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024 7 |a 10.1016/j.jplph.2013.04.017  |2 doi 
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041 |a eng 
100 1 |a Grzyb, Joanna M  |e verfasserin  |4 aut 
245 1 0 |a Visualization and characterization of prolamellar bodies with atomic force microscopy 
264 1 |c 2013 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 12.03.2014 
500 |a Date Revised 30.09.2020 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Copyright © 2013 Elsevier GmbH. All rights reserved. 
520 |a Prolamellar bodies (PLBs) isolated from etiolated wheat seedlings were studied with the use of atomic force microscopy (AFM), transmission electron microscopy (TEM) and fluorescence spectroscopy. With AFM, PLBs were seen as spherical structures about 1-2μm in diameter, more elastic than mica and poly-l-lysine substrate. TEM analyses confirmed that PLBs of wheat leaf etioplasts also had an average diameter of appr. 1μm. Illumination induced the photoreduction of photoactive protochlorophyllide (Pchlide), i.e. Pchlide bound to protochlorophyllide oxidoreductase, which was shown in fluorescence spectra. The photoreduction was followed by the disruption of PLB structures, which started with the enlargement of PLB spheres and then their fragmentation into small balls as seen with AFM. Light-induced vesicle formation and the outgrowth of lamellar (pro)thylakoid membranes on the PLB surface were also confirmed by TEM analyses, and resulted in the apparent enlargement of the PLB diameter. The blue-shift of the fluorescence emission maximum of chlorophyllide observed for PLBs at room temperature after Pchlide photoreduction was completed within 25min. However, structural changes in PLBs were still observed after the completion of the blue-shift. The incubation of PLBs in darkness with HgCl2 also resulted in PLB enlargement and a loosening of their structure. AFM provides a unique opportunity to observe PLBs at a physiological temperature without the necessity of fixation 
650 4 |a Comparative Study 
650 4 |a Evaluation Study 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a AFM 
650 4 |a Chlide 
650 4 |a F655/F633 
650 4 |a Fluorescence spectra 
650 4 |a LPOR 
650 4 |a PLB 
650 4 |a PLBs 
650 4 |a PT 
650 4 |a Pchlide 
650 4 |a Protochlorophyllide photoreduction 
650 4 |a TEM 
650 4 |a atomic force microscopy 
650 4 |a chlorophyllide 
650 4 |a light-dependent protochlorophyllide oxidoreductase 
650 4 |a prolamellar bodies 
650 4 |a prothylakoids 
650 4 |a protochlorophyllide 
650 4 |a the ratio of the fluorescence intensity at 655nm to the intensity at 633nm 
650 4 |a transmission electron microscopy 
650 7 |a Chlorophyllides  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a Protochlorophyllide  |2 NLM 
650 7 |a 20369-67-9  |2 NLM 
650 7 |a Polylysine  |2 NLM 
650 7 |a 25104-18-1  |2 NLM 
650 7 |a Mercuric Chloride  |2 NLM 
650 7 |a 53GH7MZT1R  |2 NLM 
650 7 |a Oxidoreductases Acting on CH-CH Group Donors  |2 NLM 
650 7 |a EC 1.3.-  |2 NLM 
650 7 |a protochlorophyllide reductase  |2 NLM 
650 7 |a EC 1.3.1.33  |2 NLM 
700 1 |a Solymosi, Katalin  |e verfasserin  |4 aut 
700 1 |a Strzałka, Kazimierz  |e verfasserin  |4 aut 
700 1 |a Mysliwa-Kurdziel, Beata  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Journal of plant physiology  |d 1979  |g 170(2013), 14 vom: 15. Sept., Seite 1217-27  |w (DE-627)NLM098174622  |x 1618-1328  |7 nnns 
773 1 8 |g volume:170  |g year:2013  |g number:14  |g day:15  |g month:09  |g pages:1217-27 
856 4 0 |u http://dx.doi.org/10.1016/j.jplph.2013.04.017  |3 Volltext 
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952 |d 170  |j 2013  |e 14  |b 15  |c 09  |h 1217-27