Chloroplast ultrastructure, chlorophyll fluorescence, and pigment composition in chilling-stressed soybeans [Glycine max]

Shoots of 16-day-old soybeans (Glycine max L. Merr. cv Ransom) were chilled to 10°C for 7 days and monitored for visible signs of damage, ultrastructural changes, perturbations in fluorescence of chlorophyll (Chl), and quantitative changes in Chl a and b and associated pigments. Precautions were tak...

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Veröffentlicht in:Plant physiology (Bethesda) 1984-04, Vol.74 (4), p.749-754
Hauptverfasser: MUSSER, R. L, THOMAS, S. A, WISE, R. R, PEELER, T. C, NAYLOR, A. W
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creator MUSSER, R. L
THOMAS, S. A
WISE, R. R
PEELER, T. C
NAYLOR, A. W
description Shoots of 16-day-old soybeans (Glycine max L. Merr. cv Ransom) were chilled to 10°C for 7 days and monitored for visible signs of damage, ultrastructural changes, perturbations in fluorescence of chlorophyll (Chl), and quantitative changes in Chl a and b and associated pigments. Precautions were taken to prevent the confounding effects of water stress. A technique for the separation of lutein and zeaxanthin was developed utilizing a step gradient with the high performance liquid chromatograph. Visible losses in Chl were detectable within the first day of chilling, and regreening did not occur until the shoots were returned to 25°C. Ultrastructurally, unstacking of chloroplast grana occurred, and the envelope membranes developed protrusions. Furthermore, the lipids were altered to the point that the membranes were poorly stabilized by a glutaraldehyde/osmium double-fixation procedure. Chl fluorescence rates were greatly reduced within 2 hours after chilling began and returned to normal only after rewarming. The rapid loss of Chl that occurred during chilling was accompanied by the appearance of zeaxanthin and a decline in violaxanthin. Apparently a zeaxanthin-violaxanthin epoxidation/de-epoxidation cycle was operating. When only the roots were chilled, no substantial changes were detected in ultrastructure, fluorescence rates, or pigment levels.
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A technique for the separation of lutein and zeaxanthin was developed utilizing a step gradient with the high performance liquid chromatograph. Visible losses in Chl were detectable within the first day of chilling, and regreening did not occur until the shoots were returned to 25°C. Ultrastructurally, unstacking of chloroplast grana occurred, and the envelope membranes developed protrusions. Furthermore, the lipids were altered to the point that the membranes were poorly stabilized by a glutaraldehyde/osmium double-fixation procedure. Chl fluorescence rates were greatly reduced within 2 hours after chilling began and returned to normal only after rewarming. The rapid loss of Chl that occurred during chilling was accompanied by the appearance of zeaxanthin and a decline in violaxanthin. Apparently a zeaxanthin-violaxanthin epoxidation/de-epoxidation cycle was operating. When only the roots were chilled, no substantial changes were detected in ultrastructure, fluorescence rates, or pigment levels.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Biological and medical sciences</subject><subject>Cell physiology</subject><subject>Cells, cell elements: structure and function</subject><subject>chilling</subject><subject>chlorophyll</subject><subject>Chlorophylls</subject><subject>Chloroplasts</subject><subject>Cooling</subject><subject>Economic plant physiology</subject><subject>Fluorescence</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycine max</subject><subject>Growth and development</subject><subject>Leaves</subject><subject>Natural and artificial inductions</subject><subject>Pigments</subject><subject>Plant physiology and development</subject><subject>Plant roots</subject><subject>Plants</subject><subject>Rewarming</subject><subject>Soybeans</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNpVkU2LFDEQhoMo7rh68irSB_GiPea7OxdBBl2FBQ-6J5FQnU7PZEknvUm32P_eyAyzeqkKvE-9VZVC6DnBW0IwfzdN24ZveQnqAdoQwWhNBW8fog3G5Y3bVl2gJznfYowJI_wxuiBSSiYw36B1d_AxxclDnqvFz6nktJh5SfZtZY7aYfW-GvwSk83GBlMUCH01uf1ow1yZOE4xu9nFULlQipz3LuzrYmRztn2V49pZCLn6ceVX44KtRvj98yl6NIDP9tkpX6KbTx-_7z7X11-vvuw-XNeGk2auu0H1pGESZNsP0FJDB950EjqCG8YakNQKNXBLOxC0kz0BIWVHZQEZwRLYJXp_9J2WbrR9WaAs6fWU3Ahp1RGc_l8J7qD38Zcu1bKRtBi8PhmkeLfYPOvRlX_wHoKNS9aEE6lIywv45giaFHNOdjg3IVj_PZWeJt1wzUtQhX7571z37Ok2BXh1AiAb8EOCYFw-c6rBgrC2YC-O2G2eYzrLnMpWcHbfZoCoYZ-Kw803olqBsRKSMfYHHJmyxw</recordid><startdate>19840401</startdate><enddate>19840401</enddate><creator>MUSSER, R. 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Soil science and plant productions</topic><topic>Biological and medical sciences</topic><topic>Cell physiology</topic><topic>Cells, cell elements: structure and function</topic><topic>chilling</topic><topic>chlorophyll</topic><topic>Chlorophylls</topic><topic>Chloroplasts</topic><topic>Cooling</topic><topic>Economic plant physiology</topic><topic>Fluorescence</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycine max</topic><topic>Growth and development</topic><topic>Leaves</topic><topic>Natural and artificial inductions</topic><topic>Pigments</topic><topic>Plant physiology and development</topic><topic>Plant roots</topic><topic>Plants</topic><topic>Rewarming</topic><topic>Soybeans</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MUSSER, R. L</creatorcontrib><creatorcontrib>THOMAS, S. A</creatorcontrib><creatorcontrib>WISE, R. R</creatorcontrib><creatorcontrib>PEELER, T. C</creatorcontrib><creatorcontrib>NAYLOR, A. W</creatorcontrib><creatorcontrib>Universidad Nacional Agraria, Lima (Peru). Programa Academico de Graduados</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MUSSER, R. L</au><au>THOMAS, S. A</au><au>WISE, R. R</au><au>PEELER, T. C</au><au>NAYLOR, A. W</au><aucorp>Universidad Nacional Agraria, Lima (Peru). Programa Academico de Graduados</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chloroplast ultrastructure, chlorophyll fluorescence, and pigment composition in chilling-stressed soybeans [Glycine max]</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>1984-04-01</date><risdate>1984</risdate><volume>74</volume><issue>4</issue><spage>749</spage><epage>754</epage><pages>749-754</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Shoots of 16-day-old soybeans (Glycine max L. Merr. cv Ransom) were chilled to 10°C for 7 days and monitored for visible signs of damage, ultrastructural changes, perturbations in fluorescence of chlorophyll (Chl), and quantitative changes in Chl a and b and associated pigments. Precautions were taken to prevent the confounding effects of water stress. A technique for the separation of lutein and zeaxanthin was developed utilizing a step gradient with the high performance liquid chromatograph. Visible losses in Chl were detectable within the first day of chilling, and regreening did not occur until the shoots were returned to 25°C. Ultrastructurally, unstacking of chloroplast grana occurred, and the envelope membranes developed protrusions. Furthermore, the lipids were altered to the point that the membranes were poorly stabilized by a glutaraldehyde/osmium double-fixation procedure. Chl fluorescence rates were greatly reduced within 2 hours after chilling began and returned to normal only after rewarming. The rapid loss of Chl that occurred during chilling was accompanied by the appearance of zeaxanthin and a decline in violaxanthin. Apparently a zeaxanthin-violaxanthin epoxidation/de-epoxidation cycle was operating. When only the roots were chilled, no substantial changes were detected in ultrastructure, fluorescence rates, or pigment levels.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Physiologists</pub><pmid>16663504</pmid><doi>10.1104/pp.74.4.749</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Jstor Complete Legacy; Alma/SFX Local Collection; EZB Electronic Journals Library
subjects Agronomy. Soil science and plant productions
Biological and medical sciences
Cell physiology
Cells, cell elements: structure and function
chilling
chlorophyll
Chlorophylls
Chloroplasts
Cooling
Economic plant physiology
Fluorescence
Fundamental and applied biological sciences. Psychology
Glycine max
Growth and development
Leaves
Natural and artificial inductions
Pigments
Plant physiology and development
Plant roots
Plants
Rewarming
Soybeans
title Chloroplast ultrastructure, chlorophyll fluorescence, and pigment composition in chilling-stressed soybeans [Glycine max]
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