by feeding the moss with 2‐ 14 C‐acetate and, after extraction of the lipids, counting the 14 C‐content of different lipid fractions immediately after feeding or after chase periods. Translocation of 14 C after 14 C‐feeding was st...

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Bibliographic Details
Published in:Physiologia Plantarum
Main Authors: Hakala, Kaija, Sewón, Pirjo
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1992
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Online Access:http://dx.doi.org/10.1111/j.1399-3054.1992.tb05271.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-3054.1992.tb05271.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-3054.1992.tb05271.x
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Summary:Lipid metabolism of the subarctic moss Dicranum elongatum was studied by feeding the moss with 2‐ 14 C‐acetate and, after extraction of the lipids, counting the 14 C‐content of different lipid fractions immediately after feeding or after chase periods. Translocation of 14 C after 14 C‐feeding was studied with autoradiography. Both low temperature (+6°C) and drought (at +23°C) resulted in increased incorporation of 14 C into the neutral lipid (NL) fraction and decreased incorporation of 14 C into the glycolipid (GL) fraction of the green shoot part of the moss. The distribution of radioactivity between the NL classes suggests that diacylglycerols (1, 2‐DAG) and common triacylglycerols (cTAG) are turned into acetylenic triacylglycerols (aTAG), which are accumulated preferentially. The decrease in the radioactivity of the GL fraction was due to two unknown fractions, whereas 14 C incorporation into the chloroplast membrane lipids, monogalactosyl diacylglycerol (MGDG) and digalactosyl diacylglycerol (DGDG), was very low throughout the experiments. The phospho‐lipid (PL) fraction accounted for 48–63% of total lipid radioactivity at both low and high temperatures. 2‐ 14 C‐acetate feeding to the senescent moss part resulted in vigorous 14 C incorporation into the lipids, especially into the reserve TAGs. Electron microscopic examination showed the presence of plastids, which explains the capability of the senescent part of the moss for lipid synthesis. The fact that transport of 14 C from 2‐ 14 C‐acetate took place upwards and downwards in the moss shoot, together with the capability for lipid synthesis of the senescent moss part, supports the suggestion that the senescent moss part plays a role as an energy store.